Package: a4 Version: 1.30.0 Depends: a4Base, a4Preproc, a4Classif, a4Core, a4Reporting Suggests: MLP, nlcv, ALL, Cairo License: GPL-3 MD5sum: 4e44a4273b805b3fda0cbbd476566c25 NeedsCompilation: no Title: Automated Affymetrix Array Analysis Umbrella Package Description: Automated Affymetrix Array Analysis Umbrella Package biocViews: Microarray Author: Willem Talloen, Tobias Verbeke Maintainer: Tobias Verbeke , Willem Ligtenberg git_url: https://git.bioconductor.org/packages/a4 git_branch: RELEASE_3_8 git_last_commit: 771e01a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/a4_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/a4_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/a4_1.30.0.tgz vignettes: vignettes/a4/inst/doc/a4vignette.pdf vignetteTitles: a4vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/a4/inst/doc/a4vignette.R Package: a4Base Version: 1.30.0 Depends: methods, graphics, grid, Biobase, AnnotationDbi, annaffy, mpm, genefilter, limma, multtest, glmnet, a4Preproc, a4Core, gplots Suggests: Cairo, ALL Enhances: gridSVG, JavaGD License: GPL-3 MD5sum: a8238f64848e4f0974867b0a5f3dc920 NeedsCompilation: no Title: Automated Affymetrix Array Analysis Base Package Description: Automated Affymetrix Array Analysis biocViews: Microarray Author: Willem Talloen, Tobias Verbeke, Tine Casneuf, An De Bondt, Steven Osselaer and Hinrich Goehlmann, Willem Ligtenberg Maintainer: Tobias Verbeke , Willem Ligtenberg git_url: https://git.bioconductor.org/packages/a4Base git_branch: RELEASE_3_8 git_last_commit: fc370b2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/a4Base_1.30.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/a4Base_1.30.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4 Package: a4Classif Version: 1.30.0 Depends: methods, a4Core, a4Preproc, MLInterfaces, ROCR, pamr, glmnet, varSelRF Imports: a4Core Suggests: ALL License: GPL-3 MD5sum: f3c574a15569caf4bc36badf16e2403a NeedsCompilation: no Title: Automated Affymetrix Array Analysis Classification Package Description: Automated Affymetrix Array Analysis Classification Package biocViews: Microarray Author: Willem Talloen, Tobias Verbeke Maintainer: Tobias Verbeke , Willem Ligtenberg git_url: https://git.bioconductor.org/packages/a4Classif git_branch: RELEASE_3_8 git_last_commit: b62841b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/a4Classif_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/a4Classif_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/a4Classif_1.30.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4 Package: a4Core Version: 1.30.0 Depends: methods, Biobase, glmnet License: GPL-3 MD5sum: 1c18ebb284225195642263519f84089b NeedsCompilation: no Title: Automated Affymetrix Array Analysis Core Package Description: Automated Affymetrix Array Analysis Core Package biocViews: Microarray Author: Willem Talloen, Tobias Verbeke Maintainer: Tobias Verbeke , Willem Ligtenberg git_url: https://git.bioconductor.org/packages/a4Core git_branch: RELEASE_3_8 git_last_commit: e392b1b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/a4Core_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/a4Core_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/a4Core_1.30.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4, a4Base, a4Classif importsMe: a4Classif Package: a4Preproc Version: 1.30.0 Depends: methods, AnnotationDbi Suggests: ALL, hgu95av2.db License: GPL-3 MD5sum: 79f088fcd94c8cf56ca40b40a59b8e97 NeedsCompilation: no Title: Automated Affymetrix Array Analysis Preprocessing Package Description: Automated Affymetrix Array Analysis Preprocessing Package biocViews: Microarray Author: Willem Talloen, Tobias Verbeke Maintainer: Tobias Verbeke , Willem Ligtenberg git_url: https://git.bioconductor.org/packages/a4Preproc git_branch: RELEASE_3_8 git_last_commit: e6fb9fa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/a4Preproc_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/a4Preproc_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/a4Preproc_1.30.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4, a4Base, a4Classif suggestsMe: graphite Package: a4Reporting Version: 1.30.0 Depends: methods, annaffy Imports: xtable, utils License: GPL-3 MD5sum: 4a7eb752a3ac2e746930c0166c248d3d NeedsCompilation: no Title: Automated Affymetrix Array Analysis Reporting Package Description: Automated Affymetrix Array Analysis Reporting Package biocViews: Microarray Author: Tobias Verbeke Maintainer: Tobias Verbeke , Willem Ligtenberg git_url: https://git.bioconductor.org/packages/a4Reporting git_branch: RELEASE_3_8 git_last_commit: ae9b9ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/a4Reporting_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/a4Reporting_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/a4Reporting_1.30.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4 Package: ABAEnrichment Version: 1.12.0 Depends: R (>= 3.4) Imports: Rcpp (>= 0.11.5), gplots (>= 2.14.2), gtools (>= 3.5.0), ABAData (>= 0.99.2), data.table (>= 1.10.4), GOfuncR (>= 1.1.2), grDevices, stats, utils LinkingTo: Rcpp Suggests: BiocStyle, knitr, testthat License: GPL (>= 2) Archs: i386, x64 MD5sum: f5934cab26c8b62087ed9242aa0cbf8a NeedsCompilation: yes Title: Gene expression enrichment in human brain regions Description: The package ABAEnrichment is designed to test for enrichment of user defined candidate genes in the set of expressed genes in different human brain regions. The core function 'aba_enrich' integrates the expression of the candidate gene set (averaged across donors) and the structural information of the brain using an ontology, both provided by the Allen Brain Atlas project. 'aba_enrich' interfaces the ontology enrichment software FUNC to perform the statistical analyses. Additional functions provided in this package like 'get_expression' and 'plot_expression' facilitate exploring the expression data, and besides the standard candidate vs. background gene set enrichment, also three additional tests are implemented, e.g. for cases when genes are ranked instead of divided into candidate and background. biocViews: GeneSetEnrichment, GeneExpression Author: Steffi Grote Maintainer: Steffi Grote VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ABAEnrichment git_branch: RELEASE_3_8 git_last_commit: 1320e93 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ABAEnrichment_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ABAEnrichment_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ABAEnrichment_1.12.0.tgz vignettes: vignettes/ABAEnrichment/inst/doc/ABAEnrichment.html vignetteTitles: Introduction to ABAEnrichment hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ABAEnrichment/inst/doc/ABAEnrichment.R Package: ABarray Version: 1.50.0 Imports: Biobase, graphics, grDevices, methods, multtest, stats, tcltk, utils Suggests: limma, LPE License: GPL MD5sum: 84761cfa2828e57c5ef0daa712f741d8 NeedsCompilation: no Title: Microarray QA and statistical data analysis for Applied Biosystems Genome Survey Microrarray (AB1700) gene expression data. Description: Automated pipline to perform gene expression analysis for Applied Biosystems Genome Survey Microarray (AB1700) data format. Functions include data preprocessing, filtering, control probe analysis, statistical analysis in one single function. A GUI interface is also provided. The raw data, processed data, graphics output and statistical results are organized into folders according to the analysis settings used. biocViews: Microarray, OneChannel, Preprocessing Author: Yongming Andrew Sun Maintainer: Yongming Andrew Sun git_url: https://git.bioconductor.org/packages/ABarray git_branch: RELEASE_3_8 git_last_commit: 1bd72f7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ABarray_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ABarray_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ABarray_1.50.0.tgz vignettes: vignettes/ABarray/inst/doc/ABarray.pdf, vignettes/ABarray/inst/doc/ABarrayGUI.pdf vignetteTitles: ABarray gene expression, ABarray gene expression GUI interface hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: abseqR Version: 1.0.0 Depends: R (>= 3.5.0) Imports: ggplot2, RColorBrewer, circlize, reshape2, VennDiagram, plyr, flexdashboard, BiocParallel (>= 1.1.25), png, grid, gridExtra, rmarkdown, knitr, vegan, ggcorrplot, ggdendro, plotly, BiocStyle, stringr, utils, methods, grDevices, stats, tools, graphics Suggests: testthat License: GPL-3 | file LICENSE MD5sum: de9e8be03e84433a1fc776c563ec4426 NeedsCompilation: no Title: Reporting and data analysis functionalities for Rep-Seq datasets of antibody libraries Description: AbSeq is a comprehensive bioinformatic pipeline for the analysis of sequencing datasets generated from antibody libraries and abseqR is one of its packages. abseqR empowers the users of abseqPy (https://github.com/malhamdoosh/abseqPy) with plotting and reporting capabilities and allows them to generate interactive HTML reports for the convenience of viewing and sharing with other researchers. Additionally, abseqR extends abseqPy to compare multiple repertoire analyses and perform further downstream analysis on its output. biocViews: Sequencing, Visualization, ReportWriting, QualityControl, MultipleComparison Author: JiaHong Fong [cre, aut], Monther Alhamdoosh [aut] Maintainer: JiaHong Fong URL: https://github.com/malhamdoosh/abseqR SystemRequirements: pandoc (>= 1.19.2.1) VignetteBuilder: knitr BugReports: https://github.com/malhamdoosh/abseqR/issues git_url: https://git.bioconductor.org/packages/abseqR git_branch: RELEASE_3_8 git_last_commit: b96ae63 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/abseqR_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/abseqR_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/abseqR_1.0.0.tgz vignettes: vignettes/abseqR/inst/doc/abseqR.pdf vignetteTitles: Introduction to abseqR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/abseqR/inst/doc/abseqR.R Package: ABSSeq Version: 1.36.0 Depends: R (>= 2.10), methods Imports: locfit, limma Suggests: edgeR License: GPL (>= 3) MD5sum: 030589f236271c0cfa666af69b74e223 NeedsCompilation: no Title: ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences Description: Inferring differential expression genes by absolute counts difference between two groups, utilizing Negative binomial distribution and moderating fold-change according to heterogeneity of dispersion across expression level. biocViews: DifferentialExpression Author: Wentao Yang Maintainer: Wentao Yang git_url: https://git.bioconductor.org/packages/ABSSeq git_branch: RELEASE_3_8 git_last_commit: bd41907 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ABSSeq_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ABSSeq_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ABSSeq_1.36.0.tgz vignettes: vignettes/ABSSeq/inst/doc/ABSSeq.pdf vignetteTitles: ABSSeq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ABSSeq/inst/doc/ABSSeq.R Package: acde Version: 1.12.0 Depends: R(>= 3.3), boot(>= 1.3) Imports: stats, graphics Suggests: BiocGenerics, RUnit License: GPL-3 MD5sum: f5bf1b85bb7436813020a5aec3765d12 NeedsCompilation: no Title: Artificial Components Detection of Differentially Expressed Genes Description: This package provides a multivariate inferential analysis method for detecting differentially expressed genes in gene expression data. It uses artificial components, close to the data's principal components but with an exact interpretation in terms of differential genetic expression, to identify differentially expressed genes while controlling the false discovery rate (FDR). The methods on this package are described in the vignette or in the article 'Multivariate Method for Inferential Identification of Differentially Expressed Genes in Gene Expression Experiments' by J. P. Acosta, L. Lopez-Kleine and S. Restrepo (2015, pending publication). biocViews: DifferentialExpression, TimeCourse, PrincipalComponent, GeneExpression, Microarray, mRNAMicroarray Author: Juan Pablo Acosta, Liliana Lopez-Kleine Maintainer: Juan Pablo Acosta git_url: https://git.bioconductor.org/packages/acde git_branch: RELEASE_3_8 git_last_commit: f6ce592 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/acde_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/acde_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/acde_1.12.0.tgz vignettes: vignettes/acde/inst/doc/acde.pdf vignetteTitles: Identification of Differentially Expressed Genes with Artificial Components hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/acde/inst/doc/acde.R importsMe: coexnet Package: ACE Version: 1.0.0 Depends: R (>= 3.4) Imports: Biobase, QDNAseq, ggplot2, grid, stats, utils, methods, grDevices Suggests: knitr, rmarkdown, BiocStyle License: GPL-2 MD5sum: 20953839cc1ce4ab6b8a3689954c3c74 NeedsCompilation: no Title: Absolute Copy Number Estimation from Low-coverage Whole Genome Sequencing Description: Uses segmented copy number data to estimate tumor cell percentage and produce copy number plots displaying absolute copy numbers. biocViews: CopyNumberVariation, DNASeq, Coverage, WholeGenome, Visualization, Sequencing Author: Jos B Poell Maintainer: Jos B Poell URL: https://github.com/tgac-vumc/ACE VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ACE git_branch: RELEASE_3_8 git_last_commit: a7e7ae6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ACE_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ACE_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ACE_1.0.0.tgz vignettes: vignettes/ACE/inst/doc/ACE_vignette.html vignetteTitles: ACE vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ACE/inst/doc/ACE_vignette.R Package: aCGH Version: 1.60.0 Depends: R (>= 2.10), cluster, survival, multtest Imports: Biobase, cluster, grDevices, graphics, methods, multtest, stats, survival, splines, utils License: GPL-2 Archs: i386, x64 MD5sum: 4bdcf0503d13c9393ea12593e769d165 NeedsCompilation: yes Title: Classes and functions for Array Comparative Genomic Hybridization data. Description: Functions for reading aCGH data from image analysis output files and clone information files, creation of aCGH S3 objects for storing these data. Basic methods for accessing/replacing, subsetting, printing and plotting aCGH objects. biocViews: CopyNumberVariation, DataImport, Genetics Author: Jane Fridlyand , Peter Dimitrov Maintainer: Peter Dimitrov git_url: https://git.bioconductor.org/packages/aCGH git_branch: RELEASE_3_8 git_last_commit: ae58175 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/aCGH_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/aCGH_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/aCGH_1.60.0.tgz vignettes: vignettes/aCGH/inst/doc/aCGH.pdf vignetteTitles: aCGH Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/aCGH/inst/doc/aCGH.R dependsOnMe: CRImage importsMe: ADaCGH2, snapCGH suggestsMe: beadarraySNP Package: ACME Version: 2.38.0 Depends: R (>= 2.10), Biobase (>= 2.5.5), methods, BiocGenerics Imports: graphics, stats License: GPL (>= 2) Archs: i386, x64 MD5sum: 02fba578c93d2cf28d7f548400bae520 NeedsCompilation: yes Title: Algorithms for Calculating Microarray Enrichment (ACME) Description: ACME (Algorithms for Calculating Microarray Enrichment) is a set of tools for analysing tiling array ChIP/chip, DNAse hypersensitivity, or other experiments that result in regions of the genome showing "enrichment". It does not rely on a specific array technology (although the array should be a "tiling" array), is very general (can be applied in experiments resulting in regions of enrichment), and is very insensitive to array noise or normalization methods. It is also very fast and can be applied on whole-genome tiling array experiments quite easily with enough memory. biocViews: Technology, Microarray, Normalization Author: Sean Davis Maintainer: Sean Davis URL: http://watson.nci.nih.gov/~sdavis git_url: https://git.bioconductor.org/packages/ACME git_branch: RELEASE_3_8 git_last_commit: cd03196 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ACME_2.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ACME_2.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ACME_2.38.0.tgz vignettes: vignettes/ACME/inst/doc/ACME.pdf vignetteTitles: ACME hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ACME/inst/doc/ACME.R suggestsMe: oligo Package: ADaCGH2 Version: 2.22.0 Depends: R (>= 3.2.0), parallel, ff, GLAD Imports: bit, ffbase, DNAcopy, tilingArray, waveslim, cluster, aCGH, snapCGH Suggests: CGHregions, Cairo, limma Enhances: Rmpi License: GPL (>= 3) Archs: i386, x64 MD5sum: cd000cb277c242ba358cade134fc5a4d NeedsCompilation: yes Title: Analysis of big data from aCGH experiments using parallel computing and ff objects Description: Analysis and plotting of array CGH data. Allows usage of Circular Binary Segementation, wavelet-based smoothing (both as in Liu et al., and HaarSeg as in Ben-Yaacov and Eldar), HMM, BioHMM, GLAD, CGHseg. Most computations are parallelized (either via forking or with clusters, including MPI and sockets clusters) and use ff for storing data. biocViews: Microarray, CopyNumberVariants Author: Ramon Diaz-Uriarte and Oscar M. Rueda . Wavelet-based aCGH smoothing code from Li Hsu and Douglas Grove . Imagemap code from Barry Rowlingson . HaarSeg code from Erez Ben-Yaacov; downloaded from . Maintainer: Ramon Diaz-Uriarte URL: https://github.com/rdiaz02/adacgh2 git_url: https://git.bioconductor.org/packages/ADaCGH2 git_branch: RELEASE_3_8 git_last_commit: dc1b45b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ADaCGH2_2.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ADaCGH2_2.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ADaCGH2_2.22.0.tgz vignettes: vignettes/ADaCGH2/inst/doc/ADaCGH2-long-examples.pdf, vignettes/ADaCGH2/inst/doc/ADaCGH2.pdf, vignettes/ADaCGH2/inst/doc/benchmarks.pdf vignetteTitles: ADaCGH2-long-examples.pdf, ADaCGH2 Overview, benchmarks.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ADaCGH2/inst/doc/ADaCGH2.R Package: adaptest Version: 1.2.0 Depends: R (>= 3.5.0) Imports: origami (>= 1.0.0), tmle, calibrate, methods, graphics, stats, utils, SummarizedExperiment Suggests: testthat, Matrix, SuperLearner, earth, gam, nnls, airway, rmarkdown, knitr, BiocStyle License: GPL-2 MD5sum: 1535857a21f2819c2930aded9d404325 NeedsCompilation: no Title: Data-Adaptive Statistics for High-Dimensional Multiple Testing Description: Data-adaptive test statistics represent a general methodology for performing multiple hypothesis testing on effects sizes while maintaining honest statistical inference when operating in high-dimensional settings (). The utilities provided here extend the use of this general methodology to many common data analytic challenges that arise in modern computational and genomic biology. biocViews: Genetics, GeneExpression, DifferentialExpression, Sequencing, Microarray, Regression, DimensionReduction, MultipleComparison Author: Weixin Cai [aut, cre, cph], Nima Hejazi [aut], Alan Hubbard [ctb, ths] Maintainer: Weixin Cai URL: https://github.com/wilsoncai1992/adaptest VignetteBuilder: knitr BugReports: https://github.com/wilsoncai1992/adaptest/issues git_url: https://git.bioconductor.org/packages/adaptest git_branch: RELEASE_3_8 git_last_commit: ed7093d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/adaptest_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/adaptest_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/adaptest_1.2.0.tgz vignettes: vignettes/adaptest/inst/doc/differentialExpression.html vignetteTitles: Data-Mining Biomarkers and High-Dimensional Testing hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/adaptest/inst/doc/differentialExpression.R Package: adSplit Version: 1.52.0 Depends: R (>= 2.1.0), methods (>= 2.1.0) Imports: AnnotationDbi, Biobase (>= 1.5.12), cluster (>= 1.9.1), GO.db (>= 1.8.1), graphics, grDevices, KEGG.db (>= 1.8.1), methods, multtest (>= 1.6.0), stats (>= 2.1.0) Suggests: golubEsets (>= 1.0), vsn (>= 1.5.0), hu6800.db (>= 1.8.1) License: GPL (>= 2) Archs: i386, x64 MD5sum: a5cd67644a93b10c454e0584b002e08d NeedsCompilation: yes Title: Annotation-Driven Clustering Description: This package implements clustering of microarray gene expression profiles according to functional annotations. For each term genes are annotated to, splits into two subclasses are computed and a significance of the supporting gene set is determined. biocViews: Microarray, Clustering Author: Claudio Lottaz, Joern Toedling Maintainer: Claudio Lottaz URL: http://compdiag.molgen.mpg.de/software/index.shtml git_url: https://git.bioconductor.org/packages/adSplit git_branch: RELEASE_3_8 git_last_commit: 3bd105d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/adSplit_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/adSplit_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/adSplit_1.52.0.tgz vignettes: vignettes/adSplit/inst/doc/tr_2005_02.pdf vignetteTitles: Annotation-Driven Clustering hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/adSplit/inst/doc/tr_2005_02.R Package: AffiXcan Version: 1.0.0 Depends: R (>= 3.5), SummarizedExperiment Imports: MultiAssayExperiment, BiocParallel Suggests: BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: 20b361ce24b3fbf71f7d3a032655a98d NeedsCompilation: no Title: A functional approach to impute Genetically Regulated Expression Description: Impute a GReX (Genetically Regulated Expression) for a set of genes in a sample of individuals, using a method based on the Total Binding Affinity (TBA). Statistical models to impute GReX can be trained with a training dataset where the real total expression values are known. biocViews: GeneExpression, Transcription, GeneRegulation, DimensionReduction, Regression Author: Alessandro Lussana [aut, cre] Maintainer: Alessandro Lussana VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AffiXcan git_branch: RELEASE_3_8 git_last_commit: 2349f09 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AffiXcan_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AffiXcan_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AffiXcan_1.0.0.tgz vignettes: vignettes/AffiXcan/inst/doc/AffiXcan.html vignetteTitles: AffiXcan hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AffiXcan/inst/doc/AffiXcan.R Package: affxparser Version: 1.54.0 Depends: R (>= 2.14.0) Suggests: R.oo (>= 1.22.0), R.utils (>= 2.7.0), AffymetrixDataTestFiles License: LGPL (>= 2) Archs: i386, x64 MD5sum: 1c7cbf0945cc1504d16ba19d68b0f192 NeedsCompilation: yes Title: Affymetrix File Parsing SDK Description: Package for parsing Affymetrix files (CDF, CEL, CHP, BPMAP, BAR). It provides methods for fast and memory efficient parsing of Affymetrix files using the Affymetrix' Fusion SDK. Both ASCII- and binary-based files are supported. Currently, there are methods for reading chip definition file (CDF) and a cell intensity file (CEL). These files can be read either in full or in part. For example, probe signals from a few probesets can be extracted very quickly from a set of CEL files into a convenient list structure. biocViews: Infrastructure, DataImport, Microarray, ProprietaryPlatforms, OneChannel Author: Henrik Bengtsson [aut], James Bullard [aut], Robert Gentleman [ctb], Kasper Daniel Hansen [aut, cre], Jim Hester [ctb], Martin Morgan [ctb] Maintainer: Kasper Daniel Hansen URL: https://github.com/HenrikBengtsson/affxparser BugReports: https://github.com/HenrikBengtsson/affxparser/issues git_url: https://git.bioconductor.org/packages/affxparser git_branch: RELEASE_3_8 git_last_commit: dce83d2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affxparser_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affxparser_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affxparser_1.54.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: ITALICS, pdInfoBuilder, rMAT, Starr importsMe: affyILM, cn.farms, crossmeta, EventPointer, GeneRegionScan, ITALICS, oligo, rMAT suggestsMe: TIN Package: affy Version: 1.60.0 Depends: R (>= 2.8.0), BiocGenerics (>= 0.1.12), Biobase (>= 2.5.5) Imports: affyio (>= 1.13.3), BiocManager, graphics, grDevices, methods, preprocessCore, stats, utils, zlibbioc LinkingTo: preprocessCore Suggests: tkWidgets (>= 1.19.0), affydata, widgetTools License: LGPL (>= 2.0) Archs: i386, x64 MD5sum: 0f37ad355a3b6a6b501c65a3deec2d41 NeedsCompilation: yes Title: Methods for Affymetrix Oligonucleotide Arrays Description: The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it. biocViews: Microarray, OneChannel, Preprocessing Author: Rafael A. Irizarry , Laurent Gautier , Benjamin Milo Bolstad , and Crispin Miller with contributions from Magnus Astrand , Leslie M. Cope , Robert Gentleman, Jeff Gentry, Conrad Halling , Wolfgang Huber, James MacDonald , Benjamin I. P. Rubinstein, Christopher Workman , John Zhang Maintainer: Rafael A. Irizarry git_url: https://git.bioconductor.org/packages/affy git_branch: RELEASE_3_8 git_last_commit: fcae363 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affy_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affy_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affy_1.60.0.tgz vignettes: vignettes/affy/inst/doc/affy.pdf, vignettes/affy/inst/doc/builtinMethods.pdf, vignettes/affy/inst/doc/customMethods.pdf, vignettes/affy/inst/doc/vim.pdf vignetteTitles: 1. Primer, 2. Built-in Processing Methods, 3. Custom Processing Methods, 4. Import Methods hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affy/inst/doc/affy.R, vignettes/affy/inst/doc/builtinMethods.R, vignettes/affy/inst/doc/customMethods.R, vignettes/affy/inst/doc/vim.R dependsOnMe: affyContam, AffyExpress, affyPara, affypdnn, affyPLM, affyQCReport, AffyRNADegradation, altcdfenvs, arrayMvout, ArrayTools, bgx, Cormotif, DrugVsDisease, dualKS, ExiMiR, farms, frmaTools, gcrma, LMGene, logitT, maskBAD, MLP, panp, plw, prebs, qpcrNorm, RefPlus, rHVDM, Risa, RPA, SCAN.UPC, simpleaffy, sscore, Starr, webbioc importsMe: affycoretools, affyILM, affylmGUI, affyQCReport, arrayQualityMetrics, ArrayTools, CAFE, ChIPXpress, coexnet, Cormotif, crossmeta, Doscheda, EGAD, farms, ffpe, frma, gcrma, GEOsubmission, Harshlight, HTqPCR, iCheck, lumi, LVSmiRNA, makecdfenv, mimager, MSnbase, PECA, plier, plw, puma, pvac, Rnits, simpleaffy, STATegRa, tilingArray, TurboNorm, vsn, waveTiling suggestsMe: AnnotationForge, ArrayExpress, beadarray, beadarraySNP, BiocCaseStudies, BiocGenerics, Biostrings, BufferedMatrixMethods, categoryCompare, ecolitk, ExpressionView, factDesign, gCMAPWeb, GeneRegionScan, limma, made4, paxtoolsr, piano, PREDA, qcmetrics, runibic, siggenes, TCGAbiolinks Package: affycomp Version: 1.58.0 Depends: R (>= 2.13.0), methods, Biobase (>= 2.3.3) Suggests: splines, affycompData License: GPL (>= 2) MD5sum: 76bd3762a9a1589fd157be1a543de1d7 NeedsCompilation: no Title: Graphics Toolbox for Assessment of Affymetrix Expression Measures Description: The package contains functions that can be used to compare expression measures for Affymetrix Oligonucleotide Arrays. biocViews: OneChannel, Microarray, Preprocessing Author: Rafael A. Irizarry and Zhijin Wu with contributions from Simon Cawley Maintainer: Rafael A. Irizarry git_url: https://git.bioconductor.org/packages/affycomp git_branch: RELEASE_3_8 git_last_commit: 99607b2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affycomp_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affycomp_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affycomp_1.58.0.tgz vignettes: vignettes/affycomp/inst/doc/affycomp.pdf vignetteTitles: affycomp primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affycomp/inst/doc/affycomp.R Package: AffyCompatible Version: 1.42.0 Depends: R (>= 2.7.0), XML (>= 2.8-1), RCurl (>= 0.8-1), methods Imports: Biostrings License: Artistic-2.0 MD5sum: 7d2ab32e48872dcba0cdf268543d15c9 NeedsCompilation: no Title: Affymetrix GeneChip software compatibility Description: This package provides an interface to Affymetrix chip annotation and sample attribute files. The package allows an easy way for users to download and manage local data bases of Affynmetrix NetAffx annotation files. The package also provides access to GeneChip Operating System (GCOS) and GeneChip Command Console (AGCC)-compatible sample annotation files. biocViews: Infrastructure, Microarray, OneChannel Author: Martin Morgan, Robert Gentleman Maintainer: Martin Morgan git_url: https://git.bioconductor.org/packages/AffyCompatible git_branch: RELEASE_3_8 git_last_commit: 699303c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AffyCompatible_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AffyCompatible_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AffyCompatible_1.42.0.tgz vignettes: vignettes/AffyCompatible/inst/doc/MAGEAndARR.pdf, vignettes/AffyCompatible/inst/doc/NetAffxResource.pdf vignetteTitles: Retrieving MAGE and ARR sample attributes, Annotation retrieval with NetAffxResource hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AffyCompatible/inst/doc/MAGEAndARR.R, vignettes/AffyCompatible/inst/doc/NetAffxResource.R importsMe: IdMappingRetrieval Package: affyContam Version: 1.40.0 Depends: R (>= 2.7.0), tools, methods, utils, Biobase, affy, affydata Suggests: hgu95av2cdf License: Artistic-2.0 MD5sum: a2f70361f7e473c963c0e46202b8004f NeedsCompilation: no Title: structured corruption of affymetrix cel file data Description: structured corruption of cel file data to demonstrate QA effectiveness biocViews: Infrastructure Author: V. Carey Maintainer: V. Carey git_url: https://git.bioconductor.org/packages/affyContam git_branch: RELEASE_3_8 git_last_commit: dfd5fd6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affyContam_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affyContam_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affyContam_1.40.0.tgz vignettes: vignettes/affyContam/inst/doc/affyContam.pdf vignetteTitles: affy contamination tools hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affyContam/inst/doc/affyContam.R Package: affycoretools Version: 1.54.0 Depends: Biobase, methods Imports: affy, limma, GOstats, gcrma, splines, xtable, AnnotationDbi, ggplot2, gplots, oligoClasses, ReportingTools, hwriter, lattice, S4Vectors, edgeR, RSQLite, BiocGenerics, DBI Suggests: affydata, hgfocuscdf, BiocStyle, knitr, hgu95av2.db, rgl, rmarkdown License: Artistic-2.0 MD5sum: f9ed1862b102e59df1f5177ce547cecc NeedsCompilation: no Title: Functions useful for those doing repetitive analyses with Affymetrix GeneChips Description: Various wrapper functions that have been written to streamline the more common analyses that a core Biostatistician might see. biocViews: ReportWriting, Microarray, OneChannel, GeneExpression Author: James W. MacDonald Maintainer: James W. MacDonald VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/affycoretools git_branch: RELEASE_3_8 git_last_commit: 1e1f968 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affycoretools_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affycoretools_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affycoretools_1.54.0.tgz vignettes: vignettes/affycoretools/inst/doc/RefactoredAffycoretools.html vignetteTitles: Creating annotated output with \Biocpkg{affycoretools} and ReportingTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affycoretools/inst/doc/RefactoredAffycoretools.R Package: AffyExpress Version: 1.48.0 Depends: R (>= 2.10), affy (>= 1.23.4), limma Suggests: simpleaffy, R2HTML, affyPLM, hgu95av2cdf, hgu95av2, test3cdf, genefilter, estrogen, annaffy, gcrma License: LGPL MD5sum: 4afe8bb6ec8b571cacfd6faa5cb7284c NeedsCompilation: no Title: Affymetrix Quality Assessment and Analysis Tool Description: The purpose of this package is to provide a comprehensive and easy-to-use tool for quality assessment and to identify differentially expressed genes in the Affymetrix gene expression data. biocViews: Microarray, OneChannel, QualityControl, Preprocessing, DifferentialExpression, Annotation, ReportWriting, Visualization Author: Xiwei Wu , Xuejun Arthur Li Maintainer: Xuejun Arthur Li git_url: https://git.bioconductor.org/packages/AffyExpress git_branch: RELEASE_3_8 git_last_commit: dbaed51 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AffyExpress_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AffyExpress_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AffyExpress_1.48.0.tgz vignettes: vignettes/AffyExpress/inst/doc/AffyExpress.pdf vignetteTitles: 1. Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AffyExpress/inst/doc/AffyExpress.R Package: affyILM Version: 1.34.0 Depends: R (>= 2.10.0), methods, gcrma Imports: affxparser (>= 1.16.0), affy, graphics, Biobase Suggests: AffymetrixDataTestFiles, hgfocusprobe License: GPL-3 MD5sum: 87811dbf7c0589e74a9c5858811ffb61 NeedsCompilation: no Title: Linear Model of background subtraction and the Langmuir isotherm Description: affyILM is a preprocessing tool which estimates gene expression levels for Affymetrix Gene Chips. Input from physical chemistry is employed to first background subtract intensities before calculating concentrations on behalf of the Langmuir model. biocViews: Microarray, OneChannel, Preprocessing Author: K. Myriam Kroll, Fabrice Berger, Gerard Barkema, Enrico Carlon Maintainer: Myriam Kroll and Fabrice Berger git_url: https://git.bioconductor.org/packages/affyILM git_branch: RELEASE_3_8 git_last_commit: 2c02ed2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affyILM_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affyILM_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affyILM_1.34.0.tgz vignettes: vignettes/affyILM/inst/doc/affyILM.pdf vignetteTitles: affyILM1.3.0 hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affyILM/inst/doc/affyILM.R Package: affyio Version: 1.52.0 Depends: R (>= 2.6.0) Imports: zlibbioc, methods License: LGPL (>= 2) Archs: i386, x64 MD5sum: 4f0bb750a68406e25541e19a5dd1f5a2 NeedsCompilation: yes Title: Tools for parsing Affymetrix data files Description: Routines for parsing Affymetrix data files based upon file format information. Primary focus is on accessing the CEL and CDF file formats. biocViews: Microarray, DataImport, Infrastructure Author: Ben Bolstad Maintainer: Ben Bolstad URL: https://github.com/bmbolstad/affyio git_url: https://git.bioconductor.org/packages/affyio git_branch: RELEASE_3_8 git_last_commit: 9da725a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affyio_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affyio_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affyio_1.52.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: affyPara, makecdfenv, SCAN.UPC, sscore importsMe: affy, affylmGUI, crlmm, ExiMiR, gcrma, oligo, oligoClasses, puma suggestsMe: BufferedMatrixMethods Package: affylmGUI Version: 1.56.0 Imports: grDevices, graphics, stats, utils, tcltk, tkrplot, limma, affy, affyio, affyPLM, gcrma, BiocGenerics, BiocManager, R2HTML, xtable License: GPL (>=2) MD5sum: 1c03dfb6477d26f31f544c7f60d3a0d3 NeedsCompilation: no Title: GUI for limma Package with Affymetrix Microarrays Description: A Graphical User Interface (GUI) for analysis of Affymetrix microarray gene expression data using the affy and limma packages. biocViews: GUI, GeneExpression, Transcription, DifferentialExpression, DataImport, Bayesian, Regression, TimeCourse, Microarray, mRNAMicroarray, OneChannel, ProprietaryPlatforms, BatchEffect, MultipleComparison, Normalization, Preprocessing, QualityControl Author: James Wettenhall [cre,aut], Ken Simpson [aut], Gordon Smyth [aut], Keith Satterley [ctb] Maintainer: Gordon Smyth URL: http://bioinf.wehi.edu.au/affylmGUI/ git_url: https://git.bioconductor.org/packages/affylmGUI git_branch: RELEASE_3_8 git_last_commit: 44e9ad3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affylmGUI_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affylmGUI_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affylmGUI_1.56.0.tgz vignettes: vignettes/affylmGUI/inst/doc/affylmGUI.pdf, vignettes/affylmGUI/inst/doc/extract.pdf, vignettes/affylmGUI/inst/doc/about.html, vignettes/affylmGUI/inst/doc/CustMenu.html, vignettes/affylmGUI/inst/doc/index.html, vignettes/affylmGUI/inst/doc/windowsFocus.html vignetteTitles: affylmGUI Vignette, Extracting affy and limma objects from affylmGUI files, about.html, CustMenu.html, index.html, windowsFocus.html hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affylmGUI/inst/doc/affylmGUI.R Package: affyPara Version: 1.42.0 Depends: R (>= 2.5.0), methods, affy (>= 1.20.0), snow (>= 0.2-3), vsn (>= 3.6.0), aplpack (>= 1.1.1), affyio Suggests: affydata Enhances: affy License: GPL-3 MD5sum: 7a05c33daf0b6393e7ff928bf134b47f NeedsCompilation: no Title: Parallelized preprocessing methods for Affymetrix Oligonucleotide Arrays Description: The package contains parallelized functions for exploratory oligonucleotide array analysis. The package is designed for large numbers of microarray data. biocViews: Microarray, Preprocessing Author: Markus Schmidberger , Esmeralda Vicedo , Ulrich Mansmann Maintainer: Markus Schmidberger URL: http://www.ibe.med.uni-muenchen.de git_url: https://git.bioconductor.org/packages/affyPara git_branch: RELEASE_3_8 git_last_commit: 05471d6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affyPara_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affyPara_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affyPara_1.42.0.tgz vignettes: vignettes/affyPara/inst/doc/affyPara.pdf, vignettes/affyPara/inst/doc/vsnStudy.pdf vignetteTitles: Parallelized affy functions for preprocessing, Simulation Study for VSN Add-On Normalization and Subsample Size hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affyPara/inst/doc/affyPara.R, vignettes/affyPara/inst/doc/vsnStudy.R Package: affypdnn Version: 1.56.0 Depends: R (>= 2.13.0), affy (>= 1.5) Suggests: affydata, hgu95av2probe License: LGPL MD5sum: cc5feb90eb660fee35c0cab8846cb443 NeedsCompilation: no Title: Probe Dependent Nearest Neighbours (PDNN) for the affy package Description: The package contains functions to perform the PDNN method described by Li Zhang et al. biocViews: OneChannel, Microarray, Preprocessing Author: H. Bjorn Nielsen and Laurent Gautier (Many thanks to Li Zhang early communications about the existence of the PDNN program and related publications). Maintainer: Laurent Gautier git_url: https://git.bioconductor.org/packages/affypdnn git_branch: RELEASE_3_8 git_last_commit: 5fd9c52 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affypdnn_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affypdnn_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affypdnn_1.56.0.tgz vignettes: vignettes/affypdnn/inst/doc/affypdnn.pdf vignetteTitles: affypdnn hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affypdnn/inst/doc/affypdnn.R Package: affyPLM Version: 1.58.0 Depends: R (>= 2.6.0), BiocGenerics (>= 0.3.2), affy (>= 1.11.0), Biobase (>= 2.17.8), gcrma, stats, preprocessCore (>= 1.5.1) Imports: zlibbioc, graphics, grDevices, methods LinkingTo: preprocessCore Suggests: affydata, MASS License: GPL (>= 2) Archs: i386, x64 MD5sum: 4d9e87db1f232700fec8543fc83fd8be NeedsCompilation: yes Title: Methods for fitting probe-level models Description: A package that extends and improves the functionality of the base affy package. Routines that make heavy use of compiled code for speed. Central focus is on implementation of methods for fitting probe-level models and tools using these models. PLM based quality assessment tools. biocViews: Microarray, OneChannel, Preprocessing, QualityControl Author: Ben Bolstad Maintainer: Ben Bolstad URL: https://github.com/bmbolstad/affyPLM git_url: https://git.bioconductor.org/packages/affyPLM git_branch: RELEASE_3_8 git_last_commit: 32764c7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affyPLM_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affyPLM_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affyPLM_1.58.0.tgz vignettes: vignettes/affyPLM/inst/doc/AffyExtensions.pdf, vignettes/affyPLM/inst/doc/MAplots.pdf, vignettes/affyPLM/inst/doc/QualityAssess.pdf, vignettes/affyPLM/inst/doc/ThreeStep.pdf vignetteTitles: affyPLM: Fitting Probe Level Models, affyPLM: Advanced use of the MAplot function, affyPLM: Model Based QC Assessment of Affymetrix GeneChips, affyPLM: the threestep function hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affyPLM/inst/doc/AffyExtensions.R, vignettes/affyPLM/inst/doc/MAplots.R, vignettes/affyPLM/inst/doc/QualityAssess.R, vignettes/affyPLM/inst/doc/ThreeStep.R dependsOnMe: RefPlus importsMe: affylmGUI, affyQCReport, arrayQualityMetrics, mimager suggestsMe: AffyExpress, arrayMvout, ArrayTools, BiocCaseStudies, BiocGenerics, ELBOW, frmaTools, metahdep, piano Package: affyQCReport Version: 1.60.0 Depends: Biobase (>= 1.13.16), affy, lattice Imports: affy, affyPLM, Biobase, genefilter, graphics, grDevices, lattice, RColorBrewer, simpleaffy, stats, utils, xtable Suggests: tkWidgets (>= 1.5.23), affydata (>= 1.4.1) License: LGPL (>= 2) MD5sum: 639c5ee5befbf01b8f090eacc2a81f67 NeedsCompilation: no Title: QC Report Generation for affyBatch objects Description: This package creates a QC report for an AffyBatch object. The report is intended to allow the user to quickly assess the quality of a set of arrays in an AffyBatch object. biocViews: Microarray,OneChannel,QualityControl Author: Craig Parman , Conrad Halling , Robert Gentleman Maintainer: Craig Parman git_url: https://git.bioconductor.org/packages/affyQCReport git_branch: RELEASE_3_8 git_last_commit: d0c15b1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/affyQCReport_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/affyQCReport_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/affyQCReport_1.60.0.tgz vignettes: vignettes/affyQCReport/inst/doc/affyQCReport.pdf vignetteTitles: affyQCReport: Methods for Generating Affymetrix QC Reports hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/affyQCReport/inst/doc/affyQCReport.R suggestsMe: BiocCaseStudies Package: AffyRNADegradation Version: 1.28.0 Depends: R (>= 2.9.0), methods, affy Suggests: AmpAffyExample License: GPL-2 MD5sum: cad1f5fe8dd49d21d9409975dfb9bb32 NeedsCompilation: no Title: Analyze and correct probe positional bias in microarray data due to RNA degradation Description: The package helps with the assessment and correction of RNA degradation effects in Affymetrix 3' expression arrays. The parameter d gives a robust and accurate measure of RNA integrity. The correction removes the probe positional bias, and thus improves comparability of samples that are affected by RNA degradation. biocViews: GeneExpression, Microarray, OneChannel, Preprocessing, QualityControl Author: Mario Fasold Maintainer: Mario Fasold git_url: https://git.bioconductor.org/packages/AffyRNADegradation git_branch: RELEASE_3_8 git_last_commit: aff91d7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AffyRNADegradation_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AffyRNADegradation_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AffyRNADegradation_1.28.0.tgz vignettes: vignettes/AffyRNADegradation/inst/doc/vignette.pdf vignetteTitles: AffyRNADegradation Example hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AffyRNADegradation/inst/doc/vignette.R Package: AGDEX Version: 1.30.0 Depends: R (>= 2.10), Biobase, GSEABase Imports: stats License: GPL Version 2 or later MD5sum: 0a82c526b05e7fbac77480ea0a93b42c NeedsCompilation: no Title: Agreement of Differential Expression Analysis Description: A tool to evaluate agreement of differential expression for cross-species genomics biocViews: Microarray, Genetics, GeneExpression Author: Stan Pounds ; Cuilan Lani Gao Maintainer: Cuilan lani Gao git_url: https://git.bioconductor.org/packages/AGDEX git_branch: RELEASE_3_8 git_last_commit: d6cc21e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AGDEX_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AGDEX_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AGDEX_1.30.0.tgz vignettes: vignettes/AGDEX/inst/doc/AGDEX.pdf vignetteTitles: AGDEX.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AGDEX/inst/doc/AGDEX.R Package: agilp Version: 3.14.0 Depends: R (>= 2.14.0) License: GPL-3 MD5sum: c9c79b9c0a8bf313d6426266e1cac965 NeedsCompilation: no Title: Agilent expression array processing package Description: More about what it does (maybe more than one line) Author: Benny Chain Maintainer: Benny Chain git_url: https://git.bioconductor.org/packages/agilp git_branch: RELEASE_3_8 git_last_commit: 8feb047 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/agilp_3.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/agilp_3.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/agilp_3.14.0.tgz vignettes: vignettes/agilp/inst/doc/agilp_manual.pdf vignetteTitles: An R Package for processing expression microarray data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/agilp/inst/doc/agilp_manual.R Package: AgiMicroRna Version: 2.32.0 Depends: R (>= 2.10),methods,Biobase,limma,affy (>= 1.22),preprocessCore,affycoretools Imports: Biobase Suggests: geneplotter,marray,gplots,gtools,gdata,codelink License: GPL-3 MD5sum: c28be6c85e4bf0e0fdfd1bf17df43814 NeedsCompilation: no Title: Processing and Differential Expression Analysis of Agilent microRNA chips Description: Processing and Analysis of Agilent microRNA data biocViews: Microarray, AgilentChip, OneChannel, Preprocessing, DifferentialExpression Author: Pedro Lopez-Romero Maintainer: Pedro Lopez-Romero git_url: https://git.bioconductor.org/packages/AgiMicroRna git_branch: RELEASE_3_8 git_last_commit: 681ae17 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AgiMicroRna_2.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AgiMicroRna_2.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AgiMicroRna_2.32.0.tgz vignettes: vignettes/AgiMicroRna/inst/doc/AgiMicroRna.pdf vignetteTitles: AgiMicroRna hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AgiMicroRna/inst/doc/AgiMicroRna.R Package: AIMS Version: 1.14.1 Depends: R (>= 2.10), e1071, Biobase Suggests: breastCancerVDX, hgu133a.db, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: ada00ee9705dde004d8fde37923aabd8 NeedsCompilation: no Title: AIMS : Absolute Assignment of Breast Cancer Intrinsic Molecular Subtype Description: This package contains the AIMS implementation. It contains necessary functions to assign the five intrinsic molecular subtypes (Luminal A, Luminal B, Her2-enriched, Basal-like, Normal-like). Assignments could be done on individual samples as well as on dataset of gene expression data. biocViews: ImmunoOncology, Classification, RNASeq, Microarray, Software, GeneExpression Author: Eric R. Paquet, Michael T. Hallett Maintainer: Eric R Paquet URL: http://www.bci.mcgill.ca/AIMS git_url: https://git.bioconductor.org/packages/AIMS git_branch: RELEASE_3_8 git_last_commit: fe0535e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/AIMS_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/AIMS_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AIMS_1.14.1.tgz vignettes: vignettes/AIMS/inst/doc/AIMS.pdf vignetteTitles: AIMS An Introduction (HowTo) hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AIMS/inst/doc/AIMS.R dependsOnMe: genefu Package: ALDEx2 Version: 1.14.1 Depends: methods, stats Imports: BiocParallel, GenomicRanges, IRanges, S4Vectors, SummarizedExperiment, multtest Suggests: testthat License: file LICENSE MD5sum: de6ce7be75ca2f1b8082a9c91108a046 NeedsCompilation: no Title: Analysis Of Differential Abundance Taking Sample Variation Into Account Description: A differential abundance analysis for the comparison of two or more conditions. Useful for analyzing data from standard RNA-seq or meta-RNA-seq assays as well as selected and unselected values from in-vitro sequence selections. Uses a Dirichlet-multinomial model to infer abundance from counts, optimized for three or more experimental replicates. The method infers biological and sampling variation to calculate the expected false discovery rate, given the variation, based on a Wilcox rank test or Welch t-test (via aldex.ttest), or a glm and Kruskal-Wallis test (via aldex.glm). Reports p-values and Benjamini-Hochberg corrected p-values. biocViews: ImmunoOncology, DifferentialExpression, RNASeq, DNASeq, ChIPSeq, GeneExpression, Bayesian, Sequencing, Software, Microbiome, Metagenomics Author: Greg Gloor, Ruth Grace Wong, Andrew Fernandes, Arianne Albert, Matt Links, Thomas Quinn, Jia Rong Wu Maintainer: Greg Gloor URL: https://github.com/ggloor/ALDEx2 BugReports: https://github.com/ggloor/ALDEx2/issues git_url: https://git.bioconductor.org/packages/ALDEx2 git_branch: RELEASE_3_8 git_last_commit: a8b970c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ALDEx2_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ALDEx2_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ALDEx2_1.14.1.tgz vignettes: vignettes/ALDEx2/inst/doc/ALDEx2_vignette.pdf vignetteTitles: An R Package for determining differential abundance in high throughput sequencing experiments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ALDEx2/inst/doc/ALDEx2_vignette.R importsMe: omicplotR Package: AllelicImbalance Version: 1.20.0 Depends: R (>= 3.2.0), grid, GenomicRanges (>= 1.31.8), SummarizedExperiment (>= 0.2.0), GenomicAlignments (>= 1.15.6) Imports: methods, BiocGenerics, AnnotationDbi, BSgenome (>= 1.47.3), VariantAnnotation (>= 1.25.11), Biostrings (>= 2.47.6), S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), Rsamtools (>= 1.31.2), GenomicFeatures (>= 1.31.3), Gviz, lattice, latticeExtra, gridExtra, seqinr, GenomeInfoDb, nlme Suggests: testthat, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene, SNPlocs.Hsapiens.dbSNP144.GRCh37, BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: 6a2b9b7e9957cf227690060862bd280c NeedsCompilation: no Title: Investigates Allele Specific Expression Description: Provides a framework for allelic specific expression investigation using RNA-seq data. biocViews: Genetics, Infrastructure, Sequencing Author: Jesper R Gadin, Lasse Folkersen Maintainer: Jesper R Gadin URL: https://github.com/pappewaio/AllelicImbalance VignetteBuilder: knitr BugReports: https://github.com/pappewaio/AllelicImbalance/issues git_url: https://git.bioconductor.org/packages/AllelicImbalance git_branch: RELEASE_3_8 git_last_commit: 4cd3a78 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AllelicImbalance_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AllelicImbalance_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AllelicImbalance_1.20.0.tgz vignettes: vignettes/AllelicImbalance/inst/doc/AllelicImbalance-vignette.pdf vignetteTitles: AllelicImbalance Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AllelicImbalance/inst/doc/AllelicImbalance-vignette.R Package: alpine Version: 1.8.0 Depends: R (>= 3.3) Imports: Biostrings, IRanges, GenomicRanges, GenomicAlignments, Rsamtools, SummarizedExperiment, GenomicFeatures, speedglm, splines, graph, RBGL, stringr, stats, methods, graphics, GenomeInfoDb, S4Vectors Suggests: knitr, testthat, alpineData, rtracklayer, ensembldb, BSgenome.Hsapiens.NCBI.GRCh38, RColorBrewer License: GPL (>=2) MD5sum: 2f5f6264027f585b0c8a25a7d90095a2 NeedsCompilation: no Title: alpine Description: Fragment sequence bias modeling and correction for RNA-seq transcript abundance estimation. biocViews: Sequencing, RNASeq, AlternativeSplicing, DifferentialSplicing, GeneExpression, Transcription, Coverage, BatchEffect, Normalization, Visualization, QualityControl Author: Michael Love, Rafael Irizarry Maintainer: Michael Love VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/alpine git_branch: RELEASE_3_8 git_last_commit: ddaa0b4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/alpine_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/alpine_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/alpine_1.8.0.tgz vignettes: vignettes/alpine/inst/doc/alpine.html vignetteTitles: alpine hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/alpine/inst/doc/alpine.R Package: alsace Version: 1.18.0 Depends: R (>= 2.10), ALS, ptw (>= 1.0.6) Suggests: lattice, knitr License: GPL (>= 2) MD5sum: a26103b4ba914dab96374e4e7be3b78b NeedsCompilation: no Title: ALS for the Automatic Chemical Exploration of mixtures Description: Alternating Least Squares (or Multivariate Curve Resolution) for analytical chemical data, in particular hyphenated data where the first direction is a retention time axis, and the second a spectral axis. Package builds on the basic als function from the ALS package and adds functionality for high-throughput analysis, including definition of time windows, clustering of profiles, retention time correction, etcetera. Author: Ron Wehrens Maintainer: Ron Wehrens URL: https://github.com/rwehrens/alsace VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/alsace git_branch: RELEASE_3_8 git_last_commit: c9fc43c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/alsace_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/alsace_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/alsace_1.18.0.tgz vignettes: vignettes/alsace/inst/doc/alsace.pdf vignetteTitles: alsace hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: altcdfenvs Version: 2.44.0 Depends: R (>= 2.7), methods, BiocGenerics (>= 0.1.0), S4Vectors (>= 0.9.25), Biobase (>= 2.15.1), affy, makecdfenv, Biostrings, hypergraph Suggests: plasmodiumanophelescdf, hgu95acdf, hgu133aprobe, hgu133a.db, hgu133acdf, Rgraphviz, RColorBrewer License: GPL (>= 2) MD5sum: 3d5ddd23cc69e649a27a607a98d5d4dc NeedsCompilation: no Title: alternative CDF environments (aka probeset mappings) Description: Convenience data structures and functions to handle cdfenvs biocViews: Microarray, OneChannel, QualityControl, Preprocessing, Annotation, ProprietaryPlatforms, Transcription Author: Laurent Gautier Maintainer: Laurent Gautier git_url: https://git.bioconductor.org/packages/altcdfenvs git_branch: RELEASE_3_8 git_last_commit: d804f64 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/altcdfenvs_2.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/altcdfenvs_2.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/altcdfenvs_2.44.0.tgz vignettes: vignettes/altcdfenvs/inst/doc/altcdfenvs.pdf, vignettes/altcdfenvs/inst/doc/modify.pdf, vignettes/altcdfenvs/inst/doc/ngenomeschips.pdf vignetteTitles: altcdfenvs, affy primer, affy primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/altcdfenvs/inst/doc/altcdfenvs.R, vignettes/altcdfenvs/inst/doc/modify.R, vignettes/altcdfenvs/inst/doc/ngenomeschips.R importsMe: Harshlight Package: AMOUNTAIN Version: 1.8.0 Depends: R (>= 3.3.0) Imports: stats Suggests: BiocStyle, qgraph, knitr, rmarkdown License: GPL (>= 2) Archs: i386, x64 MD5sum: 394ae847017425e30abdaf18107b02b7 NeedsCompilation: yes Title: Active modules for multilayer weighted gene co-expression networks: a continuous optimization approach Description: A pure data-driven gene network, weighted gene co-expression network (WGCN) could be constructed only from expression profile. Different layers in such networks may represent different time points, multiple conditions or various species. AMOUNTAIN aims to search active modules in multi-layer WGCN using a continuous optimization approach. biocViews: GeneExpression, Microarray, DifferentialExpression, Network Author: Dong Li, Shan He, Zhisong Pan and Guyu Hu Maintainer: Dong Li SystemRequirements: gsl VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AMOUNTAIN git_branch: RELEASE_3_8 git_last_commit: e0719dd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AMOUNTAIN_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AMOUNTAIN_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AMOUNTAIN_1.8.0.tgz vignettes: vignettes/AMOUNTAIN/inst/doc/AMOUNTAIN.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AMOUNTAIN/inst/doc/AMOUNTAIN.R importsMe: MODA Package: amplican Version: 1.4.1 Depends: R (>= 3.4.0), methods, BiocGenerics (>= 0.22.0), Biostrings (>= 2.44.2), data.table (>= 1.10.4-3) Imports: utils (>= 3.4.1), S4Vectors (>= 0.14.3), ShortRead (>= 1.34.0), IRanges (>= 2.10.2), GenomicRanges (>= 1.28.4), GenomeInfoDb (>= 1.12.2), BiocParallel (>= 1.10.1), gtable (>= 0.2.0), gridExtra (>= 2.2.1), ggplot2 (>= 2.2.0), ggforce (>= 0.1.2), ggthemes (>= 3.4.0), waffle (>= 0.7.0), stringr (>= 1.2.0), stats (>= 3.4.1), matrixStats (>= 0.52.2), Matrix (>= 1.2-10), dplyr (>= 0.7.2), rmarkdown (>= 1.6), knitr (>= 1.16), clusterCrit (>= 1.2.7) Suggests: testthat, BiocStyle, GenomicAlignments License: GPL-3 MD5sum: 251e270473582a16905798a20fa589d1 NeedsCompilation: no Title: Automated analysis of CRISPR experiments Description: `amplican` performs alignment of the amplicon reads, normalizes gathered data, calculates multiple statistics (e.g. cut rates, frameshifts) and presents results in form of aggregated reports. Data and statistics can be broken down by experiments, barcodes, user defined groups, guides and amplicons allowing for quick identification of potential problems. biocViews: ImmunoOncology, Technology, Alignment, qPCR, CRISPR Author: Kornel Labun [aut], Eivind Valen [cph, cre] Maintainer: Eivind Valen URL: https://github.com/valenlab/amplican VignetteBuilder: knitr BugReports: https://github.com/valenlab/amplican/issues git_url: https://git.bioconductor.org/packages/amplican git_branch: RELEASE_3_8 git_last_commit: ef9ebb4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/amplican_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/amplican_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/amplican_1.4.1.tgz vignettes: vignettes/amplican/inst/doc/amplicanFAQ.html, vignettes/amplican/inst/doc/amplicanOverview.html, vignettes/amplican/inst/doc/example_amplicon_report.html, vignettes/amplican/inst/doc/example_barcode_report.html, vignettes/amplican/inst/doc/example_group_report.html, vignettes/amplican/inst/doc/example_guide_report.html, vignettes/amplican/inst/doc/example_id_report.html, vignettes/amplican/inst/doc/example_index.html vignetteTitles: amplican FAQ, amplican overview, example amplicon_report report, example barcode_report report, example group_report report, example guide_report report, example id_report report, example index report hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/amplican/inst/doc/amplicanOverview.R, vignettes/amplican/inst/doc/example_amplicon_report.R, vignettes/amplican/inst/doc/example_barcode_report.R, vignettes/amplican/inst/doc/example_group_report.R, vignettes/amplican/inst/doc/example_guide_report.R, vignettes/amplican/inst/doc/example_id_report.R, vignettes/amplican/inst/doc/example_index.R Package: ampliQueso Version: 1.20.0 Depends: R (>= 2.15.0), rnaSeqMap (>= 2.17.1), knitr, rgl, ggplot2, gplots, parallel, doParallel, foreach, VariantAnnotation,genefilter,statmod,xtable Imports: edgeR, DESeq, samr License: GPL-2 MD5sum: 568c03956831cb1c2af20d9c8c78f0a0 NeedsCompilation: no Title: Analysis of amplicon enrichment panels Description: The package provides tools and reports for the analysis of amplicon sequencing panels, such as AmpliSeq biocViews: ReportWriting, Transcription, GeneExpression, DifferentialExpression, Sequencing, RNASeq, Visualization Author: Alicja Szabelska ; Marek Wiewiorka ; Michal Okoniewski Maintainer: Michal Okoniewski PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/ampliQueso git_branch: RELEASE_3_8 git_last_commit: ed064ff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ampliQueso_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ampliQueso_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ampliQueso_1.20.0.tgz vignettes: vignettes/ampliQueso/inst/doc/ampliQueso.pdf vignetteTitles: ampliQueso primer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ampliQueso/inst/doc/ampliQueso.R Package: AnalysisPageServer Version: 1.16.0 Imports: methods, log4r, tools, rjson, Biobase, graph Suggests: RUnit, XML, knitr Enhances: Rook (>= 1.1), fork, FastRWeb, ggplot2 License: Artistic-2.0 Archs: i386, x64 MD5sum: 85095095c94e346b6c74c85b3a8ee6dc NeedsCompilation: yes Title: A framework for sharing interactive data and plots from R through the web Description: AnalysisPageServer is a modular system that enables sharing of customizable R analyses via the web. biocViews: GUI, Visualization, DataRepresentation Author: Brad Friedman , Adrian Nowicki, Hunter Whitney , Matthew Brauer , Sara Moore, Konrad Debski Maintainer: Brad Friedman VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AnalysisPageServer git_branch: RELEASE_3_8 git_last_commit: 67b0635 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AnalysisPageServer_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnalysisPageServer_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnalysisPageServer_1.16.0.tgz vignettes: vignettes/AnalysisPageServer/inst/doc/AnalysisPageServer.html, vignettes/AnalysisPageServer/inst/doc/ApacheDeployment.html, vignettes/AnalysisPageServer/inst/doc/embedding.html, vignettes/AnalysisPageServer/inst/doc/ExampleServers.html, vignettes/AnalysisPageServer/inst/doc/FastRWebDeployment.html, vignettes/AnalysisPageServer/inst/doc/InteractiveApps.html, vignettes/AnalysisPageServer/inst/doc/Interactivity.html, vignettes/AnalysisPageServer/inst/doc/Licenses.html, vignettes/AnalysisPageServer/inst/doc/StaticContent.html, vignettes/AnalysisPageServer/inst/doc/TrappingConditions.html vignetteTitles: 0. AnalysisPageServer, 6. Apache Deployment, 2. Embedding APS datasets in other documents, 4. Non-interactive servers and Rook Deployment, 7. FastRWeb Deployment, 5. Interactive Apps AnalysisPageServer, 3. AnalysisPageServer Interactivity, 8. Licenses, 1. Making Static Content Interactive with AnalysisPageServer, 8. Condition Trapping hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: FALSE Rfiles: vignettes/AnalysisPageServer/inst/doc/AnalysisPageServer.R, vignettes/AnalysisPageServer/inst/doc/ApacheDeployment.R, vignettes/AnalysisPageServer/inst/doc/embedding.R, vignettes/AnalysisPageServer/inst/doc/ExampleServers.R, vignettes/AnalysisPageServer/inst/doc/FastRWebDeployment.R, vignettes/AnalysisPageServer/inst/doc/InteractiveApps.R, vignettes/AnalysisPageServer/inst/doc/Interactivity.R, vignettes/AnalysisPageServer/inst/doc/StaticContent.R, vignettes/AnalysisPageServer/inst/doc/TrappingConditions.R Package: anamiR Version: 1.10.0 Depends: R (>= 3.5) Imports: stats, DBI, limma, lumi, agricolae, RMySQL, DESeq2, SummarizedExperiment, gplots, gage, S4Vectors Suggests: knitr, rmarkdown, data.table License: GPL-2 MD5sum: 0743887caa63267607e4165602f90951 NeedsCompilation: no Title: An integrated analysis package of miRNA and mRNA expression data Description: This package is intended to identify potential interactions of miRNA-target gene interactions from miRNA and mRNA expression data. It contains functions for statistical test, databases of miRNA-target gene interaction and functional analysis. biocViews: Software, AssayDomain, GeneExpression, BiologicalQuestion, GeneSetEnrichment, GeneTarget, Normalization, Pathways, DifferentialExpression, GeneRegulation, ResearchField, Genetics, Technology, Microarray, Sequencing, miRNA, WorkflowStep Author: Ti-Tai Wang [aut, cre], Tzu-Pin Lu [aut], Chien-Yueh Lee[ctb,] Eric Y. Chuang [aut] Maintainer: Ti-Tai Wang URL: https://github.com/AllenTiTaiWang/anamiR VignetteBuilder: knitr BugReports: https://github.com/AllenTiTaiWang/anamiR/issues git_url: https://git.bioconductor.org/packages/anamiR git_branch: RELEASE_3_8 git_last_commit: 56b26a2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/anamiR_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/anamiR_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/anamiR_1.10.0.tgz vignettes: vignettes/anamiR/inst/doc/IntroductionToanamiR.html vignetteTitles: Introduction to anamiR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/anamiR/inst/doc/IntroductionToanamiR.R Package: Anaquin Version: 2.6.1 Depends: R (>= 3.3), ggplot2 (>= 2.2.0) Imports: ggplot2, ROCR, knitr, qvalue, locfit, methods, stats, utils, plyr, DESeq2 Suggests: RUnit, rmarkdown License: BSD_3_clause + file LICENSE MD5sum: 644b13c2d0da8993dbd11f52b60d2603 NeedsCompilation: no Title: Statistical analysis of sequins Description: The project is intended to support the use of sequins (synthetic sequencing spike-in controls) owned and made available by the Garvan Institute of Medical Research. The goal is to provide a standard open source library for quantitative analysis, modelling and visualization of spike-in controls. biocViews: ImmunoOncology, DifferentialExpression, Preprocessing, RNASeq, GeneExpression, Software Author: Ted Wong Maintainer: Ted Wong URL: www.sequin.xyz VignetteBuilder: knitr BugReports: https://github.com/student-t/RAnaquin/issues git_url: https://git.bioconductor.org/packages/Anaquin git_branch: RELEASE_3_8 git_last_commit: 22b6c71 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Anaquin_2.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Anaquin_2.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Anaquin_2.6.1.tgz vignettes: vignettes/Anaquin/inst/doc/Anaquin.pdf vignetteTitles: Anaquin - Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Anaquin/inst/doc/Anaquin.R Package: AneuFinder Version: 1.10.2 Depends: R (>= 3.5), GenomicRanges, cowplot, AneuFinderData Imports: methods, utils, grDevices, graphics, stats, foreach, doParallel, S4Vectors, GenomeInfoDb, IRanges, Rsamtools, bamsignals, DNAcopy, ecp, Biostrings, GenomicAlignments, ggplot2, reshape2, ggdendro, ggrepel, ReorderCluster, mclust Suggests: knitr, BiocStyle, testthat, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10 License: Artistic-2.0 Archs: i386, x64 MD5sum: 22a8604ea8b2db1b2876e79a044f669a NeedsCompilation: yes Title: Analysis of Copy Number Variation in Single-Cell-Sequencing Data Description: AneuFinder implements functions for copy-number detection, breakpoint detection, and karyotype and heterogeneity analysis in single-cell whole genome sequencing and strand-seq data. biocViews: ImmunoOncology, Software, Sequencing, SingleCell, CopyNumberVariation, GenomicVariation, HiddenMarkovModel, WholeGenome Author: Aaron Taudt, Bjorn Bakker, David Porubsky Maintainer: Aaron Taudt URL: https://github.com/ataudt/aneufinder.git VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AneuFinder git_branch: RELEASE_3_8 git_last_commit: 56578ae git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/AneuFinder_1.10.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/AneuFinder_1.10.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AneuFinder_1.10.2.tgz vignettes: vignettes/AneuFinder/inst/doc/AneuFinder.pdf vignetteTitles: A quick introduction to AneuFinder hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AneuFinder/inst/doc/AneuFinder.R Package: ANF Version: 1.4.0 Imports: igraph, Biobase, survival, MASS, stats, RColorBrewer Suggests: ExperimentHub, SNFtool, knitr, rmarkdown, testthat License: GPL-3 MD5sum: 78709ee747b31ed759c515fd36ae9960 NeedsCompilation: no Title: Affinity Network Fusion for Complex Patient Clustering Description: This package is used for complex patient clustering by integrating multi-omic data through affinity network fusion. biocViews: Clustering, GraphAndNetwork, Network Author: Tianle Ma, Aidong Zhang Maintainer: Tianle Ma VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ANF git_branch: RELEASE_3_8 git_last_commit: c82e31c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ANF_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ANF_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ANF_1.4.0.tgz vignettes: vignettes/ANF/inst/doc/ANF.html vignetteTitles: Cancer Patient Clustering with ANF hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ANF/inst/doc/ANF.R Package: annaffy Version: 1.54.0 Depends: R (>= 2.5.0), methods, Biobase, GO.db, KEGG.db Imports: AnnotationDbi (>= 0.1.15), DBI Suggests: hgu95av2.db, multtest, tcltk License: LGPL MD5sum: 1417af7e94aa576c88bb823ac42e6f9e NeedsCompilation: no Title: Annotation tools for Affymetrix biological metadata Description: Functions for handling data from Bioconductor Affymetrix annotation data packages. Produces compact HTML and text reports including experimental data and URL links to many online databases. Allows searching biological metadata using various criteria. biocViews: OneChannel, Microarray, Annotation, GO, Pathways, ReportWriting Author: Colin A. Smith Maintainer: Colin A. Smith git_url: https://git.bioconductor.org/packages/annaffy git_branch: RELEASE_3_8 git_last_commit: e1b3bf1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/annaffy_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/annaffy_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/annaffy_1.54.0.tgz vignettes: vignettes/annaffy/inst/doc/annaffy.pdf vignetteTitles: annaffy Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/annaffy/inst/doc/annaffy.R dependsOnMe: a4Base, a4Reporting, PGSEA, webbioc suggestsMe: AffyExpress, ArrayTools, BiocCaseStudies Package: annmap Version: 1.24.0 Depends: R (>= 2.15.0), methods, GenomicRanges Imports: DBI, RMySQL (>= 0.6-0), digest, Biobase, grid, lattice, Rsamtools, genefilter, IRanges, BiocGenerics Suggests: RUnit, rjson, Gviz License: GPL-2 MD5sum: 004c0c2fc7fe6be4898c97449f568b62 NeedsCompilation: no Title: Genome annotation and visualisation package pertaining to Affymetrix arrays and NGS analysis. Description: annmap provides annotation mappings for Affymetrix exon arrays and coordinate based queries to support deep sequencing data analysis. Database access is hidden behind the API which provides a set of functions such as genesInRange(), geneToExon(), exonDetails(), etc. Functions to plot gene architecture and BAM file data are also provided. Underlying data are from Ensembl. biocViews: Annotation, Microarray, OneChannel, ReportWriting, Transcription, Visualization Author: Tim Yates Maintainer: Chris Wirth URL: http://annmap.cruk.manchester.ac.uk git_url: https://git.bioconductor.org/packages/annmap git_branch: RELEASE_3_8 git_last_commit: 97425ca git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/annmap_1.24.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/annmap_1.24.0.tgz vignettes: vignettes/annmap/inst/doc/annmap.pdf, vignettes/annmap/inst/doc/cookbook.pdf, vignettes/annmap/inst/doc/INSTALL.pdf vignetteTitles: annmap primer, The Annmap Cookbook, annmap installation instruction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: annotate Version: 1.60.1 Depends: R (>= 2.10), AnnotationDbi (>= 1.27.5), XML Imports: Biobase, DBI, xtable, graphics, utils, stats, methods, BiocGenerics (>= 0.13.8), RCurl Suggests: hgu95av2.db, genefilter, Biostrings (>= 2.25.10), IRanges, rae230a.db, rae230aprobe, tkWidgets, GO.db, org.Hs.eg.db, org.Mm.eg.db, hom.Hs.inp.db, humanCHRLOC, Rgraphviz, RUnit, License: Artistic-2.0 MD5sum: 30155b2da80dedf6f9f879f440e7fac6 NeedsCompilation: no Title: Annotation for microarrays Description: Using R enviroments for annotation. biocViews: Annotation, Pathways, GO Author: R. Gentleman Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/annotate git_branch: RELEASE_3_8 git_last_commit: 9d8f87d git_last_commit_date: 2019-03-07 Date/Publication: 2019-03-07 source.ver: src/contrib/annotate_1.60.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/annotate_1.60.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/annotate_1.60.1.tgz vignettes: vignettes/annotate/inst/doc/annotate.pdf, vignettes/annotate/inst/doc/chromLoc.pdf, vignettes/annotate/inst/doc/GOusage.pdf, vignettes/annotate/inst/doc/prettyOutput.pdf, vignettes/annotate/inst/doc/query.pdf, vignettes/annotate/inst/doc/useDataPkgs.pdf, vignettes/annotate/inst/doc/useHomology.pdf, vignettes/annotate/inst/doc/useProbeInfo.pdf vignetteTitles: Annotation Overview, HowTo: use chromosomal information, Basic GO Usage, HowTo: Get HTML Output, HOWTO: Use the online query tools, Using Data Packages, Using the homology package, Using Affymetrix Probe Level Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/annotate/inst/doc/annotate.R, vignettes/annotate/inst/doc/chromLoc.R, vignettes/annotate/inst/doc/GOusage.R, vignettes/annotate/inst/doc/prettyOutput.R, vignettes/annotate/inst/doc/query.R, vignettes/annotate/inst/doc/useDataPkgs.R, vignettes/annotate/inst/doc/useHomology.R, vignettes/annotate/inst/doc/useProbeInfo.R dependsOnMe: ChromHeatMap, GeneAnswers, geneplotter, GOSim, GSEABase, idiogram, macat, MineICA, MLInterfaces, PCpheno, phenoTest, PREDA, RpsiXML, sampleClassifier, ScISI, SemDist importsMe: CAFE, Category, categoryCompare, CNEr, codelink, debrowser, DOQTL, DrugVsDisease, gCMAP, gCMAPWeb, GeneAnswers, genefilter, GlobalAncova, globaltest, GOstats, lumi, methyAnalysis, methylumi, MGFR, PathwaySplice, phenoTest, qpgraph, ScISI, splicegear, systemPipeR, tigre suggestsMe: BiocCaseStudies, BiocGenerics, biomaRt, GenomicRanges, GSAR, GSEAlm, hmdbQuery, maigesPack, metagenomeSeq, MLP, pcxn, RnBeads, siggenes, SummarizedExperiment Package: AnnotationDbi Version: 1.44.0 Depends: R (>= 2.7.0), methods, utils, stats4, BiocGenerics (>= 0.23.1), Biobase (>= 1.17.0), IRanges Imports: DBI, RSQLite, S4Vectors (>= 0.9.25) Suggests: hgu95av2.db, GO.db, org.Sc.sgd.db, org.At.tair.db, KEGG.db, RUnit, TxDb.Hsapiens.UCSC.hg19.knownGene, hom.Hs.inp.db, org.Hs.eg.db, reactome.db, AnnotationForge, graph, EnsDb.Hsapiens.v75, BiocStyle, knitr License: Artistic-2.0 MD5sum: 65b98cea76650046e4287a093092269a NeedsCompilation: no Title: Annotation Database Interface Description: Provides user interface and database connection code for annotation data packages using SQLite data storage. biocViews: Annotation, Microarray, Sequencing, GenomeAnnotation Author: Hervé Pagès, Marc Carlson, Seth Falcon, Nianhua Li Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr Video: https://www.youtube.com/watch?v=8qvGNTVz3Ik git_url: https://git.bioconductor.org/packages/AnnotationDbi git_branch: RELEASE_3_8 git_last_commit: ce191b0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AnnotationDbi_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnnotationDbi_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnnotationDbi_1.44.0.tgz vignettes: vignettes/AnnotationDbi/inst/doc/AnnotationDbi.pdf, vignettes/AnnotationDbi/inst/doc/IntroToAnnotationPackages.pdf vignetteTitles: 2. (Deprecated) How to use bimaps from the ".db" annotation packages, 1. Introduction To Bioconductor Annotation Packages hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AnnotationDbi/inst/doc/AnnotationDbi.R, vignettes/AnnotationDbi/inst/doc/IntroToAnnotationPackages.R dependsOnMe: a4Base, a4Preproc, annotate, AnnotationForge, AnnotationFuncs, attract, Category, chimera, ChromHeatMap, customProDB, DEXSeq, EGSEA, eisa, ExpressionView, GenomicFeatures, GOFunction, goProfiles, GSReg, ipdDb, miRNAtap, MLP, OrganismDbi, pathRender, PGSEA, proBAMr, RpsiXML, safe, SemDist, topGO importsMe: adSplit, affycoretools, AllelicImbalance, annaffy, AnnotationHub, AnnotationHubData, annotatr, artMS, ASpli, beadarray, biomaRt, BioNet, biovizBase, bumphunter, CancerMutationAnalysis, categoryCompare, ccmap, cellity, chimeraviz, chipenrich, ChIPpeakAnno, ChIPseeker, clusterProfiler, CoCiteStats, compEpiTools, consensusDE, crisprseekplus, CrispRVariants, crossmeta, csaw, debrowser, derfinder, DominoEffect, DOSE, dSimer, EDASeq, eegc, EnrichmentBrowser, enrichplot, ensembldb, erma, esATAC, ExpressionView, GA4GHshiny, gage, gCMAP, gCMAPWeb, genefilter, geneplotter, geneXtendeR, GenVisR, GGBase, ggbio, GGtools, GlobalAncova, globaltest, GOfuncR, GOFunction, GOpro, GOSemSim, goseq, GOSim, goSTAG, GOstats, goTools, gpart, gQTLstats, graphite, GSEABase, GSEABenchmarkeR, Gviz, gwascat, HTSanalyzeR, ideal, IMAS, InPAS, interactiveDisplay, iSEE, isomiRs, IVAS, LRBaseDbi, lumi, mAPKL, MCbiclust, mdgsa, MeSHDbi, meshes, MetaboSignal, methyAnalysis, methylGSA, methylumi, MIGSA, MineICA, MiRaGE, mirIntegrator, miRNAmeConverter, missMethyl, multiMiR, NanoStringQCPro, Onassis, ontoProc, Organism.dplyr, PADOG, pathview, PathwaySplice, pcaExplorer, pcaGoPromoter, PCpheno, PGA, phenoTest, psichomics, pwOmics, qpgraph, RCAS, ReactomePA, REDseq, restfulSE, rgsepd, rTRM, ScISI, scPipe, scruff, SGSeq, singleCellTK, SLGI, SMITE, SpidermiR, StarBioTrek, SVM2CRM, TCGAutils, tenXplore, tigre, trackViewer, trena, tximeta, UniProt.ws, VariantAnnotation, VariantFiltering suggestsMe: BiocCaseStudies, BiocGenerics, BiocOncoTK, CellTrails, cicero, DEGreport, edgeR, esetVis, FELLA, FGNet, fgsea, GA4GHclient, gCrisprTools, geecc, GeneAnswers, GeneRegionScan, GenomicRanges, limma, MmPalateMiRNA, oligo, OUTRIDER, piano, Pigengene, pRoloc, qcmetrics, R3CPET, recount, RGalaxy, sigPathway, SummarizedExperiment, TFutils, wiggleplotr Package: AnnotationFilter Version: 1.6.0 Depends: R (>= 3.4.0) Imports: utils, methods, GenomicRanges, lazyeval Suggests: BiocStyle, knitr, testthat, RSQLite, org.Hs.eg.db License: Artistic-2.0 MD5sum: 607d1a6cc3e97499cb79ff01e24f03c6 NeedsCompilation: no Title: Facilities for Filtering Bioconductor Annotation Resources Description: This package provides class and other infrastructure to implement filters for manipulating Bioconductor annotation resources. The filters will be used by ensembldb, Organism.dplyr, and other packages. biocViews: Annotation, Infrastructure, Software Author: Martin Morgan [aut], Johannes Rainer [aut], Joachim Bargsten [ctb], Daniel Van Twisk [ctb], Bioconductor Package Maintainer [cre] Maintainer: Bioconductor Package Maintainer URL: https://github.com/Bioconductor/AnnotationFilter VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/AnnotationFilter/issues git_url: https://git.bioconductor.org/packages/AnnotationFilter git_branch: RELEASE_3_8 git_last_commit: fa40a7e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AnnotationFilter_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnnotationFilter_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnnotationFilter_1.6.0.tgz vignettes: vignettes/AnnotationFilter/inst/doc/AnnotationFilter.html vignetteTitles: Facilities for Filtering Bioconductor Annotation resources hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AnnotationFilter/inst/doc/AnnotationFilter.R dependsOnMe: chimeraviz, ensembldb, Organism.dplyr importsMe: biovizBase, ggbio, Pbase, TVTB suggestsMe: TFutils, TxRegInfra, wiggleplotr Package: AnnotationForge Version: 1.24.0 Depends: R (>= 2.7.0), methods, utils, BiocGenerics (>= 0.15.10), Biobase (>= 1.17.0), AnnotationDbi (>= 1.33.14) Imports: DBI, RSQLite, XML, S4Vectors, RCurl Suggests: biomaRt, httr, GenomeInfoDb (>= 1.17.1), Biostrings, affy, hgu95av2.db, human.db0, org.Hs.eg.db, Homo.sapiens, hom.Hs.inp.db, GO.db, BiocStyle, knitr, BiocManager License: Artistic-2.0 MD5sum: 2f5509af2751bdbc94f0f08b2ec6950e NeedsCompilation: no Title: Code for Building Annotation Database Packages Description: Provides code for generating Annotation packages and their databases. Packages produced are intended to be used with AnnotationDbi. biocViews: Annotation, Infrastructure Author: Marc Carlson, Hervé Pagès Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AnnotationForge git_branch: RELEASE_3_8 git_last_commit: 3e1fe86 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AnnotationForge_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnnotationForge_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnnotationForge_1.24.0.tgz vignettes: vignettes/AnnotationForge/inst/doc/makeProbePackage.pdf, vignettes/AnnotationForge/inst/doc/MakingNewAnnotationPackages.pdf, vignettes/AnnotationForge/inst/doc/SQLForge.pdf, vignettes/AnnotationForge/inst/doc/MakingNewOrganismPackages.html vignetteTitles: Creating probe packages, AnnotationForge: Creating select Interfaces for custom Annotation resources, SQLForge: An easy way to create a new annotation package with a standard database schema., Making New Organism Packages hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AnnotationForge/inst/doc/makeProbePackage.R, vignettes/AnnotationForge/inst/doc/MakingNewAnnotationPackages.R, vignettes/AnnotationForge/inst/doc/MakingNewOrganismPackages.R, vignettes/AnnotationForge/inst/doc/SQLForge.R importsMe: AnnotationHubData, GOstats suggestsMe: AnnotationDbi, AnnotationHub Package: AnnotationFuncs Version: 1.32.0 Depends: R (>= 2.7.0), AnnotationDbi Imports: DBI Suggests: org.Bt.eg.db, GO.db, org.Hs.eg.db, hom.Hs.inp.db License: GPL-2 MD5sum: 80fb2ac0e0b19ff0abdce58fc2c53933 NeedsCompilation: no Title: Annotation translation functions Description: Functions for handling translating between different identifieres using the Biocore Data Team data-packages (e.g. org.Bt.eg.db). biocViews: AnnotationData, Software Author: Stefan McKinnon Edwards Maintainer: Stefan McKinnon Edwards URL: http://www.iysik.com/index.php?page=annotation-functions git_url: https://git.bioconductor.org/packages/AnnotationFuncs git_branch: RELEASE_3_8 git_last_commit: aa2948b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AnnotationFuncs_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnnotationFuncs_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnnotationFuncs_1.32.0.tgz vignettes: vignettes/AnnotationFuncs/inst/doc/AnnotationFuncsUserguide.pdf vignetteTitles: Annotation mapping functions hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AnnotationFuncs/inst/doc/AnnotationFuncsUserguide.R importsMe: bioCancer Package: AnnotationHub Version: 2.14.5 Depends: BiocGenerics (>= 0.15.10) Imports: utils, methods, grDevices, RSQLite, BiocManager, curl, AnnotationDbi (>= 1.31.19), S4Vectors, interactiveDisplayBase, httr, yaml Suggests: IRanges, GenomicRanges, GenomeInfoDb, VariantAnnotation, Rsamtools, rtracklayer, BiocStyle, knitr, AnnotationForge, rBiopaxParser, RUnit, GenomicFeatures, MSnbase, mzR, Biostrings, SummarizedExperiment, ExperimentHub, gdsfmt Enhances: AnnotationHubData License: Artistic-2.0 MD5sum: 7feb1f41de7753a7c4579e1eee6fa942 NeedsCompilation: yes Title: Client to access AnnotationHub resources Description: This package provides a client for the Bioconductor AnnotationHub web resource. The AnnotationHub web resource provides a central location where genomic files (e.g., VCF, bed, wig) and other resources from standard locations (e.g., UCSC, Ensembl) can be discovered. The resource includes metadata about each resource, e.g., a textual description, tags, and date of modification. The client creates and manages a local cache of files retrieved by the user, helping with quick and reproducible access. biocViews: Infrastructure, DataImport, GUI, ThirdPartyClient Author: Martin Morgan [cre], Marc Carlson [ctb], Dan Tenenbaum [ctb], Sonali Arora [ctb], Lori Shepherd [ctb] Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AnnotationHub git_branch: RELEASE_3_8 git_last_commit: 993a98c git_last_commit_date: 2019-03-14 Date/Publication: 2019-03-14 source.ver: src/contrib/AnnotationHub_2.14.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnnotationHub_2.14.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnnotationHub_2.14.5.tgz vignettes: vignettes/AnnotationHub/inst/doc/AnnotationHub-HOWTO.html, vignettes/AnnotationHub/inst/doc/AnnotationHub.html, vignettes/AnnotationHub/inst/doc/CreateAnAnnotationPackage.html vignetteTitles: AnnotationHub: AnnotationHub HOW TO's, AnnotationHub: Access the AnnotationHub Web Service, AnnotationHub: Creating An AnnotationHub Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AnnotationHub/inst/doc/AnnotationHub-HOWTO.R, vignettes/AnnotationHub/inst/doc/AnnotationHub.R dependsOnMe: AnnotationHubData, ExperimentHub, hipathia, ipdDb, ProteomicsAnnotationHubData, RefNet importsMe: annotatr, dmrseq, GenomicScores, GSEABenchmarkeR, gwascat, PathwaySplice, psichomics, pwOmics, REMP, restfulSE, scmeth, TSRchitect, Ularcirc suggestsMe: Chicago, CINdex, clusterProfiler, COCOA, DNAshapeR, dupRadar, ensembldb, epiNEM, epivizrChart, epivizrData, GenomicRanges, GOSemSim, maser, MIRA, MSnbase, OrganismDbi, Pbase, VariantAnnotation Package: AnnotationHubData Version: 1.12.0 Depends: R (>= 3.2.2), methods, utils, S4Vectors (>= 0.7.21), IRanges (>= 2.3.23), GenomicRanges, AnnotationHub (>= 2.9.14) Imports: GenomicFeatures, Rsamtools, rtracklayer, BiocGenerics, jsonlite, BiocManager, biocViews, AnnotationDbi, Biobase, Biostrings, DBI, GenomeInfoDb (>= 1.15.4), OrganismDbi, RSQLite, rBiopaxParser, AnnotationForge, futile.logger (>= 1.3.0), XML, RCurl Suggests: RUnit, knitr, BiocStyle, grasp2db, GenomeInfoDbData License: Artistic-2.0 MD5sum: 523c97f501f82a3ea206a80e4d99c3e4 NeedsCompilation: no Title: Transform public data resources into Bioconductor Data Structures Description: These recipes convert a wide variety and a growing number of public bioinformatic data sets into easily-used standard Bioconductor data structures. biocViews: DataImport Author: Martin Morgan [ctb], Marc Carlson [ctb], Dan Tenenbaum [ctb], Sonali Arora [ctb], Paul Shannon [ctb], Lori Shepherd [ctb], Bioconductor Package Maintainer [cre] Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AnnotationHubData git_branch: RELEASE_3_8 git_last_commit: f7f26c8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/AnnotationHubData_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/AnnotationHubData_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AnnotationHubData_1.12.0.tgz vignettes: vignettes/AnnotationHubData/inst/doc/CreateAnAnnotationPackage.html, vignettes/AnnotationHubData/inst/doc/IntroductionToAnnotationHubData.html vignetteTitles: AnnotationHub: Creating An AnnotationHub Package, Introduction to AnnotationHubData hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AnnotationHubData/inst/doc/CreateAnAnnotationPackage.R dependsOnMe: ExperimentHubData Package: annotationTools Version: 1.56.0 Imports: Biobase, stats License: GPL MD5sum: 9371efaf0751aa8d26710245cba18825 NeedsCompilation: no Title: Annotate microarrays and perform cross-species gene expression analyses using flat file databases. Description: Functions to annotate microarrays, find orthologs, and integrate heterogeneous gene expression profiles using annotation and other molecular biology information available as flat file database (plain text files). biocViews: Microarray, Annotation Author: Alexandre Kuhn Maintainer: Alexandre Kuhn git_url: https://git.bioconductor.org/packages/annotationTools git_branch: RELEASE_3_8 git_last_commit: f06dec8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/annotationTools_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/annotationTools_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/annotationTools_1.56.0.tgz vignettes: vignettes/annotationTools/inst/doc/annotationTools.pdf vignetteTitles: annotationTools Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/annotationTools/inst/doc/annotationTools.R importsMe: DOQTL Package: annotatr Version: 1.8.0 Depends: R (>= 3.4.0) Imports: AnnotationDbi, AnnotationHub, dplyr, GenomicFeatures, GenomicRanges, GenomeInfoDb (>= 1.10.3), ggplot2, IRanges, methods, readr, regioneR, reshape2, rtracklayer, S4Vectors (>= 0.17.5), stats, utils Suggests: BiocStyle, devtools, knitr, org.Dm.eg.db, org.Gg.eg.db, org.Hs.eg.db, org.Mm.eg.db, org.Rn.eg.db, rmarkdown, roxygen2, testthat, TxDb.Dmelanogaster.UCSC.dm3.ensGene, TxDb.Dmelanogaster.UCSC.dm6.ensGene, TxDb.Ggallus.UCSC.galGal5.refGene, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Mmusculus.UCSC.mm9.knownGene, TxDb.Mmusculus.UCSC.mm10.knownGene, TxDb.Rnorvegicus.UCSC.rn4.ensGene, TxDb.Rnorvegicus.UCSC.rn5.refGene, TxDb.Rnorvegicus.UCSC.rn6.refGene License: GPL-3 MD5sum: e91b2cc81be539c201d2c518d37b764f NeedsCompilation: no Title: Annotation of Genomic Regions to Genomic Annotations Description: Given a set of genomic sites/regions (e.g. ChIP-seq peaks, CpGs, differentially methylated CpGs or regions, SNPs, etc.) it is often of interest to investigate the intersecting genomic annotations. Such annotations include those relating to gene models (promoters, 5'UTRs, exons, introns, and 3'UTRs), CpGs (CpG islands, CpG shores, CpG shelves), or regulatory sequences such as enhancers. The annotatr package provides an easy way to summarize and visualize the intersection of genomic sites/regions with genomic annotations. biocViews: Software, Annotation, GenomeAnnotation, FunctionalGenomics, Visualization Author: Raymond G. Cavalcante [aut, cre], Maureen A. Sartor [ths] Maintainer: Raymond G. Cavalcante VignetteBuilder: knitr BugReports: https://www.github.com/rcavalcante/annotatr/issues git_url: https://git.bioconductor.org/packages/annotatr git_branch: RELEASE_3_8 git_last_commit: 15163fb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/annotatr_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/annotatr_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/annotatr_1.8.0.tgz vignettes: vignettes/annotatr/inst/doc/annotatr-vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/annotatr/inst/doc/annotatr-vignette.R importsMe: dmrseq, scmeth Package: anota Version: 1.30.0 Depends: qvalue Imports: multtest, qvalue License: GPL-3 MD5sum: c3cc7015b78f0b9283107019ce4fd4ad NeedsCompilation: no Title: ANalysis Of Translational Activity (ANOTA). Description: Genome wide studies of translational control is emerging as a tool to study verious biological conditions. The output from such analysis is both the mRNA level (e.g. cytosolic mRNA level) and the levl of mRNA actively involved in translation (the actively translating mRNA level) for each mRNA. The standard analysis of such data strives towards identifying differential translational between two or more sample classes - i.e. differences in actively translated mRNA levels that are independent of underlying differences in cytosolic mRNA levels. This package allows for such analysis using partial variances and the random variance model. As 10s of thousands of mRNAs are analyzed in parallell the library performs a number of tests to assure that the data set is suitable for such analysis. biocViews: GeneExpression, DifferentialExpression, Microarray, Sequencing Author: Ola Larsson , Nahum Sonenberg , Robert Nadon Maintainer: Ola Larsson git_url: https://git.bioconductor.org/packages/anota git_branch: RELEASE_3_8 git_last_commit: 0ca424b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/anota_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/anota_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/anota_1.30.0.tgz vignettes: vignettes/anota/inst/doc/anota.pdf vignetteTitles: ANalysis Of Translational Activity (anota) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/anota/inst/doc/anota.R dependsOnMe: tRanslatome Package: anota2seq Version: 1.4.2 Depends: R (>= 3.4.0), methods Imports: multtest,qvalue,limma,DESeq2,edgeR,RColorBrewer, grDevices, graphics, stats, utils, SummarizedExperiment Suggests: BiocStyle,knitr License: GPL-3 MD5sum: 24fb82c63bcdaa10711c1c95cc1af240 NeedsCompilation: no Title: Generally applicable transcriptome-wide analysis of translational efficiency using anota2seq Description: anota2seq provides analysis of translational efficiency and differential expression analysis for polysome-profiling and ribosome-profiling studies (two or more sample classes) quantified by RNA sequencing or DNA-microarray. Polysome-profiling and ribosome-profiling typically generate data for two RNA sources; translated mRNA and total mRNA. Analysis of differential expression is used to estimate changes within each RNA source (i.e. translated mRNA or total mRNA). Analysis of translational efficiency aims to identify changes in translation efficiency leading to altered protein levels that are independent of total mRNA levels (i.e. changes in translated mRNA that are independent of levels of total mRNA) or buffering, a mechanism regulating translational efficiency so that protein levels remain constant despite fluctuating total mRNA levels (i.e. changes in total mRNA that are independent of levels of translated mRNA). anota2seq applies analysis of partial variance and the random variance model to fulfill these tasks. biocViews: ImmunoOncology, GeneExpression, DifferentialExpression, Microarray,GenomeWideAssociation, BatchEffect, Normalization, RNASeq, Sequencing, GeneRegulation, Regression Author: Christian Oertlin , Julie Lorent , Ola Larsson Maintainer: Christian Oertlin , Julie Lorent VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/anota2seq git_branch: RELEASE_3_8 git_last_commit: 571252c git_last_commit_date: 2019-04-02 Date/Publication: 2019-04-02 source.ver: src/contrib/anota2seq_1.4.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/anota2seq_1.4.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/anota2seq_1.4.2.tgz vignettes: vignettes/anota2seq/inst/doc/anota2seq.pdf vignetteTitles: Generally applicable transcriptome-wide analysis of translational efficiency using anota2seq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/anota2seq/inst/doc/anota2seq.R Package: antiProfiles Version: 1.22.0 Depends: R (>= 3.0), matrixStats (>= 0.50.0), methods (>= 2.14), locfit (>= 1.5) Suggests: antiProfilesData, RColorBrewer License: Artistic-2.0 MD5sum: 5f45e664940f6ea8925cb91e62f3e6e7 NeedsCompilation: no Title: Implementation of gene expression anti-profiles Description: Implements gene expression anti-profiles as described in Corrada Bravo et al., BMC Bioinformatics 2012, 13:272 doi:10.1186/1471-2105-13-272. biocViews: GeneExpression,Classification Author: Hector Corrada Bravo, Rafael A. Irizarry and Jeffrey T. Leek Maintainer: Hector Corrada Bravo URL: https://github.com/HCBravoLab/antiProfiles git_url: https://git.bioconductor.org/packages/antiProfiles git_branch: RELEASE_3_8 git_last_commit: e5098f8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/antiProfiles_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/antiProfiles_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/antiProfiles_1.22.0.tgz vignettes: vignettes/antiProfiles/inst/doc/antiProfiles.pdf vignetteTitles: Introduction to antiProfiles hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/antiProfiles/inst/doc/antiProfiles.R Package: apComplex Version: 2.48.1 Depends: R (>= 2.10), graph, RBGL Imports: Rgraphviz, stats, org.Sc.sgd.db License: LGPL MD5sum: e48677d1c3143ee6f6e8517edb37b966 NeedsCompilation: no Title: Estimate protein complex membership using AP-MS protein data Description: Functions to estimate a bipartite graph of protein complex membership using AP-MS data. biocViews: ImmunoOncology, NetworkInference, MassSpectrometry, GraphAndNetwork Author: Denise Scholtens Maintainer: Denise Scholtens git_url: https://git.bioconductor.org/packages/apComplex git_branch: RELEASE_3_8 git_last_commit: 79135d0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/apComplex_2.48.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/apComplex_2.48.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/apComplex_2.48.1.tgz vignettes: vignettes/apComplex/inst/doc/apComplex.pdf vignetteTitles: apComplex hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/apComplex/inst/doc/apComplex.R dependsOnMe: ScISI suggestsMe: BiocCaseStudies Package: apeglm Version: 1.4.2 Imports: emdbook, SummarizedExperiment, GenomicRanges, methods, stats, utils, Rcpp LinkingTo: Rcpp, RcppEigen, RcppNumerical Suggests: DESeq2, airway, knitr, rmarkdown, testthat License: GPL-2 Archs: i386, x64 MD5sum: b09fdbd7241685adc593a336fd797000 NeedsCompilation: yes Title: Approximate posterior estimation for GLM coefficients Description: apeglm provides Bayesian shrinkage estimators for effect sizes for a variety of GLM models, using approximation of the posterior for individual coefficients. biocViews: ImmunoOncology, Sequencing, RNASeq, DifferentialExpression, GeneExpression, Bayesian Author: Anqi Zhu, Joseph G. Ibrahim, Michael I. Love Maintainer: Anqi Zhu VignetteBuilder: knitr, rmarkdown git_url: https://git.bioconductor.org/packages/apeglm git_branch: RELEASE_3_8 git_last_commit: 7cceea7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/apeglm_1.4.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/apeglm_1.4.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/apeglm_1.4.2.tgz vignettes: vignettes/apeglm/inst/doc/apeglm.html vignetteTitles: Effect size estimation with apeglm hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/apeglm/inst/doc/apeglm.R suggestsMe: DESeq2 Package: appreci8R Version: 1.0.0 Imports: shiny, shinyjs, DT, VariantAnnotation, BSgenome, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, Homo.sapiens, SNPlocs.Hsapiens.dbSNP144.GRCh37, XtraSNPlocs.Hsapiens.dbSNP144.GRCh37, rsnps, Biostrings, MafDb.1Kgenomes.phase3.hs37d5, MafDb.ExAC.r1.0.hs37d5, MafDb.ESP6500SI.V2.SSA137.hs37d5, MafDb.gnomADex.r2.0.1.hs37d5, COSMIC.67, rentrez, PolyPhen.Hsapiens.dbSNP131, SIFT.Hsapiens.dbSNP137, seqinr, openxlsx, Rsamtools, stringr, utils, stats, GenomicRanges, S4Vectors, GenomicFeatures, IRanges, GenomicScores, SummarizedExperiment Suggests: GO.db, org.Hs.eg.db License: LGPL-3 MD5sum: 425813a17e39960bc786393fbf3ac7ee NeedsCompilation: no Title: appreci8R: an R/Bioconductor package for filtering SNVs and short indels with high sensitivity and high PPV Description: The appreci8R is an R version of our appreci8-algorithm - A Pipeline for PREcise variant Calling Integrating 8 tools. Variant calling results of our standard appreci8-tools (GATK, Platypus, VarScan, FreeBayes, LoFreq, SNVer, samtools and VarDict), as well as up to 5 additional tools is combined, evaluated and filtered. biocViews: VariantDetection, GeneticVariability, SNP, VariantAnnotation, Sequencing, Author: Sarah Sandmann Maintainer: Sarah Sandmann git_url: https://git.bioconductor.org/packages/appreci8R git_branch: RELEASE_3_8 git_last_commit: addad71 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/appreci8R_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/appreci8R_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/appreci8R_1.0.0.tgz vignettes: vignettes/appreci8R/inst/doc/appreci8R.pdf vignetteTitles: Using appreci8R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/appreci8R/inst/doc/appreci8R.R Package: aroma.light Version: 3.12.0 Depends: R (>= 2.15.2) Imports: stats, R.methodsS3 (>= 1.7.1), R.oo (>= 1.22.0), R.utils (>= 2.7.0), matrixStats (>= 0.54.0) Suggests: princurve (>= 2.1.2) License: GPL (>= 2) MD5sum: f98a7b55b903ecd0334b7d3afed5ce95 NeedsCompilation: no Title: Light-Weight Methods for Normalization and Visualization of Microarray Data using Only Basic R Data Types Description: Methods for microarray analysis that take basic data types such as matrices and lists of vectors. These methods can be used standalone, be utilized in other packages, or be wrapped up in higher-level classes. biocViews: Infrastructure, Microarray, OneChannel, TwoChannel, MultiChannel, Visualization, Preprocessing Author: Henrik Bengtsson [aut, cre, cph], Pierre Neuvial [ctb], Aaron Lun [ctb] Maintainer: Henrik Bengtsson URL: https://github.com/HenrikBengtsson/aroma.light, http://www.aroma-project.org BugReports: https://github.com/HenrikBengtsson/aroma.light/issues git_url: https://git.bioconductor.org/packages/aroma.light git_branch: RELEASE_3_8 git_last_commit: e4cef05 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/aroma.light_3.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/aroma.light_3.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/aroma.light_3.12.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE importsMe: EDASeq, scone suggestsMe: scran, TIN Package: ArrayExpress Version: 1.42.0 Depends: R (>= 2.9.0), Biobase (>= 2.4.0) Imports: XML, oligo, limma Suggests: affy License: Artistic-2.0 MD5sum: 718b770b408424f6141d1ce8c818b00a NeedsCompilation: no Title: Access the ArrayExpress Microarray Database at EBI and build Bioconductor data structures: ExpressionSet, AffyBatch, NChannelSet Description: Access the ArrayExpress Repository at EBI and build Bioconductor data structures: ExpressionSet, AffyBatch, NChannelSet biocViews: Microarray, DataImport, OneChannel, TwoChannel Author: Audrey Kauffmann, Ibrahim Emam, Michael Schubert Maintainer: Suhaib Mohammed git_url: https://git.bioconductor.org/packages/ArrayExpress git_branch: RELEASE_3_8 git_last_commit: f550d15 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ArrayExpress_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ArrayExpress_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ArrayExpress_1.42.0.tgz vignettes: vignettes/ArrayExpress/inst/doc/ArrayExpress.pdf vignetteTitles: ArrayExpress: Import and convert ArrayExpress data sets into R object hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ArrayExpress/inst/doc/ArrayExpress.R dependsOnMe: DrugVsDisease suggestsMe: gCMAPWeb Package: ArrayExpressHTS Version: 1.32.1 Depends: sampling, Rsamtools (>= 1.19.36), snow Imports: Biobase, BiocGenerics, Biostrings, DESeq, GenomicRanges, Hmisc, IRanges (>= 2.13.11), R2HTML, RColorBrewer, Rsamtools, ShortRead, XML, biomaRt, edgeR, grDevices, graphics, methods, rJava, stats, svMisc, utils, sendmailR, bitops LinkingTo: Rsamtools License: Artistic License 2.0 MD5sum: 999bbee605ec5abb2c4328916301e33a NeedsCompilation: yes Title: ArrayExpress High Throughput Sequencing Processing Pipeline Description: RNA-Seq processing pipeline for public ArrayExpress experiments or local datasets biocViews: ImmunoOncology, RNASeq, Sequencing Author: Angela Goncalves, Andrew Tikhonov Maintainer: Angela Goncalves , Andrew Tikhonov git_url: https://git.bioconductor.org/packages/ArrayExpressHTS git_branch: RELEASE_3_8 git_last_commit: 6c778c1 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ArrayExpressHTS_1.32.1.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ArrayExpressHTS_1.32.1.tgz vignettes: vignettes/ArrayExpressHTS/inst/doc/ArrayExpressHTS.pdf vignetteTitles: ArrayExpressHTS: RNA-Seq Pipeline for transcription profiling experiments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ArrayExpressHTS/inst/doc/ArrayExpressHTS.R Package: arrayMvout Version: 1.40.0 Depends: R (>= 2.6.0), tools, methods, utils, parody, Biobase, affy, lumi Imports: simpleaffy, mdqc, affyContam, Suggests: MAQCsubset, mvoutData, lumiBarnes, affyPLM, affydata, hgu133atagcdf License: Artistic-2.0 MD5sum: c9c9ec7b5f1774bab6514b85fb9db8a8 NeedsCompilation: no Title: multivariate outlier detection for expression array QA Description: This package supports the application of diverse quality metrics to AffyBatch instances, summarizing these metrics via PCA, and then performing parametric outlier detection on the PCs to identify aberrant arrays with a fixed Type I error rate biocViews: Infrastructure, Microarray, QualityControl Author: Z. Gao, A. Asare, R. Wang, V. Carey Maintainer: V. Carey git_url: https://git.bioconductor.org/packages/arrayMvout git_branch: RELEASE_3_8 git_last_commit: 2b5461c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/arrayMvout_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/arrayMvout_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/arrayMvout_1.40.0.tgz vignettes: vignettes/arrayMvout/inst/doc/arrayMvout.pdf vignetteTitles: arrayMvout -- multivariate outlier algorithm for expression arrays hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/arrayMvout/inst/doc/arrayMvout.R Package: arrayQuality Version: 1.60.0 Depends: R (>= 2.2.0) Imports: graphics, grDevices, grid, gridBase, hexbin, limma, marray, methods, RColorBrewer, stats, utils Suggests: mclust, MEEBOdata, HEEBOdata License: LGPL MD5sum: e217db056836d45c77da1fa228ea7d87 NeedsCompilation: no Title: Assessing array quality on spotted arrays Description: Functions for performing print-run and array level quality assessment. biocViews: Microarray,TwoChannel,QualityControl,Visualization Author: Agnes Paquet and Jean Yee Hwa Yang Maintainer: Agnes Paquet URL: http://arrays.ucsf.edu/ git_url: https://git.bioconductor.org/packages/arrayQuality git_branch: RELEASE_3_8 git_last_commit: 6a053ab git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/arrayQuality_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/arrayQuality_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/arrayQuality_1.60.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: arrayQualityMetrics Version: 3.38.0 Imports: affy, affyPLM (>= 1.27.3), beadarray, Biobase, Cairo (>= 1.4-6), genefilter, graphics, grDevices, grid, gridSVG (>= 1.4-3), Hmisc, hwriter, lattice, latticeExtra, limma, methods, RColorBrewer, setRNG, stats, utils, vsn (>= 3.23.3), XML Suggests: ALLMLL, CCl4, BiocStyle, knitr License: LGPL (>= 2) MD5sum: c85ba7444832fd3da35ebeb206ac5dbc NeedsCompilation: no Title: Quality metrics report for microarray data sets Description: This package generates microarray quality metrics reports for data in Bioconductor microarray data containers (ExpressionSet, NChannelSet, AffyBatch). One and two color array platforms are supported. biocViews: Microarray, QualityControl, OneChannel, TwoChannel, ReportWriting Author: Audrey Kauffmann, Wolfgang Huber Maintainer: Mike Smith VignetteBuilder: knitr BugReports: https://github.com/grimbough/arrayQualityMetrics/issues git_url: https://git.bioconductor.org/packages/arrayQualityMetrics git_branch: RELEASE_3_8 git_last_commit: 4c80bb4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/arrayQualityMetrics_3.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/arrayQualityMetrics_3.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/arrayQualityMetrics_3.38.0.tgz vignettes: vignettes/arrayQualityMetrics/inst/doc/aqm.pdf, vignettes/arrayQualityMetrics/inst/doc/arrayQualityMetrics.pdf vignetteTitles: Advanced topics: Customizing arrayQualityMetrics reports and programmatic processing of the output, Introduction: microarray quality assessment with arrayQualityMetrics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/arrayQualityMetrics/inst/doc/aqm.R, vignettes/arrayQualityMetrics/inst/doc/arrayQualityMetrics.R importsMe: EGAD Package: ArrayTools Version: 1.42.0 Depends: R (>= 2.7.0), affy (>= 1.23.4), Biobase (>= 2.5.5), methods Imports: affy, Biobase, graphics, grDevices, limma, methods, stats, utils, xtable Suggests: simpleaffy, R2HTML, affydata, affyPLM, genefilter, annaffy, gcrma, hugene10sttranscriptcluster.db License: LGPL (>= 2.0) MD5sum: 2111784fb075319520ca6b6f1add616b NeedsCompilation: no Title: geneChip Analysis Package Description: This package is designed to provide solutions for quality assessment and to detect differentially expressed genes for the Affymetrix GeneChips, including both 3' -arrays and gene 1.0-ST arrays. The package generates comprehensive analysis reports in HTML format. Hyperlinks on the report page will lead to a series of QC plots, processed data, and differentially expressed gene lists. Differentially expressed genes are reported in tabular format with annotations hyperlinked to online biological databases. biocViews: Microarray, OneChannel, QualityControl, Preprocessing, StatisticalMethod, DifferentialExpression, Annotation, ReportWriting, Visualization Author: Xiwei Wu, Arthur Li Maintainer: Arthur Li git_url: https://git.bioconductor.org/packages/ArrayTools git_branch: RELEASE_3_8 git_last_commit: 7e8eab6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ArrayTools_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ArrayTools_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ArrayTools_1.42.0.tgz vignettes: vignettes/ArrayTools/inst/doc/ArrayTools.pdf vignetteTitles: 1. Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ArrayTools/inst/doc/ArrayTools.R Package: ArrayTV Version: 1.20.0 Depends: R (>= 2.14) Imports: methods, foreach, S4Vectors (>= 0.9.25), IRanges (>= 2.13.24), DNAcopy, oligoClasses (>= 1.21.3) Suggests: RColorBrewer, crlmm, ff, BSgenome.Hsapiens.UCSC.hg18,BSgenome.Hsapiens.UCSC.hg19, lattice, latticeExtra, RUnit, BiocGenerics Enhances: doMC, doSNOW, doParallel License: GPL (>= 2) MD5sum: 5cf6ce896c57f219ee738b6d9dfa8a7f NeedsCompilation: no Title: Implementation of wave correction for arrays Description: Wave correction for genotyping and copy number arrays biocViews: CopyNumberVariation Author: Eitan Halper-Stromberg Maintainer: Eitan Halper-Stromberg git_url: https://git.bioconductor.org/packages/ArrayTV git_branch: RELEASE_3_8 git_last_commit: 632852c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ArrayTV_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ArrayTV_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ArrayTV_1.20.0.tgz vignettes: vignettes/ArrayTV/inst/doc/ArrayTV.pdf vignetteTitles: ArrayTV Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ArrayTV/inst/doc/ArrayTV.R suggestsMe: VanillaICE Package: ARRmNormalization Version: 1.22.0 Depends: R (>= 2.15.1), ARRmData License: Artistic-2.0 MD5sum: 0007af10085c49def9f420ab8a14bfa0 NeedsCompilation: no Title: Adaptive Robust Regression normalization for Illumina methylation data Description: Perform the Adaptive Robust Regression method (ARRm) for the normalization of methylation data from the Illumina Infinium HumanMethylation 450k assay. biocViews: DNAMethylation, TwoChannel, Preprocessing, Microarray Author: Jean-Philippe Fortin, Celia M.T. Greenwood, Aurelie Labbe. Maintainer: Jean-Philippe Fortin git_url: https://git.bioconductor.org/packages/ARRmNormalization git_branch: RELEASE_3_8 git_last_commit: 3f2dc9c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ARRmNormalization_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ARRmNormalization_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ARRmNormalization_1.22.0.tgz vignettes: vignettes/ARRmNormalization/inst/doc/ARRmNormalization.pdf vignetteTitles: ARRmNormalization hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ARRmNormalization/inst/doc/ARRmNormalization.R Package: artMS Version: 1.0.12 Depends: R (>= 3.5.0) Imports: AnnotationDbi, biomaRt, bit64, circlize, cluster, ComplexHeatmap, corrplot, data.table, dplyr, factoextra, FactoMineR, getopt, ggdendro, ggplot2, gplots, ggrepel, gProfileR, graphics, grDevices, grid, limma, MSstats, openxlsx, org.Hs.eg.db, org.Mm.eg.db, PerformanceAnalytics, pheatmap, plotly, plyr, RColorBrewer, reshape2, seqinr, stats, stringr, tidyr, UpSetR, utils, VennDiagram, yaml Suggests: BiocStyle, knitr, rmarkdown, testthat License: GPL (>= 3) + file LICENSE MD5sum: 77f17057a8771f9f2596466d48360bd0 NeedsCompilation: no Title: Analytical R tools for Mass Spectrometry Description: artMS provides a set of tools for the analysis of proteomics label-free datasets. It takes as input the MaxQuant search result output (evidence.txt file) and performs quality control, relative quantification using MSstats, downstream analysis and integration. artMS also provides a set of functions to re-format and make it compatible with other analytical tools, including, SAINTq, SAINTexpress, Phosfate, and PHOTON. biocViews: Proteomics, DifferentialExpression, BiomedicalInformatics, SystemsBiology, MassSpectrometry, Annotation, QualityControl, GeneSetEnrichment, Clustering, Normalization, ImmunoOncology, MultipleComparison Author: David Jimenez-Morales, Alexandre Rosa Campos, John Von Dollen. Maintainer: David Jimenez-Morales URL: https://github.com/biodavidjm/artMS VignetteBuilder: knitr BugReports: https://github.com/biodavidjm/artMS/issues git_url: https://git.bioconductor.org/packages/artMS git_branch: RELEASE_3_8 git_last_commit: cb3b4fc git_last_commit_date: 2019-04-07 Date/Publication: 2019-04-08 source.ver: src/contrib/artMS_1.0.12.tar.gz win.binary.ver: bin/windows/contrib/3.5/artMS_1.0.12.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/artMS_1.0.12.tgz vignettes: vignettes/artMS/inst/doc/artMS_vignette.html vignetteTitles: Learn to use artMS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/artMS/inst/doc/artMS_vignette.R Package: ASAFE Version: 1.8.0 Depends: R (>= 3.2) Suggests: knitr, testthat License: Artistic-2.0 MD5sum: 514dbf478d594a68fd86ba799f35b51d NeedsCompilation: no Title: Ancestry Specific Allele Frequency Estimation Description: Given admixed individuals' bi-allelic SNP genotypes and ancestry pairs (where each ancestry can take one of three values) for multiple SNPs, perform an EM algorithm to deal with the fact that SNP genotypes are unphased with respect to ancestry pairs, in order to estimate ancestry-specific allele frequencies for all SNPs. biocViews: SNP, GenomeWideAssociation, LinkageDisequilibrium, BiomedicalInformatics, Genetics, ExperimentalDesign Author: Qian Zhang Maintainer: Qian Zhang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ASAFE git_branch: RELEASE_3_8 git_last_commit: dd07f4b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ASAFE_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASAFE_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASAFE_1.8.0.tgz vignettes: vignettes/ASAFE/inst/doc/ASAFE.pdf vignetteTitles: ASAFE (Ancestry Specific Allele Frequency Estimation) hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ASAFE/inst/doc/ASAFE.R Package: ASEB Version: 1.26.0 Depends: R (>= 2.8.0), methods Imports: graphics, methods, utils License: GPL (>= 3) Archs: i386, x64 MD5sum: 3051785401668b2ad729c669a876699e NeedsCompilation: yes Title: Predict Acetylated Lysine Sites Description: ASEB is an R package to predict lysine sites that can be acetylated by a specific KAT-family. biocViews: Proteomics Author: Likun Wang and Tingting Li . Maintainer: Likun Wang git_url: https://git.bioconductor.org/packages/ASEB git_branch: RELEASE_3_8 git_last_commit: 599765a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ASEB_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASEB_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASEB_1.26.0.tgz vignettes: vignettes/ASEB/inst/doc/ASEB.pdf vignetteTitles: ASEB hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ASEB/inst/doc/ASEB.R Package: ASGSCA Version: 1.16.0 Imports: Matrix, MASS Suggests: BiocStyle License: GPL-3 MD5sum: 1a540dfd5b527f46d89a54056ea29339 NeedsCompilation: no Title: Association Studies for multiple SNPs and multiple traits using Generalized Structured Equation Models Description: The package provides tools to model and test the association between multiple genotypes and multiple traits, taking into account the prior biological knowledge. Genes, and clinical pathways are incorporated in the model as latent variables. The method is based on Generalized Structured Component Analysis (GSCA). biocViews: StructuralEquationModels Author: Hela Romdhani, Stepan Grinek , Heungsun Hwang and Aurelie Labbe. Maintainer: Hela Romdhani git_url: https://git.bioconductor.org/packages/ASGSCA git_branch: RELEASE_3_8 git_last_commit: 925f146 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ASGSCA_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASGSCA_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASGSCA_1.16.0.tgz vignettes: vignettes/ASGSCA/inst/doc/ASGSCA.pdf vignetteTitles: Association Studies using Generalized Structured Equation Models. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ASGSCA/inst/doc/ASGSCA.R Package: ASICS Version: 1.2.0 Depends: R (>= 3.5) Imports: BiocParallel, ggplot2, grDevices, gridExtra, methods, plyr, quadprog, ropls, speaq, stats, SummarizedExperiment, utils, zoo Suggests: knitr, rmarkdown, BiocStyle, testthat, ASICSdata License: GPL (>= 2) MD5sum: 96b660a838b9d9edcf46b98c866ce4c1 NeedsCompilation: no Title: Automatic Statistical Identification in Complex Spectra Description: With a set of pure metabolite reference spectra, ASICS quantifies concentration of metabolites in a complex spectrum. The identification of metabolites is performed by fitting a mixture model to the spectra of the library with a sparse penalty. The method and its statistical properties are described in Tardivel et al. (2017) . biocViews: Software, DataImport, Cheminformatics, Metabolomics Author: Gaëlle Lefort [aut, cre], Rémi Servien [aut], Patrick Tardivel [aut], Nathalie Vialaneix [aut] Maintainer: Gaëlle Lefort VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ASICS git_branch: RELEASE_3_8 git_last_commit: 1d8644d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ASICS_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASICS_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASICS_1.2.0.tgz vignettes: vignettes/ASICS/inst/doc/ASICS.html, vignettes/ASICS/inst/doc/ASICSUsersGuide.html vignetteTitles: ASICS, ASICS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ASICS/inst/doc/ASICS.R, vignettes/ASICS/inst/doc/ASICSUsersGuide.R Package: ASpli Version: 1.8.1 Depends: methods, grDevices, stats, utils, parallel, edgeR Imports: GenomicRanges, GenomicFeatures, BiocGenerics, IRanges, GenomicAlignments, Gviz, S4Vectors, AnnotationDbi, Rsamtools, BiocStyle License: GPL MD5sum: 6d6db03f3faa099728762f6f67894b5a NeedsCompilation: no Title: Analysis of alternative splicing using RNA-Seq Description: Integrative pipeline for the analysis of alternative splicing using RNAseq. biocViews: ImmunoOncology, GeneExpression, Transcription, AlternativeSplicing, Coverage, DifferentialExpression, DifferentialSplicing, TimeCourse, RNASeq, GenomeAnnotation, Sequencing, Alignment Author: Estefania Mancini, Javier Iserte, Marcelo Yanovsky and Ariel Chernomoretz Maintainer: Estefania Mancini git_url: https://git.bioconductor.org/packages/ASpli git_branch: RELEASE_3_8 git_last_commit: a38e1df git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ASpli_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASpli_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASpli_1.8.1.tgz vignettes: vignettes/ASpli/inst/doc/ASpli.pdf vignetteTitles: Analysis of alternative splicing using ASpli hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ASpli/inst/doc/ASpli.R Package: AssessORF Version: 1.0.2 Depends: R (>= 3.5.0), DECIPHER (>= 2.8.0) Imports: Biostrings, GenomicRanges, IRanges, graphics, grDevices, methods, stats, utils Suggests: AssessORFData, BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: 2e28b613ca3a146a5e719e2ce6366ccf NeedsCompilation: no Title: Assess Gene Predictions Using Proteomics and Evolutionary Conservation Description: In order to assess the quality of a set of predicted genes for a genome, evidence must first be mapped to that genome. Next, each gene must be categorized based on how strong the evidence is for or against that gene. The AssessORF package provides the functions and class structures necessary for accomplishing those tasks, using proteomic hits and evolutionarily conserved start codons as the forms of evidence. biocViews: ComparativeGenomics, GenePrediction, GenomeAnnotation, Genetics, Proteomics, QualityControl, Visualization Author: Deepank Korandla [aut, cre], Erik Wright [aut] Maintainer: Deepank Korandla VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AssessORF git_branch: RELEASE_3_8 git_last_commit: 670115f git_last_commit_date: 2018-11-08 Date/Publication: 2018-11-08 source.ver: src/contrib/AssessORF_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/AssessORF_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AssessORF_1.0.2.tgz vignettes: vignettes/AssessORF/inst/doc/UsingAssessORF.pdf vignetteTitles: Using AssessORF hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AssessORF/inst/doc/UsingAssessORF.R Package: ASSET Version: 2.0.0 Depends: MASS, msm, rmeta Suggests: RUnit, BiocGenerics License: GPL-2 + file LICENSE MD5sum: 70928d9e0f7dac81d168732658f53b69 NeedsCompilation: no Title: An R package for subset-based association analysis of heterogeneous traits and subtypes Description: An R package for subset-based analysis of heterogeneous traits and subtypes biocViews: Software Author: Samsiddhi Bhattacharjee, Nilanjan Chatterjee and William Wheeler Maintainer: Samsiddhi Bhattacharjee git_url: https://git.bioconductor.org/packages/ASSET git_branch: RELEASE_3_8 git_last_commit: fb52c56 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ASSET_2.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASSET_2.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASSET_2.0.0.tgz vignettes: vignettes/ASSET/inst/doc/vignette.pdf vignetteTitles: ASSET Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ASSET/inst/doc/vignette.R dependsOnMe: REBET Package: ASSIGN Version: 1.18.0 Depends: R (>= 3.4) Imports: gplots, graphics, grDevices, msm, Rlab, stats, sva, utils, ggplot2, yaml Suggests: testthat, BiocStyle, knitr, rmarkdown License: MIT + file LICENSE MD5sum: cd78a27ed8e521787729a557227ceba6 NeedsCompilation: no Title: Adaptive Signature Selection and InteGratioN (ASSIGN) Description: ASSIGN is a computational tool to evaluate the pathway deregulation/activation status in individual patient samples. ASSIGN employs a flexible Bayesian factor analysis approach that adapts predetermined pathway signatures derived either from knowledge-based literature or from perturbation experiments to the cell-/tissue-specific pathway signatures. The deregulation/activation level of each context-specific pathway is quantified to a score, which represents the extent to which a patient sample encompasses the pathway deregulation/activation signature. biocViews: Software, GeneExpression, Pathways, Bayesian Author: Ying Shen, Andrea H. Bild, W. Evan Johnson, and Mumtehena Rahman Maintainer: Ying Shen , W. Evan Johnson , David Jenkins , Mumtehena Rahman URL: https://compbiomed.github.io/ASSIGN/ VignetteBuilder: knitr BugReports: https://github.com/compbiomed/ASSIGN/issues git_url: https://git.bioconductor.org/packages/ASSIGN git_branch: RELEASE_3_8 git_last_commit: 330bae8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ASSIGN_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ASSIGN_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ASSIGN_1.18.0.tgz vignettes: vignettes/ASSIGN/inst/doc/ASSIGN.vignette.html vignetteTitles: Primer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ASSIGN/inst/doc/ASSIGN.vignette.R Package: ATACseqQC Version: 1.6.4 Depends: R (>= 3.4), BiocGenerics, S4Vectors Imports: BSgenome, Biostrings, ChIPpeakAnno, IRanges, GenomicRanges, GenomicAlignments, GenomeInfoDb, GenomicScores, graphics, grid, limma, Rsamtools (>= 1.31.2), randomForest, rtracklayer, stats, motifStack, preseqR, utils, KernSmooth Suggests: BiocStyle, knitr, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, phastCons100way.UCSC.hg19, MotifDb, trackViewer, testthat License: GPL (>= 2) MD5sum: beb49cf02e2d39c45810d19cbea2dd59 NeedsCompilation: no Title: ATAC-seq Quality Control Description: ATAC-seq, an assay for Transposase-Accessible Chromatin using sequencing, is a rapid and sensitive method for chromatin accessibility analysis. It was developed as an alternative method to MNase-seq, FAIRE-seq and DNAse-seq. Comparing to the other methods, ATAC-seq requires less amount of the biological samples and time to process. In the process of analyzing several ATAC-seq dataset produced in our labs, we learned some of the unique aspects of the quality assessment for ATAC-seq data.To help users to quickly assess whether their ATAC-seq experiment is successful, we developed ATACseqQC package partially following the guideline published in Nature Method 2013 (Greenleaf et al.), including diagnostic plot of fragment size distribution, proportion of mitochondria reads, nucleosome positioning pattern, and CTCF or other Transcript Factor footprints. biocViews: Sequencing, DNASeq, ATACSeq, GeneRegulation, QualityControl, Coverage, NucleosomePositioning, ImmunoOncology Author: Jianhong Ou, Haibo Liu, Feng Yan, Jun Yu, Michelle Kelliher, Lucio Castilla, Nathan Lawson, Lihua Julie Zhu Maintainer: Jianhong Ou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ATACseqQC git_branch: RELEASE_3_8 git_last_commit: d1e2df6 git_last_commit_date: 2018-12-19 Date/Publication: 2018-12-19 source.ver: src/contrib/ATACseqQC_1.6.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/ATACseqQC_1.6.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ATACseqQC_1.6.4.tgz vignettes: vignettes/ATACseqQC/inst/doc/ATACseqQC.html vignetteTitles: ATACseqQC Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ATACseqQC/inst/doc/ATACseqQC.R Package: attract Version: 1.34.1 Depends: R (>= 3.4.0), AnnotationDbi Imports: Biobase, limma, cluster, GOstats, graphics, stats, reactome.db, KEGGREST, org.Hs.eg.db, utils, methods Suggests: illuminaHumanv1.db License: LGPL (>= 2.0) MD5sum: a4f853e6fed10a05773124a03a0bd2c8 NeedsCompilation: no Title: Methods to Find the Gene Expression Modules that Represent the Drivers of Kauffman's Attractor Landscape Description: This package contains the functions to find the gene expression modules that represent the drivers of Kauffman's attractor landscape. The modules are the core attractor pathways that discriminate between different cell types of groups of interest. Each pathway has a set of synexpression groups, which show transcriptionally-coordinated changes in gene expression. biocViews: ImmunoOncology, KEGG, Reactome, GeneExpression, Pathways, GeneSetEnrichment, Microarray, RNASeq Author: Jessica Mar Maintainer: Samuel Zimmerman git_url: https://git.bioconductor.org/packages/attract git_branch: RELEASE_3_8 git_last_commit: 9f14b65 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/attract_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/attract_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/attract_1.34.1.tgz vignettes: vignettes/attract/inst/doc/attract.pdf vignetteTitles: Tutorial on How to Use the Functions in the \texttt{attract} Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/attract/inst/doc/attract.R Package: AUCell Version: 1.4.1 Imports: data.table, graphics, grDevices, GSEABase, methods, mixtools, R.utils, shiny, stats, SummarizedExperiment, utils Suggests: Biobase, BiocStyle, devtools, DT, GEOquery, knitr, NMF, plotly, R2HTML, rbokeh, rmarkdown, Rtsne, testthat, zoo Enhances: doMC, doRNG, doParallel, foreach License: GPL-3 MD5sum: 170badbf1b074c59b28b7fb467f06897 NeedsCompilation: no Title: AUCell: Analysis of 'gene set' activity in single-cell RNA-seq data (e.g. identify cells with specific gene signatures) Description: AUCell allows to identify cells with active gene sets (e.g. signatures, gene modules...) in single-cell RNA-seq data. AUCell uses the "Area Under the Curve" (AUC) to calculate whether a critical subset of the input gene set is enriched within the expressed genes for each cell. The distribution of AUC scores across all the cells allows exploring the relative expression of the signature. Since the scoring method is ranking-based, AUCell is independent of the gene expression units and the normalization procedure. In addition, since the cells are evaluated individually, it can easily be applied to bigger datasets, subsetting the expression matrix if needed. biocViews: ImmunoOncology, SingleCell, GeneSetEnrichment, Transcriptomics, Transcription, GeneExpression, WorkflowStep, Normalization Author: Sara Aibar, Stein Aerts. Laboratory of Computational Biology. VIB-KU Leuven Center for Brain & Disease Research. Leuven, Belgium Maintainer: Sara Aibar URL: http://scenic.aertslab.org VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/AUCell git_branch: RELEASE_3_8 git_last_commit: 58b6e2a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/AUCell_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/AUCell_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/AUCell_1.4.1.tgz vignettes: vignettes/AUCell/inst/doc/AUCell.html vignetteTitles: AUCell: Identifying cells with active gene sets hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/AUCell/inst/doc/AUCell.R importsMe: RcisTarget Package: BaalChIP Version: 1.8.0 Depends: R (>= 3.3.1), GenomicRanges, IRanges, Rsamtools, Imports: GenomicAlignments, GenomeInfoDb, doParallel, parallel, doBy, reshape2, scales, coda, foreach, ggplot2, methods, utils, graphics, stats Suggests: RUnit, BiocGenerics, knitr, rmarkdown, BiocStyle License: Artistic-2.0 MD5sum: d2f63d691155d6831cae2aa3a10277a7 NeedsCompilation: no Title: BaalChIP: Bayesian analysis of allele-specific transcription factor binding in cancer genomes Description: The package offers functions to process multiple ChIP-seq BAM files and detect allele-specific events. Computes allele counts at individual variants (SNPs/SNVs), implements extensive QC steps to remove problematic variants, and utilizes a bayesian framework to identify statistically significant allele- specific events. BaalChIP is able to account for copy number differences between the two alleles, a known phenotypical feature of cancer samples. biocViews: Software, ChIPSeq, Bayesian, Sequencing Author: Ines de Santiago, Wei Liu, Ke Yuan, Martin O'Reilly, Chandra SR Chilamakuri, Bruce Ponder, Kerstin Meyer, Florian Markowetz Maintainer: Ines de Santiago VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BaalChIP git_branch: RELEASE_3_8 git_last_commit: 291c42f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BaalChIP_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BaalChIP_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BaalChIP_1.8.0.tgz vignettes: vignettes/BaalChIP/inst/doc/BaalChIP.html vignetteTitles: Analyzing ChIP-seq and FAIRE-seq data with the BaalChIP package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BaalChIP/inst/doc/BaalChIP.R Package: BAC Version: 1.42.0 Depends: R (>= 2.10) License: Artistic-2.0 Archs: i386, x64 MD5sum: 1d862459cdf5b19fa4d1f45825a2ef46 NeedsCompilation: yes Title: Bayesian Analysis of Chip-chip experiment Description: This package uses a Bayesian hierarchical model to detect enriched regions from ChIP-chip experiments biocViews: Microarray, Transcription Author: Raphael Gottardo Maintainer: Raphael Gottardo git_url: https://git.bioconductor.org/packages/BAC git_branch: RELEASE_3_8 git_last_commit: cd9afba git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BAC_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BAC_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BAC_1.42.0.tgz vignettes: vignettes/BAC/inst/doc/BAC.pdf vignetteTitles: 1. Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BAC/inst/doc/BAC.R Package: bacon Version: 1.10.1 Depends: R (>= 3.3), methods, stats, ggplot2, graphics, BiocParallel, ellipse Suggests: BiocStyle, knitr, rmarkdown, testthat, roxygen2 License: GPL (>= 2) Archs: i386, x64 MD5sum: 306b2c63ff90c3584aa904ceb4ad3c72 NeedsCompilation: yes Title: Controlling bias and inflation in association studies using the empirical null distribution Description: Bacon can be used to remove inflation and bias often observed in epigenome- and transcriptome-wide association studies. To this end bacon constructs an empirical null distribution using a Gibbs Sampling algorithm by fitting a three-component normal mixture on z-scores. biocViews: ImmunoOncology, StatisticalMethod, Bayesian, Regression, GenomeWideAssociation, Transcriptomics, RNASeq, MethylationArray, BatchEffect, MultipleComparison Author: Maarten van Iterson [aut, cre], Erik van Zwet [ctb] Maintainer: Maarten van Iterson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/bacon git_branch: RELEASE_3_8 git_last_commit: f8f5cb0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/bacon_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/bacon_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bacon_1.10.1.tgz vignettes: vignettes/bacon/inst/doc/bacon.html vignetteTitles: Controlling bias and inflation in association studies using the empirical null distribution hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bacon/inst/doc/bacon.R Package: BADER Version: 1.20.1 Suggests: pasilla (>= 0.2.10) License: GPL-2 Archs: i386, x64 MD5sum: 7cea340eb46d86d415094f8ee014a934 NeedsCompilation: yes Title: Bayesian Analysis of Differential Expression in RNA Sequencing Data Description: For RNA sequencing count data, BADER fits a Bayesian hierarchical model. The algorithm returns the posterior probability of differential expression for each gene between two groups A and B. The joint posterior distribution of the variables in the model can be returned in the form of posterior samples, which can be used for further down-stream analyses such as gene set enrichment. biocViews: ImmunoOncology, Sequencing, RNASeq, DifferentialExpression, Software, SAGE Author: Andreas Neudecker, Matthias Katzfuss Maintainer: Andreas Neudecker git_url: https://git.bioconductor.org/packages/BADER git_branch: RELEASE_3_8 git_last_commit: 05ec83c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BADER_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BADER_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BADER_1.20.1.tgz vignettes: vignettes/BADER/inst/doc/BADER.pdf vignetteTitles: Analysing RNA-Seq data with the "BADER" package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BADER/inst/doc/BADER.R Package: BadRegionFinder Version: 1.10.0 Imports: VariantAnnotation, Rsamtools, biomaRt, GenomicRanges, S4Vectors, utils, stats, grDevices, graphics Suggests: BSgenome.Hsapiens.UCSC.hg19 License: LGPL-3 MD5sum: 1e8c8450b18124340da912960d9a7d13 NeedsCompilation: no Title: BadRegionFinder: an R/Bioconductor package for identifying regions with bad coverage Description: BadRegionFinder is a package for identifying regions with a bad, acceptable and good coverage in sequence alignment data available as bam files. The whole genome may be considered as well as a set of target regions. Various visual and textual types of output are available. biocViews: Coverage, Sequencing, Alignment, WholeGenome, Classification Author: Sarah Sandmann Maintainer: Sarah Sandmann git_url: https://git.bioconductor.org/packages/BadRegionFinder git_branch: RELEASE_3_8 git_last_commit: c8a8695 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BadRegionFinder_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BadRegionFinder_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BadRegionFinder_1.10.0.tgz vignettes: vignettes/BadRegionFinder/inst/doc/BadRegionFinder.pdf vignetteTitles: Using BadRegionFinder hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BadRegionFinder/inst/doc/BadRegionFinder.R Package: BAGS Version: 2.22.0 Depends: R (>= 2.10), breastCancerVDX, Biobase License: Artistic-2.0 Archs: i386, x64 MD5sum: 2d000e29d269eb8f93a2eabcd1436182 NeedsCompilation: yes Title: A Bayesian Approach for Geneset Selection Description: R package providing functions to perform geneset significance analysis over simple cross-sectional data between 2 and 5 phenotypes of interest. biocViews: Bayesian Author: Alejandro Quiroz-Zarate Maintainer: Alejandro Quiroz-Zarate git_url: https://git.bioconductor.org/packages/BAGS git_branch: RELEASE_3_8 git_last_commit: ff9fe81 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BAGS_2.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BAGS_2.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BAGS_2.22.0.tgz vignettes: vignettes/BAGS/inst/doc/BAGS.pdf vignetteTitles: BAGS: A Bayesian Approach for Geneset Selection. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BAGS/inst/doc/BAGS.R Package: ballgown Version: 2.14.1 Depends: R (>= 3.1.1), methods Imports: GenomicRanges (>= 1.17.25), IRanges (>= 1.99.22), S4Vectors (>= 0.9.39), RColorBrewer, splines, sva, limma, rtracklayer (>= 1.29.25), Biobase (>= 2.25.0), GenomeInfoDb Suggests: testthat, knitr License: Artistic-2.0 MD5sum: 44df7a386da33b9c4f6627ff977e260d NeedsCompilation: no Title: Flexible, isoform-level differential expression analysis Description: Tools for statistical analysis of assembled transcriptomes, including flexible differential expression analysis, visualization of transcript structures, and matching of assembled transcripts to annotation. biocViews: ImmunoOncology, RNASeq, StatisticalMethod, Preprocessing, DifferentialExpression Author: Jack Fu [aut], Alyssa C. Frazee [aut, cre], Leonardo Collado-Torres [aut], Andrew E. Jaffe [aut], Jeffrey T. Leek [aut, ths] Maintainer: Jack Fu VignetteBuilder: knitr BugReports: https://github.com/alyssafrazee/ballgown/issues git_url: https://git.bioconductor.org/packages/ballgown git_branch: RELEASE_3_8 git_last_commit: aa95afd git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ballgown_2.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ballgown_2.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ballgown_2.14.1.tgz vignettes: vignettes/ballgown/inst/doc/ballgown.html vignetteTitles: Flexible isoform-level differential expression analysis with Ballgown hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ballgown/inst/doc/ballgown.R importsMe: RNASeqR suggestsMe: polyester, variancePartition Package: bamsignals Version: 1.14.0 Depends: R (>= 3.2.0) Imports: methods, BiocGenerics, Rcpp (>= 0.10.6), IRanges, GenomicRanges, zlibbioc LinkingTo: Rcpp, Rhtslib (>= 1.13.1), zlibbioc Suggests: testthat (>= 0.9), Rsamtools, BiocStyle, knitr, rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 5d36b092f1a9e17de3b7f39ea838f7dc NeedsCompilation: yes Title: Extract read count signals from bam files Description: This package allows to efficiently obtain count vectors from indexed bam files. It counts the number of reads in given genomic ranges and it computes reads profiles and coverage profiles. It also handles paired-end data. biocViews: DataImport, Sequencing, Coverage, Alignment Author: Alessandro Mammana [aut, cre], Johannes Helmuth [aut] Maintainer: Alessandro Mammana VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/bamsignals git_branch: RELEASE_3_8 git_last_commit: 3107d3a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bamsignals_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bamsignals_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bamsignals_1.14.0.tgz vignettes: vignettes/bamsignals/inst/doc/bamsignals.html vignetteTitles: Introduction to the bamsignals package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bamsignals/inst/doc/bamsignals.R importsMe: AneuFinder, chromstaR, karyoploteR, normr Package: banocc Version: 1.6.1 Depends: R (>= 3.5.1), rstan (>= 2.17.4) Imports: coda (>= 0.18.1), mvtnorm, stringr Suggests: knitr, rmarkdown, methods, testthat License: MIT + file LICENSE MD5sum: 1803b7e6681726b610bd4e7ea3f5bce3 NeedsCompilation: no Title: Bayesian ANalysis Of Compositional Covariance Description: BAnOCC is a package designed for compositional data, where each sample sums to one. It infers the approximate covariance of the unconstrained data using a Bayesian model coded with `rstan`. It provides as output the `stanfit` object as well as posterior median and credible interval estimates for each correlation element. biocViews: ImmunoOncology, Metagenomics, Software, Bayesian Author: Emma Schwager [aut, cre], Curtis Huttenhower [aut] Maintainer: George Weingart , Curtis Huttenhower SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/banocc git_branch: RELEASE_3_8 git_last_commit: b669beb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/banocc_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/banocc_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/banocc_1.6.1.tgz vignettes: vignettes/banocc/inst/doc/banocc-vignette.html vignetteTitles: BAnOCC (Bayesian Analysis of Compositional Covariance) hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/banocc/inst/doc/banocc-vignette.R Package: basecallQC Version: 1.6.0 Depends: R (>= 3.4), stats, utils, methods, rmarkdown, knitr, prettydoc, yaml Imports: ggplot2, stringr, XML, raster, dplyr, data.table, tidyr, magrittr, DT, lazyeval, ShortRead Suggests: testthat, BiocStyle License: GPL (>= 3) MD5sum: 88e03b7e9ba40099f69694c3b228bbe5 NeedsCompilation: no Title: Working with Illumina Basecalling and Demultiplexing input and output files Description: The basecallQC package provides tools to work with Illumina bcl2Fastq (versions >= 2.1.7) software.Prior to basecalling and demultiplexing using the bcl2Fastq software, basecallQC functions allow the user to update Illumina sample sheets from versions <= 1.8.9 to >= 2.1.7 standards, clean sample sheets of common problems such as invalid sample names and IDs, create read and index basemasks and the bcl2Fastq command. Following the generation of basecalled and demultiplexed data, the basecallQC packages allows the user to generate HTML tables, plots and a self contained report of summary metrics from Illumina XML output files. biocViews: Sequencing, Infrastructure, DataImport, QualityControl Author: Thomas Carroll and Marian Dore Maintainer: Thomas Carroll SystemRequirements: bcl2Fastq (versions >= 2.1.7) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/basecallQC git_branch: RELEASE_3_8 git_last_commit: 2a64547 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/basecallQC_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/basecallQC_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/basecallQC_1.6.0.tgz vignettes: vignettes/basecallQC/inst/doc/basecallQC.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/basecallQC/inst/doc/basecallQC.R Package: BaseSpaceR Version: 1.26.0 Depends: R (>= 2.15.0), RCurl, RJSONIO Imports: methods Suggests: RUnit, IRanges, Rsamtools License: Apache License 2.0 MD5sum: 25da31488eb0751ca13b4c24ef1d27f0 NeedsCompilation: no Title: R SDK for BaseSpace RESTful API Description: A rich R interface to Illumina's BaseSpace cloud computing environment, enabling the fast development of data analysis and visualisation tools. biocViews: Infrastructure, DataRepresentation, ConnectTools, Software, DataImport, HighThroughputSequencing, Sequencing, Genetics Author: Adrian Alexa Maintainer: Jared O'Connell git_url: https://git.bioconductor.org/packages/BaseSpaceR git_branch: RELEASE_3_8 git_last_commit: 122b803 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BaseSpaceR_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BaseSpaceR_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BaseSpaceR_1.26.0.tgz vignettes: vignettes/BaseSpaceR/inst/doc/BaseSpaceR.pdf vignetteTitles: BaseSpaceR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BaseSpaceR/inst/doc/BaseSpaceR.R Package: Basic4Cseq Version: 1.18.1 Depends: R (>= 3.4), Biostrings, GenomicAlignments, caTools, GenomicRanges, grDevices, graphics, stats, utils Imports: methods, RCircos, BSgenome.Ecoli.NCBI.20080805 Suggests: BSgenome.Hsapiens.UCSC.hg19 License: LGPL-3 MD5sum: 3758e6693d8be05452867aae9c139b8a NeedsCompilation: no Title: Basic4Cseq: an R/Bioconductor package for analyzing 4C-seq data Description: Basic4Cseq is an R/Bioconductor package for basic filtering, analysis and subsequent visualization of 4C-seq data. Virtual fragment libraries can be created for any BSGenome package, and filter functions for both reads and fragments and basic quality controls are included. Fragment data in the vicinity of the experiment's viewpoint can be visualized as a coverage plot based on a running median approach and a multi-scale contact profile. biocViews: ImmunoOncology, Visualization, QualityControl, Sequencing, Coverage, Alignment, RNASeq, SequenceMatching, DataImport Author: Carolin Walter Maintainer: Carolin Walter git_url: https://git.bioconductor.org/packages/Basic4Cseq git_branch: RELEASE_3_8 git_last_commit: ade9a72 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Basic4Cseq_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Basic4Cseq_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Basic4Cseq_1.18.1.tgz vignettes: vignettes/Basic4Cseq/inst/doc/vignette.pdf vignetteTitles: Basic4Cseq: an R/Bioconductor package for the analysis of 4C-seq data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Basic4Cseq/inst/doc/vignette.R Package: BASiCS Version: 1.4.7 Depends: R (>= 3.5), SingleCellExperiment, KernSmooth, ggplot2 Imports: BiocGenerics, methods, coda, data.table, graphics, grDevices, MASS, matrixStats, Rcpp (>= 0.11.3), S4Vectors, scran, stats, SummarizedExperiment, testthat, utils LinkingTo: Rcpp, RcppArmadillo Suggests: BiocStyle, knitr, rmarkdown License: GPL (>= 2) Archs: i386, x64 MD5sum: de937a3a82e68114407df790d6e46644 NeedsCompilation: yes Title: Bayesian Analysis of Single-Cell Sequencing data Description: Single-cell mRNA sequencing can uncover novel cell-to-cell heterogeneity in gene expression levels in seemingly homogeneous populations of cells. However, these experiments are prone to high levels of technical noise, creating new challenges for identifying genes that show genuine heterogeneous expression within the population of cells under study. BASiCS (Bayesian Analysis of Single-Cell Sequencing data) is an integrated Bayesian hierarchical model to perform statistical analyses of single-cell RNA sequencing datasets in the context of supervised experiments (where the groups of cells of interest are known a priori, e.g. experimental conditions or cell types). BASiCS performs built-in data normalisation (global scaling) and technical noise quantification (based on spike-in genes). BASiCS provides an intuitive detection criterion for highly (or lowly) variable genes within a single group of cells. Additionally, BASiCS can compare gene expression patterns between two or more pre-specified groups of cells. Unlike traditional differential expression tools, BASiCS quantifies changes in expression that lie beyond comparisons of means, also allowing the study of changes in cell-to-cell heterogeneity. The latter can be quantified via a biological over-dispersion parameter that measures the excess of variability that is observed with respect to Poisson sampling noise, after normalisation and technical noise removal. Due to the strong mean/over-dispersion confounding that is typically observed for scRNA-seq datasets, BASiCS also tests for changes in residual over-dispersion, defined by residual values with respect to a global mean/over-dispersion trend. biocViews: ImmunoOncology, Normalization, Sequencing, RNASeq, Software, GeneExpression, Transcriptomics, SingleCell, DifferentialExpression, Bayesian, CellBiology Author: Catalina Vallejos [aut, cre], Nils Eling [aut], Alan O'Callaghan [ctb], Sylvia Richardson [ctb], John Marioni [ctb] Maintainer: Catalina A. Vallejos , Nils Eling URL: https://github.com/catavallejos/BASiCS SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/catavallejos/BASiCS/issues git_url: https://git.bioconductor.org/packages/BASiCS git_branch: RELEASE_3_8 git_last_commit: 56a7c64 git_last_commit_date: 2019-03-22 Date/Publication: 2019-03-22 source.ver: src/contrib/BASiCS_1.4.7.tar.gz win.binary.ver: bin/windows/contrib/3.5/BASiCS_1.4.7.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BASiCS_1.4.7.tgz vignettes: vignettes/BASiCS/inst/doc/BASiCS.html vignetteTitles: Introduction to BASiCS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BASiCS/inst/doc/BASiCS.R suggestsMe: splatter Package: BasicSTARRseq Version: 1.10.0 Depends: GenomicRanges,GenomicAlignments Imports: S4Vectors,methods,IRanges,GenomeInfoDb,stats Suggests: knitr License: LGPL-3 MD5sum: 6ef49c32242bce2db8d44a695ed756a8 NeedsCompilation: no Title: Basic peak calling on STARR-seq data Description: Basic peak calling on STARR-seq data based on a method introduced in "Genome-Wide Quantitative Enhancer Activity Maps Identified by STARR-seq" Arnold et al. Science. 2013 Mar 1;339(6123):1074-7. doi: 10.1126/science. 1232542. Epub 2013 Jan 17. biocViews: PeakDetection, GeneRegulation, FunctionalPrediction, FunctionalGenomics, Coverage Author: Annika Buerger Maintainer: Annika Buerger VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BasicSTARRseq git_branch: RELEASE_3_8 git_last_commit: a5ca3a3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BasicSTARRseq_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BasicSTARRseq_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BasicSTARRseq_1.10.0.tgz vignettes: vignettes/BasicSTARRseq/inst/doc/BasicSTARRseq.pdf vignetteTitles: BasicSTARRseq.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BasicSTARRseq/inst/doc/BasicSTARRseq.R Package: BatchQC Version: 1.10.1 Depends: R (>= 3.3.0) Imports: utils, rmarkdown, knitr, pander, gplots, MCMCpack, shiny, sva, corpcor, moments, matrixStats, ggvis, d3heatmap, reshape2, limma, grDevices, graphics, stats, methods, Matrix Suggests: testthat License: GPL (>= 2) MD5sum: 5011c3bec69aa680c0d3e6130b483dcd NeedsCompilation: no Title: Batch Effects Quality Control Software Description: Sequencing and microarray samples often are collected or processed in multiple batches or at different times. This often produces technical biases that can lead to incorrect results in the downstream analysis. BatchQC is a software tool that streamlines batch preprocessing and evaluation by providing interactive diagnostics, visualizations, and statistical analyses to explore the extent to which batch variation impacts the data. BatchQC diagnostics help determine whether batch adjustment needs to be done, and how correction should be applied before proceeding with a downstream analysis. Moreover, BatchQC interactively applies multiple common batch effect approaches to the data, and the user can quickly see the benefits of each method. BatchQC is developed as a Shiny App. The output is organized into multiple tabs, and each tab features an important part of the batch effect analysis and visualization of the data. The BatchQC interface has the following analysis groups: Summary, Differential Expression, Median Correlations, Heatmaps, Circular Dendrogram, PCA Analysis, Shape, ComBat and SVA. biocViews: BatchEffect, GraphAndNetwork, Microarray, PrincipalComponent, Sequencing, Software, Visualization, QualityControl, RNASeq, Preprocessing, DifferentialExpression, ImmunoOncology Author: Solaiappan Manimaran , W. Evan Johnson , Heather Selby , Claire Ruberman , Kwame Okrah , Hector Corrada Bravo Maintainer: Solaiappan Manimaran URL: https://github.com/mani2012/BatchQC SystemRequirements: pandoc (http://pandoc.org/installing.html) for generating reports from markdown files. VignetteBuilder: knitr BugReports: https://github.com/mani2012/BatchQC/issues git_url: https://git.bioconductor.org/packages/BatchQC git_branch: RELEASE_3_8 git_last_commit: 08477be git_last_commit_date: 2018-12-01 Date/Publication: 2018-12-02 source.ver: src/contrib/BatchQC_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BatchQC_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BatchQC_1.10.1.tgz vignettes: vignettes/BatchQC/inst/doc/BatchQC_usage_advanced.pdf, vignettes/BatchQC/inst/doc/BatchQC_examples.html, vignettes/BatchQC/inst/doc/BatchQCIntro.html vignetteTitles: BatchQC_usage_advanced, BatchQC_examples, BatchQCIntro hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BatchQC/inst/doc/BatchQC_usage_advanced.R Package: BayesKnockdown Version: 1.8.0 Depends: R (>= 3.3) Imports: stats, Biobase License: GPL-3 MD5sum: 75b7426ec5da2b1e3513f9f78c739412 NeedsCompilation: no Title: BayesKnockdown: Posterior Probabilities for Edges from Knockdown Data Description: A simple, fast Bayesian method for computing posterior probabilities for relationships between a single predictor variable and multiple potential outcome variables, incorporating prior probabilities of relationships. In the context of knockdown experiments, the predictor variable is the knocked-down gene, while the other genes are potential targets. Can also be used for differential expression/2-class data. biocViews: NetworkInference, GeneExpression, GeneTarget, Network, Bayesian Author: William Chad Young Maintainer: William Chad Young git_url: https://git.bioconductor.org/packages/BayesKnockdown git_branch: RELEASE_3_8 git_last_commit: a8bd135 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BayesKnockdown_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BayesKnockdown_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BayesKnockdown_1.8.0.tgz vignettes: vignettes/BayesKnockdown/inst/doc/BayesKnockdown.pdf vignetteTitles: BayesKnockdown.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BayesKnockdown/inst/doc/BayesKnockdown.R Package: BayesPeak Version: 1.34.0 Depends: R (>= 2.14), IRanges Imports: IRanges, graphics Suggests: BiocStyle, parallel License: GPL (>= 2) Archs: i386, x64 MD5sum: e92c2c9940b0329142b613fe625eba15 NeedsCompilation: yes Title: Bayesian Analysis of ChIP-seq Data Description: This package is an implementation of the BayesPeak algorithm for peak-calling in ChIP-seq data. biocViews: ChIPSeq Author: Christiana Spyrou, Jonathan Cairns, Rory Stark, Andy Lynch, Simon Tavar\\'{e}, Maintainer: Jonathan Cairns git_url: https://git.bioconductor.org/packages/BayesPeak git_branch: RELEASE_3_8 git_last_commit: e691788 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BayesPeak_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BayesPeak_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BayesPeak_1.34.0.tgz vignettes: vignettes/BayesPeak/inst/doc/BayesPeak.pdf vignetteTitles: BayesPeak Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BayesPeak/inst/doc/BayesPeak.R Package: bayNorm Version: 1.0.9 Depends: R (>= 3.5), Imports: Rcpp (>= 0.12.12), BB, foreach, iterators, doSNOW, parallel, MASS, locfit, fitdistrplus, stats, methods, graphics, grDevices, SingleCellExperiment, SummarizedExperiment, BiocParallel, utils LinkingTo: Rcpp, RcppArmadillo,RcppProgress Suggests: knitr, rmarkdown, BiocStyle, devtools, testthat License: GPL (>= 2) Archs: i386, x64 MD5sum: 977d8286593a38b3741742c979d88798 NeedsCompilation: yes Title: Single-cell RNA sequencing data normalization Description: bayNorm is used for normalizing single-cell RNA-seq data. biocViews: ImmunoOncology, Normalization, RNASeq, SingleCell,Sequencing Author: Wenhao Tang [aut, cre], Franois Bertaux [aut], Philipp Thomas [aut], Claire Stefanelli [aut], Malika Saint [aut], Samuel Marguerat [aut], Vahid Shahrezaei [aut] Maintainer: Wenhao Tang URL: https://github.com/WT215/bayNorm VignetteBuilder: knitr BugReports: https://github.com/WT215/bayNorm/issues git_url: https://git.bioconductor.org/packages/bayNorm git_branch: RELEASE_3_8 git_last_commit: 888f4d0 git_last_commit_date: 2019-03-26 Date/Publication: 2019-03-26 source.ver: src/contrib/bayNorm_1.0.9.tar.gz win.binary.ver: bin/windows/contrib/3.5/bayNorm_1.0.9.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bayNorm_1.0.9.tgz vignettes: vignettes/bayNorm/inst/doc/bayNorm.html vignetteTitles: Introduction to bayNorm hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bayNorm/inst/doc/bayNorm.R Package: baySeq Version: 2.16.0 Depends: R (>= 2.3.0), methods, GenomicRanges, abind, parallel Imports: edgeR Suggests: BiocStyle, BiocGenerics License: GPL-3 MD5sum: 640b6b622f46258525fecc4304ffbac5 NeedsCompilation: no Title: Empirical Bayesian analysis of patterns of differential expression in count data Description: This package identifies differential expression in high-throughput 'count' data, such as that derived from next-generation sequencing machines, calculating estimated posterior likelihoods of differential expression (or more complex hypotheses) via empirical Bayesian methods. biocViews: Sequencing, DifferentialExpression, MultipleComparison, SAGE Author: Thomas J. Hardcastle Maintainer: Thomas J. Hardcastle git_url: https://git.bioconductor.org/packages/baySeq git_branch: RELEASE_3_8 git_last_commit: bc1df9c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/baySeq_2.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/baySeq_2.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/baySeq_2.16.0.tgz vignettes: vignettes/baySeq/inst/doc/baySeq_generic.pdf, vignettes/baySeq/inst/doc/baySeq.pdf vignetteTitles: Advanced baySeq analyses, baySeq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/baySeq/inst/doc/baySeq_generic.R, vignettes/baySeq/inst/doc/baySeq.R dependsOnMe: clusterSeq, Rcade, segmentSeq, TCC importsMe: EDDA, metaseqR, riboSeqR suggestsMe: compcodeR Package: BBCAnalyzer Version: 1.12.0 Imports: SummarizedExperiment, VariantAnnotation, Rsamtools, grDevices, GenomicRanges, IRanges, Biostrings Suggests: BSgenome.Hsapiens.UCSC.hg19 License: LGPL-3 MD5sum: a43ebce794b431b5600923809bbd81f8 NeedsCompilation: no Title: BBCAnalyzer: an R/Bioconductor package for visualizing base counts Description: BBCAnalyzer is a package for visualizing the relative or absolute number of bases, deletions and insertions at defined positions in sequence alignment data available as bam files in comparison to the reference bases. Markers for the relative base frequencies, the mean quality of the detected bases, known mutations or polymorphisms and variants called in the data may additionally be included in the plots. biocViews: Sequencing, Alignment, Coverage, GeneticVariability, SNP Author: Sarah Sandmann Maintainer: Sarah Sandmann git_url: https://git.bioconductor.org/packages/BBCAnalyzer git_branch: RELEASE_3_8 git_last_commit: 97364cf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BBCAnalyzer_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BBCAnalyzer_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BBCAnalyzer_1.12.0.tgz vignettes: vignettes/BBCAnalyzer/inst/doc/BBCAnalyzer.pdf vignetteTitles: Using BBCAnalyzer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BBCAnalyzer/inst/doc/BBCAnalyzer.R Package: BCRANK Version: 1.44.0 Depends: methods Imports: Biostrings Suggests: seqLogo License: GPL-2 Archs: i386, x64 MD5sum: 69400b8a8212a30ece13daec99343f3d NeedsCompilation: yes Title: Predicting binding site consensus from ranked DNA sequences Description: Functions and classes for de novo prediction of transcription factor binding consensus by heuristic search biocViews: MotifDiscovery, GeneRegulation Author: Adam Ameur Maintainer: Adam Ameur git_url: https://git.bioconductor.org/packages/BCRANK git_branch: RELEASE_3_8 git_last_commit: 4889b82 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BCRANK_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BCRANK_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BCRANK_1.44.0.tgz vignettes: vignettes/BCRANK/inst/doc/BCRANK.pdf vignetteTitles: BCRANK hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BCRANK/inst/doc/BCRANK.R suggestsMe: universalmotif Package: bcSeq Version: 1.4.1 Depends: R (>= 3.4) Imports: Rcpp (>= 0.12.12), Matrix, Biostrings LinkingTo: Rcpp, Matrix Suggests: knitr License: GPL (>= 2) Archs: i386, x64 MD5sum: c7f99bb847fa352b64aceaf3c336b081 NeedsCompilation: yes Title: Fast Sequence Mapping in High-Throughput shRNA and CRISPR Screens Description: This Rcpp-based package implements a highly efficient data structure and algorithm for performing alignment of short reads from CRISPR or shRNA screens to reference barcode library. Sequencing error are considered and matching qualities are evaluated based on Phred scores. A Bayes' classifier is employed to predict the originating barcode of a read. The package supports provision of user-defined probability models for evaluating matching qualities. The package also supports multi-threading. biocViews: ImmunoOncology, Alignment, CRISPR, Sequencing, SequenceMatching, MultipleSequenceAlignment, Software Author: Jiaxing Lin [aut, cre], Jeremy Gresham [aut], Jichun Xie [aut], Kouros Owzar [aut], Tongrong Wang [ctb], So Young Kim [ctb], James Alvarez [ctb], Jeffrey S. Damrauer [ctb], Scott Floyd [ctb], Joshua Granek [ctb], Andrew Allen [ctb], Cliburn Chan [ctb] Maintainer: Jiaxing Lin URL: https://github.com/jl354/bcSeq VignetteBuilder: knitr BugReports: https://support.bioconductor.org git_url: https://git.bioconductor.org/packages/bcSeq git_branch: RELEASE_3_8 git_last_commit: 5777ce5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/bcSeq_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/bcSeq_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bcSeq_1.4.1.tgz vignettes: vignettes/bcSeq/inst/doc/bcSeq.pdf vignetteTitles: bcSeq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bcSeq/inst/doc/bcSeq.R Package: BDMMAcorrect Version: 1.0.1 Depends: R (>= 3.5), vegan, ellipse, ggplot2, ape, SummarizedExperiment Imports: Rcpp (>= 0.12.12), RcppArmadillo, RcppEigen, stats LinkingTo: Rcpp, RcppArmadillo, RcppEigen Suggests: knitr, rmarkdown, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: 6b77eed0ed2024a6079ae76fd8a9f2bd NeedsCompilation: yes Title: Meta-analysis for the metagenomic read counts data from different cohorts Description: Metagenomic sequencing techniques enable quantitative analyses of the microbiome. However, combining the microbial data from these experiments is challenging due to the variations between experiments. The existing methods for correcting batch effects do not consider the interactions between variables—microbial taxa in microbial studies—and the overdispersion of the microbiome data. Therefore, they are not applicable to microbiome data. We develop a new method, Bayesian Dirichlet-multinomial regression meta-analysis (BDMMA), to simultaneously model the batch effects and detect the microbial taxa associated with phenotypes. BDMMA automatically models the dependence among microbial taxa and is robust to the high dimensionality of the microbiome and their association sparsity. biocViews: ImmunoOncology, BatchEffect, Microbiome, Bayesian Author: ZHENWEI DAI Maintainer: ZHENWEI DAI VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BDMMAcorrect git_branch: RELEASE_3_8 git_last_commit: 6fe7f5f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BDMMAcorrect_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BDMMAcorrect_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BDMMAcorrect_1.0.1.tgz vignettes: vignettes/BDMMAcorrect/inst/doc/Vignette.pdf vignetteTitles: BDMMAcorrect_user_guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BDMMAcorrect/inst/doc/Vignette.R Package: beachmat Version: 1.4.0 Depends: R (>= 3.5) Imports: utils, methods, Rhdf5lib (>= 1.1.4), rhdf5, HDF5Array (>= 1.9.5), DelayedArray (>= 0.7.38), Rcpp (>= 0.12.14), BiocGenerics LinkingTo: Rcpp, Rhdf5lib Suggests: testthat, BiocStyle, knitr, rmarkdown, Matrix, devtools License: GPL-3 Archs: i386, x64 MD5sum: 41e56c5e6b9366f13fca35053c15fced NeedsCompilation: yes Title: Compiling Bioconductor to Handle Each Matrix Type Description: Provides a consistent C++ class interface for a variety of commonly used matrix types, including sparse and HDF5-backed matrices. biocViews: DataRepresentation, DataImport, Infrastructure Author: Aaron Lun [aut, cre], Hervé Pagès [aut], Mike Smith [aut] Maintainer: Aaron Lun SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/beachmat git_branch: RELEASE_3_8 git_last_commit: e3b7a21 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/beachmat_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/beachmat_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/beachmat_1.4.0.tgz vignettes: vignettes/beachmat/inst/doc/external.html, vignettes/beachmat/inst/doc/input.html, vignettes/beachmat/inst/doc/linking.html, vignettes/beachmat/inst/doc/miscellaneous.html, vignettes/beachmat/inst/doc/output.html vignetteTitles: 4. Supporting arbitrary matrix classes, 2. Reading data from R matrices in C++, 1. Linking to beachmat from another package, 5. Using beachmat's helper functions, 3. Writing data into R matrix objects hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/beachmat/inst/doc/external.R, vignettes/beachmat/inst/doc/input.R, vignettes/beachmat/inst/doc/linking.R, vignettes/beachmat/inst/doc/miscellaneous.R, vignettes/beachmat/inst/doc/output.R suggestsMe: bsseq, DropletUtils, scater, scran linksToMe: bsseq, DropletUtils, scater, scran Package: beadarray Version: 2.32.0 Depends: R (>= 2.13.0), BiocGenerics (>= 0.3.2), Biobase (>= 2.17.8), methods, ggplot2 Imports: BeadDataPackR, limma, AnnotationDbi, stats4, reshape2, GenomicRanges, IRanges, illuminaio Suggests: lumi, vsn, affy, hwriter, beadarrayExampleData, illuminaHumanv3.db, gridExtra, BiocStyle, TxDb.Hsapiens.UCSC.hg19.knownGene, ggbio, Nozzle.R1, knitr License: GPL-2 Archs: i386, x64 MD5sum: 3a4e97e6601c7dd23ecc9581624fe74e NeedsCompilation: yes Title: Quality assessment and low-level analysis for Illumina BeadArray data Description: The package is able to read bead-level data (raw TIFFs and text files) output by BeadScan as well as bead-summary data from BeadStudio. Methods for quality assessment and low-level analysis are provided. biocViews: Microarray, OneChannel, QualityControl, Preprocessing Author: Mark Dunning, Mike Smith, Jonathan Cairns, Andy Lynch, Matt Ritchie Maintainer: Mark Dunning VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/beadarray git_branch: RELEASE_3_8 git_last_commit: f3f4d33 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/beadarray_2.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/beadarray_2.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/beadarray_2.32.0.tgz vignettes: vignettes/beadarray/inst/doc/beadarray.pdf, vignettes/beadarray/inst/doc/beadlevel.pdf, vignettes/beadarray/inst/doc/beadsummary.pdf, vignettes/beadarray/inst/doc/ImageProcessing.pdf vignetteTitles: beadarray.pdf, beadlevel.pdf, beadsummary.pdf, ImageProcessing.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/beadarray/inst/doc/beadarray.R, vignettes/beadarray/inst/doc/beadlevel.R, vignettes/beadarray/inst/doc/beadsummary.R, vignettes/beadarray/inst/doc/ImageProcessing.R importsMe: arrayQualityMetrics, blima, epigenomix suggestsMe: beadarraySNP, lumi Package: beadarraySNP Version: 1.48.0 Depends: methods, Biobase (>= 2.14), quantsmooth Suggests: aCGH, affy, limma, snapCGH, beadarray, DNAcopy License: GPL-2 MD5sum: 6022599758a0d8487f62868a6b0895ad NeedsCompilation: no Title: Normalization and reporting of Illumina SNP bead arrays Description: Importing data from Illumina SNP experiments and performing copy number calculations and reports. biocViews: CopyNumberVariation, SNP, GeneticVariability, TwoChannel, Preprocessing, DataImport Author: Jan Oosting Maintainer: Jan Oosting git_url: https://git.bioconductor.org/packages/beadarraySNP git_branch: RELEASE_3_8 git_last_commit: 9ad7cad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/beadarraySNP_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/beadarraySNP_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/beadarraySNP_1.48.0.tgz vignettes: vignettes/beadarraySNP/inst/doc/beadarraySNP.pdf vignetteTitles: beadarraySNP.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/beadarraySNP/inst/doc/beadarraySNP.R Package: BeadDataPackR Version: 1.34.0 Imports: stats, utils Suggests: BiocStyle, knitr License: GPL-2 Archs: i386, x64 MD5sum: 0e53726240d897ac98a7fc3044bc198e NeedsCompilation: yes Title: Compression of Illumina BeadArray data Description: Provides functionality for the compression and decompression of raw bead-level data from the Illumina BeadArray platform. biocViews: Microarray Author: Mike Smith, Andy Lynch Maintainer: Mike Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BeadDataPackR git_branch: RELEASE_3_8 git_last_commit: b0facc1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BeadDataPackR_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BeadDataPackR_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BeadDataPackR_1.34.0.tgz vignettes: vignettes/BeadDataPackR/inst/doc/BeadDataPackR.pdf vignetteTitles: BeadDataPackR.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BeadDataPackR/inst/doc/BeadDataPackR.R importsMe: beadarray Package: BEARscc Version: 1.2.1 Imports: ggplot2, SingleCellExperiment, data.table, stats, utils, graphics, compiler Suggests: testthat, cowplot, knitr, rmarkdown, BiocStyle, NMF License: GPL-3 MD5sum: 84bd147a8ea46d73805fb900af59dea2 NeedsCompilation: no Title: BEARscc (Bayesian ERCC Assesstment of Robustness of Single Cell Clusters) Description: BEARscc is a noise estimation and injection tool that is designed to assess putative single-cell RNA-seq clusters in the context of experimental noise estimated by ERCC spike-in controls. biocViews: ImmunoOncology, SingleCell, Clustering, Transcriptomics Author: David T. Severson Maintainer: Benjamin Schuster-Boeckler VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BEARscc git_branch: RELEASE_3_8 git_last_commit: b16e1c3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BEARscc_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BEARscc_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BEARscc_1.2.1.tgz vignettes: vignettes/BEARscc/inst/doc/BEARscc.pdf vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BEARscc/inst/doc/BEARscc.R Package: BEAT Version: 1.20.1 Depends: R (>= 2.13.0) Imports: GenomicRanges, ShortRead, Biostrings, BSgenome License: LGPL (>= 3.0) MD5sum: 896ce4cb9595b2d7455ded6750f5fa90 NeedsCompilation: no Title: BEAT - BS-Seq Epimutation Analysis Toolkit Description: Model-based analysis of single-cell methylation data biocViews: ImmunoOncology, Genetics, MethylSeq, Software, DNAMethylation, Epigenetics Author: Kemal Akman Maintainer: Kemal Akman git_url: https://git.bioconductor.org/packages/BEAT git_branch: RELEASE_3_8 git_last_commit: 804145f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BEAT_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BEAT_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BEAT_1.20.1.tgz vignettes: vignettes/BEAT/inst/doc/BEAT.pdf vignetteTitles: Analysing single-cell BS-Seq data with the "BEAT" package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BEAT/inst/doc/BEAT.R Package: BEclear Version: 1.14.0 Depends: BiocParallel (>= 1.15.12) Imports: futile.logger, stats, Rdpack, graphics, Matrix, utils, methods, data.table (>= 1.11.8) Suggests: testthat License: GPL-2 MD5sum: f7d173d8b8e409c822746bced7049a1e NeedsCompilation: no Title: Correct for batch effects in DNA methylation data Description: Provides some functions to detect and correct for batch effects in DNA methylation data. The core function is based on latent factor models and can also be used to predict missing values in any other matrix containing real numbers. biocViews: BatchEffect, DNAMethylation, Software, Preprocessing Author: Markus Merl, Ruslan Akulenko, David Rasp Maintainer: David Rasp URL: https://github.com/David-J-R/BEclear BugReports: https://github.com/David-J-R/BEclear/issues git_url: https://git.bioconductor.org/packages/BEclear git_branch: RELEASE_3_8 git_last_commit: e124e81 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BEclear_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BEclear_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BEclear_1.14.0.tgz vignettes: vignettes/BEclear/inst/doc/BEclear.pdf vignetteTitles: BEclear tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BEclear/inst/doc/BEclear.R Package: bgafun Version: 1.44.0 Depends: made4, seqinr,ade4 License: Artistic-2.0 MD5sum: 592bfaec5b579e3e9b2cd37afb26e9d3 NeedsCompilation: no Title: BGAfun A method to identify specifity determining residues in protein families Description: A method to identify specifity determining residues in protein families using Between Group Analysis biocViews: Classification Author: Iain Wallace Maintainer: Iain Wallace git_url: https://git.bioconductor.org/packages/bgafun git_branch: RELEASE_3_8 git_last_commit: c55e0bb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bgafun_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bgafun_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bgafun_1.44.0.tgz vignettes: vignettes/bgafun/inst/doc/bgafun.pdf vignetteTitles: bgafun.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bgafun/inst/doc/bgafun.R Package: BgeeDB Version: 2.8.0 Depends: R (>= 3.3.0), topGO, tidyr Imports: data.table, RCurl, digest, methods, stats, utils, dplyr, graph, Biobase Suggests: knitr, BiocStyle, testthat, rmarkdown License: GPL-3 MD5sum: 124a63f929213a6fc1b30f964cf3e1b5 NeedsCompilation: no Title: Annotation and gene expression data retrieval from Bgee database Description: A package for the annotation and gene expression data download from Bgee database, and TopAnat analysis: GO-like enrichment of anatomical terms, mapped to genes by expression patterns. biocViews: Software, DataImport, Sequencing, GeneExpression, Microarray, GO, GeneSetEnrichment Author: Andrea Komljenovic [aut, cre], Julien Roux [aut, cre] Maintainer: Julien Wollbrett , Julien Roux , Andrea Komljenovic , Frederic Bastian URL: https://github.com/BgeeDB/BgeeDB_R VignetteBuilder: knitr BugReports: https://github.com/BgeeDB/BgeeDB_R/issues git_url: https://git.bioconductor.org/packages/BgeeDB git_branch: RELEASE_3_8 git_last_commit: fb26014 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BgeeDB_2.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BgeeDB_2.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BgeeDB_2.8.0.tgz vignettes: vignettes/BgeeDB/inst/doc/BgeeDB_Manual.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/BgeeDB/inst/doc/BgeeDB_Manual.R importsMe: psygenet2r, RITAN Package: BGmix Version: 1.42.0 Depends: R (>= 2.3.1), KernSmooth License: GPL-2 MD5sum: 0fe9456585e4fa7c1ef2e87e2c93fd26 NeedsCompilation: yes Title: Bayesian models for differential gene expression Description: Fully Bayesian mixture models for differential gene expression biocViews: Microarray, DifferentialExpression, MultipleComparison Author: Alex Lewin, Natalia Bochkina Maintainer: Alex Lewin git_url: https://git.bioconductor.org/packages/BGmix git_branch: RELEASE_3_8 git_last_commit: 7734326 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BGmix_1.42.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BGmix_1.42.0.tgz vignettes: vignettes/BGmix/inst/doc/BGmix.pdf vignetteTitles: BGmix Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BGmix/inst/doc/BGmix.R Package: bgx Version: 1.48.1 Depends: R (>= 2.0.1), Biobase, affy (>= 1.5.0), gcrma (>= 2.4.1) Imports: Rcpp (>= 0.11.0) LinkingTo: Rcpp Suggests: affydata, hgu95av2cdf License: GPL-2 Archs: i386, x64 MD5sum: 16b83dd458322f39c457d82c63b37602 NeedsCompilation: yes Title: Bayesian Gene eXpression Description: Bayesian integrated analysis of Affymetrix GeneChips biocViews: Microarray, DifferentialExpression Author: Ernest Turro, Graeme Ambler, Anne-Mette K Hein Maintainer: Ernest Turro git_url: https://git.bioconductor.org/packages/bgx git_branch: RELEASE_3_8 git_last_commit: d5674fd git_last_commit_date: 2018-11-01 Date/Publication: 2018-11-07 source.ver: src/contrib/bgx_1.48.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/bgx_1.48.1.zip vignettes: vignettes/bgx/inst/doc/bgx.pdf vignetteTitles: HowTo BGX hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bgx/inst/doc/bgx.R Package: BHC Version: 1.34.0 License: GPL-3 Archs: i386, x64 MD5sum: 7779188efbd83088fc32df257617e208 NeedsCompilation: yes Title: Bayesian Hierarchical Clustering Description: The method performs bottom-up hierarchical clustering, using a Dirichlet Process (infinite mixture) to model uncertainty in the data and Bayesian model selection to decide at each step which clusters to merge. This avoids several limitations of traditional methods, for example how many clusters there should be and how to choose a principled distance metric. This implementation accepts multinomial (i.e. discrete, with 2+ categories) or time-series data. This version also includes a randomised algorithm which is more efficient for larger data sets. biocViews: Microarray, Clustering Author: Rich Savage, Emma Cooke, Robert Darkins, Yang Xu Maintainer: Rich Savage git_url: https://git.bioconductor.org/packages/BHC git_branch: RELEASE_3_8 git_last_commit: e183dcd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BHC_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BHC_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BHC_1.34.0.tgz vignettes: vignettes/BHC/inst/doc/bhc.pdf vignetteTitles: Bayesian Hierarchical Clustering hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BHC/inst/doc/bhc.R Package: BicARE Version: 1.40.0 Depends: R (>= 1.8.0), Biobase (>= 2.5.5), multtest, GSEABase License: GPL-2 Archs: i386, x64 MD5sum: 90878d870f7ec218fc9eea9fe9b5d839 NeedsCompilation: yes Title: Biclustering Analysis and Results Exploration Description: Biclustering Analysis and Results Exploration biocViews: Microarray, Transcription, Clustering Author: Pierre Gestraud Maintainer: Pierre Gestraud URL: http://bioinfo.curie.fr git_url: https://git.bioconductor.org/packages/BicARE git_branch: RELEASE_3_8 git_last_commit: e174d75 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BicARE_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BicARE_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BicARE_1.40.0.tgz vignettes: vignettes/BicARE/inst/doc/BicARE.pdf vignetteTitles: BicARE hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BicARE/inst/doc/BicARE.R importsMe: miRSM Package: BiFET Version: 1.2.1 Imports: stats, poibin, GenomicRanges Suggests: testthat, knitr License: GPL-3 MD5sum: 67a21d9e2b17948505b2690908752a3b NeedsCompilation: no Title: Bias-free Footprint Enrichment Test Description: BiFET identifies TFs whose footprints are over-represented in target regions compared to background regions after correcting for the bias arising from the imbalance in read counts and GC contents between the target and background regions. For a given TF k, BiFET tests the null hypothesis that the target regions have the same probability of having footprints for the TF k as the background regions while correcting for the read count and GC content bias. For this, we use the number of target regions with footprints for TF k, t_k as a test statistic and calculate the p-value as the probability of observing t_k or more target regions with footprints under the null hypothesis. biocViews: ImmunoOncology, Genetics, Epigenetics, Transcription, GeneRegulation, ATACSeq, DNaseSeq, RIPSeq, Software Author: Ahrim Youn [aut, cre], Eladio Marquez [aut], Nathan Lawlor [aut], Michael Stitzel [aut], Duygu Ucar [aut] Maintainer: Ahrim Youn VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BiFET git_branch: RELEASE_3_8 git_last_commit: 38e54a1 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BiFET_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiFET_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiFET_1.2.1.tgz vignettes: vignettes/BiFET/inst/doc/BiFET.html vignetteTitles: "A Guide to using BiFET" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiFET/inst/doc/BiFET.R Package: BiGGR Version: 1.18.0 Depends: R (>= 2.14.0), rsbml, hyperdraw, LIM,stringr Imports: hypergraph, limSolve License: file LICENSE MD5sum: c0bbb2a19b06bc77e802c9f131b5bd0e NeedsCompilation: no Title: Constraint based modeling in R using metabolic reconstruction databases Description: This package provides an interface to simulate metabolic reconstruction from the BiGG database(http://bigg.ucsd.edu/) and other metabolic reconstruction databases. The package facilitates flux balance analysis (FBA) and the sampling of feasible flux distributions. Metabolic networks and estimated fluxes can be visualized with hypergraphs. biocViews: Systems Biology,Pathway, Network,GraphAndNetwork,Visualization,Metabolomics Author: Anand K. Gavai, Hannes Hettling Maintainer: Anand K. Gavai , Hannes Hettling URL: http://www.bioconductor.org/ git_url: https://git.bioconductor.org/packages/BiGGR git_branch: RELEASE_3_8 git_last_commit: 865730c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiGGR_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiGGR_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiGGR_1.18.0.tgz vignettes: vignettes/BiGGR/inst/doc/BiGGR.pdf vignetteTitles: BiGGR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/BiGGR/inst/doc/BiGGR.R Package: bigmelon Version: 1.8.0 Depends: R (>= 3.3), wateRmelon (>= 1.25.0), gdsfmt (>= 1.0.4), methods, minfi (>= 1.21.0), Biobase, methylumi Imports: stats, utils, GEOquery, graphics, BiocGenerics Suggests: BiocGenerics, BiocStyle, minfiData, parallel, IlluminaHumanMethylation450kanno.ilmn12.hg19, IlluminaHumanMethylationEPICanno.ilm10b2.hg19, bumphunter License: GPL-3 MD5sum: 3b7456161c012f3441cffda28e3ce9ca NeedsCompilation: no Title: Illumina methylation array analysis for large experiments Description: Methods for working with Illumina arrays using gdsfmt. biocViews: DNAMethylation, Microarray, TwoChannel, Preprocessing, QualityControl, MethylationArray, DataImport, CpGIsland Author: Tyler J. Gorrie-Stone [cre, aut], Ayden Saffari [aut], Karim Malki [aut], Leonard C. Schalkwyk [aut] Maintainer: Tyler J. Gorrie-Stone git_url: https://git.bioconductor.org/packages/bigmelon git_branch: RELEASE_3_8 git_last_commit: f24aa08 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bigmelon_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bigmelon_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bigmelon_1.8.0.tgz vignettes: vignettes/bigmelon/inst/doc/bigmelon.pdf vignetteTitles: The bigmelon Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bigmelon/inst/doc/bigmelon.R Package: bigmemoryExtras Version: 1.30.0 Depends: R (>= 2.12), bigmemory (>= 4.5.31) Imports: methods Suggests: testthat, BiocGenerics, BiocStyle, knitr License: Artistic-2.0 OS_type: unix MD5sum: fea9a5d5915ed5832554e56d06b8389a NeedsCompilation: no Title: An extension of the bigmemory package with added safety, convenience, and a factor class Description: This package defines a "BigMatrix" ReferenceClass which adds safety and convenience features to the filebacked.big.matrix class from the bigmemory package. BigMatrix protects against segfaults by monitoring and gracefully restoring the connection to on-disk data and it also protects against accidental data modification with a filesystem-based permissions system. We provide utilities for using BigMatrix-derived classes as assayData matrices within the Biobase package's eSet family of classes. BigMatrix provides some optimizations related to attaching to, and indexing into, file-backed matrices with dimnames. Additionally, the package provides a "BigMatrixFactor" class, a file-backed matrix with factor properties. biocViews: Infrastructure, DataRepresentation Author: Peter M. Haverty Maintainer: Peter M. Haverty URL: https://github.com/phaverty/bigmemoryExtras VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/bigmemoryExtras git_branch: RELEASE_3_8 git_last_commit: 585a2c0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bigmemoryExtras_1.30.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bigmemoryExtras_1.30.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE importsMe: gCMAP Package: bioassayR Version: 1.20.1 Depends: R (>= 3.1.0), DBI (>= 0.3.1), RSQLite (>= 1.0.0), methods, Matrix, rjson, BiocGenerics (>= 0.13.8) Imports: XML, ChemmineR Suggests: BiocStyle, RCurl, biomaRt, cellHTS2, knitr, knitcitations, knitrBootstrap, testthat, ggplot2, rmarkdown License: Artistic-2.0 MD5sum: 19b141961cf62efabd8803e11edbc264 NeedsCompilation: no Title: Cross-target analysis of small molecule bioactivity Description: bioassayR is a computational tool that enables simultaneous analysis of thousands of bioassay experiments performed over a diverse set of compounds and biological targets. Unique features include support for large-scale cross-target analyses of both public and custom bioassays, generation of high throughput screening fingerprints (HTSFPs), and an optional preloaded database that provides access to a substantial portion of publicly available bioactivity data. biocViews: ImmunoOncology, MicrotitrePlateAssay, CellBasedAssays, Visualization, Infrastructure, DataImport, Bioinformatics, Proteomics, Metabolomics Author: Tyler Backman, Ronly Schlenk, Thomas Girke Maintainer: Tyler Backman URL: https://github.com/TylerBackman/bioassayR VignetteBuilder: knitr BugReports: https://github.com/TylerBackman/bioassayR/issues git_url: https://git.bioconductor.org/packages/bioassayR git_branch: RELEASE_3_8 git_last_commit: 022717e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/bioassayR_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/bioassayR_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bioassayR_1.20.1.tgz vignettes: vignettes/bioassayR/inst/doc/bioassayR.html vignetteTitles: Introduction and Examples hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bioassayR/inst/doc/bioassayR.R Package: Biobase Version: 2.42.0 Depends: R (>= 2.10), BiocGenerics (>= 0.27.1), utils Imports: methods Suggests: tools, tkWidgets, ALL, RUnit, golubEsets License: Artistic-2.0 Archs: i386, x64 MD5sum: a7137201a04682443ec0a418309e006b NeedsCompilation: yes Title: Biobase: Base functions for Bioconductor Description: Functions that are needed by many other packages or which replace R functions. biocViews: Infrastructure Author: R. Gentleman, V. Carey, M. Morgan, S. Falcon Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/Biobase git_branch: RELEASE_3_8 git_last_commit: 3e5bd46 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Biobase_2.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Biobase_2.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Biobase_2.42.0.tgz vignettes: vignettes/Biobase/inst/doc/BiobaseDevelopment.pdf, vignettes/Biobase/inst/doc/esApply.pdf, vignettes/Biobase/inst/doc/ExpressionSetIntroduction.pdf vignetteTitles: Notes for eSet developers, esApply Introduction, An introduction to Biobase and ExpressionSets hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Biobase/inst/doc/BiobaseDevelopment.R, vignettes/Biobase/inst/doc/esApply.R, vignettes/Biobase/inst/doc/ExpressionSetIntroduction.R dependsOnMe: a4Base, a4Core, ACME, affy, affycomp, affyContam, affycoretools, affyPLM, affyQCReport, AGDEX, AIMS, altcdfenvs, annaffy, AnnotationDbi, AnnotationForge, ArrayExpress, arrayMvout, ArrayTools, BAGS, beadarray, beadarraySNP, bgx, BicARE, bigmelon, BiocCaseStudies, BioMVCClass, BioQC, birta, BLMA, BrainStars, CAMERA, cancerclass, casper, Category, categoryCompare, CCPROMISE, cellHTS2, CGHbase, CGHcall, CGHregions, charm, chimera, chroGPS, clippda, clusterStab, CMA, cn.farms, codelink, convert, copa, covEB, covRNA, DESeq, DEXSeq, DFP, diggit, doppelgangR, DSS, dualKS, dyebias, EBarrays, EDASeq, edge, EGSEA, eisa, epigenomix, epivizrData, ExiMiR, ExpressionAtlas, fabia, factDesign, fastseg, flowBeads, frma, gaga, gCMAPWeb, GeneAnswers, GeneExpressionSignature, GeneMeta, geneplotter, geneRecommender, GeneRegionScan, GeneSelectMMD, GeneSelector, geNetClassifier, GEOquery, GOexpress, GOFunction, goProfiles, GOstats, GSEABase, GSEABenchmarkeR, GSEAlm, GWASTools, hapFabia, HELP, hopach, HTqPCR, htSeqTools, HybridMTest, iCheck, IdeoViz, idiogram, InPAS, INSPEcT, isobar, iterativeBMA, IVAS, LMGene, lumi, macat, mAPKL, massiR, MEAL, MergeMaid, metagenomeFeatures, metagenomeSeq, metavizr, MethPed, methyAnalysis, methylumi, Mfuzz, MiChip, mimager, MIMOSA, MineICA, MiRaGE, miRcomp, MLInterfaces, MmPalateMiRNA, monocle, MSnbase, Mulcom, MultiDataSet, multtest, NanoStringDiff, NOISeq, nondetects, normalize450K, NormqPCR, oligo, omicRexposome, OrderedList, OTUbase, OutlierD, pandaR, panp, pcaMethods, pcot2, pdInfoBuilder, pepStat, PGSEA, phenoTest, PLPE, plrs, prada, PREDA, pRolocGUI, PROMISE, qpcrNorm, qPLEXanalyzer, R453Plus1Toolbox, RbcBook1, rbsurv, rcellminer, ReadqPCR, reb, RefPlus, rexposome, rHVDM, Ringo, Risa, Rmagpie, rMAT, RNAinteract, rnaSeqMap, Rnits, Roleswitch, RpsiXML, RTopper, RUVSeq, safe, SCAN.UPC, SeqGSEA, sigaR, SigCheck, siggenes, simpleaffy, simulatorZ, singleCellTK, SpeCond, SPEM, spkTools, splicegear, splineTimeR, STROMA4, SummarizedExperiment, TDARACNE, tigre, tilingArray, topGO, TPP, tRanslatome, tspair, twilight, UNDO, variancePartition, VegaMC, viper, vsn, wateRmelon, waveTiling, webbioc, xcms, XDE, XINA, yarn importsMe: ABarray, ACE, aCGH, adSplit, affyILM, affyQCReport, AgiMicroRna, AnalysisPageServer, ANF, annmap, annotate, AnnotationHubData, annotationTools, ArrayExpressHTS, arrayQualityMetrics, ArrayTools, attract, ballgown, BayesKnockdown, BgeeDB, biobroom, bioCancer, biocViews, BioNet, BioSeqClass, biosigner, biosvd, birte, BiSeq, blima, BrainStars, bsseq, BubbleTree, CAFE, CAMTHC, canceR, Cardinal, CATALYST, CellScore, CellTrails, CGHnormaliter, charm, ChIPpeakAnno, ChIPQC, ChIPXpress, ChromHeatMap, chromswitch, cicero, clipper, cn.mops, COCOA, coexnet, cogena, ConsensusClusterPlus, consensusDE, consensusOV, coRdon, crlmm, crossmeta, cummeRbund, cycle, cydar, CytoML, ddCt, DEGreport, DESeq2, destiny, diffloop, discordant, DOQTL, easyRNASeq, EBarrays, ecolitk, EGAD, ensembldb, erma, esetVis, ExiMiR, farms, ffpe, FindMyFriends, flowClust, flowCore, flowFP, flowMatch, flowMeans, flowStats, flowType, flowUtils, flowViz, flowWorkspace, FourCSeq, frma, frmaTools, FunciSNP, gCMAP, gCrisprTools, gcrma, genbankr, geneClassifiers, genefilter, GeneMeta, geneRecommender, GeneRegionScan, GeneSelectMMD, GENESIS, GenomicFeatures, GenomicInteractions, GenomicScores, GEOsubmission, gep2pep, gespeR, GGBase, ggbio, GGtools, girafe, GISPA, GlobalAncova, globaltest, gmapR, GOFunction, GoogleGenomics, gQTLstats, GSRI, GSVA, Gviz, Harshlight, HEM, HTqPCR, HTSFilter, IdMappingAnalysis, imageHTS, ImmuneSpaceR, ImpulseDE2, IsoGeneGUI, isomiRs, iterClust, JunctionSeq, kimod, kissDE, lapmix, LINC, LiquidAssociation, LRBaseDbi, LVSmiRNA, maanova, makecdfenv, maSigPro, MAST, mBPCR, MCRestimate, MeSHDbi, metaArray, methyAnalysis, MethylAid, methylumi, mfa, MiChip, MIGSA, minfi, MinimumDistance, MiPP, MIRA, miRSM, MLSeq, MmPalateMiRNA, mogsa, MoonlightR, MoPS, MSnID, MTseeker, MultiAssayExperiment, multiscan, mzR, NanoStringQCPro, NormalyzerDE, npGSEA, nucleR, OGSA, oligoClasses, ontoProc, oposSOM, oppar, OrderedList, OrganismDbi, OUTRIDER, panp, PathwaySplice, Pbase, PCpheno, phantasus, PharmacoGx, phyloseq, piano, plateCore, plethy, plgem, plier, podkat, POST, PowerExplorer, ppiStats, prada, prebs, proFIA, progeny, pRoloc, PROMISE, PROPS, ProteomicsAnnotationHubData, PSEA, psygenet2r, puma, pvac, pvca, pwOmics, qcmetrics, QDNAseq, qpgraph, quantro, QuasR, qusage, randPack, readat, RGalaxy, RIVER, Rmagpie, rMAT, rols, ropls, ROTS, rqubic, Rtreemix, RUVnormalize, SAGx, scmap, SeqVarTools, ShortRead, sigsquared, SimBindProfiles, simpleaffy, singscore, SLGI, SNPchip, SomaticSignatures, spkTools, splicegear, SPONGE, STATegRa, subSeq, synapter, TEQC, TFBSTools, timecourse, TMixClust, TnT, topdownr, TSSi, TTMap, twilight, uSORT, VanillaICE, VariantAnnotation, VariantFiltering, VariantTools, vidger, vulcan, wateRmelon, XBSeq suggestsMe: AUCell, BiocCaseStudies, BiocCheck, BiocGenerics, BiocOncoTK, BSgenome, CellMapper, cellTree, clustComp, coseq, CountClust, DAPAR, DART, EpiDISH, epivizr, epivizrChart, epivizrStandalone, farms, genefu, GENIE3, GenomicRanges, GSAR, Heatplus, interactiveDisplay, kebabs, les, limma, Logolas, mCSEA, messina, msa, multiClust, nem, OSAT, pkgDepTools, RcisTarget, ROC, RTCGA, scater, scmeth, scran, SeqArray, slinky, stageR, survcomp, TargetScore, TCGAbiolinks, TFutils, TimeSeriesExperiment, tkWidgets, TypeInfo, vbmp, widgetTools Package: biobroom Version: 1.14.0 Depends: R (>= 3.0.0), broom Imports: dplyr, tidyr, Biobase Suggests: limma, DESeq2, airway, ggplot2, plyr, GenomicRanges, testthat, magrittr, edgeR, qvalue, knitr, data.table, MSnbase, SummarizedExperiment License: LGPL MD5sum: 8e8a35fc42f28c672f6f5b8b144cc2b1 NeedsCompilation: no Title: Turn Bioconductor objects into tidy data frames Description: This package contains methods for converting standard objects constructed by bioinformatics packages, especially those in Bioconductor, and converting them to tidy data. It thus serves as a complement to the broom package, and follows the same the tidy, augment, glance division of tidying methods. Tidying data makes it easy to recombine, reshape and visualize bioinformatics analyses. biocViews: MultipleComparison, DifferentialExpression, Regression, GeneExpression, Proteomics, DataImport Author: Andrew J. Bass, David G. Robinson, Steve Lianoglou, Emily Nelson, John D. Storey, with contributions from Laurent Gatto Maintainer: John D. Storey and Andrew J. Bass URL: https://github.com/StoreyLab/biobroom VignetteBuilder: knitr BugReports: https://github.com/StoreyLab/biobroom/issues git_url: https://git.bioconductor.org/packages/biobroom git_branch: RELEASE_3_8 git_last_commit: f52a4b1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biobroom_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biobroom_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biobroom_1.14.0.tgz vignettes: vignettes/biobroom/inst/doc/biobroom_vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biobroom/inst/doc/biobroom_vignette.R importsMe: TPP Package: bioCancer Version: 1.10.11 Depends: R (>= 3.4.0), radiant.data (>= 0.9.1), cgdsr(>= 1.2.6), XML(>= 3.98) Imports: DT (>= 0.3), dplyr (>= 0.7.2), shiny (>= 1.0.5), AlgDesign (>= 1.1.7.3), import (>= 1.1.0), methods, shinythemes, Biobase, geNetClassifier, AnnotationFuncs, org.Hs.eg.db, DOSE, clusterProfiler, reactome.db, ReactomePA, DiagrammeR(>= 0.7), visNetwork, htmlwidgets, plyr, tibble Suggests: BiocStyle, rmarkdown, knitr, testthat (>= 0.10.0) License: AGPL-3 | file LICENSE MD5sum: 6c6764db443b9c9c20434583b1753d7d NeedsCompilation: no Title: Interactive Multi-Omics Cancers Data Visualization and Analysis Description: bioCancer is a Shiny App to visualize and analyse interactively Multi-Assays of Cancer Genomic Data. biocViews: GUI, DataRepresentation, Network, MultipleComparison, Pathways, Reactome, Visualization,GeneExpression,GeneTarget Author: Karim Mezhoud [aut, cre] Maintainer: Karim Mezhoud URL: http://kmezhoud.github.io/bioCancer VignetteBuilder: knitr BugReports: https://github.com/kmezhoud/bioCancer/issues git_url: https://git.bioconductor.org/packages/bioCancer git_branch: RELEASE_3_8 git_last_commit: 915d797 git_last_commit_date: 2019-04-04 Date/Publication: 2019-04-04 source.ver: src/contrib/bioCancer_1.10.11.tar.gz win.binary.ver: bin/windows/contrib/3.5/bioCancer_1.10.11.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bioCancer_1.10.11.tgz vignettes: vignettes/bioCancer/inst/doc/bioCancer.html vignetteTitles: bioCancer: Interactive Multi-OMICS Cancers Data Visualization and Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/bioCancer/inst/doc/bioCancer.R Package: BiocCaseStudies Version: 1.44.0 Depends: tools, methods, utils, Biobase Suggests: affy (>= 1.17.3), affyPLM (>= 1.15.1), affyQCReport (>= 1.17.0), ALL (>= 1.4.3), annaffy (>= 1.11.1), annotate (>= 1.17.3), AnnotationDbi (>= 1.1.6), apComplex (>= 2.5.0), Biobase (>= 1.17.5), bioDist (>= 1.11.3), biocGraph (>= 1.1.1), biomaRt (>= 1.13.5), CCl4 (>= 1.0.6), CLL (>= 1.2.4), Category (>= 2.5.0), class (>= 7.2-38), cluster (>= 1.11.9), convert (>= 1.15.0), gcrma (>= 2.11.1), genefilter (>= 1.17.6), geneplotter (>= 1.17.2), GO.db (>= 2.0.2), GOstats (>= 2.5.0), graph (>= 1.17.4), GSEABase (>= 1.1.13), hgu133a.db (>= 2.0.2), hgu95av2.db, hgu95av2cdf (>= 2.0.0), hgu95av2probe (>= 2.0.0), hopach (>= 1.13.0), KEGG.db (>= 2.0.2), kohonen (>= 2.0.2), lattice (>= 0.17.2), latticeExtra (>= 0.3-1), limma (>= 2.13.1), MASS (>= 7.2-38), MLInterfaces (>= 1.13.17), multtest (>= 1.19.0), org.Hs.eg.db (>= 2.0.2), ppiStats (>= 1.5.4), randomForest (>= 4.5-20), RBGL (>= 1.15.6), RColorBrewer (>= 1.0-2), Rgraphviz (>= 1.17.11), vsn (>= 3.4.0), weaver (>= 1.5.0), xtable (>= 1.5-2), yeastExpData (>= 0.9.11) License: Artistic-2.0 MD5sum: b42e2a90273bbc029e3163dddc35656c NeedsCompilation: no Title: BiocCaseStudies: Support for the Case Studies Monograph Description: Software and data to support the case studies. biocViews: Infrastructure Author: R. Gentleman, W. Huber, F. Hahne, M. Morgan, S. Falcon Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/BiocCaseStudies git_branch: RELEASE_3_8 git_last_commit: 2b671b5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocCaseStudies_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocCaseStudies_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocCaseStudies_1.44.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: BiocCheck Version: 1.18.0 Depends: R (>= 3.5.0) Imports: biocViews (>= 1.33.7), BiocManager, stringdist, graph, httr, tools, optparse, codetools, methods, utils, knitr Suggests: RUnit, BiocGenerics, Biobase, RJSONIO, rmarkdown, devtools (>= 1.4.1) Enhances: codetoolsBioC License: Artistic-2.0 MD5sum: 89d98a97234600db83aa55aa628bbeef NeedsCompilation: no Title: Bioconductor-specific package checks Description: Executes Bioconductor-specific package checks. biocViews: Infrastructure Author: Bioconductor Package Maintainer [aut, cre], Daniel von Twisk [ctb], Lori Shepherd [ctb], Kevin Rue [ctb] Maintainer: Bioconductor Package Maintainer URL: https://github.com/Bioconductor/BiocCheck/issues VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BiocCheck git_branch: RELEASE_3_8 git_last_commit: 1ce818f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocCheck_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocCheck_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocCheck_1.18.0.tgz vignettes: vignettes/BiocCheck/inst/doc/BiocCheck.html vignetteTitles: BiocCheck: Ensuring Bioconductor package guidelines hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiocCheck/inst/doc/BiocCheck.R importsMe: ExperimentHubData suggestsMe: CNPBayes Package: BiocFileCache Version: 1.6.0 Depends: R (>= 3.4.0), dbplyr (>= 1.0.0) Imports: methods, stats, utils, dplyr, RSQLite, DBI, rappdirs, curl, httr Suggests: testthat, knitr, BiocStyle, rmarkdown, rtracklayer License: Artistic-2.0 MD5sum: c5b4282a6191a520567d03508bf46652 NeedsCompilation: no Title: Manage Files Across Sessions Description: This package creates a persistent on-disk cache of files that the user can add, update, and retrieve. It is useful for managing resources (such as custom Txdb objects) that are costly or difficult to create, web resources, and data files used across sessions. biocViews: DataImport Author: Lori Shepherd [aut, cre], Martin Morgan [aut] Maintainer: Lori Shepherd VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/BiocFileCache/issues git_url: https://git.bioconductor.org/packages/BiocFileCache git_branch: RELEASE_3_8 git_last_commit: c2de6c1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocFileCache_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocFileCache_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocFileCache_1.6.0.tgz vignettes: vignettes/BiocFileCache/inst/doc/BiocFileCache.html vignetteTitles: BiocFileCache: Managing File Resources Across Sessions hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiocFileCache/inst/doc/BiocFileCache.R importsMe: cbaf, CTDquerier, EnrichmentBrowser, GSEABenchmarkeR, HiCBricks, IMMAN, Organism.dplyr, tximeta, UniProt.ws suggestsMe: BiocOncoTK, progeny, seqsetvis, TimeSeriesExperiment Package: BiocGenerics Version: 0.28.0 Depends: methods, utils, graphics, stats, parallel Imports: methods, utils, graphics, stats, parallel Suggests: Biobase, S4Vectors, IRanges, GenomicRanges, Rsamtools, AnnotationDbi, oligoClasses, oligo, affyPLM, flowClust, affy, DESeq2, MSnbase, annotate, RUnit License: Artistic-2.0 MD5sum: 39b4dfb1f9526c64ddcb9b994130a7c0 NeedsCompilation: no Title: S4 generic functions for Bioconductor Description: S4 generic functions needed by many Bioconductor packages. biocViews: Infrastructure Author: The Bioconductor Dev Team Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/BiocGenerics git_branch: RELEASE_3_8 git_last_commit: 041fc49 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocGenerics_0.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocGenerics_0.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocGenerics_0.28.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: ACME, affy, affyPLM, altcdfenvs, amplican, AnnotationDbi, AnnotationForge, AnnotationHub, ATACseqQC, beadarray, bioassayR, Biobase, Biostrings, bnbc, BSgenome, bsseq, Cardinal, Category, categoryCompare, chipseq, ChIPseqR, ChromHeatMap, cleanUpdTSeq, clusterExperiment, codelink, consensusDE, consensusSeekeR, copynumber, CRISPRseek, cummeRbund, DelayedArray, DESeq, dexus, ensembldb, ensemblVEP, ExperimentHub, ExperimentHubData, GDSArray, geneplotter, GenomeInfoDb, genomeIntervals, GenomicAlignments, GenomicFeatures, GenomicFiles, GenomicRanges, GenomicScores, Genominator, genoset, ggbio, girafe, graph, GSEABase, GUIDEseq, HelloRanges, htSeqTools, interactiveDisplay, interactiveDisplayBase, IRanges, MBASED, MeSHDbi, methyAnalysis, MIGSA, MineICA, minfi, MLInterfaces, MotifDb, MotIV, mpra, MSnbase, multtest, NADfinder, oligo, OrganismDbi, Pbase, PICS, plethy, plyranges, PSICQUIC, PWMEnrich, RareVariantVis, REDseq, Repitools, rMAT, RNAprobR, RnBeads, RPA, rsbml, S4Vectors, scsR, shinyMethyl, ShortRead, simpleaffy, simulatorZ, soGGi, SummarizedBenchmark, TEQC, tigre, topdownr, topGO, UNDO, UniProt.ws, VanillaICE, VariantAnnotation, VariantFiltering, XVector, yamss importsMe: affycoretools, affylmGUI, AllelicImbalance, annmap, annotate, AnnotationHubData, ArrayExpressHTS, ASpli, bamsignals, BASiCS, beachmat, bigmelon, biocGraph, biosvd, biotmle, biovizBase, BiSeq, blima, brainImageR, breakpointR, BrowserViz, BSgenome, BubbleTree, bumphunter, CAGEfightR, CAGEr, casper, celaref, cellHTS2, CellTrails, cghMCR, ChemmineOB, ChemmineR, ChIC, chipenrich, ChIPpeakAnno, ChIPQC, ChIPseeker, chipseq, ChIPSeqSpike, chromVAR, cicero, clusterSeq, cn.mops, CNEr, CNPBayes, cobindR, COCOA, compEpiTools, crlmm, crossmeta, csaw, cummeRbund, cydar, dada2, 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Package: biocGraph Version: 1.44.0 Depends: Rgraphviz, graph Imports: Rgraphviz, geneplotter, graph, BiocGenerics, methods Suggests: fibroEset, geneplotter, hgu95av2.db License: Artistic-2.0 MD5sum: eca6aee70c90d6a42c92bcada35490eb NeedsCompilation: no Title: Graph examples and use cases in Bioinformatics Description: This package provides examples and code that make use of the different graph related packages produced by Bioconductor. biocViews: Visualization, GraphAndNetwork Author: Li Long , Robert Gentleman , Seth Falcon Florian Hahne Maintainer: Florian Hahne git_url: https://git.bioconductor.org/packages/biocGraph git_branch: RELEASE_3_8 git_last_commit: 974e98b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biocGraph_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biocGraph_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biocGraph_1.44.0.tgz vignettes: vignettes/biocGraph/inst/doc/biocGraph.pdf, vignettes/biocGraph/inst/doc/layingOutPathways.pdf vignetteTitles: Examples of plotting graphs Using Rgraphviz, HOWTO layout pathways hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biocGraph/inst/doc/biocGraph.R, vignettes/biocGraph/inst/doc/layingOutPathways.R importsMe: EnrichmentBrowser suggestsMe: BiocCaseStudies Package: BiocInstaller Version: 1.32.1 Depends: R (>= 3.5.0), R (< 3.6.0) Suggests: remotes, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: cc58048dad0325a2fca2a92680611c22 NeedsCompilation: no Title: Install/Update Bioconductor, CRAN, and github Packages Description: This package is used to install and update Bioconductor, CRAN, and (some) github packages. biocViews: Infrastructure Author: Dan Tenenbaum and Biocore Team Maintainer: Bioconductor Package Maintainer PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/BiocInstaller git_branch: RELEASE_3_8 git_last_commit: 4c2a39e git_last_commit_date: 2018-11-01 Date/Publication: 2018-11-01 source.ver: src/contrib/BiocInstaller_1.32.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocInstaller_1.32.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocInstaller_1.32.1.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: BiocNeighbors Version: 1.0.0 Depends: R (>= 3.5), BiocParallel Imports: Rcpp, S4Vectors, stats, methods LinkingTo: Rcpp, RcppAnnoy Suggests: testthat, BiocStyle, knitr, rmarkdown, FNN, RcppAnnoy License: GPL-3 Archs: i386, x64 MD5sum: 654e4deee2cadb9901f8137142719b16 NeedsCompilation: yes Title: Nearest Neighbor Detection for Bioconductor Packages Description: Implements exact and approximate methods for nearest neighbor detection, in a framework that allows them to be easily switched within Bioconductor packages or workflows. The exact algorithm is implemented using pre-clustering with the k-means algorithm, as described by Wang (2012). This is faster than conventional kd-trees for neighbor searching in higher (> 20) dimensional data. The approximate method uses the Annoy algorithm. Functions are also provided to search for all neighbors within a given distance. Parallelization is achieved for all methods using the BiocParallel framework. biocViews: Clustering, Classification Author: Aaron Lun [aut, cre, cph] Maintainer: Aaron Lun SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BiocNeighbors git_branch: RELEASE_3_8 git_last_commit: e252fc0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocNeighbors_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocNeighbors_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocNeighbors_1.0.0.tgz vignettes: vignettes/BiocNeighbors/inst/doc/annoy.html, vignettes/BiocNeighbors/inst/doc/kmknn.html, vignettes/BiocNeighbors/inst/doc/range.html vignetteTitles: 2. Detecting approximate nearest neighbors, 1. Detecting exact nearest neighbors, 3. Detecting neighbors within range hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiocNeighbors/inst/doc/annoy.R, vignettes/BiocNeighbors/inst/doc/kmknn.R, vignettes/BiocNeighbors/inst/doc/range.R importsMe: cydar, scran Package: BiocOncoTK Version: 1.2.1 Depends: R (>= 3.5.0), methods Imports: ComplexHeatmap, S4Vectors, bigrquery, shiny, stats, httr, rjson, dplyr, magrittr, grid, utils, DT, GenomicRanges, IRanges, ggplot2, SummarizedExperiment, DBI, GenomicFeatures Suggests: knitr, dbplyr, DBI, org.Hs.eg.db, MultiAssayExperiment, BiocStyle, ontoProc, ontologyPlot, pogos, GenomeInfoDb, restfulSE (>= 1.3.7), BiocFileCache, TxDb.Hsapiens.UCSC.hg19.knownGene, Biobase, TxDb.Hsapiens.UCSC.hg18.knownGene, reshape2, testthat, AnnotationDbi, FDb.InfiniumMethylation.hg19, EnsDb.Hsapiens.v75 License: Artistic-2.0 MD5sum: 2716434e04a3ff739ca28bfb1d569084 NeedsCompilation: no Title: Bioconductor components for general cancer genomics Description: Provide a central interface to various tools for genome-scale analysis of cancer studies. biocViews: ImmunoOncology, CopyNumberVariation, CpGIsland, DNAMethylation, GeneExpression, GeneticVariability, SNP, Transcription Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BiocOncoTK git_branch: RELEASE_3_8 git_last_commit: 078e833 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BiocOncoTK_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocOncoTK_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocOncoTK_1.2.1.tgz vignettes: vignettes/BiocOncoTK/inst/doc/BiocOncoTK.html vignetteTitles: BiocOncoTK -- cancer oriented components for Bioconductor hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiocOncoTK/inst/doc/BiocOncoTK.R Package: BioCor Version: 1.6.1 Imports: BiocParallel, Matrix, GSEABase Suggests: reactome.db, org.Hs.eg.db, WGCNA, methods, GOSemSim, testthat, knitr, rmarkdown, BiocStyle, airway, DESeq2, boot, targetscan.Hs.eg.db, Hmisc, spelling License: MIT + file LICENSE MD5sum: 47b943ebcb9f7bacaebe40f89ec48e85 NeedsCompilation: no Title: Functional similarities Description: Calculates functional similarities based on the pathways described on KEGG and REACTOME or in gene sets. These similarities can be calculated for pathways or gene sets, genes, or clusters and combined with other similarities. They can be used to improve networks, gene selection, testing relationships... biocViews: StatisticalMethod, Clustering, GeneExpression, Network, Pathways, NetworkEnrichment, SystemsBiology Author: Lluís Revilla Sancho [aut, cre] (), Pau Sancho-Bru [ths] (), Juan José Salvatella Lozano [ths] () Maintainer: Lluís Revilla Sancho URL: https://github.com/llrs/BioCor/ VignetteBuilder: knitr BugReports: https://github.com/llrs/BioCor/issues git_url: https://git.bioconductor.org/packages/BioCor git_branch: RELEASE_3_8 git_last_commit: 29376d1 git_last_commit_date: 2019-01-26 Date/Publication: 2019-01-26 source.ver: src/contrib/BioCor_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BioCor_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BioCor_1.6.1.tgz vignettes: vignettes/BioCor/inst/doc/BioCor_1_basics.html, vignettes/BioCor/inst/doc/BioCor_2_advanced.html vignetteTitles: About BioCor, Advanced usage of BioCor hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/BioCor/inst/doc/BioCor_1_basics.R, vignettes/BioCor/inst/doc/BioCor_2_advanced.R Package: BiocParallel Version: 1.16.6 Depends: methods Imports: stats, utils, futile.logger, parallel, snow LinkingTo: BH Suggests: BiocGenerics, tools, foreach, BatchJobs, BBmisc, doParallel, Rmpi, GenomicRanges, RNAseqData.HNRNPC.bam.chr14, TxDb.Hsapiens.UCSC.hg19.knownGene, VariantAnnotation, Rsamtools, GenomicAlignments, ShortRead, codetools, RUnit, BiocStyle, knitr, batchtools, data.table License: GPL-2 | GPL-3 Archs: i386, x64 MD5sum: bd95c6d6202bd09612b448e5da49bd2a NeedsCompilation: yes Title: Bioconductor facilities for parallel evaluation Description: This package provides modified versions and novel implementation of functions for parallel evaluation, tailored to use with Bioconductor objects. biocViews: Infrastructure Author: Bioconductor Package Maintainer [cre], Martin Morgan [aut], Valerie Obenchain [aut], Michel Lang [aut], Ryan Thompson [aut], Nitesh Turaga [aut] Maintainer: Bioconductor Package Maintainer URL: https://github.com/Bioconductor/BiocParallel SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/BiocParallel/issues git_url: https://git.bioconductor.org/packages/BiocParallel git_branch: RELEASE_3_8 git_last_commit: 7f7a54c git_last_commit_date: 2019-02-08 Date/Publication: 2019-02-10 source.ver: src/contrib/BiocParallel_1.16.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocParallel_1.16.6.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocParallel_1.16.6.tgz vignettes: vignettes/BiocParallel/inst/doc/BiocParallel_BatchtoolsParam.pdf, vignettes/BiocParallel/inst/doc/Errors_Logs_And_Debugging.pdf, vignettes/BiocParallel/inst/doc/Introduction_To_BiocParallel.pdf vignetteTitles: 2. 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Package vignettes illustrate use and functionality. biocViews: Software Author: Andrzej Oleś, Martin Morgan, Wolfgang Huber Maintainer: Bioconductor Package Maintainer URL: https://github.com/Bioconductor/BiocStyle VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/BiocStyle/issues git_url: https://git.bioconductor.org/packages/BiocStyle git_branch: RELEASE_3_8 git_last_commit: 8fc9460 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocStyle_2.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocStyle_2.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocStyle_2.10.0.tgz vignettes: vignettes/BiocStyle/inst/doc/LatexStyle2.pdf, vignettes/BiocStyle/inst/doc/AuthoringRmdVignettes.html vignetteTitles: Bioconductor LaTeX Style 2.0, Authoring R Markdown vignettes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiocStyle/inst/doc/AuthoringRmdVignettes.R, vignettes/BiocStyle/inst/doc/LatexStyle2.R importsMe: abseqR, ASpli, BiocWorkflowTools, BPRMeth, BubbleTree, chimeraviz, COMPASS, geneXtendeR, PathoStat, regionReport, Rmmquant, Rqc, srnadiff suggestsMe: ABAEnrichment, ACE, adaptest, AffiXcan, affycoretools, AllelicImbalance, AMOUNTAIN, amplican, AneuFinder, AnnotationDbi, AnnotationFilter, AnnotationForge, AnnotationHub, AnnotationHubData, annotatr, arrayQualityMetrics, artMS, ASGSCA, ASICS, AssessORF, ASSIGN, ATACseqQC, AUCell, BaalChIP, bacon, bamsignals, basecallQC, BASiCS, BayesPeak, bayNorm, baySeq, beachmat, beadarray, BeadDataPackR, BEARscc, BgeeDB, bigmelon, bigmemoryExtras, bioassayR, bioCancer, BiocFileCache, BiocNeighbors, BiocOncoTK, BioCor, BiocParallel, BiocPkgTools, biomaRt, biomformat, biosigner, biotmle, BitSeq, blima, bnbc, branchpointer, breakpointR, BridgeDbR, BrowserViz, bsseq, BUMHMM, BUScorrect, CAFE, CAGEfightR, CAGEr, CAMTHC, CancerInSilico, CAnD, Cardinal, CATALYST, cbaf, ccfindR, ccrepe, cellbaseR, cellity, CellMapper, cellTree, CexoR, ChemmineOB, ChemmineR, Chicago, chipenrich, ChIPexoQual, ChIPpeakAnno, ChIPQC, ChIPseeker, ChIPSeqSpike, chromstaR, chromswitch, ClassifyR, cleanUpdTSeq, cleaver, clipper, clusterExperiment, clusterSeq, ClusterSignificance, CNEr, CNPBayes, COCOA, CoGAPS, coMET, compcodeR, condcomp, CONFESS, consensusSeekeR, contiBAIT, conumee, CopywriteR, coRdon, CoRegNet, cosmiq, CountClust, covRNA, cpvSNP, CRISPRseek, CrispRVariants, CTDquerier, ctsGE, CVE, cydar, dada2, dagLogo, DaMiRseq, DAPAR, DChIPRep, ddPCRclust, decontam, DEFormats, DEGreport, DelayedArray, DelayedMatrixStats, DEP, derfinder, derfinderHelper, derfinderPlot, DEScan2, DEXSeq, DiffBind, diffcyt, diffuStats, discordant, dmrseq, DNABarcodes, doppelgangR, Doscheda, DOSE, drawProteins, DRIMSeq, DropletUtils, dSimer, DSS, dupRadar, easyRNASeq, EBImage, EDASeq, EGSEA, eiR, ELMER, EmpiricalBrownsMethod, EnrichmentBrowser, ensembldb, EpiDISH, epivizr, epivizrChart, epivizrData, epivizrServer, epivizrStandalone, erma, ERSSA, EventPointer, ExperimentHub, ExperimentHubData, FamAgg, FastqCleaner, fCCAC, fCI, FELLA, FindMyFriends, flowcatchR, flowMap, FlowSOM, fmcsR, FourCSeq, GA4GHclient, GA4GHshiny, GARS, gcapc, GDSArray, genbankr, GeneAccord, genefilter, GeneOverlap, geneplast, GeneStructureTools, GenoGAM, GenomeInfoDb, GenomicAlignments, GenomicDataCommons, GenomicFeatures, GenomicFiles, GenomicInteractions, GenomicRanges, GenomicScores, GenomicTuples, genoset, GenVisR, ggbio, Glimma, glmSparseNet, GMRP, GOexpress, GOfuncR, GoogleGenomics, GOpro, goSTAG, gpart, gQTLBase, gQTLstats, graphite, GreyListChIP, GRmetrics, groHMM, GSAR, GSEABase, GSEABenchmarkeR, GUIDEseq, Gviz, gwasurvivr, Harman, HDF5Array, HelloRanges, hipathia, HIREewas, HiTC, HPAanalyze, hpar, HTSFilter, ideal, iGC, igvR, IHW, illuminaio, imageHTS, IMAS, Imetagene, immunoClust, InPAS, INSPEcT, InTAD, InteractionSet, InterMineR, IONiseR, IRanges, iSEE, isomiRs, IVAS, JunctionSeq, karyoploteR, kissDE, Linnorm, loci2path, Logolas, LOLA, LoomExperiment, LowMACA, lpsymphony, LRBaseDbi, M3D, MACPET, MAGeCKFlute, mAPKL, maser, MAST, MatrixRider, matter, MaxContrastProjection, MBASED, MBttest, MCbiclust, mCSEA, mdgsa, MEAL, MEDIPS, messina, MetaboSignal, metagene, metagenomeFeatures, metavizr, methimpute, methInheritSim, MethPed, MethylAid, methylInheritance, MethylMix, methyvim, MetNet, mfa, microbiome, mimager, minfi, MIRA, miRcomp, miRmine, miRSM, miRsponge, missMethyl, missRows, mixOmics, MLSeq, MMDiff2, MODA, mogsa, MoonlightR, motifbreakR, motifStack, mpra, MSnbase, MSnID, msPurity, MSstats, MSstatsTMT, MTseeker, MultiAssayExperiment, MultiDataSet, multiHiCcompare, multiMiR, MutationalPatterns, MWASTools, mygene, myvariant, mzR, NADfinder, NanoStringDiff, NanoStringQCPro, NarrowPeaks, ndexr, nethet, netprioR, netReg, netSmooth, nondetects, normr, npGSEA, nucleoSim, nucleR, oligo, omicade4, omicRexposome, OmicsMarkeR, omicsPrint, Onassis, OncoScore, OncoSimulR, ontoProc, OPWeight, ORFik, Organism.dplyr, Oscope, OUTRIDER, PAA, PanVizGenerator, Path2PPI, paxtoolsr, Pbase, pcaExplorer, PCAN, PepsNMR, perturbatr, PGA, phantasus, phenopath, philr, phyloseq, Pi, Pigengene, plethy, plotGrouper, plyranges, Polyfit, powerTCR, pqsfinder, profileScoreDist, pRoloc, pRolocGUI, Prostar, ProteomicsAnnotationHubData, ProteoMM, proteoQC, PSEA, PureCN, PWMEnrich, qcmetrics, QDNAseq, qpgraph, qsea, QSutils, quantro, QuasR, R3CPET, RaggedExperiment, rain, ramwas, RandomWalkRestartMH, Rbowtie, Rcade, rcellminer, rCGH, RcisTarget, RCy3, RCyjs, ReactomePA, recount, recoup, RedeR, RefNet, regioneR, regsplice, ReQON, restfulSE, rexposome, rfPred, RGMQL, RGraph2js, RGSEA, rhdf5, rhdf5client, Rhdf5lib, Rhtslib, RiboProfiling, riboSeqR, RIVER, RJMCMCNucleosomes, RNAprobR, rnaseqcomp, RnaSeqSampleSize, Rnits, rols, ropls, rpx, rqt, Rsamtools, RTCGAToolbox, RTN, RTNduals, RTNsurvival, RUVcorr, RUVSeq, RVS, rWikiPathways, S4Vectors, sampleClassifier, sangerseqR, sapFinder, scater, scDD, SCnorm, scone, scoreInvHap, scran, scruff, segmentSeq, seqCAT, seqPattern, seqplots, seqsetvis, SeqSQC, SeqVarTools, sevenC, SGSeq, shinyMethyl, ShortRead, SIAMCAT, SigCheck, SigFuge, signet, SIMD, similaRpeak, SIMLR, simulatorZ, sincell, SingleCellExperiment, singleCellTK, slinky, SNPediaR, SNPhood, soGGi, sparseDOSSA, sparsenetgls, SparseSignatures, specL, SpidermiR, splatter, SPLINTER, SSPA, stageR, STAN, StarBioTrek, STATegRa, statTarget, strandCheckR, SummarizedBenchmark, SummarizedExperiment, sva, SVAPLSseq, swfdr, switchde, synapter, systemPipeR, TargetSearch, TCGAbiolinks, TCGAbiolinksGUI, TCGAutils, TFARM, TFBSTools, TFHAZ, TFutils, tigre, TMixClust, ToPASeq, topdownr, TPP, tracktables, trackViewer, transcriptogramer, transcriptR, Trendy, tRNA, tRNAdbImport, tRNAscanImport, TRONCO, TTMap, TurboNorm, TVTB, twoddpcr, universalmotif, variancePartition, VariantAnnotation, VariantFiltering, vidger, vsn, wavClusteR, XBSeq, xcms, yamss, YAPSA, zinbwave, mlm4omics Package: BiocVersion Version: 3.8.0 Depends: R (>= 3.5.0), R (< 3.6.0) License: Artistic-2.0 MD5sum: 7ebb61bfd78dcc1567b649a35dee075a NeedsCompilation: no Title: Set the appropriate version of Bioconductor packages Description: This package provides repository information for the appropriate version of Bioconductor. biocViews: Infrastructure Author: Martin Morgan [aut], Marcel Ramos [ctb], Bioconductor Package Maintainer [ctb, cre] Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/BiocVersion git_branch: RELEASE_3_8 git_last_commit: 4d09de4 git_last_commit_date: 2018-05-01 Date/Publication: 2018-10-31 source.ver: src/contrib/BiocVersion_3.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocVersion_3.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocVersion_3.8.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: biocViews Version: 1.50.10 Depends: R (>= 3.5.0) Imports: Biobase, graph (>= 1.9.26), methods, RBGL (>= 1.13.5), tools, utils, XML, RCurl, RUnit Suggests: BiocGenerics, knitr, commonmark License: Artistic-2.0 MD5sum: 9b66a0cdd9cebbd49c171e6b2131137a NeedsCompilation: no Title: Categorized views of R package repositories Description: Infrastructure to support Bioconductor 'views' used to classify software packages. 'biocViews' are directed acyclic graphs of terms from a controlled vocabulary. There are three major classifications, corresponding to 'software', 'annotation', and 'experiment data' packages. biocViews: Infrastructure Author: VJ Carey , BJ Harshfield , S Falcon , Sonali Arora Maintainer: Bioconductor Package Maintainer URL: http://www.bioconductor.org/packages/release/BiocViews.html git_url: https://git.bioconductor.org/packages/biocViews git_branch: RELEASE_3_8 git_last_commit: 24d1431 git_last_commit_date: 2018-12-18 Date/Publication: 2018-12-18 source.ver: src/contrib/biocViews_1.50.10.tar.gz win.binary.ver: bin/windows/contrib/3.5/biocViews_1.50.10.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biocViews_1.50.10.tgz vignettes: vignettes/biocViews/inst/doc/createReposHtml.pdf, vignettes/biocViews/inst/doc/HOWTO-BCV.pdf vignetteTitles: biocViews-CreateRepositoryHTML, biocViews-HOWTO hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biocViews/inst/doc/createReposHtml.R, vignettes/biocViews/inst/doc/HOWTO-BCV.R dependsOnMe: Risa importsMe: AnnotationHubData, BiocCheck, ExperimentHubData, monocle, sigFeature suggestsMe: BiocPkgTools Package: BiocWorkflowTools Version: 1.8.0 Depends: R (>= 3.4) Imports: BiocStyle, bookdown, devtools, git2r, httr, knitr, rmarkdown, rstudioapi, stringr, tools, utils License: MIT + file LICENSE MD5sum: 6c344c8e215be2318eca98bc8f579a67 NeedsCompilation: no Title: Tools to aid the development of Bioconductor Workflow packages Description: Provides functions to ease the transition between Rmarkdown and LaTeX documents when authoring a Bioconductor Workflow. biocViews: Software, ReportWriting Author: Mike Smith [aut, cre], Andrzej Oleś [aut] Maintainer: Mike Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BiocWorkflowTools git_branch: RELEASE_3_8 git_last_commit: 281edd0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiocWorkflowTools_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiocWorkflowTools_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiocWorkflowTools_1.8.0.tgz vignettes: vignettes/BiocWorkflowTools/inst/doc/Generate_F1000_Latex.html vignetteTitles: Converting Rmarkdown to F1000Research LaTeX Format hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/BiocWorkflowTools/inst/doc/Generate_F1000_Latex.R Package: bioDist Version: 1.54.0 Depends: R (>= 2.0), methods, Biobase,KernSmooth Suggests: locfit License: Artistic-2.0 MD5sum: fed70af697577a8e3f3f7065be6b790b NeedsCompilation: no Title: Different distance measures Description: A collection of software tools for calculating distance measures. biocViews: Clustering, Classification Author: B. Ding, R. Gentleman and Vincent Carey Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/bioDist git_branch: RELEASE_3_8 git_last_commit: a0f74b8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bioDist_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bioDist_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bioDist_1.54.0.tgz vignettes: vignettes/bioDist/inst/doc/bioDist.pdf vignetteTitles: bioDist Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bioDist/inst/doc/bioDist.R suggestsMe: BiocCaseStudies Package: biomaRt Version: 2.38.0 Depends: methods Imports: utils, XML, RCurl, AnnotationDbi, progress, stringr, httr Suggests: annotate, BiocStyle, knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: 4a9185e87108865494abcd7340cab002 NeedsCompilation: no Title: Interface to BioMart databases (i.e. Ensembl) Description: In recent years a wealth of biological data has become available in public data repositories. Easy access to these valuable data resources and firm integration with data analysis is needed for comprehensive bioinformatics data analysis. biomaRt provides an interface to a growing collection of databases implementing the BioMart software suite (http://www.biomart.org). The package enables retrieval of large amounts of data in a uniform way without the need to know the underlying database schemas or write complex SQL queries. The most prominent examples of BioMart databases are Ensembl, which provides biomaRt users direct access to a diverse set of data and enables a wide range of powerful online queries from gene annotation to database mining. biocViews: Annotation Author: Steffen Durinck [aut], Wolfgang Huber [aut], Sean Davis [ctb], Francois Pepin [ctb], Vince S Buffalo [ctb], Mike Smith [ctb, cre] Maintainer: Mike Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/biomaRt git_branch: RELEASE_3_8 git_last_commit: 16b997a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biomaRt_2.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biomaRt_2.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biomaRt_2.38.0.tgz vignettes: vignettes/biomaRt/inst/doc/biomaRt.html vignetteTitles: The biomaRt users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biomaRt/inst/doc/biomaRt.R dependsOnMe: chromPlot, coMET, customProDB, dagLogo, DrugVsDisease, GenomeGraphs, MineICA, PPInfer, PSICQUIC, Roleswitch, VegaMC importsMe: ArrayExpressHTS, artMS, BadRegionFinder, branchpointer, ChIPpeakAnno, CHRONOS, cobindR, DEXSeq, diffloop, DominoEffect, DOQTL, easyRNASeq, EDASeq, ELMER, GDCRNATools, GeneAccord, GenomicFeatures, GenVisR, gespeR, glmSparseNet, GOexpress, goSTAG, gpart, Gviz, HTSanalyzeR, IdMappingRetrieval, isobar, MAGeCKFlute, MEDIPS, MetaboSignal, metaseqR, methyAnalysis, MGFR, OncoScore, oposSOM, Pbase, pcaExplorer, PGA, phenoTest, pRoloc, ProteoMM, psygenet2r, pwOmics, R453Plus1Toolbox, ramwas, RCAS, recoup, rgsepd, RNAither, scPipe, seq2pathway, SeqGSEA, SPLINTER, SWATH2stats, TCGAbiolinks, TFEA.ChIP, transcriptogramer, trena, yarn suggestsMe: AnnotationForge, bioassayR, BiocCaseStudies, cellTree, chromstaR, ClusterJudge, cTRAP, FELLA, GeneAnswers, Genominator, h5vc, LINC, martini, massiR, MineICA, MiRaGE, MutationalPatterns, netSmooth, oligo, OrganismDbi, paxtoolsr, piano, Pigengene, progeny, R3CPET, Rcade, RIPSeeker, RnBeads, rTANDEM, rTRM, scater, ShortRead, SIM, sincell, SummarizedBenchmark, systemPipeR, trackViewer, wiggleplotr, zinbwave Package: biomformat Version: 1.10.1 Depends: R (>= 3.2), methods Imports: plyr (>= 1.8), jsonlite (>= 0.9.16), Matrix (>= 1.2), rhdf5 Suggests: testthat (>= 0.10), knitr (>= 1.10), BiocStyle (>= 1.6), rmarkdown (>= 0.7) License: GPL-2 MD5sum: 978fbb49840f53897a87e2bb95a73c0c NeedsCompilation: no Title: An interface package for the BIOM file format Description: This is an R package for interfacing with the BIOM format. This package includes basic tools for reading biom-format files, accessing and subsetting data tables from a biom object (which is more complex than a single table), as well as limited support for writing a biom-object back to a biom-format file. The design of this API is intended to match the python API and other tools included with the biom-format project, but with a decidedly "R flavor" that should be familiar to R users. This includes S4 classes and methods, as well as extensions of common core functions/methods. biocViews: ImmunoOncology, DataImport, Metagenomics, Microbiome Author: Paul J. McMurdie and Joseph N Paulson Maintainer: Paul J. McMurdie URL: https://github.com/joey711/biomformat/, http://biom-format.org/ VignetteBuilder: knitr BugReports: https://github.com/joey711/biomformat/issues git_url: https://git.bioconductor.org/packages/biomformat git_branch: RELEASE_3_8 git_last_commit: e67c6f4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/biomformat_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/biomformat_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biomformat_1.10.1.tgz vignettes: vignettes/biomformat/inst/doc/biomformat.html vignetteTitles: The biomformat package Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biomformat/inst/doc/biomformat.R importsMe: phyloseq suggestsMe: metagenomeSeq Package: BioMVCClass Version: 1.50.0 Depends: R (>= 2.1.0), methods, MVCClass, Biobase, graph, Rgraphviz License: LGPL MD5sum: a37c816ced8ff46c22e7493f9e10997f NeedsCompilation: no Title: Model-View-Controller (MVC) Classes That Use Biobase Description: Creates classes used in model-view-controller (MVC) design biocViews: Visualization, Infrastructure, GraphAndNetwork Author: Elizabeth Whalen Maintainer: Elizabeth Whalen git_url: https://git.bioconductor.org/packages/BioMVCClass git_branch: RELEASE_3_8 git_last_commit: 9f0f889 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BioMVCClass_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BioMVCClass_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BioMVCClass_1.50.0.tgz vignettes: vignettes/BioMVCClass/inst/doc/BioMVCClass.pdf vignetteTitles: BioMVCClass hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: biomvRCNS Version: 1.22.0 Depends: IRanges, GenomicRanges, Gviz Imports: methods, mvtnorm Suggests: cluster, parallel, GenomicFeatures, dynamicTreeCut, Rsamtools, TxDb.Hsapiens.UCSC.hg19.knownGene License: GPL (>= 2) Archs: i386, x64 MD5sum: 43649cec95f927eace8290ffe12e756d NeedsCompilation: yes Title: Copy Number study and Segmentation for multivariate biological data Description: In this package, a Hidden Semi Markov Model (HSMM) and one homogeneous segmentation model are designed and implemented for segmentation genomic data, with the aim of assisting in transcripts detection using high throughput technology like RNA-seq or tiling array, and copy number analysis using aCGH or sequencing. biocViews: aCGH, CopyNumberVariation, Microarray, Sequencing, Sequencing, Visualization, Genetics Author: Yang Du Maintainer: Yang Du git_url: https://git.bioconductor.org/packages/biomvRCNS git_branch: RELEASE_3_8 git_last_commit: f01fd8f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biomvRCNS_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biomvRCNS_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biomvRCNS_1.22.0.tgz vignettes: vignettes/biomvRCNS/inst/doc/biomvRCNS.pdf vignetteTitles: biomvRCNS package introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biomvRCNS/inst/doc/biomvRCNS.R Package: BioNet Version: 1.42.0 Depends: R (>= 2.10.0), graph, RBGL Imports: igraph (>= 1.0.1), AnnotationDbi, Biobase Suggests: rgl, impute, DLBCL, genefilter, xtable, ALL, limma, hgu95av2.db, XML License: GPL (>= 2) MD5sum: c87b42a860906cd6ec25b02150e4b763 NeedsCompilation: no Title: Routines for the functional analysis of biological networks Description: This package provides functions for the integrated analysis of protein-protein interaction networks and the detection of functional modules. Different datasets can be integrated into the network by assigning p-values of statistical tests to the nodes of the network. E.g. p-values obtained from the differential expression of the genes from an Affymetrix array are assigned to the nodes of the network. By fitting a beta-uniform mixture model and calculating scores from the p-values, overall scores of network regions can be calculated and an integer linear programming algorithm identifies the maximum scoring subnetwork. biocViews: Microarray, DataImport, GraphAndNetwork, Network, NetworkEnrichment, GeneExpression, DifferentialExpression Author: Marcus Dittrich and Daniela Beisser Maintainer: Marcus Dittrich URL: http://bionet.bioapps.biozentrum.uni-wuerzburg.de/ git_url: https://git.bioconductor.org/packages/BioNet git_branch: RELEASE_3_8 git_last_commit: 8721550 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BioNet_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BioNet_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BioNet_1.42.0.tgz vignettes: vignettes/BioNet/inst/doc/Tutorial.pdf vignetteTitles: BioNet Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BioNet/inst/doc/Tutorial.R importsMe: HTSanalyzeR, SMITE suggestsMe: SANTA Package: BioNetStat Version: 1.2.2 Depends: R (>= 3.5), shiny, igraph, shinyBS, pathview Imports: BiocParallel, RJSONIO, whisker, yaml, pheatmap, ggplot2, plyr, utils, stats, RColorBrewer, Hmisc, psych, knitr License: GPL (>= 3) MD5sum: d815407c6d2c3bb0387ae0e22fc2ee81 NeedsCompilation: no Title: Biological Network Analysis Description: A package to perform differential network analysis, differential node analysis (differential coexpression analysis), network and metabolic pathways view. biocViews: Network, NetworkInference, Pathways, GraphAndNetwork, Sequencing, Microarray, Metabolomics, Proteomics, GeneExpression, RNASeq, SystemsBiology, DifferentialExpression, GeneSetEnrichment, ImmunoOncology Author: Vinícius Jardim, Suzana Santos, André Fujita, and Marcos Buckeridge Maintainer: Vinicius Jardim URL: http://github.com/jardimViniciusC/BioNetStat VignetteBuilder: knitr BugReports: http://github.com/jardimViniciusC/BioNetStat/issues git_url: https://git.bioconductor.org/packages/BioNetStat git_branch: RELEASE_3_8 git_last_commit: e9b4a61 git_last_commit_date: 2018-12-17 Date/Publication: 2018-12-17 source.ver: src/contrib/BioNetStat_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/BioNetStat_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BioNetStat_1.2.2.tgz vignettes: vignettes/BioNetStat/inst/doc/BNS_tutorial_by_command_line.html, vignettes/BioNetStat/inst/doc/vignette.html vignetteTitles: 1. Line command tutorial, 2. Interface tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: BioQC Version: 1.10.0 Depends: utils, Rcpp, Biobase, methods, stats Suggests: testthat, knitr, rmarkdown, lattice, latticeExtra, rbenchmark, gplots, gridExtra, hgu133plus2.db, ineq License: GPL (>=3) Archs: i386, x64 MD5sum: 47b14e1b9485410002bb96d5346fb525 NeedsCompilation: yes Title: Detect tissue heterogeneity in expression profiles with gene sets Description: BioQC performs quality control of high-throughput expression data based on tissue gene signatures. It can detect tissue heterogeneity in gene expression data. The core algorithm is a Wilcoxon-Mann-Whitney test that is optimised for high performance. biocViews: GeneExpression,QualityControl,StatisticalMethod Author: Jitao David Zhang , Laura Badi, Gregor Sturm, Roland Ambs Maintainer: Jitao David Zhang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BioQC git_branch: RELEASE_3_8 git_last_commit: 5c71aee git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BioQC_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BioQC_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BioQC_1.10.0.tgz vignettes: vignettes/BioQC/inst/doc/bioqc-efficiency.html, vignettes/BioQC/inst/doc/bioqc-signedGenesets.html, vignettes/BioQC/inst/doc/bioqc.html vignetteTitles: BioQC Alogrithm: Speeding up the Wilcoxon-Mann-Whitney Test, Using BioQC with signed genesets, BioQC: Detect tissue heterogeneity in gene expression data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BioQC/inst/doc/bioqc-efficiency.R, vignettes/BioQC/inst/doc/bioqc-signedGenesets.R, vignettes/BioQC/inst/doc/bioqc.R Package: BioSeqClass Version: 1.40.0 Depends: R (>= 2.10), scatterplot3d Imports: Biostrings, ipred, e1071, klaR, randomForest, class, tree, nnet, rpart, party, foreign, Biobase, utils, stats, grDevices Suggests: scatterplot3d License: LGPL (>= 2.0) MD5sum: 9bb1fbea1848a6ffe2e020deaa1f3777 NeedsCompilation: no Title: Classification for Biological Sequences Description: Extracting Features from Biological Sequences and Building Classification Model biocViews: Classification Author: Li Hong sysptm@gmail.com Maintainer: Li Hong git_url: https://git.bioconductor.org/packages/BioSeqClass git_branch: RELEASE_3_8 git_last_commit: b13df85 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BioSeqClass_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BioSeqClass_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BioSeqClass_1.40.0.tgz vignettes: vignettes/BioSeqClass/inst/doc/BioSeqClass.pdf vignetteTitles: Using the BioSeqClass Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BioSeqClass/inst/doc/BioSeqClass.R Package: biosigner Version: 1.10.0 Imports: methods, e1071, randomForest, ropls, Biobase Suggests: BioMark, RUnit, BiocGenerics, BiocStyle, golubEsets, hu6800.db, knitr, rmarkdown License: CeCILL MD5sum: 5a7f57cd3552ed1c2cf21cf18f33da77 NeedsCompilation: no Title: Signature discovery from omics data Description: Feature selection is critical in omics data analysis to extract restricted and meaningful molecular signatures from complex and high-dimension data, and to build robust classifiers. This package implements a new method to assess the relevance of the variables for the prediction performances of the classifier. The approach can be run in parallel with the PLS-DA, Random Forest, and SVM binary classifiers. The signatures and the corresponding 'restricted' models are returned, enabling future predictions on new datasets. A Galaxy implementation of the package is available within the Workflow4metabolomics.org online infrastructure for computational metabolomics. biocViews: Classification, FeatureExtraction, Transcriptomics, Proteomics, Metabolomics, Lipidomics Author: Philippe Rinaudo , Etienne Thevenot Maintainer: Philippe Rinaudo , Etienne Thevenot VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/biosigner git_branch: RELEASE_3_8 git_last_commit: 3146e24 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biosigner_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biosigner_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biosigner_1.10.0.tgz vignettes: vignettes/biosigner/inst/doc/biosigner-vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biosigner/inst/doc/biosigner-vignette.R Package: Biostrings Version: 2.50.2 Depends: R (>= 3.5.0), methods, BiocGenerics, S4Vectors, IRanges, XVector Imports: graphics, methods, stats, utils LinkingTo: S4Vectors, IRanges, XVector (>= 0.21.4) Suggests: BSgenome (>= 1.13.14), BSgenome.Celegans.UCSC.ce2 (>= 1.3.11), BSgenome.Dmelanogaster.UCSC.dm3 (>= 1.3.11), BSgenome.Hsapiens.UCSC.hg18, drosophila2probe, hgu95av2probe, hgu133aprobe, GenomicFeatures (>= 1.3.14), hgu95av2cdf, affy (>= 1.41.3), affydata (>= 1.11.5), RUnit Enhances: Rmpi License: Artistic-2.0 Archs: i386, x64 MD5sum: 40233fb2ae38e2e1d5900cdd2e578ad7 NeedsCompilation: yes Title: Efficient manipulation of biological strings Description: Memory efficient string containers, string matching algorithms, and other utilities, for fast manipulation of large biological sequences or sets of sequences. biocViews: SequenceMatching, Alignment, Sequencing, Genetics, DataImport, DataRepresentation, Infrastructure Author: H. Pagès, P. Aboyoun, R. Gentleman, and S. DebRoy Maintainer: H. Pagès git_url: https://git.bioconductor.org/packages/Biostrings git_branch: RELEASE_3_8 git_last_commit: 025e734 git_last_commit_date: 2019-01-03 Date/Publication: 2019-01-03 source.ver: src/contrib/Biostrings_2.50.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/Biostrings_2.50.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Biostrings_2.50.2.tgz vignettes: vignettes/Biostrings/inst/doc/Biostrings2Classes.pdf, vignettes/Biostrings/inst/doc/BiostringsQuickOverview.pdf, vignettes/Biostrings/inst/doc/matchprobes.pdf, vignettes/Biostrings/inst/doc/MultipleAlignments.pdf, vignettes/Biostrings/inst/doc/PairwiseAlignments.pdf vignetteTitles: A short presentation of the basic classes defined in Biostrings 2, Biostrings Quick Overview, Handling probe sequence information, Multiple Alignments, Pairwise Sequence Alignments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Biostrings/inst/doc/Biostrings2Classes.R, vignettes/Biostrings/inst/doc/matchprobes.R, vignettes/Biostrings/inst/doc/MultipleAlignments.R, vignettes/Biostrings/inst/doc/PairwiseAlignments.R dependsOnMe: altcdfenvs, amplican, Basic4Cseq, BRAIN, BSgenome, chimeraviz, ChIPanalyser, ChIPpeakAnno, ChIPsim, cleaver, CODEX, CRISPRseek, DECIPHER, deepSNV, GeneRegionScan, GenomicAlignments, GOTHiC, HelloRanges, hiReadsProcessor, iPAC, kebabs, MethTargetedNGS, methVisual, minfi, MotifDb, motifRG, motifStack, msa, muscle, oligo, pcaGoPromoter, PGA, pqsfinder, qrqc, QSutils, R453Plus1Toolbox, R4RNA, REDseq, rGADEM, RiboProfiling, Roleswitch, rRDP, Rsamtools, RSVSim, sangerseqR, SCAN.UPC, scsR, SELEX, seqbias, ShortRead, SICtools, systemPipeR, topdownr, triplex, waveTiling importsMe: AffyCompatible, AllelicImbalance, alpine, AneuFinder, AnnotationHubData, appreci8R, ArrayExpressHTS, AssessORF, ATACseqQC, BBCAnalyzer, BCRANK, bcSeq, BEAT, BioSeqClass, biovizBase, branchpointer, BSgenome, bsseq, BUMHMM, charm, ChIPseqR, ChIPsim, chromVAR, CNEr, cobindR, compEpiTools, consensusDE, coRdon, CrispRVariants, customProDB, dada2, dagLogo, diffHic, DNAshapeR, DominoEffect, easyRNASeq, EDASeq, ensembldb, ensemblVEP, esATAC, eudysbiome, FastqCleaner, FindMyFriends, FourCSeq, GA4GHclient, gcapc, gcrma, genbankr, GeneRegionScan, GenoGAM, genomation, GenomicAlignments, GenomicFeatures, GenomicScores, genphen, GenVisR, ggbio, GGtools, girafe, gmapR, GoogleGenomics, GUIDEseq, Gviz, gwascat, h5vc, heatmaps, HiTC, HTSeqGenie, icetea, IMMAN, IntEREst, InterMineR, IONiseR, ipdDb, IsoformSwitchAnalyzeR, KEGGREST, Logolas, LowMACA, LymphoSeq, MACPET, MADSEQ, maftools, MatrixRider, MDTS, MEDIPS, MEDME, metagenomeFeatures, methimpute, methVisual, methylPipe, microRNA, MMDiff2, motifbreakR, motifcounter, motifmatchr, MotIV, MTseeker, MutationalPatterns, nucleR, oligoClasses, OmaDB, openPrimeR, ORFik, OTUbase, Pbase, pdInfoBuilder, phyloseq, podkat, polyester, primirTSS, proBAMr, procoil, ProteomicsAnnotationHubData, PureCN, Pviz, qPLEXanalyzer, qrqc, qsea, QuasR, r3Cseq, ramwas, RCAS, Rcpi, REDseq, regioneR, REMP, Repitools, rGADEM, RNAprobR, RNASeqR, Rqc, rSFFreader, rtracklayer, scmeth, scoreInvHap, scruff, SeqArray, seqcombo, seqPattern, seqplots, SGSeq, signeR, SNPhood, soGGi, SomaticSignatures, SparseSignatures, SPLINTER, sscu, synapter, TarSeqQC, TFBSTools, transite, trena, tRNA, tRNAdbImport, tRNAscanImport, TVTB, Ularcirc, universalmotif, VariantAnnotation, VariantFiltering, VariantTools, wavClusteR suggestsMe: annotate, AnnotationForge, AnnotationHub, CSAR, exomeCopy, GenomicFiles, GenomicRanges, genoset, GWASTools, methylumi, MiRaGE, nuCpos, rpx, rTRM, XVector linksToMe: DECIPHER, kebabs, MatrixRider, Rsamtools, rSFFreader, ShortRead, triplex, VariantAnnotation, VariantFiltering Package: biosvd Version: 2.18.0 Depends: R (>= 3.1.0) Imports: BiocGenerics, Biobase, methods, grid, graphics, NMF License: Artistic-2.0 MD5sum: aeb5728b6822575a2e87140073a2de84 NeedsCompilation: no Title: Package for high-throughput data processing, outlier detection, noise removal and dynamic modeling Description: The biosvd package contains functions to reduce the input data set from the feature x assay space to the reduced diagonalized eigenfeature x eigenassay space, with the eigenfeatures and eigenassays unique orthonormal superpositions of the features and assays, respectively. Results of SVD applied to the data can subsequently be inspected based on generated graphs, such as a heatmap of the eigenfeature x assay matrix and a bar plot with the eigenexpression fractions of all eigenfeatures. These graphs aid in deciding which eigenfeatures and eigenassays to filter out (i.e., eigenfeatures representing steady state, noise, or experimental artifacts; or when applied to the variance in the data, eigenfeatures representing steady-scale variance). After possible removal of steady state expression, steady-scale variance, noise and experimental artifacts, and after re-applying SVD to the normalized data, a summary html report of the eigensystem is generated, containing among others polar plots of the assays and features, a table with the list of features sortable according to their coordinates, radius and phase in the polar plot, and a visualization of the data sorted according to the two selected eigenfeatures and eigenassays with colored feature/assay annotation information when provided. This gives a global picture of the dynamics of expression/intensity levels, in which individual features and assays are classified in groups of similar regulation and function or similar cellular state and biological phenotype. biocViews: TimeCourse, Visualization Author: Anneleen Daemen , Matthew Brauer Maintainer: Anneleen Daemen , Matthew Brauer git_url: https://git.bioconductor.org/packages/biosvd git_branch: RELEASE_3_8 git_last_commit: ec7cd56 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biosvd_2.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biosvd_2.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biosvd_2.18.0.tgz vignettes: vignettes/biosvd/inst/doc/biosvd.pdf vignetteTitles: biosvd hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biosvd/inst/doc/biosvd.R Package: biotmle Version: 1.6.0 Depends: R (>= 3.4) Imports: dplyr, ggplot2, ggsci, superheat, doFuture, future, stats, methods, limma, S4Vectors, BiocGenerics, BiocParallel, SummarizedExperiment, tmle Suggests: testthat, knitr, rmarkdown, BiocStyle, SuperLearner, Matrix, DBI, biotmleData (>= 1.1.1) License: file LICENSE MD5sum: 19b83e8aa5038a0a939357fa63638a44 NeedsCompilation: no Title: Targeted Learning with Moderated Statistics for Biomarker Discovery Description: This package facilitates the discovery of biomarkers from biological sequencing data (e.g., microarrays, RNA-seq) based on the associations of potential biomarkers with exposure and outcome variables by implementing an estimation procedure that combines a generalization of moderated statistics with targeted minimum loss-based estimates (TMLE) of parameters defined via causal inference (e.g., Average Treatment Effect) whose estimators admit asymptotically linear representations. biocViews: GeneExpression, DifferentialExpression, Sequencing, Microarray, RNASeq Author: Nima Hejazi [aut, cre, cph], Alan Hubbard [aut, ths], Weixin Cai [ctb] Maintainer: Nima Hejazi URL: https://github.com/nhejazi/biotmle VignetteBuilder: knitr BugReports: https://github.com/nhejazi/biotmle/issues git_url: https://git.bioconductor.org/packages/biotmle git_branch: RELEASE_3_8 git_last_commit: 85d5e91 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/biotmle_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/biotmle_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biotmle_1.6.0.tgz vignettes: vignettes/biotmle/inst/doc/exposureBiomarkers.html, vignettes/biotmle/inst/doc/rnaseqProcessing.html vignetteTitles: Identifying Biomarkers from an Exposure Variable, Processing and Analyzing RNA-Seq Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/biotmle/inst/doc/exposureBiomarkers.R, vignettes/biotmle/inst/doc/rnaseqProcessing.R Package: biovizBase Version: 1.30.1 Depends: R (>= 2.10), methods Imports: grDevices, stats, scales, Hmisc, RColorBrewer, dichromat, BiocGenerics, S4Vectors (>= 0.9.25), IRanges (>= 1.99.28), GenomeInfoDb (>= 1.5.14), GenomicRanges (>= 1.23.21), SummarizedExperiment, Biostrings (>= 2.33.11), Rsamtools (>= 1.17.28), GenomicAlignments (>= 1.1.16), GenomicFeatures (>= 1.21.19), AnnotationDbi, VariantAnnotation (>= 1.11.4), ensembldb (>= 1.99.13), AnnotationFilter (>= 0.99.8), rlang Suggests: BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome, rtracklayer, EnsDb.Hsapiens.v75, RUnit License: Artistic-2.0 Archs: i386, x64 MD5sum: 43a32d6cc270b0edf67938d30f9d1ce5 NeedsCompilation: yes Title: Basic graphic utilities for visualization of genomic data. Description: The biovizBase package is designed to provide a set of utilities, color schemes and conventions for genomic data. It serves as the base for various high-level packages for biological data visualization. This saves development effort and encourages consistency. biocViews: Infrastructure, Visualization, Preprocessing Author: Tengfei Yin [aut], Michael Lawrence [aut, ths, cre], Dianne Cook [aut, ths], Johannes Rainer [ctb] Maintainer: Michael Lawrence git_url: https://git.bioconductor.org/packages/biovizBase git_branch: RELEASE_3_8 git_last_commit: b6776d0 git_last_commit_date: 2018-12-11 Date/Publication: 2018-12-11 source.ver: src/contrib/biovizBase_1.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/biovizBase_1.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/biovizBase_1.30.1.tgz vignettes: vignettes/biovizBase/inst/doc/intro.pdf vignetteTitles: An Introduction to biovizBase hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/biovizBase/inst/doc/intro.R dependsOnMe: CAFE, qrqc importsMe: BubbleTree, ChIPexoQual, ggbio, Gviz, karyoploteR, Pviz, qrqc, Rqc suggestsMe: CINdex, derfinder, derfinderPlot, R3CPET, regionReport, TxRegInfra Package: BiRewire Version: 3.14.0 Depends: igraph, slam, tsne, Matrix Suggests: RUnit, BiocGenerics License: GPL-3 Archs: i386, x64 MD5sum: dfa755b6535050e3c39865feedb53c55 NeedsCompilation: yes Title: High-performing routines for the randomization of a bipartite graph (or a binary event matrix), undirected and directed signed graph preserving degree distribution (or marginal totals) Description: Fast functions for bipartite network rewiring through N consecutive switching steps (See References) and for the computation of the minimal number of switching steps to be performed in order to maximise the dissimilarity with respect to the original network. Includes functions for the analysis of the introduced randomness across the switching steps and several other routines to analyse the resulting networks and their natural projections. Extension to undirected networks and directed signed networks is also provided. Starting from version 1.9.7 a more precise bound (especially for small network) has been implemented. Starting from version 2.2.0 the analysis routine is more complete and a visual montioring of the underlying Markov Chain has been implemented. Starting from 3.6.0 the library can handle also matrices with NA (not for the directed signed graphs). biocViews: Network Author: Andrea Gobbi [aut], Francesco Iorio [aut], Giuseppe Jurman [cbt], Davide Albanese [cbt], Julio Saez-Rodriguez [cbt]. Maintainer: Andrea Gobbi URL: http://www.ebi.ac.uk/~iorio/BiRewire git_url: https://git.bioconductor.org/packages/BiRewire git_branch: RELEASE_3_8 git_last_commit: f0cbc88 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiRewire_3.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiRewire_3.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiRewire_3.14.0.tgz vignettes: vignettes/BiRewire/inst/doc/BiRewire.pdf vignetteTitles: BiRewire hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiRewire/inst/doc/BiRewire.R Package: birta Version: 1.26.0 Depends: limma, MASS, R(>= 2.10), Biobase, methods License: GPL (>= 2) Archs: i386, x64 MD5sum: 16a30ffecfc786f5ba64e8796f4a8266 NeedsCompilation: yes Title: Bayesian Inference of Regulation of Transcriptional Activity Description: Expression levels of mRNA molecules are regulated by different processes, comprising inhibition or activation by transcription factors and post-transcriptional degradation by microRNAs. birta (Bayesian Inference of Regulation of Transcriptional Activity) uses the regulatory networks of TFs and miRNAs together with mRNA and miRNA expression data to predict switches in regulatory activity between two conditions. A Bayesian network is used to model the regulatory structure and Markov-Chain-Monte-Carlo is applied to sample the activity states. biocViews: Microarray, Sequencing, GeneExpression, Transcription, GraphAndNetwork Author: Benedikt Zacher, Khalid Abnaof, Stephan Gade, Erfan Younesi, Achim Tresch, Holger Froehlich Maintainer: Benedikt Zacher , Holger Froehlich git_url: https://git.bioconductor.org/packages/birta git_branch: RELEASE_3_8 git_last_commit: 43cffee git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/birta_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/birta_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/birta_1.26.0.tgz vignettes: vignettes/birta/inst/doc/birta.pdf vignetteTitles: Bayesian Inference of Regulation of Transcriptional Activity hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/birta/inst/doc/birta.R Package: birte Version: 1.18.0 Depends: R(>= 3.0.0), RcppArmadillo (>= 0.3.6.1), Rcpp Imports: MASS, limma(>= 3.22.0), glmnet, Biobase, nem, graphics, stats, utils LinkingTo: RcppArmadillo, Rcpp Suggests: knitr Enhances: Rgraphviz License: GPL (>= 2) Archs: i386, x64 MD5sum: b36a82163e94932b5fc3c7bf23b0fa3f NeedsCompilation: yes Title: Bayesian Inference of Regulatory Influence on Expression (biRte) Description: Expression levels of mRNA molecules are regulated by different processes, comprising inhibition or activation by transcription factors and post-transcriptional degradation by microRNAs. biRte uses regulatory networks of TFs, miRNAs and possibly other factors, together with mRNA, miRNA and other available expression data to predict the relative influence of a regulator on the expression of its target genes. Inference is done in a Bayesian modeling framework using Markov-Chain-Monte-Carlo. A special feature is the possibility for follow-up network reverse engineering between active regulators. biocViews: Microarray, Sequencing, GeneExpression, Transcription, Network, Bayesian, Regression, NetworkInference Author: Holger Froehlich, contributions by Benedikt Zacher Maintainer: Holger Froehlich SystemRequirements: BLAS, LAPACK VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/birte git_branch: RELEASE_3_8 git_last_commit: c460d0e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/birte_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/birte_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/birte_1.18.0.tgz vignettes: vignettes/birte/inst/doc/birte.pdf vignetteTitles: Bayesian Inference of Regulation of Transcriptional Activity hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/birte/inst/doc/birte.R Package: BiSeq Version: 1.22.0 Depends: R (>= 2.15.2), methods, S4Vectors, IRanges (>= 1.17.24), GenomicRanges, SummarizedExperiment (>= 0.2.0), Formula Imports: methods, BiocGenerics, Biobase, S4Vectors, IRanges, GenomeInfoDb, GenomicRanges, SummarizedExperiment, rtracklayer, parallel, betareg, lokern, Formula, globaltest License: LGPL-3 MD5sum: 2a92d9e431dba31d85eb4b55a7239214 NeedsCompilation: no Title: Processing and analyzing bisulfite sequencing data Description: The BiSeq package provides useful classes and functions to handle and analyze targeted bisulfite sequencing (BS) data such as reduced-representation bisulfite sequencing (RRBS) data. In particular, it implements an algorithm to detect differentially methylated regions (DMRs). The package takes already aligned BS data from one or multiple samples. biocViews: Genetics, Sequencing, MethylSeq, DNAMethylation Author: Katja Hebestreit, Hans-Ulrich Klein Maintainer: Katja Hebestreit git_url: https://git.bioconductor.org/packages/BiSeq git_branch: RELEASE_3_8 git_last_commit: ca0eb05 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BiSeq_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BiSeq_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BiSeq_1.22.0.tgz vignettes: vignettes/BiSeq/inst/doc/BiSeq.pdf vignetteTitles: An Introduction to BiSeq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BiSeq/inst/doc/BiSeq.R importsMe: M3D Package: BitSeq Version: 1.26.1 Depends: Rsamtools, zlibbioc Imports: S4Vectors, IRanges LinkingTo: Rsamtools (>= 1.19.38), zlibbioc Suggests: edgeR, DESeq, BiocStyle License: Artistic-2.0 + file LICENSE Archs: i386, x64 MD5sum: bd6e7540ecca693034a832584b1244c1 NeedsCompilation: yes Title: Transcript expression inference and differential expression analysis for RNA-seq data Description: The BitSeq package is targeted for transcript expression analysis and differential expression analysis of RNA-seq data in two stage process. In the first stage it uses Bayesian inference methodology to infer expression of individual transcripts from individual RNA-seq experiments. The second stage of BitSeq embraces the differential expression analysis of transcript expression. Providing expression estimates from replicates of multiple conditions, Log-Normal model of the estimates is used for inferring the condition mean transcript expression and ranking the transcripts based on the likelihood of differential expression. biocViews: ImmunoOncology, GeneExpression, DifferentialExpression, Sequencing, RNASeq, Bayesian, AlternativeSplicing, DifferentialSplicing, Transcription Author: Peter Glaus, Antti Honkela and Magnus Rattray Maintainer: Antti Honkela , Panagiotis Papastamoulis git_url: https://git.bioconductor.org/packages/BitSeq git_branch: RELEASE_3_8 git_last_commit: 1f44958 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BitSeq_1.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BitSeq_1.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BitSeq_1.26.1.tgz vignettes: vignettes/BitSeq/inst/doc/BitSeq.pdf vignetteTitles: BitSeq User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/BitSeq/inst/doc/BitSeq.R Package: blima Version: 1.16.0 Depends: R(>= 3.3) Imports: beadarray(>= 2.0.0), Biobase(>= 2.0.0), Rcpp (>= 0.12.8), BiocGenerics, grDevices, stats, graphics LinkingTo: Rcpp Suggests: xtable, blimaTestingData, BiocStyle, illuminaHumanv4.db, lumi, knitr License: GPL-3 Archs: i386, x64 MD5sum: a12b89fa5b76052797843be0affdd48c NeedsCompilation: yes Title: Tools for the preprocessing and analysis of the Illumina microarrays on the detector (bead) level Description: Package blima includes several algorithms for the preprocessing of Illumina microarray data. It focuses to the bead level analysis and provides novel approach to the quantile normalization of the vectors of unequal lengths. It provides variety of the methods for background correction including background subtraction, RMA like convolution and background outlier removal. It also implements variance stabilizing transformation on the bead level. There are also implemented methods for data summarization. It also provides the methods for performing T-tests on the detector (bead) level and on the probe level for differential expression testing. biocViews: Microarray, Preprocessing, Normalization, DifferentialExpression, GeneRegulation, GeneExpression Author: Vojtěch Kulvait Maintainer: Vojtěch Kulvait URL: https://bitbucket.org/kulvait/blima VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/blima git_branch: RELEASE_3_8 git_last_commit: b368eaf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/blima_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/blima_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/blima_1.16.0.tgz vignettes: vignettes/blima/inst/doc/blima.pdf vignetteTitles: blima.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/blima/inst/doc/blima.R Package: BLMA Version: 1.6.0 Depends: ROntoTools, GSA, PADOG, limma, graph, stats, utils, parallel, Biobase Suggests: RUnit, BiocGenerics License: GPL (>=2) MD5sum: 42b39994812056f775ef77969f32ccdc NeedsCompilation: no Title: BLMA: A package for bi-level meta-analysis Description: Suit of tools for bi-level meta-analysis. The package can be used in a wide range of applications, including general hypothesis testings, differential expression analysis, functional analysis, and pathway analysis. biocViews: GeneSetEnrichment, Pathways, DifferentialExpression, Microarray Author: Tin Nguyen and Sorin Draghici Maintainer: Tin Nguyen git_url: https://git.bioconductor.org/packages/BLMA git_branch: RELEASE_3_8 git_last_commit: bb6599e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BLMA_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BLMA_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BLMA_1.6.0.tgz vignettes: vignettes/BLMA/inst/doc/BLMA.pdf vignetteTitles: BLMA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BLMA/inst/doc/BLMA.R importsMe: multiHiCcompare Package: bnbc Version: 1.4.0 Depends: R (>= 3.4.0), methods, BiocGenerics, SummarizedExperiment, GenomicRanges Imports: Rcpp (>= 0.12.12), IRanges, GenomeInfoDb, S4Vectors, matrixStats, preprocessCore, sva, parallel, EBImage, utils LinkingTo: Rcpp Suggests: BiocStyle, knitr, rmarkdown, RUnit License: Artistic-2.0 Archs: i386, x64 MD5sum: 5aa07b96e10124cc3d9ce6f1b30aa935 NeedsCompilation: yes Title: Bandwise normalization and batch correction of Hi-C data Description: Tools to normalize (several) Hi-C data from replicates. biocViews: HiC, Preprocessing, Normalization, Software Author: Kipper Fletez-Brant [cre, aut], Kasper Daniel Hansen [aut] Maintainer: Kipper Fletez-Brant URL: https://github.com/hansenlab/bnbc VignetteBuilder: knitr BugReports: https://github.com/hansenlab/bnbc/issues git_url: https://git.bioconductor.org/packages/bnbc git_branch: RELEASE_3_8 git_last_commit: 22ba7b3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bnbc_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bnbc_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bnbc_1.4.0.tgz vignettes: vignettes/bnbc/inst/doc/bnbc.html vignetteTitles: bnbc User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bnbc/inst/doc/bnbc.R Package: BPRMeth Version: 1.8.1 Depends: R (>= 3.4.0), GenomicRanges Imports: assertthat, methods, MASS, doParallel, parallel, e1071, earth, foreach, randomForest, stats, IRanges, S4Vectors, data.table, graphics, truncnorm, mvtnorm, Rcpp (>= 0.12.14), matrixcalc, magrittr, kernlab, ggplot2, cowplot, BiocStyle LinkingTo: Rcpp, RcppArmadillo Suggests: testthat, knitr, rmarkdown License: GPL-3 Archs: i386, x64 MD5sum: 06448d58568d7bd992940a07b65acc79 NeedsCompilation: yes Title: Model higher-order methylation profiles Description: The BPRMeth package is a probabilistic method to quantify explicit features of methylation profiles, in a way that would make it easier to formally use such profiles in downstream modelling efforts, such as predicting gene expression levels or clustering genomic regions or cells according to their methylation profiles. biocViews: ImmunoOncology, DNAMethylation, GeneExpression, GeneRegulation, Epigenetics, Genetics, Clustering, FeatureExtraction, Regression, RNASeq, Bayesian, KEGG, Sequencing, Coverage, SingleCell Author: Chantriolnt-Andreas Kapourani [aut, cre] Maintainer: Chantriolnt-Andreas Kapourani VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BPRMeth git_branch: RELEASE_3_8 git_last_commit: 8e33e6c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BPRMeth_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BPRMeth_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BPRMeth_1.8.1.tgz vignettes: vignettes/BPRMeth/inst/doc/BPRMeth_vignette.html vignetteTitles: BPRMeth: Model higher-order methylation profiles hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/BPRMeth/inst/doc/BPRMeth_vignette.R Package: BRAIN Version: 1.28.1 Depends: R (>= 2.8.1), PolynomF, Biostrings, lattice License: GPL-2 MD5sum: 363be3229f287c660f2150891538bf4d NeedsCompilation: no Title: Baffling Recursive Algorithm for Isotope distributioN calculations Description: Package for calculating aggregated isotopic distribution and exact center-masses for chemical substances (in this version composed of C, H, N, O and S). This is an implementation of the BRAIN algorithm described in the paper by J. Claesen, P. Dittwald, T. Burzykowski and D. Valkenborg. biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Piotr Dittwald, with contributions of Dirk Valkenborg and Jurgen Claesen Maintainer: Piotr Dittwald git_url: https://git.bioconductor.org/packages/BRAIN git_branch: RELEASE_3_8 git_last_commit: c66ad77 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/BRAIN_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BRAIN_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BRAIN_1.28.1.tgz vignettes: vignettes/BRAIN/inst/doc/BRAIN-vignette.pdf vignetteTitles: BRAIN Usage hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BRAIN/inst/doc/BRAIN-vignette.R suggestsMe: cleaver, synapter Package: brainImageR Version: 1.0.0 Depends: R (>= 3.5) Imports: BiocGenerics, ExperimentHub, ggplot2, grDevices, grid, gridExtra, methods, randomForest, RColorBrewer, stats, testthat Suggests: knitr, rmarkdown License: CC BY-SA 4.0 MD5sum: c77706bbf26dc837b806693cba2728d3 NeedsCompilation: no Title: A Framework for visualizing gene set enrichment throughout neurodevelopment Description: BrainImageR is a package that provides the user with information of where in the human brain their gene set corresponds to. This is provided both as a continuous variable and as a easily-interpretable image. BrainImageR has additional functionality of identifying approximately when in developmental time that a gene expression dataset corresponds to. Both the spatial gene set enrichment and the developmental time point prediction are assessed in comparison to the Allen Brain Atlas reference data. biocViews: Software, Transcription, GeneSetEnrichment, GeneExpression, GenePrediction Author: Sara Linker [aut, cre] Maintainer: Sara B Linker URL: https://github.com/saralinker/brainImageR VignetteBuilder: knitr BugReports: https://github.com/saralinker/brainImageR/issues git_url: https://git.bioconductor.org/packages/brainImageR git_branch: RELEASE_3_8 git_last_commit: d830d5c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/brainImageR_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/brainImageR_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/brainImageR_1.0.0.tgz vignettes: vignettes/brainImageR/inst/doc/brainImageR.html vignetteTitles: brainImageR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/brainImageR/inst/doc/brainImageR.R Package: BrainStars Version: 1.26.0 Depends: RCurl, Biobase, methods Imports: RJSONIO, Biobase License: Artistic-2.0 MD5sum: 163e6ff00d0a1c573ddbcc5631fb1c1e NeedsCompilation: no Title: query gene expression data and plots from BrainStars (B*) Description: This package can search and get gene expression data and plots from BrainStars (B*). BrainStars is a quantitative expression database of the adult mouse brain. The database has genome-wide expression profile at 51 adult mouse CNS regions. biocViews: Microarray, OneChannel, DataImport Author: Itoshi NIKAIDO Maintainer: Itoshi NIKAIDO git_url: https://git.bioconductor.org/packages/BrainStars git_branch: RELEASE_3_8 git_last_commit: 19e5320 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BrainStars_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BrainStars_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BrainStars_1.26.0.tgz vignettes: vignettes/BrainStars/inst/doc/BrainStars.pdf vignetteTitles: BrainStars hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BrainStars/inst/doc/BrainStars.R Package: branchpointer Version: 1.8.0 Depends: caret, R(>= 3.4) Imports: plyr, kernlab, gbm, stringr, cowplot, ggplot2, biomaRt, Biostrings, parallel, utils, stats, BSgenome.Hsapiens.UCSC.hg38, rtracklayer, GenomicRanges, GenomeInfoDb, IRanges, S4Vectors, data.table Suggests: knitr, BiocStyle License: BSD_3_clause + file LICENSE MD5sum: 6632b483e3c0cbcf604ec23b145ce82a NeedsCompilation: no Title: Prediction of intronic splicing branchpoints Description: Predicts branchpoint probability for sites in intronic branchpoint windows. Queries can be supplied as intronic regions; or to evaluate the effects of mutations, SNPs. biocViews: Software, GenomeAnnotation, GenomicVariation, MotifAnnotation Author: Beth Signal Maintainer: Beth Signal VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/branchpointer git_branch: RELEASE_3_8 git_last_commit: 8b8e8a7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/branchpointer_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/branchpointer_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/branchpointer_1.8.0.tgz vignettes: vignettes/branchpointer/inst/doc/branchpointer.pdf vignetteTitles: Using Branchpointer for annotation of intronic human splicing branchpoints hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/branchpointer/inst/doc/branchpointer.R Package: breakpointR Version: 1.0.0 Depends: R (>= 3.5), GenomicRanges, cowplot, breakpointRdata Imports: methods, utils, grDevices, stats, S4Vectors, GenomeInfoDb (>= 1.12.3), IRanges, Rsamtools, GenomicAlignments, ggplot2, BiocGenerics, gtools, doParallel, foreach Suggests: knitr, BiocStyle, testthat License: file LICENSE MD5sum: a9e609669b8ffbc8116345d14dc59e42 NeedsCompilation: no Title: Find breakpoints in Strand-seq data Description: This package implements functions for finding breakpoints, plotting and export of Strand-seq data. biocViews: Software, Sequencing, DNASeq, SingleCell, Coverage Author: David Porubsky, Ashley Sanders, Aaron Taudt Maintainer: David Porubsky URL: https://github.com/daewoooo/BreakPointR VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/breakpointR git_branch: RELEASE_3_8 git_last_commit: 1e59604 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/breakpointR_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/breakpointR_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/breakpointR_1.0.0.tgz vignettes: vignettes/breakpointR/inst/doc/breakpointR.pdf vignetteTitles: How to use breakpointR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/breakpointR/inst/doc/breakpointR.R Package: bridge Version: 1.46.0 Depends: R (>= 1.9.0), rama License: GPL (>= 2) Archs: i386, x64 MD5sum: 6c1d00b6b26a2ba3ae999dac684e71eb NeedsCompilation: yes Title: Bayesian Robust Inference for Differential Gene Expression Description: Test for differentially expressed genes with microarray data. This package can be used with both cDNA microarrays or Affymetrix chip. The packge fits a robust Bayesian hierarchical model for testing for differential expression. Outliers are modeled explicitly using a $t$-distribution. The model includes an exchangeable prior for the variances which allow different variances for the genes but still shrink extreme empirical variances. Our model can be used for testing for differentially expressed genes among multiple samples, and can distinguish between the different possible patterns of differential expression when there are three or more samples. Parameter estimation is carried out using a novel version of Markov Chain Monte Carlo that is appropriate when the model puts mass on subspaces of the full parameter space. biocViews: Microarray,OneChannel,TwoChannel,DifferentialExpression Author: Raphael Gottardo Maintainer: Raphael Gottardo git_url: https://git.bioconductor.org/packages/bridge git_branch: RELEASE_3_8 git_last_commit: 558dd74 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bridge_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bridge_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bridge_1.46.0.tgz vignettes: vignettes/bridge/inst/doc/bridge.pdf vignetteTitles: bridge Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bridge/inst/doc/bridge.R Package: BridgeDbR Version: 1.16.1 Depends: R (>= 3.3.0), rJava Imports: RCurl Suggests: BiocStyle, knitr, rmarkdown, testthat License: AGPL-3 MD5sum: b83ee15b26b1686871641054744343b8 NeedsCompilation: no Title: Code for using BridgeDb identifier mapping framework from within R Description: Use BridgeDb functions and load identifier mapping databases in R. biocViews: Software, Annotation, Metabolomics, Cheminformatics Author: Christ Leemans , Egon Willighagen , Anwesha Bohler , Lars Eijssen Maintainer: Egon Willighagen URL: https://github.com/bridgedb/BridgeDbR VignetteBuilder: knitr BugReports: https://github.com/egonw/BridgeDbR/issues git_url: https://git.bioconductor.org/packages/BridgeDbR git_branch: RELEASE_3_8 git_last_commit: f4919d3 git_last_commit_date: 2018-12-16 Date/Publication: 2018-12-16 source.ver: src/contrib/BridgeDbR_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/BridgeDbR_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BridgeDbR_1.16.1.tgz vignettes: vignettes/BridgeDbR/inst/doc/tutorial.html vignetteTitles: Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BridgeDbR/inst/doc/tutorial.R Package: BrowserViz Version: 2.4.0 Depends: R (>= 3.4.0), jsonlite (>= 1.5), httpuv(>= 1.4.0) Imports: methods, BiocGenerics Suggests: RUnit, BiocStyle License: GPL-2 MD5sum: bb0a3c4799dfc95dc9b9467437ccb23c NeedsCompilation: no Title: BrowserViz: interactive R/browser graphics using websockets and JSON Description: Interactvive graphics in a web browser from R, using websockets and JSON. biocViews: Visualization, ThirdPartyClient Author: Paul Shannon Maintainer: Paul Shannon git_url: https://git.bioconductor.org/packages/BrowserViz git_branch: RELEASE_3_8 git_last_commit: b0b2b0b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BrowserViz_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BrowserViz_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BrowserViz_2.4.0.tgz vignettes: vignettes/BrowserViz/inst/doc/BrowserViz.pdf vignetteTitles: BrowserViz hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BrowserViz/inst/doc/BrowserViz.R dependsOnMe: igvR, RCyjs Package: BSgenome Version: 1.50.0 Depends: R (>= 2.8.0), methods, BiocGenerics (>= 0.13.8), S4Vectors (>= 0.17.28), IRanges (>= 2.13.16), GenomeInfoDb (>= 1.15.2), GenomicRanges (>= 1.31.10), Biostrings (>= 2.47.6), rtracklayer (>= 1.39.7) Imports: methods, utils, stats, BiocGenerics, S4Vectors, IRanges, XVector, GenomeInfoDb, GenomicRanges, Biostrings, Rsamtools, rtracklayer Suggests: BiocManager, Biobase, BSgenome.Celegans.UCSC.ce2, BSgenome.Hsapiens.UCSC.hg38, BSgenome.Hsapiens.UCSC.hg38.masked, BSgenome.Mmusculus.UCSC.mm10, BSgenome.Rnorvegicus.UCSC.rn5, BSgenome.Scerevisiae.UCSC.sacCer1, TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Mmusculus.UCSC.mm10.knownGene, SNPlocs.Hsapiens.dbSNP144.GRCh38, XtraSNPlocs.Hsapiens.dbSNP144.GRCh38, hgu95av2probe, RUnit License: Artistic-2.0 MD5sum: f395bece508475220d86ec87f694436b NeedsCompilation: no Title: Software infrastructure for efficient representation of full genomes and their SNPs Description: Infrastructure shared by all the Biostrings-based genome data packages. biocViews: Genetics, Infrastructure, DataRepresentation, SequenceMatching, Annotation, SNP Author: Hervé Pagès Maintainer: H. Pagès git_url: https://git.bioconductor.org/packages/BSgenome git_branch: RELEASE_3_8 git_last_commit: 4391075 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BSgenome_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BSgenome_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BSgenome_1.50.0.tgz vignettes: vignettes/BSgenome/inst/doc/BSgenomeForge.pdf, vignettes/BSgenome/inst/doc/GenomeSearching.pdf vignetteTitles: How to forge a BSgenome data package, Efficient genome searching with Biostrings and the BSgenome data packages hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BSgenome/inst/doc/BSgenomeForge.R, vignettes/BSgenome/inst/doc/GenomeSearching.R dependsOnMe: ChIPanalyser, cleanUpdTSeq, GOTHiC, HelloRanges, htSeqTools, MEDIPS, motifRG, REDseq, rGADEM importsMe: AllelicImbalance, appreci8R, ATACseqQC, BEAT, bsseq, CAGEr, charm, ChIPpeakAnno, chromVAR, cobindR, CRISPRseek, crisprseekplus, diffHic, esATAC, gcapc, genomation, GenomicScores, GenVisR, ggbio, gmapR, GreyListChIP, GUIDEseq, Gviz, hiAnnotator, InPAS, IsoformSwitchAnalyzeR, MADSEQ, maftools, MethylSeekR, MMDiff2, motifbreakR, motifmatchr, msgbsR, PING, podkat, qsea, QuasR, R453Plus1Toolbox, RareVariantVis, regioneR, REMP, Repitools, scmeth, seqplots, SparseSignatures, TFBSTools, trena, Ularcirc, VariantAnnotation, VariantFiltering, VariantTools suggestsMe: Biostrings, biovizBase, chipseq, easyRNASeq, GeneRegionScan, GenomeInfoDb, GenomicAlignments, GenomicFeatures, GenomicRanges, genoset, metaseqR, MiRaGE, MutationalPatterns, ORFik, QDNAseq, recoup, rtracklayer, waveTiling Package: bsseq Version: 1.18.0 Depends: R (>= 3.5), methods, BiocGenerics, GenomicRanges (>= 1.29.14), SummarizedExperiment (>= 1.9.18) Imports: IRanges (>= 2.11.16), GenomeInfoDb, scales, stats, graphics, Biobase, locfit, gtools, data.table (>= 1.11.8), S4Vectors, R.utils (>= 2.0.0), DelayedMatrixStats (>= 1.3.6), permute, limma, DelayedArray (>= 0.7.15), Rcpp, BiocParallel, BSgenome, Biostrings, utils, HDF5Array, rhdf5 LinkingTo: Rcpp, Rhdf5lib, beachmat Suggests: testthat, bsseqData, BiocStyle, rmarkdown, knitr, Matrix, doParallel, rtracklayer, BSgenome.Hsapiens.UCSC.hg38, beachmat License: Artistic-2.0 Archs: i386, x64 MD5sum: 27d165f57d1a2fdfd2fb2af640039d90 NeedsCompilation: yes Title: Analyze, manage and store bisulfite sequencing data Description: A collection of tools for analyzing and visualizing bisulfite sequencing data. biocViews: DNAMethylation Author: Kasper Daniel Hansen [aut, cre], Peter Hickey [aut] Maintainer: Kasper Daniel Hansen URL: https://github.com/kasperdanielhansen/bsseq SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/kasperdanielhansen/bsseq/issues git_url: https://git.bioconductor.org/packages/bsseq git_branch: RELEASE_3_8 git_last_commit: aa2e1a9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/bsseq_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/bsseq_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bsseq_1.18.0.tgz vignettes: vignettes/bsseq/inst/doc/bsseq_analysis.html, vignettes/bsseq/inst/doc/bsseq.html vignetteTitles: Analyzing WGBS data with bsseq, bsseq User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bsseq/inst/doc/bsseq_analysis.R, vignettes/bsseq/inst/doc/bsseq.R dependsOnMe: dmrseq, DSS importsMe: MIRA, scmeth Package: BubbleTree Version: 2.12.0 Depends: R (>= 3.3), IRanges, GenomicRanges, plyr, dplyr, magrittr Imports: BiocGenerics (>= 0.7.5), BiocStyle, Biobase, ggplot2, WriteXLS, gtools, RColorBrewer, limma, grid, gtable, gridExtra, biovizBase, e1071, methods, grDevices, stats, utils Suggests: knitr, rmarkdown License: LGPL (>= 3) MD5sum: 7a76991a141f4d831fbea768e01d76bd NeedsCompilation: no Title: BubbleTree: an intuitive visualization to elucidate tumoral aneuploidy and clonality in somatic mosaicism using next generation sequencing data Description: CNV analysis in groups of tumor samples. biocViews: CopyNumberVariation, Software, Sequencing, Coverage Author: Wei Zhu , Michael Kuziora , Todd Creasy , Brandon Higgs Maintainer: Todd Creasy , Wei Zhu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BubbleTree git_branch: RELEASE_3_8 git_last_commit: 4eeb280 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BubbleTree_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BubbleTree_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BubbleTree_2.12.0.tgz vignettes: vignettes/BubbleTree/inst/doc/BubbleTree-vignette.html vignetteTitles: BubbleTree Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BubbleTree/inst/doc/BubbleTree-vignette.R Package: BufferedMatrix Version: 1.46.0 Depends: R (>= 2.6.0), methods License: LGPL (>= 2) Archs: i386, x64 MD5sum: ac35d5e400ae81406bd70ca1f631b593 NeedsCompilation: yes Title: A matrix data storage object held in temporary files Description: A tabular style data object where most data is stored outside main memory. A buffer is used to speed up access to data. biocViews: Infrastructure Author: Ben Bolstad Maintainer: Ben Bolstad URL: https://github.com/bmbolstad/BufferedMatrix git_url: https://git.bioconductor.org/packages/BufferedMatrix git_branch: RELEASE_3_8 git_last_commit: 9fb17da git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BufferedMatrix_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BufferedMatrix_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BufferedMatrix_1.46.0.tgz vignettes: vignettes/BufferedMatrix/inst/doc/BufferedMatrix.pdf vignetteTitles: BufferedMatrix: Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BufferedMatrix/inst/doc/BufferedMatrix.R dependsOnMe: BufferedMatrixMethods linksToMe: BufferedMatrixMethods Package: BufferedMatrixMethods Version: 1.46.0 Depends: R (>= 2.6.0), BufferedMatrix (>= 1.3.0), methods LinkingTo: BufferedMatrix Suggests: affyio, affy License: GPL (>= 2) Archs: i386, x64 MD5sum: fd0c01ee09b195d76b9b4e76ccda07ca NeedsCompilation: yes Title: Microarray Data related methods that utlize BufferedMatrix objects Description: Microarray analysis methods that use BufferedMatrix objects biocViews: Infrastructure Author: Ben Bolstad Maintainer: Ben Bolstad URL: https://github.bom/bmbolstad/BufferedMatrixMethods git_url: https://git.bioconductor.org/packages/BufferedMatrixMethods git_branch: RELEASE_3_8 git_last_commit: 2e0a6b2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BufferedMatrixMethods_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BufferedMatrixMethods_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BufferedMatrixMethods_1.46.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: BUMHMM Version: 1.6.2 Depends: R (>= 3.4) Imports: devtools, stringi, gtools, stats, utils, SummarizedExperiment, Biostrings, IRanges Suggests: testthat, knitr, BiocStyle License: GPL-3 MD5sum: 7796c620a9d0a07a9672a398e52705c8 NeedsCompilation: no Title: Computational pipeline for computing probability of modification from structure probing experiment data Description: This is a probabilistic modelling pipeline for computing per- nucleotide posterior probabilities of modification from the data collected in structure probing experiments. The model supports multiple experimental replicates and empirically corrects coverage- and sequence-dependent biases. The model utilises the measure of a "drop-off rate" for each nucleotide, which is compared between replicates through a log-ratio (LDR). The LDRs between control replicates define a null distribution of variability in drop-off rate observed by chance and LDRs between treatment and control replicates gets compared to this distribution. Resulting empirical p-values (probability of being "drawn" from the null distribution) are used as observations in a Hidden Markov Model with a Beta-Uniform Mixture model used as an emission model. The resulting posterior probabilities indicate the probability of a nucleotide of having being modified in a structure probing experiment. biocViews: ImmunoOncology, GeneticVariability, Transcription, GeneExpression, GeneRegulation, Coverage, Genetics, StructuralPrediction, Transcriptomics, Bayesian, Classification, FeatureExtraction, HiddenMarkovModel, Regression, RNASeq, Sequencing Author: Alina Selega (alina.selega@gmail.com), Sander Granneman, Guido Sanguinetti Maintainer: Alina Selega VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BUMHMM git_branch: RELEASE_3_8 git_last_commit: 9903e7d git_last_commit_date: 2019-04-10 Date/Publication: 2019-04-14 source.ver: src/contrib/BUMHMM_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/BUMHMM_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BUMHMM_1.6.2.tgz vignettes: vignettes/BUMHMM/inst/doc/BUMHMM.pdf vignetteTitles: An Introduction to the BUMHMM pipeline hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BUMHMM/inst/doc/BUMHMM.R Package: bumphunter Version: 1.24.5 Depends: R (>= 3.5), S4Vectors (>= 0.9.25), IRanges (>= 2.3.23), GenomeInfoDb, GenomicRanges, foreach, iterators, methods, parallel, locfit Imports: matrixStats, limma, doRNG, BiocGenerics, utils, GenomicFeatures, AnnotationDbi, stats Suggests: testthat, RUnit, doParallel, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene License: Artistic-2.0 MD5sum: 7c38a75e34594b999dbe13f58de13d2d NeedsCompilation: no Title: Bump Hunter Description: Tools for finding bumps in genomic data biocViews: DNAMethylation, Epigenetics, Infrastructure, MultipleComparison, ImmunoOncology Author: Rafael A. Irizarry [cre, aut], Martin Aryee [aut], Kasper Daniel Hansen [aut], Hector Corrada Bravo [aut], Shan Andrews [ctb], Andrew E. Jaffe [ctb], Harris Jaffee [ctb], Leonardo Collado-Torres [ctb] Maintainer: Rafael A. Irizarry URL: https://github.com/ririzarr/bumphunter git_url: https://git.bioconductor.org/packages/bumphunter git_branch: RELEASE_3_8 git_last_commit: 29b8740 git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/bumphunter_1.24.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/bumphunter_1.24.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/bumphunter_1.24.5.tgz vignettes: vignettes/bumphunter/inst/doc/bumphunter.pdf vignetteTitles: The bumphunter user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/bumphunter/inst/doc/bumphunter.R dependsOnMe: minfi importsMe: derfinder, dmrseq, methyvim suggestsMe: bigmelon, derfinderPlot, epivizrData, regionReport Package: BUS Version: 1.38.0 Depends: R (>= 2.3.0), minet Imports: stats, infotheo License: GPL-3 Archs: i386, x64 MD5sum: ebdfc2420596f5fdc284694c57183488 NeedsCompilation: yes Title: Gene network reconstruction Description: This package can be used to compute associations among genes (gene-networks) or between genes and some external traits (i.e. clinical). biocViews: Preprocessing Author: Yin Jin, Hesen Peng, Lei Wang, Raffaele Fronza, Yuanhua Liu and Christine Nardini Maintainer: Yuanhua Liu git_url: https://git.bioconductor.org/packages/BUS git_branch: RELEASE_3_8 git_last_commit: 9864b59 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BUS_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BUS_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BUS_1.38.0.tgz vignettes: vignettes/BUS/inst/doc/bus.pdf vignetteTitles: bus.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BUS/inst/doc/bus.R Package: BUScorrect Version: 1.0.0 Depends: R (>= 3.5.0) Imports: gplots, methods, grDevices, stats, SummarizedExperiment Suggests: BiocStyle, knitr, RUnit, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: aadd22d922c6821cf37445835612c4b7 NeedsCompilation: yes Title: Batch Effects Correction with Unknown Subtypes Description: High-throughput experimental data are accumulating exponentially in public databases. However, mining valid scientific discoveries from these abundant resources is hampered by technical artifacts and inherent biological heterogeneity. The former are usually termed "batch effects," and the latter is often modelled by "subtypes." The R package BUScorrect fits a Bayesian hierarchical model, the Batch-effects-correction-with-Unknown-Subtypes model (BUS), to correct batch effects in the presence of unknown subtypes. BUS is capable of (a) correcting batch effects explicitly, (b) grouping samples that share similar characteristics into subtypes, (c) identifying features that distinguish subtypes, and (d) enjoying a linear-order computation complexity. biocViews: GeneExpression, StatisticalMethod, Bayesian, Clustering, FeatureExtraction, BatchEffect Author: Xiangyu Luo , Yingying Wei Maintainer: Xiangyu Luo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/BUScorrect git_branch: RELEASE_3_8 git_last_commit: 17ac036 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/BUScorrect_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/BUScorrect_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/BUScorrect_1.0.0.tgz vignettes: vignettes/BUScorrect/inst/doc/BUScorrect_user_guide.pdf vignetteTitles: BUScorrect_user_guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/BUScorrect/inst/doc/BUScorrect_user_guide.R Package: CAFE Version: 1.18.0 Depends: R (>= 2.10), biovizBase, GenomicRanges, IRanges, ggbio Imports: affy, ggplot2, annotate, grid, gridExtra, tcltk, Biobase Suggests: RUnit, BiocGenerics, BiocStyle License: GPL-3 MD5sum: db87b028e56b69c3372cf9e8b0f04836 NeedsCompilation: no Title: Chromosmal Aberrations Finder in Expression data Description: Detection and visualizations of gross chromosomal aberrations using Affymetrix expression microarrays as input biocViews: GeneExpression, Microarray, OneChannel, GeneSetEnrichment Author: Sander Bollen Maintainer: Sander Bollen git_url: https://git.bioconductor.org/packages/CAFE git_branch: RELEASE_3_8 git_last_commit: 06606c5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CAFE_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CAFE_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CAFE_1.18.0.tgz vignettes: vignettes/CAFE/inst/doc/CAFE-manual.pdf vignetteTitles: Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CAFE/inst/doc/CAFE-manual.R Package: CAGEfightR Version: 1.2.0 Depends: R (>= 3.5), GenomicRanges (>= 1.30.1), rtracklayer (>= 1.38.2), SummarizedExperiment (>= 1.8.1) Imports: pryr(>= 0.1.3), assertthat(>= 0.2.0), methods, Matrix(>= 1.2-12), Matrix.utils(>= 0.9.6), grr(>= 0.9.5), BiocGenerics(>= 0.24.0), S4Vectors(>= 0.16.0), IRanges(>= 2.12.0), GenomeInfoDb(>= 1.14.0), GenomicFeatures(>= 1.29.11), BiocParallel(>= 1.12.0), GenomicFiles(>= 1.14.0), Gviz(>= 1.22.2), InteractionSet(>= 1.9.4), GenomicInteractions(>= 1.15.1) Suggests: knitr, rmarkdown, BiocStyle, org.Mm.eg.db, TxDb.Mmusculus.UCSC.mm9.knownGene License: GPL-3 + file LICENSE MD5sum: bed28d787f521b9fb0ee568b6188041f NeedsCompilation: no Title: Analysis of Cap Analysis of Gene Expression (CAGE) data using Bioconductor Description: CAGE is a widely used high throughput assay for measuring transcription start site (TSS) activity. CAGEfightR is an R/Bioconductor package for performing a wide range of common data analysis tasks for CAGE and 5'-end data in general. Core functionality includes: import of CAGE TSSs (CTSSs), tag (or unidirectional) clustering for TSS identification, bidirectional clustering for enhancer identification, annotation with transcript and gene models, correlation of TSS and enhancer expression, calculation of TSS shapes, quantification of CAGE expression as expression matrices and genome brower visualization. biocViews: Software, Transcription, Coverage, GeneExpression, GeneRegulation, PeakDetection, DataImport, DataRepresentation, Transcriptomics, Sequencing, Annotation, GenomeBrowsers, Normalization, Preprocessing, Visualization Author: Malte Thodberg Maintainer: Malte Thodberg URL: https://github.com/MalteThodberg/CAGEfightR VignetteBuilder: knitr BugReports: https://github.com/MalteThodberg/CAGEfightR/issues git_url: https://git.bioconductor.org/packages/CAGEfightR git_branch: RELEASE_3_8 git_last_commit: a324636 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CAGEfightR_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CAGEfightR_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CAGEfightR_1.2.0.tgz vignettes: vignettes/CAGEfightR/inst/doc/Introduction_to_CAGEfightR.html vignetteTitles: Introduction to CAGEfightR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/CAGEfightR/inst/doc/Introduction_to_CAGEfightR.R Package: CAGEr Version: 1.24.0 Depends: methods, R (>= 2.15.0) Imports: beanplot, BiocGenerics, BiocParallel, BSgenome, data.table, DelayedArray, formula.tools, GenomeInfoDb, GenomicAlignments, GenomicRanges (>= 1.23.16), ggplot2 (>= 2.2.0), gtools, IRanges (>= 2.5.27), KernSmooth, memoise, MultiAssayExperiment, plyr, Rsamtools, reshape, rtracklayer, S4Vectors, som, stringdist, stringi, SummarizedExperiment, utils, vegan, VGAM Suggests: BSgenome.Drerio.UCSC.danRer7, DESeq2, FANTOM3and4CAGE, BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: 9ecbf3e0bb2fb6d00e1de0a3652d845e NeedsCompilation: no Title: Analysis of CAGE (Cap Analysis of Gene Expression) sequencing data for precise mapping of transcription start sites and promoterome mining Description: Preprocessing of CAGE sequencing data, identification and normalization of transcription start sites and downstream analysis of transcription start sites clusters (promoters). biocViews: Preprocessing, Sequencing, Normalization, FunctionalGenomics, Transcription, GeneExpression, Clustering, Visualization Author: Vanja Haberle Maintainer: Vanja Haberle , Charles Plessy VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CAGEr git_branch: RELEASE_3_8 git_last_commit: 420fec4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/CAGEr_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CAGEr_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CAGEr_1.24.0.tgz vignettes: vignettes/CAGEr/inst/doc/CAGEexp.html vignetteTitles: CAGEr: an R package for CAGE data analysis and promoterome mining hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CAGEr/inst/doc/CAGEexp.R suggestsMe: seqPattern Package: CALIB Version: 1.48.0 Depends: R (>= 2.10), limma, methods Imports: limma, methods, graphics, stats, utils License: LGPL Archs: i386, x64 MD5sum: 1b50dd84b955b6ca81e18509167b4896 NeedsCompilation: yes Title: Calibration model for estimating absolute expression levels from microarray data Description: This package contains functions for normalizing spotted microarray data, based on a physically motivated calibration model. The model parameters and error distributions are estimated from external control spikes. biocViews: Microarray,TwoChannel,Preprocessing Author: Hui Zhao, Kristof Engelen, Bart De Moor and Kathleen Marchal Maintainer: Hui Zhao git_url: https://git.bioconductor.org/packages/CALIB git_branch: RELEASE_3_8 git_last_commit: 2ef1085 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CALIB_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CALIB_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CALIB_1.48.0.tgz vignettes: vignettes/CALIB/inst/doc/quickstart.pdf vignetteTitles: CALIB Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CALIB/inst/doc/quickstart.R Package: CAMERA Version: 1.38.1 Depends: R (>= 2.1.0), methods, Biobase, xcms (>= 1.13.5) Imports: methods, xcms, RBGL, graph, graphics, grDevices, stats, utils, Hmisc, igraph Suggests: faahKO, RUnit, BiocGenerics Enhances: Rmpi, snow License: GPL (>= 2) Archs: i386, x64 MD5sum: f4ebd02dfe4bf266473696c109d86544 NeedsCompilation: yes Title: Collection of annotation related methods for mass spectrometry data Description: Annotation of peaklists generated by xcms, rule based annotation of isotopes and adducts, isotope validation, EIC correlation based tagging of unknown adducts and fragments biocViews: ImmunoOncology, MassSpectrometry, Metabolomics Author: Carsten Kuhl, Ralf Tautenhahn, Hendrik Treutler, Steffen Neumann {ckuhl|htreutle|sneumann}@ipb-halle.de, rtautenh@scripps.edu Maintainer: Steffen Neumann URL: http://msbi.ipb-halle.de/msbi/CAMERA/ BugReports: https://github.com/sneumann/CAMERA/issues/new git_url: https://git.bioconductor.org/packages/CAMERA git_branch: RELEASE_3_8 git_last_commit: fa6deea git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CAMERA_1.38.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CAMERA_1.38.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CAMERA_1.38.1.tgz vignettes: vignettes/CAMERA/inst/doc/CAMERA.pdf, vignettes/CAMERA/inst/doc/compoundQuantilesVignette.pdf, vignettes/CAMERA/inst/doc/IsotopeDetectionVignette.pdf vignetteTitles: Molecule Identification with CAMERA, Isotope pattern validation with CAMERA, Isotope pattern validation with CAMERA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CAMERA/inst/doc/CAMERA.R dependsOnMe: flagme, IPO, LOBSTAHS, MAIT, metaMS suggestsMe: msPurity, RMassBank Package: CAMTHC Version: 1.0.0 Depends: R (>= 3.5) Imports: methods, rJava, BiocParallel, stats, Biobase, SummarizedExperiment, corpcor, geometry, NMF, DMwR, pcaPP, apcluster, graphics Suggests: knitr, rmarkdown, BiocStyle, testthat, GEOquery, rgl License: GPL-2 MD5sum: cb62c6d7934584f5d24869db7d927437 NeedsCompilation: no Title: Convex Analysis of Mixtures for Tissue Heterogeneity Characterization Description: An R package for tissue heterogeneity characterization by convex analysis of mixtures (CAM). It provides basic functions to perform unsupervised deconvolution on mixture expression profiles by CAM and some auxiliary functions to help understand the subpopulation-specific results. It also implements functions to perform supervised deconvolution based on prior knowledge of molecular markers, S matrix or A matrix. Combining molecular markers from CAM and from prior knowledge can achieve semi-supervised deconvolution of mixtures. biocViews: Software, CellBiology, GeneExpression Author: Lulu Chen Maintainer: Lulu Chen SystemRequirements: Java (>= 1.8) VignetteBuilder: knitr BugReports: https://github.com/Lululuella/CAMTHC/issues git_url: https://git.bioconductor.org/packages/CAMTHC git_branch: RELEASE_3_8 git_last_commit: 381fbfa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CAMTHC_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CAMTHC_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CAMTHC_1.0.0.tgz vignettes: vignettes/CAMTHC/inst/doc/camthc.html vignetteTitles: CAMTHC User Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CAMTHC/inst/doc/camthc.R Package: canceR Version: 1.16.02 Depends: R (>= 3.4), tcltk, tcltk2, cgdsr Imports: GSEABase, GSEAlm, tkrplot, geNetClassifier, RUnit, Formula, rpart, survival, Biobase, phenoTest, circlize, plyr, graphics, stats, utils Suggests: testthat (>= 0.10.0), R.rsp License: GPL-2 MD5sum: 26c92ab34c7b27449bfb832584d6561d NeedsCompilation: no Title: A Graphical User Interface for accessing and modeling the Cancer Genomics Data of MSKCC Description: The package is user friendly interface based on the cgdsr and other modeling packages to explore, compare, and analyse all available Cancer Data (Clinical data, Gene Mutation, Gene Methylation, Gene Expression, Protein Phosphorylation, Copy Number Alteration) hosted by the Computational Biology Center at Memorial-Sloan-Kettering Cancer Center (MSKCC). biocViews: GUI, GeneExpression, Software Author: Karim Mezhoud. Nuclear Safety & Security Department. Nuclear Science Center of Tunisia. Maintainer: Karim Mezhoud VignetteBuilder: R.rsp git_url: https://git.bioconductor.org/packages/canceR git_branch: RELEASE_3_8 git_last_commit: da04e10 git_last_commit_date: 2019-04-04 Date/Publication: 2019-04-04 source.ver: src/contrib/canceR_1.16.02.tar.gz win.binary.ver: bin/windows/contrib/3.5/canceR_1.16.02.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/canceR_1.16.02.tgz vignettes: vignettes/canceR/inst/doc/canceR.pdf vignetteTitles: canceR Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: cancerclass Version: 1.26.0 Depends: R (>= 2.14.0), Biobase, binom, methods, stats Suggests: cancerdata License: GPL 3 Archs: i386, x64 MD5sum: 046f83f4ae882a6cc05716c51e2cfee2 NeedsCompilation: yes Title: Development and validation of diagnostic tests from high-dimensional molecular data Description: The classification protocol starts with a feature selection step and continues with nearest-centroid classification. The accurarcy of the predictor can be evaluated using training and test set validation, leave-one-out cross-validation or in a multiple random validation protocol. Methods for calculation and visualization of continuous prediction scores allow to balance sensitivity and specificity and define a cutoff value according to clinical requirements. biocViews: Cancer, Microarray, Classification, Visualization Author: Jan Budczies, Daniel Kosztyla Maintainer: Daniel Kosztyla git_url: https://git.bioconductor.org/packages/cancerclass git_branch: RELEASE_3_8 git_last_commit: 6b7e745 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cancerclass_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cancerclass_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cancerclass_1.26.0.tgz vignettes: vignettes/cancerclass/inst/doc/vignette_cancerclass.pdf vignetteTitles: Cancerclass: An R package for development and validation of diagnostic tests from high-dimensional molecular data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cancerclass/inst/doc/vignette_cancerclass.R Package: CancerInSilico Version: 2.2.1 Depends: R (>= 3.4), Rcpp Imports: methods, utils, graphics, stats LinkingTo: Rcpp, BH Suggests: testthat, knitr, rmarkdown, BiocStyle, Rtsne, viridis, rgl License: GPL-2 Archs: i386, x64 MD5sum: a87a2d1778e80e9df154575bc9bc05d0 NeedsCompilation: yes Title: An R interface for computational modeling of tumor progression Description: The CancerInSilico package provides an R interface for running mathematical models of tumor progresson and generating gene expression data from the results. This package has the underlying models implemented in C++ and the output and analysis features implemented in R. biocViews: ImmunoOncology, MathematicalBiology, SystemsBiology, CellBiology, BiomedicalInformatics, GeneExpression, RNASeq, SingleCell Author: Thomas D. Sherman, Raymond Cheng, Elana J. Fertig Maintainer: Thomas D. Sherman , Elana J. Fertig VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CancerInSilico git_branch: RELEASE_3_8 git_last_commit: e7cf62c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CancerInSilico_2.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CancerInSilico_2.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CancerInSilico_2.2.1.tgz vignettes: vignettes/CancerInSilico/inst/doc/CancerInSilico.html vignetteTitles: The CancerInSilico Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CancerInSilico/inst/doc/CancerInSilico.R Package: CancerMutationAnalysis Version: 1.24.0 Depends: R (>= 2.10.0), qvalue Imports: AnnotationDbi, limma, methods, stats Suggests: KEGG.db License: GPL (>= 2) + file LICENSE Archs: i386, x64 MD5sum: 6b4c874482fba54cb147332073586193 NeedsCompilation: yes Title: Cancer mutation analysis Description: This package implements gene and gene-set level analysis methods for somatic mutation studies of cancer. The gene-level methods distinguish between driver genes (which play an active role in tumorigenesis) and passenger genes (which are mutated in tumor samples, but have no role in tumorigenesis) and incorporate a two-stage study design. The gene-set methods implement a patient-oriented approach, which calculates gene-set scores for each sample, then combines them across samples; a gene-oriented approach which uses the Wilcoxon test is also provided for comparison. biocViews: Genetics, Software Author: Giovanni Parmigiani, Simina M. Boca Maintainer: Simina M. Boca git_url: https://git.bioconductor.org/packages/CancerMutationAnalysis git_branch: RELEASE_3_8 git_last_commit: a256566 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CancerMutationAnalysis_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CancerMutationAnalysis_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CancerMutationAnalysis_1.24.0.tgz vignettes: vignettes/CancerMutationAnalysis/inst/doc/CancerMutationAnalysis.pdf vignetteTitles: CancerMutationAnalysisTutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/CancerMutationAnalysis/inst/doc/CancerMutationAnalysis.R Package: CancerSubtypes Version: 1.8.0 Depends: R (>= 3.4), sigclust, NMF Imports: SNFtool, iCluster, cluster, impute, limma, ConsensusClusterPlus, grDevices, survival Suggests: BiocGenerics, RUnit, knitr, RTCGA.mRNA, RTCGA.clinical License: GPL (>= 2) MD5sum: f5f9711de5b16e3b4f2ddb908bc44aa7 NeedsCompilation: no Title: Cancer subtypes identification, validation and visualization based on multiple genomic data sets Description: CancerSubtypes integrates the current common computational biology methods for cancer subtypes identification and provides a standardized framework for cancer subtype analysis based multi-omics data, such as gene expression, miRNA expression, DNA methylation and others. biocViews: Clustering, Software, Visualization, GeneExpression Author: Taosheng Xu, Thuc Le Maintainer: Taosheng Xu URL: https://github.com/taoshengxu/CancerSubtypes VignetteBuilder: knitr BugReports: https://github.com/taoshengxu/CancerSubtypes/issues git_url: https://git.bioconductor.org/packages/CancerSubtypes git_branch: RELEASE_3_8 git_last_commit: d37e05a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CancerSubtypes_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CancerSubtypes_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CancerSubtypes_1.8.0.tgz vignettes: vignettes/CancerSubtypes/inst/doc/CancerSubtypes-vignette.html vignetteTitles: CancerSubtypes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CancerSubtypes/inst/doc/CancerSubtypes-vignette.R Package: CAnD Version: 1.14.0 Imports: methods, ggplot2, reshape Suggests: RUnit, BiocGenerics, BiocStyle License: Artistic-2.0 MD5sum: fd13a36a530e102aa5f1b9c2ba8eb65f NeedsCompilation: no Title: Perform Chromosomal Ancestry Differences (CAnD) Analyses Description: Functions to perform the CAnD test on a set of ancestry proportions. For a particular ancestral subpopulation, a user will supply the estimated ancestry proportion for each sample, and each chromosome or chromosomal segment of interest. A p-value for each chromosome as well as an overall CAnD p-value will be returned for each test. Plotting functions are also available. biocViews: Genetics, StatisticalMethod, GeneticVariability, SNP Author: Caitlin McHugh, Timothy Thornton Maintainer: Caitlin McHugh git_url: https://git.bioconductor.org/packages/CAnD git_branch: RELEASE_3_8 git_last_commit: daa1736 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CAnD_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CAnD_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CAnD_1.14.0.tgz vignettes: vignettes/CAnD/inst/doc/CAnD.pdf vignetteTitles: Detecting heterogenity in population structure across chromosomes with the "CAnD" package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CAnD/inst/doc/CAnD.R Package: caOmicsV Version: 1.12.1 Depends: R (>= 3.2), igraph (>= 0.7.1), bc3net (>= 1.0.2) License: GPL (>=2.0) MD5sum: 1557453c140c78a3dde7d88e542031c7 NeedsCompilation: no Title: Visualization of multi-dimentional cancer genomics data Description: caOmicsV package provides methods to visualize multi-dimentional cancer genomics data including of patient information, gene expressions, DNA methylations, DNA copy number variations, and SNP/mutations in matrix layout or network layout. biocViews: ImmunoOncology, Visualization, Network, RNASeq Author: Henry Zhang Maintainer: Henry Zhang git_url: https://git.bioconductor.org/packages/caOmicsV git_branch: RELEASE_3_8 git_last_commit: f92bd6f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/caOmicsV_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/caOmicsV_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/caOmicsV_1.12.1.tgz vignettes: vignettes/caOmicsV/inst/doc/Introduction_to_caOmicsV.pdf vignetteTitles: Intrudoction_to_caOmicsV hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/caOmicsV/inst/doc/Introduction_to_caOmicsV.R Package: Cardinal Version: 2.0.4 Depends: BiocGenerics, BiocParallel, EBImage, graphics, methods, S4Vectors, stats, ProtGenerics Imports: Biobase, dplyr, grid, irlba, lattice, magrittr, matter, signal, sp, stats4, utils Suggests: BiocStyle, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: 5456db9f83d6de8accaef5fe13a63733 NeedsCompilation: yes Title: A mass spectrometry imaging toolbox for statistical analysis Description: Implements statistical & computational tools for analyzing mass spectrometry imaging datasets, including methods for efficient pre-processing, spatial segmentation, and classification. biocViews: Software, Infrastructure, Proteomics, Lipidomics, MassSpectrometry, ImagingMassSpectrometry, ImmunoOncology, Normalization, Clustering, Classification Author: Kylie A. Bemis Maintainer: Kylie A. Bemis URL: http://www.cardinalmsi.org git_url: https://git.bioconductor.org/packages/Cardinal git_branch: RELEASE_3_8 git_last_commit: 215a754 git_last_commit_date: 2019-02-21 Date/Publication: 2019-02-21 source.ver: src/contrib/Cardinal_2.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/Cardinal_2.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Cardinal_2.0.4.tgz vignettes: vignettes/Cardinal/inst/doc/Cardinal-2-guide.pdf, vignettes/Cardinal/inst/doc/Cardinal-development.pdf, vignettes/Cardinal/inst/doc/Cardinal-walkthrough.pdf vignetteTitles: Cardinal 2.0: User's Guide, Cardinal design and development, Cardinal: Analytic tools for mass spectrometry imaging hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Cardinal/inst/doc/Cardinal-2-guide.R, vignettes/Cardinal/inst/doc/Cardinal-development.R, vignettes/Cardinal/inst/doc/Cardinal-walkthrough.R Package: casper Version: 2.16.1 Depends: R (>= 2.14.1), Biobase, IRanges, methods, GenomicRanges Imports: BiocGenerics, coda, EBarrays, gaga, gtools, GenomeInfoDb, GenomicFeatures, limma, mgcv, Rsamtools, rtracklayer, S4Vectors (>= 0.9.25), sqldf, survival, VGAM Enhances: parallel License: GPL (>=2) Archs: i386, x64 MD5sum: b221ac361dc269e55668bcd663dc812a NeedsCompilation: yes Title: Characterization of Alternative Splicing based on Paired-End Reads Description: Infer alternative splicing from paired-end RNA-seq data. The model is based on counting paths across exons, rather than pairwise exon connections, and estimates the fragment size and start distributions non-parametrically, which improves estimation precision. biocViews: ImmunoOncology, GeneExpression, DifferentialExpression, Transcription, RNASeq, Sequencing Author: David Rossell, Camille Stephan-Otto, Manuel Kroiss, Miranda Stobbe, Victor Pena Maintainer: David Rossell git_url: https://git.bioconductor.org/packages/casper git_branch: RELEASE_3_8 git_last_commit: 7207efd git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/casper_2.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/casper_2.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/casper_2.16.1.tgz vignettes: vignettes/casper/inst/doc/casper.pdf, vignettes/casper/inst/doc/DesignRNASeq.pdf vignetteTitles: Manual for the casper library, DesignRNASeq.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/casper/inst/doc/casper.R Package: CATALYST Version: 1.6.7 Depends: R (>= 3.5) Imports: Biobase, circlize, ComplexHeatmap, ConsensusClusterPlus, data.table, dplyr, drc, DT, flowCore, FlowSOM, ggplot2, ggrepel, ggridges, graphics, grDevices, grid, gridExtra, htmltools, limma, magrittr, matrixStats, methods, nnls, plotly, purrr, RColorBrewer, reshape2, Rtsne, S4Vectors, scales, scater, shiny, shinydashboard, shinyBS, shinyjs, SingleCellExperiment, stats, SummarizedExperiment, utils Suggests: BiocStyle, knitr, rmarkdown, testthat, diffcyt, umap License: GPL (>=2) MD5sum: a69d58e6b5e8dd986d6af31c5a9c0ff9 NeedsCompilation: no Title: Cytometry dATa anALYSis Tools Description: Mass cytometry (CyTOF) uses heavy metal isotopes rather than fluorescent tags as reporters to label antibodies, thereby substantially decreasing spectral overlap and allowing for examination of over 50 parameters at the single cell level. While spectral overlap is significantly less pronounced in CyTOF than flow cytometry, spillover due to detection sensitivity, isotopic impurities, and oxide formation can impede data interpretability. We designed CATALYST (Cytometry dATa anALYSis Tools) to provide a pipeline for preprocessing of cytometry data, including i) normalization using bead standards, ii) single-cell deconvolution, and iii) bead-based compensation. biocViews: DifferentialExpression, FlowCytometry, ImmunoOncology, MassSpectrometry, Normalization, Preprocessing, SingleCell, Software, StatisticalMethod, Visualization Author: Helena L. Crowell [aut, cre], Vito R.T. Zanotelli [aut], Stéphane Chevrier [aut, dtc], Mark D. Robinson [aut, fnd], Bernd Bodenmiller [fnd] Maintainer: Helena L. Crowell URL: https://github.com/HelenaLC/CATALYST VignetteBuilder: knitr BugReports: https://github.com/HelenaLC/CATALYST/issues git_url: https://git.bioconductor.org/packages/CATALYST git_branch: RELEASE_3_8 git_last_commit: 88805f2 git_last_commit_date: 2019-03-21 Date/Publication: 2019-03-21 source.ver: src/contrib/CATALYST_1.6.7.tar.gz win.binary.ver: bin/windows/contrib/3.5/CATALYST_1.6.7.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CATALYST_1.6.7.tgz vignettes: vignettes/CATALYST/inst/doc/differential_analysis.html, vignettes/CATALYST/inst/doc/preprocessing.html vignetteTitles: "Differential analysis with CATALYST", "Preprocessing with CATALYST" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CATALYST/inst/doc/differential_analysis.R, vignettes/CATALYST/inst/doc/preprocessing.R suggestsMe: diffcyt Package: Category Version: 2.48.1 Depends: methods, stats4, BiocGenerics, AnnotationDbi, Biobase, Matrix Imports: utils, stats, graph, RBGL, GSEABase, genefilter, annotate, DBI Suggests: EBarrays, ALL, Rgraphviz, RColorBrewer, xtable (>= 1.4-6), hgu95av2.db, KEGG.db, SNPchip, geneplotter, limma, lattice, RUnit, org.Sc.sgd.db, GOstats, GO.db License: Artistic-2.0 MD5sum: 6aa5fff26b63625be66eeaa725f6c446 NeedsCompilation: no Title: Category Analysis Description: A collection of tools for performing category (gene set enrichment) analysis. biocViews: Annotation, GO, Pathways, GeneSetEnrichment Author: Robert Gentleman [aut], Seth Falcon [ctb], Deepayan Sarkar [ctb], Robert Castelo [ctb], Bioconductor Package Maintainer [cre] Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/Category git_branch: RELEASE_3_8 git_last_commit: 941819a git_last_commit_date: 2019-03-07 Date/Publication: 2019-03-07 source.ver: src/contrib/Category_2.48.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Category_2.48.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Category_2.48.1.tgz vignettes: vignettes/Category/inst/doc/Category.pdf, vignettes/Category/inst/doc/ChromBand.pdf vignetteTitles: Using Categories to Analyze Microarray Data, Using Chromosome Bands as Categories hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Category/inst/doc/Category.R, vignettes/Category/inst/doc/ChromBand.R dependsOnMe: GOstats, PCpheno importsMe: categoryCompare, cellHTS2, eisa, gCMAP, interactiveDisplay, meshr, miRLAB, PCpheno, phenoTest, ppiStats, RDAVIDWebService suggestsMe: BiocCaseStudies, MmPalateMiRNA, qpgraph, RnBeads Package: categoryCompare Version: 1.26.0 Depends: R (>= 2.10), Biobase, BiocGenerics (>= 0.13.8), Imports: AnnotationDbi, hwriter, GSEABase, Category (>= 2.33.1), GOstats, annotate, colorspace, graph, RCy3 (>= 1.99.29), methods, grDevices, utils Suggests: knitr, GO.db, KEGG.db, estrogen, org.Hs.eg.db, hgu95av2.db, limma, affy, genefilter License: GPL-2 MD5sum: 0651838e9b5b0d85c2100aee6deca3c7 NeedsCompilation: no Title: Meta-analysis of high-throughput experiments using feature annotations Description: Calculates significant annotations (categories) in each of two (or more) feature (i.e. gene) lists, determines the overlap between the annotations, and returns graphical and tabular data about the significant annotations and which combinations of feature lists the annotations were found to be significant. Interactive exploration is facilitated through the use of RCytoscape (heavily suggested). biocViews: Annotation, GO, MultipleComparison, Pathways, GeneExpression Author: Robert M. Flight Maintainer: Robert M. Flight URL: https://github.com/rmflight/categoryCompare SystemRequirements: Cytoscape (>= 3.6.1) (if used for visualization of results, heavily suggested) VignetteBuilder: knitr BugReports: https://github.com/rmflight/categoryCompare/issues git_url: https://git.bioconductor.org/packages/categoryCompare git_branch: RELEASE_3_8 git_last_commit: 3cef693 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/categoryCompare_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/categoryCompare_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/categoryCompare_1.26.0.tgz vignettes: vignettes/categoryCompare/inst/doc/categoryCompare_vignette.html vignetteTitles: categoryCompare: High-throughput data meta-analysis using gene annotations hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/categoryCompare/inst/doc/categoryCompare_vignette.R Package: CausalR Version: 1.14.1 Depends: R (>= 3.2.0) Imports: igraph Suggests: knitr, RUnit, BiocGenerics License: GPL (>= 2) MD5sum: b28781d608123d026005d9388166057d NeedsCompilation: no Title: Causal network analysis methods Description: Causal network analysis methods for regulator prediction and network reconstruction from genome scale data. biocViews: ImmunoOncology, SystemsBiology, Network, GraphAndNetwork, Network Inference, Transcriptomics, Proteomics, DifferentialExpression, RNASeq, Microarray Author: Glyn Bradley, Steven Barrett, Chirag Mistry, Mark Pipe, David Wille, David Riley, Bhushan Bonde, Peter Woollard Maintainer: Glyn Bradley , Steven Barrett VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CausalR git_branch: RELEASE_3_8 git_last_commit: a315e1e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CausalR_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CausalR_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CausalR_1.14.1.tgz vignettes: vignettes/CausalR/inst/doc/CausalR.pdf vignetteTitles: CausalR.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CausalR/inst/doc/CausalR.R Package: cbaf Version: 1.4.1 Imports: BiocFileCache, RColorBrewer, cgdsr, genefilter, gplots, grDevices, stats, utils, xlsx Suggests: knitr, rmarkdown, BiocStyle License: Artistic-2.0 MD5sum: 40053098c4afaa1f0ca60a4c894e8789 NeedsCompilation: no Title: Multiple automated functions for cbioportal.org Description: This package contains functions that allow analysing and comparing various gene groups from different cancers/cancer subgroups easily. So far, it is compatible with RNA-seq, microRNA-seq, microarray and methylation datasets that are stored on cbioportal.org. biocViews: Technology Author: Arman Shahrisa [aut, cre, cph], Maryam Tahmasebi Birgani [aut] Maintainer: Arman Shahrisa VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cbaf git_branch: RELEASE_3_8 git_last_commit: 13efbdf git_last_commit_date: 2019-02-23 Date/Publication: 2019-02-27 source.ver: src/contrib/cbaf_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cbaf_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cbaf_1.4.1.tgz vignettes: vignettes/cbaf/inst/doc/cbaf.html vignetteTitles: cbaf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cbaf/inst/doc/cbaf.R Package: ccfindR Version: 1.2.1 Depends: R (>= 3.5.1) Imports: stats, S4Vectors, utils, methods, Matrix, SummarizedExperiment, SingleCellExperiment, Rtsne, graphics, grDevices, gtools, RColorBrewer, ape, Rmpi, irlba, Rcpp LinkingTo: Rcpp, RcppEigen Suggests: BiocStyle, knitr, rmarkdown License: GPL (>= 2) Archs: i386, x64 MD5sum: 51f3cc3a014689bc33680de200f5b425 NeedsCompilation: yes Title: Cancer Clone Finder Description: A collection of tools for cancer genomic data clustering analyses, including those for single cell RNA-seq. Cell clustering and feature gene selection analysis employ Bayesian (and maximum likelihood) non-negative matrix factorization (NMF) algorithm. Input data set consists of RNA count matrix, gene, and cell bar code annotations. Analysis outputs are factor matrices for multiple ranks and marginal likelihood values for each rank. The package includes utilities for downstream analyses, including meta-gene identification, visualization, and construction of rank-based trees for clusters. biocViews: Transcriptomics, SingleCell, ImmunoOncology, Bayesian, Clustering Author: Jun Woo [aut, cre], Jinhua Wang [aut] Maintainer: Jun Woo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ccfindR git_branch: RELEASE_3_8 git_last_commit: b13e377 git_last_commit_date: 2019-01-03 Date/Publication: 2019-01-03 source.ver: src/contrib/ccfindR_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ccfindR_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ccfindR_1.2.1.tgz vignettes: vignettes/ccfindR/inst/doc/ccfindR.html vignetteTitles: ccfindR: single-cell RNA-seq analysis using Bayesian non-negative matrix factorization hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ccfindR/inst/doc/ccfindR.R Package: ccmap Version: 1.8.0 Imports: AnnotationDbi (>= 1.36.2), BiocManager (>= 1.24.0), ccdata (>= 1.1.2), doParallel (>= 1.0.10), data.table (>= 1.10.4), foreach (>= 1.4.3), parallel (>= 3.3.3), xgboost (>= 0.6.4), lsa (>= 0.73.1) Suggests: crossmeta, knitr, rmarkdown, testthat, lydata License: MIT + file LICENSE MD5sum: d603b7771a6fac35514db7eb9818bf57 NeedsCompilation: no Title: Combination Connectivity Mapping Description: Finds drugs and drug combinations that are predicted to reverse or mimic gene expression signatures. These drugs might reverse diseases or mimic healthy lifestyles. biocViews: GeneExpression, Transcription, Microarray, DifferentialExpression Author: Alex Pickering Maintainer: Alex Pickering VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ccmap git_branch: RELEASE_3_8 git_last_commit: bd17d6d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ccmap_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ccmap_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ccmap_1.8.0.tgz vignettes: vignettes/ccmap/inst/doc/ccmap-vignette.html vignetteTitles: ccmap vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ccmap/inst/doc/ccmap-vignette.R importsMe: crossmeta Package: CCPROMISE Version: 1.8.0 Depends: R (>= 3.3.0), stats, methods, CCP, PROMISE, Biobase, GSEABase, utils License: GPL (>= 2) MD5sum: 73f58481f1fabc4fbd97d0b1e9647071 NeedsCompilation: no Title: PROMISE analysis with Canonical Correlation for Two Forms of High Dimensional Genetic Data Description: Perform Canonical correlation between two forms of high demensional genetic data, and associate the first compoent of each form of data with a specific biologically interesting pattern of associations with multiple endpoints. A probe level analysis is also implemented. biocViews: Microarray, GeneExpression Author: Xueyuan Cao and Stanley.pounds Maintainer: Xueyuan Cao git_url: https://git.bioconductor.org/packages/CCPROMISE git_branch: RELEASE_3_8 git_last_commit: 1051e30 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CCPROMISE_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CCPROMISE_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CCPROMISE_1.8.0.tgz vignettes: vignettes/CCPROMISE/inst/doc/CCPROMISE.pdf vignetteTitles: An introduction to CCPROMISE hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CCPROMISE/inst/doc/CCPROMISE.R Package: ccrepe Version: 1.18.1 Imports: infotheo (>= 1.1) Suggests: knitr, BiocStyle, BiocGenerics, testthat License: MIT + file LICENSE MD5sum: 4a8ab1db992aa0909e6bc3917d7900b7 NeedsCompilation: no Title: ccrepe_and_nc.score Description: The CCREPE (Compositionality Corrected by REnormalizaion and PErmutation) package is designed to assess the significance of general similarity measures in compositional datasets. In microbial abundance data, for example, the total abundances of all microbes sum to one; CCREPE is designed to take this constraint into account when assigning p-values to similarity measures between the microbes. The package has two functions: ccrepe: Calculates similarity measures, p-values and q-values for relative abundances of bugs in one or two body sites using bootstrap and permutation matrices of the data. nc.score: Calculates species-level co-variation and co-exclusion patterns based on an extension of the checkerboard score to ordinal data. biocViews: ImmunoOncology, Statistics, Metagenomics, Bioinformatics, Software Author: Emma Schwager ,Craig Bielski, George Weingart Maintainer: Emma Schwager ,Craig Bielski, George Weingart VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ccrepe git_branch: RELEASE_3_8 git_last_commit: f52af11 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ccrepe_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ccrepe_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ccrepe_1.18.1.tgz vignettes: vignettes/ccrepe/inst/doc/ccrepe.pdf vignetteTitles: ccrepe hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ccrepe/inst/doc/ccrepe.R Package: celaref Version: 1.0.1 Depends: R (>= 3.5.0), SummarizedExperiment Imports: MAST, ggplot2, Matrix, dplyr, magrittr, stats, utils, rlang, BiocGenerics, S4Vectors, readr, tibble Suggests: limma, parallel, knitr, rmarkdown, ExperimentHub License: GPL-3 MD5sum: 8df08bd73275d2e6cd4829f6722c6bdf NeedsCompilation: no Title: Single-cell RNAseq cell cluster labelling by reference Description: After the clustering step of a single-cell RNAseq experiment, this package aims to suggest labels/cell types for the clusters, on the basis of similarity to a reference dataset. It requires a table of read counts per cell per gene, and a list of the cells belonging to each of the clusters, (for both test and reference data). biocViews: ImmunoOncology, SingleCell Author: Sarah Williams [aut, cre] Maintainer: Sarah Williams VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/celaref git_branch: RELEASE_3_8 git_last_commit: 5e4a446 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/celaref_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/celaref_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/celaref_1.0.1.tgz vignettes: vignettes/celaref/inst/doc/celaref_doco.html vignetteTitles: Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/celaref/inst/doc/celaref_doco.R Package: cellbaseR Version: 1.6.1 Depends: R(>= 3.4) Imports: methods, jsonlite, httr, data.table, pbapply, tidyr, R.utils, Rsamtools, BiocParallel, foreach, utils, parallel, doParallel Suggests: BiocStyle, knitr, rmarkdown, Gviz, VariantAnnotation License: Apache License (== 2.0) MD5sum: 3073faebd9ff023b2460082636024a97 NeedsCompilation: no Title: Querying annotation data from the high performance Cellbase web Description: This R package makes use of the exhaustive RESTful Web service API that has been implemented for the Cellabase database. It enable researchers to query and obtain a wealth of biological information from a single database saving a lot of time. Another benefit is that researchers can easily make queries about different biological topics and link all this information together as all information is integrated. biocViews: Annotation, VariantAnnotation Author: Mohammed OE Abdallah Maintainer: Mohammed OE Abdallah URL: https://github.com/melsiddieg/cellbaseR VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cellbaseR git_branch: RELEASE_3_8 git_last_commit: f01f468 git_last_commit_date: 2019-04-08 Date/Publication: 2019-04-08 source.ver: src/contrib/cellbaseR_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cellbaseR_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cellbaseR_1.6.1.tgz vignettes: vignettes/cellbaseR/inst/doc/cellbaseR.html vignetteTitles: "Simplifying Genomic Annotations in R" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cellbaseR/inst/doc/cellbaseR.R Package: cellGrowth Version: 1.26.1 Depends: R (>= 2.12.0), locfit (>= 1.5-4) Imports: lattice License: Artistic-2.0 MD5sum: 1d0750c5cdb6784f3a972f2e195377c6 NeedsCompilation: no Title: Fitting cell population growth models Description: This package provides functionalities for the fitting of cell population growth models on experimental OD curves. biocViews: ImmunoOncology, CellBasedAssays, MicrotitrePlateAssay, DataImport, Visualization, TimeCourse Author: Julien Gagneur , Andreas Neudecker Maintainer: Julien Gagneur git_url: https://git.bioconductor.org/packages/cellGrowth git_branch: RELEASE_3_8 git_last_commit: b4320c2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cellGrowth_1.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cellGrowth_1.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cellGrowth_1.26.1.tgz vignettes: vignettes/cellGrowth/inst/doc/cellGrowth.pdf vignetteTitles: Overview of the cellGrowth package. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cellGrowth/inst/doc/cellGrowth.R Package: cellHTS2 Version: 2.46.1 Depends: R (>= 2.10), RColorBrewer, Biobase, methods, genefilter, splots, vsn, hwriter, locfit, grid Imports: prada, GSEABase, Category, stats4, BiocGenerics Suggests: ggplot2 License: Artistic-2.0 MD5sum: 12a210af5dd19fd0148cf4dbe1aba5d0 NeedsCompilation: no Title: Analysis of cell-based screens - revised version of cellHTS Description: This package provides tools for the analysis of high-throughput assays that were performed in microtitre plate formats (including but not limited to 384-well plates). The functionality includes data import and management, normalisation, quality assessment, replicate summarisation and statistical scoring. A webpage that provides a detailed graphical overview over the data and analysis results is produced. In our work, we have applied the package to RNAi screens on fly and human cells, and for screens of yeast libraries. See ?cellHTS2 for a brief introduction. biocViews: ImmunoOncology, CellBasedAssays, Preprocessing, Visualization Author: Ligia Bras, Wolfgang Huber , Michael Boutros , Gregoire Pau , Florian Hahne Maintainer: Joseph Barry URL: http://www.dkfz.de/signaling, http://www.ebi.ac.uk/huber git_url: https://git.bioconductor.org/packages/cellHTS2 git_branch: RELEASE_3_8 git_last_commit: 20da04e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cellHTS2_2.46.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cellHTS2_2.46.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cellHTS2_2.46.1.tgz vignettes: vignettes/cellHTS2/inst/doc/cellhts2.pdf, vignettes/cellHTS2/inst/doc/cellhts2Complete.pdf, vignettes/cellHTS2/inst/doc/twoChannels.pdf, vignettes/cellHTS2/inst/doc/twoWay.pdf vignetteTitles: Main vignette: End-to-end analysis of cell-based screens, Main vignette (complete version): End-to-end analysis of cell-based screens, Supplement: multi-channel assays, Supplement: enhancer-suppressor screens hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cellHTS2/inst/doc/cellhts2.R, vignettes/cellHTS2/inst/doc/cellhts2Complete.R, vignettes/cellHTS2/inst/doc/twoChannels.R, vignettes/cellHTS2/inst/doc/twoWay.R dependsOnMe: imageHTS, staRank importsMe: gespeR, HTSanalyzeR, RNAinteract suggestsMe: bioassayR, prada Package: cellity Version: 1.10.1 Depends: R (>= 3.3) Imports: AnnotationDbi, e1071, ggplot2, graphics, grDevices, grid, mvoutlier, org.Hs.eg.db, org.Mm.eg.db, robustbase, stats, topGO, utils Suggests: BiocStyle, caret, knitr, testthat, rmarkdown License: GPL (>= 2) MD5sum: 3bc80ac8a158088c911972d9a7baebe6 NeedsCompilation: no Title: Quality Control for Single-Cell RNA-seq Data Description: A support vector machine approach to identifying and filtering low quality cells from single-cell RNA-seq datasets. biocViews: ImmunoOncology, RNASeq, QualityControl, Preprocessing, Normalization, Visualization, DimensionReduction, Transcriptomics, GeneExpression, Sequencing, Software, SupportVectorMachine Author: Tomislav Illicic, Davis McCarthy Maintainer: Tomislav Ilicic VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cellity git_branch: RELEASE_3_8 git_last_commit: fe9e809 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cellity_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cellity_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cellity_1.10.1.tgz vignettes: vignettes/cellity/inst/doc/cellity_vignette.html vignetteTitles: An introduction to the cellity package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cellity/inst/doc/cellity_vignette.R Package: CellMapper Version: 1.8.0 Depends: S4Vectors, methods Imports: stats, utils Suggests: CellMapperData, Biobase, HumanAffyData, ALL, BiocStyle, ExperimentHub License: Artistic-2.0 MD5sum: a7a9cd05f7a9f5fad346faf0cdbd8224 NeedsCompilation: no Title: Predict genes expressed selectively in specific cell types Description: Infers cell type-specific expression based on co-expression similarity with known cell type marker genes. Can make accurate predictions using publicly available expression data, even when a cell type has not been isolated before. biocViews: Microarray, Software, GeneExpression Author: Brad Nelms Maintainer: Brad Nelms git_url: https://git.bioconductor.org/packages/CellMapper git_branch: RELEASE_3_8 git_last_commit: d6f4e23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CellMapper_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CellMapper_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CellMapper_1.8.0.tgz vignettes: vignettes/CellMapper/inst/doc/CellMapper.pdf vignetteTitles: CellMapper Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CellMapper/inst/doc/CellMapper.R Package: CellNOptR Version: 1.28.1 Depends: R (>= 2.15.0), RBGL, graph, methods, hash, RCurl, Rgraphviz, XML, ggplot2 Suggests: RUnit, BiocGenerics, igraph, stringi, stringr License: GPL-3 Archs: i386, x64 MD5sum: c4099cae660f639dbe56caef3cfb8336 NeedsCompilation: yes Title: Training of boolean logic models of signalling networks using prior knowledge networks and perturbation data Description: This package does optimisation of boolean logic networks of signalling pathways based on a previous knowledge network and a set of data upon perturbation of the nodes in the network. biocViews: ImmunoOncology, CellBasedAssays, CellBiology, Proteomics, Bioinformatics, TimeCourse Author: T.Cokelaer, F.Eduati, A.MacNamara, S.Schrier, C.Terfve Maintainer: A.Gabor SystemRequirements: Graphviz version >= 2.2 git_url: https://git.bioconductor.org/packages/CellNOptR git_branch: RELEASE_3_8 git_last_commit: aa83d18 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CellNOptR_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CellNOptR_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CellNOptR_1.28.1.tgz vignettes: vignettes/CellNOptR/inst/doc/CellNOptR-vignette.pdf, vignettes/CellNOptR/inst/doc/CellNOptR0_1flowchart.pdf, vignettes/CellNOptR/inst/doc/Fig2.pdf, vignettes/CellNOptR/inst/doc/Fig3.pdf, vignettes/CellNOptR/inst/doc/Fig4.pdf, vignettes/CellNOptR/inst/doc/Fig6.pdf, vignettes/CellNOptR/inst/doc/Fig7.pdf, vignettes/CellNOptR/inst/doc/Fig8.pdf vignetteTitles: Main vignette:Playing with networks using CellNOptR, CellNOptR0_1flowchart.pdf, Fig2.pdf, Fig3.pdf, Fig4.pdf, Fig6.pdf, Fig7.pdf, Fig8.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CellNOptR/inst/doc/CellNOptR-examples.R, vignettes/CellNOptR/inst/doc/CellNOptR-vignette.R dependsOnMe: CNORdt, CNORfeeder, CNORfuzzy, CNORode suggestsMe: MEIGOR Package: cellscape Version: 1.6.0 Depends: R (>= 3.3) Imports: htmlwidgets (>= 0.5), jsonlite (>= 0.9.19), reshape2 (>= 1.4.1), stringr (>= 1.0.0), plyr (>= 1.8.3), dplyr (>= 0.4.3), gtools (>= 3.5.0) Suggests: knitr, rmarkdown License: GPL-3 MD5sum: fca7882d296832aed78b674d1bb92f18 NeedsCompilation: no Title: Explores single cell copy number profiles in the context of a single cell tree Description: CellScape facilitates interactive browsing of single cell clonal evolution datasets. The tool requires two main inputs: (i) the genomic content of each single cell in the form of either copy number segments or targeted mutation values, and (ii) a single cell phylogeny. Phylogenetic formats can vary from dendrogram-like phylogenies with leaf nodes to evolutionary model-derived phylogenies with observed or latent internal nodes. The CellScape phylogeny is flexibly input as a table of source-target edges to support arbitrary representations, where each node may or may not have associated genomic data. The output of CellScape is an interactive interface displaying a single cell phylogeny and a cell-by-locus genomic heatmap representing the mutation status in each cell for each locus. biocViews: Visualization Author: Maia Smith [aut, cre] Maintainer: Maia Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cellscape git_branch: RELEASE_3_8 git_last_commit: 56305f7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cellscape_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cellscape_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cellscape_1.6.0.tgz vignettes: vignettes/cellscape/inst/doc/cellscape_vignette.html vignetteTitles: CellScape vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cellscape/inst/doc/cellscape_vignette.R Package: CellScore Version: 1.2.0 Depends: R (>= 3.5.0) Imports: Biobase (>= 2.39.1), graphics (>= 3.5.0), grDevices (>= 3.5.0), gplots (>= 3.0.1), lsa (>= 0.73.1), methods (>= 3.5.0), RColorBrewer(>= 1.1-2), squash (>= 1.0.8), stats (>= 3.5.0), utils(>= 3.5.0) Suggests: hgu133plus2CellScore, knitr License: GPL-3 MD5sum: e9b84c8c0cbd7bbe43cbe7c71af89342 NeedsCompilation: no Title: Tool for Evaluation of Cell Identity from Transcription Profiles Description: The CellScore package contains functions to evaluate the cell identity of a test sample, given a cell transition defined with a starting (donor) cell type and a desired target cell type. The evaluation is based upon a scoring system, which uses a set of standard samples of known cell types, as the reference set. The functions have been carried out on a large set of microarray data from one platform (Affymetrix Human Genome U133 Plus 2.0). In principle, the method could be applied to any expression dataset, provided that there are a sufficient number of standard samples and that the data are normalized. biocViews: GeneExpression, Transcription, Microarray, MultipleComparison, ReportWriting, DataImport, Visualization Author: Nancy Mah, Katerina Taskova Maintainer: Nancy Mah VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CellScore git_branch: RELEASE_3_8 git_last_commit: 483ebd7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CellScore_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CellScore_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CellScore_1.2.0.tgz vignettes: vignettes/CellScore/inst/doc/CellScoreVignette.pdf vignetteTitles: R packages: CellScore hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CellScore/inst/doc/CellScoreVignette.R Package: CellTrails Version: 1.0.1 Depends: R (>= 3.5), SingleCellExperiment Imports: BiocGenerics, Biobase, cba, dendextend, dtw, EnvStats, ggplot2, ggrepel, grDevices, igraph, maptree, methods, mgcv, reshape2, Rtsne, stats, splines, SummarizedExperiment, utils Suggests: AnnotationDbi, destiny, RUnit, scater, scran, knitr, org.Mm.eg.db, rmarkdown License: Artistic-2.0 MD5sum: 79853754f3fb8a943cb643dc1711afa7 NeedsCompilation: no Title: Reconstruction, visualization and analysis of branching trajectories Description: CellTrails is an unsupervised algorithm for the de novo chronological ordering, visualization and analysis of single-cell expression data. CellTrails makes use of a geometrically motivated concept of lower-dimensional manifold learning, which exhibits a multitude of virtues that counteract intrinsic noise of single cell data caused by drop-outs, technical variance, and redundancy of predictive variables. CellTrails enables the reconstruction of branching trajectories and provides an intuitive graphical representation of expression patterns along all branches simultaneously. It allows the user to define and infer the expression dynamics of individual and multiple pathways towards distinct phenotypes. biocViews: ImmunoOncology, Clustering, DataRepresentation, DifferentialExpression, DimensionReduction, GeneExpression, Sequencing, SingleCell, Software, TimeCourse Author: Daniel Ellwanger [aut, cre, cph] Maintainer: Daniel Ellwanger VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CellTrails git_branch: RELEASE_3_8 git_last_commit: 548bced git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CellTrails_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CellTrails_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CellTrails_1.0.1.tgz vignettes: vignettes/CellTrails/inst/doc/vignette.pdf vignetteTitles: CellTrails: Reconstruction,, visualization,, and analysis of branching trajectories from single-cell expression data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CellTrails/inst/doc/vignette.R Package: cellTree Version: 1.12.1 Depends: R (>= 3.3), topGO Imports: topicmodels, slam, maptpx, igraph, xtable, gplots Suggests: BiocStyle, knitr, HSMMSingleCell, biomaRt, org.Hs.eg.db, Biobase, tools License: Artistic-2.0 MD5sum: ee3a7f134b2933c644889a907a4206f4 NeedsCompilation: no Title: Inference and visualisation of Single-Cell RNA-seq data as a hierarchical tree structure Description: This packages computes a Latent Dirichlet Allocation (LDA) model of single-cell RNA-seq data and builds a compact tree modelling the relationship between individual cells over time or space. biocViews: ImmunoOncology, Sequencing, RNASeq, Clustering, GraphAndNetwork, Visualization, GeneExpression, GeneSetEnrichment, BiomedicalInformatics, CellBiology, FunctionalGenomics, SystemsBiology, GO, TimeCourse, Microarray Author: David duVerle [aut, cre], Koji Tsuda [aut] Maintainer: David duVerle URL: http://tsudalab.org VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cellTree git_branch: RELEASE_3_8 git_last_commit: 6034cb5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cellTree_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cellTree_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cellTree_1.12.1.tgz vignettes: vignettes/cellTree/inst/doc/cellTree-vignette.pdf vignetteTitles: Inference and visualisation of Single-Cell RNA-seq Data data as a hierarchical tree structure hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cellTree/inst/doc/cellTree-vignette.R Package: CEMiTool Version: 1.6.11 Depends: R (>= 3.5) Imports: methods, scales, gRbase, dplyr, data.table (>= 1.9.4), WGCNA, grid, ggplot2, ggpmisc, ggthemes, ggrepel, sna, clusterProfiler, fgsea, stringr, knitr, rmarkdown, igraph, DT, htmltools, pracma, intergraph, grDevices, utils, network, matrixStats, ggdendro, gridExtra, gtable, GeneOverlap, limma, tidyr, plyr, ff, ffbase, RColorBrewer Suggests: testthat, BiocManager License: GPL-3 MD5sum: 944d0be3f6bc6d33d9b48045f1363d63 NeedsCompilation: no Title: Co-expression Modules identification Tool Description: The CEMiTool package unifies the discovery and the analysis of coexpression gene modules in a fully automatic manner, while providing a user-friendly html report with high quality graphs. Our tool evaluates if modules contain genes that are over-represented by specific pathways or that are altered in a specific sample group. Additionally, CEMiTool is able to integrate transcriptomic data with interactome information, identifying the potential hubs on each network. biocViews: GeneExpression, Transcriptomics, GraphAndNetwork, mRNAMicroarray, RNASeq, Network, NetworkEnrichment, Pathways, ImmunoOncology Author: Pedro Russo [aut], Gustavo Ferreira [aut], Matheus Bürger [aut], Lucas Cardozo [aut], Diogenes Lima [aut], Thiago Hirata [aut], Melissa Lever [aut], Helder Nakaya [aut, cre] Maintainer: Helder Nakaya VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CEMiTool git_branch: RELEASE_3_8 git_last_commit: d4c4ae4 git_last_commit_date: 2019-03-15 Date/Publication: 2019-03-15 source.ver: src/contrib/CEMiTool_1.6.11.tar.gz win.binary.ver: bin/windows/contrib/3.5/CEMiTool_1.6.11.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CEMiTool_1.6.11.tgz vignettes: vignettes/CEMiTool/inst/doc/CEMiTool.html vignetteTitles: CEMiTool: Co-expression Modules Identification Tool hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CEMiTool/inst/doc/CEMiTool.R Package: CexoR Version: 1.20.0 Depends: R (>= 2.10.0), S4Vectors, IRanges Imports: Rsamtools, GenomeInfoDb, GenomicRanges, rtracklayer, idr, RColorBrewer, genomation Suggests: RUnit, BiocGenerics, BiocStyle License: Artistic-2.0 | GPL-2 + file LICENSE MD5sum: adc301c13a685ebcb765a611268f6612 NeedsCompilation: no Title: An R package to uncover high-resolution protein-DNA interactions in ChIP-exo replicates Description: Strand specific peak-pair calling in ChIP-exo replicates. The cumulative Skellam distribution function (package 'skellam') is used to detect significant normalised count differences of opposed sign at each DNA strand (peak-pairs). Irreproducible discovery rate for overlapping peak-pairs across biological replicates is estimated using the package 'idr'. biocViews: Transcription, Genetics, Sequencing Author: Pedro Madrigal Maintainer: Pedro Madrigal git_url: https://git.bioconductor.org/packages/CexoR git_branch: RELEASE_3_8 git_last_commit: d23e629 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CexoR_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CexoR_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CexoR_1.20.0.tgz vignettes: vignettes/CexoR/inst/doc/CexoR.pdf vignetteTitles: CexoR Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/CexoR/inst/doc/CexoR.R Package: CFAssay Version: 1.16.1 Depends: R (>= 2.10.0) License: LGPL MD5sum: 8ed2b2e9908e3cf38d77a8747dd6a409 NeedsCompilation: no Title: Statistical analysis for the Colony Formation Assay Description: The package provides functions for calculation of linear-quadratic cell survival curves and for ANOVA of experimental 2-way designs along with the colony formation assay. biocViews: ImmunoOncology, CellBasedAssays, CellBiology, Regression, Survival Author: Herbert Braselmann Maintainer: Herbert Braselmann git_url: https://git.bioconductor.org/packages/CFAssay git_branch: RELEASE_3_8 git_last_commit: 9d0521b git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CFAssay_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CFAssay_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CFAssay_1.16.1.tgz vignettes: vignettes/CFAssay/inst/doc/cfassay.pdf vignetteTitles: CFAssay hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CFAssay/inst/doc/cfassay.R Package: CGEN Version: 3.18.0 Depends: R (>= 2.10.1), survival, mvtnorm Suggests: cluster License: GPL-2 + file LICENSE Archs: i386, x64 MD5sum: 8de652a5e02f957223ebbe1923ed9886 NeedsCompilation: yes Title: An R package for analysis of case-control studies in genetic epidemiology Description: An R package for analysis of case-control studies in genetic epidemiology. biocViews: SNP, MultipleComparisons, Clustering Author: Samsiddhi Bhattacharjee, Nilanjan Chatterjee, Summer Han and William Wheeler Maintainer: William Wheeler git_url: https://git.bioconductor.org/packages/CGEN git_branch: RELEASE_3_8 git_last_commit: 6454ffc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CGEN_3.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CGEN_3.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CGEN_3.18.0.tgz vignettes: vignettes/CGEN/inst/doc/vignette_GxE.pdf, vignettes/CGEN/inst/doc/vignette.pdf vignetteTitles: CGEN Vignette, CGEN Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/CGEN/inst/doc/vignette_GxE.R, vignettes/CGEN/inst/doc/vignette.R Package: CGHbase Version: 1.42.0 Depends: R (>= 2.10), methods, Biobase (>= 2.5.5), marray License: GPL MD5sum: 8e5a1db8a434a7a03a7f0298a6e466a1 NeedsCompilation: no Title: CGHbase: Base functions and classes for arrayCGH data analysis. Description: Contains functions and classes that are needed by arrayCGH packages. biocViews: Infrastructure, Microarray, CopyNumberVariation Author: Sjoerd Vosse, Mark van de Wiel Maintainer: Mark van de Wiel URL: https://github.com/tgac-vumc/CGHbase BugReports: https://github.com/tgac-vumc/CGHbase/issues git_url: https://git.bioconductor.org/packages/CGHbase git_branch: RELEASE_3_8 git_last_commit: 56c1525 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CGHbase_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CGHbase_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CGHbase_1.42.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: CGHcall, CGHnormaliter, CGHregions, GeneBreak, sigaR importsMe: CGHnormaliter, plrs, QDNAseq Package: CGHcall Version: 2.44.0 Depends: R (>= 2.0.0), impute(>= 1.8.0), DNAcopy (>= 1.6.0), methods, Biobase, CGHbase (>= 1.15.1), snowfall License: GPL (http://www.gnu.org/copyleft/gpl.html) MD5sum: 6adfe221a755373d03ab61d68c575c06 NeedsCompilation: no Title: Calling aberrations for array CGH tumor profiles. Description: Calls aberrations for array CGH data using a six state mixture model as well as several biological concepts that are ignored by existing algorithms. Visualization of profiles is also provided. biocViews: Microarray,Preprocessing,Visualization Author: Mark van de Wiel, Sjoerd Vosse Maintainer: Mark van de Wiel git_url: https://git.bioconductor.org/packages/CGHcall git_branch: RELEASE_3_8 git_last_commit: 1730063 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CGHcall_2.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CGHcall_2.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CGHcall_2.44.0.tgz vignettes: vignettes/CGHcall/inst/doc/CGHcall.pdf vignetteTitles: CGHcall hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CGHcall/inst/doc/CGHcall.R dependsOnMe: CGHnormaliter, focalCall, GeneBreak importsMe: CGHnormaliter, QDNAseq suggestsMe: sigaR Package: cghMCR Version: 1.40.0 Depends: methods, DNAcopy, CNTools, limma Imports: BiocGenerics (>= 0.1.6), stats4 License: LGPL MD5sum: ee9010fd0cda4e0454890e547be251fa NeedsCompilation: no Title: Find chromosome regions showing common gains/losses Description: This package provides functions to identify genomic regions of interests based on segmented copy number data from multiple samples. biocViews: Microarray, CopyNumberVariation Author: J. Zhang and B. Feng Maintainer: J. Zhang git_url: https://git.bioconductor.org/packages/cghMCR git_branch: RELEASE_3_8 git_last_commit: c433190 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cghMCR_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cghMCR_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cghMCR_1.40.0.tgz vignettes: vignettes/cghMCR/inst/doc/findMCR.pdf vignetteTitles: cghMCR findMCR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cghMCR/inst/doc/findMCR.R Package: CGHnormaliter Version: 1.36.0 Depends: CGHcall (>= 2.17.0), CGHbase (>= 1.15.0) Imports: Biobase, CGHbase, CGHcall, methods, stats, utils License: GPL (>= 3) MD5sum: 864c1f86399bde28c8deea6390e8f03f NeedsCompilation: no Title: Normalization of array CGH data with imbalanced aberrations. Description: Normalization and centralization of array comparative genomic hybridization (aCGH) data. The algorithm uses an iterative procedure that effectively eliminates the influence of imbalanced copy numbers. This leads to a more reliable assessment of copy number alterations (CNAs). biocViews: Microarray, Preprocessing Author: Bart P.P. van Houte, Thomas W. Binsl, Hannes Hettling Maintainer: Bart P.P. van Houte git_url: https://git.bioconductor.org/packages/CGHnormaliter git_branch: RELEASE_3_8 git_last_commit: e68bd33 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CGHnormaliter_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CGHnormaliter_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CGHnormaliter_1.36.0.tgz vignettes: vignettes/CGHnormaliter/inst/doc/CGHnormaliter.pdf vignetteTitles: CGHnormaliter hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CGHnormaliter/inst/doc/CGHnormaliter.R Package: CGHregions Version: 1.40.0 Depends: R (>= 2.0.0), methods, Biobase, CGHbase License: GPL (http://www.gnu.org/copyleft/gpl.html) MD5sum: 83a3b0748e057ec4ca72aa1866f9b030 NeedsCompilation: no Title: Dimension Reduction for Array CGH Data with Minimal Information Loss. Description: Dimension Reduction for Array CGH Data with Minimal Information Loss biocViews: Microarray, CopyNumberVariation, Visualization Author: Sjoerd Vosse & Mark van de Wiel Maintainer: Sjoerd Vosse git_url: https://git.bioconductor.org/packages/CGHregions git_branch: RELEASE_3_8 git_last_commit: 759b445 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CGHregions_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CGHregions_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CGHregions_1.40.0.tgz vignettes: vignettes/CGHregions/inst/doc/CGHregions.pdf vignetteTitles: CGHcall hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CGHregions/inst/doc/CGHregions.R suggestsMe: ADaCGH2 Package: ChAMP Version: 2.12.4 Depends: R (>= 3.3), minfi, ChAMPdata (>= 2.6.0), FEM (>= 3.1),DMRcate, Illumina450ProbeVariants.db,IlluminaHumanMethylationEPICmanifest Imports: prettydoc,Hmisc,globaltest,sva,illuminaio,rmarkdown,IlluminaHumanMethylation450kmanifest,IlluminaHumanMethylationEPICanno.ilm10b2.hg19, limma,RPMM, DNAcopy, preprocessCore,impute, marray, wateRmelon, plyr,goseq,missMethyl,kpmt, GenomicRanges,qvalue,isva,doParallel,bumphunter,quadprog,shiny,shinythemes,plotly (>= 4.5.6),RColorBrewer,dendextend, matrixStats,combinat Suggests: knitr,rmarkdown License: GPL-3 MD5sum: fe30953a17a828908bc158dc69a8ad88 NeedsCompilation: no Title: Chip Analysis Methylation Pipeline for Illumina HumanMethylation450 and EPIC Description: The package includes quality control metrics, a selection of normalization methods and novel methods to identify differentially methylated regions and to highlight copy number alterations. biocViews: Microarray, MethylationArray, Normalization, TwoChannel, CopyNumber, DNAMethylation Author: Yuan Tian [cre,aut], Tiffany Morris [ctb], Lee Stirling [ctb], Andrew Feber [ctb], Andrew Teschendorff [ctb], Ankur Chakravarthy [ctb] Maintainer: Yuan Tian VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ChAMP git_branch: RELEASE_3_8 git_last_commit: 45372e6 git_last_commit_date: 2019-02-05 Date/Publication: 2019-02-06 source.ver: src/contrib/ChAMP_2.12.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChAMP_2.12.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChAMP_2.12.4.tgz vignettes: vignettes/ChAMP/inst/doc/ChAMP.html vignetteTitles: ChAMP: The Chip Analysis Methylation Pipeline hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChAMP/inst/doc/ChAMP.R Package: CHARGE Version: 1.2.0 Depends: R (>= 3.5), GenomicRanges, methods Imports: SummarizedExperiment, FactoMineR, factoextra, IRanges, graphics, modes, parallel, plyr, cluster, diptest, stats, matrixStats Suggests: roxygen2, EnsDb.Hsapiens.v86 License: GPL-2 MD5sum: 5c4c8debe46ce9db6a724b4bc94e6f06 NeedsCompilation: no Title: CHARGE: CHromosome Assessment in R from Gene Expression data Description: Identifies genomic duplications or deletions from gene expression data. biocViews: GeneExpression, Clustering Author: Benjamin Mayne Maintainer: Benjamin Mayne git_url: https://git.bioconductor.org/packages/CHARGE git_branch: RELEASE_3_8 git_last_commit: 136a83c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CHARGE_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CHARGE_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CHARGE_1.2.0.tgz vignettes: vignettes/CHARGE/inst/doc/CHARGE_Vignette.pdf vignetteTitles: CHARGE_Example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CHARGE/inst/doc/CHARGE_Vignette.R Package: charm Version: 2.28.0 Depends: R (>= 2.14.0), Biobase, SQN, fields, RColorBrewer, genefilter Imports: BSgenome, Biobase, oligo (>= 1.11.31), oligoClasses(>= 1.17.39), ff, preprocessCore, methods, stats, Biostrings, IRanges, siggenes, nor1mix, gtools, grDevices, graphics, utils, limma, parallel, sva(>= 3.1.2) Suggests: charmData, BSgenome.Hsapiens.UCSC.hg18, corpcor License: LGPL (>= 2) MD5sum: 63fa78f4ef43f5c8ea4f2fe33885e184 NeedsCompilation: no Title: Analysis of DNA methylation data from CHARM microarrays Description: This package implements analysis tools for DNA methylation data generated using Nimblegen microarrays and the McrBC protocol. It finds differentially methylated regions between samples, calculates percentage methylation estimates and includes array quality assessment tools. biocViews: Microarray, DNAMethylation Author: Martin Aryee, Peter Murakami, Harris Jaffee, Rafael Irizarry Maintainer: Peter Murakami git_url: https://git.bioconductor.org/packages/charm git_branch: RELEASE_3_8 git_last_commit: f6e6e9b git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/charm_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/charm_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/charm_2.28.0.tgz vignettes: vignettes/charm/inst/doc/charm.pdf vignetteTitles: charm Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/charm/inst/doc/charm.R Package: ChemmineOB Version: 1.20.0 Depends: R (>= 2.15.1), methods Imports: BiocGenerics, zlibbioc, Rcpp (>= 0.11.0) LinkingTo: BH, Rcpp Suggests: ChemmineR, BiocStyle, knitr, knitcitations, knitrBootstrap, BiocManager Enhances: ChemmineR (>= 2.13.0) License: file LICENSE Archs: i386, x64 MD5sum: e22ab70101dfc90ee6432269eb9d2adb NeedsCompilation: yes Title: R interface to a subset of OpenBabel functionalities Description: ChemmineOB provides an R interface to a subset of cheminformatics functionalities implemented by the OpelBabel C++ project. OpenBabel is an open source cheminformatics toolbox that includes utilities for structure format interconversions, descriptor calculations, compound similarity searching and more. ChemineOB aims to make a subset of these utilities available from within R. For non-developers, ChemineOB is primarily intended to be used from ChemmineR as an add-on package rather than used directly. biocViews: Cheminformatics, BiomedicalInformatics, Pharmacogenetics, Pharmacogenomics, MicrotitrePlateAssay, CellBasedAssays, Visualization, Infrastructure, DataImport, Clustering, Proteomics, Metabolomics Author: Kevin Horan, Thomas Girke Maintainer: Thomas Girke URL: https://github.com/girke-lab/ChemmineOB SystemRequirements: OpenBabel (>= 2.3.1) with headers (http://openbabel.org). VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ChemmineOB git_branch: RELEASE_3_8 git_last_commit: 312f828 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChemmineOB_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChemmineOB_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChemmineOB_1.20.0.tgz vignettes: vignettes/ChemmineOB/inst/doc/ChemmineOB.html vignetteTitles: ChemmineOB hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: TRUE Rfiles: vignettes/ChemmineOB/inst/doc/ChemmineOB.R suggestsMe: ChemmineR Package: ChemmineR Version: 3.34.1 Depends: R (>= 2.10.0), methods Imports: rjson, graphics, stats, RCurl, DBI, digest, BiocGenerics, Rcpp (>= 0.11.0), ggplot2,grid,gridExtra, png,base64enc,DT,rsvg LinkingTo: Rcpp, BH Suggests: RSQLite, scatterplot3d, gplots, fmcsR, snow, RPostgreSQL, BiocStyle, knitr, knitcitations, knitrBootstrap, ChemmineOB (>= 1.16.1), ChemmineDrugs, png,rmarkdown, BiocManager Enhances: ChemmineOB License: Artistic-2.0 Archs: i386, x64 MD5sum: e271de186e07cdbb5195645bbab04f13 NeedsCompilation: yes Title: Cheminformatics Toolkit for R Description: ChemmineR is a cheminformatics package for analyzing drug-like small molecule data in R. Its latest version contains functions for efficient processing of large numbers of molecules, physicochemical/structural property predictions, structural similarity searching, classification and clustering of compound libraries with a wide spectrum of algorithms. In addition, it offers visualization functions for compound clustering results and chemical structures. biocViews: Cheminformatics, BiomedicalInformatics, Pharmacogenetics, Pharmacogenomics, MicrotitrePlateAssay, CellBasedAssays, Visualization, Infrastructure, DataImport, Clustering, Proteomics,Metabolomics Author: Y. Eddie Cao, Kevin Horan, Tyler Backman, Thomas Girke Maintainer: Thomas Girke URL: https://github.com/girke-lab/ChemmineR SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ChemmineR git_branch: RELEASE_3_8 git_last_commit: a8b1e28 git_last_commit_date: 2018-11-14 Date/Publication: 2018-11-15 source.ver: src/contrib/ChemmineR_3.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChemmineR_3.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChemmineR_3.34.1.tgz vignettes: vignettes/ChemmineR/inst/doc/ChemmineR.html vignetteTitles: ChemmineR hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChemmineR/inst/doc/ChemmineR.R dependsOnMe: eiR, fmcsR importsMe: bioassayR, eiR, fmcsR, MetID, Rchemcpp, Rcpi suggestsMe: ChemmineOB Package: ChIC Version: 1.2.0 Depends: spp, R (>= 3.5) Imports: ChIC.data (>= 1.1.4), caTools, methods,GenomicRanges, IRanges, parallel, progress, caret, grDevices, stats, utils, graphics, S4Vectors, BiocGenerics License: GPL-2 MD5sum: dcf74f7e88f59bb8965f1d0202651109 NeedsCompilation: no Title: Quality Control Pipeline for ChIP-Seq Data Description: Quality control (QC) pipeline for ChIP-seq data using a comprehensive set of QC metrics, including previously proposed metrics as well as novel ones, based on local characteristics of the enrichment profile. The package provides functions to calculate a set of QC metrics, a compendium with reference values and machine learning models to score sample quality. biocViews: ChIPSeq, QualityControl Author: Carmen Maria Livi Maintainer: Carmen Maria Livi git_url: https://git.bioconductor.org/packages/ChIC git_branch: RELEASE_3_8 git_last_commit: 57469d4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIC_1.2.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIC_1.2.0.tgz vignettes: vignettes/ChIC/inst/doc/ChIC-Vignette.pdf vignetteTitles: ChIC hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIC/inst/doc/ChIC-Vignette.R Package: Chicago Version: 1.10.1 Depends: R (>= 3.2), data.table Imports: matrixStats, MASS, Hmisc, Delaporte, methods, grDevices, graphics, stats, utils Suggests: argparser, BiocStyle, knitr, rmarkdown, PCHiCdata, testthat, Rsamtools, GenomicInteractions, GenomicRanges, IRanges, AnnotationHub License: Artistic-2.0 MD5sum: 4dd883d54c606ec9c47a78bc942ca5bb NeedsCompilation: no Title: CHiCAGO: Capture Hi-C Analysis of Genomic Organization Description: A pipeline for analysing Capture Hi-C data. biocViews: ImmunoOncology, Epigenetics, HiC, Sequencing, Software Author: Jonathan Cairns, Paula Freire Pritchett, Steven Wingett, Mikhail Spivakov Maintainer: Mikhail Spivakov VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Chicago git_branch: RELEASE_3_8 git_last_commit: 1a21c85 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Chicago_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Chicago_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Chicago_1.10.1.tgz vignettes: vignettes/Chicago/inst/doc/Chicago.html vignetteTitles: CHiCAGO Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Chicago/inst/doc/Chicago.R Package: chimera Version: 1.24.0 Depends: Biobase, GenomicRanges (>= 1.13.3), Rsamtools (>= 1.13.1), GenomicAlignments, methods, AnnotationDbi, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, Homo.sapiens Suggests: BiocParallel, geneplotter Enhances: Rsubread, BSgenome.Mmusculus.UCSC.mm9, TxDb.Mmusculus.UCSC.mm9.knownGene, BSgenome.Mmusculus.UCSC.mm10, TxDb.Mmusculus.UCSC.mm10.knownGene, Mus.musculus, BSgenome.Hsapiens.NCBI.GRCh38, TxDb.Hsapiens.UCSC.hg38.knownGene License: Artistic-2.0 Archs: i386, x64 MD5sum: 3245d0c076c17bc1b850d377cf15070a NeedsCompilation: yes Title: A package for secondary analysis of fusion products Description: This package facilitates the characterisation of fusion products events. It allows to import fusion data results from the following fusion finders: chimeraScan, bellerophontes, deFuse, FusionFinder, FusionHunter, mapSplice, tophat-fusion, FusionMap, STAR, Rsubread, fusionCatcher. biocViews: Infrastructure Author: Raffaele A Calogero, Matteo Carrara, Marco Beccuti, Francesca Cordero Maintainer: Raffaele A Calogero SystemRequirements: STAR, TopHat, bowtie and samtools are required for some functionalities git_url: https://git.bioconductor.org/packages/chimera git_branch: RELEASE_3_8 git_last_commit: ec9ab96 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/chimera_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/chimera_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chimera_1.24.0.tgz vignettes: vignettes/chimera/inst/doc/chimera.pdf vignetteTitles: chimera hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chimera/inst/doc/chimera.R Package: chimeraviz Version: 1.8.5 Depends: Biostrings, GenomicRanges, IRanges, Gviz, S4Vectors, ensembldb, AnnotationFilter, data.table Imports: methods, grid, Rsamtools, GenomeInfoDb, GenomicAlignments, RColorBrewer, graphics, AnnotationDbi, RCircos, org.Hs.eg.db, org.Mm.eg.db, rmarkdown, graph, Rgraphviz, DT, plyr, dplyr, BiocStyle, ArgumentCheck, gtools Suggests: testthat, roxygen2, devtools, knitr, lintr License: Artistic-2.0 MD5sum: 5b9f413b1e399944247c6fa76565e680 NeedsCompilation: no Title: Visualization tools for gene fusions Description: chimeraviz manages data from fusion gene finders and provides useful visualization tools. biocViews: Infrastructure, Alignment Author: Stian Lågstad [aut, cre], Sen Zhao [ctb], Andreas M. Hoff [ctb], Bjarne Johannessen [ctb], Ole Christian Lingjærde [ctb], Rolf Skotheim [ctb] Maintainer: Stian Lågstad URL: https://github.com/stianlagstad/chimeraviz SystemRequirements: bowtie, samtools, and egrep are required for some functionalities VignetteBuilder: knitr BugReports: https://github.com/stianlagstad/chimeraviz/issues git_url: https://git.bioconductor.org/packages/chimeraviz git_branch: RELEASE_3_8 git_last_commit: 90aa749 git_last_commit_date: 2019-03-22 Date/Publication: 2019-03-23 source.ver: src/contrib/chimeraviz_1.8.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/chimeraviz_1.8.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chimeraviz_1.8.5.tgz vignettes: vignettes/chimeraviz/inst/doc/chimeraviz-vignette.html vignetteTitles: chimeraviz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chimeraviz/inst/doc/chimeraviz-vignette.R Package: ChIPanalyser Version: 1.4.0 Depends: R (>= 3.5.1),GenomicRanges, Biostrings, BSgenome, RcppRoll, parallel Imports: methods, IRanges, S4Vectors,grDevices,graphics,stats,utils,rtracklayer,ROCR, BiocManager,GenomeInfoDb Suggests: BSgenome.Dmelanogaster.UCSC.dm3,knitr, RUnit, BiocGenerics License: GPL-3 MD5sum: 4f3fdeed3fb1ba02a78e56d70f1a9098 NeedsCompilation: no Title: ChIPanalyser: Predicting Transcription Factor Binding Sites Description: Based on a statistical thermodynamic framework, ChIPanalyser tries to produce ChIP-seq like profile. The model relies on four consideration: TF binding sites can be scored using a Position weight Matrix, DNA accessibility plays a role in Transcription Factor binding, binding profiles are dependant on the number of transcription factors bound to DNA and finally binding energy (another way of describing PWM's) or binding specificity should be modulated (hence the introduction of a binding specificity modulator). The end result of ChIPanalyser is to produce profiles simulating real ChIP-seq profile and provide accuracy measurements of these predicted profiles after being compared to real ChIP-seq data. The ultimate goal is to produce ChIP-seq like profiles predicting ChIP-seq like profile to circumvent the need to produce costly ChIP-seq experiments. biocViews: Software, BiologicalQuestion, WorkflowStep, Transcription, Sequencing, ChipOnChip, Coverage, Alignment, ChIPSeq, SequenceMatching, DataImport ,PeakDetection Author: Patrick C.N.Martin & Nicolae Radu Zabet Maintainer: Patrick C.N. Martin VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ChIPanalyser git_branch: RELEASE_3_8 git_last_commit: b5a2283 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPanalyser_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPanalyser_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPanalyser_1.4.0.tgz vignettes: vignettes/ChIPanalyser/inst/doc/ChIPanalyser.pdf vignetteTitles: ChIPanalyser User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPanalyser/inst/doc/ChIPanalyser.R Package: ChIPComp Version: 1.12.0 Depends: R (>= 3.2.0),GenomicRanges,IRanges,rtracklayer,GenomeInfoDb,S4Vectors Imports: Rsamtools,limma,BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm9,BiocGenerics Suggests: BiocStyle,RUnit License: GPL Archs: i386, x64 MD5sum: de5f56eb79ef4dab25dd22ac8aa20b0e NeedsCompilation: yes Title: Quantitative comparison of multiple ChIP-seq datasets Description: ChIPComp detects differentially bound sharp binding sites across multiple conditions considering matching control. biocViews: ChIPSeq, Sequencing, Transcription, Genetics,Coverage, MultipleComparison, DataImport Author: Hao Wu, Li Chen, Zhaohui S.Qin, Chi Wang Maintainer: Li Chen git_url: https://git.bioconductor.org/packages/ChIPComp git_branch: RELEASE_3_8 git_last_commit: 3bc42ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPComp_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPComp_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPComp_1.12.0.tgz vignettes: vignettes/ChIPComp/inst/doc/ChIPComp.pdf vignetteTitles: ChIPComp hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPComp/inst/doc/ChIPComp.R Package: chipenrich Version: 2.6.1 Depends: R (>= 3.4.0) Imports: AnnotationDbi, BiocGenerics, chipenrich.data, GenomeInfoDb, GenomicRanges, grDevices, grid, IRanges, lattice, latticeExtra, methods, mgcv, org.Dm.eg.db, org.Dr.eg.db, org.Hs.eg.db, org.Mm.eg.db, org.Rn.eg.db, parallel, plyr, rms, rtracklayer, S4Vectors, stats, stringr, utils Suggests: BiocStyle, devtools, knitr, rmarkdown, roxygen2, testthat License: GPL-3 MD5sum: ccc78d06d9b671a09d5ddac46d7917a9 NeedsCompilation: no Title: Gene Set Enrichment For ChIP-seq Peak Data Description: ChIP-Enrich performs gene set enrichment testing using peaks called from a ChIP-seq experiment. The method empirically corrects for confounding factors such as the length of genes, and the mappability of the sequence surrounding genes. biocViews: ImmunoOncology, ChIPSeq, Epigenetics, FunctionalGenomics, GeneSetEnrichment, HistoneModification, Regression Author: Ryan P. Welch [aut, cph], Chee Lee [aut], Raymond G. Cavalcante [aut, cre], Chris Lee [aut], Laura J. Scott [ths], Maureen A. Sartor [ths] Maintainer: Raymond G. Cavalcante VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/chipenrich git_branch: RELEASE_3_8 git_last_commit: 3b0d5f2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/chipenrich_2.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/chipenrich_2.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chipenrich_2.6.1.tgz vignettes: vignettes/chipenrich/inst/doc/chipenrich-vignette.html vignetteTitles: chipenrich_vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chipenrich/inst/doc/chipenrich-vignette.R Package: ChIPexoQual Version: 1.6.0 Depends: R (>= 3.4.0), GenomicAlignments (>= 1.0.1) Imports: methods, utils, GenomeInfoDb, stats, BiocParallel, GenomicRanges (>= 1.14.4), ggplot2 (>= 1.0), data.table (>= 1.9.6), Rsamtools (>= 1.16.1), IRanges (>= 1.6), S4Vectors (>= 0.8), biovizBase (>= 1.18), broom (>= 0.4), RColorBrewer (>= 1.1), dplyr (>= 0.5), scales (>= 0.4.0), viridis (>= 0.3), hexbin (>= 1.27), rmarkdown Suggests: ChIPexoQualExample (>= 0.99.1), knitr (>= 1.10), BiocStyle, gridExtra (>= 2.2), testthat License: GPL (>=2) MD5sum: 611bcc06f4a538ad75e2233cbf3c88ec NeedsCompilation: no Title: ChIPexoQual Description: Package with a quality control pipeline for ChIP-exo/nexus data. biocViews: ChIPSeq, Sequencing, Transcription, Visualization, QualityControl, Coverage, Alignment Author: Rene Welch, Dongjun Chung, Sunduz Keles Maintainer: Rene Welch URL: https:github.com/keleslab/ChIPexoQual VignetteBuilder: knitr BugReports: https://github.com/welch16/ChIPexoQual/issues git_url: https://git.bioconductor.org/packages/ChIPexoQual git_branch: RELEASE_3_8 git_last_commit: 74ec35d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPexoQual_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPexoQual_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPexoQual_1.6.0.tgz vignettes: vignettes/ChIPexoQual/inst/doc/vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPexoQual/inst/doc/vignette.R Package: ChIPpeakAnno Version: 3.16.1 Depends: R (>= 3.2), methods, grid, IRanges (>= 2.13.12), Biostrings (>= 2.47.6), GenomicRanges (>= 1.31.8), S4Vectors (>= 0.17.25), VennDiagram Imports: BiocGenerics (>= 0.1.0), GO.db, biomaRt, BSgenome, GenomicFeatures, GenomeInfoDb, matrixStats, AnnotationDbi, limma, multtest, RBGL, graph, BiocManager, stats, regioneR, DBI, ensembldb, Biobase, seqinr, idr, GenomicAlignments, DelayedArray, SummarizedExperiment, Rsamtools Suggests: reactome.db, BSgenome.Ecoli.NCBI.20080805, BSgenome.Hsapiens.UCSC.hg19, org.Ce.eg.db, org.Hs.eg.db, BSgenome.Celegans.UCSC.ce10, BSgenome.Drerio.UCSC.danRer7, EnsDb.Hsapiens.v75, EnsDb.Hsapiens.v79, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Hsapiens.UCSC.hg38.knownGene, gplots, BiocStyle, rtracklayer, knitr, rmarkdown, testthat, trackViewer, motifStack, OrganismDbi License: GPL (>= 2) MD5sum: 933dd6a74b8d94c65f86341763119ccb NeedsCompilation: no Title: Batch annotation of the peaks identified from either ChIP-seq, ChIP-chip experiments or any experiments resulted in large number of chromosome ranges Description: The package includes functions to retrieve the sequences around the peak, obtain enriched Gene Ontology (GO) terms, find the nearest gene, exon, miRNA or custom features such as most conserved elements and other transcription factor binding sites supplied by users. Starting 2.0.5, new functions have been added for finding the peaks with bi-directional promoters with summary statistics (peaksNearBDP), for summarizing the occurrence of motifs in peaks (summarizePatternInPeaks) and for adding other IDs to annotated peaks or enrichedGO (addGeneIDs). This package leverages the biomaRt, IRanges, Biostrings, BSgenome, GO.db, multtest and stat packages. biocViews: Annotation, ChIPSeq, ChIPchip Author: Lihua Julie Zhu, Jianhong Ou, Jun Yu, Hervé Pagès, Claude Gazin, Nathan Lawson, Ryan Thompson, Simon Lin, David Lapointe and Michael Green Maintainer: Lihua Julie Zhu , Jianhong Ou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ChIPpeakAnno git_branch: RELEASE_3_8 git_last_commit: 924626e git_last_commit_date: 2019-01-09 Date/Publication: 2019-01-10 source.ver: src/contrib/ChIPpeakAnno_3.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPpeakAnno_3.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPpeakAnno_3.16.1.tgz vignettes: vignettes/ChIPpeakAnno/inst/doc/ChIPpeakAnno.html, vignettes/ChIPpeakAnno/inst/doc/FAQs.html, vignettes/ChIPpeakAnno/inst/doc/pipeline.html, vignettes/ChIPpeakAnno/inst/doc/quickStart.html vignetteTitles: ChIPpeakAnno Vignette, ChIPpeakAnno FAQs, ChIPpeakAnno Annotation Pipeline, ChIPpeakAnno Quick Start hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPpeakAnno/inst/doc/ChIPpeakAnno.R, vignettes/ChIPpeakAnno/inst/doc/FAQs.R, vignettes/ChIPpeakAnno/inst/doc/pipeline.R, vignettes/ChIPpeakAnno/inst/doc/quickStart.R dependsOnMe: REDseq importsMe: ATACseqQC, DChIPRep, DEScan2, FunciSNP, GUIDEseq, REDseq suggestsMe: R3CPET, RIPSeeker, seqsetvis Package: ChIPQC Version: 1.18.2 Depends: R (>= 3.0.0), ggplot2, DiffBind, GenomicRanges (>= 1.17.19) Imports: BiocGenerics (>= 0.11.3), S4Vectors (>= 0.1.0), IRanges (>= 1.99.17), Rsamtools (>= 1.17.28), GenomicAlignments (>= 1.1.16), chipseq (>= 1.12.0), gtools, BiocParallel, methods, reshape2, Nozzle.R1, Biobase, grDevices, stats, utils, GenomicFeatures, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Hsapiens.UCSC.hg18.knownGene, TxDb.Mmusculus.UCSC.mm10.knownGene, TxDb.Mmusculus.UCSC.mm9.knownGene, TxDb.Rnorvegicus.UCSC.rn4.ensGene, TxDb.Celegans.UCSC.ce6.ensGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene Suggests: BiocStyle License: GPL (>= 3) MD5sum: 16de65710a6d40872b208d6bdad77a9f NeedsCompilation: no Title: Quality metrics for ChIPseq data Description: Quality metrics for ChIPseq data. biocViews: Sequencing, ChIPSeq, QualityControl, ReportWriting Author: Tom Carroll, Wei Liu, Ines de Santiago, Rory Stark Maintainer: Tom Carroll , Rory Stark git_url: https://git.bioconductor.org/packages/ChIPQC git_branch: RELEASE_3_8 git_last_commit: ea078ba git_last_commit_date: 2019-02-28 Date/Publication: 2019-03-01 source.ver: src/contrib/ChIPQC_1.18.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPQC_1.18.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPQC_1.18.2.tgz vignettes: vignettes/ChIPQC/inst/doc/ChIPQC.pdf, vignettes/ChIPQC/inst/doc/ChIPQCSampleReport.pdf vignetteTitles: Assessing ChIP-seq sample quality with ChIPQC, ChIPQCSampleReport.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPQC/inst/doc/ChIPQC.R Package: ChIPseeker Version: 1.18.0 Depends: R (>= 3.4.0) Imports: AnnotationDbi, BiocGenerics, boot, enrichplot, IRanges (>= 2.13.12), GenomeInfoDb, GenomicRanges (>= 1.31.8), GenomicFeatures (>= 1.31.3), ggplot2 (>= 2.2.0), gplots, graphics, grDevices, grid, gridBase, gtools, methods, plotrix, dplyr, parallel, magrittr, RColorBrewer, rtracklayer, S4Vectors (>= 0.17.25), stats, TxDb.Hsapiens.UCSC.hg19.knownGene, UpSetR, utils Suggests: clusterProfiler, ReactomePA, org.Hs.eg.db, knitr, BiocStyle, rmarkdown, testthat License: Artistic-2.0 MD5sum: ef4405a995f3e80a672528ddb20d0279 NeedsCompilation: no Title: ChIPseeker for ChIP peak Annotation, Comparison, and Visualization Description: This package implements functions to retrieve the nearest genes around the peak, annotate genomic region of the peak, statstical methods for estimate the significance of overlap among ChIP peak data sets, and incorporate GEO database for user to compare the own dataset with those deposited in database. The comparison can be used to infer cooperative regulation and thus can be used to generate hypotheses. Several visualization functions are implemented to summarize the coverage of the peak experiment, average profile and heatmap of peaks binding to TSS regions, genomic annotation, distance to TSS, and overlap of peaks or genes. biocViews: Annotation, ChIPSeq, Software, Visualization, MultipleComparison Author: Guangchuang Yu [aut, cre] (), Yun Yan [ctb], Hervé Pagès [ctb], Michael Kluge [ctb], Thomas Schwarzl [ctb] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/ChIPseeker VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/ChIPseeker/issues git_url: https://git.bioconductor.org/packages/ChIPseeker git_branch: RELEASE_3_8 git_last_commit: 6d54183 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPseeker_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPseeker_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPseeker_1.18.0.tgz vignettes: vignettes/ChIPseeker/inst/doc/ChIPseeker.html vignetteTitles: ChIPseeker: an R package for ChIP peak Annotation,, Comparison and Visualization hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPseeker/inst/doc/ChIPseeker.R importsMe: esATAC Package: chipseq Version: 1.32.0 Depends: R (>= 2.10), methods, BiocGenerics (>= 0.1.0), S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), GenomicRanges (>= 1.31.8), ShortRead Imports: methods, stats, lattice, BiocGenerics, IRanges, GenomicRanges, ShortRead Suggests: BSgenome, GenomicFeatures, TxDb.Mmusculus.UCSC.mm9.knownGene License: Artistic-2.0 Archs: i386, x64 MD5sum: 290f7ce079aa0d77772ce81d8499f3af NeedsCompilation: yes Title: chipseq: A package for analyzing chipseq data Description: Tools for helping process short read data for chipseq experiments biocViews: ChIPSeq, Sequencing, Coverage, QualityControl, DataImport Author: Deepayan Sarkar, Robert Gentleman, Michael Lawrence, Zizhen Yao Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/chipseq git_branch: RELEASE_3_8 git_last_commit: a7e65a9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/chipseq_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/chipseq_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chipseq_1.32.0.tgz vignettes: vignettes/chipseq/inst/doc/Workflow.pdf vignetteTitles: A Sample ChIP-Seq analysis workflow hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chipseq/inst/doc/Workflow.R dependsOnMe: PING importsMe: ChIPQC, CopywriteR, HTSeqGenie, soGGi, transcriptR suggestsMe: GenoGAM, ggbio Package: ChIPseqR Version: 1.36.0 Depends: R (>= 2.10.0), methods, BiocGenerics, S4Vectors (>= 0.9.25) Imports: Biostrings, fBasics, GenomicRanges, IRanges (>= 2.5.14), graphics, grDevices, HilbertVis, ShortRead, stats, timsac, utils License: GPL (>= 2) Archs: i386, x64 MD5sum: 546c295c55884109a0a1e834b58c41b2 NeedsCompilation: yes Title: Identifying Protein Binding Sites in High-Throughput Sequencing Data Description: ChIPseqR identifies protein binding sites from ChIP-seq and nucleosome positioning experiments. The model used to describe binding events was developed to locate nucleosomes but should flexible enough to handle other types of experiments as well. biocViews: ChIPSeq, Infrastructure Author: Peter Humburg Maintainer: Peter Humburg git_url: https://git.bioconductor.org/packages/ChIPseqR git_branch: RELEASE_3_8 git_last_commit: 10219bd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPseqR_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPseqR_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPseqR_1.36.0.tgz vignettes: vignettes/ChIPseqR/inst/doc/Introduction.pdf vignetteTitles: Introduction to ChIPseqR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPseqR/inst/doc/Introduction.R Package: ChIPSeqSpike Version: 1.2.1 Depends: R (>= 3.5), rtracklayer (>= 1.37.6) Imports: tools, stringr, Rsamtools, GenomicRanges, IRanges, seqplots, ggplot2, LSD, corrplot, methods, stats, grDevices, graphics, utils, BiocGenerics, S4Vectors Suggests: BiocStyle, knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: a37e46a63ee063dd972881beb78030b9 NeedsCompilation: no Title: ChIP-Seq data scaling according to spike-in control Description: Chromatin Immuno-Precipitation followed by Sequencing (ChIP-Seq) is used to determine the binding sites of any protein of interest, such as transcription factors or histones with or without a specific modification, at a genome scale. The many steps of the protocol can introduce biases that make ChIP-Seq more qualitative than quantitative. For instance, it was shown that global histone modification differences are not caught by traditional downstream data normalization techniques. A case study reported no differences in histone H3 lysine-27 trimethyl (H3K27me3) upon Ezh2 inhibitor treatment. To tackle this problem, external spike-in control were used to keep track of technical biases between conditions. Exogenous DNA from a different non-closely related species was inserted during the protocol to infer scaling factors that enabled an accurate normalization, thus revealing the inhibitor effect. ChIPSeqSpike offers tools for ChIP-Seq spike-in normalization. Ready to use scaled bigwig files and scaling factors values are obtained as output. ChIPSeqSpike also provides tools for ChIP-Seq spike-in assessment and analysis through a versatile collection of graphical functions. biocViews: ImmunoOncology, ChIPSeq, Sequencing, Normalization, Transcription, Coverage, DifferentialMethylation, Epigenetics, DataImport, HistoneModification Author: Nicolas Descostes Maintainer: Nicolas Descostes VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ChIPSeqSpike git_branch: RELEASE_3_8 git_last_commit: 9daf589 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ChIPSeqSpike_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPSeqSpike_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPSeqSpike_1.2.1.tgz vignettes: vignettes/ChIPSeqSpike/inst/doc/ChIPSeqSpike.pdf vignetteTitles: ChIPSeqSpike hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPSeqSpike/inst/doc/ChIPSeqSpike.R Package: ChIPsim Version: 1.36.0 Depends: Biostrings (>= 2.29.2) Imports: IRanges, XVector, Biostrings, ShortRead, graphics, methods, stats, utils Suggests: actuar, zoo License: GPL (>= 2) MD5sum: 807aa8e54aeac47c04e3b4173118482a NeedsCompilation: no Title: Simulation of ChIP-seq experiments Description: A general framework for the simulation of ChIP-seq data. Although currently focused on nucleosome positioning the package is designed to support different types of experiments. biocViews: Infrastructure, ChIPSeq Author: Peter Humburg Maintainer: Peter Humburg git_url: https://git.bioconductor.org/packages/ChIPsim git_branch: RELEASE_3_8 git_last_commit: a894f41 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPsim_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChIPsim_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPsim_1.36.0.tgz vignettes: vignettes/ChIPsim/inst/doc/ChIPsimIntro.pdf vignetteTitles: Simulating ChIP-seq experiments hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPsim/inst/doc/ChIPsimIntro.R Package: ChIPXpress Version: 1.26.0 Depends: R (>= 2.10), ChIPXpressData Imports: Biobase, GEOquery, frma, affy, bigmemory, biganalytics Suggests: mouse4302frmavecs, mouse4302.db, mouse4302cdf, RUnit, BiocGenerics License: GPL(>=2) MD5sum: 42bb787851b0c8b7875266dff5128c4e NeedsCompilation: no Title: ChIPXpress: enhanced transcription factor target gene identification from ChIP-seq and ChIP-chip data using publicly available gene expression profiles Description: ChIPXpress takes as input predicted TF bound genes from ChIPx data and uses a corresponding database of gene expression profiles downloaded from NCBI GEO to rank the TF bound targets in order of which gene is most likely to be functional TF target. biocViews: ChIPchip, ChIPSeq Author: George Wu Maintainer: George Wu git_url: https://git.bioconductor.org/packages/ChIPXpress git_branch: RELEASE_3_8 git_last_commit: 90b90c9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChIPXpress_1.26.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChIPXpress_1.26.0.tgz vignettes: vignettes/ChIPXpress/inst/doc/ChIPXpress.pdf vignetteTitles: ChIPXpress hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChIPXpress/inst/doc/ChIPXpress.R Package: chopsticks Version: 1.48.0 Imports: graphics, stats, utils, methods, survival Suggests: hexbin License: GPL-3 Archs: i386, x64 MD5sum: b808bcd49f1f23d35a2189e46df3a6de NeedsCompilation: yes Title: The 'snp.matrix' and 'X.snp.matrix' Classes Description: Implements classes and methods for large-scale SNP association studies biocViews: Microarray, SNPsAndGeneticVariability, SNP, GeneticVariability Author: Hin-Tak Leung Maintainer: Hin-Tak Leung URL: http://outmodedbonsai.sourceforge.net/ git_url: https://git.bioconductor.org/packages/chopsticks git_branch: RELEASE_3_8 git_last_commit: 3c44af4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/chopsticks_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/chopsticks_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chopsticks_1.48.0.tgz vignettes: vignettes/chopsticks/inst/doc/chopsticks-vignette.pdf vignetteTitles: snpMatrix hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chopsticks/inst/doc/chopsticks-vignette.R Package: chroGPS Version: 2.0.1 Depends: R (>= 3.2.0), GenomicRanges, IRanges, methods, Biobase, MASS, graphics, stats, changepoint Imports: cluster, DPpackage, ICSNP, ellipse, vegan Enhances: parallel, XML, rgl, gplots, pheatmap, ChIPpeakAnno, org.Dm.eg.db, caTools, plotly License: GPL (>=2.14) MD5sum: e2d2fbcc1addfcf53cac565380b86399 NeedsCompilation: no Title: chroGPS2: Generation, visualization and differential analysis of epigenome maps Description: We provide intuitive maps to visualize, analyze and compare the association between genetic elements based on their epigenetic profiles. The approach is based on Multi-Dimensional Scaling, and includes a parallelized implementation for handling high dimensional datasets. We provide several sensible distance metrics, and adjustment procedures to remove systematic biases typically observed when merging data obtained under different technologies or genetic backgrounds. We also provide functions and methods to perform differential analysis of epigenome maps at factor and gene level. biocViews: Epigenetics, Clustering, ChIPchip, ChIPSeq, HistoneModification, Visualization, DataRepresentation, ImmunoOncology Author: Oscar Reina, David Rossell Maintainer: Oscar Reina git_url: https://git.bioconductor.org/packages/chroGPS git_branch: RELEASE_3_8 git_last_commit: ac7ff10 git_last_commit_date: 2018-12-10 Date/Publication: 2018-12-10 source.ver: src/contrib/chroGPS_2.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/chroGPS_2.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chroGPS_2.0.1.tgz vignettes: vignettes/chroGPS/inst/doc/chroGPS.pdf vignetteTitles: Manual for the chroGPS library hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chroGPS/inst/doc/chroGPS.R Package: chromDraw Version: 2.12.0 Depends: R (>= 3.0.0) Imports: Rcpp (>= 0.11.1), GenomicRanges (>= 1.17.46) LinkingTo: Rcpp License: GPL-3 Archs: i386, x64 MD5sum: c54bc321ee938793b8fcbb474ef540f1 NeedsCompilation: yes Title: chromDraw is a R package for drawing the schemes of karyotypes in the linear and circular fashion. Description: ChromDraw is a R package for drawing the schemes of karyotype(s) in the linear and circular fashion. It is possible to visualized cytogenetic marsk on the chromosomes. This tool has own input data format. Input data can be imported from the GenomicRanges data structure. This package can visualized the data in the BED file format. Here is requirement on to the first nine fields of the BED format. Output files format are *.eps and *.svg. biocViews: Software Author: Jan Janecka, Ing., Mgr. CEITEC Masaryk University Maintainer: Jan Janecka URL: www.plantcytogenomics.org/chromDraw SystemRequirements: Rtools (>= 3.1) git_url: https://git.bioconductor.org/packages/chromDraw git_branch: RELEASE_3_8 git_last_commit: 090b98c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/chromDraw_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/chromDraw_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chromDraw_2.12.0.tgz vignettes: vignettes/chromDraw/inst/doc/chromDraw.pdf vignetteTitles: chromDraw hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chromDraw/inst/doc/chromDraw.R Package: ChromHeatMap Version: 1.36.0 Depends: R (>= 2.9.0), BiocGenerics (>= 0.3.2), annotate (>= 1.20.0), AnnotationDbi (>= 1.4.0) Imports: Biobase (>= 2.17.8), graphics, grDevices, methods, stats, IRanges, rtracklayer, GenomicRanges Suggests: ALL, hgu95av2.db License: Artistic-2.0 MD5sum: 8c849b949219b4a16234dc8850dd594e NeedsCompilation: no Title: Heat map plotting by genome coordinate Description: The ChromHeatMap package can be used to plot genome-wide data (e.g. expression, CGH, SNP) along each strand of a given chromosome as a heat map. The generated heat map can be used to interactively identify probes and genes of interest. biocViews: Visualization Author: Tim F. Rayner Maintainer: Tim F. Rayner git_url: https://git.bioconductor.org/packages/ChromHeatMap git_branch: RELEASE_3_8 git_last_commit: a78830f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ChromHeatMap_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ChromHeatMap_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ChromHeatMap_1.36.0.tgz vignettes: vignettes/ChromHeatMap/inst/doc/ChromHeatMap.pdf vignetteTitles: Plotting expression data with ChromHeatMap hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ChromHeatMap/inst/doc/ChromHeatMap.R Package: chromPlot Version: 1.10.0 Depends: stats, utils, graphics, grDevices, datasets, base, biomaRt, GenomicRanges, R (>= 3.1.0) Suggests: qtl, GenomicFeatures, TxDb.Hsapiens.UCSC.hg19.knownGene License: GPL (>= 2) MD5sum: fd2da81e6c20c564f5b23a49c65e6847 NeedsCompilation: no Title: Global visualization tool of genomic data Description: Package designed to visualize genomic data along the chromosomes, where the vertical chromosomes are sorted by number, with sex chromosomes at the end. biocViews: DataRepresentation, FunctionalGenomics, Genetics, Sequencing, Annotation, Visualization Author: Ricardo A. Verdugo and Karen Y. Orostica Maintainer: Karen Y. Orostica git_url: https://git.bioconductor.org/packages/chromPlot git_branch: RELEASE_3_8 git_last_commit: 5946cb1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/chromPlot_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/chromPlot_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chromPlot_1.10.0.tgz vignettes: vignettes/chromPlot/inst/doc/chromPlot.pdf vignetteTitles: General Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chromPlot/inst/doc/chromPlot.R Package: chromstaR Version: 1.8.1 Depends: R (>= 3.3), GenomicRanges, ggplot2, chromstaRData Imports: methods, utils, grDevices, graphics, stats, foreach, doParallel, S4Vectors, GenomeInfoDb, IRanges, reshape2, Rsamtools, GenomicAlignments, bamsignals, mvtnorm Suggests: knitr, BiocStyle, testthat, biomaRt License: Artistic-2.0 Archs: i386, x64 MD5sum: 55388dee59d7db8dd9042778d0ff9f79 NeedsCompilation: yes Title: Combinatorial and Differential Chromatin State Analysis for ChIP-Seq Data Description: This package implements functions for combinatorial and differential analysis of ChIP-seq data. It includes uni- and multivariate peak-calling, export to genome browser viewable files, and functions for enrichment analyses. biocViews: ImmunoOncology, Software, DifferentialPeakCalling, HiddenMarkovModel, ChIPSeq, HistoneModification, MultipleComparison, Sequencing, PeakDetection, ATACSeq Author: Aaron Taudt, Maria Colome Tatche, Matthias Heinig, Minh Anh Nguyen Maintainer: Aaron Taudt URL: https://github.com/ataudt/chromstaR VignetteBuilder: knitr BugReports: https://github.com/ataudt/chromstaR/issues git_url: https://git.bioconductor.org/packages/chromstaR git_branch: RELEASE_3_8 git_last_commit: 2d75cac git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/chromstaR_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/chromstaR_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chromstaR_1.8.1.tgz vignettes: vignettes/chromstaR/inst/doc/chromstaR.pdf vignetteTitles: The chromstaR user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/chromstaR/inst/doc/chromstaR.R Package: chromswitch Version: 1.4.1 Depends: R (>= 3.4), GenomicRanges (>= 1.26.4) Imports: cluster (>= 2.0.6), Biobase (>= 2.36.2), BiocParallel (>= 1.8.2), dplyr (>= 0.5.0), gplots(>= 3.0.1), graphics, grDevices, IRanges (>= 2.4.8), lazyeval (>= 0.2.0), matrixStats (>= 0.52), magrittr (>= 1.5), methods, NMF (>= 0.20.6), rtracklayer (>= 1.36.4), S4Vectors (>= 0.14.4), stats, tidyr (>= 0.6.3) Suggests: BiocStyle, DescTools (>= 0.99.19), devtools (>= 1.13.3), GenomeInfoDb (>= 1.16.0), knitr, rmarkdown, mclust (>= 5.3), testthat License: MIT + file LICENSE MD5sum: 36c5d3dc74c17ed9d82bc8f1bc7b46df NeedsCompilation: no Title: An R package to detect chromatin state switches from epigenomic data Description: Chromswitch implements a flexible method to detect chromatin state switches between samples in two biological conditions in a specific genomic region of interest given peaks or chromatin state calls from ChIP-seq data. biocViews: ImmunoOncology, MultipleComparison, Transcription, GeneExpression, DifferentialPeakCalling, HistoneModification, Epigenetics, FunctionalGenomics, Clustering Author: Selin Jessa [aut, cre], Claudia L. Kleinman [aut] Maintainer: Selin Jessa URL: https://github.com/sjessa/chromswitch VignetteBuilder: knitr BugReports: https://github.com/sjessa/chromswitch/issues git_url: https://git.bioconductor.org/packages/chromswitch git_branch: RELEASE_3_8 git_last_commit: 0f4b655 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/chromswitch_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/chromswitch_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chromswitch_1.4.1.tgz vignettes: vignettes/chromswitch/inst/doc/chromswitch_intro.html vignetteTitles: An introduction to `chromswitch` for detecting chromatin state switches hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/chromswitch/inst/doc/chromswitch_intro.R Package: chromVAR Version: 1.4.1 Depends: R (>= 3.4) Imports: IRanges, GenomeInfoDb, GenomicRanges, ggplot2, nabor, BiocParallel, BiocGenerics, Biostrings, TFBSTools, Rsamtools, S4Vectors, methods, Rcpp, grid, plotly, shiny, miniUI, stats, utils, graphics, DT, Rtsne, Matrix, SummarizedExperiment, RColorBrewer, BSgenome LinkingTo: Rcpp, RcppArmadillo Suggests: JASPAR2016, BSgenome.Hsapiens.UCSC.hg19, readr, testthat, knitr, rmarkdown, pheatmap, motifmatchr License: MIT + file LICENSE Archs: i386, x64 MD5sum: 7dcbe9c69e7956109f77d47d3a69edea NeedsCompilation: yes Title: Chromatin Variation Across Regions Description: Determine variation in chromatin accessibility across sets of annotations or peaks. Designed primarily for single-cell or sparse chromatin accessibility data, e.g. from scATAC-seq or sparse bulk ATAC or DNAse-seq experiments. biocViews: ImmunoOncology, SingleCell, Sequencing, GeneRegulation Author: Alicia Schep [aut, cre], Jason Buenrostro [ctb], Caleb Lareau [ctb], William Greenleaf [ths], Stanford University [cph] Maintainer: Alicia Schep SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/chromVAR git_branch: RELEASE_3_8 git_last_commit: e185549 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/chromVAR_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/chromVAR_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/chromVAR_1.4.1.tgz vignettes: vignettes/chromVAR/inst/doc/Introduction.html vignetteTitles: Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/chromVAR/inst/doc/Introduction.R Package: CHRONOS Version: 1.10.1 Depends: R (>= 3.5) Imports: XML, RCurl, RBGL, parallel, foreach, doParallel, openxlsx, igraph, circlize, graph, stats, utils, grDevices, graphics, methods, biomaRt Suggests: RUnit, BiocGenerics, knitr License: GPL-2 MD5sum: ee6e35b4baf3c1f3b898dd5b414afb39 NeedsCompilation: no Title: CHRONOS: A time-varying method for microRNA-mediated sub-pathway enrichment analysis Description: A package used for efficient unraveling of the inherent dynamic properties of pathways. MicroRNA-mediated subpathway topologies are extracted and evaluated by exploiting the temporal transition and the fold change activity of the linked genes/microRNAs. biocViews: SystemsBiology, GraphAndNetwork, Pathways, KEGG Author: Aristidis G. Vrahatis, Konstantina Dimitrakopoulou, Panos Balomenos Maintainer: Panos Balomenos SystemRequirements: Java version >= 1.7, Pandoc VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CHRONOS git_branch: RELEASE_3_8 git_last_commit: 84084b5 git_last_commit_date: 2019-03-28 Date/Publication: 2019-03-29 source.ver: src/contrib/CHRONOS_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CHRONOS_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CHRONOS_1.10.1.tgz vignettes: vignettes/CHRONOS/inst/doc/CHRONOS.pdf vignetteTitles: CHRONOS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CHRONOS/inst/doc/CHRONOS.R Package: cicero Version: 1.0.15 Depends: R (>= 3.5.0), monocle, Gviz (>= 1.22.3) Imports: assertthat (>= 0.2.0), Biobase (>= 2.37.2), BiocGenerics (>= 0.23.0), data.table (>= 1.10.4), dplyr (>= 0.7.4), FNN (>= 1.1), GenomicRanges (>= 1.30.3), ggplot2 (>= 2.2.1), glasso (>= 1.8), grDevices, igraph (>= 1.1.0), IRanges (>= 2.10.5), Matrix (>= 1.2-12), methods, parallel, plyr (>= 1.8.4), reshape2 (>= 1.4.3), S4Vectors (>= 0.14.7), stats, stringr (>= 1.2.0), tibble (>= 1.4.2), VGAM (>= 1.0-5), utils Suggests: AnnotationDbi (>= 1.38.2), knitr, rmarkdown, rtracklayer (>= 1.36.6), testthat, vdiffr (>= 0.2.3), covr License: MIT + file LICENSE MD5sum: c39a5a62a35b38033889c12fcabc058d NeedsCompilation: no Title: Precict cis-co-accessibility from single-cell chromatin accessibility data Description: Cicero computes putative cis-regulatory maps from single-cell chromatin accessibility data. It also extends monocle 2 for use in chromatin accessibility data. biocViews: Sequencing, Clustering, CellBasedAssays, ImmunoOncology GeneRegulation, GeneTarget, Epigenetics, ATACSeq, SingleCell Author: Hannah Pliner [aut, cre], Cole Trapnell [aut] Maintainer: Hannah Pliner VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cicero git_branch: RELEASE_3_8 git_last_commit: 99b142a git_last_commit_date: 2019-02-19 Date/Publication: 2019-02-20 source.ver: src/contrib/cicero_1.0.15.tar.gz win.binary.ver: bin/windows/contrib/3.5/cicero_1.0.15.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cicero_1.0.15.tgz vignettes: vignettes/cicero/inst/doc/website.html vignetteTitles: Vignette from Cicero Website hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/cicero/inst/doc/website.R Package: CINdex Version: 1.10.0 Depends: R (>= 3.3), GenomicRanges Imports: bitops,gplots,grDevices,som, dplyr,gridExtra,png,stringr,S4Vectors, IRanges, GenomeInfoDb,graphics, stats, utils Suggests: knitr, testthat, ReactomePA, RUnit, BiocGenerics, AnnotationHub, rtracklayer, pd.genomewidesnp.6, org.Hs.eg.db, biovizBase, TxDb.Hsapiens.UCSC.hg18.knownGene, methods, Biostrings,Homo.sapiens License: GPL (>= 2) MD5sum: 429ec61774d457ec691f01d418bb6ff1 NeedsCompilation: no Title: Chromosome Instability Index Description: The CINdex package addresses important area of high-throughput genomic analysis. It allows the automated processing and analysis of the experimental DNA copy number data generated by Affymetrix SNP 6.0 arrays or similar high throughput technologies. It calculates the chromosome instability (CIN) index that allows to quantitatively characterize genome-wide DNA copy number alterations as a measure of chromosomal instability. This package calculates not only overall genomic instability, but also instability in terms of copy number gains and losses separately at the chromosome and cytoband level. biocViews: Software, CopyNumberVariation, GenomicVariation, aCGH, Microarray, Genetics, Sequencing Author: Lei Song, Krithika Bhuvaneshwar, Yue Wang, Yuanjian Feng, Ie-Ming Shih, Subha Madhavan, Yuriy Gusev Maintainer: Yuriy Gusev VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CINdex git_branch: RELEASE_3_8 git_last_commit: 0e2509c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CINdex_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CINdex_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CINdex_1.10.0.tgz vignettes: vignettes/CINdex/inst/doc/CINdex.pdf, vignettes/CINdex/inst/doc/PrepareInputData.pdf vignetteTitles: CINdex Tutorial, Prepare input data for CINdex hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CINdex/inst/doc/CINdex.R, vignettes/CINdex/inst/doc/PrepareInputData.R Package: cisPath Version: 1.22.0 Depends: R (>= 2.10.0) Imports: methods, utils License: GPL (>= 3) Archs: i386, x64 MD5sum: f599dcd8049193817764ff0114785078 NeedsCompilation: yes Title: Visualization and management of the protein-protein interaction networks. Description: cisPath is an R package that uses web browsers to visualize and manage protein-protein interaction networks. biocViews: Proteomics Author: Likun Wang Maintainer: Likun Wang git_url: https://git.bioconductor.org/packages/cisPath git_branch: RELEASE_3_8 git_last_commit: b138f04 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cisPath_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cisPath_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cisPath_1.22.0.tgz vignettes: vignettes/cisPath/inst/doc/cisPath.pdf vignetteTitles: cisPath hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cisPath/inst/doc/cisPath.R Package: ClassifyR Version: 2.2.6 Depends: R (>= 3.5.0), methods, S4Vectors (>= 0.18.0), MultiAssayExperiment (>= 1.6.0), BiocParallel Imports: locfit, grid, utils, plyr Suggests: limma, genefilter, edgeR, car, Rmixmod, ggplot2 (>= 3.0.0), gridExtra (>= 2.0.0), cowplot, BiocStyle, pamr, PoiClaClu, parathyroidSE, knitr, htmltools, gtable, scales, e1071, rmarkdown, IRanges, randomForest, robustbase, glmnet, class License: GPL-3 MD5sum: 5e17ba0d5c16354d00145a3dc9adbb79 NeedsCompilation: no Title: A framework for cross-validated classification problems, with applications to differential variability and differential distribution testing Description: The software formalises a framework for classification in R. There are four stages; Data transformation, feature selection, classifier training, and prediction. The requirements of variable types and names are fixed, but specialised variables for functions can also be provided. The classification framework is wrapped in a driver loop, that reproducibly carries out a number of cross-validation schemes. Functions for differential expression, differential variability, and differential distribution are included. Additional functions may be developed by the user, by creating an interface to the framework. biocViews: Classification, Survival Author: Dario Strbenac, John Ormerod, Graham Mann, Jean Yang Maintainer: Dario Strbenac VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ClassifyR git_branch: RELEASE_3_8 git_last_commit: f4f1b0a git_last_commit_date: 2019-02-14 Date/Publication: 2019-02-15 source.ver: src/contrib/ClassifyR_2.2.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/ClassifyR_2.2.6.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ClassifyR_2.2.6.tgz vignettes: vignettes/ClassifyR/inst/doc/ClassifyR.html, vignettes/ClassifyR/inst/doc/wrapper.html vignetteTitles: An Introduction to the ClassifyR Package, Example: Creating a Wrapper Function for the k-NN Classifier hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ClassifyR/inst/doc/ClassifyR.R, vignettes/ClassifyR/inst/doc/wrapper.R Package: cleanUpdTSeq Version: 1.20.1 Depends: R (>= 2.15), BiocGenerics (>= 0.1.0), methods, BSgenome, BSgenome.Drerio.UCSC.danRer7, GenomicRanges, seqinr, e1071 Suggests: BiocStyle, knitr, RUnit License: GPL-2 MD5sum: a58a193e02534e58852db4ce98ce602b NeedsCompilation: no Title: This package classifies putative polyadenylation sites as true or false/internally oligodT primed Description: This package uses the Naive Bayes classifier (from e1071) to assign probability values to putative polyadenylation sites (pA sites) based on training data from zebrafish. This will allow the user to separate true, biologically relevant pA sites from false, oligodT primed pA sites. biocViews: Sequencing, SequenceMatching, Genetics, GeneRegulation Author: Sarah Sheppard, Jianhong Ou, Nathan Lawson, Lihua Julie Zhu Maintainer: Jianhong Ou ; Lihua Julie Zhu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cleanUpdTSeq git_branch: RELEASE_3_8 git_last_commit: aa0569e git_last_commit_date: 2019-04-09 Date/Publication: 2019-04-09 source.ver: src/contrib/cleanUpdTSeq_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cleanUpdTSeq_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cleanUpdTSeq_1.20.1.tgz vignettes: vignettes/cleanUpdTSeq/inst/doc/cleanUpdTSeq.html vignetteTitles: cleanUpdTSeq Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cleanUpdTSeq/inst/doc/cleanUpdTSeq.R importsMe: InPAS Package: cleaver Version: 1.20.0 Depends: R (>= 3.0.0), methods, Biostrings (>= 1.29.8) Imports: S4Vectors, IRanges Suggests: testthat (>= 0.8), knitr, BiocStyle (>= 0.0.14), BRAIN, UniProt.ws (>= 2.1.4) License: GPL (>= 3) MD5sum: 3ac18493a9e15c2f5e9679b96d9d3da7 NeedsCompilation: no Title: Cleavage of Polypeptide Sequences Description: In-silico cleavage of polypeptide sequences. The cleavage rules are taken from: http://web.expasy.org/peptide_cutter/peptidecutter_enzymes.html biocViews: Proteomics Author: Sebastian Gibb [aut, cre] Maintainer: Sebastian Gibb URL: https://github.com/sgibb/cleaver/ VignetteBuilder: knitr BugReports: https://github.com/sgibb/cleaver/issues/ git_url: https://git.bioconductor.org/packages/cleaver git_branch: RELEASE_3_8 git_last_commit: e9242ec git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cleaver_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cleaver_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cleaver_1.20.0.tgz vignettes: vignettes/cleaver/inst/doc/cleaver.pdf vignetteTitles: in-silico cleavage of polypeptides hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cleaver/inst/doc/cleaver.R importsMe: Pbase, synapter Package: clippda Version: 1.32.0 Depends: R (>= 2.13.1),limma, statmod, rgl, lattice, scatterplot3d, graphics, grDevices, stats, utils, Biobase, tools, methods License: GPL (>=2) MD5sum: 0d4835a20f6d5153606e6338f6933a85 NeedsCompilation: no Title: A package for the clinical proteomic profiling data analysis Description: Methods for the nalysis of data from clinical proteomic profiling studies. The focus is on the studies of human subjects, which are often observational case-control by design and have technical replicates. A method for sample size determination for planning these studies is proposed. It incorporates routines for adjusting for the expected heterogeneities and imbalances in the data and the within-sample replicate correlations. biocViews: Proteomics, OneChannel, Preprocessing, DifferentialExpression, MultipleComparison Author: Stephen Nyangoma Maintainer: Stephen Nyangoma URL: http://www.cancerstudies.bham.ac.uk/crctu/CLIPPDA.shtml git_url: https://git.bioconductor.org/packages/clippda git_branch: RELEASE_3_8 git_last_commit: dbb0b23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clippda_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clippda_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clippda_1.32.0.tgz vignettes: vignettes/clippda/inst/doc/clippda.pdf vignetteTitles: Sample Size Calculation hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clippda/inst/doc/clippda.R Package: clipper Version: 1.22.0 Depends: R (>= 2.15.0), Matrix, graph Imports: methods, Biobase, Rcpp, igraph, gRbase (>= 1.6.6), qpgraph, KEGGgraph, corpcor, RBGL Suggests: RUnit, BiocGenerics, graphite, ALL, hgu95av2.db, MASS, BiocStyle Enhances: RCy3 License: AGPL-3 MD5sum: eb3ea7c60842da6cb778e932d303688f NeedsCompilation: no Title: Gene Set Analysis Exploiting Pathway Topology Description: Implements topological gene set analysis using a two-step empirical approach. It exploits graph decomposition theory to create a junction tree and reconstruct the most relevant signal path. In the first step clipper selects significant pathways according to statistical tests on the means and the concentration matrices of the graphs derived from pathway topologies. Then, it "clips" the whole pathway identifying the signal paths having the greatest association with a specific phenotype. Author: Paolo Martini , Gabriele Sales , Chiara Romualdi Maintainer: Paolo Martini git_url: https://git.bioconductor.org/packages/clipper git_branch: RELEASE_3_8 git_last_commit: e798b1c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clipper_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clipper_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clipper_1.22.0.tgz vignettes: vignettes/clipper/inst/doc/clipper.pdf vignetteTitles: clipper hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clipper/inst/doc/clipper.R suggestsMe: graphite Package: Clomial Version: 1.18.1 Depends: R (>= 2.10), matrixStats Imports: methods, permute License: GPL (>= 2) MD5sum: 6b28f8d222ff2b4d8101cf3f2bd0c670 NeedsCompilation: no Title: Infers clonal composition of a tumor Description: Clomial fits binomial distributions to counts obtained from Next Gen Sequencing data of multiple samples of the same tumor. The trained parameters can be interpreted to infer the clonal structure of the tumor. biocViews: ImmunoOncology, Genetics, GeneticVariability, Sequencing, Clustering, MultipleComparison, Bayesian, DNASeq, ExomeSeq, TargetedResequencing Author: Habil Zare and Alex Hu Maintainer: Habil Zare git_url: https://git.bioconductor.org/packages/Clomial git_branch: RELEASE_3_8 git_last_commit: b45ab1e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Clomial_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Clomial_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Clomial_1.18.1.tgz vignettes: vignettes/Clomial/inst/doc/Clonal_decomposition_by_Clomial.pdf vignetteTitles: A likelihood maximization approach to infer the clonal structure of a cancer using multiple tumor samples hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Clomial/inst/doc/Clonal_decomposition_by_Clomial.R Package: Clonality Version: 1.30.0 Depends: R (>= 2.12.2), DNAcopy Imports: grDevices, graphics, stats, utils Suggests: gdata License: GPL-3 MD5sum: aa1dccf7e9baf578b9be782ec99278e2 NeedsCompilation: no Title: Clonality testing Description: Statistical tests for clonality versus independence of tumors from the same patient based on their LOH or genomewide copy number profiles biocViews: Microarray, CopyNumberVariation, Classification, aCGH Author: Irina Ostrovnaya Maintainer: Irina Ostrovnaya git_url: https://git.bioconductor.org/packages/Clonality git_branch: RELEASE_3_8 git_last_commit: 7ae80f0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Clonality_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Clonality_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Clonality_1.30.0.tgz vignettes: vignettes/Clonality/inst/doc/Clonality.pdf vignetteTitles: Clonality hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Clonality/inst/doc/Clonality.R Package: clonotypeR Version: 1.20.0 Imports: methods Suggests: BiocGenerics, edgeR, knitr, pvclust, RUnit, vegan License: file LICENSE MD5sum: ce60c01fcc6b07e75ad0047f74e308ec NeedsCompilation: no Title: High throughput analysis of T cell antigen receptor sequences Description: High throughput analysis of T cell antigen receptor sequences The genes encoding T cell receptors are created by somatic recombination, generating an immense combination of V, (D) and J segments. Additional processes during the recombination create extra sequence diversity between the V an J segments. Collectively, this hyper-variable region is called the CDR3 loop. The purpose of this package is to process and quantitatively analyse millions of V-CDR3-J combination, called clonotypes, from multiple sequence libraries. biocViews: Sequencing Author: Charles Plessy Maintainer: Charles Plessy URL: http://clonotyper.branchable.com/ VignetteBuilder: knitr BugReports: http://clonotyper.branchable.com/Bugs/ git_url: https://git.bioconductor.org/packages/clonotypeR git_branch: RELEASE_3_8 git_last_commit: cbe6d72 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clonotypeR_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clonotypeR_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clonotypeR_1.20.0.tgz vignettes: vignettes/clonotypeR/inst/doc/clonotypeR.html vignetteTitles: clonotypeR User's Guide hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/clonotypeR/inst/doc/clonotypeR.R Package: clst Version: 1.30.0 Depends: R (>= 2.10) Imports: ROC, lattice Suggests: RUnit License: GPL-3 MD5sum: 03379c8704e8e7843e96d8feb82ac307 NeedsCompilation: no Title: Classification by local similarity threshold Description: Package for modified nearest-neighbor classification based on calculation of a similarity threshold distinguishing within-group from between-group comparisons. biocViews: Classification Author: Noah Hoffman Maintainer: Noah Hoffman git_url: https://git.bioconductor.org/packages/clst git_branch: RELEASE_3_8 git_last_commit: f80d648 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clst_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clst_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clst_1.30.0.tgz vignettes: vignettes/clst/inst/doc/clstDemo.pdf vignetteTitles: clst hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clst/inst/doc/clstDemo.R dependsOnMe: clstutils Package: clstutils Version: 1.30.0 Depends: R (>= 2.10), clst, rjson, ape Imports: lattice, RSQLite Suggests: RUnit, RSVGTipsDevice License: GPL-3 MD5sum: e63fa92d5f3812877f3c9904b7530fe7 NeedsCompilation: no Title: Tools for performing taxonomic assignment. Description: Tools for performing taxonomic assignment based on phylogeny using pplacer and clst. biocViews: Sequencing, Classification, Visualization, QualityControl Author: Noah Hoffman Maintainer: Noah Hoffman git_url: https://git.bioconductor.org/packages/clstutils git_branch: RELEASE_3_8 git_last_commit: 84f9bcf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clstutils_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clstutils_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clstutils_1.30.0.tgz vignettes: vignettes/clstutils/inst/doc/pplacerDemo.pdf, vignettes/clstutils/inst/doc/refSet.pdf vignetteTitles: clst, clstutils hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clstutils/inst/doc/pplacerDemo.R, vignettes/clstutils/inst/doc/refSet.R Package: clustComp Version: 1.10.0 Depends: R (>= 3.3) Imports: sm, stats, graphics, grDevices Suggests: Biobase, colonCA, RUnit, BiocGenerics License: GPL (>= 2) MD5sum: e6750fcee97be0e5706cb50e8d87f610 NeedsCompilation: no Title: Clustering Comparison Package Description: clustComp is a package that implements several techniques for the comparison and visualisation of relationships between different clustering results, either flat versus flat or hierarchical versus flat. These relationships among clusters are displayed using a weighted bi-graph, in which the nodes represent the clusters and the edges connect pairs of nodes with non-empty intersection; the weight of each edge is the number of elements in that intersection and is displayed through the edge thickness. The best layout of the bi-graph is provided by the barycentre algorithm, which minimises the weighted number of crossings. In the case of comparing a hierarchical and a non-hierarchical clustering, the dendrogram is pruned at different heights, selected by exploring the tree by depth-first search, starting at the root. Branches are decided to be split according to the value of a scoring function, that can be based either on the aesthetics of the bi-graph or on the mutual information between the hierarchical and the flat clusterings. A mapping between groups of clusters from each side is constructed with a greedy algorithm, and can be additionally visualised. biocViews: GeneExpression, Clustering, Visualization Author: Aurora Torrente and Alvis Brazma. Maintainer: Aurora Torrente git_url: https://git.bioconductor.org/packages/clustComp git_branch: RELEASE_3_8 git_last_commit: 71b3b58 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clustComp_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clustComp_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clustComp_1.10.0.tgz vignettes: vignettes/clustComp/inst/doc/clustComp.pdf vignetteTitles: The clustComp Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clustComp/inst/doc/clustComp.R Package: clusterExperiment Version: 2.2.0 Depends: R (>= 3.5.0), SingleCellExperiment, SummarizedExperiment, BiocGenerics Imports: methods, NMF, RColorBrewer, ape (>= 5.0), phylobase, cluster, stats, limma, dendextend, howmany, locfdr, matrixStats, graphics, parallel, RSpectra, kernlab, stringr, S4Vectors, grDevices, Rcpp, HDF5Array (>= 1.7.10), DelayedArray (>= 0.5.31), edgeR, scales, zinbwave LinkingTo: Rcpp Suggests: BiocStyle, knitr, testthat, scRNAseq, MAST, Rtsne, scran, igraph License: Artistic-2.0 Archs: i386, x64 MD5sum: d8125f0b838d2d47f45701e1ee5fc54a NeedsCompilation: yes Title: Compare Clusterings for Single-Cell Sequencing Description: Provides functionality for running and comparing many different clusterings of single-cell sequencing data or other large mRNA Expression data sets. biocViews: Clustering, RNASeq, Sequencing, Software, SingleCell Author: Elizabeth Purdom [aut, cre, cph], Davide Risso [aut], Marla Johnson [ctb] Maintainer: Elizabeth Purdom VignetteBuilder: knitr BugReports: https://github.com/epurdom/clusterExperiment/issues git_url: https://git.bioconductor.org/packages/clusterExperiment git_branch: RELEASE_3_8 git_last_commit: 05e03ba git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clusterExperiment_2.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clusterExperiment_2.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clusterExperiment_2.2.0.tgz vignettes: vignettes/clusterExperiment/inst/doc/clusterExperimentTutorial.html vignetteTitles: clusterExperiment Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clusterExperiment/inst/doc/clusterExperimentTutorial.R dependsOnMe: netSmooth importsMe: slingshot Package: ClusterJudge Version: 1.4.0 Depends: R (>= 3.4), stats, utils, graphics, infotheo, lattice, latticeExtra, httr, jsonlite Suggests: yeastExpData, knitr, rmarkdown, devtools, testthat, biomaRt License: Artistic-2.0 MD5sum: 87cb47cba4bc6d197a97d2e50b814e0c NeedsCompilation: no Title: Judging Quality of Clustering Methods using Mutual Information Description: ClusterJudge implements the functions, examples and other software published as an algorithm by Gibbons, FD and Roth FP. The article is called "Judging the Quality of Gene Expression-Based Clustering Methods Using Gene Annotation" and it appeared in Genome Research, vol. 12, pp1574-1581 (2002). See package?ClusterJudge for an overview. biocViews: Software, StatisticalMethod, Clustering, GeneExpression, GO Author: Adrian Pasculescu Maintainer: Adrian Pasculescu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ClusterJudge git_branch: RELEASE_3_8 git_last_commit: a30d0af git_last_commit_date: 2018-11-06 Date/Publication: 2018-11-06 source.ver: src/contrib/ClusterJudge_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ClusterJudge_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ClusterJudge_1.4.0.tgz vignettes: vignettes/ClusterJudge/inst/doc/ClusterJudge-intro.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ClusterJudge/inst/doc/ClusterJudge-intro.R Package: clusterProfiler Version: 3.10.1 Depends: R (>= 3.4.0) Imports: AnnotationDbi, DOSE (>= 3.5.1), enrichplot (>= 0.99.7), ggplot2, GO.db, GOSemSim, magrittr, methods, plyr, qvalue, rvcheck, stats, tidyr, utils Suggests: AnnotationHub, GSEABase, KEGG.db, knitr, org.Hs.eg.db, prettydoc, pathview, ReactomePA, testthat License: Artistic-2.0 MD5sum: 4b67eff75b931da94b8862db7f9e8776 NeedsCompilation: no Title: statistical analysis and visualization of functional profiles for genes and gene clusters Description: This package implements methods to analyze and visualize functional profiles (GO and KEGG) of gene and gene clusters. biocViews: Annotation, Clustering, GeneSetEnrichment, GO, KEGG, MultipleComparison, Pathways, Reactome, Visualization Author: Guangchuang Yu [aut, cre, cph] (), Li-Gen Wang [ctb], Giovanni Dall'Olio [ctb] (formula interface of compareCluster) Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/clusterProfiler VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/clusterProfiler/issues git_url: https://git.bioconductor.org/packages/clusterProfiler git_branch: RELEASE_3_8 git_last_commit: 39927ef git_last_commit_date: 2018-12-20 Date/Publication: 2018-12-20 source.ver: src/contrib/clusterProfiler_3.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/clusterProfiler_3.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clusterProfiler_3.10.1.tgz vignettes: vignettes/clusterProfiler/inst/doc/clusterProfiler.html vignetteTitles: Statistical analysis and visualization of functional profiles for genes and gene clusters hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clusterProfiler/inst/doc/clusterProfiler.R importsMe: bioCancer, CEMiTool, DAPAR, debrowser, eegc, esATAC, GDCRNATools, LINC, MAGeCKFlute, methylGSA, miRsponge, MoonlightR, RNASeqR, TCGAbiolinksGUI suggestsMe: ChIPseeker, DOSE, enrichplot, GOSemSim, ReactomePA, TCGAbiolinks Package: clusterSeq Version: 1.6.0 Depends: R (>= 3.0.0), methods, BiocParallel, baySeq, graphics, stats, utils Imports: BiocGenerics Suggests: BiocStyle License: GPL-3 MD5sum: de87aa6662095dfe988eff1c8c2c6bce NeedsCompilation: no Title: Clustering of high-throughput sequencing data by identifying co-expression patterns Description: Identification of clusters of co-expressed genes based on their expression across multiple (replicated) biological samples. biocViews: Sequencing, DifferentialExpression, MultipleComparison, Clustering, GeneExpression Author: Thomas J. Hardcastle & Irene Papatheodorou Maintainer: Thomas J. Hardcastle git_url: https://git.bioconductor.org/packages/clusterSeq git_branch: RELEASE_3_8 git_last_commit: bc978ee git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clusterSeq_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clusterSeq_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clusterSeq_1.6.0.tgz vignettes: vignettes/clusterSeq/inst/doc/clusterSeq.pdf vignetteTitles: Advanced baySeq analyses hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clusterSeq/inst/doc/clusterSeq.R Package: ClusterSignificance Version: 1.10.0 Depends: R (>= 3.3.0) Imports: methods, pracma, princurve (>= 2.0.5), scatterplot3d, RColorBrewer, grDevices, graphics, utils, stats Suggests: knitr, rmarkdown, testthat, BiocStyle, ggplot2, plsgenomics, covr License: GPL-3 MD5sum: e9d0e4317b1a056b26796c4158d5b63f NeedsCompilation: no Title: The ClusterSignificance package provides tools to assess if class clusters in dimensionality reduced data representations have a separation different from permuted data Description: The ClusterSignificance package provides tools to assess if class clusters in dimensionality reduced data representations have a separation different from permuted data. The term class clusters here refers to, clusters of points representing known classes in the data. This is particularly useful to determine if a subset of the variables, e.g. genes in a specific pathway, alone can separate samples into these established classes. ClusterSignificance accomplishes this by, projecting all points onto a one dimensional line. Cluster separations are then scored and the probability of the seen separation being due to chance is evaluated using a permutation method. biocViews: Clustering, Classification, PrincipalComponent, StatisticalMethod Author: Jason T. Serviss [aut, cre], Jesper R. Gadin [aut] Maintainer: Jason T Serviss URL: https://github.com/jasonserviss/ClusterSignificance/ VignetteBuilder: knitr BugReports: https://github.com/jasonserviss/ClusterSignificance/issues git_url: https://git.bioconductor.org/packages/ClusterSignificance git_branch: RELEASE_3_8 git_last_commit: 9f726b4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ClusterSignificance_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ClusterSignificance_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ClusterSignificance_1.10.0.tgz vignettes: vignettes/ClusterSignificance/inst/doc/ClusterSignificance-vignette.html vignetteTitles: ClusterSignificance Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ClusterSignificance/inst/doc/ClusterSignificance-vignette.R Package: clusterStab Version: 1.54.0 Depends: Biobase (>= 1.4.22), R (>= 1.9.0), methods Suggests: fibroEset, genefilter License: Artistic-2.0 MD5sum: 13e2412428edb769e74ebf828778f9e0 NeedsCompilation: no Title: Compute cluster stability scores for microarray data Description: This package can be used to estimate the number of clusters in a set of microarray data, as well as test the stability of these clusters. biocViews: Clustering Author: James W. MacDonald, Debashis Ghosh, Mark Smolkin Maintainer: James W. MacDonald git_url: https://git.bioconductor.org/packages/clusterStab git_branch: RELEASE_3_8 git_last_commit: 274e010 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/clusterStab_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/clusterStab_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/clusterStab_1.54.0.tgz vignettes: vignettes/clusterStab/inst/doc/clusterStab.pdf vignetteTitles: clusterStab Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/clusterStab/inst/doc/clusterStab.R Package: CMA Version: 1.40.0 Depends: R (>= 2.10), methods, stats, Biobase Suggests: MASS, class, nnet, glmnet, e1071, randomForest, plsgenomics, gbm, mgcv, corpcor, limma, st, mvtnorm License: GPL (>= 2) MD5sum: ae7cd551d9e6cf48713f81726e421044 NeedsCompilation: no Title: Synthesis of microarray-based classification Description: This package provides a comprehensive collection of various microarray-based classification algorithms both from Machine Learning and Statistics. Variable Selection, Hyperparameter tuning, Evaluation and Comparison can be performed combined or stepwise in a user-friendly environment. biocViews: Classification, DecisionTree Author: Martin Slawski , Anne-Laure Boulesteix , Christoph Bernau . Maintainer: Christoph Bernau git_url: https://git.bioconductor.org/packages/CMA git_branch: RELEASE_3_8 git_last_commit: 70adf88 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CMA_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CMA_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CMA_1.40.0.tgz vignettes: vignettes/CMA/inst/doc/CMA_vignette.pdf vignetteTitles: CMA_vignette.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CMA/inst/doc/CMA_vignette.R Package: cn.farms Version: 1.30.0 Depends: R (>= 3.0), Biobase, methods, ff, oligoClasses, snow Imports: DBI, affxparser, oligo, DNAcopy, preprocessCore, lattice Suggests: pd.mapping250k.sty, pd.mapping250k.nsp, pd.genomewidesnp.5, pd.genomewidesnp.6 License: LGPL (>= 2.0) Archs: i386, x64 MD5sum: 0182f9e0aa8c1ab548b761a264cf0926 NeedsCompilation: yes Title: cn.FARMS - factor analysis for copy number estimation Description: This package implements the cn.FARMS algorithm for copy number variation (CNV) analysis. cn.FARMS allows to analyze the most common Affymetrix (250K-SNP6.0) array types, supports high-performance computing using snow and ff. biocViews: Microarray, CopyNumberVariation Author: Andreas Mitterecker, Djork-Arne Clevert Maintainer: Andreas Mitterecker URL: http://www.bioinf.jku.at/software/cnfarms/cnfarms.html git_url: https://git.bioconductor.org/packages/cn.farms git_branch: RELEASE_3_8 git_last_commit: bd2c539 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cn.farms_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cn.farms_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cn.farms_1.30.0.tgz vignettes: vignettes/cn.farms/inst/doc/cn.farms.pdf vignetteTitles: cn.farms: Manual for the R package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cn.farms/inst/doc/cn.farms.R Package: cn.mops Version: 1.28.0 Depends: R (>= 2.12), methods, utils, stats, graphics, parallel, GenomicRanges Imports: BiocGenerics, Biobase, IRanges, Rsamtools, GenomeInfoDb, S4Vectors, exomeCopy Suggests: DNAcopy License: LGPL (>= 2.0) Archs: i386, x64 MD5sum: c6736a533b5a4a5832b974bf0f33389b NeedsCompilation: yes Title: cn.mops - Mixture of Poissons for CNV detection in NGS data Description: cn.mops (Copy Number estimation by a Mixture Of PoissonS) is a data processing pipeline for copy number variations and aberrations (CNVs and CNAs) from next generation sequencing (NGS) data. The package supplies functions to convert BAM files into read count matrices or genomic ranges objects, which are the input objects for cn.mops. cn.mops models the depths of coverage across samples at each genomic position. Therefore, it does not suffer from read count biases along chromosomes. Using a Bayesian approach, cn.mops decomposes read variations across samples into integer copy numbers and noise by its mixture components and Poisson distributions, respectively. cn.mops guarantees a low FDR because wrong detections are indicated by high noise and filtered out. cn.mops is very fast and written in C++. biocViews: Sequencing, CopyNumberVariation, Homo_sapiens, CellBiology, HapMap, Genetics Author: Guenter Klambauer Maintainer: Guenter Klambauer URL: http://www.bioinf.jku.at/software/cnmops/cnmops.html git_url: https://git.bioconductor.org/packages/cn.mops git_branch: RELEASE_3_8 git_last_commit: f953d10 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cn.mops_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cn.mops_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cn.mops_1.28.0.tgz vignettes: vignettes/cn.mops/inst/doc/cn.mops.pdf vignetteTitles: cn.mops: Manual for the R package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cn.mops/inst/doc/cn.mops.R dependsOnMe: panelcn.mops Package: CNAnorm Version: 1.28.0 Depends: R (>= 2.10.1), methods Imports: DNAcopy License: GPL-2 Archs: i386, x64 MD5sum: edd5ffe29a6af7360a99b61e85ae5292 NeedsCompilation: yes Title: A normalization method for Copy Number Aberration in cancer samples Description: Performs ratio, GC content correction and normalization of data obtained using low coverage (one read every 100-10,000 bp) high troughput sequencing. It performs a "discrete" normalization looking for the ploidy of the genome. It will also provide tumour content if at least two ploidy states can be found. biocViews: CopyNumberVariation, Sequencing, Coverage, Normalization, WholeGenome, DNASeq, GenomicVariation Author: Stefano Berri , Henry M. Wood , Arief Gusnanto Maintainer: Stefano Berri URL: http://www.r-project.org, git_url: https://git.bioconductor.org/packages/CNAnorm git_branch: RELEASE_3_8 git_last_commit: 3650df3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNAnorm_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNAnorm_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNAnorm_1.28.0.tgz vignettes: vignettes/CNAnorm/inst/doc/CNAnorm.pdf vignetteTitles: CNAnorm.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNAnorm/inst/doc/CNAnorm.R Package: CNEr Version: 1.18.1 Depends: R (>= 3.4) Imports: Biostrings (>= 2.33.4), DBI (>= 0.7), RSQLite (>= 0.11.4), GenomeInfoDb (>= 1.1.3), GenomicRanges (>= 1.23.16), rtracklayer (>= 1.25.5), XVector (>= 0.5.4), GenomicAlignments (>= 1.1.9), methods, S4Vectors (>= 0.13.13), IRanges (>= 2.5.27), readr (>= 0.2.2), BiocGenerics, tools, parallel, reshape2 (>= 1.4.1), ggplot2 (>= 2.1.0), poweRlaw (>= 0.60.3), annotate (>= 1.50.0), GO.db (>= 3.3.0), R.utils (>= 2.3.0), KEGGREST (>= 1.14.0) LinkingTo: S4Vectors, IRanges, XVector Suggests: Gviz (>= 1.7.4), BiocStyle, knitr, rmarkdown, testthat, BSgenome.Drerio.UCSC.danRer10, BSgenome.Hsapiens.UCSC.hg38, TxDb.Drerio.UCSC.danRer10.refGene, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Ggallus.UCSC.galGal3 License: GPL-2 | file LICENSE License_restricts_use: yes Archs: i386, x64 MD5sum: d14b070544db2a224af7ddacd34e24ad NeedsCompilation: yes Title: CNE Detection and Visualization Description: Large-scale identification and advanced visualization of sets of conserved noncoding elements. biocViews: GeneRegulation, Visualization, DataImport Author: Ge Tan Maintainer: Ge Tan URL: https://github.com/ge11232002/CNEr VignetteBuilder: knitr BugReports: https://github.com/ge11232002/CNEr/issues git_url: https://git.bioconductor.org/packages/CNEr git_branch: RELEASE_3_8 git_last_commit: 66aa88a git_last_commit_date: 2018-11-01 Date/Publication: 2018-11-01 source.ver: src/contrib/CNEr_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNEr_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNEr_1.18.1.tgz vignettes: vignettes/CNEr/inst/doc/CNEr.html, vignettes/CNEr/inst/doc/PairwiseWholeGenomeAlignment.html vignetteTitles: CNE identification and visualisation, Pairwise whole genome alignment hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/CNEr/inst/doc/CNEr.R, vignettes/CNEr/inst/doc/PairwiseWholeGenomeAlignment.R importsMe: TFBSTools Package: CNORdt Version: 1.24.1 Depends: R (>= 1.8.0), CellNOptR (>= 0.99), abind License: GPL-2 Archs: i386, x64 MD5sum: cf70dff7dc7563f6896b09d7af84d9fd NeedsCompilation: yes Title: Add-on to CellNOptR: Discretized time treatments Description: This add-on to the package CellNOptR handles time-course data, as opposed to steady state data in CellNOptR. It scales the simulation step to allow comparison and model fitting for time-course data. Future versions will optimize delays and strengths for each edge. biocViews: ImmunoOncology, CellBasedAssays, CellBiology, Proteomics, TimeCourse Author: A. MacNamara Maintainer: A. MacNamara git_url: https://git.bioconductor.org/packages/CNORdt git_branch: RELEASE_3_8 git_last_commit: 018589c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CNORdt_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNORdt_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNORdt_1.24.1.tgz vignettes: vignettes/CNORdt/inst/doc/CNORdt-vignette.pdf vignetteTitles: Using multiple time points to train logic models to data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNORdt/inst/doc/CNORdt-vignette-example.R, vignettes/CNORdt/inst/doc/CNORdt-vignette.R Package: CNORfeeder Version: 1.22.1 Depends: R (>= 2.15.0), CellNOptR (>= 1.4.0), graph Suggests: minet, catnet, Rgraphviz, RUnit, BiocGenerics, igraph License: GPL-3 MD5sum: 2218d31a7dbfebe08bc5160024d8f1be NeedsCompilation: no Title: Integration of CellNOptR to add missing links Description: This package integrates literature-constrained and data-driven methods to infer signalling networks from perturbation experiments. It permits to extends a given network with links derived from the data via various inference methods and uses information on physical interactions of proteins to guide and validate the integration of links. biocViews: ImmunoOncology, CellBasedAssays, CellBiology, Proteomics, Bioinformatics, NetworkInference Author: F.Eduati Maintainer: F.Eduati git_url: https://git.bioconductor.org/packages/CNORfeeder git_branch: RELEASE_3_8 git_last_commit: 9bde560 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CNORfeeder_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNORfeeder_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNORfeeder_1.22.1.tgz vignettes: vignettes/CNORfeeder/inst/doc/CNORfeeder-vignette.pdf vignetteTitles: Main vignette:Playing with networks using CNORfeeder hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNORfeeder/inst/doc/CNORfeeder-vignette.R Package: CNORfuzzy Version: 1.24.0 Depends: R (>= 2.15.0), CellNOptR (>= 1.4.0), nloptr (>= 0.8.5) Suggests: xtable, Rgraphviz, RUnit, BiocGenerics License: GPL-2 Archs: i386, x64 MD5sum: a81e01df30c7acdb9a966953fa009109 NeedsCompilation: yes Title: Addon to CellNOptR: Fuzzy Logic Description: This package is an extension to CellNOptR. It contains additional functionality needed to simulate and train a prior knowledge network to experimental data using constrained fuzzy logic (cFL, rather than Boolean logic as is the case in CellNOptR). Additionally, this package will contain functions to use for the compilation of multiple optimization results (either Boolean or cFL). biocViews: Network Author: M. Morris, T. Cokelaer Maintainer: T. Cokelaer git_url: https://git.bioconductor.org/packages/CNORfuzzy git_branch: RELEASE_3_8 git_last_commit: 709045d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNORfuzzy_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNORfuzzy_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNORfuzzy_1.24.0.tgz vignettes: vignettes/CNORfuzzy/inst/doc/CNORfuzzy-vignette.pdf vignetteTitles: Main vignette:Playing with networks using CNORfuzzyl hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNORfuzzy/inst/doc/CNORfuzzy-vignette.R Package: CNORode Version: 1.24.1 Depends: CellNOptR (>= 1.5.14), genalg Enhances: MEIGOR License: GPL-2 Archs: i386, x64 MD5sum: 8d640141018332b3b5506a6ee64d4e12 NeedsCompilation: yes Title: ODE add-on to CellNOptR Description: ODE add-on to CellNOptR biocViews: ImmunoOncology, CellBasedAssays, CellBiology, Proteomics, Bioinformatics, TimeCourse Author: David Henriques, Thomas Cokelaer Maintainer: David Henriques git_url: https://git.bioconductor.org/packages/CNORode git_branch: RELEASE_3_8 git_last_commit: bbe578e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CNORode_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNORode_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNORode_1.24.1.tgz vignettes: vignettes/CNORode/inst/doc/CNORode-vignette.pdf vignetteTitles: Main vignette:Playing with networks using CNORode hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNORode/inst/doc/CNORode-vignette.R dependsOnMe: MEIGOR Package: CNPBayes Version: 1.12.0 Depends: R (>= 3.4.0), IRanges, GenomicRanges Imports: Rcpp (>= 0.12.1), S4Vectors, matrixStats, RColorBrewer, gtools, combinat, GenomeInfoDb (>= 1.11.6), methods, BiocGenerics, graphics, stats, coda, SummarizedExperiment, mclust, reshape2, ggplot2, magrittr, purrr, tidyr, dplyr, tibble, scales LinkingTo: Rcpp Suggests: testthat, knitr, BiocStyle, rmarkdown, BiocCheck, MASS, VanillaICE, tidyverse License: Artistic-2.0 Archs: i386, x64 MD5sum: b9231a3d34f0e502f273043d299f125d NeedsCompilation: yes Title: Bayesian mixture models for copy number polymorphisms Description: Bayesian hierarchical mixture models for batch effects and copy number. biocViews: CopyNumberVariation, Bayesian Author: Stephen Cristiano, Robert Scharpf, and Jacob Carey Maintainer: Jacob Carey URL: https://github.com/scristia/CNPBayes VignetteBuilder: knitr BugReports: https://github.com/scristia/CNPBayes/issues git_url: https://git.bioconductor.org/packages/CNPBayes git_branch: RELEASE_3_8 git_last_commit: 01190fc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNPBayes_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNPBayes_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNPBayes_1.12.0.tgz vignettes: vignettes/CNPBayes/inst/doc/Convergence.pdf, vignettes/CNPBayes/inst/doc/Implementation.pdf, vignettes/CNPBayes/inst/doc/Overview.pdf vignetteTitles: Overview of CNPBayes package, Implementation of Bayesian mixture models for copy number estimation, Overview of CNPBayes package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNPBayes/inst/doc/Convergence.R, vignettes/CNPBayes/inst/doc/Implementation.R, vignettes/CNPBayes/inst/doc/Overview.R Package: CNTools Version: 1.38.0 Depends: R (>= 2.10), methods, tools, stats, genefilter License: LGPL Archs: i386, x64 MD5sum: 0a41c86ddaddf77e73f344fe7fa3c915 NeedsCompilation: yes Title: Convert segment data into a region by sample matrix to allow for other high level computational analyses. Description: This package provides tools to convert the output of segmentation analysis using DNAcopy to a matrix structure with overlapping segments as rows and samples as columns so that other computational analyses can be applied to segmented data biocViews: Microarray, CopyNumberVariation Author: Jianhua Zhang Maintainer: J. Zhang git_url: https://git.bioconductor.org/packages/CNTools git_branch: RELEASE_3_8 git_last_commit: 0691a5d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNTools_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNTools_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNTools_1.38.0.tgz vignettes: vignettes/CNTools/inst/doc/HowTo.pdf vignetteTitles: NCTools HowTo hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNTools/inst/doc/HowTo.R dependsOnMe: cghMCR Package: cnvGSA Version: 1.26.0 Depends: brglm, doParallel, foreach, GenomicRanges, methods, splitstackshape Suggests: cnvGSAdata, org.Hs.eg.db License: LGPL MD5sum: f178bf3793415071fcb3504af847f843 NeedsCompilation: no Title: Gene Set Analysis of (Rare) Copy Number Variants Description: This package is intended to facilitate gene-set association with rare CNVs in case-control studies. biocViews: MultipleComparison Author: Daniele Merico , Robert Ziman ; packaged by Joseph Lugo Maintainer: Joseph Lugo git_url: https://git.bioconductor.org/packages/cnvGSA git_branch: RELEASE_3_8 git_last_commit: db6759f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cnvGSA_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cnvGSA_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cnvGSA_1.26.0.tgz vignettes: vignettes/cnvGSA/inst/doc/cnvGSA-vignette.pdf, vignettes/cnvGSA/inst/doc/cnvGSAUsersGuide.pdf vignetteTitles: cnvGSA - Gene-Set Analysis of Rare Copy Number Variants, cnvGSAUsersGuide.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: CNVPanelizer Version: 1.14.0 Depends: R (>= 3.2.0), GenomicRanges Imports: S4Vectors, grDevices, stats, utils, NOISeq, IRanges, Rsamtools, exomeCopy, foreach, ggplot2, plyr, GenomeInfoDb, gplots, reshape2, stringr, testthat, graphics, methods, shiny, shinyFiles, shinyjs, grid, openxlsx Suggests: knitr, RUnit, BiocGenerics License: GPL-3 MD5sum: 98e25515072bab932fb127f75cbfe980 NeedsCompilation: no Title: Reliable CNV detection in targeted sequencing applications Description: A method that allows for the use of a collection of non-matched normal tissue samples. Our approach uses a non-parametric bootstrap subsampling of the available reference samples to estimate the distribution of read counts from targeted sequencing. As inspired by random forest, this is combined with a procedure that subsamples the amplicons associated with each of the targeted genes. The obtained information allows us to reliably classify the copy number aberrations on the gene level. biocViews: Classification, Sequencing, Normalization, CopyNumberVariation, Coverage Author: Cristiano Oliveira [aut], Thomas Wolf [aut, cre], Albrecht Stenzinger [ctb], Volker Endris [ctb], Nicole Pfarr [ctb], Benedikt Brors [ths], Wilko Weichert [ths] Maintainer: Thomas Wolf VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CNVPanelizer git_branch: RELEASE_3_8 git_last_commit: 8779375 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNVPanelizer_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNVPanelizer_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNVPanelizer_1.14.0.tgz vignettes: vignettes/CNVPanelizer/inst/doc/CNVPanelizer.pdf vignetteTitles: CNVPanelizer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNVPanelizer/inst/doc/CNVPanelizer.R Package: CNVrd2 Version: 1.20.0 Depends: R (>= 3.0.0), methods, VariantAnnotation, parallel, rjags, ggplot2, gridExtra Imports: DNAcopy, IRanges, Rsamtools Suggests: knitr License: GPL-2 MD5sum: 43748a826e927c6f6c8a24789b709688 NeedsCompilation: no Title: CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data. Description: CNVrd2 uses next-generation sequencing data to measure human gene copy number for multiple samples, indentify SNPs tagging copy number variants and detect copy number polymorphic genomic regions. biocViews: CopyNumberVariation, SNP, Sequencing, Software, Coverage, LinkageDisequilibrium, Clustering. Author: Hoang Tan Nguyen, Tony R Merriman and Mik Black Maintainer: Hoang Tan Nguyen URL: https://github.com/hoangtn/CNVrd2 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CNVrd2 git_branch: RELEASE_3_8 git_last_commit: f0332cc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNVrd2_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNVrd2_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNVrd2_1.20.0.tgz vignettes: vignettes/CNVrd2/inst/doc/CNVrd2.pdf vignetteTitles: A Markdown Vignette with knitr hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNVrd2/inst/doc/CNVrd2.R Package: CNVtools Version: 1.76.0 Depends: R (>= 2.10), survival License: GPL-3 Archs: i386, x64 MD5sum: 8c7a391861a596b79dec372a8ed5fd92 NeedsCompilation: yes Title: A package to test genetic association with CNV data Description: This package is meant to facilitate the testing of Copy Number Variant data for genetic association, typically in case-control studies. biocViews: GeneticVariability Author: Chris Barnes and Vincent Plagnol Maintainer: Chris Barnes git_url: https://git.bioconductor.org/packages/CNVtools git_branch: RELEASE_3_8 git_last_commit: ece5748 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CNVtools_1.76.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CNVtools_1.76.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CNVtools_1.76.0.tgz vignettes: vignettes/CNVtools/inst/doc/CNVtools-vignette.pdf vignetteTitles: Copy Number Variation Tools hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CNVtools/inst/doc/CNVtools-vignette.R Package: cobindR Version: 1.20.0 Imports: methods, seqinr, yaml, rtfbs, gplots, mclust, gmp, BiocGenerics (>= 0.13.8), IRanges, Biostrings, BSgenome, biomaRt Suggests: RUnit Enhances: rGADEM, seqLogo, genoPlotR, parallel, VennDiagram, RColorBrewer, vcd, MotifDb, snowfall License: Artistic-2.0 MD5sum: a311dfeeec28c8f77c993ace8a77b5c7 NeedsCompilation: no Title: Finding Co-occuring motifs of transcription factor binding sites Description: Finding and analysing co-occuring motifs of transcription factor binding sites in groups of genes biocViews: ChIPSeq, CellBiology, MultipleComparison, SequenceMatching Author: Manuela Benary, Stefan Kroeger, Yuehien Lee, Robert Lehmann Maintainer: Manuela Benary git_url: https://git.bioconductor.org/packages/cobindR git_branch: RELEASE_3_8 git_last_commit: c45cc5e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cobindR_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cobindR_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cobindR_1.20.0.tgz vignettes: vignettes/cobindR/inst/doc/cobindR.pdf vignetteTitles: Using cobindR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cobindR/inst/doc/cobindR.R Package: CoCiteStats Version: 1.54.0 Depends: R (>= 2.0), org.Hs.eg.db Imports: AnnotationDbi License: CPL MD5sum: 631d2c987e3945ab37065b400165fd2f NeedsCompilation: no Title: Different test statistics based on co-citation. Description: A collection of software tools for dealing with co-citation data. biocViews: Software Author: B. Ding and R. Gentleman Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/CoCiteStats git_branch: RELEASE_3_8 git_last_commit: abb51f2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CoCiteStats_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CoCiteStats_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CoCiteStats_1.54.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: COCOA Version: 1.0.2 Depends: R (>= 3.5), GenomicRanges Imports: BiocGenerics, S4Vectors, IRanges, data.table, ggplot2, Biobase, stats, methods, ComplexHeatmap, MIRA, tidyr, grid, grDevices Suggests: knitr, parallel, testthat, BiocStyle, rmarkdown, AnnotationHub, LOLA License: GPL-3 MD5sum: ab8b8c2ca9c7ce6bce78d86d557de5e9 NeedsCompilation: no Title: Coordinate Covariation Analysis Description: COCOA is a method for understanding variation among samples and can be used with data that includes genomic coordinates such as DNA methylation. On a high level, COCOA uses a database of "region sets" and principal component analysis (PCA) of your data to identify sources of variation among samples. A region set is a set of genomic regions that share a biological annotation, for instance, transcription factor binding regions, histone modification regions, or open chromatin regions. COCOA works in both supervised (known groups of samples) and unsupervised (no groups) situations and can be used as a complement to "differential" methods that find discrete differences between groups. COCOA can identify biologically meaningful sources of variation between samples and increase understanding of variation in your data. biocViews: PrincipalComponent, GenomicVariation, DNAMethylation, GeneRegulation, GenomeAnnotation, SystemsBiology, FunctionalGenomics, ChIPSeq, MethylSeq, Sequencing, Epigenetics, ImmunoOncology Author: John Lawson [aut, cre], Nathan Sheffield [aut] (http://www.databio.org) Maintainer: John Lawson URL: http://code.databio.org/COCOA/ VignetteBuilder: knitr BugReports: https://github.com/databio/COCOA git_url: https://git.bioconductor.org/packages/COCOA git_branch: RELEASE_3_8 git_last_commit: aa24dba git_last_commit_date: 2019-03-06 Date/Publication: 2019-03-06 source.ver: src/contrib/COCOA_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/COCOA_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/COCOA_1.0.2.tgz vignettes: vignettes/COCOA/inst/doc/COCOA_Workflow.html, vignettes/COCOA/inst/doc/IntroToCOCOA.html vignetteTitles: COCOA Workflow, Introduction to Coordinate Covariation Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/COCOA/inst/doc/COCOA_Workflow.R, vignettes/COCOA/inst/doc/IntroToCOCOA.R Package: codelink Version: 1.50.0 Depends: R (>= 2.10), BiocGenerics (>= 0.3.2), methods, Biobase (>= 2.17.8), limma Imports: annotate Suggests: genefilter, parallel, knitr License: GPL-2 MD5sum: 581f0dafd469d47a78e5c59c019d20fc NeedsCompilation: no Title: Manipulation of Codelink microarray data Description: This package facilitates reading, preprocessing and manipulating Codelink microarray data. The raw data must be exported as text file using the Codelink software. biocViews: Microarray, OneChannel, DataImport, Preprocessing Author: Diego Diez Maintainer: Diego Diez URL: https://github.com/ddiez/codelink VignetteBuilder: knitr BugReports: https://github.com/ddiez/codelink/issues git_url: https://git.bioconductor.org/packages/codelink git_branch: RELEASE_3_8 git_last_commit: aadfb3e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/codelink_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/codelink_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/codelink_1.50.0.tgz vignettes: vignettes/codelink/inst/doc/Codelink_Introduction.pdf, vignettes/codelink/inst/doc/Codelink_Legacy.pdf vignetteTitles: Codelink Intruction, Codelink Legacy hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/codelink/inst/doc/Codelink_Introduction.R, vignettes/codelink/inst/doc/Codelink_Legacy.R Package: CODEX Version: 1.14.1 Depends: R (>= 3.2.3), Rsamtools, GenomeInfoDb, BSgenome.Hsapiens.UCSC.hg19, IRanges, Biostrings, S4Vectors Suggests: WES.1KG.WUGSC License: GPL-2 MD5sum: 0fd82fd8f53602dd31e7859cf7e9c831 NeedsCompilation: no Title: A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing Description: A normalization and copy number variation calling procedure for whole exome DNA sequencing data. CODEX relies on the availability of multiple samples processed using the same sequencing pipeline for normalization, and does not require matched controls. The normalization model in CODEX includes terms that specifically remove biases due to GC content, exon length and targeting and amplification efficiency, and latent systemic artifacts. CODEX also includes a Poisson likelihood-based recursive segmentation procedure that explicitly models the count-based exome sequencing data. biocViews: ImmunoOncology, ExomeSeq, Normalization, QualityControl, CopyNumberVariation Author: Yuchao Jiang, Nancy R. Zhang Maintainer: Yuchao Jiang git_url: https://git.bioconductor.org/packages/CODEX git_branch: RELEASE_3_8 git_last_commit: d4c7d54 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CODEX_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CODEX_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CODEX_1.14.1.tgz vignettes: vignettes/CODEX/inst/doc/CODEX_vignettes.pdf vignetteTitles: Using CODEX hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CODEX/inst/doc/CODEX_vignettes.R dependsOnMe: iCNV Package: coexnet Version: 1.4.0 Depends: R (>= 3.4) Imports: affy, siggenes, GEOquery, vsn, igraph, acde, Biobase, limma, graphics, stats, utils, STRINGdb, SummarizedExperiment, minet, rmarkdown Suggests: RUnit, BiocGenerics, knitr License: LGPL MD5sum: 9d8e6b5ab48da4a1ca2db90f2160c94f NeedsCompilation: no Title: coexnet: An R package to build CO-EXpression NETworks from Microarray Data Description: Extracts the gene expression matrix from GEO DataSets (.CEL files) as a AffyBatch object. Additionally, can make the normalization process using two different methods (vsn and rma). The summarization (pass from multi-probe to one gene) uses two different criteria (Maximum value and Median of the samples expression data) and the process of gene differentially expressed analisys using two methods (sam and acde). The construction of the co-expression network can be conduced using two different methods, Pearson Correlation Coefficient (PCC) or Mutual Information (MI) and choosing a threshold value using a graph theory approach. biocViews: GeneExpression, Microarray, DifferentialExpression, GraphAndNetwork, NetworkInference, SystemsBiology, Normalization, Network Author: Juan David Henao [aut,cre], Liliana Lopez-Kleine [aut], Andres Pinzon-Velasco [aut] Maintainer: Juan David Henao VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/coexnet git_branch: RELEASE_3_8 git_last_commit: 053d9b7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/coexnet_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/coexnet_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/coexnet_1.4.0.tgz vignettes: vignettes/coexnet/inst/doc/coexnet.pdf vignetteTitles: The title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/coexnet/inst/doc/coexnet.R Package: CoGAPS Version: 3.2.40 Depends: R (>= 3.5.0) Imports: BiocParallel, cluster, data.table, methods, gplots, graphics, grDevices, RColorBrewer, Rcpp, S4Vectors, SingleCellExperiment, stats, SummarizedExperiment, tools, utils, rhdf5 LinkingTo: Rcpp Suggests: testthat, knitr, rmarkdown, BiocStyle License: GPL (==2) Archs: i386, x64 MD5sum: ca19b32b5950c6ed6efc215073df2d17 NeedsCompilation: yes Title: Coordinated Gene Activity in Pattern Sets Description: Coordinated Gene Activity in Pattern Sets (CoGAPS) implements a Bayesian MCMC matrix factorization algorithm, GAPS, and links it to gene set statistic methods to infer biological process activity. It can be used to perform sparse matrix factorization on any data, and when this data represents biomolecules, to do gene set analysis. biocViews: ImmunoOncology, GeneExpression, Transcription, GeneSetEnrichment, DifferentialExpression, Bayesian, Clustering, TimeCourse, RNASeq, Microarray, MultipleComparison, DimensionReduction, ImmunoOncology Author: Thomas Sherman, Wai-shing Lee, Conor Kelton, Ondrej Maxian, Jacob Carey, Genevieve Stein-O'Brien, Michael Considine, Maggie Wodicka, John Stansfield, Shawn Sivy, Carlo Colantuoni, Alexander Favorov, Mike Ochs, Elana Fertig Maintainer: Elana J. Fertig , Thomas D. Sherman VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CoGAPS git_branch: RELEASE_3_8 git_last_commit: 0bb2e91 git_last_commit_date: 2019-02-23 Date/Publication: 2019-02-27 source.ver: src/contrib/CoGAPS_3.2.40.tar.gz win.binary.ver: bin/windows/contrib/3.5/CoGAPS_3.2.40.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CoGAPS_3.2.40.tgz vignettes: vignettes/CoGAPS/inst/doc/CoGAPS.html vignetteTitles: CoGAPS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CoGAPS/inst/doc/CoGAPS.R Package: cogena Version: 1.16.0 Depends: R (>= 3.4), cluster, ggplot2, kohonen Imports: methods, class, gplots, mclust, amap, apcluster, foreach, parallel, doParallel, fastcluster, corrplot, biwt, Biobase, reshape2, dplyr, devtools Suggests: knitr, rmarkdown License: LGPL-3 MD5sum: e2c7d73b261ab79838296c26f8b38878 NeedsCompilation: no Title: co-expressed gene-set enrichment analysis Description: cogena is a workflow for co-expressed gene-set enrichment analysis. It aims to discovery smaller scale, but highly correlated cellular events that may be of great biological relevance. A novel pipeline for drug discovery and drug repositioning based on the cogena workflow is proposed. Particularly, candidate drugs can be predicted based on the gene expression of disease-related data, or other similar drugs can be identified based on the gene expression of drug-related data. Moreover, the drug mode of action can be disclosed by the associated pathway analysis. In summary, cogena is a flexible workflow for various gene set enrichment analysis for co-expressed genes, with a focus on pathway/GO analysis and drug repositioning. biocViews: Clustering, GeneSetEnrichment, GeneExpression, Visualization, Pathways, KEGG, GO, Microarray, Sequencing, SystemsBiology, DataRepresentation, DataImport Author: Zhilong Jia [aut, cre], Michael Barnes [aut] Maintainer: Zhilong Jia URL: https://github.com/zhilongjia/cogena VignetteBuilder: knitr BugReports: https://github.com/zhilongjia/cogena/issues git_url: https://git.bioconductor.org/packages/cogena git_branch: RELEASE_3_8 git_last_commit: e6f596c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cogena_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cogena_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cogena_1.16.0.tgz vignettes: vignettes/cogena/inst/doc/cogena-vignette_pdf.pdf, vignettes/cogena/inst/doc/cogena-vignette_html.html vignetteTitles: cogena Tutorial, cogena Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cogena/inst/doc/cogena-vignette_html.R, vignettes/cogena/inst/doc/cogena-vignette_pdf.R Package: coGPS Version: 1.26.0 Depends: R (>= 2.13.0) Imports: graphics, grDevices Suggests: limma License: GPL-2 MD5sum: e471e9f7a0a57988cbe0729d35712e77 NeedsCompilation: no Title: cancer outlier Gene Profile Sets Description: Gene Set Enrichment Analysis of P-value based statistics for outlier gene detection in dataset merged from multiple studies biocViews: Microarray, DifferentialExpression Author: Yingying Wei, Michael Ochs Maintainer: Yingying Wei git_url: https://git.bioconductor.org/packages/coGPS git_branch: RELEASE_3_8 git_last_commit: 5ed0a73 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/coGPS_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/coGPS_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/coGPS_1.26.0.tgz vignettes: vignettes/coGPS/inst/doc/coGPS.pdf vignetteTitles: coGPS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/coGPS/inst/doc/coGPS.R Package: COHCAP Version: 1.28.1 Depends: WriteXLS, COHCAPanno, RColorBrewer, gplots Imports: Rcpp, RcppArmadillo, BH LinkingTo: Rcpp, BH License: GPL-3 Archs: i386, x64 MD5sum: a00f1b04b6e4a464ab245bf79ebbb764 NeedsCompilation: yes Title: CpG Island Analysis Pipeline for Illumina Methylation Array and Targeted BS-Seq Data Description: This package provides a pipeline to analyze single-nucleotide resolution methylation data (Illumina 450k/EPIC methylation array, targeted BS-Seq, etc.). It provides differential methylation for CpG Sites, differential methylation for CpG Islands, integration with gene expression data, with visualizaton options. Discussion Group: https://sourceforge.net/p/cohcap/discussion/bioconductor/ biocViews: DNAMethylation, Microarray, MethylSeq, Epigenetics, DifferentialMethylation Author: Charles Warden , Yate-Ching Yuan , Xiwei Wu Maintainer: Charles Warden SystemRequirements: Perl git_url: https://git.bioconductor.org/packages/COHCAP git_branch: RELEASE_3_8 git_last_commit: 5bd856f git_last_commit_date: 2018-11-09 Date/Publication: 2018-11-09 source.ver: src/contrib/COHCAP_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/COHCAP_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/COHCAP_1.28.1.tgz vignettes: vignettes/COHCAP/inst/doc/COHCAP.pdf vignetteTitles: COHCAP Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/COHCAP/inst/doc/COHCAP.R Package: coMET Version: 1.14.0 Depends: R (>= 3.4.0), grid, utils, biomaRt, Gviz, psych Imports: colortools, hash,grDevices, gridExtra, rtracklayer, IRanges, S4Vectors, GenomicRanges, stats, corrplot Suggests: BiocStyle, knitr, RUnit, BiocGenerics License: GPL (>= 2) MD5sum: 47824d638de57c2c0bc0c22a624fb0f2 NeedsCompilation: no Title: coMET: visualisation of regional epigenome-wide association scan (EWAS) results and DNA co-methylation patterns Description: Visualisation of EWAS results in a genomic region. In addition to phenotype-association P-values, coMET also generates plots of co-methylation patterns and provides a series of annotation tracks. It can be used to other omic-wide association scans as long as the data can be translated to genomic level and for any species. biocViews: Software, DifferentialMethylation, Visualization, Sequencing, Genetics, FunctionalGenomics, Microarray, MethylationArray, MethylSeq, ChIPSeq, DNASeq, RiboSeq, RNASeq, ExomeSeq, DNAMethylation, GenomeWideAssociation, MotifAnnotation Author: Tiphaine C. Martin [aut,cre], Thomas Hardiman [aut], Idil Yet [aut], Pei-Chien Tsai [aut], Jordana T. Bell [aut] Maintainer: Tiphaine Martin URL: http://epigen.kcl.ac.uk/comet VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/coMET git_branch: RELEASE_3_8 git_last_commit: 2833a76 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/coMET_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/coMET_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/coMET_1.14.0.tgz vignettes: vignettes/coMET/inst/doc/coMET.pdf vignetteTitles: coMET users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/coMET/inst/doc/coMET.R Package: compartmap Version: 1.0.3 Depends: R (>= 3.5.0), minfi, Homo.sapiens, mixOmics Imports: SummarizedExperiment, GenomicRanges, gtools, parallel Suggests: covr, testthat, knitr License: GPL-3 + file LICENSE MD5sum: 5aac6ba1795650d064da234ab073232e NeedsCompilation: no Title: A/B compartment inference from ATAC-seq and methylation array data Description: Compartmap performs shrunken A/B compartment inference from ATAC-seq and methylation arrays. biocViews: ImmunoOncology, Genetics, Epigenetics, ATACSeq, MethylSeq, MethylationArray Author: Benjamin Johnson [aut, cre], Tim Triche [aut], Kasper Hansen [aut], Jean-Philippe Fortin [aut] Maintainer: Benjamin Johnson URL: https://github.com/biobenkj/compartmap VignetteBuilder: knitr BugReports: https://github.com/biobenkj/compartmap/issues git_url: https://git.bioconductor.org/packages/compartmap git_branch: RELEASE_3_8 git_last_commit: fd8e478 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/compartmap_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/compartmap_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/compartmap_1.0.3.tgz vignettes: vignettes/compartmap/inst/doc/compartmap_vignette.html vignetteTitles: A/B compartment inference with compartmap hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/compartmap/inst/doc/compartmap_vignette.R Package: COMPASS Version: 1.20.1 Depends: R (>= 3.0.3) Imports: methods, Rcpp, data.table, RColorBrewer, scales, grid, plyr, knitr, abind, clue, grDevices, utils, pdist, magrittr, reshape2, dplyr, tidyr, rlang, BiocStyle, rmarkdown LinkingTo: Rcpp (>= 0.11.0) Suggests: flowWorkspace (>= 3.9.66), flowCore, ncdfFlow, shiny, testthat, devtools, flowWorkspaceData License: Artistic-2.0 Archs: i386, x64 MD5sum: 6283483b5d380ba8065652cc0b9bc292 NeedsCompilation: yes Title: Combinatorial Polyfunctionality Analysis of Single Cells Description: COMPASS is a statistical framework that enables unbiased analysis of antigen-specific T-cell subsets. COMPASS uses a Bayesian hierarchical framework to model all observed cell-subsets and select the most likely to be antigen-specific while regularizing the small cell counts that often arise in multi-parameter space. The model provides a posterior probability of specificity for each cell subset and each sample, which can be used to profile a subject's immune response to external stimuli such as infection or vaccination. biocViews: ImmunoOncology, FlowCytometry Author: Lynn Lin, Kevin Ushey, Greg Finak, Ravio Kolde (pheatmap) Maintainer: Greg Finak VignetteBuilder: knitr BugReports: https://github.com/RGLab/COMPASS/issues git_url: https://git.bioconductor.org/packages/COMPASS git_branch: RELEASE_3_8 git_last_commit: 8c13ec8 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/COMPASS_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/COMPASS_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/COMPASS_1.20.1.tgz vignettes: vignettes/COMPASS/inst/doc/SimpleCOMPASS.pdf, vignettes/COMPASS/inst/doc/COMPASS.html vignetteTitles: SimpleCOMPASS, COMPASS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/COMPASS/inst/doc/COMPASS.R, vignettes/COMPASS/inst/doc/SimpleCOMPASS.R Package: compcodeR Version: 1.18.1 Depends: R (>= 3.0.2), sm Imports: tcltk, knitr (>= 1.2), markdown, ROCR, lattice (>= 0.16), gplots, gtools, gdata, caTools, grid, KernSmooth, MASS, ggplot2, stringr, modeest, edgeR, limma, vioplot, methods Suggests: BiocStyle, EBSeq, DESeq, DESeq2 (>= 1.1.31), baySeq (>= 2.2.0), genefilter, NOISeq, TCC, NBPSeq (>= 0.3.0) Enhances: rpanel, DSS License: GPL (>= 2) MD5sum: 8dc1027420fcf4a670918068cc2cab37 NeedsCompilation: no Title: RNAseq data simulation, differential expression analysis and performance comparison of differential expression methods Description: This package provides extensive functionality for comparing results obtained by different methods for differential expression analysis of RNAseq data. It also contains functions for simulating count data and interfaces to several packages for performing the differential expression analysis. biocViews: ImmunoOncology, RNASeq, DifferentialExpression Author: Charlotte Soneson Maintainer: Charlotte Soneson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/compcodeR git_branch: RELEASE_3_8 git_last_commit: 9df43ba git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/compcodeR_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/compcodeR_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/compcodeR_1.18.1.tgz vignettes: vignettes/compcodeR/inst/doc/compcodeR.pdf vignetteTitles: compcodeR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/compcodeR/inst/doc/compcodeR.R Package: compEpiTools Version: 1.16.0 Depends: R (>= 3.1.1), methods, topGO, GenomicRanges Imports: AnnotationDbi, BiocGenerics, Biostrings, Rsamtools, parallel, grDevices, gplots, IRanges, GenomicFeatures, XVector, methylPipe, GO.db, S4Vectors, GenomeInfoDb Suggests: BSgenome.Mmusculus.UCSC.mm9, TxDb.Mmusculus.UCSC.mm9.knownGene, org.Mm.eg.db, knitr, rtracklayer License: GPL MD5sum: fb61333b079671d747268fb10a6b1188 NeedsCompilation: no Title: Tools for computational epigenomics Description: Tools for computational epigenomics developed for the analysis, integration and simultaneous visualization of various (epi)genomics data types across multiple genomic regions in multiple samples. biocViews: GeneExpression, Sequencing, Visualization, GenomeAnnotation, Coverage Author: Mattia Pelizzola [aut], Kamal Kishore [aut, cre] Maintainer: Kamal Kishore VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/compEpiTools git_branch: RELEASE_3_8 git_last_commit: bfc46e8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/compEpiTools_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/compEpiTools_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/compEpiTools_1.16.0.tgz vignettes: vignettes/compEpiTools/inst/doc/compEpiTools.pdf vignetteTitles: compEpiTools.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/compEpiTools/inst/doc/compEpiTools.R Package: CompGO Version: 1.18.0 Depends: RDAVIDWebService Imports: rtracklayer, Rgraphviz, ggplot2, GenomicFeatures, TxDb.Mmusculus.UCSC.mm9.knownGene, pcaMethods, reshape2, pathview License: GPL-2 MD5sum: 8d55397e57562db724c8714f2ca5b0c1 NeedsCompilation: no Title: An R pipeline for .bed file annotation, comparing GO term enrichment between gene sets and data visualisation Description: This package contains functions to accomplish several tasks. It is able to download full genome databases from UCSC, import .bed files easily, annotate these .bed file regions with genes (plus distance) from aforementioned database dumps, interface with DAVID to create functional annotation and gene ontology enrichment charts based on gene lists (such as those generated from input .bed files) and finally visualise and compare these enrichments using either directed acyclic graphs or scatterplots. biocViews: GeneSetEnrichment, MultipleComparison, GO, Visualization Author: Sam D. Bassett [aut], Ashley J. Waardenberg [aut, cre] Maintainer: Ashley J. Waardenberg git_url: https://git.bioconductor.org/packages/CompGO git_branch: RELEASE_3_8 git_last_commit: 3bd7acb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CompGO_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CompGO_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CompGO_1.18.0.tgz vignettes: vignettes/CompGO/inst/doc/CompGO-Intro.pdf vignetteTitles: Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CompGO/inst/doc/CompGO-Intro.R Package: ComplexHeatmap Version: 1.20.0 Depends: R (>= 3.1.2), methods, grid, graphics, stats, grDevices Imports: circlize (>= 0.4.1), GetoptLong, colorspace, RColorBrewer, GlobalOptions (>= 0.1.0) Suggests: testthat (>= 0.3), knitr, markdown, cluster, MASS, pvclust, dendsort, HilbertCurve, Cairo, png, jpeg, tiff, fastcluster, dendextend (>= 1.0.1) License: MIT + file LICENSE MD5sum: 456f36170972af9de5e366781054c561 NeedsCompilation: no Title: Making Complex Heatmaps Description: Complex heatmaps are efficient to visualize associations between different sources of data sets and reveal potential structures. Here the ComplexHeatmap package provides a highly flexible way to arrange multiple heatmaps and supports self-defined annotation graphics. biocViews: Software, Visualization, Sequencing Author: Zuguang Gu Maintainer: Zuguang Gu URL: https://github.com/jokergoo/ComplexHeatmap VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ComplexHeatmap git_branch: RELEASE_3_8 git_last_commit: 1501ecc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ComplexHeatmap_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ComplexHeatmap_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ComplexHeatmap_1.20.0.tgz vignettes: vignettes/ComplexHeatmap/inst/doc/s1.introduction.html, vignettes/ComplexHeatmap/inst/doc/s2.single_heatmap.html, vignettes/ComplexHeatmap/inst/doc/s3.a_list_of_heatmaps.html, vignettes/ComplexHeatmap/inst/doc/s4.heatmap_annotation.html, vignettes/ComplexHeatmap/inst/doc/s5.legend.html, vignettes/ComplexHeatmap/inst/doc/s6.heatmap_decoration.html, vignettes/ComplexHeatmap/inst/doc/s7.interactive.html, vignettes/ComplexHeatmap/inst/doc/s8.oncoprint.html, vignettes/ComplexHeatmap/inst/doc/s9.examples.html vignetteTitles: 1. Introduction to ComplexHeatmap package, 2. Making a single heatmap, 3. Making a list of Heatmaps, 4. Heatmap Annotations, 5. Heatmap and Annotation Legends, 6. Heatmap Decoration, 7. Interactive with Heatmaps, 8. OncoPrint, 9. More Examples hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ComplexHeatmap/inst/doc/s1.introduction.R, vignettes/ComplexHeatmap/inst/doc/s2.single_heatmap.R, vignettes/ComplexHeatmap/inst/doc/s3.a_list_of_heatmaps.R, vignettes/ComplexHeatmap/inst/doc/s4.heatmap_annotation.R, vignettes/ComplexHeatmap/inst/doc/s5.legend.R, vignettes/ComplexHeatmap/inst/doc/s6.heatmap_decoration.R, vignettes/ComplexHeatmap/inst/doc/s7.interactive.R, vignettes/ComplexHeatmap/inst/doc/s8.oncoprint.R, vignettes/ComplexHeatmap/inst/doc/s9.examples.R dependsOnMe: EnrichedHeatmap, recoup importsMe: artMS, BiocOncoTK, CATALYST, COCOA, DEComplexDisease, DEGreport, DEP, diffcyt, ELMER, EnrichmentBrowser, fCCAC, ImpulseDE2, LineagePulse, maftools, MWASTools, PathoStat, singleCellTK, TCGAbiolinks, YAPSA suggestsMe: gtrellis, HilbertCurve, TimeSeriesExperiment Package: condcomp Version: 1.0.1 Depends: R (>= 3.5.0) Imports: cluster, ggplot2, ggrepel, outliers Suggests: testthat, knitr, rmarkdown, BiocStyle, Matrix, Seurat, monocle, HSMMSingleCell License: GPL (>=2) | file LICENSE MD5sum: 19e58e283d0ffc5e9a5fccf562513f20 NeedsCompilation: no Title: Condition Comparison in scRNA-seq Data Description: For a given clustered data, which can also be split into two conditions, this package provides a way to perform a condition comparison on said clustered data. The comparison is performed on each cluster. Several statistics are used and, when analysed in conjunction, they might give some insight regarding the heterogeneity of some of the clusters. biocViews: ImmunoOncology, Clustering, SingleCell, Visualization Author: Diogo P. P. Branco [aut, cre] Maintainer: Diogo P. P. Branco VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/condcomp git_branch: RELEASE_3_8 git_last_commit: 8dafee7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/condcomp_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/condcomp_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/condcomp_1.0.1.tgz vignettes: vignettes/condcomp/inst/doc/condcomp.html vignetteTitles: scRNA-seq data heterogeneity with condcomp hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/condcomp/inst/doc/condcomp.R Package: CONFESS Version: 1.10.1 Depends: R (>= 3.3),grDevices,utils,stats,graphics Imports: methods,changepoint,cluster,contrast,data.table(>= 1.9.7),ecp,EBImage,flexmix,flowCore,flowClust,flowMeans,flowMerge,flowPeaks,foreach,ggplot2,grid,limma,MASS,moments,outliers,parallel,plotrix,raster,readbitmap,reshape2,SamSPECTRAL,waveslim,wavethresh,zoo Suggests: BiocStyle, knitr, rmarkdown, CONFESSdata License: GPL-2 MD5sum: 5fa9f3d2b4d02fdf8964f10fa9bf83b0 NeedsCompilation: no Title: Cell OrderiNg by FluorEScence Signal Description: Single Cell Fluidigm Spot Detector. biocViews: ImmunoOncology, GeneExpression,DataImport,CellBiology,Clustering,RNASeq,QualityControl,Visualization,TimeCourse,Regression,Classification Author: Diana LOW and Efthimios MOTAKIS Maintainer: Diana LOW VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CONFESS git_branch: RELEASE_3_8 git_last_commit: 8e722e9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CONFESS_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CONFESS_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CONFESS_1.10.1.tgz vignettes: vignettes/CONFESS/inst/doc/vignette_tex.pdf, vignettes/CONFESS/inst/doc/vignette.html vignetteTitles: CONFESS, CONFESS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CONFESS/inst/doc/vignette_tex.R, vignettes/CONFESS/inst/doc/vignette.R Package: consensus Version: 1.0.3 Depends: R (>= 3.5), RColorBrewer Imports: matrixStats, gplots, grDevices, methods, graphics, stats, utils Suggests: knitr, RUnit, rmarkdown, BiocGenerics License: BSD_3_clause + file LICENSE MD5sum: f99a2435304184087002c5c50f04d732 NeedsCompilation: no Title: Cross-platform consensus analysis of genomic measurements via interlaboratory testing method Description: An implementation of the American Society for Testing and Materials (ASTM) Standard E691 for interlaboratory testing procedures, designed for cross-platform genomic measurements. Given three (3) or more genomic platforms or laboratory protocols, this package provides interlaboratory testing procedures giving per-locus comparisons for sensitivity and precision between platforms. biocViews: ImmunoOncology, QualityControl, Regression, DataRepresentation, GeneExpression, Microarray, RNASeq Author: Tim Peters Maintainer: Tim Peters VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/consensus git_branch: RELEASE_3_8 git_last_commit: ff11338 git_last_commit_date: 2019-03-05 Date/Publication: 2019-03-06 source.ver: src/contrib/consensus_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/consensus_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/consensus_1.0.3.tgz vignettes: vignettes/consensus/inst/doc/consensus.pdf vignetteTitles: Fitting and visualising row-linear models with \texttt{consensus} hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/consensus/inst/doc/consensus.R Package: ConsensusClusterPlus Version: 1.46.0 Imports: Biobase, ALL, graphics, stats, utils, cluster License: GPL version 2 MD5sum: e53f78c29f4dc2a0a9feaf93acb4c71f NeedsCompilation: no Title: ConsensusClusterPlus Description: algorithm for determining cluster count and membership by stability evidence in unsupervised analysis biocViews: Software, Clustering Author: Matt Wilkerson , Peter Waltman Maintainer: Matt Wilkerson git_url: https://git.bioconductor.org/packages/ConsensusClusterPlus git_branch: RELEASE_3_8 git_last_commit: ed23703 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ConsensusClusterPlus_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ConsensusClusterPlus_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ConsensusClusterPlus_1.46.0.tgz vignettes: vignettes/ConsensusClusterPlus/inst/doc/ConsensusClusterPlus.pdf vignetteTitles: ConsensusClusterPlus Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ConsensusClusterPlus/inst/doc/ConsensusClusterPlus.R importsMe: CancerSubtypes, CATALYST, CVE, DEGreport, FlowSOM, TCGAbiolinks Package: consensusDE Version: 1.0.6 Depends: R (>= 3.5), BiocGenerics Imports: limma, AnnotationDbi, Biobase, edgeR, BiocParallel, GenomicAlignments, EDASeq, RColorBrewer, GenomicFeatures, SummarizedExperiment, DESeq2 (>= 1.20.0), pcaMethods, dendextend, RUVSeq, Rsamtools, S4Vectors, stats, TxDb.Dmelanogaster.UCSC.dm3.ensGene, airway, Biostrings Suggests: knitr, rmarkdown License: GPL-3 MD5sum: 23aac5279f7b644e139838a24e69fc6c NeedsCompilation: no Title: RNA-seq analysis using multiple algorithms Description: This package allows users to perform DE analysis using multiple algorithms. It seeks consensus from multiple methods. Currently it supports "Voom", "EdgeR" and "DESeq". It uses RUV-seq (optional) to remove batch effects. biocViews: Transcriptomics, MultipleComparison, Clustering Author: Ashley J. Waardenberg Maintainer: Ashley J. Waardenberg VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/consensusDE git_branch: RELEASE_3_8 git_last_commit: 8b922fe git_last_commit_date: 2019-01-31 Date/Publication: 2019-01-31 source.ver: src/contrib/consensusDE_1.0.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/consensusDE_1.0.6.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/consensusDE_1.0.6.tgz vignettes: vignettes/consensusDE/inst/doc/consensusDE.html vignetteTitles: consensusDE hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/consensusDE/inst/doc/consensusDE.R Package: consensusOV Version: 1.4.1 Depends: R (>= 3.4) Imports: Biobase, GSVA, gdata, genefu, limma, matrixStats, randomForest, stats, utils Suggests: knitr, ggplot2 License: Artistic-2.0 MD5sum: bae7c5cf0c2d5174dcde8cba046e1222 NeedsCompilation: no Title: Gene expression-based subtype classification for high-grade serous ovarian cancer Description: This package implements four major subtype classifiers for high-grade serous (HGS) ovarian cancer as described by Helland et al. (PLoS One, 2011), Bentink et al. (PLoS One, 2012), Verhaak et al. (J Clin Invest, 2013), and Konecny et al. (J Natl Cancer Inst, 2014). In addition, the package implements a consensus classifier, which consolidates and improves on the robustness of the proposed subtype classifiers, thereby providing reliable stratification of patients with HGS ovarian tumors of clearly defined subtype. biocViews: Classification, Clustering, DifferentialExpression, GeneExpression, Microarray, Transcriptomics Author: Gregory M Chen, Lavanya Kannan, Ludwig Geistlinger, Victor Kofia, Levi Waldron, Benjamin Haibe-Kains Maintainer: Benjamin Haibe-Kains URL: http://www.pmgenomics.ca/bhklab/software/consensusOV VignetteBuilder: knitr BugReports: https://github.com/bhklab/consensusOV/issues git_url: https://git.bioconductor.org/packages/consensusOV git_branch: RELEASE_3_8 git_last_commit: 861d677 git_last_commit_date: 2018-11-01 Date/Publication: 2018-11-01 source.ver: src/contrib/consensusOV_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/consensusOV_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/consensusOV_1.4.1.tgz vignettes: vignettes/consensusOV/inst/doc/consensusOV.html vignetteTitles: Molecular subtyping for ovarian cancer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/consensusOV/inst/doc/consensusOV.R Package: consensusSeekeR Version: 1.10.0 Depends: R (>= 2.10), BiocGenerics, IRanges, GenomicRanges, BiocParallel Imports: GenomeInfoDb, rtracklayer, stringr, S4Vectors, methods Suggests: BiocStyle, ggplot2, knitr, rmarkdown, RUnit License: Artistic-2.0 MD5sum: 32baf724416cf72420acc402a030cc1a NeedsCompilation: no Title: Detection of consensus regions inside a group of experiences using genomic positions and genomic ranges Description: This package compares genomic positions and genomic ranges from multiple experiments to extract common regions. The size of the analyzed region is adjustable as well as the number of experiences in which a feature must be present in a potential region to tag this region as a consensus region. biocViews: BiologicalQuestion, ChIPSeq, Genetics, MultipleComparison, Transcription, PeakDetection, Sequencing, Coverage Author: Astrid Deschenes [cre, aut], Fabien Claude Lamaze [ctb], Pascal Belleau [aut], Arnaud Droit [aut] Maintainer: Astrid Deschenes URL: https://github.com/ArnaudDroitLab/consensusSeekeR VignetteBuilder: knitr BugReports: https://github.com/ArnaudDroitLab/consensusSeekeR/issues git_url: https://git.bioconductor.org/packages/consensusSeekeR git_branch: RELEASE_3_8 git_last_commit: c44b75d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/consensusSeekeR_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/consensusSeekeR_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/consensusSeekeR_1.10.0.tgz vignettes: vignettes/consensusSeekeR/inst/doc/consensusSeekeR.html vignetteTitles: Detection of consensus regions inside a group of experiments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/consensusSeekeR/inst/doc/consensusSeekeR.R importsMe: RJMCMCNucleosomes Package: contiBAIT Version: 1.10.1 Depends: BH (>= 1.51.0-3), Rsamtools (>= 1.21) Imports: data.table, grDevices, clue, cluster, gplots, IRanges, GenomicRanges, S4Vectors, Rcpp, TSP, GenomicFiles, gtools, rtracklayer, BiocParallel, DNAcopy, colorspace, reshape2, ggplot2, methods, exomeCopy, GenomicAlignments, diagram LinkingTo: Rcpp, BH Suggests: BiocStyle License: BSD_2_clause + file LICENSE Archs: i386, x64 MD5sum: 77b17205ae95443880fe579df528c755 NeedsCompilation: yes Title: Improves Early Build Genome Assemblies using Strand-Seq Data Description: Using strand inheritance data from multiple single cells from the organism whose genome is to be assembled, contiBAIT can cluster unbridged contigs together into putative chromosomes, and order the contigs within those chromosomes. biocViews: ImmunoOncology, CellBasedAssays, QualityControl, WholeGenome, Genetics, GenomeAssembly Author: Kieran O'Neill, Mark Hills, Mike Gottlieb Maintainer: Kieran O'Neill git_url: https://git.bioconductor.org/packages/contiBAIT git_branch: RELEASE_3_8 git_last_commit: 750bd27 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/contiBAIT_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/contiBAIT_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/contiBAIT_1.10.1.tgz vignettes: vignettes/contiBAIT/inst/doc/contiBAIT.pdf vignetteTitles: flowBi hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/contiBAIT/inst/doc/contiBAIT.R Package: conumee Version: 1.16.0 Depends: R (>= 3.0), minfi, IlluminaHumanMethylation450kanno.ilmn12.hg19, IlluminaHumanMethylation450kmanifest, IlluminaHumanMethylationEPICanno.ilm10b2.hg19, IlluminaHumanMethylationEPICmanifest Imports: methods, stats, DNAcopy, rtracklayer, GenomicRanges, IRanges, GenomeInfoDb Suggests: BiocStyle, knitr, rmarkdown, minfiData, RCurl License: GPL (>= 2) MD5sum: cbf7b1712e25b8433f543f3d9d6459a1 NeedsCompilation: no Title: Enhanced copy-number variation analysis using Illumina DNA methylation arrays Description: This package contains a set of processing and plotting methods for performing copy-number variation (CNV) analysis using Illumina 450k or EPIC methylation arrays. biocViews: CopyNumberVariation, DNAMethylation, MethylationArray, Microarray, Normalization, Preprocessing, QualityControl, Software Author: Volker Hovestadt, Marc Zapatka Maintainer: Volker Hovestadt VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/conumee git_branch: RELEASE_3_8 git_last_commit: 4720c4a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/conumee_1.16.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/conumee_1.16.0.tgz vignettes: vignettes/conumee/inst/doc/conumee.html vignetteTitles: conumee hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/conumee/inst/doc/conumee.R Package: convert Version: 1.58.0 Depends: R (>= 2.6.0), Biobase (>= 1.15.33), limma (>= 1.7.0), marray, utils, methods License: LGPL MD5sum: 315f0cead1c62a2d4e898a1d7136c625 NeedsCompilation: no Title: Convert Microarray Data Objects Description: Define coerce methods for microarray data objects. biocViews: Infrastructure, Microarray, TwoChannel Author: Gordon Smyth , James Wettenhall , Yee Hwa (Jean Yang) , Martin Morgan Maintainer: Yee Hwa (Jean) Yang URL: http://bioinf.wehi.edu.au/limma/convert.html git_url: https://git.bioconductor.org/packages/convert git_branch: RELEASE_3_8 git_last_commit: df27c24 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/convert_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/convert_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/convert_1.58.0.tgz vignettes: vignettes/convert/inst/doc/convert.pdf vignetteTitles: Converting Between Microarray Data Classes hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: maigesPack, TurboNorm suggestsMe: BiocCaseStudies, dyebias, OLIN Package: copa Version: 1.50.0 Depends: Biobase, methods Suggests: colonCA License: Artistic-2.0 Archs: i386, x64 MD5sum: 0b6d430c7136ee40abaae1d099d2dfd1 NeedsCompilation: yes Title: Functions to perform cancer outlier profile analysis. Description: COPA is a method to find genes that undergo recurrent fusion in a given cancer type by finding pairs of genes that have mutually exclusive outlier profiles. biocViews: OneChannel, TwoChannel, DifferentialExpression, Visualization Author: James W. MacDonald Maintainer: James W. MacDonald git_url: https://git.bioconductor.org/packages/copa git_branch: RELEASE_3_8 git_last_commit: 070f7ae git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/copa_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/copa_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/copa_1.50.0.tgz vignettes: vignettes/copa/inst/doc/copa.pdf vignetteTitles: copa Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/copa/inst/doc/copa.R Package: copynumber Version: 1.22.0 Depends: R (>= 2.10), BiocGenerics Imports: S4Vectors, IRanges, GenomicRanges License: Artistic-2.0 MD5sum: d2ce25bf392279699524af3cf45cf4c2 NeedsCompilation: no Title: Segmentation of single- and multi-track copy number data by penalized least squares regression. Description: Penalized least squares regression is applied to fit piecewise constant curves to copy number data to locate genomic regions of constant copy number. Procedures are available for individual segmentation of each sample, joint segmentation of several samples and joint segmentation of the two data tracks from SNP-arrays. Several plotting functions are available for visualization of the data and the segmentation results. biocViews: aCGH, SNP, CopyNumberVariation, Genetics, Visualization Author: Gro Nilsen, Knut Liestoel and Ole Christian Lingjaerde. Maintainer: Gro Nilsen git_url: https://git.bioconductor.org/packages/copynumber git_branch: RELEASE_3_8 git_last_commit: 9273073 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/copynumber_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/copynumber_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/copynumber_1.22.0.tgz vignettes: vignettes/copynumber/inst/doc/copynumber.pdf vignetteTitles: copynumber.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/copynumber/inst/doc/copynumber.R Package: CopywriteR Version: 2.14.1 Depends: R(>= 3.2), BiocParallel Imports: matrixStats, gtools, data.table, S4Vectors, chipseq, IRanges, Rsamtools, DNAcopy, GenomicAlignments, GenomicRanges, CopyhelpeR, GenomeInfoDb, futile.logger Suggests: BiocStyle, SCLCBam, snow License: GPL-2 MD5sum: c1e89845437d840811120d8c955a9bd7 NeedsCompilation: no Title: Copy number information from targeted sequencing using off-target reads Description: CopywriteR extracts DNA copy number information from targeted sequencing by utiizing off-target reads. It allows for extracting uniformly distributed copy number information, can be used without reference, and can be applied to sequencing data obtained from various techniques including chromatin immunoprecipitation and target enrichment on small gene panels. Thereby, CopywriteR constitutes a widely applicable alternative to available copy number detection tools. biocViews: ImmunoOncology, TargetedResequencing, ExomeSeq, CopyNumberVariation, Preprocessing, Visualization, Coverage Author: Thomas Kuilman Maintainer: Oscar Krijgsman URL: https://github.com/PeeperLab/CopywriteR git_url: https://git.bioconductor.org/packages/CopywriteR git_branch: RELEASE_3_8 git_last_commit: b024236 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CopywriteR_2.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CopywriteR_2.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CopywriteR_2.14.1.tgz vignettes: vignettes/CopywriteR/inst/doc/CopywriteR.pdf vignetteTitles: CopywriteR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CopywriteR/inst/doc/CopywriteR.R Package: coRdon Version: 1.0.3 Depends: R (>= 3.5) Imports: methods, stats, utils, Biostrings, Biobase, dplyr, stringr, purrr, ggplot2, data.table Suggests: BiocStyle, testthat, knitr, rmarkdown License: Artistic-2.0 MD5sum: 42c868d02d1810af10e49bcfe0a53325 NeedsCompilation: no Title: Codon Usage Analysis and Prediction of Gene Expressivity Description: Tool for analysis of codon usage in various unannotated or KEGG/COG annotated DNA sequences. Calculates different measures of CU bias and CU-based predictors of gene expressivity, and performs gene set enrichment analysis for annotated sequences. Implements several methods for visualization of CU and enrichment analysis results. biocViews: Software, Metagenomics, GeneExpression, GeneSetEnrichment, GenePrediction, Visualization, KEGG, Pathways, Genetics CellBiology, BiomedicalInformatics, ImmunoOncology Author: Anamaria Elek [cre, aut], Maja Kuzman [aut], Kristian Vlahovicek [aut] Maintainer: Anamaria Elek URL: https://github.com/BioinfoHR/coRdon VignetteBuilder: knitr BugReports: https://github.com/BioinfoHR/coRdon/issues git_url: https://git.bioconductor.org/packages/coRdon git_branch: RELEASE_3_8 git_last_commit: d08a56a git_last_commit_date: 2019-01-02 Date/Publication: 2019-01-02 source.ver: src/contrib/coRdon_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/coRdon_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/coRdon_1.0.3.tgz vignettes: vignettes/coRdon/inst/doc/coRdon.html vignetteTitles: coRdon hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/coRdon/inst/doc/coRdon.R Package: CoRegNet Version: 1.20.0 Depends: R (>= 2.14), igraph, shiny, arules, methods Suggests: RColorBrewer, gplots, BiocStyle, knitr License: GPL-3 Archs: i386, x64 MD5sum: 9271a02c25c486a3becae3002e02590a NeedsCompilation: yes Title: CoRegNet : reconstruction and integrated analysis of co-regulatory networks Description: This package provides methods to identify active transcriptional programs. Methods and classes are provided to import or infer large scale co-regulatory network from transcriptomic data. The specificity of the encoded networks is to model Transcription Factor cooperation. External regulation evidences (TFBS, ChIP,...) can be integrated to assess the inferred network and refine it if necessary. Transcriptional activity of the regulators in the network can be estimated using an measure of their influence in a given sample. Finally, an interactive UI can be used to navigate through the network of cooperative regulators and to visualize their activity in a specific sample or subgroup sample. The proposed visualization tool can be used to integrate gene expression, transcriptional activity, copy number status, sample classification and a transcriptional network including co-regulation information. biocViews: NetworkInference, NetworkEnrichment, GeneRegulation, GeneExpression, GraphAndNetwork,SystemsBiology, Network, Visualization, Transcription Author: Remy Nicolle, Thibault Venzac and Mohamed Elati Maintainer: Remy Nicolle VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CoRegNet git_branch: RELEASE_3_8 git_last_commit: e355448 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CoRegNet_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CoRegNet_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CoRegNet_1.20.0.tgz vignettes: vignettes/CoRegNet/inst/doc/CoRegNet.html vignetteTitles: Custom Print Methods hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CoRegNet/inst/doc/CoRegNet.R Package: Cormotif Version: 1.28.0 Depends: R (>= 2.12.0), affy, limma Imports: affy, graphics, grDevices License: GPL-2 MD5sum: 23da3810b5bd4632e8cec7e5a23d132f NeedsCompilation: no Title: Correlation Motif Fit Description: It fits correlation motif model to multiple studies to detect study specific differential expression patterns. biocViews: Microarray, DifferentialExpression Author: Hongkai Ji, Yingying Wei Maintainer: Yingying Wei git_url: https://git.bioconductor.org/packages/Cormotif git_branch: RELEASE_3_8 git_last_commit: 24775d3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Cormotif_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Cormotif_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Cormotif_1.28.0.tgz vignettes: vignettes/Cormotif/inst/doc/CormotifVignette.pdf vignetteTitles: Cormotif Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Cormotif/inst/doc/CormotifVignette.R Package: CorMut Version: 1.24.0 Depends: methods,seqinr,igraph License: GPL-2 MD5sum: 87d0c12fe94d44ee994cf211b377db63 NeedsCompilation: no Title: Detect the correlated mutations based on selection pressure Description: CorMut provides functions for computing kaks for individual sites or specific amino acids and detecting correlated mutations among them. Three methods are provided for detecting correlated mutations ,including conditional selection pressure, mutual information and Jaccard index. The computation consists of two steps: First, the positive selection sites are detected; Second, the mutation correlations are computed among the positive selection sites. Note that the first step is optional. Meanwhile, CorMut facilitates the comparison of the correlated mutations between two conditions by the means of correlated mutation network. The reference sequence should be the first sequence of the sequence file, and does not allow the presence of gap. biocViews: Sequencing Author: Zhenpeng Li Maintainer: Zhenpeng Li git_url: https://git.bioconductor.org/packages/CorMut git_branch: RELEASE_3_8 git_last_commit: 78e4af6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CorMut_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CorMut_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CorMut_1.24.0.tgz vignettes: vignettes/CorMut/inst/doc/CorMut.pdf vignetteTitles: CorMut hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CorMut/inst/doc/CorMut.R Package: CORREP Version: 1.48.0 Imports: e1071, stats Suggests: cluster, MASS License: GPL (>= 2) MD5sum: bb75ae6c927d9b6ab112864dad047cf5 NeedsCompilation: no Title: Multivariate Correlation Estimator and Statistical Inference Procedures. Description: Multivariate correlation estimation and statistical inference. See package vignette. biocViews: Microarray, Clustering, GraphAndNetwork Author: Dongxiao Zhu and Youjuan Li Maintainer: Dongxiao Zhu git_url: https://git.bioconductor.org/packages/CORREP git_branch: RELEASE_3_8 git_last_commit: 7176b2f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CORREP_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CORREP_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CORREP_1.48.0.tgz vignettes: vignettes/CORREP/inst/doc/CORREP.pdf vignetteTitles: Multivariate Correlation Estimator hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CORREP/inst/doc/CORREP.R Package: coseq Version: 1.6.1 Depends: R (>= 3.4.0), SummarizedExperiment, S4Vectors Imports: edgeR, DESeq2, capushe, Rmixmod, e1071, BiocParallel, ggplot2 (>= 2.1.0), scales, HTSFilter, corrplot, HTSCluster (>= 2.0.8), grDevices, graphics, stats, methods, compositions, mvtnorm Suggests: Biobase, knitr, rmarkdown, testthat License: GPL (>=3) MD5sum: 1a9d9633f5eba88e917a491069f1f83c NeedsCompilation: no Title: Co-Expression Analysis of Sequencing Data Description: Co-expression analysis for expression profiles arising from high-throughput sequencing data. Feature (e.g., gene) profiles are clustered using adapted transformations and mixture models or a K-means algorithm, and model selection criteria (to choose an appropriate number of clusters) are provided. biocViews: ImmunoOncology, GeneExpression, RNASeq, Sequencing, Software Author: Andrea Rau, Cathy Maugis-Rabusseau, Antoine Godichon-Baggioni Maintainer: Andrea Rau VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/coseq git_branch: RELEASE_3_8 git_last_commit: 169b805 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/coseq_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/coseq_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/coseq_1.6.1.tgz vignettes: vignettes/coseq/inst/doc/coseq.html vignetteTitles: coseq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/coseq/inst/doc/coseq.R Package: cosmiq Version: 1.16.1 Depends: R (>= 3.0.2), Rcpp Imports: pracma, xcms, MassSpecWavelet, faahKO Suggests: RUnit, BiocGenerics, BiocStyle License: GPL-3 Archs: i386, x64 MD5sum: b26dc394e45a3ce9eac78550972aae03 NeedsCompilation: yes Title: cosmiq - COmbining Single Masses Into Quantities Description: cosmiq is a tool for the preprocessing of liquid- or gas - chromatography mass spectrometry (LCMS/GCMS) data with a focus on metabolomics or lipidomics applications. To improve the detection of low abundant signals, cosmiq generates master maps of the mZ/RT space from all acquired runs before a peak detection algorithm is applied. The result is a more robust identification and quantification of low-intensity MS signals compared to conventional approaches where peak picking is performed in each LCMS/GCMS file separately. The cosmiq package builds on the xcmsSet object structure and can be therefore integrated well with the package xcms as an alternative preprocessing step. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics Author: David Fischer , Christian Panse , Endre Laczko Maintainer: David Fischer , Christian Panse URL: http://www.bioconductor.org/packages/devel/bioc/html/cosmiq.html git_url: https://git.bioconductor.org/packages/cosmiq git_branch: RELEASE_3_8 git_last_commit: 5b7a4fc git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cosmiq_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cosmiq_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cosmiq_1.16.1.tgz vignettes: vignettes/cosmiq/inst/doc/cosmiq.pdf vignetteTitles: cosmiq primer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cosmiq/inst/doc/cosmiq.R Package: COSNet Version: 1.16.0 Suggests: bionetdata, PerfMeas, RUnit, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: ca0dbf84990b9770b2179ff397e5c407 NeedsCompilation: yes Title: Cost Sensitive Network for node label prediction on graphs with highly unbalanced labelings Description: Package that implements the COSNet classification algorithm. The algorithm predicts node labels in partially labeled graphs where few positives are available for the class being predicted. biocViews: GraphAndNetwork, Classification,Network, NeuralNetwork Author: Marco Frasca and Giorgio Valentini -- Universita' degli Studi di Milano Maintainer: Marco Frasca URL: https://github.com/m1frasca/COSNet_GitHub git_url: https://git.bioconductor.org/packages/COSNet git_branch: RELEASE_3_8 git_last_commit: c8939d8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/COSNet_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/COSNet_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/COSNet_1.16.0.tgz vignettes: vignettes/COSNet/inst/doc/COSNet_v.pdf vignetteTitles: An R Package for Predicting Binary Labels in Partially-Labeled Graphs hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/COSNet/inst/doc/COSNet_v.R Package: CountClust Version: 1.10.1 Depends: R (>= 3.4), ggplot2 (>= 2.1.0) Imports: SQUAREM, slam, maptpx, plyr(>= 1.7.1), cowplot, gtools, flexmix, picante, limma, parallel, reshape2, stats, utils, graphics, grDevices Suggests: knitr, kableExtra, BiocStyle, Biobase, roxygen2, RColorBrewer, devtools, xtable License: GPL (>= 2) MD5sum: 03a0134a9a835113a2614adafdc6ed3b NeedsCompilation: no Title: Clustering and Visualizing RNA-Seq Expression Data using Grade of Membership Models Description: Fits grade of membership models (GoM, also known as admixture models) to cluster RNA-seq gene expression count data, identifies characteristic genes driving cluster memberships, and provides a visual summary of the cluster memberships. biocViews: ImmunoOncology, RNASeq, GeneExpression, Clustering, Sequencing, StatisticalMethod, Software, Visualization Author: Kushal Dey [aut, cre], Joyce Hsiao [aut], Matthew Stephens [aut] Maintainer: Kushal Dey URL: https://github.com/kkdey/CountClust VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CountClust git_branch: RELEASE_3_8 git_last_commit: 3ab58f4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CountClust_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CountClust_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CountClust_1.10.1.tgz vignettes: vignettes/CountClust/inst/doc/count-clust.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CountClust/inst/doc/count-clust.R Package: countsimQC Version: 1.0.1 Depends: R (>= 3.5) Imports: rmarkdown (>= 0.9.5), edgeR, DESeq2 (>= 1.16.0), dplyr, tidyr, ggplot2, grDevices, tools, SummarizedExperiment, genefilter, DT, GenomeInfoDbData, caTools, randtests, stats, utils, methods Suggests: knitr, testthat License: GPL (>=2) MD5sum: 3ad101e19f6282334ef36193bff470b5 NeedsCompilation: no Title: Compare Characteristic Features of Count Data Sets Description: countsimQC provides functionality to create a comprehensive report comparing a broad range of characteristics across a collection of count matrices. One important use case is the comparison of one or more synthetic count matrices to a real count matrix, possibly the one underlying the simulations. However, any collection of count matrices can be compared. biocViews: ImmunoOncology, Microbiome, RNASeq, SingleCell, ExperimentalDesign, QualityControl, ReportWriting, Visualization Author: Charlotte Soneson Maintainer: Charlotte Soneson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/countsimQC git_branch: RELEASE_3_8 git_last_commit: 47669e3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/countsimQC_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/countsimQC_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/countsimQC_1.0.1.tgz vignettes: vignettes/countsimQC/inst/doc/countsimQC.html vignetteTitles: countsimQC User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/countsimQC/inst/doc/countsimQC.R Package: covEB Version: 1.8.1 Depends: R (>= 3.3), mvtnorm, igraph, gsl, Biobase, stats, LaplacesDemon, Matrix Suggests: curatedBladderData License: GPL-3 MD5sum: 4182aa09e1d296f5afda14d7b1d0adb1 NeedsCompilation: no Title: Empirical Bayes estimate of block diagonal covariance matrices Description: Using bayesian methods to estimate correlation matrices assuming that they can be written and estimated as block diagonal matrices. These block diagonal matrices are determined using shrinkage parameters that values below this parameter to zero. biocViews: ImmunoOncology, Bayesian, Microarray, RNASeq, Preprocessing, Software, GeneExpression, StatisticalMethod Author: C. Pacini Maintainer: C. Pacini git_url: https://git.bioconductor.org/packages/covEB git_branch: RELEASE_3_8 git_last_commit: 7f4ad82 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/covEB_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/covEB_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/covEB_1.8.1.tgz vignettes: vignettes/covEB/inst/doc/covEB.pdf vignetteTitles: covEB hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/covEB/inst/doc/covEB.R Package: CoverageView Version: 1.20.1 Depends: R (>= 2.10), methods, Rsamtools (>= 1.19.17), rtracklayer Imports: S4Vectors (>= 0.7.21), IRanges(>= 2.3.23), GenomicRanges, GenomicAlignments, parallel, tools License: Artistic-2.0 MD5sum: 68629ded2b4507bf473a5acfd9e27205 NeedsCompilation: no Title: Coverage visualization package for R Description: This package provides a framework for the visualization of genome coverage profiles. It can be used for ChIP-seq experiments, but it can be also used for genome-wide nucleosome positioning experiments or other experiment types where it is important to have a framework in order to inspect how the coverage distributed across the genome biocViews: ImmunoOncology, Visualization,RNASeq,ChIPSeq,Sequencing,Technology,Software Author: Ernesto Lowy Maintainer: Ernesto Lowy git_url: https://git.bioconductor.org/packages/CoverageView git_branch: RELEASE_3_8 git_last_commit: d5e37d9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CoverageView_1.20.1.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CoverageView_1.20.1.tgz vignettes: vignettes/CoverageView/inst/doc/CoverageView.pdf vignetteTitles: Easy visualization of the read coverage hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CoverageView/inst/doc/CoverageView.R Package: covRNA Version: 1.8.0 Depends: ade4, Biobase Imports: parallel, genefilter, grDevices, stats, graphics Suggests: BiocStyle, knitr, rmarkdown License: GPL (>= 2) MD5sum: 808e8c797079d7a87f802b5d45935d73 NeedsCompilation: no Title: Multivariate Analysis of Transcriptomic Data Description: This package provides the analysis methods fourthcorner and RLQ analysis for large-scale transcriptomic data. biocViews: GeneExpression, Transcription Author: Lara Urban Maintainer: Lara Urban VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/covRNA git_branch: RELEASE_3_8 git_last_commit: 7863700 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/covRNA_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/covRNA_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/covRNA_1.8.0.tgz vignettes: vignettes/covRNA/inst/doc/covRNA.html vignetteTitles: An Introduction to covRNA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/covRNA/inst/doc/covRNA.R Package: cpvSNP Version: 1.14.0 Depends: R (>= 2.10), GenomicFeatures, GSEABase (>= 1.24.0) Imports: methods, corpcor, BiocParallel, ggplot2, plyr Suggests: TxDb.Hsapiens.UCSC.hg19.knownGene, RUnit, BiocGenerics, ReportingTools, BiocStyle License: Artistic-2.0 MD5sum: 398ce7f3fde5ae72b9a0c171902351b0 NeedsCompilation: no Title: Gene set analysis methods for SNP association p-values that lie in genes in given gene sets Description: Gene set analysis methods exist to combine SNP-level association p-values into gene sets, calculating a single association p-value for each gene set. This package implements two such methods that require only the calculated SNP p-values, the gene set(s) of interest, and a correlation matrix (if desired). One method (GLOSSI) requires independent SNPs and the other (VEGAS) can take into account correlation (LD) among the SNPs. Built-in plotting functions are available to help users visualize results. biocViews: Genetics, StatisticalMethod, Pathways, GeneSetEnrichment, GenomicVariation Author: Caitlin McHugh, Jessica Larson, and Jason Hackney Maintainer: Caitlin McHugh git_url: https://git.bioconductor.org/packages/cpvSNP git_branch: RELEASE_3_8 git_last_commit: 483b769 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cpvSNP_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cpvSNP_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cpvSNP_1.14.0.tgz vignettes: vignettes/cpvSNP/inst/doc/cpvSNP.pdf vignetteTitles: Running gene set analyses with the "cpvSNP" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cpvSNP/inst/doc/cpvSNP.R Package: cqn Version: 1.28.1 Depends: R (>= 2.10.0), mclust, nor1mix, stats, preprocessCore, splines, quantreg Imports: splines Suggests: scales, edgeR License: Artistic-2.0 MD5sum: 10f10966d2d261d5414153e73eaa0618 NeedsCompilation: no Title: Conditional quantile normalization Description: A normalization tool for RNA-Seq data, implementing the conditional quantile normalization method. biocViews: ImmunoOncology, RNASeq, Preprocessing, DifferentialExpression Author: Jean (Zhijin) Wu, Kasper Daniel Hansen Maintainer: Kasper Daniel Hansen git_url: https://git.bioconductor.org/packages/cqn git_branch: RELEASE_3_8 git_last_commit: e51ca3e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cqn_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cqn_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cqn_1.28.1.tgz vignettes: vignettes/cqn/inst/doc/cqn.pdf vignetteTitles: CQN (Conditional Quantile Normalization) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cqn/inst/doc/cqn.R importsMe: tweeDEseq Package: CRImage Version: 1.30.0 Depends: EBImage, DNAcopy, aCGH Imports: MASS, e1071, foreach, sgeostat License: Artistic-2.0 MD5sum: fcab4dae1b32b2a00aedf7c509307ac9 NeedsCompilation: no Title: CRImage a package to classify cells and calculate tumour cellularity Description: CRImage provides functionality to process and analyze images, in particular to classify cells in biological images. Furthermore, in the context of tumor images, it provides functionality to calculate tumour cellularity. biocViews: CellBiology, Classification Author: Henrik Failmezger , Yinyin Yuan , Oscar Rueda , Florian Markowetz Maintainer: Henrik Failmezger , Yinyin Yuan git_url: https://git.bioconductor.org/packages/CRImage git_branch: RELEASE_3_8 git_last_commit: 8444e4e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CRImage_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CRImage_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CRImage_1.30.0.tgz vignettes: vignettes/CRImage/inst/doc/CRImage.pdf vignetteTitles: CRImage Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CRImage/inst/doc/CRImage.R Package: CRISPRseek Version: 1.22.1 Depends: R (>= 3.0.1), BiocGenerics, Biostrings Imports: parallel, data.table, seqinr, S4Vectors (>= 0.9.25), IRanges, BSgenome, BiocParallel, hash Suggests: RUnit, BiocStyle, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db License: GPL (>= 2) MD5sum: 6cc20a2e3dc2d57d8a1f6ee6b7f21da3 NeedsCompilation: no Title: Design of target-specific guide RNAs in CRISPR-Cas9, genome-editing systems Description: The package includes functions to find potential guide RNAs for input target sequences, optionally filter guide RNAs without restriction enzyme cut site, or without paired guide RNAs, genome-wide search for off-targets, score, rank, fetch flank sequence and indicate whether the target and off-targets are located in exon region or not. Potential guide RNAs are annotated with total score of the top5 and topN off-targets, detailed topN mismatch sites, restriction enzyme cut sites, and paired guide RNAs. This package leverages Biostrings and BSgenome packages. biocViews: ImmunoOncology, GeneRegulation, SequenceMatching, CRISPR Author: Lihua Julie Zhu, Benjamin R. Holmes, Hervé Pagès, Michael Lawrence, Isana Veksler-Lublinsky, Victor Ambros, Neil Aronin and Michael Brodsky Maintainer: Lihua Julie Zhu git_url: https://git.bioconductor.org/packages/CRISPRseek git_branch: RELEASE_3_8 git_last_commit: 23b3bb4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CRISPRseek_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CRISPRseek_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CRISPRseek_1.22.1.tgz vignettes: vignettes/CRISPRseek/inst/doc/CRISPRseek.pdf vignetteTitles: CRISPRseek Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CRISPRseek/inst/doc/CRISPRseek.R dependsOnMe: crisprseekplus importsMe: GUIDEseq Package: crisprseekplus Version: 1.8.0 Depends: R (>= 3.3.0), shiny, shinyjs, CRISPRseek Imports: DT, utils, GUIDEseq, GenomicRanges, GenomicFeatures, BiocManager, BSgenome, AnnotationDbi, hash Suggests: testthat, rmarkdown, knitr, R.rsp License: GPL-3 + file LICENSE MD5sum: 555d70d98d046f584dc4ec325ba9c6cd NeedsCompilation: no Title: crisprseekplus Description: Bioinformatics platform containing interface to work with offTargetAnalysis and compare2Sequences in the CRISPRseek package, and GUIDEseqAnalysis. biocViews: GeneRegulation, SequenceMatching, Software Author: Sophie Wigmore , Alper Kucukural , Lihua Julie Zhu , Michael Brodsky , Manuel Garber Maintainer: Alper Kucukural URL: https://github.com/UMMS-Biocore/crisprseekplus VignetteBuilder: knitr, R.rsp BugReports: https://github.com/UMMS-Biocore/crisprseekplus/issues/new git_url: https://git.bioconductor.org/packages/crisprseekplus git_branch: RELEASE_3_8 git_last_commit: 17b4034 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/crisprseekplus_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/crisprseekplus_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/crisprseekplus_1.8.0.tgz vignettes: vignettes/crisprseekplus/inst/doc/crisprseekplus.html vignetteTitles: DEBrowser Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/crisprseekplus/inst/doc/crisprseekplus.R Package: CrispRVariants Version: 1.10.1 Depends: R (>= 3.5), ggplot2 (>= 2.2.0) Imports: AnnotationDbi, BiocParallel, Biostrings, methods, GenomeInfoDb, GenomicAlignments, GenomicRanges, grDevices, grid, gridExtra, IRanges, reshape2, Rsamtools, S4Vectors (>= 0.9.38), utils Suggests: BiocStyle, gdata, GenomicFeatures, knitr, rmarkdown, rtracklayer, sangerseqR, testthat, VariantAnnotation License: GPL-2 MD5sum: 40f8efb7e795e313e6e13ff4dc506a6d NeedsCompilation: no Title: Tools for counting and visualising mutations in a target location Description: CrispRVariants provides tools for analysing the results of a CRISPR-Cas9 mutagenesis sequencing experiment, or other sequencing experiments where variants within a given region are of interest. These tools allow users to localize variant allele combinations with respect to any genomic location (e.g. the Cas9 cut site), plot allele combinations and calculate mutation rates with flexible filtering of unrelated variants. biocViews: ImmunoOncology, CRISPR, GenomicVariation, VariantDetection, GeneticVariability, DataRepresentation, Visualization Author: Helen Lindsay [aut, cre] Maintainer: Helen Lindsay VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CrispRVariants git_branch: RELEASE_3_8 git_last_commit: 8269b06 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CrispRVariants_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CrispRVariants_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CrispRVariants_1.10.1.tgz vignettes: vignettes/CrispRVariants/inst/doc/user_guide.pdf vignetteTitles: CrispRVariants hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CrispRVariants/inst/doc/user_guide.R Package: crlmm Version: 1.40.0 Depends: R (>= 2.14.0), oligoClasses (>= 1.21.12), preprocessCore (>= 1.17.7) Imports: methods, Biobase (>= 2.15.4), BiocGenerics, affyio (>= 1.23.2), illuminaio, ellipse, mvtnorm, splines, stats, SNPchip, utils, lattice, ff, foreach, RcppEigen (>= 0.3.1.2.1), matrixStats, VGAM, parallel, graphics, limma, beanplot LinkingTo: preprocessCore (>= 1.17.7) Suggests: hapmapsnp6, genomewidesnp6Crlmm (>= 1.0.7), GGdata, snpStats, RUnit License: Artistic-2.0 Archs: i386, x64 MD5sum: 0297a5176d679d97b5465292552b151b NeedsCompilation: yes Title: Genotype Calling (CRLMM) and Copy Number Analysis tool for Affymetrix SNP 5.0 and 6.0 and Illumina arrays Description: Faster implementation of CRLMM specific to SNP 5.0 and 6.0 arrays, as well as a copy number tool specific to 5.0, 6.0, and Illumina platforms. biocViews: Microarray, Preprocessing, SNP, CopyNumberVariation Author: Benilton S Carvalho, Robert Scharpf, Matt Ritchie, Ingo Ruczinski, Rafael A Irizarry Maintainer: Benilton S Carvalho , Robert Scharpf , Matt Ritchie git_url: https://git.bioconductor.org/packages/crlmm git_branch: RELEASE_3_8 git_last_commit: 95b6fe6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/crlmm_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/crlmm_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/crlmm_1.40.0.tgz vignettes: vignettes/crlmm/inst/doc/AffyGW.pdf, vignettes/crlmm/inst/doc/CopyNumberOverview.pdf, vignettes/crlmm/inst/doc/genotyping.pdf, vignettes/crlmm/inst/doc/gtypeDownstream.pdf, vignettes/crlmm/inst/doc/IlluminaPreprocessCN.pdf, vignettes/crlmm/inst/doc/Infrastructure.pdf vignetteTitles: Copy number estimation, Overview of copy number vignettes, crlmm Vignette - Genotyping, crlmm Vignette - Downstream Analysis, Preprocessing and genotyping Illumina arrays for copy number analysis, Infrastructure for copy number analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/crlmm/inst/doc/genotyping.R importsMe: VanillaICE suggestsMe: ArrayTV, oligoClasses, SNPchip Package: crossmeta Version: 1.8.0 Depends: R (>= 3.3) Imports: affy (>= 1.52.0), affxparser (>= 1.46.0), AnnotationDbi (>= 1.36.2), Biobase (>= 2.34.0), BiocGenerics (>= 0.20.0), BiocManager (>= 1.24.0), ccmap, DT (>= 0.2), data.table (>= 1.10.4), doParallel (>= 1.0.10), doRNG (>= 1.6), fdrtool (>= 1.2.15), foreach (>= 1.4.3), ggplot2 (>= 2.2.1), GEOquery (>= 2.40.0), limma (>= 3.30.13), matrixStats (>= 0.51.0), metaMA (>= 3.1.2), metap (>= 0.8), miniUI (>= 0.1.1), oligo (>= 1.38.0), pander (>= 0.6.0), plotly(>= 4.5.6), reshape (>= 0.8.6), RColorBrewer (>= 1.1.2), rdrop2 (>= 0.7.0), stringr (>= 1.2.0), sva (>= 3.22.0), shiny (>= 1.0.0), stats (>= 3.3.3) Suggests: knitr, rmarkdown, lydata, org.Hs.eg.db, testthat, ccdata License: MIT + file LICENSE MD5sum: 8ca286bce5ef78116e67a41eea184ed2 NeedsCompilation: no Title: Cross Platform Meta-Analysis of Microarray Data Description: Implements cross-platform and cross-species meta-analyses of Affymentrix, Illumina, and Agilent microarray data. This package automates common tasks such as downloading, normalizing, and annotating raw GEO data. The user then selects control and treatment samples in order to perform differential expression/pathway analyses for all comparisons. After analysing each contrast seperately, the user can select tissue sources for each contrast and specify any tissue sources that should be grouped for the subsequent meta-analyses. Finally, effect size and pathway meta-analyses can proceed and the results graphically explored. biocViews: GeneExpression, Transcription, DifferentialExpression, Microarray, TissueMicroarray, OneChannel, Annotation, BatchEffect, Preprocessing, GUI Author: Alex Pickering Maintainer: Alex Pickering VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/crossmeta git_branch: RELEASE_3_8 git_last_commit: 032522f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/crossmeta_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/crossmeta_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/crossmeta_1.8.0.tgz vignettes: vignettes/crossmeta/inst/doc/crossmeta-vignette.html vignetteTitles: crossmeta vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/crossmeta/inst/doc/crossmeta-vignette.R suggestsMe: ccmap Package: CSAR Version: 1.34.0 Depends: R (>= 2.15.0), S4Vectors, IRanges, GenomeInfoDb, GenomicRanges Imports: stats, utils Suggests: ShortRead, Biostrings License: Artistic-2.0 Archs: i386, x64 MD5sum: cb843cd969ee7b70323486c565279993 NeedsCompilation: yes Title: Statistical tools for the analysis of ChIP-seq data Description: Statistical tools for ChIP-seq data analysis. The package includes the statistical method described in Kaufmann et al. (2009) PLoS Biology: 7(4):e1000090. Briefly, Taking the average DNA fragment size subjected to sequencing into account, the software calculates genomic single-nucleotide read-enrichment values. After normalization, sample and control are compared using a test based on the Poisson distribution. Test statistic thresholds to control the false discovery rate are obtained through random permutation. biocViews: ChIPSeq, Transcription, Genetics Author: Jose M Muino Maintainer: Jose M Muino git_url: https://git.bioconductor.org/packages/CSAR git_branch: RELEASE_3_8 git_last_commit: 5df1841 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CSAR_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CSAR_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CSAR_1.34.0.tgz vignettes: vignettes/CSAR/inst/doc/CSAR.pdf vignetteTitles: CSAR Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CSAR/inst/doc/CSAR.R importsMe: NarrowPeaks suggestsMe: NarrowPeaks Package: csaw Version: 1.16.1 Depends: R (>= 3.5), GenomicRanges, SummarizedExperiment, BiocParallel Imports: Rcpp, BiocGenerics, Rsamtools, edgeR, limma, GenomicFeatures, AnnotationDbi, methods, S4Vectors, IRanges, GenomeInfoDb, stats LinkingTo: Rhtslib (>= 1.13.1), zlibbioc, Rcpp Suggests: org.Mm.eg.db, TxDb.Mmusculus.UCSC.mm10.knownGene, testthat License: GPL-3 Archs: i386, x64 MD5sum: 82d3daa64a0e7d2fc765c0194bae718a NeedsCompilation: yes Title: ChIP-Seq Analysis with Windows Description: Detection of differentially bound regions in ChIP-seq data with sliding windows, with methods for normalization and proper FDR control. biocViews: MultipleComparison, ChIPSeq, Normalization, Sequencing, Coverage, Genetics, Annotation, DifferentialPeakCalling Author: Aaron Lun [aut, cre], Gordon Smyth [aut] Maintainer: Aaron Lun SystemRequirements: C++11 git_url: https://git.bioconductor.org/packages/csaw git_branch: RELEASE_3_8 git_last_commit: 63ef4a6 git_last_commit_date: 2018-12-20 Date/Publication: 2018-12-21 source.ver: src/contrib/csaw_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/csaw_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/csaw_1.16.1.tgz vignettes: vignettes/csaw/inst/doc/csaw.pdf, vignettes/csaw/inst/doc/csawUserGuide.pdf vignetteTitles: csaw Vignette, csawUserGuide.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE importsMe: diffHic, icetea, NADfinder, vulcan Package: CSSP Version: 1.20.0 Imports: methods, splines, stats, utils Suggests: testthat License: GPL-2 Archs: i386, x64 MD5sum: 80255d123a4ba68f4b7bc8eafa0f30f8 NeedsCompilation: yes Title: ChIP-Seq Statistical Power Description: Power computation for ChIP-Seq data based on Bayesian estimation for local poisson counting process. biocViews: ChIPSeq, Sequencing, QualityControl, Bayesian Author: Chandler Zuo, Sunduz Keles Maintainer: Chandler Zuo git_url: https://git.bioconductor.org/packages/CSSP git_branch: RELEASE_3_8 git_last_commit: cbae27d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CSSP_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CSSP_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CSSP_1.20.0.tgz vignettes: vignettes/CSSP/inst/doc/cssp.pdf vignetteTitles: cssp.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CSSP/inst/doc/cssp.R Package: ctc Version: 1.56.0 Depends: amap License: GPL-2 MD5sum: fe42ef0d23d5e1861c71b74a423f17e6 NeedsCompilation: no Title: Cluster and Tree Conversion. Description: Tools for export and import classification trees and clusters to other programs biocViews: Microarray, Clustering, Classification, DataImport, Visualization Author: Antoine Lucas , Laurent Gautier Maintainer: Antoine Lucas URL: http://antoinelucas.free.fr/ctc git_url: https://git.bioconductor.org/packages/ctc git_branch: RELEASE_3_8 git_last_commit: cbd5bef git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ctc_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ctc_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ctc_1.56.0.tgz vignettes: vignettes/ctc/inst/doc/ctc.pdf vignetteTitles: Introduction to ctc hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ctc/inst/doc/ctc.R importsMe: miRLAB, multiClust Package: CTDquerier Version: 1.2.0 Depends: R (>= 3.4.0) Imports: RCurl, stringr, S4Vectors, stringdist, ggplot2, igraph, utils, grid, gridExtra, methods, stats, BiocFileCache, rappdirs Suggests: BiocStyle, knitr License: MIT + file LICENSE MD5sum: 30fbafbd91f9c7191e26145edd756856 NeedsCompilation: no Title: Package for CTDbase data query, visualization and downstream analysis Description: Package to retrieve and visualize data from the Comparative Toxicogenomics Database (http://ctdbase.org/). The downloaded data is formated as DataFrames for further downstream analyses. biocViews: Software, BiomedicalInformatics, Infrastructure, DataImport, DataRepresentation, GeneSetEnrichment, NetworkEnrichment, Pathways, Network, GO, KEGG Author: Carles Hernandez-Ferrer [aut, cre], Jaun R. Gonzalez [aut] Maintainer: Carles Hernandez-Ferrer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CTDquerier git_branch: RELEASE_3_8 git_last_commit: fd2eb0a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CTDquerier_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CTDquerier_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CTDquerier_1.2.0.tgz vignettes: vignettes/CTDquerier/inst/doc/batch_query.html, vignettes/CTDquerier/inst/doc/case_study.html, vignettes/CTDquerier/inst/doc/vignette.html vignetteTitles: Simple comparison between CTDquerier R package and CTDbase Batch Query web tool, Case study on Environmental Chemicals and asthma-related genes, CTDquerier: A package to retrieve CTDbase data for downstream analysis and data visualization hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/CTDquerier/inst/doc/batch_query.R, vignettes/CTDquerier/inst/doc/case_study.R, vignettes/CTDquerier/inst/doc/vignette.R Package: cTRAP Version: 1.0.3 Depends: R (>= 3.5.0) Imports: data.table, limma, stats, fgsea, pbapply, plyr, cowplot, ggplot2, rhdf5, R.utils, httr, methods, piano, readr, utils, graphics Suggests: testthat, knitr, covr, biomaRt License: MIT + file LICENSE MD5sum: df4aabaf7896ba049296d92bd7885506 NeedsCompilation: no Title: Identification of candidate causal perturbations from differential gene expression data Description: Compare differential gene expression results with those from known cellular perturbations (such as gene knock-down, overexpression or small molecules) derived from the Connectivity Map. Such analyses allow not only to infer the molecular causes of the observed difference in gene expression but also to identify small molecules that could drive or revert specific transcriptomic alterations. biocViews: DifferentialExpression, GeneExpression, RNASeq, Transcriptomics, Pathways, ImmunoOncology Author: Bernardo P. de Almeida [aut], Nuno Saraiva-Agostinho [aut, cre], Nuno L. Barbosa-Morais [aut, led] Maintainer: Nuno Saraiva-Agostinho URL: https://github.com/nuno-agostinho/cTRAP VignetteBuilder: knitr BugReports: https://github.com/nuno-agostinho/cTRAP/issues git_url: https://git.bioconductor.org/packages/cTRAP git_branch: RELEASE_3_8 git_last_commit: e97c3f1 git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/cTRAP_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/cTRAP_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cTRAP_1.0.3.tgz vignettes: vignettes/cTRAP/inst/doc/comparing_DGE_with_perturbations.html vignetteTitles: cTRAP: DGE comparison with cellular perturbations hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/cTRAP/inst/doc/comparing_DGE_with_perturbations.R Package: ctsGE Version: 1.8.1 Depends: R (>= 3.2) Imports: ccaPP, ggplot2, limma, reshape2, shiny, stats, stringr, utils Suggests: BiocStyle, dplyr, DT, GEOquery, knitr, pander, rmarkdown, testthat License: GPL-2 MD5sum: e0f29236a970966649b051d60ad320b1 NeedsCompilation: no Title: Clustering of Time Series Gene Expression data Description: Methodology for supervised clustering of potentially many predictor variables, such as genes etc., in time series datasets Provides functions that help the user assigning genes to predefined set of model profiles. biocViews: ImmunoOncology, GeneExpression, Transcription, DifferentialExpression, GeneSetEnrichment, Genetics, Bayesian, Clustering, TimeCourse, Sequencing, RNASeq Author: Michal Sharabi-Schwager [aut, cre], Ron Ophir [aut] Maintainer: Michal Sharabi-Schwager URL: https://github.com/michalsharabi/ctsGE VignetteBuilder: knitr BugReports: https://github.com/michalsharabi/ctsGE/issues git_url: https://git.bioconductor.org/packages/ctsGE git_branch: RELEASE_3_8 git_last_commit: dafd431 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ctsGE_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ctsGE_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ctsGE_1.8.1.tgz vignettes: vignettes/ctsGE/inst/doc/ctsGE.html vignetteTitles: ctsGE Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ctsGE/inst/doc/ctsGE.R Package: cummeRbund Version: 2.24.0 Depends: R (>= 2.7.0), BiocGenerics (>= 0.3.2), RSQLite, ggplot2, reshape2, fastcluster, rtracklayer, Gviz Imports: methods, plyr, BiocGenerics, S4Vectors (>= 0.9.25), Biobase Suggests: cluster, plyr, NMFN, stringr, GenomicFeatures, GenomicRanges, rjson License: Artistic-2.0 MD5sum: a713a35d1c8f2a837d9c5a8ab86b8f72 NeedsCompilation: no Title: Analysis, exploration, manipulation, and visualization of Cufflinks high-throughput sequencing data. Description: Allows for persistent storage, access, exploration, and manipulation of Cufflinks high-throughput sequencing data. In addition, provides numerous plotting functions for commonly used visualizations. biocViews: HighThroughputSequencing, HighThroughputSequencingData, RNAseq, RNAseqData, GeneExpression, DifferentialExpression, Infrastructure, DataImport, DataRepresentation, Visualization, Bioinformatics, Clustering, MultipleComparisons, QualityControl Author: L. Goff, C. Trapnell, D. Kelley Maintainer: Loyal A. Goff git_url: https://git.bioconductor.org/packages/cummeRbund git_branch: RELEASE_3_8 git_last_commit: 8287661 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cummeRbund_2.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cummeRbund_2.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cummeRbund_2.24.0.tgz vignettes: vignettes/cummeRbund/inst/doc/cummeRbund-example-workflow.pdf, vignettes/cummeRbund/inst/doc/cummeRbund-manual.pdf vignetteTitles: Sample cummeRbund workflow, CummeRbund User Guide hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cummeRbund/inst/doc/cummeRbund-example-workflow.R, vignettes/cummeRbund/inst/doc/cummeRbund-manual.R importsMe: meshr suggestsMe: IsoformSwitchAnalyzeR Package: customProDB Version: 1.22.1 Depends: R (>= 3.0.1), IRanges, AnnotationDbi, biomaRt(>= 2.17.1) Imports: S4Vectors (>= 0.9.25), DBI, GenomeInfoDb, GenomicRanges, Rsamtools (>= 1.10.2), GenomicAlignments, Biostrings (>= 2.26.3), GenomicFeatures (>= 1.32.0), stringr, RCurl, plyr, VariantAnnotation (>= 1.13.44), rtracklayer, RSQLite, AhoCorasickTrie, methods Suggests: RMariaDB, BSgenome.Hsapiens.UCSC.hg19 License: Artistic-2.0 MD5sum: 887c6d09551b4e59eb364a2067db556d NeedsCompilation: no Title: Generate customized protein database from NGS data, with a focus on RNA-Seq data, for proteomics search Description: Database search is the most widely used approach for peptide and protein identification in mass spectrometry-based proteomics studies. Our previous study showed that sample-specific protein databases derived from RNA-Seq data can better approximate the real protein pools in the samples and thus improve protein identification. More importantly, single nucleotide variations, short insertion and deletions and novel junctions identified from RNA-Seq data make protein database more complete and sample-specific. Here, we report an R package customProDB that enables the easy generation of customized databases from RNA-Seq data for proteomics search. This work bridges genomics and proteomics studies and facilitates cross-omics data integration. biocViews: ImmunoOncology, Sequencing, MassSpectrometry, Proteomics, SNP, RNASeq, Software, Transcription, AlternativeSplicing, FunctionalGenomics Author: Xiaojing Wang Maintainer: Xiaojing Wang Bo Wen git_url: https://git.bioconductor.org/packages/customProDB git_branch: RELEASE_3_8 git_last_commit: ce87d06 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/customProDB_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/customProDB_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/customProDB_1.22.1.tgz vignettes: vignettes/customProDB/inst/doc/customProDB.pdf vignetteTitles: Introduction to customProDB hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/customProDB/inst/doc/customProDB.R importsMe: PGA Package: CVE Version: 1.8.0 Depends: R (>= 3.4.0), tidyverse, plyr, ggplot2 Imports: shiny, ConsensusClusterPlus, RColorBrewer, gplots, jsonlite, ape, WGCNA Suggests: knitr, rmarkdown, RTCGAToolbox, testthat, BiocStyle License: GPL-3 MD5sum: b21a70bfa5c7401ffd91e3eb8be07d39 NeedsCompilation: no Title: Cancer Variant Explorer Description: Shiny app for interactive variant prioritisation in precision oncology. The input file for CVE is the output file of the recently released Oncotator Variant Annotation tool summarising variant-centric information from 14 different publicly available resources relevant for cancer researches. Interactive priortisation in CVE is based on known germline and cancer variants, DNA repair genes and functional prediction scores. An optional feature of CVE is the exploration of the tumour-specific pathway context that is facilitated using co-expression modules generated from publicly available transcriptome data. Finally druggability of prioritised variants is assessed using the Drug Gene Interaction Database (DGIdb). biocViews: BiomedicalInformatics Author: Andreas Mock [aut, cre] Maintainer: Andreas Mock VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CVE git_branch: RELEASE_3_8 git_last_commit: 3985d5c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/CVE_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/CVE_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CVE_1.8.0.tgz vignettes: vignettes/CVE/inst/doc/CVE_tutorial.html, vignettes/CVE/inst/doc/WGCNA_from_TCGA_RNAseq.html vignetteTitles: Cancer Variant Explorer (CVE) tutorial, Weighted gene co-expression network analysis with TCGA RNAseq data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CVE/inst/doc/CVE_tutorial.R, vignettes/CVE/inst/doc/WGCNA_from_TCGA_RNAseq.R Package: cycle Version: 1.36.0 Depends: R (>= 2.10.0), Mfuzz Imports: Biobase, stats License: GPL-2 MD5sum: 20c0540915e76d5897c280c086256c36 NeedsCompilation: no Title: Significance of periodic expression pattern in time-series data Description: Package for assessing the statistical significance of periodic expression based on Fourier analysis and comparison with data generated by different background models biocViews: Microarray, TimeCourse Author: Matthias Futschik Maintainer: Matthias Futschik URL: http://cycle.sysbiolab.eu git_url: https://git.bioconductor.org/packages/cycle git_branch: RELEASE_3_8 git_last_commit: c0d50b6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/cycle_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/cycle_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cycle_1.36.0.tgz vignettes: vignettes/cycle/inst/doc/cycle.pdf vignetteTitles: Introduction to cycle hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cycle/inst/doc/cycle.R Package: cydar Version: 1.6.1 Depends: BiocParallel, SingleCellExperiment Imports: viridis, methods, shiny, graphics, stats, grDevices, utils, BiocGenerics, S4Vectors, flowCore, Biobase, Rcpp, BiocNeighbors, SummarizedExperiment LinkingTo: Rcpp Suggests: ncdfFlow, testthat, knitr, edgeR, limma, glmnet, BiocStyle, flowStats License: GPL-3 Archs: i386, x64 MD5sum: 847f2c5b9d209029f56c40fb79261d4b NeedsCompilation: yes Title: Using Mass Cytometry for Differential Abundance Analyses Description: Identifies differentially abundant populations between samples and groups in mass cytometry data. Provides methods for counting cells into hyperspheres, controlling the spatial false discovery rate, and visualizing changes in abundance in the high-dimensional marker space. biocViews: ImmunoOncology, FlowCytometry, MultipleComparison, Proteomics, SingleCell Author: Aaron Lun [aut, cre] Maintainer: Aaron Lun SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cydar git_branch: RELEASE_3_8 git_last_commit: cce42fb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cydar_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cydar_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cydar_1.6.1.tgz vignettes: vignettes/cydar/inst/doc/cydar.html vignetteTitles: Detecting differentially abundant subpopulations in mass cytometry data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cydar/inst/doc/cydar.R Package: CytoDx Version: 1.2.1 Depends: R (>= 3.5) Imports: doParallel, dplyr, glmnet, rpart, rpart.plot, stats, flowCore,grDevices, graphics, utils Suggests: knitr License: GPL-2 MD5sum: 9e2a90f9e0816c38eb2c0d4c17a146e7 NeedsCompilation: no Title: Robust prediction of clinical outcomes using cytometry data without cell gating Description: This package provides functions that predict clinical outcomes using single cell data (such as flow cytometry data, RNA single cell sequencing data) without the requirement of cell gating or clustering. biocViews: ImmunoOncology, CellBiology, FlowCytometry, StatisticalMethod, Software, CellBasedAssays, Regression, Classification, Survival Author: Zicheng Hu Maintainer: Zicheng Hu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/CytoDx git_branch: RELEASE_3_8 git_last_commit: 5c2959e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CytoDx_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CytoDx_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CytoDx_1.2.1.tgz vignettes: vignettes/CytoDx/inst/doc/CytoDx_Vignette.pdf vignetteTitles: Introduction to CytoDx hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CytoDx/inst/doc/CytoDx_Vignette.R Package: cytolib Version: 1.4.1 Depends: R (>= 3.4) LinkingTo: BH(>= 1.62.0-1), RProtoBufLib(>= 1.1.7) Suggests: knitr License: Artistic-2.0 MD5sum: 3b9d823ae09d6d83d05e088afc955e4b NeedsCompilation: no Title: C++ infrastructure for representing and interacting with the gated cytometry Description: This package provides the core data structure and API to represent and interact with the gated cytometry data. biocViews: ImmunoOncology, FlowCytometry, DataImport, Preprocessing, DataRepresentation Author: Mike Jiang Maintainer: Mike Jiang SystemRequirements: GNU make, C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/cytolib git_branch: RELEASE_3_8 git_last_commit: c34a194 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/cytolib_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/cytolib_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/cytolib_1.4.1.tgz vignettes: vignettes/cytolib/inst/doc/cytolib.html vignetteTitles: Using cytolib hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/cytolib/inst/doc/cytolib.R linksToMe: flowWorkspace Package: CytoML Version: 1.8.1 Imports: flowCore (>= 1.43.10), flowWorkspace (>= 3.29.10), openCyto (>= 1.11.3), XML, data.table, flowUtils (>= 1.35.7), jsonlite, RBGL, ncdfFlow, Rgraphviz, Biobase, methods, graph, graphics, utils, base64enc, plyr, grDevices, methods, ggcyto (>= 1.9.3) Suggests: testthat, flowWorkspaceData (>= 2.11.1), knitr, parallel License: Artistic-2.0 MD5sum: 9be209a388efba16dd699e4c85542c51 NeedsCompilation: no Title: A GatingML Interface for Cross Platform Cytometry Data Sharing Description: Uses platform-specific implemenations of the GatingML2.0 standard to exchange gated cytometry data with other software platforms. biocViews: ImmunoOncology, FlowCytometry, DataImport, DataRepresentation Author: Mike Jiang Maintainer: Mike Jiang URL: https://github.com/RGLab/CytoML VignetteBuilder: knitr BugReports: https://github.com/RGLab/CytoML/issues git_url: https://git.bioconductor.org/packages/CytoML git_branch: RELEASE_3_8 git_last_commit: b12fab2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/CytoML_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/CytoML_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/CytoML_1.8.1.tgz vignettes: vignettes/CytoML/inst/doc/HowToExportGatingSet.html, vignettes/CytoML/inst/doc/HowToParseGatingML.html vignetteTitles: How to export a GatingSet to GatingML, How to parse gatingML into a GatingSet hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/CytoML/inst/doc/HowToExportGatingSet.R, vignettes/CytoML/inst/doc/HowToParseGatingML.R Package: dada2 Version: 1.10.1 Depends: R (>= 3.2.0), Rcpp (>= 0.11.2), methods (>= 3.2.0) Imports: Biostrings (>= 2.42.1), ggplot2 (>= 2.1.0), data.table (>= 1.9.4), reshape2 (>= 1.4.1), ShortRead (>= 1.32.0), RcppParallel (>= 4.3.0), parallel (>= 3.2.0), IRanges (>= 2.6.0), XVector (>= 0.16.0), BiocGenerics (>= 0.22.0) LinkingTo: Rcpp, RcppParallel Suggests: BiocStyle, knitr, rmarkdown License: LGPL-3 Archs: i386, x64 MD5sum: b64676d261a184dbf1152d01c1572c85 NeedsCompilation: yes Title: Accurate, high-resolution sample inference from amplicon sequencing data Description: The dada2 package infers exact amplicon sequence variants (ASVs) from high-throughput amplicon sequencing data, replacing the coarser and less accurate OTU clustering approach. The dada2 pipeline takes as input demultiplexed fastq files, and outputs the sequence variants and their sample-wise abundances after removing substitution and chimera errors. Taxonomic classification is available via a native implementation of the RDP naive Bayesian classifier, and species-level assignment to 16S rRNA gene fragments by exact matching. biocViews: ImmunoOncology, Microbiome, Sequencing, Classification, Metagenomics Author: Benjamin Callahan , Paul McMurdie, Susan Holmes Maintainer: Benjamin Callahan URL: http://benjjneb.github.io/dada2/ SystemRequirements: GNU make VignetteBuilder: knitr BugReports: https://github.com/benjjneb/dada2/issues git_url: https://git.bioconductor.org/packages/dada2 git_branch: RELEASE_3_8 git_last_commit: 322b76d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/dada2_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/dada2_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dada2_1.10.1.tgz vignettes: vignettes/dada2/inst/doc/dada2-intro.html vignetteTitles: Introduction to dada2 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/dada2/inst/doc/dada2-intro.R Package: dagLogo Version: 1.20.0 Depends: R (>= 3.0.1), methods, biomaRt, grImport, grid, motifStack Imports: pheatmap, Biostrings Suggests: XML, BiocStyle, knitr, rmarkdown, testthat, UniProt.ws License: GPL (>=2) MD5sum: eb5d6fe6ff233fd79d7c1ed8fff34965 NeedsCompilation: no Title: dagLogo Description: Visualize significant conserved amino acid sequence pattern in groups based on probability theory. biocViews: SequenceMatching, Visualization Author: Jianhong Ou, Alexey Stukalov, Niraj Nirala, Usha Acharya, Lihua Julie Zhu Maintainer: Jianhong Ou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/dagLogo git_branch: RELEASE_3_8 git_last_commit: 11fe9fb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/dagLogo_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/dagLogo_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dagLogo_1.20.0.tgz vignettes: vignettes/dagLogo/inst/doc/dagLogo.html vignetteTitles: dagLogo Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/dagLogo/inst/doc/dagLogo.R Package: daMA Version: 1.54.0 Imports: MASS, stats License: GPL (>= 2) MD5sum: 51df11f7dc90a9ac4ab8f24e61584a0a NeedsCompilation: no Title: Efficient design and analysis of factorial two-colour microarray data Description: This package contains functions for the efficient design of factorial two-colour microarray experiments and for the statistical analysis of factorial microarray data. Statistical details are described in Bretz et al. (2003, submitted) biocViews: Microarray, TwoChannel, DifferentialExpression Author: Jobst Landgrebe and Frank Bretz Maintainer: Jobst Landgrebe URL: http://www.microarrays.med.uni-goettingen.de git_url: https://git.bioconductor.org/packages/daMA git_branch: RELEASE_3_8 git_last_commit: 3015ade git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/daMA_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/daMA_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/daMA_1.54.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: DaMiRseq Version: 1.6.2 Depends: R (>= 3.4), SummarizedExperiment, ggplot2 Imports: DESeq2, limma, EDASeq, RColorBrewer, sva, Hmisc, pheatmap, FactoMineR, corrplot, randomForest, e1071, caret, MASS, lubridate, plsVarSel, kknn, FSelector, methods, stats, utils, graphics, grDevices, reshape2, ineq, arm, pls, RSNNS, edgeR Suggests: BiocStyle, knitr, testthat License: GPL (>= 2) MD5sum: 4cd2d065024ce3981840b0bfa27d2e2e NeedsCompilation: no Title: Data Mining for RNA-seq data: normalization, feature selection and classification Description: The DaMiRseq package offers a tidy pipeline of data mining procedures to identify transcriptional biomarkers and exploit them for both binary and multi-class classification purposes. The package accepts any kind of data presented as a table of raw counts and allows including both continous and factorial variables that occur with the experimental setting. A series of functions enable the user to clean up the data by filtering genomic features and samples, to adjust data by identifying and removing the unwanted source of variation (i.e. batches and confounding factors) and to select the best predictors for modeling. Finally, a "stacking" ensemble learning technique is applied to build a robust classification model. Every step includes a checkpoint that the user may exploit to assess the effects of data management by looking at diagnostic plots, such as clustering and heatmaps, RLE boxplots, MDS or correlation plot. biocViews: Sequencing, RNASeq, Classification, ImmunoOncology Author: Mattia Chiesa , Luca Piacentini Maintainer: Mattia Chiesa VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DaMiRseq git_branch: RELEASE_3_8 git_last_commit: f5f6030 git_last_commit_date: 2019-01-16 Date/Publication: 2019-01-16 source.ver: src/contrib/DaMiRseq_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DaMiRseq_1.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DaMiRseq_1.6.2.tgz vignettes: vignettes/DaMiRseq/inst/doc/DaMiRseq.pdf vignetteTitles: Data Mining for RNA-seq data: normalization,, features selection and classification - DaMiRseq package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DaMiRseq/inst/doc/DaMiRseq.R importsMe: GARS Package: DAPAR Version: 1.14.5 Depends: R (>= 3.5), foreach, parallel, doParallel Imports: MSnbase, RColorBrewer,stats,preprocessCore,Cairo,png, lattice,reshape2,gplots,pcaMethods,ggplot2, limma,knitr,tmvtnorm,norm,impute, stringr, grDevices, graphics, openxlsx, utils, cp4p (>= 0.3.5), scales, Matrix, vioplot, imp4p (>= 0.7), highcharter (>= 0.5.0), DAPARdata (>= 1.11.2), siggenes, graph, lme4, readxl, clusterProfiler, dplyr, tidyr,AnnotationDbi, tidyverse, vsn, FactoMineR, factoextra Suggests: BiocGenerics, Biobase, testthat, BiocStyle License: Artistic-2.0 MD5sum: 9a026117593c83d2fbf6fb85425eedb6 NeedsCompilation: no Title: Tools for the Differential Analysis of Proteins Abundance with R Description: This package contains a collection of functions for the visualisation and the statistical analysis of proteomic data. biocViews: ImmunoOncology, Proteomics, Normalization, Preprocessing, MassSpectrometry, QualityControl, GO, DataImport Author: Samuel Wieczorek [cre,aut], Florence Combes [aut], Thomas Burger [aut], Cosmin Lazar [ctb], Alexia Dorffer [ctb] Maintainer: Samuel Wieczorek VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DAPAR git_branch: RELEASE_3_8 git_last_commit: 4425fb4 git_last_commit_date: 2019-02-09 Date/Publication: 2019-02-10 source.ver: src/contrib/DAPAR_1.14.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/DAPAR_1.14.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DAPAR_1.14.5.tgz vignettes: vignettes/DAPAR/inst/doc/intro.pdf, vignettes/DAPAR/inst/doc/Prostar_UserManual.pdf vignetteTitles: DAPAR One Page Introduction, Prostar user manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DAPAR/inst/doc/Prostar_UserManual.R importsMe: Prostar Package: DART Version: 1.30.0 Depends: R (>= 2.10.0), igraph (>= 0.6.0) Suggests: breastCancerVDX, breastCancerMAINZ, Biobase License: GPL-2 MD5sum: a2c0ddeb30154385e9b4672c8d137fac NeedsCompilation: no Title: Denoising Algorithm based on Relevance network Topology Description: Denoising Algorithm based on Relevance network Topology (DART) is an algorithm designed to evaluate the consistency of prior information molecular signatures (e.g in-vitro perturbation expression signatures) in independent molecular data (e.g gene expression data sets). If consistent, a pruning network strategy is then used to infer the activation status of the molecular signature in individual samples. biocViews: GeneExpression, DifferentialExpression, GraphAndNetwork, Pathways Author: Yan Jiao, Katherine Lawler, Andrew E Teschendorff, Charles Shijie Zheng Maintainer: Charles Shijie Zheng git_url: https://git.bioconductor.org/packages/DART git_branch: RELEASE_3_8 git_last_commit: aa5767f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DART_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DART_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DART_1.30.0.tgz vignettes: vignettes/DART/inst/doc/DART.pdf vignetteTitles: DART Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DART/inst/doc/DART.R Package: DBChIP Version: 1.26.0 Depends: R (>= 2.15.0), edgeR, DESeq Suggests: ShortRead, BiocGenerics License: GPL (>= 2) MD5sum: d2ca8f6a4e640074c6de45eba4db9a50 NeedsCompilation: no Title: Differential Binding of Transcription Factor with ChIP-seq Description: DBChIP detects differentially bound sharp binding sites across multiple conditions, with or without matching control samples. biocViews: ChIPSeq, Sequencing, Transcription, Genetics Author: Kun Liang Maintainer: Kun Liang git_url: https://git.bioconductor.org/packages/DBChIP git_branch: RELEASE_3_8 git_last_commit: 8ac8e13 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DBChIP_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DBChIP_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DBChIP_1.26.0.tgz vignettes: vignettes/DBChIP/inst/doc/DBChIP.pdf vignetteTitles: DBChIP hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DBChIP/inst/doc/DBChIP.R importsMe: metagene Package: dcGSA Version: 1.10.1 Depends: R (>= 3.3), Matrix Imports: BiocParallel Suggests: knitr License: GPL-2 MD5sum: b5ee3b5f18c045b2a72cee81195409c2 NeedsCompilation: no Title: Distance-correlation based Gene Set Analysis for longitudinal gene expression profiles Description: Distance-correlation based Gene Set Analysis for longitudinal gene expression profiles. In longitudinal studies, the gene expression profiles were collected at each visit from each subject and hence there are multiple measurements of the gene expression profiles for each subject. The dcGSA package could be used to assess the associations between gene sets and clinical outcomes of interest by fully taking advantage of the longitudinal nature of both the gene expression profiles and clinical outcomes. biocViews: ImmunoOncology, GeneSetEnrichment,Microarray, StatisticalMethod, Sequencing, RNASeq, GeneExpression Author: Jiehuan Sun [aut, cre], Jose Herazo-Maya [aut], Xiu Huang [aut], Naftali Kaminski [aut], and Hongyu Zhao [aut] Maintainer: Jiehuan sun VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/dcGSA git_branch: RELEASE_3_8 git_last_commit: 34dca44 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/dcGSA_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/dcGSA_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dcGSA_1.10.1.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: DChIPRep Version: 1.12.0 Depends: R (>= 3.4), DESeq2 Imports: methods, stats, utils, ggplot2, fdrtool, reshape2, GenomicRanges, SummarizedExperiment, smoothmest, plyr, tidyr, assertthat, S4Vectors, purrr, soGGi, ChIPpeakAnno Suggests: mgcv, testthat, BiocStyle, knitr, rmarkdown License: MIT + file LICENCE MD5sum: 16c51ba26b30d3f5466e7aa8676a4441 NeedsCompilation: no Title: DChIPRep - Analysis of chromatin modification ChIP-Seq data with replication Description: The DChIPRep package implements a methodology to assess differences between chromatin modification profiles in replicated ChIP-Seq studies as described in Chabbert et. al - http://www.dx.doi.org/10.15252/msb.20145776. A detailed description of the method is given in the software paper at https://doi.org/10.7717/peerj.1981 biocViews: Sequencing, ChIPSeq, WholeGenome Author: Bernd Klaus [aut, cre], Christophe Chabbert [aut], Sebastian Gibb [ctb] Maintainer: Bernd Klaus VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DChIPRep git_branch: RELEASE_3_8 git_last_commit: ece1f25 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DChIPRep_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DChIPRep_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DChIPRep_1.12.0.tgz vignettes: vignettes/DChIPRep/inst/doc/DChIPRepVignette.html vignetteTitles: DChIPRepVignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DChIPRep/inst/doc/DChIPRepVignette.R Package: ddCt Version: 1.38.0 Depends: R (>= 2.3.0), methods Imports: Biobase (>= 1.10.0), RColorBrewer (>= 0.1-3), xtable, lattice, BiocGenerics Suggests: RUnit License: LGPL-3 MD5sum: a0d6affcd7f9fac5b22389a3657bba99 NeedsCompilation: no Title: The ddCt Algorithm for the Analysis of Quantitative Real-Time PCR (qRT-PCR) Description: The Delta-Delta-Ct (ddCt) Algorithm is an approximation method to determine relative gene expression with quantitative real-time PCR (qRT-PCR) experiments. Compared to other approaches, it requires no standard curve for each primer-target pair, therefore reducing the working load and yet returning accurate enough results as long as the assumptions of the amplification efficiency hold. The ddCt package implements a pipeline to collect, analyse and visualize qRT-PCR results, for example those from TaqMan SDM software, mainly using the ddCt method. The pipeline can be either invoked by a script in command-line or through the API consisting of S4-Classes, methods and functions. biocViews: GeneExpression, DifferentialExpression, MicrotitrePlateAssay, qPCR Author: Jitao David Zhang, Rudolf Biczok, and Markus Ruschhaupt Maintainer: Jitao David Zhang git_url: https://git.bioconductor.org/packages/ddCt git_branch: RELEASE_3_8 git_last_commit: e42a7c5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ddCt_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ddCt_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ddCt_1.38.0.tgz vignettes: vignettes/ddCt/inst/doc/RT-PCR-Script-ddCt.pdf, vignettes/ddCt/inst/doc/rtPCR-usage.pdf, vignettes/ddCt/inst/doc/rtPCR.pdf vignetteTitles: How to apply the ddCt method, Analyse RT-PCR data with the end-to-end script in ddCt package, Introduction to the ddCt method for qRT-PCR data analysis: background,, algorithm and example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ddCt/inst/doc/RT-PCR-Script-ddCt.R, vignettes/ddCt/inst/doc/rtPCR-usage.R, vignettes/ddCt/inst/doc/rtPCR.R Package: ddPCRclust Version: 1.2.0 Depends: R (>= 3.5) Imports: plotrix, clue, parallel, ggplot2, openxlsx, R.utils, flowCore, flowDensity (>= 1.13.3), SamSPECTRAL, flowPeaks Suggests: BiocStyle License: Artistic-2.0 MD5sum: cf65901cbc08efe813fa358b52244059 NeedsCompilation: no Title: Clustering algorithm for ddPCR data Description: The ddPCRclust algorithm can automatically quantify the CPDs of non-orthogonal ddPCR reactions with up to four targets. In order to determine the correct droplet count for each target, it is crucial to both identify all clusters and label them correctly based on their position. For more information on what data can be analyzed and how a template needs to be formatted, please check the vignette. biocViews: ddPCR, Clustering Author: Benedikt G. Brink [aut, cre], Justin Meskas [ctb], Ryan R. Brinkman [ctb] Maintainer: Benedikt G. Brink URL: https://github.com/bgbrink/ddPCRclust BugReports: https://github.com/bgbrink/ddPCRclust/issues git_url: https://git.bioconductor.org/packages/ddPCRclust git_branch: RELEASE_3_8 git_last_commit: 85f5df4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ddPCRclust_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ddPCRclust_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ddPCRclust_1.2.0.tgz vignettes: vignettes/ddPCRclust/inst/doc/ddPCRclust.pdf vignetteTitles: Bioconductor LaTeX Style hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ddPCRclust/inst/doc/ddPCRclust.R Package: debrowser Version: 1.10.9 Depends: R (>= 3.5.0), Imports: shiny, jsonlite, shinyjs, shinydashboard, shinyBS, gplots, DT, ggplot2, RColorBrewer, annotate, AnnotationDbi, DESeq2, DOSE, igraph, grDevices, graphics, stats, utils, GenomicRanges, IRanges, S4Vectors, SummarizedExperiment, stringi, reshape2, d3heatmap, org.Hs.eg.db, org.Mm.eg.db, limma, edgeR, clusterProfiler, methods, sva, RCurl, enrichplot, colourpicker, plotly, heatmaply, Harman, pathview Suggests: testthat, rmarkdown, knitr, R.rsp License: GPL-3 + file LICENSE MD5sum: a6058292a60cc4fe2c376b0c26c7b764 NeedsCompilation: no Title: Interactive Differential Expresion Analysis Browser Description: Bioinformatics platform containing interactive plots and tables for differential gene and region expression studies. Allows visualizing expression data much more deeply in an interactive and faster way. By changing the parameters, users can easily discover different parts of the data that like never have been done before. Manually creating and looking these plots takes time. With DEBrowser users can prepare plots without writing any code. Differential expression, PCA and clustering analysis are made on site and the results are shown in various plots such as scatter, bar, box, volcano, ma plots and Heatmaps. biocViews: Sequencing, ChIPSeq, RNASeq, DifferentialExpression, GeneExpression, Clustering, ImmunoOncology Author: Alper Kucukural , Onur Yukselen , Manuel Garber Maintainer: Alper Kucukural URL: https://github.com/UMMS-Biocore/debrowser VignetteBuilder: knitr, R.rsp BugReports: https://github.com/UMMS-Biocore/debrowser/issues/new git_url: https://git.bioconductor.org/packages/debrowser git_branch: RELEASE_3_8 git_last_commit: 02d3a86 git_last_commit_date: 2019-02-02 Date/Publication: 2019-02-03 source.ver: src/contrib/debrowser_1.10.9.tar.gz win.binary.ver: bin/windows/contrib/3.5/debrowser_1.10.9.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/debrowser_1.10.9.tgz vignettes: vignettes/debrowser/inst/doc/DEBrowser.html vignetteTitles: DEBrowser Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/debrowser/inst/doc/DEBrowser.R Package: DECIPHER Version: 2.10.2 Depends: R (>= 3.3.0), Biostrings (>= 2.35.12), RSQLite (>= 1.1), stats, parallel Imports: methods, DBI, S4Vectors, IRanges, XVector LinkingTo: Biostrings, S4Vectors, IRanges, XVector License: GPL-3 Archs: i386, x64 MD5sum: c72447ea5d1e14081bb277564ab7e470 NeedsCompilation: yes Title: Tools for curating, analyzing, and manipulating biological sequences Description: A toolset for deciphering and managing biological sequences. biocViews: ImmunoOncology, Clustering, Genetics, Sequencing, DataImport, Visualization, Microarray, QualityControl, qPCR, Alignment, WholeGenome, Microbiome Author: Erik Wright Maintainer: Erik Wright git_url: https://git.bioconductor.org/packages/DECIPHER git_branch: RELEASE_3_8 git_last_commit: db7b017 git_last_commit_date: 2019-01-21 Date/Publication: 2019-02-07 source.ver: src/contrib/DECIPHER_2.10.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DECIPHER_2.10.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DECIPHER_2.10.2.tgz vignettes: vignettes/DECIPHER/inst/doc/ArtOfAlignmentInR.pdf, vignettes/DECIPHER/inst/doc/ClassifySequences.pdf, vignettes/DECIPHER/inst/doc/DECIPHERing.pdf, vignettes/DECIPHER/inst/doc/DesignMicroarray.pdf, vignettes/DECIPHER/inst/doc/DesignPrimers.pdf, vignettes/DECIPHER/inst/doc/DesignProbes.pdf, vignettes/DECIPHER/inst/doc/DesignSignatures.pdf, vignettes/DECIPHER/inst/doc/FindChimeras.pdf vignetteTitles: The Art of Multiple Sequence Alignment in R, Classify Sequences, Getting Started DECIPHERing, Design Microarray Probes, Design Group-Specific Primers, Design Group-Specific FISH Probes, Design Primers That Yield Group-Specific Signatures, Finding Chimeric Sequences hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DECIPHER/inst/doc/ArtOfAlignmentInR.R, vignettes/DECIPHER/inst/doc/ClassifySequences.R, vignettes/DECIPHER/inst/doc/DECIPHERing.R, vignettes/DECIPHER/inst/doc/DesignMicroarray.R, vignettes/DECIPHER/inst/doc/DesignPrimers.R, vignettes/DECIPHER/inst/doc/DesignProbes.R, vignettes/DECIPHER/inst/doc/DesignSignatures.R, vignettes/DECIPHER/inst/doc/FindChimeras.R dependsOnMe: AssessORF importsMe: metagenomeFeatures, openPrimeR Package: DEComplexDisease Version: 1.2.0 Depends: R (>= 3.3.3) Imports: Rcpp (>= 0.12.7), DESeq2, edgeR, SummarizedExperiment, ComplexHeatmap, grid, parallel, BiocParallel, grDevices, graphics, stats, methods, utils LinkingTo: Rcpp Suggests: knitr License: GPL-3 Archs: i386, x64 MD5sum: 8939bc37f0e9520bb74d734800f681d7 NeedsCompilation: yes Title: A tool for differential expression analysis and DEGs based investigation to complex diseases by bi-clustering analysis Description: It is designed to find the differential expressed genes (DEGs) for complex disease, which is characterized by the heterogeneous genomic expression profiles. Different from the established DEG analysis tools, it does not assume the patients of complex diseases to share the common DEGs. By applying a bi-clustering algorithm, DECD finds the DEGs shared by as many patients. In this way, DECD describes the DEGs of complex disease in a novel syntax, e.g. a gene list composed of 200 genes are differentially expressed in 30% percent of studied complex disease. Applying the DECD analysis results, users are possible to find the patients affected by the same mechanism based on the shared signatures. biocViews: DNASeq, WholeGenome, FunctionalGenomics, DifferentialExpression,GeneExpression, Clustering Author: Guofeng Meng Maintainer: Guofeng Meng VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DEComplexDisease git_branch: RELEASE_3_8 git_last_commit: 9785cef git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DEComplexDisease_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEComplexDisease_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEComplexDisease_1.2.0.tgz vignettes: vignettes/DEComplexDisease/inst/doc/vignettes.pdf, vignettes/DEComplexDisease/inst/doc/decd.html vignetteTitles: DEComplexDisease: a R package for DE analysis, DEComplexDisease: a R package for DE analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEComplexDisease/inst/doc/decd.R Package: DeconRNASeq Version: 1.24.0 Depends: R (>= 2.14.0), limSolve, pcaMethods, ggplot2, grid License: GPL-2 MD5sum: 22cb44d707c7ce74ce46d782949aaad7 NeedsCompilation: no Title: Deconvolution of Heterogeneous Tissue Samples for mRNA-Seq data Description: DeconSeq is an R package for deconvolution of heterogeneous tissues based on mRNA-Seq data. It modeled expression levels from heterogeneous cell populations in mRNA-Seq as the weighted average of expression from different constituting cell types and predicted cell type proportions of single expression profiles. biocViews: DifferentialExpression Author: Ting Gong Joseph D. Szustakowski Maintainer: Ting Gong git_url: https://git.bioconductor.org/packages/DeconRNASeq git_branch: RELEASE_3_8 git_last_commit: 590bd50 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DeconRNASeq_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DeconRNASeq_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DeconRNASeq_1.24.0.tgz vignettes: vignettes/DeconRNASeq/inst/doc/DeconRNASeq.pdf vignetteTitles: DeconRNASeq Demo hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DeconRNASeq/inst/doc/DeconRNASeq.R Package: decontam Version: 1.2.1 Depends: R (>= 3.4.1), methods (>= 3.4.1) Imports: ggplot2 (>= 2.1.0), reshape2 (>= 1.4.1), stats Suggests: BiocStyle, knitr, rmarkdown, phyloseq License: Artistic-2.0 MD5sum: 9ff6703e6bc65320f3eeffb89ef3a097 NeedsCompilation: no Title: Identify Contaminants in Marker-gene and Metagenomics Sequencing Data Description: Simple statistical identification of contaminating sequence features in marker-gene or metagenomics data. Works on any kind of feature derived from environmental sequencing data (e.g. ASVs, OTUs, taxonomic groups, MAGs,...). Requires DNA quantitation data or sequenced negative control samples. biocViews: ImmunoOncology, Microbiome, Sequencing, Classification, Metagenomics Author: Benjamin Callahan , Nicole Marie Davis Maintainer: Benjamin Callahan URL: https://github.com/benjjneb/decontam VignetteBuilder: knitr BugReports: https://github.com/benjjneb/decontam/issues git_url: https://git.bioconductor.org/packages/decontam git_branch: RELEASE_3_8 git_last_commit: 2123320 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/decontam_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/decontam_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/decontam_1.2.1.tgz vignettes: vignettes/decontam/inst/doc/decontam_intro.html vignetteTitles: Introduction to dada2 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/decontam/inst/doc/decontam_intro.R Package: DEDS Version: 1.56.0 Depends: R (>= 1.7.0) License: LGPL Archs: i386, x64 MD5sum: 520ca60c57d58412dd6eaede77dcd215 NeedsCompilation: yes Title: Differential Expression via Distance Summary for Microarray Data Description: This library contains functions that calculate various statistics of differential expression for microarray data, including t statistics, fold change, F statistics, SAM, moderated t and F statistics and B statistics. It also implements a new methodology called DEDS (Differential Expression via Distance Summary), which selects differentially expressed genes by integrating and summarizing a set of statistics using a weighted distance approach. biocViews: Microarray, DifferentialExpression Author: Yuanyuan Xiao , Jean Yee Hwa Yang . Maintainer: Yuanyuan Xiao git_url: https://git.bioconductor.org/packages/DEDS git_branch: RELEASE_3_8 git_last_commit: 6b88d43 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DEDS_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEDS_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEDS_1.56.0.tgz vignettes: vignettes/DEDS/inst/doc/DEDS.pdf vignetteTitles: DEDS.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEDS/inst/doc/DEDS.R Package: DeepBlueR Version: 1.8.1 Depends: R (>= 3.3), XML, RCurl Imports: GenomicRanges, data.table, stringr, diffr, dplyr, methods, rjson, utils, R.utils, foreach, withr, rtracklayer, GenomeInfoDb, settings, filehash Suggests: knitr, rmarkdown, LOLA, Gviz, gplots, ggplot2, tidyr, RColorBrewer, matrixStats License: GPL (>=2.0) MD5sum: 018f4595b05dc18852ae9f59c2b999e8 NeedsCompilation: no Title: DeepBlueR Description: Accessing the DeepBlue Epigenetics Data Server through R. biocViews: DataImport, DataRepresentation, ThirdPartyClient, GeneRegulation, GenomeAnnotation, CpGIsland, DNAMethylation, Epigenetics, Annotation, Preprocessing, ImmunoOncology Author: Felipe Albrecht, Markus List Maintainer: Felipe Albrecht , Markus List VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DeepBlueR git_branch: RELEASE_3_8 git_last_commit: 43a471f git_last_commit_date: 2019-04-12 Date/Publication: 2019-04-12 source.ver: src/contrib/DeepBlueR_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DeepBlueR_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DeepBlueR_1.8.1.tgz vignettes: vignettes/DeepBlueR/inst/doc/DeepBlueR.html vignetteTitles: The DeepBlue epigenomic data server - R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DeepBlueR/inst/doc/DeepBlueR.R Package: deepSNV Version: 1.28.0 Depends: R (>= 2.13.0), methods, graphics, parallel, Rhtslib, IRanges, GenomicRanges, SummarizedExperiment, Biostrings, VGAM, VariantAnnotation (>= 1.13.44), Imports: Rhtslib LinkingTo: Rhtslib (>= 1.13.1) Suggests: RColorBrewer, knitr, rmarkdown License: GPL-3 Archs: i386, x64 MD5sum: e75cbb2a6a32b486dd4f525de48d8f40 NeedsCompilation: yes Title: Detection of subclonal SNVs in deep sequencing data. Description: This package provides provides quantitative variant callers for detecting subclonal mutations in ultra-deep (>=100x coverage) sequencing experiments. The deepSNV algorithm is used for a comparative setup with a control experiment of the same loci and uses a beta-binomial model and a likelihood ratio test to discriminate sequencing errors and subclonal SNVs. The shearwater algorithm computes a Bayes classifier based on a beta-binomial model for variant calling with multiple samples for precisely estimating model parameters - such as local error rates and dispersion - and prior knowledge, e.g. from variation data bases such as COSMIC. biocViews: GeneticVariability, SNP, Sequencing, Genetics, DataImport Author: Niko Beerenwinkel [ths], David Jones [ctb], Inigo Martincorena [ctb], Moritz Gerstung [aut, cre] Maintainer: Moritz Gerstung URL: http://github.com/gerstung-lab/deepSNV VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/deepSNV git_branch: RELEASE_3_8 git_last_commit: 9b6d747 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/deepSNV_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/deepSNV_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/deepSNV_1.28.0.tgz vignettes: vignettes/deepSNV/inst/doc/deepSNV.pdf, vignettes/deepSNV/inst/doc/shearwater.pdf, vignettes/deepSNV/inst/doc/shearwaterML.html vignetteTitles: An R package for detecting low frequency variants in deep sequencing experiments, Subclonal variant calling with multiple samples and prior knowledge using shearwater, Shearwater ML hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/deepSNV/inst/doc/deepSNV.R, vignettes/deepSNV/inst/doc/shearwater.R, vignettes/deepSNV/inst/doc/shearwaterML.R suggestsMe: GenomicFiles Package: DEFormats Version: 1.10.1 Imports: checkmate, data.table, DESeq2, edgeR (>= 3.13.4), GenomicRanges, methods, S4Vectors, stats, SummarizedExperiment Suggests: BiocStyle (>= 1.8.0), knitr, rmarkdown, testthat License: GPL-3 MD5sum: 6658bf4cfd04a498b2f9ffe3efafb880 NeedsCompilation: no Title: Differential gene expression data formats converter Description: Convert between different data formats used by differential gene expression analysis tools. biocViews: ImmunoOncology, DifferentialExpression, GeneExpression, RNASeq, Sequencing, Transcription Author: Andrzej Oleś Maintainer: Andrzej Oleś URL: https://github.com/aoles/DEFormats VignetteBuilder: knitr BugReports: https://github.com/aoles/DEFormats/issues git_url: https://git.bioconductor.org/packages/DEFormats git_branch: RELEASE_3_8 git_last_commit: 9cf213e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DEFormats_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEFormats_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEFormats_1.10.1.tgz vignettes: vignettes/DEFormats/inst/doc/DEFormats.html vignetteTitles: Differential gene expression data formats converter hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEFormats/inst/doc/DEFormats.R importsMe: regionReport suggestsMe: ideal Package: DEGraph Version: 1.34.0 Depends: R (>= 2.10.0), R.utils Imports: graph, KEGGgraph, lattice, mvtnorm, R.methodsS3, RBGL, Rgraphviz, rrcov, NCIgraph Suggests: corpcor, fields, graph, KEGGgraph, lattice, marray, RBGL, rrcov, Rgraphviz, NCIgraph License: GPL-3 MD5sum: 51a9e855c83c270117e9cd3ed052d86e NeedsCompilation: no Title: Two-sample tests on a graph Description: DEGraph implements recent hypothesis testing methods which directly assess whether a particular gene network is differentially expressed between two conditions. This is to be contrasted with the more classical two-step approaches which first test individual genes, then test gene sets for enrichment in differentially expressed genes. These recent methods take into account the topology of the network to yield more powerful detection procedures. DEGraph provides methods to easily test all KEGG pathways for differential expression on any gene expression data set and tools to visualize the results. biocViews: Microarray, DifferentialExpression, GraphAndNetwork, Network, NetworkEnrichment, DecisionTree Author: Laurent Jacob, Pierre Neuvial and Sandrine Dudoit Maintainer: Laurent Jacob git_url: https://git.bioconductor.org/packages/DEGraph git_branch: RELEASE_3_8 git_last_commit: b79d101 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DEGraph_1.34.0.tar.gz vignettes: vignettes/DEGraph/inst/doc/DEGraph.pdf vignetteTitles: DEGraph: differential expression testing for gene networks hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEGraph/inst/doc/DEGraph.R Package: DEGreport Version: 1.18.1 Depends: R (>= 3.4.0) Imports: utils, methods, Biobase, BiocGenerics, broom, circlize, ComplexHeatmap, cowplot, ConsensusClusterPlus, cluster, DESeq2, dplyr, edgeR, ggplot2, ggdendro, grid, ggrepel, grDevices, knitr, logging, lasso2, magrittr, Nozzle.R1, psych, RColorBrewer, reshape, rlang, scales, stats, stringr, S4Vectors, SummarizedExperiment, tidyr, tibble Suggests: BiocStyle, AnnotationDbi, limma, pheatmap, knitr, rmarkdown, statmod, testthat License: MIT + file LICENSE MD5sum: 9891853b99027e641881c720ebd96980 NeedsCompilation: no Title: Report of DEG analysis Description: Creation of a HTML report of differential expression analyses of count data. It integrates some of the code mentioned in DESeq2 and edgeR vignettes, and report a ranked list of genes according to the fold changes mean and variability for each selected gene. biocViews: ImmunoOncology, DifferentialExpression, Visualization, RNASeq, ReportWriting, GeneExpression Author: Lorena Pantano [aut, cre], John Hutchinson [ctb], Victor Barrera [ctb], Mary Piper [ctb], Radhika Khetani [ctb], Kenneth Daily [ctb], Thanneer Malai Perumal [ctb], Rory Kirchner [ctb], Michael Steinbaugh [ctb] Maintainer: Lorena Pantano URL: http://lpantano.github.io/DEGreport/ VignetteBuilder: knitr BugReports: https://github.com/lpantano/DEGreport/issues git_url: https://git.bioconductor.org/packages/DEGreport git_branch: RELEASE_3_8 git_last_commit: 9d5c08e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DEGreport_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEGreport_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEGreport_1.18.1.tgz vignettes: vignettes/DEGreport/inst/doc/DEGreport.html vignetteTitles: QC and downstream analysis for differential expression RNA-seq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/DEGreport/inst/doc/DEGreport.R importsMe: isomiRs Package: DEGseq Version: 1.36.1 Depends: R (>= 2.8.0), qvalue, methods Imports: graphics, grDevices, methods, stats, utils License: LGPL (>=2) Archs: i386, x64 MD5sum: b8923f545fdf7ddeece5e9abd038cc00 NeedsCompilation: yes Title: Identify Differentially Expressed Genes from RNA-seq data Description: DEGseq is an R package to identify differentially expressed genes from RNA-Seq data. biocViews: RNASeq, Preprocessing, GeneExpression, DifferentialExpression, ImmunoOncology Author: Likun Wang and Xi Wang . Maintainer: Likun Wang git_url: https://git.bioconductor.org/packages/DEGseq git_branch: RELEASE_3_8 git_last_commit: 780902e git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/DEGseq_1.36.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEGseq_1.36.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEGseq_1.36.1.tgz vignettes: vignettes/DEGseq/inst/doc/DEGseq.pdf vignetteTitles: DEGseq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEGseq/inst/doc/DEGseq.R Package: DelayedArray Version: 0.8.0 Depends: R (>= 3.4), methods, stats4, matrixStats, BiocGenerics (>= 0.27.1), S4Vectors (>= 0.19.15), IRanges (>= 2.11.17), BiocParallel Imports: stats LinkingTo: S4Vectors Suggests: Matrix, HDF5Array, genefilter, SummarizedExperiment, airway, pryr, DelayedMatrixStats, knitr, BiocStyle, RUnit License: Artistic-2.0 Archs: i386, x64 MD5sum: f8365083bd320d946db08c9aa34c335c NeedsCompilation: yes Title: Delayed operations on array-like objects Description: Wrapping an array-like object (typically an on-disk object) in a DelayedArray object allows one to perform common array operations on it without loading the object in memory. In order to reduce memory usage and optimize performance, operations on the object are either delayed or executed using a block processing mechanism. Note that this also works on in-memory array-like objects like DataFrame objects (typically with Rle columns), Matrix objects, and ordinary arrays and data frames. biocViews: Infrastructure, DataRepresentation, Annotation, GenomeAnnotation Author: Hervé Pagès , with contributions from Peter Hickey Maintainer: Hervé Pagès VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DelayedArray git_branch: RELEASE_3_8 git_last_commit: 7c23cf4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DelayedArray_0.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DelayedArray_0.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DelayedArray_0.8.0.tgz vignettes: vignettes/DelayedArray/inst/doc/01-Working_with_large_arrays.pdf, vignettes/DelayedArray/inst/doc/02-Implementing_a_backend.html vignetteTitles: Working with large arrays in R, Implementing A DelayedArray Backend hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DelayedArray/inst/doc/01-Working_with_large_arrays.R dependsOnMe: DelayedMatrixStats, GDSArray, HDF5Array, rhdf5client, singleCellTK, SummarizedExperiment importsMe: beachmat, bsseq, CAGEr, ChIPpeakAnno, clusterExperiment, DEScan2, DSS, ELMER, GenoGAM, hipathia, LoomExperiment, minfi, RTCGAToolbox, scater, scmeth, scran suggestsMe: iSEE, S4Vectors Package: DelayedMatrixStats Version: 1.4.0 Depends: DelayedArray (>= 0.7.37) Imports: methods, matrixStats (>= 0.53.1), Matrix, S4Vectors (>= 0.17.5), IRanges, HDF5Array (>= 1.7.10), BiocParallel Suggests: testthat, knitr, rmarkdown, covr, BiocStyle, microbenchmark, profmem License: MIT + file LICENSE MD5sum: 7393b93bd0df9dfc1964e1d05f3e474b NeedsCompilation: no Title: Functions that Apply to Rows and Columns of 'DelayedMatrix' Objects Description: A port of the 'matrixStats' API for use with DelayedMatrix objects from the 'DelayedArray' package. High-performing functions operating on rows and columns of DelayedMatrix objects, e.g. col / rowMedians(), col / rowRanks(), and col / rowSds(). Functions optimized per data type and for subsetted calculations such that both memory usage and processing time is minimized. biocViews: Infrastructure, DataRepresentation, Software Author: Peter Hickey Maintainer: Peter Hickey URL: https://github.com/PeteHaitch/DelayedMatrixStats VignetteBuilder: knitr BugReports: https://github.com/PeteHaitch/DelayedMatrixStats/issues git_url: https://git.bioconductor.org/packages/DelayedMatrixStats git_branch: RELEASE_3_8 git_last_commit: eb5b390 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DelayedMatrixStats_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DelayedMatrixStats_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DelayedMatrixStats_1.4.0.tgz vignettes: vignettes/DelayedMatrixStats/inst/doc/DelayedMatrixStatsOverview.html vignetteTitles: Overview of DelayedMatrixStats hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/DelayedMatrixStats/inst/doc/DelayedMatrixStatsOverview.R importsMe: bsseq, dmrseq, minfi, scater, scran suggestsMe: DelayedArray Package: deltaGseg Version: 1.22.0 Depends: R (>= 2.15.1), methods, ggplot2, changepoint, wavethresh, tseries, pvclust, fBasics, grid, reshape, scales Suggests: knitr License: GPL-2 MD5sum: fa281178cf227dc36cbc08c12954a7cb NeedsCompilation: no Title: deltaGseg Description: Identifying distinct subpopulations through multiscale time series analysis biocViews: Proteomics, TimeCourse, Visualization, Clustering Author: Diana Low, Efthymios Motakis Maintainer: Diana Low VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/deltaGseg git_branch: RELEASE_3_8 git_last_commit: 98e4a72 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/deltaGseg_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/deltaGseg_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/deltaGseg_1.22.0.tgz vignettes: vignettes/deltaGseg/inst/doc/deltaGseg.pdf vignetteTitles: deltaGseg hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/deltaGseg/inst/doc/deltaGseg.R Package: DeMAND Version: 1.12.0 Depends: R (>= 2.14.0), KernSmooth, methods License: file LICENSE MD5sum: 7407289aa62fd7f774451b158ee89d6d NeedsCompilation: no Title: DeMAND Description: DEMAND predicts Drug MoA by interrogating a cell context specific regulatory network with a small number (N >= 6) of compound-induced gene expression signatures, to elucidate specific proteins whose interactions in the network is dysregulated by the compound. biocViews: SystemsBiology, NetworkEnrichment, GeneExpression, StatisticalMethod, Network Author: Jung Hoon Woo , Yishai Shimoni Maintainer: Jung Hoon Woo , Mariano Alvarez git_url: https://git.bioconductor.org/packages/DeMAND git_branch: RELEASE_3_8 git_last_commit: c0662c7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DeMAND_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DeMAND_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DeMAND_1.12.0.tgz vignettes: vignettes/DeMAND/inst/doc/DeMAND.pdf vignetteTitles: Using DeMAND hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/DeMAND/inst/doc/DeMAND.R Package: DEP Version: 1.4.1 Depends: R (>= 3.5) Imports: ggplot2, dplyr, purrr, readr, tibble, tidyr, SummarizedExperiment (>= 1.11.5), MSnbase, limma, vsn, fdrtool, ggrepel, ComplexHeatmap, RColorBrewer, circlize, shiny, shinydashboard, DT, rmarkdown, assertthat, gridExtra, grid, stats, imputeLCMD, cluster Suggests: testthat, enrichR, knitr, BiocStyle License: Artistic-2.0 MD5sum: 946fc6af73e0379dafb4e49e23e7260f NeedsCompilation: no Title: Differential Enrichment analysis of Proteomics data Description: This package provides an integrated analysis workflow for robust and reproducible analysis of mass spectrometry proteomics data for differential protein expression or differential enrichment. It requires tabular input (e.g. txt files) as generated by quantitative analysis softwares of raw mass spectrometry data, such as MaxQuant or IsobarQuant. Functions are provided for data preparation, filtering, variance normalization and imputation of missing values, as well as statistical testing of differentially enriched / expressed proteins. It also includes tools to check intermediate steps in the workflow, such as normalization and missing values imputation. Finally, visualization tools are provided to explore the results, including heatmap, volcano plot and barplot representations. For scientists with limited experience in R, the package also contains wrapper functions that entail the complete analysis workflow and generate a report. Even easier to use are the interactive Shiny apps that are provided by the package. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, DifferentialExpression, DataRepresentation Author: Arne Smits [cre, aut], Wolfgang Huber [aut] Maintainer: Arne Smits VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DEP git_branch: RELEASE_3_8 git_last_commit: e024011 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DEP_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEP_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEP_1.4.1.tgz vignettes: vignettes/DEP/inst/doc/DEP.html, vignettes/DEP/inst/doc/MissingValues.html vignetteTitles: DEP: Introduction, DEP: Missing value handling hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEP/inst/doc/DEP.R, vignettes/DEP/inst/doc/MissingValues.R Package: DEqMS Version: 1.0.1 Depends: R(>= 3.5),graphics,stats,ggplot2,limma(>= 3.34) Suggests: BiocStyle,knitr,rmarkdown,plyr,matrixStats,reshape2,farms,RColorBrewer,utils,ggrepel,pheatmap,ExperimentHub License: LGPL MD5sum: 59963b019c076b54dd5168f46c86588d NeedsCompilation: no Title: a tool to perform statistical analysis of differential protein expression for quantitative proteomics data. Description: DEqMS is developped on top of Limma. However, Limma assumes same prior variance for all genes. In proteomics, the accuracy of protein abundance estimates varies by the number of peptides/PSMs quantified in both label-free and labelled data. Proteins quantification by multiple peptides or PSMs are more accurate. DEqMS package is able to estimate different prior variances for proteins quantified by different number of PSMs/peptides, therefore acchieving better accuracy. The package can be applied to analyze both label-free and labelled proteomics data. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, Preprocessing, DifferentialExpression, MultipleComparison,Normalization,Bayesian Author: Yafeng Zhu Maintainer: Yafeng Zhu VignetteBuilder: knitr BugReports: https://github.com/yafeng/DEqMS/issues git_url: https://git.bioconductor.org/packages/DEqMS git_branch: RELEASE_3_8 git_last_commit: f13e048 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DEqMS_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEqMS_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEqMS_1.0.1.tgz vignettes: vignettes/DEqMS/inst/doc/DEqMS-package-vignette.html vignetteTitles: DEqMS R Markdown vignettes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEqMS/inst/doc/DEqMS-package-vignette.R Package: derfinder Version: 1.16.1 Depends: R(>= 3.2) Imports: BiocGenerics (>= 0.25.1), AnnotationDbi (>= 1.27.9), BiocParallel (>= 1.15.15), bumphunter (>= 1.9.2), derfinderHelper (>= 1.1.0), GenomeInfoDb (>= 1.3.3), GenomicAlignments, GenomicFeatures, GenomicFiles, GenomicRanges (>= 1.17.40), Hmisc, IRanges (>= 2.3.23), methods, qvalue (>= 1.99.0), Rsamtools (>= 1.25.0), rtracklayer, S4Vectors (>= 0.9.38) Suggests: BiocStyle (>= 2.5.19), biovizBase, sessioninfo, derfinderData (>= 0.99.0), derfinderPlot, DESeq2, ggplot2, knitcitations (>= 1.0.1), knitr (>= 1.6), limma, RefManageR, rmarkdown (>= 0.3.3), testthat, TxDb.Hsapiens.UCSC.hg19.knownGene License: Artistic-2.0 MD5sum: 7899d9344b5d359f2fb65d88a8bd3bfc NeedsCompilation: no Title: Annotation-agnostic differential expression analysis of RNA-seq data at base-pair resolution via the DER Finder approach Description: This package provides functions for annotation-agnostic differential expression analysis of RNA-seq data. Two implementations of the DER Finder approach are included in this package: (1) single base-level F-statistics and (2) DER identification at the expressed regions-level. The DER Finder approach can also be used to identify differentially bounded ChIP-seq peaks. biocViews: DifferentialExpression, Sequencing, RNASeq, ChIPSeq, DifferentialPeakCalling, Software, ImmunoOncology Author: Leonardo Collado-Torres [aut, cre], Alyssa C. Frazee [ctb], Andrew E. Jaffe [aut], Jeffrey T. Leek [aut, ths] Maintainer: Leonardo Collado-Torres URL: https://github.com/lcolladotor/derfinder VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/derfinder/ git_url: https://git.bioconductor.org/packages/derfinder git_branch: RELEASE_3_8 git_last_commit: fbc7300 git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/derfinder_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/derfinder_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/derfinder_1.16.1.tgz vignettes: vignettes/derfinder/inst/doc/derfinder-quickstart.html, vignettes/derfinder/inst/doc/derfinder-users-guide.html vignetteTitles: derfinder quick start guide, derfinder users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/derfinder/inst/doc/derfinder-quickstart.R, vignettes/derfinder/inst/doc/derfinder-users-guide.R importsMe: derfinderPlot, recount, regionReport Package: derfinderHelper Version: 1.16.1 Depends: R(>= 3.2.2) Imports: IRanges (>= 1.99.27), Matrix, methods, S4Vectors (>= 0.2.2) Suggests: sessioninfo, knitcitations (>= 1.0.1), knitr (>= 1.6), BiocStyle (>= 2.5.19), rmarkdown (>= 0.3.3), testthat License: Artistic-2.0 MD5sum: 0aa279c6fed199400564d6cdc3f1ffd3 NeedsCompilation: no Title: derfinder helper package Description: Helper package for speeding up the derfinder package when using multiple cores. biocViews: DifferentialExpression, Sequencing, RNASeq, Software, ImmunoOncology Author: Leonardo Collado-Torres [aut, cre], Andrew E. Jaffe [aut], Jeffrey T. Leek [aut, ths] Maintainer: Leonardo Collado-Torres URL: https://github.com/leekgroup/derfinderHelper VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/derfinderHelper git_url: https://git.bioconductor.org/packages/derfinderHelper git_branch: RELEASE_3_8 git_last_commit: 92894af git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/derfinderHelper_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/derfinderHelper_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/derfinderHelper_1.16.1.tgz vignettes: vignettes/derfinderHelper/inst/doc/derfinderHelper.html vignetteTitles: Introduction to derfinderHelper hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/derfinderHelper/inst/doc/derfinderHelper.R importsMe: derfinder Package: derfinderPlot Version: 1.16.1 Depends: R(>= 3.2) Imports: derfinder (>= 1.1.0), GenomeInfoDb (>= 1.3.3), GenomicFeatures, GenomicRanges (>= 1.17.40), ggbio (>= 1.13.13), ggplot2, graphics, grDevices, IRanges (>= 1.99.28), limma, methods, plyr, RColorBrewer, RefManageR, reshape2, S4Vectors (>= 0.9.38), scales, utils Suggests: biovizBase (>= 1.27.2), bumphunter (>= 1.7.6), derfinderData (>= 0.99.0), sessioninfo, knitcitations (>= 1.0.1), knitr (>= 1.6), BiocStyle (>= 2.5.19), org.Hs.eg.db, rmarkdown (>= 0.3.3), testthat, TxDb.Hsapiens.UCSC.hg19.knownGene License: Artistic-2.0 MD5sum: fb39127239320c43ca5180870017ecb2 NeedsCompilation: no Title: Plotting functions for derfinder Description: This package provides plotting functions for results from the derfinder package. biocViews: DifferentialExpression, Sequencing, RNASeq, Software, Visualization, ImmunoOncology Author: Leonardo Collado-Torres [aut, cre], Andrew E. Jaffe [aut], Jeffrey T. Leek [aut, ths] Maintainer: Leonardo Collado-Torres URL: https://github.com/leekgroup/derfinderPlot VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/derfinderPlot git_url: https://git.bioconductor.org/packages/derfinderPlot git_branch: RELEASE_3_8 git_last_commit: 119db18 git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/derfinderPlot_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/derfinderPlot_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/derfinderPlot_1.16.1.tgz vignettes: vignettes/derfinderPlot/inst/doc/derfinderPlot.html vignetteTitles: Introduction to derfinderPlot hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/derfinderPlot/inst/doc/derfinderPlot.R suggestsMe: derfinder, regionReport Package: DEScan2 Version: 1.2.1 Depends: R (>= 3.5), GenomicRanges Imports: BiocParallel, BiocGenerics, ChIPpeakAnno, data.table, DelayedArray, GenomeInfoDb, GenomicAlignments, glue, IRanges, plyr, Rcpp (>= 0.12.13), rtracklayer, S4Vectors, SummarizedExperiment, tools, utils LinkingTo: Rcpp, RcppArmadillo Suggests: BiocStyle, knitr, rmarkdown, testthat, edgeR, limma, EDASeq, RUVSeq, RColorBrewer, statmod License: Artistic-2.0 Archs: i386, x64 MD5sum: ef5dd1a45ba5ba03dfb624128e418803 NeedsCompilation: yes Title: Differential Enrichment Scan 2 Description: Integrated peak and differential caller, specifically designed for broad epigenomic signals. biocViews: ImmunoOncology, PeakDetection, Epigenetics, Software, Sequencing, Coverage Author: Dario Righelli [aut, cre], John Koberstein [aut], Bruce Gomes [aut], Nancy Zhang [aut], Claudia Angelini [aut], Lucia Peixoto [aut], Davide Risso [aut] Maintainer: Dario Righelli VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DEScan2 git_branch: RELEASE_3_8 git_last_commit: 2b9414c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DEScan2_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEScan2_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEScan2_1.2.1.tgz vignettes: vignettes/DEScan2/inst/doc/DEScan2.html vignetteTitles: DEScan2 Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEScan2/inst/doc/DEScan2.R Package: DESeq Version: 1.34.1 Depends: BiocGenerics (>= 0.7.5), Biobase (>= 2.21.7), locfit, lattice Imports: genefilter, geneplotter, methods, MASS, RColorBrewer Suggests: pasilla (>= 0.2.10), vsn, gplots License: GPL (>= 3) Archs: i386, x64 MD5sum: f8cea5de200c9d10a3e956bc0fdb0c0e NeedsCompilation: yes Title: Differential gene expression analysis based on the negative binomial distribution Description: Estimate variance-mean dependence in count data from high-throughput sequencing assays and test for differential expression based on a model using the negative binomial distribution biocViews: ImmunoOncology, Sequencing, ChIPSeq, RNASeq, SAGE, DifferentialExpression Author: Simon Anders, EMBL Heidelberg Maintainer: Simon Anders URL: http://www-huber.embl.de/users/anders/DESeq git_url: https://git.bioconductor.org/packages/DESeq git_branch: RELEASE_3_8 git_last_commit: e86f1b0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DESeq_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DESeq_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DESeq_1.34.1.tgz vignettes: vignettes/DESeq/inst/doc/DESeq.pdf vignetteTitles: Analysing RNA-Seq data with the "DESeq" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DESeq/inst/doc/DESeq.R dependsOnMe: DBChIP, metaseqR, Polyfit, SeqGSEA, TCC, tRanslatome importsMe: ampliQueso, ArrayExpressHTS, DEsubs, easyRNASeq, EDASeq, EDDA, gCMAP, HTSFilter, rnaSeqMap, vulcan suggestsMe: BitSeq, compcodeR, dexus, DiffBind, ELBOW, gage, genefilter, regionReport, SSPA, XBSeq Package: DESeq2 Version: 1.22.2 Depends: S4Vectors (>= 0.9.25), IRanges, GenomicRanges, SummarizedExperiment (>= 1.1.6) Imports: BiocGenerics (>= 0.7.5), Biobase, BiocParallel, genefilter, methods, locfit, geneplotter, ggplot2, Hmisc, Rcpp (>= 0.11.0) LinkingTo: Rcpp, RcppArmadillo Suggests: testthat, knitr, rmarkdown, vsn, pheatmap, RColorBrewer, IHW, apeglm, ashr, tximport, tximportData, readr, pbapply, airway, pasilla (>= 0.2.10) License: LGPL (>= 3) Archs: i386, x64 MD5sum: f1237166b176ba1df536e5c19f86d322 NeedsCompilation: yes Title: Differential gene expression analysis based on the negative binomial distribution Description: Estimate variance-mean dependence in count data from high-throughput sequencing assays and test for differential expression based on a model using the negative binomial distribution. biocViews: ImmunoOncology, Sequencing, RNASeq, ChIPSeq, Microbiome, GeneExpression, Transcription, Normalization, DifferentialExpression, Bayesian, Regression, PrincipalComponent, Clustering Author: Michael Love, Simon Anders, Wolfgang Huber Maintainer: Michael Love URL: https://github.com/mikelove/DESeq2 VignetteBuilder: knitr, rmarkdown git_url: https://git.bioconductor.org/packages/DESeq2 git_branch: RELEASE_3_8 git_last_commit: 3c6a89b git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DESeq2_1.22.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DESeq2_1.22.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DESeq2_1.22.2.tgz vignettes: vignettes/DESeq2/inst/doc/DESeq2.html vignetteTitles: Analyzing RNA-seq data with DESeq2 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DESeq2/inst/doc/DESeq2.R dependsOnMe: DChIPRep, DEXSeq, FourCSeq, rgsepd, TCC, XBSeq importsMe: anamiR, Anaquin, consensusDE, coseq, countsimQC, DaMiRseq, debrowser, DEComplexDisease, DEFormats, DEGreport, DEsubs, DiffBind, eegc, EnrichmentBrowser, ERSSA, FourCSeq, GDCRNATools, GenoGAM, HTSFilter, ideal, ImpulseDE2, INSPEcT, IntEREst, isomiRs, JunctionSeq, kissDE, MLSeq, OUTRIDER, PathoStat, pcaExplorer, PowerExplorer, regionReport, ReportingTools, Rmmquant, RNASeqR, singleCellTK, SNPhood, srnadiff, systemPipeR, TimeSeriesExperiment, vidger suggestsMe: apeglm, biobroom, BiocGenerics, BioCor, CAGEr, compcodeR, derfinder, diffloop, EnhancedVolcano, gage, GenomicAlignments, GenomicRanges, Glimma, IHW, miRmine, OPWeight, phyloseq, progeny, recount, RUVSeq, scran, subSeq, SummarizedBenchmark, TFEA.ChIP, tximeta, tximport, variancePartition, Wrench, zinbwave Package: DEsingle Version: 1.2.1 Depends: R (>= 3.4.0) Imports: stats, Matrix (>= 1.2-14), MASS (>= 7.3-45), VGAM (>= 1.0-2), bbmle (>= 1.0.18), gamlss (>= 4.4-0), maxLik (>= 1.3-4), pscl (>= 1.4.9), BiocParallel (>= 1.12.0), Suggests: knitr, rmarkdown, SingleCellExperiment License: GPL-2 MD5sum: 8d446c9bd3e760ae2c67426a1911e42c NeedsCompilation: no Title: DEsingle for detecting three types of differential expression in single-cell RNA-seq data Description: DEsingle is an R package for differential expression (DE) analysis of single-cell RNA-seq (scRNA-seq) data. It defines and detects 3 types of differentially expressed genes between two groups of single cells, with regard to different expression status (DEs), differential expression abundance (DEa), and general differential expression (DEg). DEsingle employs Zero-Inflated Negative Binomial model to estimate the proportion of real and dropout zeros and to define and detect the 3 types of DE genes. Results showed that DEsingle outperforms existing methods for scRNA-seq DE analysis, and can reveal different types of DE genes that are enriched in different biological functions. biocViews: DifferentialExpression, GeneExpression, SingleCell, ImmunoOncology, RNASeq, Transcriptomics, Sequencing, Preprocessing, Software Author: Zhun Miao Maintainer: Zhun Miao URL: https://miaozhun.github.io/DEsingle/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DEsingle git_branch: RELEASE_3_8 git_last_commit: bf1cd87 git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/DEsingle_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEsingle_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEsingle_1.2.1.tgz vignettes: vignettes/DEsingle/inst/doc/DEsingle.html vignetteTitles: DEsingle hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEsingle/inst/doc/DEsingle.R Package: destiny Version: 2.12.0 Depends: R (>= 3.3.0) Imports: methods, graphics, grDevices, utils, stats, Matrix, Rcpp (>= 0.10.3), RcppEigen, Biobase, BiocGenerics, SummarizedExperiment, ggplot2, ggthemes, VIM, proxy, igraph, smoother, scales, scatterplot3d LinkingTo: Rcpp, RcppEigen, grDevices Suggests: nbconvertR, testthat, FNN, tidyr, SingleCellExperiment Enhances: rgl, SingleCellExperiment License: GPL Archs: i386, x64 MD5sum: ac5c9847de79461d53d1ad996f155d19 NeedsCompilation: yes Title: Creates diffusion maps Description: Create and plot diffusion maps. biocViews: CellBiology, CellBasedAssays, Clustering, Software, Visualization Author: Philipp Angerer [cre, aut] (), Laleh Haghverdi [ctb], Maren Büttner [ctb] (), Fabian Theis [ctb] (), Carsten Marr [ctb] (), Florian Büttner [ctb] () Maintainer: Philipp Angerer URL: https://github.com/theislab/destiny SystemRequirements: C++11 VignetteBuilder: nbconvertR BugReports: https://github.com/theislab/destiny/issues git_url: https://git.bioconductor.org/packages/destiny git_branch: RELEASE_3_8 git_last_commit: fd8c2e5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/destiny_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/destiny_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/destiny_2.12.0.tgz vignettes: vignettes/destiny/inst/doc/Diffusion-Map-recap.pdf, vignettes/destiny/inst/doc/Diffusion-Maps.pdf, vignettes/destiny/inst/doc/DPT.pdf, vignettes/destiny/inst/doc/Global-Sigma.pdf, vignettes/destiny/inst/doc/tidyverse.pdf vignetteTitles: Diffusion-Map-recap.pdf, Diffusion-Maps.pdf, DPT.pdf, Global-Sigma.pdf, tidyverse.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE suggestsMe: CellTrails, monocle, scater, slingshot Package: DEsubs Version: 1.8.1 Depends: R (>= 3.3), locfit Imports: graph, igraph, RBGL, circlize, limma, edgeR, EBSeq, NBPSeq, DESeq, stats, grDevices, graphics, pheatmap, utils, ggplot2, Matrix, jsonlite, tools, DESeq2, methods Suggests: RUnit, BiocGenerics, knitr License: GPL-3 MD5sum: 90cc0ee693e5b17182604558c98ab38a NeedsCompilation: no Title: DEsubs: an R package for flexible identification of differentially expressed subpathways using RNA-seq expression experiments Description: DEsubs is a network-based systems biology package that extracts disease-perturbed subpathways within a pathway network as recorded by RNA-seq experiments. It contains an extensive and customizable framework covering a broad range of operation modes at all stages of the subpathway analysis, enabling a case-specific approach. The operation modes refer to the pathway network construction and processing, the subpathway extraction, visualization and enrichment analysis with regard to various biological and pharmacological features. Its capabilities render it a tool-guide for both the modeler and experimentalist for the identification of more robust systems-level biomarkers for complex diseases. biocViews: SystemsBiology, GraphAndNetwork, Pathways, KEGG, GeneExpression, NetworkEnrichment, Network, RNASeq, DifferentialExpression, Normalization, ImmunoOncology Author: Aristidis G. Vrahatis and Panos Balomenos Maintainer: Aristidis G. Vrahatis , Panos Balomenos VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DEsubs git_branch: RELEASE_3_8 git_last_commit: 226e86e git_last_commit_date: 2018-11-28 Date/Publication: 2018-11-29 source.ver: src/contrib/DEsubs_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEsubs_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEsubs_1.8.1.tgz vignettes: vignettes/DEsubs/inst/doc/DEsubs.pdf vignetteTitles: DEsubs hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEsubs/inst/doc/DEsubs.R Package: DEXSeq Version: 1.28.3 Depends: BiocParallel, Biobase, SummarizedExperiment, IRanges (>= 2.5.17), GenomicRanges (>= 1.23.7), DESeq2 (>= 1.9.11), AnnotationDbi, RColorBrewer, S4Vectors Imports: BiocGenerics, biomaRt, hwriter, methods, stringr, Rsamtools, statmod, geneplotter, genefilter Suggests: GenomicFeatures (>= 1.13.29), pasilla (>= 0.2.22), parathyroidSE, BiocStyle, knitr License: GPL (>= 3) MD5sum: 30b0a8576fa6a56ba52fe0f2a9512619 NeedsCompilation: no Title: Inference of differential exon usage in RNA-Seq Description: The package is focused on finding differential exon usage using RNA-seq exon counts between samples with different experimental designs. It provides functions that allows the user to make the necessary statistical tests based on a model that uses the negative binomial distribution to estimate the variance between biological replicates and generalized linear models for testing. The package also provides functions for the visualization and exploration of the results. biocViews: ImmunoOncology, Sequencing, RNASeq, DifferentialExpression, AlternativeSplicing, DifferentialSplicing, GeneExpression, Visualization Author: Simon Anders and Alejandro Reyes Maintainer: Alejandro Reyes VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DEXSeq git_branch: RELEASE_3_8 git_last_commit: 4f592da git_last_commit_date: 2019-03-11 Date/Publication: 2019-03-11 source.ver: src/contrib/DEXSeq_1.28.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/DEXSeq_1.28.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DEXSeq_1.28.3.tgz vignettes: vignettes/DEXSeq/inst/doc/DEXSeq.pdf vignetteTitles: Analyzing RNA-seq data for differential exon usage with the "DEXSeq" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DEXSeq/inst/doc/DEXSeq.R dependsOnMe: IsoformSwitchAnalyzeR importsMe: IntEREst suggestsMe: GenomicRanges, stageR, subSeq Package: dexus Version: 1.22.1 Depends: R (>= 2.15), methods, BiocGenerics Imports: stats Suggests: parallel, statmod, DESeq, RColorBrewer License: LGPL (>= 2.0) Archs: i386, x64 MD5sum: df149bdc24e61ffbe4bdb9f9ed34095c NeedsCompilation: yes Title: DEXUS - Identifying Differential Expression in RNA-Seq Studies with Unknown Conditions or without Replicates Description: DEXUS identifies differentially expressed genes in RNA-Seq data under all possible study designs such as studies without replicates, without sample groups, and with unknown conditions. DEXUS works also for known conditions, for example for RNA-Seq data with two or multiple conditions. RNA-Seq read count data can be provided both by the S4 class Count Data Set and by read count matrices. Differentially expressed transcripts can be visualized by heatmaps, in which unknown conditions, replicates, and samples groups are also indicated. This software is fast since the core algorithm is written in C. For very large data sets, a parallel version of DEXUS is provided in this package. DEXUS is a statistical model that is selected in a Bayesian framework by an EM algorithm. DEXUS does not need replicates to detect differentially expressed transcripts, since the replicates (or conditions) are estimated by the EM method for each transcript. The method provides an informative/non-informative value to extract differentially expressed transcripts at a desired significance level or power. biocViews: ImmunoOncology, Sequencing, RNASeq, GeneExpression, DifferentialExpression, CellBiology, Classification, QualityControl Author: Guenter Klambauer Maintainer: Guenter Klambauer git_url: https://git.bioconductor.org/packages/dexus git_branch: RELEASE_3_8 git_last_commit: 36b7c42 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/dexus_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/dexus_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dexus_1.22.1.tgz vignettes: vignettes/dexus/inst/doc/dexus.pdf vignetteTitles: dexus: Manual for the R package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/dexus/inst/doc/dexus.R Package: DFP Version: 1.40.0 Depends: methods, Biobase (>= 2.5.5) License: GPL-2 MD5sum: 12981b09b4c4c8d2738eb7d9ae20e399 NeedsCompilation: no Title: Gene Selection Description: This package provides a supervised technique able to identify differentially expressed genes, based on the construction of \emph{Fuzzy Patterns} (FPs). The Fuzzy Patterns are built by means of applying 3 Membership Functions to discretized gene expression values. biocViews: Microarray, DifferentialExpression Author: R. Alvarez-Gonzalez, D. Glez-Pena, F. Diaz, F. Fdez-Riverola Maintainer: Rodrigo Alvarez-Glez git_url: https://git.bioconductor.org/packages/DFP git_branch: RELEASE_3_8 git_last_commit: 856ab59 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DFP_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DFP_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DFP_1.40.0.tgz vignettes: vignettes/DFP/inst/doc/DFP.pdf vignetteTitles: Howto: Discriminat Fuzzy Pattern hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DFP/inst/doc/DFP.R Package: DiffBind Version: 2.10.0 Depends: R (>= 3.5), GenomicRanges, SummarizedExperiment Imports: RColorBrewer, amap, edgeR, gplots, grDevices, limma, GenomicAlignments, locfit, stats, utils, IRanges, zlibbioc, lattice, systemPipeR, tools, Rcpp, dplyr, ggplot2, BiocParallel, parallel, S4Vectors, Rsamtools, DESeq2, methods, graphics, ggrepel LinkingTo: Rsamtools (>= 1.19.38), Rcpp Suggests: DESeq, BiocStyle, testthat Enhances: rgl, XLConnect License: Artistic-2.0 Archs: i386, x64 MD5sum: cebf717d82d269302bb10819892d6b6e NeedsCompilation: yes Title: Differential Binding Analysis of ChIP-Seq Peak Data Description: Compute differentially bound sites from multiple ChIP-seq experiments using affinity (quantitative) data. Also enables occupancy (overlap) analysis and plotting functions. biocViews: Sequencing, ChIPSeq, DifferentialPeakCalling Author: Rory Stark, Gord Brown Maintainer: Rory Stark git_url: https://git.bioconductor.org/packages/DiffBind git_branch: RELEASE_3_8 git_last_commit: 4631fd7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DiffBind_2.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DiffBind_2.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DiffBind_2.10.0.tgz vignettes: vignettes/DiffBind/inst/doc/DiffBind.pdf vignetteTitles: DiffBind: Differential binding analysis of ChIP-Seq peak data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DiffBind/inst/doc/DiffBind.R dependsOnMe: ChIPQC, vulcan Package: diffcoexp Version: 1.2.0 Depends: R (>= 3.5), WGCNA, SummarizedExperiment Imports: stats, DiffCorr, psych, igraph, BiocGenerics Suggests: GEOquery License: GPL (>2) MD5sum: 84d4b05956389705839485018b5aa33c NeedsCompilation: no Title: Differential Co-expression Analysis Description: A tool for the identification of differentially coexpressed links (DCLs) and differentially coexpressed genes (DCGs). DCLs are gene pairs with significantly different correlation coefficients under two conditions. DCGs are genes with significantly more DCLs than by chance. biocViews: GeneExpression, DifferentialExpression, Transcription, Microarray, OneChannel, TwoChannel, RNASeq, Sequencing, Coverage Author: Wenbin Wei, Sandeep Amberkar, Winston Hide Maintainer: Wenbin Wei URL: https://github.com/hidelab/diffcoexp git_url: https://git.bioconductor.org/packages/diffcoexp git_branch: RELEASE_3_8 git_last_commit: 8cf0c79 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/diffcoexp_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/diffcoexp_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diffcoexp_1.2.0.tgz vignettes: vignettes/diffcoexp/inst/doc/diffcoexp.pdf vignetteTitles: About diffcoexp hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/diffcoexp/inst/doc/diffcoexp.R Package: diffcyt Version: 1.2.23 Depends: R (>= 3.4.0) Imports: flowCore, FlowSOM, SummarizedExperiment, S4Vectors, limma, edgeR, lme4, multcomp, dplyr, tidyr, reshape2, magrittr, stats, methods, utils, grDevices, graphics, ComplexHeatmap, circlize, grid Suggests: BiocStyle, knitr, rmarkdown, testthat, HDCytoData, CATALYST License: MIT + file LICENSE MD5sum: 1aaf7d62abe990792f52e699dc1777f1 NeedsCompilation: no Title: Differential discovery in high-dimensional cytometry via high-resolution clustering Description: Statistical methods for differential discovery analyses in high-dimensional cytometry data (including flow cytometry, mass cytometry or CyTOF, and oligonucleotide-tagged cytometry), based on a combination of high-resolution clustering and empirical Bayes moderated tests adapted from transcriptomics. biocViews: ImmunoOncology, FlowCytometry, Proteomics, SingleCell, CellBasedAssays, CellBiology, Clustering, FeatureExtraction, Software Author: Lukas M. Weber [aut, cre] () Maintainer: Lukas M. Weber URL: https://github.com/lmweber/diffcyt VignetteBuilder: knitr BugReports: https://github.com/lmweber/diffcyt/issues git_url: https://git.bioconductor.org/packages/diffcyt git_branch: RELEASE_3_8 git_last_commit: 8bdfd18 git_last_commit_date: 2019-04-04 Date/Publication: 2019-04-04 source.ver: src/contrib/diffcyt_1.2.23.tar.gz win.binary.ver: bin/windows/contrib/3.5/diffcyt_1.2.23.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diffcyt_1.2.23.tgz vignettes: vignettes/diffcyt/inst/doc/diffcyt_workflow.html vignetteTitles: diffcyt workflow hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/diffcyt/inst/doc/diffcyt_workflow.R suggestsMe: CATALYST Package: diffGeneAnalysis Version: 1.64.0 Imports: graphics, grDevices, minpack.lm (>= 1.0-4), stats, utils License: GPL MD5sum: 506fc6d4eb0b4d2d23cee89b0f19c704 NeedsCompilation: no Title: Performs differential gene expression Analysis Description: Analyze microarray data biocViews: Microarray, DifferentialExpression Author: Choudary Jagarlamudi Maintainer: Choudary Jagarlamudi git_url: https://git.bioconductor.org/packages/diffGeneAnalysis git_branch: RELEASE_3_8 git_last_commit: 19c980d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/diffGeneAnalysis_1.64.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/diffGeneAnalysis_1.64.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diffGeneAnalysis_1.64.0.tgz vignettes: vignettes/diffGeneAnalysis/inst/doc/diffGeneAnalysis.pdf vignetteTitles: Documentation on diffGeneAnalysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/diffGeneAnalysis/inst/doc/diffGeneAnalysis.R Package: diffHic Version: 1.14.0 Depends: R (>= 3.5), GenomicRanges, InteractionSet, SummarizedExperiment Imports: Rsamtools, Rhtslib, Biostrings, BSgenome, rhdf5, edgeR, limma, csaw, locfit, methods, IRanges, S4Vectors, GenomeInfoDb, BiocGenerics, grDevices, graphics, stats, utils, Rcpp, rtracklayer LinkingTo: Rhtslib (>= 1.13.1), zlibbioc, Rcpp Suggests: BSgenome.Ecoli.NCBI.20080805, Matrix, testthat License: GPL-3 Archs: i386, x64 MD5sum: b3a4a022ba4b42c3c84d13a12a2e3e79 NeedsCompilation: yes Title: Differential Analyis of Hi-C Data Description: Detects differential interactions across biological conditions in a Hi-C experiment. Methods are provided for read alignment and data pre-processing into interaction counts. Statistical analysis is based on edgeR and supports normalization and filtering. Several visualization options are also available. biocViews: MultipleComparison, Preprocessing, Sequencing, Coverage, Alignment, Normalization, Clustering, HiC Author: Aaron Lun [aut, cre], Gordon Smyth [aut] Maintainer: Aaron Lun SystemRequirements: C++11 git_url: https://git.bioconductor.org/packages/diffHic git_branch: RELEASE_3_8 git_last_commit: eb331b6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/diffHic_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/diffHic_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diffHic_1.14.0.tgz vignettes: vignettes/diffHic/inst/doc/diffHic.pdf, vignettes/diffHic/inst/doc/diffHicUsersGuide.pdf vignetteTitles: diffHic Vignette, diffHicUsersGuide.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: DiffLogo Version: 2.6.0 Depends: R (>= 3.4), stats, cba Imports: grDevices, graphics, utils, tools Suggests: knitr, testthat, seqLogo, MotifDb License: GPL (>= 2) MD5sum: 7135a21ee77702fa93080a7076f9d314 NeedsCompilation: no Title: DiffLogo: A comparative visualisation of biooligomer motifs Description: DiffLogo is an easy-to-use tool to visualize motif differences. biocViews: Software, SequenceMatching, MultipleComparison, MotifAnnotation, Visualization, Alignment Author: c( person("Martin", "Nettling", role = c("aut", "cre"), email = "martin.nettling@informatik.uni-halle.de"), person("Hendrik", "Treutler", role = c("aut", "cre"), email = "hendrik.treutler@ipb-halle.de"), person("Jan", "Grau", role = c("aut", "ctb"), email = "grau@informatik.uni-halle.de"), person("Andrey", "Lando", role = c("aut", "ctb"), email = "dronte@autosome.ru"), person("Jens", "Keilwagen", role = c("aut", "ctb"), email = "jens.keilwagen@julius-kuehn.de"), person("Stefan", "Posch", role = "aut", email = "posch@informatik.uni-halle.de"), person("Ivo", "Grosse", role = "aut", email = "grosse@informatik.uni-halle.de")) Maintainer: Hendrik Treutler URL: https://github.com/mgledi/DiffLogo/ VignetteBuilder: knitr BugReports: https://github.com/mgledi/DiffLogo/issues git_url: https://git.bioconductor.org/packages/DiffLogo git_branch: RELEASE_3_8 git_last_commit: b40ac15 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DiffLogo_2.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DiffLogo_2.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DiffLogo_2.6.0.tgz vignettes: vignettes/DiffLogo/inst/doc/DiffLogoBasics.pdf vignetteTitles: Basics of the DiffLogo package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DiffLogo/inst/doc/DiffLogoBasics.R Package: diffloop Version: 1.10.0 Imports: methods, GenomicRanges, foreach, plyr, dplyr, reshape2, ggplot2, matrixStats, Sushi, edgeR, locfit, statmod, biomaRt, GenomeInfoDb, S4Vectors, IRanges, grDevices, graphics, stats, utils, Biobase, readr, data.table, rtracklayer, pbapply, limma Suggests: DESeq2, diffloopdata, ggrepel, knitr, rmarkdown, testthat License: MIT + file LICENSE MD5sum: a5f0e706ebe5ef31bbea8c497fe7ad90 NeedsCompilation: no Title: Identifying differential DNA loops from chromatin topology data Description: A suite of tools for subsetting, visualizing, annotating, and statistically analyzing the results of one or more ChIA-PET experiments or other assays that infer chromatin loops. biocViews: Preprocessing, QualityControl, Visualization, DataImport, DataRepresentation, GO Author: Caleb Lareau [aut, cre], Martin Aryee [aut] Maintainer: Caleb Lareau URL: https://github.com/aryeelab/diffloop VignetteBuilder: knitr BugReports: https://github.com/aryeelab/diffloop/issues git_url: https://git.bioconductor.org/packages/diffloop git_branch: RELEASE_3_8 git_last_commit: 442a0b0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/diffloop_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/diffloop_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diffloop_1.10.0.tgz vignettes: vignettes/diffloop/inst/doc/diffloop.html vignetteTitles: diffloop: Identifying differential DNA loops from chromatin topology data. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/diffloop/inst/doc/diffloop.R Package: diffuStats Version: 1.2.0 Depends: R (>= 3.4) Imports: grDevices, stats, methods, Matrix, MASS, expm, igraph, Rcpp, RcppArmadillo, RcppParallel, plyr, precrec LinkingTo: Rcpp, RcppArmadillo, RcppParallel Suggests: testthat, knitr, rmarkdown, ggplot2, ggsci, igraphdata, BiocStyle, reshape2 License: GPL-3 Archs: i386, x64 MD5sum: 98921980a28a6e7ce21bf8b1d83eb6f3 NeedsCompilation: yes Title: Diffusion scores on biological networks Description: Label propagation approaches are a widely used procedure in computational biology for giving context to molecular entities using network data. Node labels, which can derive from gene expression, genome-wide association studies, protein domains or metabolomics profiling, are propagated to their neighbours in the network, effectively smoothing the scores through prior annotated knowledge and prioritising novel candidates. The R package diffuStats contains a collection of diffusion kernels and scoring approaches that facilitates their computation and benchmarking. biocViews: Network, GeneExpression, GraphAndNetwork Author: Sergio Picart-Armada and Alexandre Perera-Lluna Maintainer: Sergio Picart-Armada SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/diffuStats git_branch: RELEASE_3_8 git_last_commit: 176ff48 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/diffuStats_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/diffuStats_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diffuStats_1.2.0.tgz vignettes: vignettes/diffuStats/inst/doc/diffuStats.pdf, vignettes/diffuStats/inst/doc/intro.html vignetteTitles: Case study: predicting protein function, Quick start hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/diffuStats/inst/doc/diffuStats.R, vignettes/diffuStats/inst/doc/intro.R Package: diggit Version: 1.14.0 Depends: R (>= 3.0.2), Biobase, methods Imports: ks, viper(>= 1.3.1), parallel Suggests: diggitdata License: file LICENSE MD5sum: a21bdc5d8e8cbb24df4dd989df2d1450 NeedsCompilation: no Title: Inference of Genetic Variants Driving Cellular Phenotypes Description: Inference of Genetic Variants Driving Cellullar Phenotypes by the DIGGIT algorithm biocViews: SystemsBiology, NetworkEnrichment, GeneExpression, FunctionalPrediction, GeneRegulation Author: Mariano J Alvarez Maintainer: Mariano J Alvarez git_url: https://git.bioconductor.org/packages/diggit git_branch: RELEASE_3_8 git_last_commit: 038aa4d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/diggit_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/diggit_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/diggit_1.14.0.tgz vignettes: vignettes/diggit/inst/doc/diggit.pdf vignetteTitles: Using DIGGIT hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/diggit/inst/doc/diggit.R Package: Director Version: 1.8.0 Depends: R (>= 3.3) Imports: htmltools, utils, grDevices License: GPL-3 + file LICENSE MD5sum: 2f4bce6a06d8920880b28603880e9284 NeedsCompilation: no Title: A dynamic visualization tool of multi-level data Description: Director is an R package designed to streamline the visualization of molecular effects in regulatory cascades. It utilizes the R package htmltools and a modified Sankey plugin of the JavaScript library D3 to provide a fast and easy, browser-enabled solution to discovering potentially interesting downstream effects of regulatory and/or co-expressed molecules. The diagrams are robust, interactive, and packaged as highly-portable HTML files that eliminate the need for third-party software to view. This enables a straightforward approach for scientists to interpret the data produced, and bioinformatics developers an alternative means to present relevant data. biocViews: Visualization Author: Katherine Icay [aut, cre] Maintainer: Katherine Icay URL: https://github.com/kzouchka/Director BugReports: https://github.com/kzouchka/Director/issues git_url: https://git.bioconductor.org/packages/Director git_branch: RELEASE_3_8 git_last_commit: 15d3d23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Director_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Director_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Director_1.8.0.tgz vignettes: vignettes/Director/inst/doc/vignette.pdf vignetteTitles: Using Director hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Director/inst/doc/vignette.R Package: DirichletMultinomial Version: 1.24.1 Depends: S4Vectors, IRanges Imports: stats4, methods, BiocGenerics Suggests: lattice, parallel, MASS, RColorBrewer, xtable License: LGPL-3 Archs: i386, x64 MD5sum: fdd42970564b1cc75fc254ea88a1ad7e NeedsCompilation: yes Title: Dirichlet-Multinomial Mixture Model Machine Learning for Microbiome Data Description: Dirichlet-multinomial mixture models can be used to describe variability in microbial metagenomic data. This package is an interface to code originally made available by Holmes, Harris, and Quince, 2012, PLoS ONE 7(2): 1-15, as discussed further in the man page for this package, ?DirichletMultinomial. biocViews: ImmunoOncology, Microbiome, Sequencing, Clustering, Classification, Metagenomics Author: Martin Morgan Maintainer: Martin Morgan SystemRequirements: gsl git_url: https://git.bioconductor.org/packages/DirichletMultinomial git_branch: RELEASE_3_8 git_last_commit: 50195d9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DirichletMultinomial_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DirichletMultinomial_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DirichletMultinomial_1.24.1.tgz vignettes: vignettes/DirichletMultinomial/inst/doc/DirichletMultinomial.pdf vignetteTitles: An introduction to DirichletMultinomial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DirichletMultinomial/inst/doc/DirichletMultinomial.R importsMe: TFBSTools Package: discordant Version: 1.6.1 Depends: R (>= 3.4) Imports: Biobase, stats, biwt, gtools, MASS, tools Suggests: BiocStyle, knitr License: GPL (>= 2) Archs: i386, x64 MD5sum: b7dcaaed12c47dc87d38d25f5254e9cd NeedsCompilation: yes Title: The Discordant Method: A Novel Approach for Differential Correlation Description: Discordant is a method to determine differential correlation of molecular feature pairs from -omics data using mixture models. Algorithm is explained further in Siska et al. biocViews: ImmunoOncology, BiologicalQuestion, StatisticalMethod, mRNAMicroarray, Microarray, Genetics, RNASeq Author: Charlotte Siska [cre,aut], Katerina Kechris [aut] Maintainer: Charlotte Siska URL: https://github.com/siskac/discordant VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/discordant git_branch: RELEASE_3_8 git_last_commit: d3336f0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/discordant_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/discordant_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/discordant_1.6.1.tgz vignettes: vignettes/discordant/inst/doc/Discordant_vignette.pdf vignetteTitles: Discordant hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/discordant/inst/doc/Discordant_vignette.R Package: dks Version: 1.28.0 Depends: R (>= 2.8) Imports: cubature License: GPL MD5sum: 5ef3fc109a885dd0a57afc15b4e1892e NeedsCompilation: no Title: The double Kolmogorov-Smirnov package for evaluating multiple testing procedures. Description: The dks package consists of a set of diagnostic functions for multiple testing methods. The functions can be used to determine if the p-values produced by a multiple testing procedure are correct. These functions are designed to be applied to simulated data. The functions require the entire set of p-values from multiple simulated studies, so that the joint distribution can be evaluated. biocViews: MultipleComparison, QualityControl Author: Jeffrey T. Leek Maintainer: Jeffrey T. Leek git_url: https://git.bioconductor.org/packages/dks git_branch: RELEASE_3_8 git_last_commit: 6e0e955 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/dks_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/dks_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dks_1.28.0.tgz vignettes: vignettes/dks/inst/doc/dks.pdf vignetteTitles: dksTutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/dks/inst/doc/dks.R Package: DMCHMM Version: 1.4.0 Depends: R (>= 3.5.0), SummarizedExperiment, methods, S4Vectors, BiocParallel, GenomicRanges, IRanges, fdrtool Imports: utils, stats, grDevices, rtracklayer, multcomp, calibrate, graphics Suggests: testthat, knitr License: GPL-3 MD5sum: 18d395ae88598cefb95eefe00606bef5 NeedsCompilation: no Title: Differentially Methylated CpG using Hidden Markov Model Description: A pipeline for identifying differentially methylated CpG sites using Hidden Markov Model in bisulfite sequencing data. biocViews: DifferentialMethylation, Sequencing, HiddenMarkovModel, Coverage Author: Farhad Shokoohi Maintainer: Farhad Shokoohi VignetteBuilder: knitr BugReports: https://github.com/shokoohi/DMCHMM/issues git_url: https://git.bioconductor.org/packages/DMCHMM git_branch: RELEASE_3_8 git_last_commit: 5f583ec git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DMCHMM_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DMCHMM_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DMCHMM_1.4.0.tgz vignettes: vignettes/DMCHMM/inst/doc/DMCHMM.html vignetteTitles: DMCHMM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DMCHMM/inst/doc/DMCHMM.R Package: DMRcaller Version: 1.14.2 Depends: R (>= 3.5), GenomicRanges, IRanges, S4Vectors Imports: parallel, Rcpp, RcppRoll, betareg, grDevices, graphics, methods, stats, utils Suggests: knitr, RUnit, BiocGenerics License: GPL-3 MD5sum: 42155127d7b103c963b0443683e8e531 NeedsCompilation: no Title: Differentially Methylated Regions caller Description: Uses Bisulfite sequencing data in two conditions and identifies differentially methylated regions between the conditions in CG and non-CG context. The input is the CX report files produced by Bismark and the output is a list of DMRs stored as GRanges objects. biocViews: DifferentialMethylation, DNAMethylation, Software, Sequencing, Coverage Author: Nicolae Radu Zabet , Jonathan Michael Foonlan Tsang , Alessandro Pio Greco and Ryan Merritt Maintainer: Nicolae Radu Zabet VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DMRcaller git_branch: RELEASE_3_8 git_last_commit: bf03ca3 git_last_commit_date: 2019-02-15 Date/Publication: 2019-02-15 source.ver: src/contrib/DMRcaller_1.14.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DMRcaller_1.14.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DMRcaller_1.14.2.tgz vignettes: vignettes/DMRcaller/inst/doc/DMRcaller.pdf vignetteTitles: DMRcaller hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DMRcaller/inst/doc/DMRcaller.R Package: DMRcate Version: 1.18.0 Depends: R (>= 3.3.0), minfi, DSS, DMRcatedata Imports: limma, missMethyl, GenomicRanges, parallel, methods, graphics, plyr, Gviz, IRanges, stats, utils, S4Vectors Suggests: knitr, RUnit, BiocGenerics, IlluminaHumanMethylation450kanno.ilmn12.hg19, IlluminaHumanMethylationEPICanno.ilm10b4.hg19 License: file LICENSE MD5sum: 4bfe58dbc6445926f73996a187c6aa1f NeedsCompilation: no Title: Methylation array and sequencing spatial analysis methods Description: De novo identification and extraction of differentially methylated regions (DMRs) from the human genome using Whole Genome Bisulphite Sequencing (WGBS) and Illumina Infinium Array (450K and EPIC) data. Provides functionality for filtering probes possibly confounded by SNPs and cross-hybridisation. Includes GRanges generation and plotting functions. biocViews: DifferentialMethylation, GeneExpression, Microarray, MethylationArray, Genetics, DifferentialExpression, GenomeAnnotation, DNAMethylation, OneChannel, TwoChannel, MultipleComparison, QualityControl, TimeCourse Author: Tim Peters Maintainer: Tim Peters VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DMRcate git_branch: RELEASE_3_8 git_last_commit: 533acd1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DMRcate_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DMRcate_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DMRcate_1.18.0.tgz vignettes: vignettes/DMRcate/inst/doc/DMRcate.pdf vignetteTitles: The DMRcate package user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/DMRcate/inst/doc/DMRcate.R importsMe: MEAL Package: DMRforPairs Version: 1.18.0 Depends: R (>= 2.15.2), Gviz (>= 1.2.1), R2HTML (>= 2.2.1), GenomicRanges (>= 1.10.7), parallel License: GPL (>= 2) MD5sum: 0f972e67a117c8be0dc1cc2fcf831ab7 NeedsCompilation: no Title: DMRforPairs: identifying Differentially Methylated Regions between unique samples using array based methylation profiles Description: DMRforPairs (formerly DMR2+) allows researchers to compare n>=2 unique samples with regard to their methylation profile. The (pairwise) comparison of n unique single samples distinguishes DMRforPairs from other existing pipelines as these often compare groups of samples in either single CpG locus or region based analysis. DMRforPairs defines regions of interest as genomic ranges with sufficient probes located in close proximity to each other. Probes in one region are optionally annotated to the same functional class(es). Differential methylation is evaluated by comparing the methylation values within each region between individual samples and (if the difference is sufficiently large), testing this difference formally for statistical significance. biocViews: Microarray, DNAMethylation, DifferentialMethylation, ReportWriting, Visualization, Annotation Author: Martin Rijlaarsdam [aut, cre], Yvonne vd Zwan [aut], Lambert Dorssers [aut], Leendert Looijenga [aut] Maintainer: Martin Rijlaarsdam URL: http://www.martinrijlaarsdam.nl, http://www.erasmusmc.nl/pathologie/research/lepo/3898639/ git_url: https://git.bioconductor.org/packages/DMRforPairs git_branch: RELEASE_3_8 git_last_commit: 6d98e69 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DMRforPairs_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DMRforPairs_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DMRforPairs_1.18.0.tgz vignettes: vignettes/DMRforPairs/inst/doc/DMRforPairs_vignette.pdf vignetteTitles: DMRforPairs_vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DMRforPairs/inst/doc/DMRforPairs_vignette.R Package: DMRScan Version: 1.8.0 Depends: R (>= 3.4.0) Imports: Matrix, MASS, RcppRoll,GenomicRanges, IRanges, GenomeInfoDb, methods, mvtnorm, stats, parallel Suggests: testthat, knitr, rmarkdown License: GPL-3 MD5sum: 0e746f249607060c44d9f4591fc72a1d NeedsCompilation: no Title: Detection of Differentially Methylated Regions Description: This package detects significant differentially methylated regions (for both qualitative and quantitative traits), using a scan statistic with underlying Poisson heuristics. The scan statistic will depend on a sequence of window sizes (# of CpGs within each window) and on a threshold for each window size. This threshold can be calculated by three different means: i) analytically using Siegmund et.al (2012) solution (preferred), ii) an important sampling as suggested by Zhang (2008), and a iii) full MCMC modeling of the data, choosing between a number of different options for modeling the dependency between each CpG. biocViews: Software, Technology, Sequencing, WholeGenome Author: Christian M Page [aut, cre], Linda Vos [aut], Trine B Rounge [ctb, dtc], Hanne F Harbo [ths], Bettina K Andreassen [aut] Maintainer: Christian M Page URL: https://github.com/christpa/DMRScan VignetteBuilder: knitr BugReports: https://github.com/christpa/DMRScan/issues PackageStatus: Active git_url: https://git.bioconductor.org/packages/DMRScan git_branch: RELEASE_3_8 git_last_commit: 28195a7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DMRScan_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DMRScan_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DMRScan_1.8.0.tgz vignettes: vignettes/DMRScan/inst/doc/DMRScan_vignette.pdf vignetteTitles: DMRScan.Rmd hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DMRScan/inst/doc/DMRScan_vignette.R Package: dmrseq Version: 1.2.5 Depends: R (>= 3.5), bsseq Imports: GenomicRanges, nlme, ggplot2, S4Vectors, RColorBrewer, bumphunter, DelayedMatrixStats (>= 1.1.13), matrixStats, BiocParallel, outliers, methods, locfit, IRanges, grDevices, graphics, stats, utils, annotatr, AnnotationHub, rtracklayer, GenomeInfoDb, splines Suggests: knitr, rmarkdown, BiocStyle License: MIT + file LICENSE MD5sum: cb52ecb7e623ec1eb5cd85dbedc656e9 NeedsCompilation: no Title: Detection and inference of differentially methylated regions from Whole Genome Bisulfite Sequencing Description: This package implements an approach for scanning the genome to detect and perform accurate inference on differentially methylated regions from Whole Genome Bisulfite Sequencing data. The method is based on comparing detected regions to a pooled null distribution, that can be implemented even when as few as two samples per population are available. Region-level statistics are obtained by fitting a generalized least squares (GLS) regression model with a nested autoregressive correlated error structure for the effect of interest on transformed methylation proportions. biocViews: ImmunoOncology, DNAMethylation, Epigenetics, MultipleComparison, Software, Sequencing, DifferentialMethylation, WholeGenome, Regression, FunctionalGenomics Author: Keegan Korthauer , Sutirtha Chakraborty , Yuval Benjamini , Rafael Irizarry Maintainer: Keegan Korthauer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/dmrseq git_branch: RELEASE_3_8 git_last_commit: 467248f git_last_commit_date: 2019-03-25 Date/Publication: 2019-03-25 source.ver: src/contrib/dmrseq_1.2.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/dmrseq_1.2.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dmrseq_1.2.5.tgz vignettes: vignettes/dmrseq/inst/doc/dmrseq.html vignetteTitles: Analyzing Bisulfite-seq data with dmrseq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/dmrseq/inst/doc/dmrseq.R Package: DNABarcodes Version: 1.12.0 Depends: Matrix, parallel Imports: Rcpp (>= 0.11.2), BH LinkingTo: Rcpp, BH Suggests: knitr, BiocStyle, rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 7c3ceda6d5afa1322c928dab20a28f74 NeedsCompilation: yes Title: A tool for creating and analysing DNA barcodes used in Next Generation Sequencing multiplexing experiments Description: The package offers a function to create DNA barcode sets capable of correcting insertion, deletion, and substitution errors. Existing barcodes can be analysed regarding their minimal, maximal and average distances between barcodes. Finally, reads that start with a (possibly mutated) barcode can be demultiplexed, i.e., assigned to their original reference barcode. biocViews: Preprocessing, Sequencing Author: Tilo Buschmann Maintainer: Tilo Buschmann VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DNABarcodes git_branch: RELEASE_3_8 git_last_commit: fc16fa4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DNABarcodes_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DNABarcodes_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DNABarcodes_1.12.0.tgz vignettes: vignettes/DNABarcodes/inst/doc/DNABarcodes.html vignetteTitles: DNABarcodes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DNABarcodes/inst/doc/DNABarcodes.R Package: DNAcopy Version: 1.56.0 License: GPL (>= 2) Archs: i386, x64 MD5sum: 184fc2c7f242fcfe49504ad1e135f34f NeedsCompilation: yes Title: DNA copy number data analysis Description: Implements the circular binary segmentation (CBS) algorithm to segment DNA copy number data and identify genomic regions with abnormal copy number. biocViews: Microarray, CopyNumberVariation Author: Venkatraman E. Seshan, Adam Olshen Maintainer: Venkatraman E. Seshan git_url: https://git.bioconductor.org/packages/DNAcopy git_branch: RELEASE_3_8 git_last_commit: e521826 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DNAcopy_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DNAcopy_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DNAcopy_1.56.0.tgz vignettes: vignettes/DNAcopy/inst/doc/DNAcopy.pdf vignetteTitles: DNAcopy hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DNAcopy/inst/doc/DNAcopy.R dependsOnMe: CGHcall, cghMCR, Clonality, CRImage, PureCN, snapCGH importsMe: ADaCGH2, AneuFinder, ArrayTV, ChAMP, cn.farms, CNAnorm, CNVrd2, contiBAIT, conumee, CopywriteR, GWASTools, MDTS, MEDIPS, MinimumDistance, QDNAseq, Repitools, sesame, snapCGH suggestsMe: beadarraySNP, cn.mops, fastseg, genoset Package: DNAshapeR Version: 1.10.0 Depends: R (>= 3.4), GenomicRanges Imports: Rcpp (>= 0.12.1), Biostrings, fields LinkingTo: Rcpp Suggests: AnnotationHub, knitr, rmarkdown, testthat, BSgenome.Scerevisiae.UCSC.sacCer3, BSgenome.Hsapiens.UCSC.hg19, caret License: GPL-2 Archs: i386, x64 MD5sum: d0da206934c751b45cc8606a22dbeb6d NeedsCompilation: yes Title: High-throughput prediction of DNA shape features Description: DNAhapeR is an R/BioConductor package for ultra-fast, high-throughput predictions of DNA shape features. The package allows to predict, visualize and encode DNA shape features for statistical learning. biocViews: StructuralPrediction, DNA3DStructure, Software Author: Tsu-Pei Chiu and Federico Comoglio Maintainer: Tsu-Pei Chiu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DNAshapeR git_branch: RELEASE_3_8 git_last_commit: d61d7d8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DNAshapeR_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DNAshapeR_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DNAshapeR_1.10.0.tgz vignettes: vignettes/DNAshapeR/inst/doc/DNAshapeR.html vignetteTitles: DNAshapeR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DNAshapeR/inst/doc/DNAshapeR.R Package: DominoEffect Version: 1.2.1 Depends: R(>= 3.5) Imports: biomaRt, data.table, utils, stats, Biostrings, SummarizedExperiment, VariantAnnotation, AnnotationDbi, GenomeInfoDb, IRanges, GenomicRanges Suggests: knitr, testthat License: GPL (>= 3) MD5sum: b4ff1d47e6409ad76352e13709577d25 NeedsCompilation: no Title: Identification and Annotation of Protein Hotspot Residues Description: The functions support identification and annotation of hotspot residues in proteins. These are individual amino acids that accumulate mutations at a much higher rate than their surrounding regions. biocViews: Software, SomaticMutation, Proteomics, SequenceMatching, Alignment Author: Marija Buljan and Peter Blattmann Maintainer: Marija Buljan , Peter Blattmann VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DominoEffect git_branch: RELEASE_3_8 git_last_commit: f16db7f git_last_commit_date: 2019-02-22 Date/Publication: 2019-02-22 source.ver: src/contrib/DominoEffect_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DominoEffect_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DominoEffect_1.2.1.tgz vignettes: vignettes/DominoEffect/inst/doc/Vignette.html vignetteTitles: Vignette for DominoEffect package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DominoEffect/inst/doc/Vignette.R Package: doppelgangR Version: 1.10.1 Depends: R (>= 3.5.0), Biobase, BiocParallel Imports: sva, impute, digest, mnormt, methods, grDevices, graphics, stats, SummarizedExperiment, utils Suggests: BiocStyle, knitr, rmarkdown, curatedOvarianData, ROCR, pROC, RUnit, simulatorZ, proxy License: GPL (>=2.0) MD5sum: 81743278a4db71d5b8881189df2c08af NeedsCompilation: no Title: Identify likely duplicate samples from genomic or meta-data Description: The main function is doppelgangR(), which takes as minimal input a list of ExpressionSet object, and searches all list pairs for duplicated samples. The search is based on the genomic data (exprs(eset)), phenotype/clinical data (pData(eset)), and "smoking guns" - supposedly unique identifiers found in pData(eset). biocViews: ImmunoOncology, RNASeq, Microarray, GeneExpression, QualityControl Author: Levi Waldron [aut, cre], Markus Reister [aut, ctb], Marcel Ramos [ctb] Maintainer: Levi Waldron URL: https://github.com/lwaldron/doppelgangR VignetteBuilder: knitr BugReports: https://github.com/lwaldron/doppelgangR/issues git_url: https://git.bioconductor.org/packages/doppelgangR git_branch: RELEASE_3_8 git_last_commit: 7424747 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/doppelgangR_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/doppelgangR_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/doppelgangR_1.10.1.tgz vignettes: vignettes/doppelgangR/inst/doc/doppelgangR.html vignetteTitles: doppelgangR vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/doppelgangR/inst/doc/doppelgangR.R Package: DOQTL Version: 1.18.0 Depends: R (>= 3.0.0), BSgenome.Mmusculus.UCSC.mm10, GenomicRanges, VariantAnnotation Imports: annotate, annotationTools, biomaRt, Biobase, BiocGenerics, corpcor, doParallel, foreach, fpc, hwriter, IRanges, iterators, mclust, QTLRel, regress, rhdf5, Rsamtools, RUnit, XML Suggests: MUGAExampleData License: GPL-3 Archs: i386, x64 MD5sum: 8b15a6d126d98936877e94434c13b3b5 NeedsCompilation: yes Title: Genotyping and QTL Mapping in DO Mice Description: DOQTL is a quantitative trait locus (QTL) mapping pipeline designed for Diversity Outbred mice and other multi-parent outbred populations. The package reads in data from genotyping arrays and perform haplotype reconstruction using a hidden Markov model (HMM). The haplotype probabilities from the HMM are then used to perform linkage mapping. When founder sequences are available, DOQTL can use the haplotype reconstructions to impute the founder sequences onto DO genomes and perform association mapping. biocViews: GeneticVariability, SNP, Genetics, HiddenMarkovModel Author: Daniel Gatti, Karl Broman, Andrey Shabalin, Petr Simecek Maintainer: Daniel Gatti URL: http://do.jax.org git_url: https://git.bioconductor.org/packages/DOQTL git_branch: RELEASE_3_8 git_last_commit: 5e629bd git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/DOQTL_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DOQTL_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DOQTL_1.18.0.tgz vignettes: vignettes/DOQTL/inst/doc/QTL_Mapping_DO_Mice.pdf vignetteTitles: QTL Mapping using Diversity Outbred Mice hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DOQTL/inst/doc/QTL_Mapping_DO_Mice.R Package: Doscheda Version: 1.4.1 Depends: R (>= 3.4) Imports: methods, drc, stats, httr, jsonlite, reshape2 , vsn, affy, limma, stringr, ggplot2, graphics, grDevices, calibrate, corrgram, gridExtra, DT, shiny, shinydashboard, readxl, d3heatmap, prodlim, matrixStats Suggests: BiocStyle, knitr, rmarkdown, testthat License: GPL-3 MD5sum: 619cfec033e9cc2010002d3c51fcb0ed NeedsCompilation: no Title: A DownStream Chemo-Proteomics Analysis Pipeline Description: Doscheda focuses on quantitative chemoproteomics used to determine protein interaction profiles of small molecules from whole cell or tissue lysates using Mass Spectrometry data. The package provides a shiny application to run the pipeline, several visualisations and a downloadable report of an experiment. biocViews: ImmunoOncology, Proteomics, Normalization, Preprocessing, MassSpectrometry, QualityControl, DataImport, Regression Author: Bruno Contrino, Piero Ricchiuto Maintainer: Bruno Contrino VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Doscheda git_branch: RELEASE_3_8 git_last_commit: 61b8284 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Doscheda_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Doscheda_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Doscheda_1.4.1.tgz vignettes: vignettes/Doscheda/inst/doc/Doscheda.html vignetteTitles: Doscheda hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Doscheda/inst/doc/Doscheda.R Package: DOSE Version: 3.8.2 Depends: R (>= 3.4.0) Imports: AnnotationDbi, BiocParallel, DO.db, fgsea, ggplot2, GOSemSim (>= 2.0.0), methods, qvalue, reshape2, S4Vectors, stats, utils Suggests: BiocStyle, clusterProfiler, knitr, org.Hs.eg.db, testthat License: Artistic-2.0 MD5sum: 72f683cea0ec82490a7c2893a66d002c NeedsCompilation: no Title: Disease Ontology Semantic and Enrichment analysis Description: This package implements five methods proposed by Resnik, Schlicker, Jiang, Lin and Wang respectively for measuring semantic similarities among DO terms and gene products. Enrichment analyses including hypergeometric model and gene set enrichment analysis are also implemented for discovering disease associations of high-throughput biological data. biocViews: Annotation, Visualization, MultipleComparison, GeneSetEnrichment, Pathways, Software Author: Guangchuang Yu [aut, cre], Li-Gen Wang [ctb], Vladislav Petyuk [ctb], Giovanni Dall'Olio [ctb] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/DOSE VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/DOSE/issues git_url: https://git.bioconductor.org/packages/DOSE git_branch: RELEASE_3_8 git_last_commit: 4d3d1ca git_last_commit_date: 2019-01-14 Date/Publication: 2019-01-14 source.ver: src/contrib/DOSE_3.8.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DOSE_3.8.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DOSE_3.8.2.tgz vignettes: vignettes/DOSE/inst/doc/DOSE.html, vignettes/DOSE/inst/doc/enrichmentAnalysis.html, vignettes/DOSE/inst/doc/GSEA.html, vignettes/DOSE/inst/doc/semanticAnalysis.html vignetteTitles: 00 DOSE introduction, 02 Disease enrichment analysis, 03 Disease GSEA, 01 DOSE semantic similarity analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DOSE/inst/doc/DOSE.R, vignettes/DOSE/inst/doc/enrichmentAnalysis.R, vignettes/DOSE/inst/doc/GSEA.R, vignettes/DOSE/inst/doc/semanticAnalysis.R importsMe: bioCancer, clusterProfiler, debrowser, eegc, enrichplot, GDCRNATools, LINC, MAGeCKFlute, meshes, miRsponge, MoonlightR, PathwaySplice, ReactomePA, RNASeqR suggestsMe: GOSemSim Package: drawProteins Version: 1.2.0 Depends: R (>= 3.4) Imports: ggplot2, httr, dplyr, readr, stringr Suggests: covr, testthat, knitr, rmarkdown, BiocStyle License: MIT + file LICENSE MD5sum: 206c89be262e17a9c1f9611aa69272c5 NeedsCompilation: no Title: Package to Draw Protein Schematics from Uniprot API output Description: This package draws protein schematics from Uniprot API output. From the JSON returned by the GET command, it creates a dataframe from the Uniprot Features API. This dataframe can then be used by geoms based on ggplot2 and base R to draw protein schematics. biocViews: Visualization, FunctionalPrediction, Proteomics Author: Paul Brennan [aut, cre] Maintainer: Paul Brennan URL: https://github.com/brennanpincardiff/drawProteins VignetteBuilder: knitr BugReports: https://github.com/brennanpincardiff/drawProteins/issues/new git_url: https://git.bioconductor.org/packages/drawProteins git_branch: RELEASE_3_8 git_last_commit: 7870417 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/drawProteins_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/drawProteins_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/drawProteins_1.2.0.tgz vignettes: vignettes/drawProteins/inst/doc/drawProteins_BiocStyle.html, vignettes/drawProteins/inst/doc/drawProteins_extract_transcripts_BiocStyle.html vignetteTitles: Using drawProteins, Using drawProteins hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/drawProteins/inst/doc/drawProteins_BiocStyle.R, vignettes/drawProteins/inst/doc/drawProteins_extract_transcripts_BiocStyle.R Package: DRIMSeq Version: 1.10.1 Depends: R (>= 3.4.0) Imports: utils, stats, MASS, GenomicRanges, IRanges, S4Vectors, BiocGenerics, methods, BiocParallel, limma, edgeR, ggplot2, reshape2 Suggests: PasillaTranscriptExpr, GeuvadisTranscriptExpr, grid, BiocStyle, knitr, testthat License: GPL (>= 3) MD5sum: 42ed0703c4a75da4d21dbf1ab3c689d2 NeedsCompilation: no Title: Differential transcript usage and tuQTL analyses with Dirichlet-multinomial model in RNA-seq Description: The package provides two frameworks. One for the differential transcript usage analysis between different conditions and one for the tuQTL analysis. Both are based on modeling the counts of genomic features (i.e., transcripts) with the Dirichlet-multinomial distribution. The package also makes available functions for visualization and exploration of the data and results. biocViews: ImmunoOncology, SNP, AlternativeSplicing, DifferentialSplicing, Genetics, RNASeq, Sequencing, WorkflowStep, MultipleComparison, GeneExpression, DifferentialExpression Author: Malgorzata Nowicka [aut, cre] Maintainer: Malgorzata Nowicka VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DRIMSeq git_branch: RELEASE_3_8 git_last_commit: 333b72b git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DRIMSeq_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DRIMSeq_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DRIMSeq_1.10.1.tgz vignettes: vignettes/DRIMSeq/inst/doc/DRIMSeq.pdf vignetteTitles: Differential transcript usage and transcript usage QTL analyses in RNA-seq with the DRIMSeq package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DRIMSeq/inst/doc/DRIMSeq.R importsMe: IsoformSwitchAnalyzeR Package: DriverNet Version: 1.22.0 Depends: R (>= 2.10), methods License: GPL-3 MD5sum: 0a220e7958f082c4c716ee19f77f735a NeedsCompilation: no Title: Drivernet: uncovering somatic driver mutations modulating transcriptional networks in cancer Description: DriverNet is a package to predict functional important driver genes in cancer by integrating genome data (mutation and copy number variation data) and transcriptome data (gene expression data). The different kinds of data are combined by an influence graph, which is a gene-gene interaction network deduced from pathway data. A greedy algorithm is used to find the possible driver genes, which may mutated in a larger number of patients and these mutations will push the gene expression values of the connected genes to some extreme values. biocViews: Network Author: Ali Bashashati, Reza Haffari, Jiarui Ding, Gavin Ha, Kenneth Liu, Jamie Rosner and Sohrab Shah Maintainer: Jiarui Ding git_url: https://git.bioconductor.org/packages/DriverNet git_branch: RELEASE_3_8 git_last_commit: 65eb5d0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DriverNet_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DriverNet_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DriverNet_1.22.0.tgz vignettes: vignettes/DriverNet/inst/doc/DriverNet-Overview.pdf vignetteTitles: An introduction to DriverNet hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DriverNet/inst/doc/DriverNet-Overview.R Package: DropletUtils Version: 1.2.2 Depends: R (>= 3.5), BiocParallel, SingleCellExperiment Imports: S4Vectors, Matrix, methods, utils, stats, edgeR, Rcpp, rhdf5, HDF5Array LinkingTo: Rcpp, beachmat, Rhdf5lib Suggests: testthat, beachmat, knitr, BiocStyle, rmarkdown License: GPL-3 Archs: i386, x64 MD5sum: 8f93b2bd3148dbc41728e1410b18d645 NeedsCompilation: yes Title: Utilities for Handling Single-Cell Droplet Data Description: Provides a number of utility functions for handling single-cell (RNA-seq) data from droplet technologies such as 10X Genomics. This includes data loading, identification of cells from empty droplets, removal of barcode-swapped pseudo-cells, and downsampling of the count matrix. biocViews: ImmunoOncology, SingleCell, Sequencing, RNASeq, GeneExpression, Transcriptomics, DataImport, Coverage Author: Aaron Lun [aut, cre], Jonathan Griffiths [ctb], Davis McCarthy [ctb] Maintainer: Aaron Lun SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DropletUtils git_branch: RELEASE_3_8 git_last_commit: 1424ff5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DropletUtils_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DropletUtils_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DropletUtils_1.2.2.tgz vignettes: vignettes/DropletUtils/inst/doc/DropletUtils.html vignetteTitles: Utilities for handling droplet-based single-cell RNA-seq data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DropletUtils/inst/doc/DropletUtils.R Package: DrugVsDisease Version: 2.24.2 Depends: R (>= 2.10), affy, limma, biomaRt, ArrayExpress, GEOquery, DrugVsDiseasedata, cMap2data, qvalue Imports: annotate, hgu133a.db, hgu133a2.db, hgu133plus2.db, RUnit, BiocGenerics, xtable License: GPL-3 MD5sum: 70b3c0ce3a8af1afa7f2d08b718092f8 NeedsCompilation: no Title: Comparison of disease and drug profiles using Gene set Enrichment Analysis Description: This package generates ranked lists of differential gene expression for either disease or drug profiles. Input data can be downloaded from Array Express or GEO, or from local CEL files. Ranked lists of differential expression and associated p-values are calculated using Limma. Enrichment scores (Subramanian et al. PNAS 2005) are calculated to a reference set of default drug or disease profiles, or a set of custom data supplied by the user. Network visualisation of significant scores are output in Cytoscape format. biocViews: Microarray, GeneExpression, Clustering Author: C. Pacini Maintainer: j. Saez-Rodriguez git_url: https://git.bioconductor.org/packages/DrugVsDisease git_branch: RELEASE_3_8 git_last_commit: c129fb3 git_last_commit_date: 2018-12-08 Date/Publication: 2018-12-08 source.ver: src/contrib/DrugVsDisease_2.24.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/DrugVsDisease_2.24.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DrugVsDisease_2.24.2.tgz vignettes: vignettes/DrugVsDisease/inst/doc/DrugVsDisease.pdf vignetteTitles: DrugVsDisease hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DrugVsDisease/inst/doc/DrugVsDisease.R Package: dSimer Version: 1.8.0 Depends: R (>= 3.3.0), igraph (>= 1.0.1) Imports: stats, Rcpp (>= 0.11.3), ggplot2, reshape2, GO.db, org.Hs.eg.db, AnnotationDbi, graphics LinkingTo: Rcpp Suggests: knitr, rmarkdown, BiocStyle License: GPL (>= 2) Archs: i386, x64 MD5sum: 6f09cfd76372e623ef50b24ad7bd076f NeedsCompilation: yes Title: Integration of Disease Similarity Methods Description: dSimer is an R package which provides computation of nine methods for measuring disease-disease similarity, including a standard cosine similarity measure and eight function-based methods. The disease similarity matrix obtained from these nine methods can be visualized through heatmap and network. Biological data widely used in disease-disease associations study are also provided by dSimer. biocViews: Software, Visualization, Network Author: Min Li , Peng Ni with contributions from Zhihui Fei and Ping Huang. Maintainer: Peng Ni VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/dSimer git_branch: RELEASE_3_8 git_last_commit: 78df868 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/dSimer_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/dSimer_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dSimer_1.8.0.tgz vignettes: vignettes/dSimer/inst/doc/dSimer.html vignetteTitles: Integration of Disease Similarity Methods hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/dSimer/inst/doc/dSimer.R Package: DSS Version: 2.30.1 Depends: R (>= 3.3), Biobase, bsseq, splines, methods Imports: stats, graphics, DelayedArray Suggests: BiocStyle License: GPL Archs: i386, x64 MD5sum: f234d3bc11132379d64b03c3dd493b25 NeedsCompilation: yes Title: Dispersion shrinkage for sequencing data Description: DSS is an R library performing differntial analysis for count-based sequencing data. It detectes differentially expressed genes (DEGs) from RNA-seq, and differentially methylated loci or regions (DML/DMRs) from bisulfite sequencing (BS-seq). The core of DSS is a new dispersion shrinkage method for estimating the dispersion parameter from Gamma-Poisson or Beta-Binomial distributions. biocViews: ImmunoOncology, Sequencing, RNASeq, ChIPSeq, DNAMethylation,GeneExpression, DifferentialExpression,DifferentialMethylation Author: Hao Wu Maintainer: Hao Wu git_url: https://git.bioconductor.org/packages/DSS git_branch: RELEASE_3_8 git_last_commit: 6420932 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/DSS_2.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/DSS_2.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DSS_2.30.1.tgz vignettes: vignettes/DSS/inst/doc/DSS.pdf vignetteTitles: Differential expression for RNA-seq data with dispersion shrinkage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DSS/inst/doc/DSS.R dependsOnMe: DMRcate importsMe: kissDE Package: DTA Version: 2.28.0 Depends: R (>= 2.10), LSD Imports: scatterplot3d License: Artistic-2.0 MD5sum: 7af46c4b3ca3d98a4c9398b0d68a1c71 NeedsCompilation: no Title: Dynamic Transcriptome Analysis Description: Dynamic Transcriptome Analysis (DTA) can monitor the cellular response to perturbations with higher sensitivity and temporal resolution than standard transcriptomics. The package implements the underlying kinetic modeling approach capable of the precise determination of synthesis- and decay rates from individual microarray or RNAseq measurements. biocViews: Microarray, DifferentialExpression, GeneExpression, Transcription Author: Bjoern Schwalb, Benedikt Zacher, Sebastian Duemcke, Achim Tresch Maintainer: Bjoern Schwalb git_url: https://git.bioconductor.org/packages/DTA git_branch: RELEASE_3_8 git_last_commit: 4b7f7b1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DTA_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DTA_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DTA_2.28.0.tgz vignettes: vignettes/DTA/inst/doc/DTA.pdf vignetteTitles: A guide to Dynamic Transcriptome Analysis (DTA) hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DTA/inst/doc/DTA.R Package: dualKS Version: 1.42.0 Depends: R (>= 2.6.0), Biobase (>= 1.15.0), affy, methods Imports: graphics License: LGPL (>= 2.0) MD5sum: aef440fc9d6a7971b3ca41a51f7368c1 NeedsCompilation: no Title: Dual KS Discriminant Analysis and Classification Description: This package implements a Kolmogorov Smirnov rank-sum based algorithm for training (i.e. discriminant analysis--identification of genes that discriminate between classes) and classification of gene expression data sets. One of the chief strengths of this approach is that it is amenable to the "multiclass" problem. That is, it can discriminate between more than 2 classes. biocViews: Microarray, Classification Author: Eric J. Kort, Yarong Yang Maintainer: Eric J. Kort , Yarong Yang git_url: https://git.bioconductor.org/packages/dualKS git_branch: RELEASE_3_8 git_last_commit: e00107d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/dualKS_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/dualKS_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dualKS_1.42.0.tgz vignettes: vignettes/dualKS/inst/doc/dualKS.pdf vignetteTitles: dualKS.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/dualKS/inst/doc/dualKS.R Package: DupChecker Version: 1.20.0 Imports: tools, R.utils, RCurl Suggests: knitr License: GPL (>= 2) MD5sum: c5867bb93e37d69cb72527f796de4e0f NeedsCompilation: no Title: a package for checking high-throughput genomic data redundancy in meta-analysis Description: Meta-analysis has become a popular approach for high-throughput genomic data analysis because it often can significantly increase power to detect biological signals or patterns in datasets. However, when using public-available databases for meta-analysis, duplication of samples is an often encountered problem, especially for gene expression data. Not removing duplicates would make study results questionable. We developed a Bioconductor package DupChecker that efficiently identifies duplicated samples by generating MD5 fingerprints for raw data. biocViews: Preprocessing Author: Quanhu Sheng, Yu Shyr, Xi Chen Maintainer: "Quanhu SHENG" VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/DupChecker git_branch: RELEASE_3_8 git_last_commit: 6d629a3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DupChecker_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DupChecker_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DupChecker_1.20.0.tgz vignettes: vignettes/DupChecker/inst/doc/DupChecker.pdf vignetteTitles: Validate genomic data with "DupChecker" package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/DupChecker/inst/doc/DupChecker.R Package: dupRadar Version: 1.12.1 Depends: R (>= 3.2.0) Imports: Rsubread (>= 1.14.1) Suggests: BiocStyle, knitr, rmarkdown, AnnotationHub License: GPL-3 MD5sum: 58ff3f96c44230db7e9483621a213421 NeedsCompilation: no Title: Assessment of duplication rates in RNA-Seq datasets Description: Duplication rate quality control for RNA-Seq datasets. biocViews: Technology, Sequencing, RNASeq, QualityControl, ImmunoOncology Author: Sergi Sayols , Holger Klein Maintainer: Sergi Sayols , Holger Klein VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/dupRadar git_branch: RELEASE_3_8 git_last_commit: fc184d1 git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/dupRadar_1.12.1.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dupRadar_1.12.1.tgz vignettes: vignettes/dupRadar/inst/doc/dupRadar.html vignetteTitles: Using dupRadar hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/dupRadar/inst/doc/dupRadar.R Package: dyebias Version: 1.42.0 Depends: R (>= 1.4.1), marray, Biobase Suggests: limma, convert, GEOquery, dyebiasexamples, methods License: GPL-3 MD5sum: a5c7c84939a73cac498807188f7c8ee8 NeedsCompilation: no Title: The GASSCO method for correcting for slide-dependent gene-specific dye bias Description: Many two-colour hybridizations suffer from a dye bias that is both gene-specific and slide-specific. The former depends on the content of the nucleotide used for labeling; the latter depends on the labeling percentage. The slide-dependency was hitherto not recognized, and made addressing the artefact impossible. Given a reasonable number of dye-swapped pairs of hybridizations, or of same vs. same hybridizations, both the gene- and slide-biases can be estimated and corrected using the GASSCO method (Margaritis et al., Mol. Sys. Biol. 5:266 (2009), doi:10.1038/msb.2009.21) biocViews: Microarray, TwoChannel, QualityControl, Preprocessing Author: Philip Lijnzaad and Thanasis Margaritis Maintainer: Philip Lijnzaad URL: http://www.holstegelab.nl/publications/margaritis_lijnzaad git_url: https://git.bioconductor.org/packages/dyebias git_branch: RELEASE_3_8 git_last_commit: 07f6958 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/dyebias_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/dyebias_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/dyebias_1.42.0.tgz vignettes: vignettes/dyebias/inst/doc/dyebias-vignette.pdf vignetteTitles: dye bias correction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/dyebias/inst/doc/dyebias-vignette.R Package: DynDoc Version: 1.60.0 Depends: methods, utils Imports: methods License: Artistic-2.0 MD5sum: 9ab4d310071f59bab69bad2f75c152e7 NeedsCompilation: no Title: Dynamic document tools Description: A set of functions to create and interact with dynamic documents and vignettes. biocViews: ReportWriting, Infrastructure Author: R. Gentleman, Jeff Gentry Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/DynDoc git_branch: RELEASE_3_8 git_last_commit: 8b21d20 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/DynDoc_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/DynDoc_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/DynDoc_1.60.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: tkWidgets Package: EasyqpcR Version: 1.24.0 Imports: plyr, matrixStats, plotrix, gWidgetsRGtk2 Suggests: SLqPCR, qpcrNorm, qpcR, knitr License: GPL (>=2) MD5sum: 858ce6239d7775d581f9dd188ea167df NeedsCompilation: no Title: EasyqpcR for low-throughput real-time quantitative PCR data analysis Description: This package is based on the qBase algorithms published by Hellemans et al. in 2007. The EasyqpcR package allows you to import easily qPCR data files as described in the vignette. Thereafter, you can calculate amplification efficiencies, relative quantities and their standard errors, normalization factors based on the best reference genes choosen (using the SLqPCR package), and then the normalized relative quantities, the NRQs scaled to your control and their standard errors. This package has been created for low-throughput qPCR data analysis. biocViews: qPCR, GeneExpression Author: Le Pape Sylvain Maintainer: Le Pape Sylvain git_url: https://git.bioconductor.org/packages/EasyqpcR git_branch: RELEASE_3_8 git_last_commit: 2342a77 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EasyqpcR_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EasyqpcR_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EasyqpcR_1.24.0.tgz vignettes: vignettes/EasyqpcR/inst/doc/vignette_EasyqpcR.pdf vignetteTitles: EasyqpcR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EasyqpcR/inst/doc/vignette_EasyqpcR.R Package: easyRNASeq Version: 2.18.4 Imports: Biobase (>= 2.39.1), BiocGenerics (>= 0.25.1), BiocParallel (>= 1.13.1), biomaRt (>= 2.35.8), Biostrings (>= 2.47.6), DESeq (>= 1.31.0), edgeR (>= 3.21.6), GenomeInfoDb (>= 1.15.2), genomeIntervals (>= 1.35.1), GenomicAlignments (>= 1.15.6), GenomicRanges (>= 1.31.8), SummarizedExperiment (>= 1.9.9), graphics, IRanges (>= 2.13.13), LSD (>= 3.0), locfit, methods, parallel, Rsamtools (>= 1.31.2), S4Vectors (>= 0.17.25), ShortRead (>= 1.37.1), utils Suggests: BiocStyle (>= 2.7.8), BSgenome (>= 1.39.0), BSgenome.Dmelanogaster.UCSC.dm3 (>= 1.4.0), curl, knitr, rmarkdown, RUnit (>= 0.4.31) License: Artistic-2.0 MD5sum: c98fbdefb1bde53dbdde8042611e5672 NeedsCompilation: no Title: Count summarization and normalization for RNA-Seq data Description: Calculates the coverage of high-throughput short-reads against a genome of reference and summarizes it per feature of interest (e.g. exon, gene, transcript). The data can be normalized as 'RPKM' or by the 'DESeq' or 'edgeR' package. biocViews: ImmunoOncology, GeneExpression, RNASeq, Genetics, Preprocessing Author: Nicolas Delhomme, Ismael Padioleau, Bastian Schiffthaler, Niklas Maehler Maintainer: Nicolas Delhomme VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/easyRNASeq git_branch: RELEASE_3_8 git_last_commit: 0931ba8 git_last_commit_date: 2019-04-13 Date/Publication: 2019-04-14 source.ver: src/contrib/easyRNASeq_2.18.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/easyRNASeq_2.18.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/easyRNASeq_2.18.4.tgz vignettes: vignettes/easyRNASeq/inst/doc/easyRNASeq.pdf, vignettes/easyRNASeq/inst/doc/simpleRNASeq.html vignetteTitles: R / Bioconductor for High Throughput Sequence Analysis, geneNetworkR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/easyRNASeq/inst/doc/easyRNASeq.R, vignettes/easyRNASeq/inst/doc/simpleRNASeq.R importsMe: msgbsR suggestsMe: SeqGSEA Package: EBarrays Version: 2.46.0 Depends: R (>= 1.8.0), Biobase, lattice, methods Imports: Biobase, cluster, graphics, grDevices, lattice, methods, stats License: GPL (>= 2) Archs: i386, x64 MD5sum: 4a42f6740313e671fbd0433896b6f227 NeedsCompilation: yes Title: Unified Approach for Simultaneous Gene Clustering and Differential Expression Identification Description: EBarrays provides tools for the analysis of replicated/unreplicated microarray data. biocViews: Clustering, DifferentialExpression Author: Ming Yuan, Michael Newton, Deepayan Sarkar and Christina Kendziorski Maintainer: Ming Yuan git_url: https://git.bioconductor.org/packages/EBarrays git_branch: RELEASE_3_8 git_last_commit: 182aee9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EBarrays_2.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EBarrays_2.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EBarrays_2.46.0.tgz vignettes: vignettes/EBarrays/inst/doc/vignette.pdf vignetteTitles: Introduction to EBarrays hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EBarrays/inst/doc/vignette.R dependsOnMe: EBcoexpress, gaga, geNetClassifier importsMe: casper suggestsMe: Category Package: EBcoexpress Version: 1.26.0 Depends: EBarrays, mclust, minqa Suggests: graph, igraph, colorspace License: GPL (>= 2) Archs: i386, x64 MD5sum: 391a4f44e4fc3c4578121104a30877c6 NeedsCompilation: yes Title: EBcoexpress for Differential Co-Expression Analysis Description: An Empirical Bayesian Approach to Differential Co-Expression Analysis at the Gene-Pair Level biocViews: Bayesian Author: John A. Dawson Maintainer: John A. Dawson git_url: https://git.bioconductor.org/packages/EBcoexpress git_branch: RELEASE_3_8 git_last_commit: 095c479 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EBcoexpress_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EBcoexpress_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EBcoexpress_1.26.0.tgz vignettes: vignettes/EBcoexpress/inst/doc/EBcoexpressVignette.pdf vignetteTitles: EBcoexpress Demo hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EBcoexpress/inst/doc/EBcoexpressVignette.R dependsOnMe: SRGnet Package: EBImage Version: 4.24.0 Depends: methods Imports: BiocGenerics (>= 0.7.1), graphics, grDevices, stats, abind, tiff, jpeg, png, locfit, fftwtools (>= 0.9-7), utils, htmltools, htmlwidgets, RCurl Suggests: BiocStyle, digest, knitr, rmarkdown, shiny License: LGPL Archs: i386, x64 MD5sum: 3ddadf0e47dfe26013b10378dee62c55 NeedsCompilation: yes Title: Image processing and analysis toolbox for R Description: EBImage provides general purpose functionality for image processing and analysis. In the context of (high-throughput) microscopy-based cellular assays, EBImage offers tools to segment cells and extract quantitative cellular descriptors. This allows the automation of such tasks using the R programming language and facilitates the use of other tools in the R environment for signal processing, statistical modeling, machine learning and visualization with image data. biocViews: Visualization Author: Andrzej Oleś, Gregoire Pau, Mike Smith, Oleg Sklyar, Wolfgang Huber, with contributions from Joseph Barry and Philip A. Marais Maintainer: Andrzej Oleś URL: https://github.com/aoles/EBImage VignetteBuilder: knitr BugReports: https://github.com/aoles/EBImage/issues git_url: https://git.bioconductor.org/packages/EBImage git_branch: RELEASE_3_8 git_last_commit: 2d41204 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EBImage_4.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EBImage_4.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EBImage_4.24.0.tgz vignettes: vignettes/EBImage/inst/doc/EBImage-introduction.html vignetteTitles: Introduction to EBImage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EBImage/inst/doc/EBImage-introduction.R dependsOnMe: Cardinal, CRImage, flowcatchR, imageHTS importsMe: bnbc, flowCHIC, heatmaps, MaxContrastProjection, yamss suggestsMe: HilbertVis, tofsims Package: EBSEA Version: 1.10.0 Imports: edgeR, limma, graphics, stats, plyr License: GPL-2 MD5sum: 6e9147314c2308892969992ca042ddec NeedsCompilation: no Title: Exon Based Strategy for Expression Analysis of genes Description: Calculates differential expression of genes based on exon counts of genes obtained from RNA-seq sequencing data. biocViews: Software, DifferentialExpression, GeneExpression, Sequencing Author: Arfa Mehmood, Asta Laiho, Laura L. Elo Maintainer: Arfa Mehmood git_url: https://git.bioconductor.org/packages/EBSEA git_branch: RELEASE_3_8 git_last_commit: 8779479 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EBSEA_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EBSEA_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EBSEA_1.10.0.tgz vignettes: vignettes/EBSEA/inst/doc/EBSEA.pdf vignetteTitles: EBSEA: Exon Based Strategy for Expression Analysis of genes hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EBSEA/inst/doc/EBSEA.R Package: EBSeq Version: 1.22.1 Depends: blockmodeling, gplots, testthat, R (>= 3.0.0) License: Artistic-2.0 MD5sum: e1c4b6272a6aff94cfc115d6ba0af8cc NeedsCompilation: no Title: An R package for gene and isoform differential expression analysis of RNA-seq data Description: Differential Expression analysis at both gene and isoform level using RNA-seq data biocViews: ImmunoOncology, StatisticalMethod, DifferentialExpression, MultipleComparison, RNASeq, Sequencing Author: Ning Leng, Christina Kendziorski Maintainer: Ning Leng git_url: https://git.bioconductor.org/packages/EBSeq git_branch: RELEASE_3_8 git_last_commit: b431657 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/EBSeq_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EBSeq_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EBSeq_1.22.1.tgz vignettes: vignettes/EBSeq/inst/doc/EBSeq_Vignette.pdf vignetteTitles: EBSeq Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EBSeq/inst/doc/EBSeq_Vignette.R dependsOnMe: EBSeqHMM, Oscope importsMe: DEsubs, scDD suggestsMe: compcodeR Package: EBSeqHMM Version: 1.16.1 Depends: EBSeq License: Artistic-2.0 MD5sum: 99b65375abb77bed298bebc6fcffcfe9 NeedsCompilation: no Title: Bayesian analysis for identifying gene or isoform expression changes in ordered RNA-seq experiments Description: The EBSeqHMM package implements an auto-regressive hidden Markov model for statistical analysis in ordered RNA-seq experiments (e.g. time course or spatial course data). The EBSeqHMM package provides functions to identify genes and isoforms that have non-constant expression profile over the time points/positions, and cluster them into expression paths. biocViews: ImmunoOncology, StatisticalMethod, DifferentialExpression, MultipleComparison, RNASeq, Sequencing, GeneExpression, Bayesian, HiddenMarkovModel, TimeCourse Author: Ning Leng, Christina Kendziorski Maintainer: Ning Leng git_url: https://git.bioconductor.org/packages/EBSeqHMM git_branch: RELEASE_3_8 git_last_commit: 8e14b5f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/EBSeqHMM_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EBSeqHMM_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EBSeqHMM_1.16.1.tgz vignettes: vignettes/EBSeqHMM/inst/doc/EBSeqHMM_vignette.pdf vignetteTitles: HMM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EBSeqHMM/inst/doc/EBSeqHMM_vignette.R Package: ecolitk Version: 1.54.0 Depends: R (>= 2.10) Imports: Biobase, graphics, methods Suggests: ecoliLeucine, ecolicdf, graph, multtest, affy License: GPL (>= 2) MD5sum: a0d9620024909dcbb12b20e3b5ebf92f NeedsCompilation: no Title: Meta-data and tools for E. coli Description: Meta-data and tools to work with E. coli. The tools are mostly plotting functions to work with circular genomes. They can used with other genomes/plasmids. biocViews: Annotation, Visualization Author: Laurent Gautier Maintainer: Laurent Gautier git_url: https://git.bioconductor.org/packages/ecolitk git_branch: RELEASE_3_8 git_last_commit: 2849ebd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ecolitk_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ecolitk_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ecolitk_1.54.0.tgz vignettes: vignettes/ecolitk/inst/doc/ecolitk.pdf vignetteTitles: ecolitk hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ecolitk/inst/doc/ecolitk.R Package: EDASeq Version: 2.16.3 Depends: Biobase (>= 2.15.1), ShortRead (>= 1.11.42) Imports: methods, graphics, BiocGenerics, IRanges (>= 1.13.9), DESeq, aroma.light, Rsamtools (>= 1.5.75), biomaRt, Biostrings, AnnotationDbi, GenomicFeatures, GenomicRanges, BiocManager Suggests: BiocStyle, knitr, yeastRNASeq, leeBamViews, edgeR, KernSmooth, testthat License: Artistic-2.0 MD5sum: 6b89211e4e1ade48127524b54a8d5a2a NeedsCompilation: no Title: Exploratory Data Analysis and Normalization for RNA-Seq Description: Numerical and graphical summaries of RNA-Seq read data. Within-lane normalization procedures to adjust for GC-content effect (or other gene-level effects) on read counts: loess robust local regression, global-scaling, and full-quantile normalization (Risso et al., 2011). Between-lane normalization procedures to adjust for distributional differences between lanes (e.g., sequencing depth): global-scaling and full-quantile normalization (Bullard et al., 2010). biocViews: ImmunoOncology, Sequencing, RNASeq, Preprocessing, QualityControl, DifferentialExpression Author: Davide Risso [aut, cre, cph], Sandrine Dudoit [aut], Ludwig Geistlinger [ctb] Maintainer: Davide Risso URL: https://github.com/drisso/EDASeq VignetteBuilder: knitr BugReports: https://github.com/drisso/EDASeq/issues git_url: https://git.bioconductor.org/packages/EDASeq git_branch: RELEASE_3_8 git_last_commit: abf1b7c git_last_commit_date: 2019-01-10 Date/Publication: 2019-01-10 source.ver: src/contrib/EDASeq_2.16.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/EDASeq_2.16.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EDASeq_2.16.3.tgz vignettes: vignettes/EDASeq/inst/doc/EDASeq.html vignetteTitles: EDASeq Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EDASeq/inst/doc/EDASeq.R dependsOnMe: metaseqR, RUVSeq importsMe: consensusDE, DaMiRseq, EnrichmentBrowser, TCGAbiolinks suggestsMe: DEScan2, HTSFilter Package: EDDA Version: 1.20.1 Depends: Rcpp (>= 0.10.4),parallel,methods,ROCR,DESeq,baySeq,snow,edgeR Imports: graphics, stats, utils, parallel, methods, ROCR, DESeq, baySeq, snow, edgeR LinkingTo: Rcpp License: GPL (>= 2) Archs: i386, x64 MD5sum: 28bedf0b293d64808ba970c681b891f7 NeedsCompilation: yes Title: Experimental Design in Differential Abundance analysis Description: EDDA can aid in the design of a range of common experiments such as RNA-seq, Nanostring assays, RIP-seq and Metagenomic sequencing, and enables researchers to comprehensively investigate the impact of experimental decisions on the ability to detect differential abundance. This work was published on 3 December 2014 at Genome Biology under the title "The importance of study design for detecting differentially abundant features in high-throughput experiments" (http://genomebiology.com/2014/15/12/527). biocViews: ImmunoOncology, Sequencing, ExperimentalDesign, Normalization, RNASeq, ChIPSeq Author: Li Juntao, Luo Huaien, Chia Kuan Hui Burton, Niranjan Nagarajan Maintainer: Chia Kuan Hui Burton , Niranjan Nagarajan URL: http://edda.gis.a-star.edu.sg/, http://genomebiology.com/2014/15/12/527 git_url: https://git.bioconductor.org/packages/EDDA git_branch: RELEASE_3_8 git_last_commit: 1328485 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/EDDA_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EDDA_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EDDA_1.20.1.tgz vignettes: vignettes/EDDA/inst/doc/EDDA.pdf vignetteTitles: EDDA Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: edge Version: 2.14.0 Depends: R(>= 3.1.0), Biobase Imports: methods, splines, sva, snm, jackstraw, qvalue(>= 1.99.0), MASS Suggests: testthat, knitr, ggplot2, reshape2 License: MIT + file LICENSE Archs: i386, x64 MD5sum: 6797ccce69d0cfc8d172ead461d3cec7 NeedsCompilation: yes Title: Extraction of Differential Gene Expression Description: The edge package implements methods for carrying out differential expression analyses of genome-wide gene expression studies. Significance testing using the optimal discovery procedure and generalized likelihood ratio tests (equivalent to F-tests and t-tests) are implemented for general study designs. Special functions are available to facilitate the analysis of common study designs, including time course experiments. Other packages such as snm, sva, and qvalue are integrated in edge to provide a wide range of tools for gene expression analysis. biocViews: MultipleComparison, DifferentialExpression, TimeCourse, Regression, GeneExpression, DataImport Author: John D. Storey, Jeffrey T. Leek and Andrew J. Bass Maintainer: John D. Storey , Andrew J. Bass URL: https://github.com/jdstorey/edge VignetteBuilder: knitr BugReports: https://github.com/jdstorey/edge/issues git_url: https://git.bioconductor.org/packages/edge git_branch: RELEASE_3_8 git_last_commit: 17fa86d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/edge_2.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/edge_2.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/edge_2.14.0.tgz vignettes: vignettes/edge/inst/doc/edge.pdf vignetteTitles: edge Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/edge/inst/doc/edge.R Package: edgeR Version: 3.24.3 Depends: R (>= 2.15.0), limma (>= 3.34.5) Imports: graphics, stats, utils, methods, locfit, Rcpp LinkingTo: Rcpp Suggests: AnnotationDbi, jsonlite, org.Hs.eg.db, readr, rhdf5, splines License: GPL (>=2) Archs: i386, x64 MD5sum: 4ceb5925b1cb40cfe5560a734174a6a9 NeedsCompilation: yes Title: Empirical Analysis of Digital Gene Expression Data in R Description: Differential expression analysis of RNA-seq expression profiles with biological replication. Implements a range of statistical methodology based on the negative binomial distributions, including empirical Bayes estimation, exact tests, generalized linear models and quasi-likelihood tests. As well as RNA-seq, it be applied to differential signal analysis of other types of genomic data that produce counts, including ChIP-seq, Bisulfite-seq, SAGE and CAGE. biocViews: GeneExpression, Transcription, AlternativeSplicing, Coverage, DifferentialExpression, DifferentialSplicing, DifferentialMethylation, GeneSetEnrichment, Pathways, Genetics, DNAMethylation, Bayesian, Clustering, ChIPSeq, Regression, TimeCourse, Sequencing, RNASeq, BatchEffect, SAGE, Normalization, QualityControl, MultipleComparison, BiomedicalInformatics, CellBiology, FunctionalGenomics, Epigenetics, Genetics, ImmunoOncology, SystemsBiology, Transcriptomics Author: Yunshun Chen , Aaron Lun , Davis McCarthy , Xiaobei Zhou , Mark Robinson , Gordon Smyth Maintainer: Yunshun Chen , Aaron Lun , Mark Robinson , Davis McCarthy , Gordon Smyth URL: http://bioinf.wehi.edu.au/edgeR SystemRequirements: C++11 git_url: https://git.bioconductor.org/packages/edgeR git_branch: RELEASE_3_8 git_last_commit: d1260a2 git_last_commit_date: 2019-01-01 Date/Publication: 2019-01-02 source.ver: src/contrib/edgeR_3.24.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/edgeR_3.24.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/edgeR_3.24.3.tgz vignettes: vignettes/edgeR/inst/doc/edgeR.pdf, vignettes/edgeR/inst/doc/edgeRUsersGuide.pdf vignetteTitles: edgeR Vignette, edgeRUsersGuide.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: ASpli, DBChIP, IntEREst, manta, methylMnM, RNASeqR, RUVSeq, TCC, tRanslatome importsMe: affycoretools, ampliQueso, ArrayExpressHTS, baySeq, clusterExperiment, compcodeR, consensusDE, coseq, countsimQC, csaw, DaMiRseq, debrowser, DEComplexDisease, DEFormats, DEGreport, DEsubs, DiffBind, diffcyt, diffHic, diffloop, DRIMSeq, DropletUtils, easyRNASeq, EBSEA, EDDA, eegc, EGSEA, EnrichmentBrowser, erccdashboard, ERSSA, GDCRNATools, Glimma, GSEABenchmarkeR, HTSFilter, icetea, IsoformSwitchAnalyzeR, MEDIPS, metaseqR, MIGSA, MLSeq, msgbsR, msmsTests, multiHiCcompare, NBSplice, PathoStat, PROPER, psichomics, regsplice, Repitools, rnaSeqMap, scde, scone, scran, SIMD, singscore, splatter, STATegRa, SVAPLSseq, systemPipeR, TCGAbiolinks, TCseq, TimeSeriesExperiment, tweeDEseq, vidger, yarn, zinbwave suggestsMe: ABSSeq, biobroom, BitSeq, ClassifyR, clonotypeR, cqn, cydar, DEScan2, EDASeq, gage, gCrisprTools, GenomicAlignments, GenomicRanges, goseq, groHMM, GSAR, GSVA, ideal, missMethyl, multiMiR, regionReport, SSPA, stageR, subSeq, SummarizedBenchmark, tximport, variancePartition, Wrench, zFPKM Package: eegc Version: 1.8.1 Depends: R (>= 3.4.0) Imports: R.utils, gplots, sna, wordcloud, igraph, pheatmap, edgeR, DESeq2, clusterProfiler, S4Vectors, ggplot2, org.Hs.eg.db, org.Mm.eg.db, limma, DOSE, AnnotationDbi Suggests: knitr License: GPL-2 MD5sum: acac7f97fcfcc9641aab15beda10c60c NeedsCompilation: no Title: Engineering Evaluation by Gene Categorization (eegc) Description: This package has been developed to evaluate cellular engineering processes for direct differentiation of stem cells or conversion (transdifferentiation) of somatic cells to primary cells based on high throughput gene expression data screened either by DNA microarray or RNA sequencing. The package takes gene expression profiles as inputs from three types of samples: (i) somatic or stem cells to be (trans)differentiated (input of the engineering process), (ii) induced cells to be evaluated (output of the engineering process) and (iii) target primary cells (reference for the output). The package performs differential gene expression analysis for each pair-wise sample comparison to identify and evaluate the transcriptional differences among the 3 types of samples (input, output, reference). The ideal goal is to have induced and primary reference cell showing overlapping profiles, both very different from the original cells. biocViews: ImmunoOncology, Microarray, Sequencing, RNASeq, DifferentialExpression, GeneRegulation, GeneSetEnrichment, GeneExpression, GeneTarget Author: Xiaoyuan Zhou, Guofeng Meng, Christine Nardini, Hongkang Mei Maintainer: Xiaoyuan Zhou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/eegc git_branch: RELEASE_3_8 git_last_commit: 33d0080 git_last_commit_date: 2018-12-21 Date/Publication: 2018-12-21 source.ver: src/contrib/eegc_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/eegc_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/eegc_1.8.1.tgz vignettes: vignettes/eegc/inst/doc/eegc.pdf vignetteTitles: Engineering Evaluation by Gene Categorization (eegc) hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/eegc/inst/doc/eegc.R Package: EGAD Version: 1.10.0 Depends: R(>= 3.3) Imports: gplots, Biobase, GEOquery, limma, arrayQualityMetrics, impute, RColorBrewer, zoo, igraph, plyr, Matrix, MASS, RCurl, affy Suggests: knitr, rmarkdown, testthat License: GPL-2 MD5sum: 798b2f43513b64bec9a70c5a6b387efe NeedsCompilation: no Title: Extending guilt by association by degree Description: The package implements a series of highly efficient tools to calculate functional properties of networks based on guilt by association methods. biocViews: Software, FunctionalGenomics, SystemsBiology, GenePrediction, FunctionalPrediction, NetworkEnrichment, GraphAndNetwork, Network Author: Sara Ballouz [aut, cre], Melanie Weber [aut, ctb], Paul Pavlidis [aut], Jesse Gillis [aut, ctb] Maintainer: Sara Ballouz VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EGAD git_branch: RELEASE_3_8 git_last_commit: 93a1288 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EGAD_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EGAD_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EGAD_1.10.0.tgz vignettes: vignettes/EGAD/inst/doc/EGAD.pdf vignetteTitles: "EGAD user guide" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EGAD/inst/doc/EGAD.R Package: EGSEA Version: 1.10.1 Depends: R (>= 3.5), Biobase, gage (>= 2.14.4), AnnotationDbi, topGO (>= 2.16.0), pathview (>= 1.4.2) Imports: PADOG (>= 1.6.0), GSVA (>= 1.12.0), globaltest (>= 5.18.0), limma (>= 3.20.9), edgeR (>= 3.6.8), HTMLUtils (>= 0.1.5), hwriter (>= 1.2.2), gplots (>= 2.14.2), ggplot2 (>= 1.0.0), safe (>= 3.4.0), stringi (>= 0.5.0), parallel, stats, metap, grDevices, graphics, utils, org.Hs.eg.db, org.Mm.eg.db, org.Rn.eg.db, RColorBrewer, methods, EGSEAdata (>= 1.3.1), Glimma (>= 1.4.0), htmlwidgets, plotly, DT Suggests: BiocStyle, knitr, testthat License: GPL-3 MD5sum: d5fc8fd276ef0ef99b7798257f8dc0c1 NeedsCompilation: no Title: Ensemble of Gene Set Enrichment Analyses Description: This package implements the Ensemble of Gene Set Enrichment Analyses (EGSEA) method for gene set testing. biocViews: ImmunoOncology, DifferentialExpression, GO, GeneExpression, GeneSetEnrichment, Genetics, Microarray, MultipleComparison, OneChannel, Pathways, RNASeq, Sequencing, Software, SystemsBiology, TwoChannel,Metabolomics, Proteomics, KEGG, GraphAndNetwork, GeneSignaling, GeneTarget, NetworkEnrichment, Network, Classification Author: Monther Alhamdoosh, Luyi Tian, Milica Ng and Matthew Ritchie Maintainer: Monther Alhamdoosh VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EGSEA git_branch: RELEASE_3_8 git_last_commit: ac649ee git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/EGSEA_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EGSEA_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EGSEA_1.10.1.tgz vignettes: vignettes/EGSEA/inst/doc/EGSEA.pdf vignetteTitles: EGSEA vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EGSEA/inst/doc/EGSEA.R Package: eiR Version: 1.22.0 Depends: R (>= 2.10.0), ChemmineR (>= 2.15.15), methods, DBI Imports: snow, tools, snowfall, RUnit, methods, ChemmineR, RCurl, digest, BiocGenerics, gespeR,RcppAnnoy (>= 0.0.9) Suggests: BiocStyle, knitcitations, knitr, knitrBootstrap License: Artistic-2.0 Archs: x64 MD5sum: 02df663489eb5a3924b07e84a86f38e4 NeedsCompilation: yes Title: Accelerated similarity searching of small molecules Description: The eiR package provides utilities for accelerated structure similarity searching of very large small molecule data sets using an embedding and indexing approach. biocViews: Cheminformatics, BiomedicalInformatics, Pharmacogenetics, Pharmacogenomics, MicrotitrePlateAssay, CellBasedAssays, Visualization, Infrastructure, DataImport, Clustering, Proteomics, Metabolomics Author: Kevin Horan, Yiqun Cao and Tyler Backman Maintainer: Thomas Girke URL: https://github.com/girke-lab/eiR VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/eiR git_branch: RELEASE_3_8 git_last_commit: f11bf8f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/eiR_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/eiR_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/eiR_1.22.0.tgz vignettes: vignettes/eiR/inst/doc/eiR.html vignetteTitles: eiR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: TRUE Rfiles: vignettes/eiR/inst/doc/eiR.R Package: eisa Version: 1.34.0 Depends: isa2, Biobase (>= 2.17.8), AnnotationDbi, methods Imports: BiocGenerics, Category, genefilter, DBI Suggests: igraph (>= 0.6), Matrix, GOstats, GO.db, KEGG.db, biclust, MASS, xtable, ALL, hgu95av2.db, targetscan.Hs.eg.db, org.Hs.eg.db License: GPL (>= 2) MD5sum: 114415b5b584378e8c2f93e081833045 NeedsCompilation: no Title: Expression data analysis via the Iterative Signature Algorithm Description: The Iterative Signature Algorithm (ISA) is a biclustering method; it finds correlated blocks (transcription modules) in gene expression (or other tabular) data. The ISA is capable of finding overlapping modules and it is resilient to noise. This package provides a convenient interface to the ISA, using standard BioConductor data structures; and also contains various visualization tools that can be used with other biclustering algorithms. biocViews: Classification, Visualization, Microarray, GeneExpression Author: Gabor Csardi Maintainer: Gabor Csardi git_url: https://git.bioconductor.org/packages/eisa git_branch: RELEASE_3_8 git_last_commit: d164cb0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/eisa_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/eisa_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/eisa_1.34.0.tgz vignettes: vignettes/eisa/inst/doc/EISA_tutorial.pdf vignetteTitles: The Iterative Signature Algorithm for Gene Expression Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/eisa/inst/doc/EISA_tutorial.R dependsOnMe: ExpressionView importsMe: ExpressionView Package: ELBOW Version: 1.18.1 Depends: R (>= 2.15.0) Imports: graphics, stats, utils Suggests: DESeq, GEOquery, limma, simpleaffy, affyPLM, RColorBrewer, hgu133plus2cdf, hgu133plus2probe License: file LICENSE License_is_FOSS: yes License_restricts_use: no MD5sum: 66a2e8881b2fb3ea5cd7d76785a8c123 NeedsCompilation: no Title: ELBOW - Evaluating foLd change By the lOgit Way Description: Elbow an improved fold change test that uses cluster analysis and pattern recognition to set cut off limits that are derived directly from intrareplicate variance without assuming a normal distribution for as few as 2 biological replicates. Elbow also provides the same consistency as fold testing in cross platform analysis. Elbow has lower false positive and false negative rates than standard fold testing when both are evaluated using T testing and Statistical Analysis of Microarray using 12 replicates (six replicates each for initial and final conditions). Elbow provides a null value based on initial condition replicates and gives error bounds for results to allow better evaluation of significance. biocViews: ImmunoOncology, Technology, Microarray, RNASeq, Sequencing, Sequencing, Software, MultiChannel, OneChannel, TwoChannel, GeneExpression Author: Xiangli Zhang, Natalie Bjorklund, Graham Alvare, Tom Ryzdak, Richard Sparling, Brian Fristensky Maintainer: Graham Alvare , Xiangli Zhang git_url: https://git.bioconductor.org/packages/ELBOW git_branch: RELEASE_3_8 git_last_commit: 89932af git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ELBOW_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ELBOW_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ELBOW_1.18.1.tgz vignettes: vignettes/ELBOW/inst/doc/Elbow_tutorial_vignette.pdf vignetteTitles: Using ELBOW --- the definitive ELBOW tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ELBOW/inst/doc/Elbow_tutorial_vignette.R Package: ELMER Version: 2.6.3 Depends: R (>= 3.4.0), ELMER.data Imports: GenomicRanges, ggplot2, reshape, grid, grDevices, graphics, methods, parallel, stats, utils, IRanges, GenomeInfoDb, S4Vectors, GenomicFeatures, TCGAbiolinks (>= 2.9.2), plyr, Matrix, dplyr, Gviz, ComplexHeatmap, circlize, MultiAssayExperiment, SummarizedExperiment, biomaRt, doParallel, downloader, ggrepel, lattice, magrittr, readr, rvest, xml2, plotly, gridExtra, rmarkdown, stringr, tibble, tidyr, progress, purrr, rtracklayer, DelayedArray Suggests: BiocStyle, knitr, testthat, data.table, DT, GenomicInteractions, webshot, R.utils, covr License: GPL-3 MD5sum: 288f66fe079a76907bdee1b730d35957 NeedsCompilation: no Title: Inferring Regulatory Element Landscapes and Transcription Factor Networks Using Cancer Methylomes Description: ELMER is designed to use DNA methylation and gene expression from a large number of samples to infere regulatory element landscape and transcription factor network in primary tissue. biocViews: DNAMethylation, GeneExpression, MotifAnnotation, Software, GeneRegulation, Transcription, Network Author: Tiago Chedraoui Silva [aut, cre], Lijing Yao [aut], Simon Coetzee [aut], Nicole Gull [ctb], Hui Shen [ctb], Peter Laird [ctb], Peggy Farnham [aut], Dechen Li [ctb], Benjamin Berman [aut] Maintainer: Tiago Chedraoui Silva VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ELMER git_branch: RELEASE_3_8 git_last_commit: 684c8d9 git_last_commit_date: 2019-04-02 Date/Publication: 2019-04-02 source.ver: src/contrib/ELMER_2.6.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/ELMER_2.6.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ELMER_2.6.3.tgz vignettes: vignettes/ELMER/inst/doc/analysis_data_input.html, vignettes/ELMER/inst/doc/analysis_diff_meth.html, vignettes/ELMER/inst/doc/analysis_get_pair.html, vignettes/ELMER/inst/doc/analysis_gui.html, vignettes/ELMER/inst/doc/analysis_motif_enrichment.html, vignettes/ELMER/inst/doc/analysis_regulatory_tf.html, vignettes/ELMER/inst/doc/index.html, vignettes/ELMER/inst/doc/input.html, vignettes/ELMER/inst/doc/pipe.html, vignettes/ELMER/inst/doc/plots_heatmap.html, vignettes/ELMER/inst/doc/plots_motif_enrichment.html, vignettes/ELMER/inst/doc/plots_scatter.html, vignettes/ELMER/inst/doc/plots_schematic.html, vignettes/ELMER/inst/doc/plots_TF.html, vignettes/ELMER/inst/doc/usecase.html vignetteTitles: "3.1 - Data input - Creating MAE object", "3.2 - Identifying differentially methylated probes", "3.3 - Identifying putative probe-gene pairs", 5 - Integrative analysis workshop with TCGAbiolinks and ELMER - Analysis GUI, "3.4 - Motif enrichment analysis on the selected probes", "3.5 - Identifying regulatory TFs", "1 - ELMER v.2: An R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles", "2 - Introduction: Input data", "3.6 - TCGA.pipe: Running ELMER for TCGA data in a compact way", "4.5 - Heatmap plots", "4.3 - Motif enrichment plots", "4.1 - Scatter plots", "4.2 - Schematic plots", "4.4 - Regulatory TF plots", "11 - ELMER: Use case" hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ELMER/inst/doc/analysis_data_input.R, vignettes/ELMER/inst/doc/analysis_diff_meth.R, vignettes/ELMER/inst/doc/analysis_get_pair.R, vignettes/ELMER/inst/doc/analysis_gui.R, vignettes/ELMER/inst/doc/analysis_motif_enrichment.R, vignettes/ELMER/inst/doc/analysis_regulatory_tf.R, vignettes/ELMER/inst/doc/index.R, vignettes/ELMER/inst/doc/input.R, vignettes/ELMER/inst/doc/pipe.R, vignettes/ELMER/inst/doc/plots_heatmap.R, vignettes/ELMER/inst/doc/plots_motif_enrichment.R, vignettes/ELMER/inst/doc/plots_scatter.R, vignettes/ELMER/inst/doc/plots_schematic.R, vignettes/ELMER/inst/doc/plots_TF.R, vignettes/ELMER/inst/doc/usecase.R importsMe: TCGAbiolinksGUI Package: EMDomics Version: 2.12.0 Depends: R (>= 3.2.1) Imports: emdist, BiocParallel, matrixStats, ggplot2, CDFt, preprocessCore Suggests: knitr License: MIT + file LICENSE MD5sum: 0f9d117d39c59207bccc6f6ecad2f5e9 NeedsCompilation: no Title: Earth Mover's Distance for Differential Analysis of Genomics Data Description: The EMDomics algorithm is used to perform a supervised multi-class analysis to measure the magnitude and statistical significance of observed continuous genomics data between groups. Usually the data will be gene expression values from array-based or sequence-based experiments, but data from other types of experiments can also be analyzed (e.g. copy number variation). Traditional methods like Significance Analysis of Microarrays (SAM) and Linear Models for Microarray Data (LIMMA) use significance tests based on summary statistics (mean and standard deviation) of the distributions. This approach lacks power to identify expression differences between groups that show high levels of intra-group heterogeneity. The Earth Mover's Distance (EMD) algorithm instead computes the "work" needed to transform one distribution into another, thus providing a metric of the overall difference in shape between two distributions. Permutation of sample labels is used to generate q-values for the observed EMD scores. This package also incorporates the Komolgorov-Smirnov (K-S) test and the Cramer von Mises test (CVM), which are both common distribution comparison tests. biocViews: Software, DifferentialExpression, GeneExpression, Microarray Author: Sadhika Malladi [aut, cre], Daniel Schmolze [aut, cre], Andrew Beck [aut], Sheida Nabavi [aut] Maintainer: Sadhika Malladi and Daniel Schmolze VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EMDomics git_branch: RELEASE_3_8 git_last_commit: cf2c6f2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EMDomics_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EMDomics_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EMDomics_2.12.0.tgz vignettes: vignettes/EMDomics/inst/doc/EMDomics.html vignetteTitles: EMDomics Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/EMDomics/inst/doc/EMDomics.R Package: EmpiricalBrownsMethod Version: 1.10.0 Depends: R (>= 3.2.0) Suggests: BiocStyle, testthat, knitr, rmarkdown License: MIT + file LICENSE MD5sum: 2d91e211bf843eefad77a8526c65a370 NeedsCompilation: no Title: Uses Brown's method to combine p-values from dependent tests Description: Combining P-values from multiple statistical tests is common in bioinformatics. However, this procedure is non-trivial for dependent P-values. This package implements an empirical adaptation of Brown’s Method (an extension of Fisher’s Method) for combining dependent P-values which is appropriate for highly correlated data sets found in high-throughput biological experiments. biocViews: StatisticalMethod, GeneExpression, Pathways Author: William Poole Maintainer: David Gibbs URL: https://github.com/IlyaLab/CombiningDependentPvaluesUsingEBM.git VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EmpiricalBrownsMethod git_branch: RELEASE_3_8 git_last_commit: bf39ac6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EmpiricalBrownsMethod_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EmpiricalBrownsMethod_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EmpiricalBrownsMethod_1.10.0.tgz vignettes: vignettes/EmpiricalBrownsMethod/inst/doc/ebmVignette.html vignetteTitles: Empirical Browns Method hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/EmpiricalBrownsMethod/inst/doc/ebmVignette.R Package: ENCODExplorer Version: 2.8.0 Depends: R (>= 3.3), shiny, DT, shinythemes Imports: tools, jsonlite, parallel, RCurl, tidyr, data.table, dplyr, stringr, stringi Suggests: RUnit,BiocGenerics,knitr, curl, httr License: Artistic-2.0 MD5sum: 6bd1aa3aa9897fbd1d85c19d47c9aaaf NeedsCompilation: no Title: A compilation of ENCODE metadata Description: This package allows user to quickly access ENCODE project files metadata and give access to helper functions to query the ENCODE rest api, download ENCODE datasets and save the database in SQLite format. biocViews: Infrastructure, DataImport Author: Charles Joly Beauparlant , Audrey Lemacon , Louis Gendron Astrid-Louise Deschenes, and Arnaud Droit Maintainer: Charles Joly Beauparlant VignetteBuilder: knitr BugReports: https://github.com/CharlesJB/ENCODExplorer/issues git_url: https://git.bioconductor.org/packages/ENCODExplorer git_branch: RELEASE_3_8 git_last_commit: 8bd4290 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ENCODExplorer_2.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ENCODExplorer_2.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ENCODExplorer_2.8.0.tgz vignettes: vignettes/ENCODExplorer/inst/doc/DataUpdate.html, vignettes/ENCODExplorer/inst/doc/DBmodel.html, vignettes/ENCODExplorer/inst/doc/ENCODExplorer.html vignetteTitles: Data update, Database model, Introduction to ENCODExplorer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ENCODExplorer/inst/doc/DataUpdate.R, vignettes/ENCODExplorer/inst/doc/DBmodel.R, vignettes/ENCODExplorer/inst/doc/ENCODExplorer.R suggestsMe: TSRchitect Package: EnhancedVolcano Version: 1.0.1 Depends: R (>= 3.5.0), ggplot2, ggrepel Suggests: RUnit, BiocGenerics, knitr, DESeq2, pasilla, airway, gridExtra, magrittr License: GPL-3 MD5sum: 2981aa06d982fff46fbbf4728e8d957e NeedsCompilation: no Title: Publication-ready volcano plots with enhanced colouring and labeling Description: Volcano plots represent a useful way to visualise the results of differential expression analyses. Here, we present a highly-configurable function that produces publication-ready volcano plots. EnhancedVolcano will attempt to fit as many transcript names in the plot window as possible, thus avoiding 'clogging' up the plot with labels that could not otherwise have been read. biocViews: ImmunoOncology, RNASeq, GeneExpression, Transcription, DifferentialExpression Author: Kevin Blighe Maintainer: Kevin Blighe URL: https://github.com/kevinblighe/EnhancedVolcano VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EnhancedVolcano git_branch: RELEASE_3_8 git_last_commit: 45c76cc git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/EnhancedVolcano_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EnhancedVolcano_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EnhancedVolcano_1.0.1.tgz vignettes: vignettes/EnhancedVolcano/inst/doc/EnhancedVolcano.html vignetteTitles: Publication-ready volcano plots with enhanced colouring and labeling hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EnhancedVolcano/inst/doc/EnhancedVolcano.R Package: ENmix Version: 1.18.2 Depends: parallel,doParallel,foreach, SummarizedExperiment (>= 1.1.6),minfi (>= 1.22.0) Imports: MASS,preprocessCore,wateRmelon,sva,geneplotter,impute,grDevices,graphics,stats Suggests: minfiData (>= 0.4.1), RPMM, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: b5264f50c08d7d6b6cf3fd55b9628303 NeedsCompilation: no Title: Data preprocessing and quality control for Illumina HumanMethylation450 and MethylationEPIC BeadChip Description: The ENmix package provides a set of quality control and data pre-processing tools for Illumina HumanMethylation450 and MethylationEPIC Beadchips. It includes ENmix background correction, RELIC dye bias correction, RCP probe-type bias adjustment, along with a number of additional tools. These functions can be used to remove unwanted experimental noise and thus to improve accuracy and reproducibility of methylation measures. ENmix functions are flexible and transparent. Users have option to choose a single pipeline command to finish all data pre-processing steps (including background correction, dye-bias adjustment, inter-array normalization and probe-type bias correction) or to use individual functions sequentially to perform data pre-processing in a more customized manner. In addition the ENmix package has selectable complementary functions for efficient data visualization (such as data distribution plots); quality control (identifing and filtering low quality data points, samples, probes, and outliers, along with imputation of missing values); identification of probes with multimodal distributions due to SNPs or other factors; exploration of data variance structure using principal component regression analysis plot; preparation of experimental factors related surrogate control variables to be adjusted in downstream statistical analysis; and an efficient algorithm oxBS-MLE to estimate 5-methylcytosine and 5-hydroxymethylcytosine level. biocViews: ImmunoOncology, DNAMethylation, Preprocessing, QualityControl, TwoChannel, Microarray, OneChannel, MethylationArray, BatchEffect, Normalization, DataImport, Regression, PrincipalComponent,Epigenetics, MultiChannel, DifferentialMethylation Author: Zongli Xu [cre, aut], Liang Niu [aut], Leping Li [ctb], Jack Taylor [ctb] Maintainer: Zongli Xu git_url: https://git.bioconductor.org/packages/ENmix git_branch: RELEASE_3_8 git_last_commit: e2cea15 git_last_commit_date: 2019-03-06 Date/Publication: 2019-03-06 source.ver: src/contrib/ENmix_1.18.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/ENmix_1.18.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ENmix_1.18.2.tgz vignettes: vignettes/ENmix/inst/doc/ENmix.pdf vignetteTitles: ENmix User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ENmix/inst/doc/ENmix.R Package: EnrichedHeatmap Version: 1.12.0 Depends: R (>= 3.1.2), methods, grid, ComplexHeatmap (>= 1.15.2), GenomicRanges Imports: matrixStats, stats, GetoptLong, Rcpp, utils, locfit, circlize (>= 0.4.1), IRanges LinkingTo: Rcpp Suggests: testthat (>= 0.3), knitr, markdown, genefilter, RColorBrewer License: MIT + file LICENSE Archs: i386, x64 MD5sum: 7e80d59a04785ab940be2ecb1c3b942e NeedsCompilation: yes Title: Making Enriched Heatmaps Description: Enriched heatmap is a special type of heatmap which visualizes the enrichment of genomic signals on specific target regions. Here we implement enriched heatmap by ComplexHeatmap package. Since this type of heatmap is just a normal heatmap but with some special settings, with the functionality of ComplexHeatmap, it would be much easier to customize the heatmap as well as concatenating to a list of heatmaps to show correspondance between different data sources. biocViews: Software, Visualization, Sequencing, GenomeAnnotation, Coverage Author: Zuguang Gu Maintainer: Zuguang Gu URL: https://github.com/jokergoo/EnrichedHeatmap VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EnrichedHeatmap git_branch: RELEASE_3_8 git_last_commit: 4deed55 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/EnrichedHeatmap_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/EnrichedHeatmap_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EnrichedHeatmap_1.12.0.tgz vignettes: vignettes/EnrichedHeatmap/inst/doc/EnrichedHeatmap.html, vignettes/EnrichedHeatmap/inst/doc/roadmap.html, vignettes/EnrichedHeatmap/inst/doc/row_odering.html, vignettes/EnrichedHeatmap/inst/doc/visualize_categorical_signals_wrapper.html vignetteTitles: Make Enriched Heatmaps, Visualize Comprehensive Associations in Roadmap dataset, Compare row ordering methods, Visualize Categorical Signals hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/EnrichedHeatmap/inst/doc/EnrichedHeatmap.R, vignettes/EnrichedHeatmap/inst/doc/roadmap.R, vignettes/EnrichedHeatmap/inst/doc/row_odering.R, vignettes/EnrichedHeatmap/inst/doc/visualize_categorical_signals_wrapper.R Package: EnrichmentBrowser Version: 2.12.1 Depends: R(>= 3.5.0), SummarizedExperiment, graph Imports: AnnotationDbi, BiocFileCache, BiocManager, ComplexHeatmap, DESeq2, EDASeq, GSEABase, GO.db, KEGGREST, KEGGgraph, MASS, ReportingTools, Rgraphviz, S4Vectors, SPIA, biocGraph, edgeR, geneplotter, graphite, hwriter, limma, methods, pathview, rappdirs, safe, topGO Suggests: ALL, BiocStyle, airway, hgu95av2.db, knitr License: Artistic-2.0 MD5sum: 8c02cbd1fae903943ca5cbd763724e6c NeedsCompilation: no Title: Seamless navigation through combined results of set-based and network-based enrichment analysis Description: The EnrichmentBrowser package implements essential functionality for the enrichment analysis of gene expression data. The analysis combines the advantages of set-based and network-based enrichment analysis in order to derive high-confidence gene sets and biological pathways that are differentially regulated in the expression data under investigation. Besides, the package facilitates the visualization and exploration of such sets and pathways. biocViews: ImmunoOncology, Microarray, RNASeq, GeneExpression, DifferentialExpression, Pathways, GraphAndNetwork, Network, GeneSetEnrichment, NetworkEnrichment, Visualization, ReportWriting Author: Ludwig Geistlinger [aut, cre], Gergely Csaba [aut], Mara Santarelli [ctb], Marcel Ramos [ctb], Levi Waldron [ctb], Ralf Zimmer [aut] Maintainer: Ludwig Geistlinger VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/EnrichmentBrowser git_branch: RELEASE_3_8 git_last_commit: 9b180b3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/EnrichmentBrowser_2.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EnrichmentBrowser_2.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EnrichmentBrowser_2.12.1.tgz vignettes: vignettes/EnrichmentBrowser/inst/doc/EnrichmentBrowser.pdf vignetteTitles: EnrichmentBrowser Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EnrichmentBrowser/inst/doc/EnrichmentBrowser.R importsMe: GSEABenchmarkeR, PathwaySplice suggestsMe: ToPASeq Package: enrichplot Version: 1.2.0 Depends: R (>= 3.4.0) Imports: AnnotationDbi, cowplot, DOSE (>= 3.5.1), europepmc, ggplot2, ggplotify, ggraph, ggridges, GOSemSim, graphics, grDevices, grid, gridExtra, igraph, methods, purrr, RColorBrewer, reshape2, stats, UpSetR, utils Suggests: clusterProfiler, knitr, org.Hs.eg.db, prettydoc License: Artistic-2.0 MD5sum: 27648033d0cf6a3a71f8ecbef075b0b8 NeedsCompilation: no Title: Visualization of Functional Enrichment Result Description: The 'enrichplot' package implements several visualization methods for interpreting functional enrichment results obtained from ORA or GSEA analysis. All the visualization methods are developed based on 'ggplot2' graphics. biocViews: Annotation, GeneSetEnrichment, GO, KEGG, Pathways, Software, Visualization Author: Guangchuang Yu [aut, cre] () Maintainer: Guangchuang Yu URL: https://github.com/GuangchuangYu/enrichplot VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/enrichplot/issues git_url: https://git.bioconductor.org/packages/enrichplot git_branch: RELEASE_3_8 git_last_commit: 2eeaafb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/enrichplot_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/enrichplot_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/enrichplot_1.2.0.tgz vignettes: vignettes/enrichplot/inst/doc/enrichplot.html vignetteTitles: enrichplot introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/enrichplot/inst/doc/enrichplot.R importsMe: ChIPseeker, clusterProfiler, debrowser, meshes, ReactomePA suggestsMe: methylGSA Package: ensembldb Version: 2.6.8 Depends: BiocGenerics (>= 0.15.10), GenomicRanges (>= 1.31.18), GenomicFeatures (>= 1.29.10), AnnotationFilter (>= 1.5.2) Imports: methods, RSQLite (>= 1.1), DBI, Biobase, GenomeInfoDb, AnnotationDbi (>= 1.31.19), rtracklayer, S4Vectors, Rsamtools, IRanges (>= 2.13.24), ProtGenerics, Biostrings (>= 2.47.9), curl Suggests: BiocStyle, knitr, EnsDb.Hsapiens.v86 (>= 0.99.8), testthat, BSgenome.Hsapiens.NCBI.GRCh38, ggbio (>= 1.24.0), Gviz (>= 1.20.0), magrittr, AnnotationHub Enhances: RMariaDB, shiny License: LGPL MD5sum: ee524e752ed627105a4a55acbe2358c3 NeedsCompilation: no Title: Utilities to create and use Ensembl-based annotation databases Description: The package provides functions to create and use transcript centric annotation databases/packages. The annotation for the databases are directly fetched from Ensembl using their Perl API. The functionality and data is similar to that of the TxDb packages from the GenomicFeatures package, but, in addition to retrieve all gene/transcript models and annotations from the database, ensembldb provides a filter framework allowing to retrieve annotations for specific entries like genes encoded on a chromosome region or transcript models of lincRNA genes. EnsDb databases built with ensembldb contain also protein annotations and mappings between proteins and their encoding transcripts. Finally, ensembldb provides functions to map between genomic, transcript and protein coordinates. biocViews: Genetics, AnnotationData, Sequencing, Coverage Author: Johannes Rainer with contributions from Tim Triche, Sebastian Gibb, Laurent Gatto and Christian Weichenberger. Maintainer: Johannes Rainer URL: https://github.com/jorainer/ensembldb VignetteBuilder: knitr BugReports: https://github.com/jorainer/ensembldb/issues git_url: https://git.bioconductor.org/packages/ensembldb git_branch: RELEASE_3_8 git_last_commit: c2c4f41 git_last_commit_date: 2019-04-03 Date/Publication: 2019-04-03 source.ver: src/contrib/ensembldb_2.6.8.tar.gz win.binary.ver: bin/windows/contrib/3.5/ensembldb_2.6.8.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ensembldb_2.6.8.tgz vignettes: vignettes/ensembldb/inst/doc/coordinate-mapping-use-cases.html, vignettes/ensembldb/inst/doc/coordinate-mapping.html, vignettes/ensembldb/inst/doc/ensembldb.html, vignettes/ensembldb/inst/doc/MySQL-backend.html, vignettes/ensembldb/inst/doc/proteins.html vignetteTitles: Use cases for coordinate mapping with ensembldb, Mapping between genome,, transcript and protein coordinates, Generating an using Ensembl based annotation packages, Using a MariaDB/MySQL server backend, Querying protein features hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ensembldb/inst/doc/coordinate-mapping-use-cases.R, vignettes/ensembldb/inst/doc/coordinate-mapping.R, vignettes/ensembldb/inst/doc/ensembldb.R, vignettes/ensembldb/inst/doc/MySQL-backend.R, vignettes/ensembldb/inst/doc/proteins.R dependsOnMe: chimeraviz importsMe: biovizBase, ChIPpeakAnno, epivizrData, ggbio, metagene, PathwaySplice, Pbase, TVTB, tximeta suggestsMe: alpine, GenomicFeatures, TxRegInfra, wiggleplotr Package: ensemblVEP Version: 1.24.2 Depends: methods, BiocGenerics, GenomicRanges, VariantAnnotation Imports: S4Vectors (>= 0.9.25), Biostrings, SummarizedExperiment, GenomeInfoDb, stats Suggests: RUnit License: Artistic-2.0 MD5sum: 65e4db8e4cac226db97b2158948c409e NeedsCompilation: no Title: R Interface to Ensembl Variant Effect Predictor Description: Query the Ensembl Variant Effect Predictor via the perl API. biocViews: Annotation, VariantAnnotation, SNP Author: Valerie Obenchain and Lori Shepherd Maintainer: Bioconductor Package Maintainer SystemRequirements: Ensembl VEP (API version 96) and the Perl modules DBI and DBD::mysql must be installed. See the package README and Ensembl installation instructions: http://www.ensembl.org/info/docs/tools/vep/script/vep_download.html#installer git_url: https://git.bioconductor.org/packages/ensemblVEP git_branch: RELEASE_3_8 git_last_commit: 11761fb git_last_commit_date: 2019-04-11 Date/Publication: 2019-04-11 source.ver: src/contrib/ensemblVEP_1.24.2.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ensemblVEP_1.24.2.tgz vignettes: vignettes/ensemblVEP/inst/doc/ensemblVEP.pdf, vignettes/ensemblVEP/inst/doc/PreV90EnsemblVEP.pdf vignetteTitles: ensemblVEP, PreV90EnsemblVEP hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ensemblVEP/inst/doc/ensemblVEP.R, vignettes/ensemblVEP/inst/doc/PreV90EnsemblVEP.R importsMe: TVTB Package: ENVISIONQuery Version: 1.30.0 Depends: rJava, XML, utils License: GPL-2 MD5sum: c5c1fc6faa77de4dce984b8311aad152 NeedsCompilation: no Title: Retrieval from the ENVISION bioinformatics data portal into R Description: Tools to retrieve data from ENVISION, the Database for Annotation, Visualization and Integrated Discovery portal biocViews: Annotation Author: Alex Lisovich, Roger Day Maintainer: Alex Lisovich , Roger Day git_url: https://git.bioconductor.org/packages/ENVISIONQuery git_branch: RELEASE_3_8 git_last_commit: 34d719f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ENVISIONQuery_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ENVISIONQuery_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ENVISIONQuery_1.30.0.tgz vignettes: vignettes/ENVISIONQuery/inst/doc/ENVISIONQuery.pdf vignetteTitles: An R Package for retrieving data from EnVision into R objects. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ENVISIONQuery/inst/doc/ENVISIONQuery.R importsMe: IdMappingRetrieval Package: EpiDISH Version: 1.4.1 Depends: R (>= 3.4) Imports: MASS, e1071, quadprog Suggests: roxygen2, GEOquery, BiocStyle, knitr, rmarkdown, Biobase, testthat License: GPL-2 MD5sum: 4acbfaf1f6e45ca12fef51b9b3e8f1eb NeedsCompilation: no Title: Epigenetic Dissection of Intra-Sample-Heterogeneity Description: EpiDISH is a R package to infer the proportions of a priori known cell subtypes present in a sample representing a mixture of such cell-types. Inference proceeds via one of 3 methods (Robust Partial Correlations-RPC, Cibersort (CBS), Constrained Projection (CP)), as determined by user. biocViews: DNAMethylation, MethylationArray, Epigenetics, DifferentialMethylation, ImmunoOncology Author: Andrew E. Teschendorff , Shijie C. Zheng Maintainer: Shijie Charles Zheng URL: https://github.com/sjczheng/EpiDISH VignetteBuilder: knitr BugReports: https://github.com/sjczheng/EpiDISH/issues git_url: https://git.bioconductor.org/packages/EpiDISH git_branch: RELEASE_3_8 git_last_commit: dd291ba git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/EpiDISH_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EpiDISH_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EpiDISH_1.4.1.tgz vignettes: vignettes/EpiDISH/inst/doc/EpiDISH.html vignetteTitles: Epigenetic Dissection of Intra-Sample-Heterogeneity - R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EpiDISH/inst/doc/EpiDISH.R Package: epigenomix Version: 1.22.0 Depends: R (>= 3.2.0), methods, Biobase, S4Vectors, IRanges, GenomicRanges, SummarizedExperiment Imports: BiocGenerics, MCMCpack, Rsamtools, parallel, GenomeInfoDb, beadarray License: LGPL-3 MD5sum: 290798e17819a26cfa3171ecefab0307 NeedsCompilation: no Title: Epigenetic and gene transcription data normalization and integration with mixture models Description: A package for the integrative analysis of RNA-seq or microarray based gene transcription and histone modification data obtained by ChIP-seq. The package provides methods for data preprocessing and matching as well as methods for fitting bayesian mixture models in order to detect genes with differences in both data types. biocViews: ChIPSeq, GeneExpression, DifferentialExpression, Classification Author: Hans-Ulrich Klein, Martin Schaefer Maintainer: Hans-Ulrich Klein git_url: https://git.bioconductor.org/packages/epigenomix git_branch: RELEASE_3_8 git_last_commit: 88ee03f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/epigenomix_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epigenomix_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epigenomix_1.22.0.tgz vignettes: vignettes/epigenomix/inst/doc/epigenomix.pdf vignetteTitles: epigenomix package vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/epigenomix/inst/doc/epigenomix.R Package: epiNEM Version: 1.6.0 Depends: R (>= 3.4) Imports: BoolNet, e1071, gtools, stats, igraph, nem, utils, lattice, latticeExtra, RColorBrewer, pcalg, minet, grDevices, graph Suggests: knitr, RUnit, BiocGenerics, STRINGdb, devtools, rmarkdown, GOSemSim, AnnotationHub, org.Sc.sgd.db License: GPL-3 MD5sum: 6e8ad9c7f2ce1f6fa87bc01d4b0ab653 NeedsCompilation: no Title: epiNEM Description: epiNEM is an extension of the original Nested Effects Models (NEM). EpiNEM is able to take into account double knockouts and infer more complex network signalling pathways. biocViews: Pathways, SystemsBiology, NetworkInference, Network Author: Madeline Diekmann & Martin Pirkl Maintainer: Martin Pirkl VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/epiNEM git_branch: RELEASE_3_8 git_last_commit: 2172c08 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/epiNEM_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epiNEM_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epiNEM_1.6.0.tgz vignettes: vignettes/epiNEM/inst/doc/epiNEM.pdf vignetteTitles: epiNEM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/epiNEM/inst/doc/epiNEM.R Package: epivizr Version: 2.12.0 Depends: R (>= 3.0), methods, Imports: epivizrServer (>= 1.1.1), epivizrData (>= 1.3.4), GenomicRanges, S4Vectors, IRanges Suggests: testthat, roxygen2, knitr, Biobase, SummarizedExperiment, antiProfilesData, hgu133plus2.db, Mus.musculus, BiocStyle License: Artistic-2.0 MD5sum: 598be3e3e7c653398de1a63851e204e1 NeedsCompilation: no Title: R Interface to epiviz web app Description: This package provides connections to the epiviz web app (http://epiviz.cbcb.umd.edu) for interactive visualization of genomic data. Objects in R/bioc interactive sessions can be displayed in genome browser tracks or plots to be explored by navigation through genomic regions. Fundamental Bioconductor data structures are supported (e.g., GenomicRanges and RangedSummarizedExperiment objects), while providing an easy mechanism to support other data structures (through package epivizrData). Visualizations (using d3.js) can be easily added to the web app as well. biocViews: Visualization, Infrastructure, GUI Author: Hector Corrada Bravo, Florin Chelaru, Llewellyn Smith, Naomi Goldstein, Jayaram Kancherla, Morgan Walter, Brian Gottfried Maintainer: Hector Corrada Bravo VignetteBuilder: knitr Video: https://www.youtube.com/watch?v=099c4wUxozA git_url: https://git.bioconductor.org/packages/epivizr git_branch: RELEASE_3_8 git_last_commit: 2fdb68c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/epivizr_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epivizr_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epivizr_2.12.0.tgz vignettes: vignettes/epivizr/inst/doc/IntroToEpivizr.html vignetteTitles: Introduction to epivizr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/epivizr/inst/doc/IntroToEpivizr.R dependsOnMe: epivizrStandalone importsMe: metavizr Package: epivizrChart Version: 1.4.0 Depends: R (>= 3.4.0) Imports: epivizrData (>= 1.5.1), epivizrServer, htmltools, rjson, methods, BiocGenerics Suggests: testthat, roxygen2, knitr, Biobase, GenomicRanges, S4Vectors, IRanges, SummarizedExperiment, antiProfilesData, hgu133plus2.db, Mus.musculus, BiocStyle, Homo.sapiens, shiny, minfi, Rsamtools, rtracklayer, RColorBrewer, magrittr, AnnotationHub License: Artistic-2.0 MD5sum: a0c65f110f53a24eb774b181b4cd21b7 NeedsCompilation: no Title: R interface to epiviz web components Description: This package provides an API for interactive visualization of genomic data using epiviz web components. Objects in R/BioConductor can be used to generate interactive R markdown/notebook documents or can be visualized in the R Studio's default viewer. biocViews: Visualization, GUI Author: Brian Gottfried [aut], Jayaram Kancherla [aut], Hector Corrada Bravo [aut, cre] Maintainer: Hector Corrada Bravo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/epivizrChart git_branch: RELEASE_3_8 git_last_commit: f3a9202 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/epivizrChart_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epivizrChart_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epivizrChart_1.4.0.tgz vignettes: vignettes/epivizrChart/inst/doc/IntegrationWithIGVjs.html, vignettes/epivizrChart/inst/doc/IntegrationWithShiny.html, vignettes/epivizrChart/inst/doc/IntroToEpivizrChart.html, vignettes/epivizrChart/inst/doc/VisualizeSumExp.html vignetteTitles: Visualizing Files with epivizrChart, Visualizing genomic data in Shiny Apps using epivizrChart, Introduction to epivizrChart, Visualizing `RangeSummarizedExperiment` objects Shiny Apps using epivizrChart hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/epivizrChart/inst/doc/IntegrationWithIGVjs.R, vignettes/epivizrChart/inst/doc/IntegrationWithShiny.R, vignettes/epivizrChart/inst/doc/IntroToEpivizrChart.R, vignettes/epivizrChart/inst/doc/VisualizeSumExp.R Package: epivizrData Version: 1.10.0 Depends: R (>= 3.4), methods, epivizrServer (>= 1.1.1), Biobase Imports: S4Vectors, GenomicRanges, SummarizedExperiment (>= 0.2.0), OrganismDbi, GenomicFeatures, GenomeInfoDb, IRanges, ensembldb Suggests: testthat, roxygen2, bumphunter, hgu133plus2.db, Mus.musculus, TxDb.Mmusculus.UCSC.mm10.knownGene, rjson, knitr, rmarkdown, BiocStyle, EnsDb.Mmusculus.v79, AnnotationHub, rtracklayer, utils, RMySQL, DBI License: MIT + file LICENSE MD5sum: a9fd3870de8f49edaf48ebfbc400d35b NeedsCompilation: no Title: Data Management API for epiviz interactive visualization app Description: Serve data from Bioconductor Objects through a WebSocket connection. biocViews: Infrastructure, Visualization Author: Hector Corrada Bravo [aut, cre], Florin Chelaru [aut] Maintainer: Hector Corrada Bravo URL: http://epiviz.github.io VignetteBuilder: knitr BugReports: https://github.com/epiviz/epivizrData/issues git_url: https://git.bioconductor.org/packages/epivizrData git_branch: RELEASE_3_8 git_last_commit: 1d39e16 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/epivizrData_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epivizrData_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epivizrData_1.10.0.tgz vignettes: vignettes/epivizrData/inst/doc/epivizrData.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/epivizrData/inst/doc/epivizrData.R importsMe: epivizr, epivizrChart, metavizr Package: epivizrServer Version: 1.10.0 Depends: R (>= 3.2.3), methods Imports: httpuv (>= 1.3.0), R6 (>= 2.0.0), rjson, mime (>= 0.2) Suggests: testthat, knitr, rmarkdown, BiocStyle License: MIT + file LICENSE MD5sum: 537fc02d780e78830cd3d470cdee219a NeedsCompilation: no Title: WebSocket server infrastructure for epivizr apps and packages Description: This package provides objects to manage WebSocket connections to epiviz apps. Other epivizr package use this infrastructure. biocViews: Infrastructure, Visualization Author: Hector Corrada Bravo [aut, cre] Maintainer: Hector Corrada Bravo URL: https://epiviz.github.io VignetteBuilder: knitr BugReports: https://github.com/epiviz/epivizrServer git_url: https://git.bioconductor.org/packages/epivizrServer git_branch: RELEASE_3_8 git_last_commit: ddd65ec git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/epivizrServer_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epivizrServer_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epivizrServer_1.10.0.tgz vignettes: vignettes/epivizrServer/inst/doc/epivizrServer.html vignetteTitles: epivizrServer Usage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE dependsOnMe: epivizrData importsMe: epivizr, epivizrChart, epivizrStandalone, metavizr Package: epivizrStandalone Version: 1.10.0 Depends: R (>= 3.2.3), epivizr (>= 2.3.6), methods Imports: git2r, epivizrServer, GenomeInfoDb, BiocGenerics, GenomicFeatures, S4Vectors Suggests: testthat, knitr, rmarkdown, OrganismDbi (>= 1.13.9), Mus.musculus, Biobase, BiocStyle License: MIT + file LICENSE MD5sum: 1c5b85237ceb90203bab2c0e7e9f5f7c NeedsCompilation: no Title: Run Epiviz Interactive Genomic Data Visualization App within R Description: This package imports the epiviz visualization JavaScript app for genomic data interactive visualization. The 'epivizrServer' package is used to provide a web server running completely within R. This standalone version allows to browse arbitrary genomes through genome annotations provided by Bioconductor packages. biocViews: Visualization, Infrastructure, GUI Author: Hector Corrada Bravo, Jayaram Kancherla Maintainer: Hector Corrada Bravo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/epivizrStandalone git_branch: RELEASE_3_8 git_last_commit: 43f1245 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/epivizrStandalone_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/epivizrStandalone_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/epivizrStandalone_1.10.0.tgz vignettes: vignettes/epivizrStandalone/inst/doc/EpivizrStandalone.html vignetteTitles: Introduction to epivizrStandalone hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE importsMe: metavizr Package: erccdashboard Version: 1.16.1 Depends: R (>= 3.2), ggplot2 (>= 2.1.0), gridExtra (>= 2.0.0) Imports: edgeR, gplots, grid, gtools, limma, locfit, MASS, plyr, qvalue, reshape2, ROCR, scales, stringr License: GPL (>=2) MD5sum: fd9fb02157320d565a9cc58fa0109123 NeedsCompilation: no Title: Assess Differential Gene Expression Experiments with ERCC Controls Description: Technical performance metrics for differential gene expression experiments using External RNA Controls Consortium (ERCC) spike-in ratio mixtures. biocViews: ImmunoOncology, GeneExpression, Transcription, AlternativeSplicing, DifferentialExpression, DifferentialSplicing, Genetics, Microarray, mRNAMicroarray, RNASeq, BatchEffect, MultipleComparison, QualityControl Author: Sarah Munro, Steve Lund Maintainer: Sarah Munro URL: https://github.com/munrosa/erccdashboard, http://tinyurl.com/erccsrm BugReports: https://github.com/munrosa/erccdashboard/issues git_url: https://git.bioconductor.org/packages/erccdashboard git_branch: RELEASE_3_8 git_last_commit: 503a11a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/erccdashboard_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/erccdashboard_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/erccdashboard_1.16.1.tgz vignettes: vignettes/erccdashboard/inst/doc/erccdashboard.pdf vignetteTitles: erccdashboard examples hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/erccdashboard/inst/doc/erccdashboard.R Package: erma Version: 0.14.0 Depends: R (>= 3.1), methods, Homo.sapiens, GenomicFiles (>= 1.5.2) Imports: rtracklayer (>= 1.38.1), S4Vectors, BiocGenerics, GenomicRanges, SummarizedExperiment, ggplot2, GenomeInfoDb, Biobase, shiny, BiocParallel, IRanges, AnnotationDbi Suggests: rmarkdown, BiocStyle, knitr, GO.db, png, DT, doParallel License: Artistic-2.0 MD5sum: 4cba185c4cd0cc49bf6d10bc4864f2f9 NeedsCompilation: no Title: epigenomic road map adventures Description: Software and data to support epigenomic road map adventures. Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/erma git_branch: RELEASE_3_8 git_last_commit: 6f52851 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/erma_0.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/erma_0.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/erma_0.14.0.tgz vignettes: vignettes/erma/inst/doc/erma.html vignetteTitles: ermaInteractive hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/erma/inst/doc/erma.R importsMe: gQTLstats, ldblock suggestsMe: gQTLBase Package: ERSSA Version: 1.0.1 Depends: R (>= 3.5.0) Imports: edgeR (>= 3.23.3), DESeq2 (>= 1.21.16), ggplot2 (>= 3.0.0), RColorBrewer (>= 1.1-2), plyr (>= 1.8.4), BiocParallel (>= 1.15.8), grDevices, stats, utils Suggests: BiocStyle, knitr, rmarkdown License: GPL-3 | file LICENSE MD5sum: e2436e391cb263447e0bcfe871646c2d NeedsCompilation: no Title: Empirical RNA-seq Sample Size Analysis Description: The ERSSA package takes user supplied RNA-seq differential expression dataset and calculates the number of differentially expressed genes at varying biological replicate levels. This allows the user to determine, without relying on any a priori assumptions, whether sufficient differential detection has been acheived with their RNA-seq dataset. biocViews: ImmunoOncology, GeneExpression, Transcription, DifferentialExpression, RNASeq, MultipleComparison, QualityControl Author: Zixuan Shao [aut, cre] Maintainer: Zixuan Shao URL: https://github.com/zshao1/ERSSA VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ERSSA git_branch: RELEASE_3_8 git_last_commit: 9d61d00 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ERSSA_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ERSSA_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ERSSA_1.0.1.tgz vignettes: vignettes/ERSSA/inst/doc/ERSSA.html vignetteTitles: ERSSA Package Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ERSSA/inst/doc/ERSSA.R Package: esATAC Version: 1.4.5 Depends: R (>= 3.5), Rsamtools, GenomicRanges, ShortRead Imports: Rcpp (>= 0.12.11), methods, knitr, Rbowtie2, rtracklayer, ggplot2, Biostrings, ChIPseeker, clusterProfiler, igraph, rJava, DiagrammeR, magrittr, digest, BSgenome, AnnotationDbi, GenomicFeatures, R.utils, GenomeInfoDb, BiocGenerics, S4Vectors, IRanges, rmarkdown, tools, VennDiagram, grid, JASPAR2016, TFBSTools, grDevices, graphics, stats, utils, parallel, corrplot, BiocManager, motifmatchr LinkingTo: Rcpp Suggests: BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db, DiagrammeRsvg, testthat, webshot License: GPL-3 | file LICENSE Archs: x64 MD5sum: fc5682ae85bf7d685a31f9384c2be54d NeedsCompilation: yes Title: An Easy-to-use Systematic pipeline for ATACseq data analysis Description: This package provides a framework and complete preset pipeline for quantification and analysis of ATAC-seq Reads. It covers raw sequencing reads preprocessing (FASTQ files), reads alignment (Rbowtie2), aligned reads file operations (SAM, BAM, and BED files), peak calling (F-seq), genome annotations (Motif, GO, SNP analysis) and quality control report. The package is managed by dataflow graph. It is easy for user to pass variables seamlessly between processes and understand the workflow. Users can process FASTQ files through end-to-end preset pipeline which produces a pretty HTML report for quality control and preliminary statistical results, or customize workflow starting from any intermediate stages with esATAC functions easily and flexibly. biocViews: ImmunoOncology, Sequencing, DNASeq, QualityControl, Alignment, Preprocessing, Coverage, ATACSeq, DNaseSeq Author: Zheng Wei, Wei Zhang Maintainer: Zheng Wei URL: https://github.com/wzthu/esATAC SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/wzthu/esATAC/issues git_url: https://git.bioconductor.org/packages/esATAC git_branch: RELEASE_3_8 git_last_commit: f9ec1c4 git_last_commit_date: 2019-03-22 Date/Publication: 2019-03-22 source.ver: src/contrib/esATAC_1.4.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/esATAC_1.4.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/esATAC_1.4.5.tgz vignettes: vignettes/esATAC/inst/doc/esATAC-Introduction.html vignetteTitles: An Introduction to esATAC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/esATAC/inst/doc/esATAC-Introduction.R Package: esetVis Version: 1.8.0 Imports: mpm, hexbin, Rtsne, MLP, grid, Biobase, MASS, stats, utils, grDevices, methods Suggests: ggplot2, ggvis, rbokeh, ggrepel, knitr, rmarkdown, ALL, hgu95av2.db, AnnotationDbi, pander, SummarizedExperiment License: GPL-3 MD5sum: 00dabd51d6f8ed126f3c6a53ef514e96 NeedsCompilation: no Title: Visualizations of expressionSet Bioconductor object Description: Utility functions for visualization of expressionSet (or SummarizedExperiment) Bioconductor object, including spectral map, tsne and linear discriminant analysis. Static plot via the ggplot2 package or interactive via the ggvis or rbokeh packages are available. biocViews: Visualization, DataRepresentation, DimensionReduction, PrincipalComponent, Pathways Author: Laure Cougnaud Maintainer: Laure Cougnaud VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/esetVis git_branch: RELEASE_3_8 git_last_commit: fc2bebc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/esetVis_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/esetVis_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/esetVis_1.8.0.tgz vignettes: vignettes/esetVis/inst/doc/esetVis-vignette.html vignetteTitles: esetVis package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/esetVis/inst/doc/esetVis-vignette.R Package: eudysbiome Version: 1.12.0 Depends: R (>= 3.1.0) Imports: plyr, Rsamtools, R.utils, Biostrings License: GPL-2 MD5sum: b8a7504e2d5c6793c7d82819f060cd3c NeedsCompilation: no Title: Cartesian plot and contingency test on 16S Microbial data Description: eudysbiome a package that permits to annotate the differential genera as harmful/harmless based on their ability to contribute to host diseases (as indicated in literature) or unknown based on their ambiguous genus classification. Further, the package statistically measures the eubiotic (harmless genera increase or harmful genera decrease) or dysbiotic(harmless genera decrease or harmful genera increase) impact of a given treatment or environmental change on the (gut-intestinal, GI) microbiome in comparison to the microbiome of the reference condition. Author: Xiaoyuan Zhou, Christine Nardini Maintainer: Xiaoyuan Zhou git_url: https://git.bioconductor.org/packages/eudysbiome git_branch: RELEASE_3_8 git_last_commit: 35df0c3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/eudysbiome_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/eudysbiome_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/eudysbiome_1.12.0.tgz vignettes: vignettes/eudysbiome/inst/doc/eudysbiome.pdf vignetteTitles: eudysbiome User Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/eudysbiome/inst/doc/eudysbiome.R Package: EventPointer Version: 2.0.1 Depends: R (>= 3.4), SGSeq, Matrix, SummarizedExperiment Imports: GenomicFeatures, stringr, GenomeInfoDb, igraph, MASS, nnls, limma, matrixStats, RBGL, prodlim, graph, methods, utils, stats, doParallel, foreach, affxparser, GenomicRanges, S4Vectors, IRanges, qvalue, cobs, rhdf5 Suggests: knitr, rmarkdown, BiocStyle, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: ecd974e8c801868993f80115b6dc07fe NeedsCompilation: no Title: An effective identification of alternative splicing events using junction arrays and RNA-Seq data Description: EventPointer is an R package to identify alternative splicing events that involve either simple (case-control experiment) or complex experimental designs such as time course experiments and studies including paired-samples. The algorithm can be used to analyze data from either junction arrays (Affymetrix Arrays) or sequencing data (RNA-Seq). The software returns a data.frame with the detected alternative splicing events: gene name, type of event (cassette, alternative 3',...,etc), genomic position, statistical significance and increment of the percent spliced in (Delta PSI) for all the events. The algorithm can generate a series of files to visualize the detected alternative splicing events in IGV. This eases the interpretation of results and the design of primers for standard PCR validation. biocViews: AlternativeSplicing, DifferentialSplicing, mRNAMicroarray, RNASeq, Transcription, Sequencing, TimeCourse, ImmunoOncology Author: Juan Pablo Romero, Juan Ferrer-Bonsoms, Ander Muniategui, Fernando Carazo, Ander Aramburu, Angel Rubio Maintainer: Juan Pablo Romero VignetteBuilder: knitr BugReports: https://github.com/jpromeror/EventPointer/issues git_url: https://git.bioconductor.org/packages/EventPointer git_branch: RELEASE_3_8 git_last_commit: e700729 git_last_commit_date: 2018-12-05 Date/Publication: 2018-12-05 source.ver: src/contrib/EventPointer_2.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/EventPointer_2.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/EventPointer_2.0.1.tgz vignettes: vignettes/EventPointer/inst/doc/EventPointer.html vignetteTitles: EventPointer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/EventPointer/inst/doc/EventPointer.R Package: ExCluster Version: 1.0.1 Depends: Rsubread, GenomicRanges, rtracklayer, matrixStats, IRanges Imports: stats, methods, grDevices, graphics, utils License: GPL-3 MD5sum: 59239b879afa6addd1da819ac9e8461e NeedsCompilation: no Title: ExCluster robustly detects differentially expressed exons between two conditions of RNA-seq data, requiring at least two independent biological replicates per condition Description: ExCluster flattens Ensembl and GENCODE GTF files into GFF files, which are used to count reads per non-overlapping exon bin from BAM files. This read counting is done using the function featureCounts from the package Rsubread. Library sizes are normalized across all biological replicates, and ExCluster then compares two different conditions to detect signifcantly differentially spliced genes. This process requires at least two independent biological repliates per condition, and ExCluster accepts only exactly two conditions at a time. ExCluster ultimately produces false discovery rates (FDRs) per gene, which are used to detect significance. Exon log2 fold change (log2FC) means and variances may be plotted for each significantly differentially spliced gene, which helps scientists develop hypothesis and target differential splicing events for RT-qPCR validation in the wet lab. biocViews: ImmunoOncology, DifferentialSplicing, RNASeq, Software Author: R. Matthew Tanner, William L. Stanford, and Theodore J. Perkins Maintainer: R. Matthew Tanner git_url: https://git.bioconductor.org/packages/ExCluster git_branch: RELEASE_3_8 git_last_commit: cee329a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ExCluster_1.0.1.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ExCluster_1.0.1.tgz vignettes: vignettes/ExCluster/inst/doc/ExCluster.pdf vignetteTitles: ExCluster Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ExCluster/inst/doc/ExCluster.R Package: ExiMiR Version: 2.24.0 Depends: R (>= 2.10), Biobase (>= 2.5.5), affy (>= 1.26.1), limma Imports: affyio(>= 1.13.3), Biobase(>= 2.5.5), preprocessCore(>= 1.10.0) Suggests: mirna10cdf License: GPL-2 MD5sum: 541711a5a0c2f740bc70a23b50d3b432 NeedsCompilation: no Title: R functions for the normalization of Exiqon miRNA array data Description: This package contains functions for reading raw data in ImaGene TXT format obtained from Exiqon miRCURY LNA arrays, annotating them with appropriate GAL files, and normalizing them using a spike-in probe-based method. Other platforms and data formats are also supported. biocViews: Microarray, OneChannel, TwoChannel, Preprocessing, GeneExpression, Transcription Author: Sylvain Gubian , Alain Sewer , PMP SA Maintainer: Sylvain Gubian git_url: https://git.bioconductor.org/packages/ExiMiR git_branch: RELEASE_3_8 git_last_commit: 29af803 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ExiMiR_2.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ExiMiR_2.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ExiMiR_2.24.0.tgz vignettes: vignettes/ExiMiR/inst/doc/ExiMiR-vignette.pdf vignetteTitles: Description of ExiMiR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ExiMiR/inst/doc/ExiMiR-vignette.R Package: exomeCopy Version: 1.28.0 Depends: IRanges (>= 2.5.27), GenomicRanges (>= 1.23.16), Rsamtools Imports: stats4, methods, GenomeInfoDb Suggests: Biostrings License: GPL (>= 2) Archs: i386, x64 MD5sum: 4512e1db1fe55da16916eccd3a45fd14 NeedsCompilation: yes Title: Copy number variant detection from exome sequencing read depth Description: Detection of copy number variants (CNV) from exome sequencing samples, including unpaired samples. The package implements a hidden Markov model which uses positional covariates, such as background read depth and GC-content, to simultaneously normalize and segment the samples into regions of constant copy count. biocViews: CopyNumberVariation, Sequencing, Genetics Author: Michael Love Maintainer: Michael Love git_url: https://git.bioconductor.org/packages/exomeCopy git_branch: RELEASE_3_8 git_last_commit: d4e5674 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/exomeCopy_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/exomeCopy_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/exomeCopy_1.28.0.tgz vignettes: vignettes/exomeCopy/inst/doc/exomeCopy.pdf vignetteTitles: Copy number variant detection in exome sequencing data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/exomeCopy/inst/doc/exomeCopy.R importsMe: cn.mops, CNVPanelizer, contiBAIT, Rariant Package: exomePeak Version: 2.16.0 Depends: Rsamtools, GenomicFeatures (>= 1.14.5), rtracklayer, GenomicAlignments License: GPL-2 MD5sum: 966b325c0553337d4f866c6ad8978bd4 NeedsCompilation: no Title: exome-based anlaysis of MeRIP-Seq data: peak calling and differential analysis Description: The package is developed for the analysis of affinity-based epitranscriptome shortgun sequencing data from MeRIP-seq (maA-seq). It was built on the basis of the exomePeak MATLAB package (Meng, Jia, et al. "Exome-based analysis for RNA epigenome sequencing data." Bioinformatics 29.12 (2013): 1565-1567.) with new functions for differential analysis of two experimental conditions to unveil the dynamics in post-transcriptional regulation of the RNA methylome. The exomePeak R-package accepts and statistically supports multiple biological replicates, internally removes PCR artifacts and multi-mapping reads, outputs exome-based binding sites (RNA methylation sites) and detects differential post-transcriptional RNA modification sites between two experimental conditions in term of percentage rather the absolute amount. The package is still under active development, and we welcome all biology and computation scientist for all kinds of collaborations and communications. Please feel free to contact Dr. Jia Meng if you have any questions. biocViews: Sequencing, HighThroughputSequencing, Methylseq, RNAseq Author: Lin Zhang , Lian Liu , Jia Meng Maintainer: Lin Zhang , Lian Liu , Jia Meng git_url: https://git.bioconductor.org/packages/exomePeak git_branch: RELEASE_3_8 git_last_commit: 014e65f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/exomePeak_2.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/exomePeak_2.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/exomePeak_2.16.0.tgz vignettes: vignettes/exomePeak/inst/doc/exomePeak-Overview.pdf vignetteTitles: An introduction to exomePeak hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/exomePeak/inst/doc/exomePeak-Overview.R Package: ExperimentHub Version: 1.8.0 Depends: methods, BiocGenerics (>= 0.15.10), AnnotationHub (>= 2.13.4) Imports: utils, S4Vectors, BiocManager, curl Suggests: knitr, BiocStyle Enhances: ExperimentHubData License: Artistic-2.0 MD5sum: c4a23733d1283fbc667b67cb0a630110 NeedsCompilation: no Title: Client to access ExperimentHub resources Description: This package provides a client for the Bioconductor ExperimentHub web resource. ExperimentHub provides a central location where curated data from experiments, publications or training courses can be accessed. Each resource has associated metadata, tags and date of modification. The client creates and manages a local cache of files retrieved enabling quick and reproducible access. biocViews: Infrastructure, DataImport, GUI, ThirdPartyClient Author: Bioconductor Package Maintainer Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ExperimentHub git_branch: RELEASE_3_8 git_last_commit: 8c4fbb2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ExperimentHub_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ExperimentHub_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ExperimentHub_1.8.0.tgz vignettes: vignettes/ExperimentHub/inst/doc/CreateAnExperimentHubPackage.html, vignettes/ExperimentHub/inst/doc/ExperimentHub.html vignetteTitles: Creating An ExperimentHub Package, ExperimentHub: Access the ExperimentHub Web Service hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ExperimentHub/inst/doc/CreateAnExperimentHubPackage.R, vignettes/ExperimentHub/inst/doc/ExperimentHub.R dependsOnMe: SeqSQC importsMe: brainImageR, ExperimentHubData, GSEABenchmarkeR, restfulSE suggestsMe: ANF, AnnotationHub, celaref, CellMapper, HDF5Array Package: ExperimentHubData Version: 1.8.0 Depends: utils, BiocGenerics (>= 0.15.10), S4Vectors, AnnotationHubData (>= 1.11.6) Imports: methods, ExperimentHub, BiocManager, DBI, BiocCheck, httr, curl, biocViews, graph Suggests: GenomeInfoDb, RUnit, knitr, BiocStyle License: Artistic-2.0 MD5sum: d12ea3b540ea4e10072c39cf6637d576 NeedsCompilation: no Title: Add resources to ExperimentHub Description: Functions to add metadata to ExperimentHub db and resource files to AWS S3 buckets. biocViews: Infrastructure, DataImport, GUI, ThirdPartyClient Author: Bioconductor Maintainer [cre] Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ExperimentHubData git_branch: RELEASE_3_8 git_last_commit: 2bc4d99 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ExperimentHubData_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ExperimentHubData_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ExperimentHubData_1.8.0.tgz vignettes: vignettes/ExperimentHubData/inst/doc/CreateAnExperimentHubPackage.html, vignettes/ExperimentHubData/inst/doc/ExperimentHubData.html vignetteTitles: Creating An ExperimentHub Package, Introduction to ExperimentHubData hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ExperimentHubData/inst/doc/CreateAnExperimentHubPackage.R Package: explorase Version: 1.46.0 Depends: R (>= 2.6.2) Imports: limma, rggobi, RGtk2 Suggests: cairoDevice License: GPL-2 MD5sum: 2064b8b45518a6a033abc5e46c312bf7 NeedsCompilation: no Title: GUI for exploratory data analysis of systems biology data Description: explore and analyze *omics data with R and GGobi biocViews: Visualization,Microarray,GUI Author: Michael Lawrence, Eun-kyung Lee, Dianne Cook, Jihong Kim, Hogeun An, and Dongshin Kim Maintainer: Michael Lawrence URL: http://www.metnetdb.org/MetNet_exploRase.htm git_url: https://git.bioconductor.org/packages/explorase git_branch: RELEASE_3_8 git_last_commit: 7cff865 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/explorase_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/explorase_1.46.0.zip vignettes: vignettes/explorase/inst/doc/explorase.pdf vignetteTitles: Introduction to exploRase hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: ExpressionAtlas Version: 1.10.0 Depends: R (>= 3.2.0), methods, Biobase, SummarizedExperiment, limma, S4Vectors, xml2 Imports: utils, XML, httr Suggests: knitr, testthat, rmarkdown License: GPL (>= 3) MD5sum: fa4131206692f3b828491081f9468738 NeedsCompilation: no Title: Download datasets from EMBL-EBI Expression Atlas Description: This package is for searching for datasets in EMBL-EBI Expression Atlas, and downloading them into R for further analysis. Each Expression Atlas dataset is represented as a SimpleList object with one element per platform. Sequencing data is contained in a SummarizedExperiment object, while microarray data is contained in an ExpressionSet or MAList object. biocViews: ExpressionData, ExperimentData, SequencingData, MicroarrayData, ArrayExpress Author: Maria Keays Maintainer: Suhaib Mohammed VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ExpressionAtlas git_branch: RELEASE_3_8 git_last_commit: 1ec74d6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ExpressionAtlas_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ExpressionAtlas_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ExpressionAtlas_1.10.0.tgz vignettes: vignettes/ExpressionAtlas/inst/doc/ExpressionAtlas.html vignetteTitles: ExpressionAtlas hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ExpressionAtlas/inst/doc/ExpressionAtlas.R suggestsMe: Pi Package: ExpressionView Version: 1.34.0 Depends: caTools, bitops, methods, isa2, eisa, GO.db, KEGG.db, AnnotationDbi Imports: methods, isa2, eisa, GO.db, KEGG.db, AnnotationDbi Suggests: ALL, hgu95av2.db, biclust, affy License: GPL (>= 2) Archs: i386, x64 MD5sum: 24263ace50dde80c1d85d8382ca5a612 NeedsCompilation: yes Title: Visualize biclusters identified in gene expression data Description: ExpressionView visualizes possibly overlapping biclusters in a gene expression matrix. It can use the result of the ISA method (eisa package) or the algorithms in the biclust package or others. The viewer itself was developed using Adobe Flex and runs in a flash-enabled web browser. biocViews: Classification, Visualization, Microarray, GeneExpression, GO, KEGG Author: Andreas Luscher Maintainer: Gabor Csardi git_url: https://git.bioconductor.org/packages/ExpressionView git_branch: RELEASE_3_8 git_last_commit: 45752ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ExpressionView_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ExpressionView_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ExpressionView_1.34.0.tgz vignettes: vignettes/ExpressionView/inst/doc/ExpressionView.format.pdf, vignettes/ExpressionView/inst/doc/ExpressionView.ordering.pdf, vignettes/ExpressionView/inst/doc/ExpressionView.tutorial.pdf vignetteTitles: ExpressionView file format, How the ordering algorithm works, ExpressionView hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ExpressionView/inst/doc/ExpressionView.ordering.R, vignettes/ExpressionView/inst/doc/ExpressionView.tutorial.R Package: fabia Version: 2.28.0 Depends: R (>= 2.8.0), Biobase Imports: methods, graphics, grDevices, stats, utils License: LGPL (>= 2.1) Archs: i386, x64 MD5sum: f98407e943a5d51e71b5d14cda70fa18 NeedsCompilation: yes Title: FABIA: Factor Analysis for Bicluster Acquisition Description: Biclustering by "Factor Analysis for Bicluster Acquisition" (FABIA). FABIA is a model-based technique for biclustering, that is clustering rows and columns simultaneously. Biclusters are found by factor analysis where both the factors and the loading matrix are sparse. FABIA is a multiplicative model that extracts linear dependencies between samples and feature patterns. It captures realistic non-Gaussian data distributions with heavy tails as observed in gene expression measurements. FABIA utilizes well understood model selection techniques like the EM algorithm and variational approaches and is embedded into a Bayesian framework. FABIA ranks biclusters according to their information content and separates spurious biclusters from true biclusters. The code is written in C. biocViews: StatisticalMethod, Microarray, DifferentialExpression, MultipleComparison, Clustering, Visualization Author: Sepp Hochreiter Maintainer: Sepp Hochreiter URL: http://www.bioinf.jku.at/software/fabia/fabia.html git_url: https://git.bioconductor.org/packages/fabia git_branch: RELEASE_3_8 git_last_commit: bb79dbf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fabia_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fabia_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fabia_2.28.0.tgz vignettes: vignettes/fabia/inst/doc/fabia.pdf vignetteTitles: FABIA: Manual for the R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fabia/inst/doc/fabia.R dependsOnMe: hapFabia importsMe: miRSM Package: factDesign Version: 1.58.0 Depends: Biobase (>= 2.5.5) Imports: stats Suggests: affy, genefilter, multtest License: LGPL MD5sum: 19e692c687b778b8a0a5cb377ba8b4ac NeedsCompilation: no Title: Factorial designed microarray experiment analysis Description: This package provides a set of tools for analyzing data from a factorial designed microarray experiment, or any microarray experiment for which a linear model is appropriate. The functions can be used to evaluate tests of contrast of biological interest and perform single outlier detection. biocViews: Microarray, DifferentialExpression Author: Denise Scholtens Maintainer: Denise Scholtens git_url: https://git.bioconductor.org/packages/factDesign git_branch: RELEASE_3_8 git_last_commit: c2a9e80 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/factDesign_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/factDesign_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/factDesign_1.58.0.tgz vignettes: vignettes/factDesign/inst/doc/factDesign.pdf vignetteTitles: factDesign hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/factDesign/inst/doc/factDesign.R Package: FamAgg Version: 1.10.4 Depends: methods, kinship2, igraph Imports: gap (>= 1.1-17), Matrix, BiocGenerics, utils, survey Suggests: BiocStyle, knitr, RUnit, rmarkdown License: MIT + file LICENSE MD5sum: ecf13a04eebf80d684942046c2db560b NeedsCompilation: no Title: Pedigree Analysis and Familial Aggregation Description: Framework providing basic pedigree analysis and plotting utilities as well as a variety of methods to evaluate familial aggregation of traits in large pedigrees. biocViews: Genetics Author: J. Rainer, D. Taliun, C.X. Weichenberger Maintainer: Johannes Rainer URL: https://github.com/EuracBiomedicalResearch/FamAgg VignetteBuilder: knitr BugReports: https://github.com/EuracBiomedicalResearch/FamAgg/issues git_url: https://git.bioconductor.org/packages/FamAgg git_branch: RELEASE_3_8 git_last_commit: fba0bfc git_last_commit_date: 2019-03-26 Date/Publication: 2019-03-26 source.ver: src/contrib/FamAgg_1.10.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/FamAgg_1.10.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FamAgg_1.10.4.tgz vignettes: vignettes/FamAgg/inst/doc/FamAgg.html vignetteTitles: Pedigree Analysis and Familial Aggregation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/FamAgg/inst/doc/FamAgg.R Package: farms Version: 1.34.0 Depends: R (>= 2.8), affy (>= 1.20.0), MASS, methods Imports: affy, MASS, Biobase (>= 1.13.41), methods, graphics Suggests: affydata, Biobase, utils License: LGPL (>= 2.1) MD5sum: a16c7d5833eabebebe06a37ab2c92ead NeedsCompilation: no Title: FARMS - Factor Analysis for Robust Microarray Summarization Description: The package provides the summarization algorithm called Factor Analysis for Robust Microarray Summarization (FARMS) and a novel unsupervised feature selection criterion called "I/NI-calls" biocViews: GeneExpression, Microarray, Preprocessing, QualityControl Author: Djork-Arne Clevert Maintainer: Djork-Arne Clevert URL: http://www.bioinf.jku.at/software/farms/farms.html git_url: https://git.bioconductor.org/packages/farms git_branch: RELEASE_3_8 git_last_commit: c52437f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/farms_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/farms_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/farms_1.34.0.tgz vignettes: vignettes/farms/inst/doc/farms.pdf vignetteTitles: Using farms hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/farms/inst/doc/farms.R Package: fastLiquidAssociation Version: 1.18.0 Depends: methods, LiquidAssociation, parallel, doParallel, stats, Hmisc, utils Imports: WGCNA, impute, preprocessCore Suggests: GOstats, yeastCC, org.Sc.sgd.db License: GPL-2 MD5sum: f264e290f452047d63defed48f91ada0 NeedsCompilation: no Title: functions for genome-wide application of Liquid Association Description: This package extends the function of the LiquidAssociation package for genome-wide application. It integrates a screening method into the LA analysis to reduce the number of triplets to be examined for a high LA value and provides code for use in subsequent significance analyses. biocViews: Software, GeneExpression, Genetics, Pathways, CellBiology Author: Tina Gunderson Maintainer: Tina Gunderson git_url: https://git.bioconductor.org/packages/fastLiquidAssociation git_branch: RELEASE_3_8 git_last_commit: 870b564 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fastLiquidAssociation_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fastLiquidAssociation_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fastLiquidAssociation_1.18.0.tgz vignettes: vignettes/fastLiquidAssociation/inst/doc/fastLiquidAssociation.pdf vignetteTitles: fastLiquidAssociation Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fastLiquidAssociation/inst/doc/fastLiquidAssociation.R Package: FastqCleaner Version: 1.0.0 Imports: methods, shiny, stats, IRanges, Biostrings, ShortRead, DT, methods, S4Vectors, graphics, htmltools, shinyBS, Rcpp (>= 0.12.12) LinkingTo: Rcpp Suggests: BiocStyle, testthat, knitr, rmarkdown License: GPL (>= 2) Archs: i386, x64 MD5sum: 24a7168bea8c5d1abfd726fd43e53484 NeedsCompilation: yes Title: A Shiny Application for Quality Control, Filtering and Trimming of FASTQ Files Description: An interactive web application for quality control, filtering and trimming of FASTQ files. This user-friendly tool combines a pipeline for data processing based on Biostrings and ShortRead infrastructure, with a cutting-edge visual environment. Single-Read and Paired-End files can be locally processed. Diagnostic interactive plots (CG content, per-base sequence quality, etc.) are provided for both the input and output files. biocViews: QualityControl,Sequencing,Software,SangerSeq,SequenceMatching Author: Leandro Roser [aut, cre], Fernán Agüero [aut], Daniel Sánchez [aut] Maintainer: Leandro Roser VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FastqCleaner git_branch: RELEASE_3_8 git_last_commit: f86fbf1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FastqCleaner_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FastqCleaner_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FastqCleaner_1.0.0.tgz vignettes: vignettes/FastqCleaner/inst/doc/Overview.pdf vignetteTitles: An Introduction to FastqCleaner hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FastqCleaner/inst/doc/Overview.R Package: fastseg Version: 1.28.0 Depends: R (>= 2.13), GenomicRanges, Biobase Imports: methods, graphics, stats, BiocGenerics, S4Vectors, IRanges Suggests: DNAcopy, oligo License: LGPL (>= 2.0) Archs: i386, x64 MD5sum: f47179909801546c1b8cbadd9d487295 NeedsCompilation: yes Title: fastseg - a fast segmentation algorithm Description: fastseg implements a very fast and efficient segmentation algorithm. It has similar functionality as DNACopy (Olshen and Venkatraman 2004), but is considerably faster and more flexible. fastseg can segment data from DNA microarrays and data from next generation sequencing for example to detect copy number segments. Further it can segment data from RNA microarrays like tiling arrays to identify transcripts. Most generally, it can segment data given as a matrix or as a vector. Various data formats can be used as input to fastseg like expression set objects for microarrays or GRanges for sequencing data. The segmentation criterion of fastseg is based on a statistical test in a Bayesian framework, namely the cyber t-test (Baldi 2001). The speed-up arises from the facts, that sampling is not necessary in for fastseg and that a dynamic programming approach is used for calculation of the segments' first and higher order moments. biocViews: Classification, CopyNumberVariation Author: Guenter Klambauer Maintainer: Guenter Klambauer URL: http://www.bioinf.jku.at/software/fastseg/fastseg.html git_url: https://git.bioconductor.org/packages/fastseg git_branch: RELEASE_3_8 git_last_commit: d6877e2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fastseg_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fastseg_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fastseg_1.28.0.tgz vignettes: vignettes/fastseg/inst/doc/fastseg.pdf vignetteTitles: fastseg: Manual for the R package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fastseg/inst/doc/fastseg.R importsMe: methylKit Package: FCBF Version: 1.0.1 Depends: R (>= 3.5.0) Imports: ggplot2, gridExtra, SummarizedExperiment Suggests: caret, mlbench, SingleCellExperiment, knitr, rmarkdown, testthat, BiocManager License: MIT + file LICENSE MD5sum: 28449b73200091dccba49241087286f0 NeedsCompilation: no Title: Fast Correlation Based Filter for Feature Selection Description: This package provides a simple R implementation for the Fast Correlation Based Filter described in Yu, L. and Liu, H.; Feature Selection for High-Dimensional Data: A Fast Correlation Based Filter Solution,Proc. 20th Intl. Conf. Mach. Learn. (ICML-2003), Washington DC, 2003 The current package is an intent to make easier for bioinformaticians to use FCBF for feature selection, especially regarding transcriptomic data.This implies discretizing expression (function discretize_exprs) before calculating the features that explain the class, but are not predictable by other features. The functions are implemented based on the algorithm of Yu and Liu, 2003 and Rajarshi Guha's implementation from 13/05/2005 available (as of 26/08/2018) at http://www.rguha.net/code/R/fcbf.R . biocViews: ImmunoOncology, GeneTarget, FeatureExtraction, Classification, GeneExpression, SingleCell Author: Tiago Lubiana [aut, cre], Helder Nakaya [aut, ths] Maintainer: Tiago Lubiana VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FCBF git_branch: RELEASE_3_8 git_last_commit: 2e9e337 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/FCBF_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/FCBF_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FCBF_1.0.1.tgz vignettes: vignettes/FCBF/inst/doc/FCBF-Vignette.html vignetteTitles: FCBF : Fast Correlation Based Filter for Feature Selection hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/FCBF/inst/doc/FCBF-Vignette.R Package: fCCAC Version: 1.8.0 Depends: R (>= 3.3.0), S4Vectors, IRanges, GenomicRanges, grid Imports: fda, RColorBrewer, genomation, ggplot2, ComplexHeatmap, grDevices, stats, utils Suggests: RUnit, BiocGenerics, BiocStyle License: Artistic-2.0 MD5sum: 20e26204e5c9d0726a0a060b5c2e41cd NeedsCompilation: no Title: functional Canonical Correlation Analysis to evaluate Covariance between nucleic acid sequencing datasets Description: An application of functional canonical correlation analysis to assess covariance of nucleic acid sequencing datasets such as chromatin immunoprecipitation followed by deep sequencing (ChIP-seq). The package can be used as well with other types of sequencing data such as neMeRIP-seq (PMID: 29489750) or with single cell RNA-seq or epigenome data provided in bigWig format. biocViews: Transcription, Genetics, Sequencing, Coverage Author: Pedro Madrigal Maintainer: Pedro Madrigal git_url: https://git.bioconductor.org/packages/fCCAC git_branch: RELEASE_3_8 git_last_commit: f89fef1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fCCAC_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fCCAC_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fCCAC_1.8.0.tgz vignettes: vignettes/fCCAC/inst/doc/fCCAC.pdf vignetteTitles: fCCAC Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fCCAC/inst/doc/fCCAC.R Package: fCI Version: 1.12.0 Depends: R (>= 3.1),FNN, psych, gtools, zoo, rgl, grid, VennDiagram Suggests: knitr, rmarkdown, BiocStyle License: GPL (>= 2) MD5sum: a3c20a38535de3aeba64aa906ac0d37a NeedsCompilation: no Title: f-divergence Cutoff Index for Differential Expression Analysis in Transcriptomics and Proteomics Description: (f-divergence Cutoff Index), is to find DEGs in the transcriptomic & proteomic data, and identify DEGs by computing the difference between the distribution of fold-changes for the control-control and remaining (non-differential) case-control gene expression ratio data. fCI provides several advantages compared to existing methods. biocViews: Proteomics Author: Shaojun Tang Maintainer: Shaojun Tang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/fCI git_branch: RELEASE_3_8 git_last_commit: 1d158e8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fCI_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fCI_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fCI_1.12.0.tgz vignettes: vignettes/fCI/inst/doc/fCI.html vignetteTitles: fCI hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fCI/inst/doc/fCI.R Package: fdrame Version: 1.54.0 Imports: tcltk, graphics, grDevices, stats, utils License: GPL (>= 2) Archs: i386, x64 MD5sum: 1cb9ad63d92d24dae60d42ba7ed28916 NeedsCompilation: yes Title: FDR adjustments of Microarray Experiments (FDR-AME) Description: This package contains two main functions. The first is fdr.ma which takes normalized expression data array, experimental design and computes adjusted p-values It returns the fdr adjusted p-values and plots, according to the methods described in (Reiner, Yekutieli and Benjamini 2002). The second, is fdr.gui() which creates a simple graphic user interface to access fdr.ma biocViews: Microarray, DifferentialExpression, MultipleComparison Author: Yoav Benjamini, Effi Kenigsberg, Anat Reiner, Daniel Yekutieli Maintainer: Effi Kenigsberg git_url: https://git.bioconductor.org/packages/fdrame git_branch: RELEASE_3_8 git_last_commit: 8f023f0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fdrame_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fdrame_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fdrame_1.54.0.tgz vignettes: vignettes/fdrame/inst/doc/fdrame.pdf vignetteTitles: Annotation Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: FELLA Version: 1.2.0 Depends: R (>= 3.5.0) Imports: methods, igraph, Matrix, KEGGREST, plyr, stats, graphics, utils Suggests: shiny, DT, magrittr, visNetwork, knitr, BiocStyle, rmarkdown, testthat, biomaRt, org.Hs.eg.db, org.Mm.eg.db, AnnotationDbi, GOSemSim License: GPL-3 MD5sum: 57cc316a2cfa0eed827576e28c8e7fd6 NeedsCompilation: no Title: Interpretation and enrichment for metabolomics data Description: Enrichment of metabolomics data using KEGG entries. Given a set of affected compounds, FELLA suggests affected reactions, enzymes, modules and pathways using label propagation in a knowledge model network. The resulting subnetwork can be visualised and exported. biocViews: Software, Metabolomics, GraphAndNetwork, KEGG, GO, Pathways, Network, NetworkEnrichment Author: Sergio Picart-Armada [aut, cre], Francesc Fernandez-Albert [aut], Alexandre Perera-Lluna [aut] Maintainer: Sergio Picart-Armada VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FELLA git_branch: RELEASE_3_8 git_last_commit: b5dd13e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FELLA_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FELLA_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FELLA_1.2.0.tgz vignettes: vignettes/FELLA/inst/doc/FELLA.pdf, vignettes/FELLA/inst/doc/musmusculus.pdf, vignettes/FELLA/inst/doc/zebrafish.pdf, vignettes/FELLA/inst/doc/quickstart.html vignetteTitles: FELLA, Example: a fatty liver study on Mus musculus, Example: oxybenzone exposition in gilt-head bream, Quick start hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FELLA/inst/doc/FELLA.R, vignettes/FELLA/inst/doc/musmusculus.R, vignettes/FELLA/inst/doc/quickstart.R, vignettes/FELLA/inst/doc/zebrafish.R Package: FEM Version: 3.10.0 Depends: AnnotationDbi,Matrix,marray,corrplot,igraph,impute,limma,org.Hs.eg.db,graph,BiocGenerics Imports: graph License: GPL (>=2) MD5sum: bdcb6f1671541b2849ed9ca57a974b9b NeedsCompilation: no Title: Identification of Functional Epigenetic Modules Description: The FEM package performs a systems-level integrative analysis of DNA methylation and gene expression data. It seeks modules of functionally related genes which exhibit differential promoter DNA methylation and differential expression, where an inverse association between promoter DNA methylation and gene expression is assumed. For full details, see Jiao et al Bioinformatics 2014. biocViews: SystemsBiology,NetworkEnrichment,DifferentialMethylation,DifferentialExpression Author: Andrew E. Teschendorff and Zhen Yang Maintainer: Zhen Yang git_url: https://git.bioconductor.org/packages/FEM git_branch: RELEASE_3_8 git_last_commit: 99fd00d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FEM_3.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FEM_3.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FEM_3.10.0.tgz vignettes: vignettes/FEM/inst/doc/IntroDoFEM.pdf vignetteTitles: The FEM package performs a systems-level integrative analysis of DNA methylationa and gene expression. It seeks modules of functionally related genes which exhibit differential promoter DNA methylation and differential expression,, where an inverse association between promoter DNA methylation and gene expression is assumed. For full details,, see Jiao et al Bioinformatics 2014. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FEM/inst/doc/IntroDoFEM.R dependsOnMe: ChAMP Package: ffpe Version: 1.26.0 Depends: R (>= 2.10.0), TTR, methods Imports: Biobase, BiocGenerics, affy, lumi, methylumi, sfsmisc Suggests: genefilter, ffpeExampleData License: GPL (>2) MD5sum: 0854fb74a6463f5e5c6fd54a18ad20e8 NeedsCompilation: no Title: Quality assessment and control for FFPE microarray expression data Description: Identify low-quality data using metrics developed for expression data derived from Formalin-Fixed, Paraffin-Embedded (FFPE) data. Also a function for making Concordance at the Top plots (CAT-plots). biocViews: Microarray, GeneExpression, QualityControl Author: Levi Waldron Maintainer: Levi Waldron git_url: https://git.bioconductor.org/packages/ffpe git_branch: RELEASE_3_8 git_last_commit: 35b9c9a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ffpe_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ffpe_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ffpe_1.26.0.tgz vignettes: vignettes/ffpe/inst/doc/ffpe.pdf vignetteTitles: ffpe package user guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ffpe/inst/doc/ffpe.R Package: FGNet Version: 3.16.0 Depends: R (>= 2.15) Imports: igraph (>= 0.6), hwriter, R.utils, XML, plotrix, reshape2, RColorBrewer, png Suggests: RCurl, RDAVIDWebService, gage, topGO, GO.db, KEGG.db, reactome.db, RUnit, BiocGenerics, org.Sc.sgd.db, knitr, rmarkdown, AnnotationDbi, RGtk2, BiocManager License: GPL (>= 2) MD5sum: 8e0ffafc6f001f952cf23b176de7d099 NeedsCompilation: no Title: Functional Gene Networks derived from biological enrichment analyses Description: Build and visualize functional gene and term networks from clustering of enrichment analyses in multiple annotation spaces. The package includes a graphical user interface (GUI) and functions to perform the functional enrichment analysis through DAVID, GeneTerm Linker, gage (GSEA) and topGO. biocViews: Annotation, GO, Pathways, GeneSetEnrichment, Network, Visualization, FunctionalGenomics, NetworkEnrichment, Clustering Author: Sara Aibar, Celia Fontanillo, Conrad Droste and Javier De Las Rivas. Maintainer: Sara Aibar URL: http://www.cicancer.org VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FGNet git_branch: RELEASE_3_8 git_last_commit: f26ca32 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FGNet_3.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FGNet_3.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FGNet_3.16.0.tgz vignettes: vignettes/FGNet/inst/doc/FGNet.html vignetteTitles: FGNet hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FGNet/inst/doc/FGNet.R importsMe: IntramiRExploreR Package: fgsea Version: 1.8.0 Depends: R (>= 3.3), Rcpp Imports: data.table, BiocParallel, stats, ggplot2 (>= 2.2.0), gridExtra, grid, fastmatch, Matrix, utils LinkingTo: Rcpp Suggests: testthat, knitr, rmarkdown, reactome.db, AnnotationDbi, parallel, org.Mm.eg.db, limma, GEOquery License: MIT + file LICENCE Archs: i386, x64 MD5sum: 1ede6d5cb80ae8f3832581da55ee5cc0 NeedsCompilation: yes Title: Fast Gene Set Enrichment Analysis Description: The package implements an algorithm for fast gene set enrichment analysis. Using the fast algorithm allows to make more permutations and get more fine grained p-values, which allows to use accurate stantard approaches to multiple hypothesis correction. biocViews: GeneExpression, DifferentialExpression, GeneSetEnrichment, Pathways Author: Gennady Korotkevich [ctb], Alexey Sergushichev [aut, cre] Maintainer: Alexey Sergushichev URL: https://github.com/ctlab/fgsea/ SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/ctlab/fgsea/issues git_url: https://git.bioconductor.org/packages/fgsea git_branch: RELEASE_3_8 git_last_commit: bb2898a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fgsea_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fgsea_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fgsea_1.8.0.tgz vignettes: vignettes/fgsea/inst/doc/fgsea-tutorial.html vignetteTitles: Using fgsea package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fgsea/inst/doc/fgsea-tutorial.R dependsOnMe: gsean, PPInfer importsMe: CEMiTool, cTRAP, DOSE, mCSEA, phantasus, piano suggestsMe: mdp, Pi Package: FindMyFriends Version: 1.12.0 Imports: methods, BiocGenerics, Biobase, tools, dplyr, IRanges, Biostrings, S4Vectors, kebabs, igraph, Matrix, digest, filehash, Rcpp, ggplot2, gtable, grid, reshape2, ggdendro, BiocParallel, utils, stats LinkingTo: Rcpp Suggests: BiocStyle, testthat, knitr, rmarkdown, reutils License: GPL (>=2) Archs: i386, x64 MD5sum: 1b49ddefa018ab07f89bc316d119f099 NeedsCompilation: yes Title: Microbial Comparative Genomics in R Description: A framework for doing microbial comparative genomics in R. The main purpose of the package is assisting in the creation of pangenome matrices where genes from related organisms are grouped by similarity, as well as the analysis of these data. FindMyFriends provides many novel approaches to doing pangenome analysis and supports a gene grouping algorithm that scales linearly, thus making the creation of huge pangenomes feasible. biocViews: ComparativeGenomics, Clustering, DataRepresentation, GenomicVariation, SequenceMatching, GraphAndNetwork Author: Thomas Lin Pedersen Maintainer: Thomas Lin Pedersen URL: https://github.com/thomasp85/FindMyFriends VignetteBuilder: knitr BugReports: https://github.com/thomasp85/FindMyFriends/issues git_url: https://git.bioconductor.org/packages/FindMyFriends git_branch: RELEASE_3_8 git_last_commit: 2f71bd7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FindMyFriends_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FindMyFriends_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FindMyFriends_1.12.0.tgz vignettes: vignettes/FindMyFriends/inst/doc/FindMyFriends_intro.html vignetteTitles: Creating pangenomes using FindMyFriends hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FindMyFriends/inst/doc/FindMyFriends_intro.R importsMe: PanVizGenerator Package: FISHalyseR Version: 1.16.0 Depends: EBImage,abind Suggests: knitr License: Artistic-2.0 MD5sum: 18f4ac8d3e1695713f0953102e3105f5 NeedsCompilation: no Title: FISHalyseR a package for automated FISH quantification Description: FISHalyseR provides functionality to process and analyse digital cell culture images, in particular to quantify FISH probes within nuclei. Furthermore, it extract the spatial location of each nucleus as well as each probe enabling spatial co-localisation analysis. biocViews: CellBiology Author: Karesh Arunakirinathan , Andreas Heindl Maintainer: Karesh Arunakirinathan , Andreas Heindl VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FISHalyseR git_branch: RELEASE_3_8 git_last_commit: 05c6979 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FISHalyseR_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FISHalyseR_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FISHalyseR_1.16.0.tgz vignettes: vignettes/FISHalyseR/inst/doc/FISHalyseR.pdf vignetteTitles: FISHAlyseR Automated fluorescence in situ hybridisation quantification in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FISHalyseR/inst/doc/FISHalyseR.R Package: FitHiC Version: 1.8.0 Imports: data.table, fdrtool, grDevices, graphics, Rcpp, stats, utils LinkingTo: Rcpp Suggests: knitr, rmarkdown License: GPL (>= 2) Archs: i386, x64 MD5sum: e61cb471638915e53858418b543fe1af NeedsCompilation: yes Title: Confidence estimation for intra-chromosomal contact maps Description: Fit-Hi-C is a tool for assigning statistical confidence estimates to intra-chromosomal contact maps produced by genome-wide genome architecture assays such as Hi-C. biocViews: DNA3DStructure, Software Author: Ferhat Ay [aut] (Python original, https://noble.gs.washington.edu/proj/fit-hi-c/), Timothy L. Bailey [aut], William S. Noble [aut], Ruyu Tan [aut, cre, trl] (R port) Maintainer: Ruyu Tan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FitHiC git_branch: RELEASE_3_8 git_last_commit: 087a7bb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FitHiC_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FitHiC_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FitHiC_1.8.0.tgz vignettes: vignettes/FitHiC/inst/doc/fithic.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FitHiC/inst/doc/fithic.R Package: flagme Version: 1.38.1 Depends: gcspikelite, xcms, CAMERA Imports: gplots, graphics, MASS, methods, SparseM, stats, utils License: LGPL (>= 2) Archs: i386, x64 MD5sum: 6a2fbf22b7ee2036539b05d38295b111 NeedsCompilation: yes Title: Analysis of Metabolomics GC/MS Data Description: Fragment-level analysis of gas chromatography - mass spectrometry metabolomics data biocViews: ImmunoOncology, DifferentialExpression, MassSpectrometry Author: Mark Robinson , Riccardo Romoli Maintainer: Mark Robinson , Riccardo Romoli git_url: https://git.bioconductor.org/packages/flagme git_branch: RELEASE_3_8 git_last_commit: 35fcae3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flagme_1.38.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flagme_1.38.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flagme_1.38.1.tgz vignettes: vignettes/flagme/inst/doc/flagme.pdf vignetteTitles: Using flagme -- Fragment-level analysis of GC-MS-based metabolomics data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flagme/inst/doc/flagme.R Package: flipflop Version: 1.20.0 Depends: R (>= 2.10.0) Imports: methods, Matrix, IRanges, GenomicRanges, parallel Suggests: GenomicFeatures License: GPL-3 Archs: i386, x64 MD5sum: 6d7199d947a60eb70e2ce165f468bb82 NeedsCompilation: yes Title: Fast lasso-based isoform prediction as a flow problem Description: Flipflop discovers which isoforms of a gene are expressed in a given sample together with their abundances, based on RNA-Seq read data. It takes an alignment file in SAM format as input. It can also discover transcripts from several samples simultaneously, increasing statistical power. biocViews: RNASeq, RNASeqData, AlternativeSplicing, Regression Author: Elsa Bernard, Laurent Jacob, Julien Mairal and Jean-Philippe Vert Maintainer: Elsa Bernard URL: http://cbio.ensmp.fr/flipflop SystemRequirements: GNU make git_url: https://git.bioconductor.org/packages/flipflop git_branch: RELEASE_3_8 git_last_commit: 5e4e92e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/flipflop_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/flipflop_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flipflop_1.20.0.tgz vignettes: vignettes/flipflop/inst/doc/flipflop.pdf vignetteTitles: FlipFlop: Fast Lasso-based Isoform Prediction as a Flow Problem hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flipflop/inst/doc/flipflop.R Package: flowAI Version: 1.12.7 Depends: R (>= 3.4) Imports: ggplot2, flowCore, plyr, changepoint, knitr, reshape2, RColorBrewer, scales, methods, graphics, stats, utils, rmarkdown Suggests: testthat, shiny License: GPL (>= 2) MD5sum: 291cf1a37cb848533f7109b324f2d788 NeedsCompilation: no Title: Automatic and interactive quality control for flow cytometry data Description: The package is able to perform an automatic or interactive quality control on FCS data acquired using flow cytometry instruments. By evaluating three different properties: 1) flow rate, 2) signal acquisition, 3) dynamic range, the quality control enables the detection and removal of anomalies. biocViews: FlowCytometry, QualityControl, BiomedicalInformatics, ImmunoOncology Author: Gianni Monaco, Hao Chen Maintainer: Gianni Monaco VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowAI git_branch: RELEASE_3_8 git_last_commit: 25587df git_last_commit_date: 2019-03-04 Date/Publication: 2019-03-04 source.ver: src/contrib/flowAI_1.12.7.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowAI_1.12.7.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowAI_1.12.7.tgz vignettes: vignettes/flowAI/inst/doc/flowAI.html vignetteTitles: Automatic and GUI methods to do quality control on Flow cytometry Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowAI/inst/doc/flowAI.R Package: flowBeads Version: 1.20.1 Depends: R (>= 2.15.0), methods, Biobase, rrcov, flowCore Imports: flowCore, rrcov, knitr, xtable Suggests: flowViz License: Artistic-2.0 MD5sum: 33c0faeae8a8c36f559ebe55a708e55e NeedsCompilation: no Title: flowBeads: Analysis of flow bead data Description: This package extends flowCore to provide functionality specific to bead data. One of the goals of this package is to automate analysis of bead data for the purpose of normalisation. biocViews: ImmunoOncology, Infrastructure, FlowCytometry, CellBasedAssays Author: Nikolas Pontikos Maintainer: Nikolas Pontikos git_url: https://git.bioconductor.org/packages/flowBeads git_branch: RELEASE_3_8 git_last_commit: f1f1b24 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowBeads_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowBeads_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowBeads_1.20.1.tgz vignettes: vignettes/flowBeads/inst/doc/HowTo-flowBeads.pdf vignetteTitles: Analysis of Flow Cytometry Bead Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowBeads/inst/doc/HowTo-flowBeads.R Package: flowBin Version: 1.18.1 Depends: methods, flowCore, flowFP, R (>= 2.10) Imports: class, limma, snow, BiocGenerics Suggests: parallel License: Artistic-2.0 MD5sum: d6daea839a985f6407a2fe2a8ee134c1 NeedsCompilation: no Title: Combining multitube flow cytometry data by binning Description: Software to combine flow cytometry data that has been multiplexed into multiple tubes with common markers between them, by establishing common bins across tubes in terms of the common markers, then determining expression within each tube for each bin in terms of the tube-specific markers. biocViews: ImmunoOncology, CellBasedAssays, FlowCytometry Author: Kieran O'Neill Maintainer: Kieran O'Neill git_url: https://git.bioconductor.org/packages/flowBin git_branch: RELEASE_3_8 git_last_commit: 11091fe git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowBin_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowBin_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowBin_1.18.1.tgz vignettes: vignettes/flowBin/inst/doc/flowBin.pdf vignetteTitles: flowBin hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowBin/inst/doc/flowBin.R Package: flowcatchR Version: 1.16.0 Depends: R (>= 2.10), methods, EBImage Imports: colorRamps, abind, BiocParallel, graphics, stats, utils, plotly, shiny Suggests: BiocStyle, knitr, rmarkdown License: BSD_3_clause + file LICENSE MD5sum: e6cce882873b92da15dcc28e0bff415d NeedsCompilation: no Title: Tools to analyze in vivo microscopy imaging data focused on tracking flowing blood cells Description: flowcatchR is a set of tools to analyze in vivo microscopy imaging data, focused on tracking flowing blood cells. It guides the steps from segmentation to calculation of features, filtering out particles not of interest, providing also a set of utilities to help checking the quality of the performed operations (e.g. how good the segmentation was). It allows investigating the issue of tracking flowing cells such as in blood vessels, to categorize the particles in flowing, rolling and adherent. This classification is applied in the study of phenomena such as hemostasis and study of thrombosis development. Moreover, flowcatchR presents an integrated workflow solution, based on the integration with a Shiny App and Jupyter notebooks, which is delivered alongside the package, and can enable fully reproducible bioimage analysis in the R environment. biocViews: Software, Visualization, CellBiology, Classification, Infrastructure, GUI Author: Federico Marini [aut, cre] () Maintainer: Federico Marini URL: https://github.com/federicomarini/flowcatchR, https://federicomarini.github.io/flowcatchR/ SystemRequirements: ImageMagick VignetteBuilder: knitr BugReports: https://github.com/federicomarini/flowcatchR/issues git_url: https://git.bioconductor.org/packages/flowcatchR git_branch: RELEASE_3_8 git_last_commit: 4cdcf2d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/flowcatchR_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowcatchR_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowcatchR_1.16.0.tgz vignettes: vignettes/flowcatchR/inst/doc/flowcatchr_vignette.html vignetteTitles: flowcatchR: tracking and analyzing cells in time lapse microscopy images hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/flowcatchR/inst/doc/flowcatchr_vignette.R Package: flowCHIC Version: 1.16.1 Depends: R (>= 3.1.0) Imports: methods, flowCore, EBImage, vegan, hexbin, ggplot2, grid License: GPL-2 MD5sum: a9c06ce1fe876415dbc45ca4cf376e9f NeedsCompilation: no Title: Analyze flow cytometric data using histogram information Description: A package to analyze flow cytometric data of complex microbial communities based on histogram images biocViews: ImmunoOncology, CellBasedAssays, Clustering, FlowCytometry, Software, Visualization Author: Joachim Schumann , Christin Koch , Ingo Fetzer , Susann Müller Maintainer: Author: Joachim Schumann URL: http://www.ufz.de/index.php?en=16773 git_url: https://git.bioconductor.org/packages/flowCHIC git_branch: RELEASE_3_8 git_last_commit: 824c93f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowCHIC_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowCHIC_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowCHIC_1.16.1.tgz vignettes: vignettes/flowCHIC/inst/doc/flowCHICmanual.pdf vignetteTitles: Analyze flow cytometric data using histogram information hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowCHIC/inst/doc/flowCHICmanual.R Package: flowCL Version: 1.20.1 Depends: R (>= 3.4), Rgraphviz, SPARQL Imports: methods, grDevices, utils, graph Suggests: RUnit, BiocGenerics License: Artistic-2.0 MD5sum: cb31d847de5e1c0582c3b12d778a1931 NeedsCompilation: no Title: Semantic labelling of flow cytometric cell populations Description: Semantic labelling of flow cytometric cell populations. biocViews: FlowCytometry, ImmunoOncology Author: Justin Meskas, Radina Droumeva Maintainer: Justin Meskas git_url: https://git.bioconductor.org/packages/flowCL git_branch: RELEASE_3_8 git_last_commit: dda2334 git_last_commit_date: 2018-11-29 Date/Publication: 2018-11-29 source.ver: src/contrib/flowCL_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowCL_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowCL_1.20.1.tgz vignettes: vignettes/flowCL/inst/doc/flowCL.pdf vignetteTitles: flowCL package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowCL/inst/doc/flowCL.R Package: flowClean Version: 1.20.0 Depends: R (>= 2.15.0), flowCore Imports: bit, changepoint, sfsmisc Suggests: flowViz, grid, gridExtra License: Artistic-2.0 MD5sum: 5aee35d8d33660b091d930a61da84b11 NeedsCompilation: no Title: flowClean Description: A quality control tool for flow cytometry data based on compositional data analysis. biocViews: FlowCytometry, QualityControl Author: Kipper Fletez-Brant Maintainer: Kipper Fletez-Brant git_url: https://git.bioconductor.org/packages/flowClean git_branch: RELEASE_3_8 git_last_commit: 101bcfc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/flowClean_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowClean_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowClean_1.20.0.tgz vignettes: vignettes/flowClean/inst/doc/flowClean.pdf vignetteTitles: flowClean hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowClean/inst/doc/flowClean.R Package: flowClust Version: 3.20.1 Depends: R(>= 2.5.0) Imports: BiocGenerics, methods, Biobase, graph, ellipse, flowViz, flowCore, clue, corpcor, mnormt Suggests: testthat, flowWorkspace, flowWorkspaceData License: Artistic-2.0 Archs: i386, x64 MD5sum: 06e05655300595c09293509689e86c5f NeedsCompilation: yes Title: Clustering for Flow Cytometry Description: Robust model-based clustering using a t-mixture model with Box-Cox transformation. Note: users should have GSL installed. Windows users: 'consult the README file available in the inst directory of the source distribution for necessary configuration instructions'. biocViews: ImmunoOncology, Clustering, Visualization, FlowCytometry Author: Raphael Gottardo , Kenneth Lo , Greg Finak Maintainer: Greg Finak , Mike Jiang SystemRequirements: GNU make git_url: https://git.bioconductor.org/packages/flowClust git_branch: RELEASE_3_8 git_last_commit: abd7e0f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowClust_3.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowClust_3.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowClust_3.20.1.tgz vignettes: vignettes/flowClust/inst/doc/flowClust.pdf vignetteTitles: flowClust package hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowClust/inst/doc/flowClust.R importsMe: flowTrans, flowType suggestsMe: BiocGenerics Package: flowCore Version: 1.48.1 Depends: R (>= 3.0.2) Imports: Biobase, BiocGenerics (>= 0.1.14), graph, grDevices, graphics, methods, rrcov, stats, utils, stats4, corpcor, Rcpp, matrixStats, MASS LinkingTo: Rcpp, BH(>= 1.65.0.1) Suggests: Rgraphviz, flowViz, flowStats, testthat, flowWorkspace, flowWorkspaceData, openCyto, knitr, ggcyto, gridExtra License: Artistic-2.0 Archs: i386, x64 MD5sum: 2426fd7ed62f7b846dd5dc999b403779 NeedsCompilation: yes Title: flowCore: Basic structures for flow cytometry data Description: Provides S4 data structures and basic functions to deal with flow cytometry data. biocViews: ImmunoOncology, Infrastructure, FlowCytometry, CellBasedAssays Author: B Ellis [aut], Perry Haaland [aut], Florian Hahne [aut], Nathan Le Meur [aut], Nishant Gopalakrishnan [aut], Josef Spidlen [aut], Mike Jiang [aut, cre], Greg Finak [aut], Samuel Granjeaud [ctb] Maintainer: Mike Jiang SystemRequirements: GNU make, C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowCore git_branch: RELEASE_3_8 git_last_commit: 154bfd9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowCore_1.48.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowCore_1.48.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowCore_1.48.1.tgz vignettes: vignettes/flowCore/inst/doc/HowTo-flowCore.pdf, vignettes/flowCore/inst/doc/fcs3.html, vignettes/flowCore/inst/doc/hyperlog.notice.html vignetteTitles: Basic Functions for Flow Cytometry Data, fcs3.html, hyperlog.notice.html hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowCore/inst/doc/HowTo-flowCore.R dependsOnMe: flowBeads, flowBin, flowClean, flowFP, flowMatch, flowStats, flowTime, flowTrans, flowViz, flowVS, ggcyto, immunoClust, ncdfFlow, plateCore importsMe: CATALYST, cydar, CytoML, ddPCRclust, diffcyt, flowAI, flowBeads, flowCHIC, flowClust, flowDensity, flowFit, flowMeans, flowPloidy, flowQB, FlowSOM, flowTrans, flowType, flowUtils, flowViz, GateFinder, ImmuneSpaceR, MetaCyto, oneSENSE, plateCore, Sconify suggestsMe: COMPASS, FlowRepositoryR, RchyOptimyx Package: flowCyBar Version: 1.18.1 Depends: R (>= 3.0.0) Imports: gplots, vegan, methods License: GPL-2 MD5sum: 6a4ece4b4aa8ca2d846ec89e431a9abc NeedsCompilation: no Title: Analyze flow cytometric data using gate information Description: A package to analyze flow cytometric data using gate information to follow population/community dynamics biocViews: ImmunoOncology, CellBasedAssays, Clustering, FlowCytometry, Software, Visualization Author: Joachim Schumann , Christin Koch , Susanne Günther , Ingo Fetzer , Susann Müller Maintainer: Joachim Schumann URL: http://www.ufz.de/index.php?de=16773 git_url: https://git.bioconductor.org/packages/flowCyBar git_branch: RELEASE_3_8 git_last_commit: f2ac74c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowCyBar_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowCyBar_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowCyBar_1.18.1.tgz vignettes: vignettes/flowCyBar/inst/doc/flowCyBar-manual.pdf vignetteTitles: Analyze flow cytometric data using gate information hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowCyBar/inst/doc/flowCyBar-manual.R Package: flowDensity Version: 1.16.1 Imports: flowCore, graphics, car, sp, rgeos, gplots, RFOC, flowWorkspace (>= 3.20.5), methods, stats, grDevices License: Artistic-2.0 MD5sum: 3bb912f71bc2d0b7342ab5e3718f608e NeedsCompilation: no Title: Sequential Flow Cytometry Data Gating Description: This package provides tools for automated sequential gating analogous to the manual gating strategy based on the density of the data. biocViews: ImmunoOncology, Bioinformatics, FlowCytometry, CellBiology, Clustering, Cancer, FlowCytData, StemCells, DensityGating Author: Mehrnoush Malek,M. Jafar Taghiyar Maintainer: Mehrnoush Malek SystemRequirements: GEOS (>= 3.2.0);for building from source: GEOS from http://trac.osgeo.org/geos/; GEOS OSX frameworks built by William Kyngesburye at http://www.kyngchaos.com/ may be used for source installs on OSX. git_url: https://git.bioconductor.org/packages/flowDensity git_branch: RELEASE_3_8 git_last_commit: e2655a2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowDensity_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowDensity_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowDensity_1.16.1.tgz vignettes: vignettes/flowDensity/inst/doc/flowDensity.pdf, vignettes/flowDensity/inst/doc/flowDensityVignette.pdf vignetteTitles: Automated alternative to the current manual gating practice, Automated alternative to the current manual gating practice hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowDensity/inst/doc/flowDensity.R, vignettes/flowDensity/inst/doc/flowDensityVignette.R importsMe: ddPCRclust Package: flowFit Version: 1.20.1 Depends: R (>= 2.12.2) Imports: flowCore, flowViz, graphics, kza, methods, minpack.lm, gplots Suggests: flowFitExampleData License: Artistic-2.0 MD5sum: 175d3d9b13e2263b591cbf40ccbbae37 NeedsCompilation: no Title: Estimate proliferation in cell-tracking dye studies Description: This package estimate the proliferation of a cell population in cell-tracking dye studies. The package uses an R implementation of the Levenberg-Marquardt algorithm (minpack.lm) to fit a set of peaks (corresponding to different generations of cells) over the proliferation-tracking dye distribution in a FACS experiment. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays Author: Davide Rambaldi Maintainer: Davide Rambaldi BugReports: Davide Rambaldi git_url: https://git.bioconductor.org/packages/flowFit git_branch: RELEASE_3_8 git_last_commit: dfa5ee7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowFit_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowFit_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowFit_1.20.1.tgz vignettes: vignettes/flowFit/inst/doc/HowTo-flowFit.pdf vignetteTitles: Fitting Functions for Flow Cytometry Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowFit/inst/doc/HowTo-flowFit.R Package: flowFP Version: 1.40.1 Depends: R (>= 2.10), flowCore, flowViz Imports: Biobase, BiocGenerics (>= 0.1.6), graphics, grDevices, methods, stats, stats4 Suggests: RUnit License: Artistic-2.0 Archs: i386, x64 MD5sum: 75a7fc1ceb1255d443afa907bc36e9bd NeedsCompilation: yes Title: Fingerprinting for Flow Cytometry Description: Fingerprint generation of flow cytometry data, used to facilitate the application of machine learning and datamining tools for flow cytometry. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays, Clustering, Visualization Author: Herb Holyst , Wade Rogers Maintainer: Herb Holyst git_url: https://git.bioconductor.org/packages/flowFP git_branch: RELEASE_3_8 git_last_commit: 9c0cf57 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowFP_1.40.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowFP_1.40.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowFP_1.40.1.tgz vignettes: vignettes/flowFP/inst/doc/flowFP_HowTo.pdf vignetteTitles: Fingerprinting for Flow Cytometry hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowFP/inst/doc/flowFP_HowTo.R dependsOnMe: flowBin Package: flowMap Version: 1.20.1 Depends: R (>= 3.0.1), ade4(>= 1.5-2), doParallel(>= 1.0.3), abind(>= 1.4.0), reshape2(>= 1.2.2), scales(>= 0.2.3), Matrix(>= 1.1-4), methods (>= 2.14) Suggests: BiocStyle, knitr License: GPL (>=2) MD5sum: b92e0c86d27f34410419826317e8277f NeedsCompilation: no Title: Mapping cell populations in flow cytometry data for cross-sample comparisons using the Friedman-Rafsky Test Description: flowMap quantifies the similarity of cell populations across multiple flow cytometry samples using a nonparametric multivariate statistical test. The method is able to map cell populations of different size, shape, and proportion across multiple flow cytometry samples. The algorithm can be incorporate in any flow cytometry work flow that requires accurat quantification of similarity between cell populations. biocViews: ImmunoOncology, MultipleComparison, FlowCytometry Author: Chiaowen Joyce Hsiao, Yu Qian, and Richard H. Scheuermann Maintainer: Chiaowen Joyce Hsiao VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowMap git_branch: RELEASE_3_8 git_last_commit: 849e0eb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowMap_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowMap_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowMap_1.20.1.tgz vignettes: vignettes/flowMap/inst/doc/flowMap.pdf vignetteTitles: Mapping cell populations in flow cytometry data flowMap-FR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowMap/inst/doc/flowMap.R Package: flowMatch Version: 1.18.1 Depends: R (>= 3.0.0), Rcpp (>= 0.11.0), methods, flowCore Imports: Biobase LinkingTo: Rcpp Suggests: healthyFlowData License: Artistic-2.0 Archs: i386, x64 MD5sum: b41ebcacfb26f3613dd1099e343aaea9 NeedsCompilation: yes Title: Matching and meta-clustering in flow cytometry Description: Matching cell populations and building meta-clusters and templates from a collection of FC samples. biocViews: ImmunoOncology, Clustering, FlowCytometry Author: Ariful Azad Maintainer: Ariful Azad git_url: https://git.bioconductor.org/packages/flowMatch git_branch: RELEASE_3_8 git_last_commit: 85c1c5e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowMatch_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowMatch_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowMatch_1.18.1.tgz vignettes: vignettes/flowMatch/inst/doc/flowMatch.pdf vignetteTitles: flowMatch: Cell population matching and meta-clustering in Flow Cytometry hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowMatch/inst/doc/flowMatch.R Package: flowMeans Version: 1.42.1 Depends: R (>= 2.10.0) Imports: Biobase, graphics, grDevices, methods, rrcov, stats, feature, flowCore License: Artistic-2.0 MD5sum: 0b5ac87aa94096b505c62a49f57a0252 NeedsCompilation: no Title: Non-parametric Flow Cytometry Data Gating Description: Identifies cell populations in Flow Cytometry data using non-parametric clustering and segmented-regression-based change point detection. Note: R 2.11.0 or newer is required. biocViews: ImmunoOncology, FlowCytometry, CellBiology, Clustering Author: Nima Aghaeepour Maintainer: Nima Aghaeepour git_url: https://git.bioconductor.org/packages/flowMeans git_branch: RELEASE_3_8 git_last_commit: 5cb2385 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowMeans_1.42.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowMeans_1.42.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowMeans_1.42.1.tgz vignettes: vignettes/flowMeans/inst/doc/flowMeans.pdf vignetteTitles: flowMeans: Non-parametric Flow Cytometry Data Gating hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowMeans/inst/doc/flowMeans.R importsMe: flowType Package: flowMerge Version: 2.30.1 Depends: graph,feature,flowClust,Rgraphviz,foreach,snow Imports: rrcov,flowCore, graphics, methods, stats, utils Enhances: doMC, multicore License: Artistic-2.0 MD5sum: 6594ae374303f35932dca812d021147b NeedsCompilation: no Title: Cluster Merging for Flow Cytometry Data Description: Merging of mixture components for model-based automated gating of flow cytometry data using the flowClust framework. Note: users should have a working copy of flowClust 2.0 installed. biocViews: ImmunoOncology, Clustering, FlowCytometry Author: Greg Finak , Raphael Gottardo Maintainer: Greg Finak git_url: https://git.bioconductor.org/packages/flowMerge git_branch: RELEASE_3_8 git_last_commit: e08748c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowMerge_2.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowMerge_2.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowMerge_2.30.1.tgz vignettes: vignettes/flowMerge/inst/doc/flowMerge.pdf vignetteTitles: flowMerge package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowMerge/inst/doc/flowMerge.R importsMe: flowType Package: flowPeaks Version: 1.28.1 Depends: R (>= 2.12.0) Enhances: flowCore License: Artistic-1.0 Archs: i386, x64 MD5sum: 8883a936581c7af8c579b73440a17852 NeedsCompilation: yes Title: An R package for flow data clustering Description: A fast and automatic clustering to classify the cells into subpopulations based on finding the peaks from the overall density function generated by K-means. biocViews: ImmunoOncology, FlowCytometry, Clustering, Gating Author: Yongchao Ge Maintainer: Yongchao Ge SystemRequirements: gsl git_url: https://git.bioconductor.org/packages/flowPeaks git_branch: RELEASE_3_8 git_last_commit: 32d9195 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowPeaks_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowPeaks_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowPeaks_1.28.1.tgz vignettes: vignettes/flowPeaks/inst/doc/flowPeaks-guide.pdf vignetteTitles: Tutorial of flowPeaks package hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowPeaks/inst/doc/flowPeaks-guide.R importsMe: ddPCRclust Package: flowPloidy Version: 1.8.0 Depends: R (>= 3.4) Imports: flowCore, car, caTools, knitr, rmarkdown, minpack.lm, shiny, methods, graphics, stats, utils Suggests: flowPloidyData, testthat License: GPL-3 MD5sum: 4866ee71a93962a34151e674a0a26895 NeedsCompilation: no Title: Analyze flow cytometer data to determine sample ploidy Description: Determine sample ploidy via flow cytometry histogram analysis. Reads Flow Cytometry Standard (FCS) files via the flowCore bioconductor package, and provides functions for determining the DNA ploidy of samples based on internal standards. biocViews: FlowCytometry, GUI, Regression, Visualization Author: Tyler Smith Maintainer: Tyler Smith URL: https://github.com/plantarum/flowPloidy VignetteBuilder: knitr BugReports: https://github.com/plantarum/flowPloidy/issues git_url: https://git.bioconductor.org/packages/flowPloidy git_branch: RELEASE_3_8 git_last_commit: 3c5dcce git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/flowPloidy_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowPloidy_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowPloidy_1.8.0.tgz vignettes: vignettes/flowPloidy/inst/doc/flowPloidy-gettingStarted.pdf, vignettes/flowPloidy/inst/doc/histogram-tour.pdf vignetteTitles: flowPloidy: Getting Started, flowPloidy: FCM Histograms hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowPloidy/inst/doc/flowPloidy-gettingStarted.R, vignettes/flowPloidy/inst/doc/histogram-tour.R Package: flowPlots Version: 1.30.1 Depends: R (>= 2.13.0), methods Suggests: vcd License: Artistic-2.0 MD5sum: 99408a38d1bddc7dca85ef37e60d4b27 NeedsCompilation: no Title: flowPlots: analysis plots and data class for gated flow cytometry data Description: Graphical displays with embedded statistical tests for gated ICS flow cytometry data, and a data class which stores "stacked" data and has methods for computing summary measures on stacked data, such as marginal and polyfunctional degree data. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays, Visualization, DataRepresentation Author: N. Hawkins, S. Self Maintainer: N. Hawkins git_url: https://git.bioconductor.org/packages/flowPlots git_branch: RELEASE_3_8 git_last_commit: 62bf533 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowPlots_1.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowPlots_1.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowPlots_1.30.1.tgz vignettes: vignettes/flowPlots/inst/doc/flowPlots.pdf vignetteTitles: Plots with Embedded Tests for Gated Flow Cytometry Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowPlots/inst/doc/flowPlots.R Package: flowQB Version: 2.10.1 Imports: methods, flowCore (>= 1.32.0), stats, extremevalues Suggests: flowQBData, FlowRepositoryR, xlsx, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: a324990ad4dec51636d4d825b3161215 NeedsCompilation: no Title: Automated Quadratic Characterization of Flow Cytometer Instrument Sensitivity: Q, B and CV instrinsic calculations Description: flowQB is a fully automated R Bioconductor package to calculate automatically the detector efficiency (Q), optical background (B) and intrinsic CV of the beads. biocViews: ImmunoOncology, FlowCytometry, Regression, PeakDetection, QualityControl, MultiChannel, OneChannel Author: Josef Spidlen, Faysal El Khettabi, Wayne Moore, David Parks, Ryan Brinkman Maintainer: Josef Spidlen git_url: https://git.bioconductor.org/packages/flowQB git_branch: RELEASE_3_8 git_last_commit: 1f80a6c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowQB_2.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowQB_2.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowQB_2.10.1.tgz vignettes: vignettes/flowQB/inst/doc/flowQBVignettes.pdf vignetteTitles: flowQB package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowQB/inst/doc/flowQBVignettes.R Package: FlowRepositoryR Version: 1.14.1 Depends: R (>= 3.2) Imports: XML, RCurl, tools, utils, jsonlite Suggests: RUnit, BiocGenerics, flowCore, methods License: Artistic-2.0 MD5sum: e634ffe0fd712764deadd08271b7bc2e NeedsCompilation: no Title: FlowRepository R Interface Description: This package provides an interface to search and download data and annotations from FlowRepository (flowrepository.org). It uses the FlowRepository programming interface to communicate with a FlowRepository server. biocViews: ImmunoOncology, Infrastructure, FlowCytometry Author: Josef Spidlen [aut, cre] Maintainer: Josef Spidlen git_url: https://git.bioconductor.org/packages/FlowRepositoryR git_branch: RELEASE_3_8 git_last_commit: 37c66d7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/FlowRepositoryR_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/FlowRepositoryR_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FlowRepositoryR_1.14.1.tgz vignettes: vignettes/FlowRepositoryR/inst/doc/HowTo-FlowRepositoryR.pdf vignetteTitles: FlowRepository R Interface hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FlowRepositoryR/inst/doc/HowTo-FlowRepositoryR.R suggestsMe: flowQB Package: FlowSOM Version: 1.14.1 Depends: R (>= 3.2), igraph Imports: flowCore, ConsensusClusterPlus, BiocGenerics, tsne, XML, flowUtils Suggests: BiocStyle License: GPL (>= 2) Archs: i386, x64 MD5sum: 2fa394ebb0e8fee9342974dd7f83bc94 NeedsCompilation: yes Title: Using self-organizing maps for visualization and interpretation of cytometry data Description: FlowSOM offers visualization options for cytometry data, by using Self-Organizing Map clustering and Minimal Spanning Trees. biocViews: ImmunoOncology, CellBiology, FlowCytometry, Clustering, Visualization, Software, CellBasedAssays Author: Sofie Van Gassen, Britt Callebaut and Yvan Saeys Maintainer: Sofie Van Gassen URL: http://www.r-project.org, http://dambi.ugent.be git_url: https://git.bioconductor.org/packages/FlowSOM git_branch: RELEASE_3_8 git_last_commit: 9c69691 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/FlowSOM_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/FlowSOM_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FlowSOM_1.14.1.tgz vignettes: vignettes/FlowSOM/inst/doc/FlowSOM.pdf vignetteTitles: FlowSOM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FlowSOM/inst/doc/FlowSOM.R importsMe: CATALYST, diffcyt Package: flowStats Version: 3.40.1 Depends: R (>= 2.10), flowCore, cluster, flowWorkspace, ncdfFlow(>= 2.19.5) Imports: BiocGenerics, MASS, flowViz, fda (>= 2.2.6), Biobase, methods, grDevices, graphics, stats, utils, KernSmooth, lattice,ks, RColorBrewer Suggests: xtable Enhances: RBGL,graph License: Artistic-2.0 MD5sum: 43c7c4367a8c80d147feb7030425e5fc NeedsCompilation: no Title: Statistical methods for the analysis of flow cytometry data Description: Methods and functionality to analyse flow data that is beyond the basic infrastructure provided by the flowCore package. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays Author: Florian Hahne, Nishant Gopalakrishnan, Alireza Hadj Khodabakhshi, Chao-Jen Wong, Kyongryun Lee Maintainer: Greg Finak and Mike Jiang URL: http://www.github.com/RGLab/flowStats BugReports: http://www.github.com/RGLab/flowStats/issues git_url: https://git.bioconductor.org/packages/flowStats git_branch: RELEASE_3_8 git_last_commit: b65676d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowStats_3.40.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowStats_3.40.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowStats_3.40.1.tgz vignettes: vignettes/flowStats/inst/doc/GettingStartedWithFlowStats.pdf vignetteTitles: flowStats Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowStats/inst/doc/GettingStartedWithFlowStats.R dependsOnMe: flowVS importsMe: plateCore suggestsMe: cydar, flowCore, ggcyto Package: flowTime Version: 1.6.1 Depends: R (>= 3.4), flowCore, plyr Imports: utils Suggests: knitr, rmarkdown, flowViz, ggplot2, BiocGenerics, moments, stats License: Artistic-2.0 MD5sum: 0c21c0faa092028214b2a125cd9cd140 NeedsCompilation: no Title: Annotation and analysis of biological dynamical systems using flow cytometry Description: This package was developed for analysis of both dynamic and steady state experiments examining the function of gene regulatory networks in yeast (strain W303) expressing fluorescent reporter proteins using a BD Accuri C6 and SORP cytometers. However, the functions are for the most part general and may be adapted for analysis of other organisms using other flow cytometers. Functions in this package facilitate the annotation of flow cytometry data with experimental metadata, as is requisite for dissemination and general ease-of-use. Functions for creating, saving and loading gate sets are also included. In the past, we have typically generated summary statistics for each flowset for each timepoint and then annotated and analyzed these summary statistics. This method loses a great deal of the power that comes from the large amounts of individual cell data generated in flow cytometry, by essentially collapsing this data into a bulk measurement after subsetting. In addition to these summary functions, this package also contains functions to facilitate annotation and analysis of steady-state or time-lapse data utilizing all of the data collected from the thousands of individual cells in each sample. biocViews: ImmunoOncology, FlowCytometry, TimeCourse, Visualization, DataImport, CellBasedAssays Author: R. Clay Wright [aut, cre], Nick Bolten [aut], Edith Pierre-Jerome [aut] Maintainer: R. Clay Wright VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowTime git_branch: RELEASE_3_8 git_last_commit: f25b1c3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowTime_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowTime_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowTime_1.6.1.tgz vignettes: vignettes/flowTime/inst/doc/steady-state-vignette.html, vignettes/flowTime/inst/doc/time-course-vignette.html vignetteTitles: Steady-state analysis of flow cytometry data, Time course analysis of flow cytometry data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowTime/inst/doc/steady-state-vignette.R, vignettes/flowTime/inst/doc/time-course-vignette.R Package: flowTrans Version: 1.34.1 Depends: R (>= 2.11.0), flowCore, flowViz,flowClust Imports: flowCore, methods, flowViz, stats, flowClust License: Artistic-2.0 MD5sum: 730f66324a0ebc90acce32fd909d9042 NeedsCompilation: no Title: Parameter Optimization for Flow Cytometry Data Transformation Description: Profile maximum likelihood estimation of parameters for flow cytometry data transformations. biocViews: ImmunoOncology, FlowCytometry Author: Greg Finak , Juan Manuel-Perez , Raphael Gottardo Maintainer: Greg Finak git_url: https://git.bioconductor.org/packages/flowTrans git_branch: RELEASE_3_8 git_last_commit: 4172564 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowTrans_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowTrans_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowTrans_1.34.1.tgz vignettes: vignettes/flowTrans/inst/doc/flowTrans.pdf vignetteTitles: flowTrans package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowTrans/inst/doc/flowTrans.R Package: flowType Version: 2.20.1 Depends: R (>= 2.10), Rcpp (>= 0.10.4), BH (>= 1.51.0-3) Imports: Biobase, graphics, grDevices, methods, flowCore, flowMeans, sfsmisc, rrcov, flowClust, flowMerge, stats LinkingTo: Rcpp, BH Suggests: xtable License: Artistic-2.0 Archs: i386, x64 MD5sum: 49e8b8b49790cb4941b43a831022fc89 NeedsCompilation: yes Title: Phenotyping Flow Cytometry Assays Description: Phenotyping Flow Cytometry Assays using multidimentional expansion of single dimentional partitions. biocViews: ImmunoOncology, FlowCytometry Author: Nima Aghaeepour, Kieran O'Neill, Adrin Jalali Maintainer: Nima Aghaeepour git_url: https://git.bioconductor.org/packages/flowType git_branch: RELEASE_3_8 git_last_commit: ffccd19 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowType_2.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowType_2.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowType_2.20.1.tgz vignettes: vignettes/flowType/inst/doc/flowType.pdf vignetteTitles: flowType package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowType/inst/doc/flowType.R importsMe: RchyOptimyx Package: flowUtils Version: 1.46.1 Depends: R (>= 2.2.0) Imports: Biobase, graph, methods, stats, utils, corpcor, RUnit, XML, flowCore (>= 1.32.0) Suggests: gatingMLData License: Artistic-2.0 MD5sum: 747407cfc4ad8f0e460eb32054488c33 NeedsCompilation: no Title: Utilities for flow cytometry Description: Provides utilities for flow cytometry data. biocViews: ImmunoOncology, Infrastructure, FlowCytometry, CellBasedAssays, DecisionTree Author: J. Spidlen., N. Gopalakrishnan, F. Hahne, B. Ellis, R. Gentleman, M. Dalphin, N. Le Meur, B. Purcell, W. Jiang Maintainer: Josef Spidlen URL: https://github.com/jspidlen/flowUtils BugReports: https://github.com/jspidlen/flowUtils/issues git_url: https://git.bioconductor.org/packages/flowUtils git_branch: RELEASE_3_8 git_last_commit: f4279da git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowUtils_1.46.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowUtils_1.46.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowUtils_1.46.1.tgz vignettes: vignettes/flowUtils/inst/doc/HowTo-flowUtils.pdf vignetteTitles: Gating-ML support in R hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowUtils/inst/doc/HowTo-flowUtils.R importsMe: CytoML, FlowSOM suggestsMe: GateFinder Package: flowViz Version: 1.46.1 Depends: R (>= 2.7.0), flowCore(>= 1.41.9), lattice Imports: stats4, Biobase, flowCore, graphics, grDevices, grid, KernSmooth, lattice, latticeExtra, MASS, methods, RColorBrewer, stats, utils, hexbin,IDPmisc Suggests: colorspace, flowStats,knitr License: Artistic-2.0 MD5sum: 06b341a37ed1e786610a96c03cd4093d NeedsCompilation: no Title: Visualization for flow cytometry Description: Provides visualization tools for flow cytometry data. biocViews: ImmunoOncology, Infrastructure, FlowCytometry, CellBasedAssays, Visualization Author: B. Ellis, R. Gentleman, F. Hahne, N. Le Meur, D. Sarkar, M. Jiang Maintainer: Mike Jiang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowViz git_branch: RELEASE_3_8 git_last_commit: ae31755 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowViz_1.46.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowViz_1.46.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowViz_1.46.1.tgz vignettes: vignettes/flowViz/inst/doc/filters.html vignetteTitles: Visualizing Gates with Flow Cytometry Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowViz/inst/doc/filters.R dependsOnMe: flowFP, flowVS, plateCore importsMe: flowClust, flowFit, flowStats, flowTrans, flowWorkspace suggestsMe: flowBeads, flowClean, flowCore, flowTime, ggcyto Package: flowVS Version: 1.14.1 Depends: R (>= 3.2), methods, flowCore, flowViz, flowStats Suggests: knitr, vsn, License: Artistic-2.0 MD5sum: a1f53e1a4431e5172e5ca33be1584e08 NeedsCompilation: no Title: Variance stabilization in flow cytometry (and microarrays) Description: Per-channel variance stabilization from a collection of flow cytometry samples by Bertlett test for homogeneity of variances. The approach is applicable to microarrays data as well. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays, Microarray Author: Ariful Azad Maintainer: Ariful Azad VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowVS git_branch: RELEASE_3_8 git_last_commit: 8527e3b git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowVS_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowVS_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowVS_1.14.1.tgz vignettes: vignettes/flowVS/inst/doc/flowVS.pdf vignetteTitles: flowVS: Cell population matching and meta-clustering in Flow Cytometry hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/flowVS/inst/doc/flowVS.R Package: flowWorkspace Version: 3.30.2 Depends: R (>= 2.16.0),flowCore(>= 1.45.14),ncdfFlow(>= 2.25.4) Imports: Biobase, BiocGenerics, graph, graphics, grDevices, lattice, methods, stats, stats4, utils, RBGL, XML, tools, gridExtra, Rgraphviz, data.table, dplyr, latticeExtra, Rcpp, RColorBrewer, stringr, scales, flowViz, matrixStats LinkingTo: Rcpp, BH(>= 1.62.0-1), RProtoBufLib(>= 1.3.7), cytolib(>= 1.3.2) Suggests: testthat, flowWorkspaceData, knitr, ggcyto, parallel License: Artistic-2.0 Archs: i386, x64 MD5sum: ecb8071bcc22758099390af1e6dc5026 NeedsCompilation: yes Title: Infrastructure for representing and interacting with gated and ungated cytometry data sets. Description: This package is designed to facilitate comparison of automated gating methods against manual gating done in flowJo. This package allows you to import basic flowJo workspaces into BioConductor and replicate the gating from flowJo using the flowCore functionality. Gating hierarchies, groups of samples, compensation, and transformation are performed so that the output matches the flowJo analysis. biocViews: ImmunoOncology, FlowCytometry, DataImport, Preprocessing, DataRepresentation Author: Greg Finak, Mike Jiang Maintainer: Greg Finak ,Mike Jiang SystemRequirements: xml2, GNU make, C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/flowWorkspace git_branch: RELEASE_3_8 git_last_commit: eac7b2d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/flowWorkspace_3.30.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/flowWorkspace_3.30.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/flowWorkspace_3.30.2.tgz vignettes: vignettes/flowWorkspace/inst/doc/flowWorkspace-Introduction.html, vignettes/flowWorkspace/inst/doc/HowToMergeGatingSet.html, vignettes/flowWorkspace/inst/doc/plotGate.html vignetteTitles: flowWorkspace Introduction: A Package to store and maninpulate gated flow data, How to merge GatingSets, How to plot gated data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: FALSE Rfiles: vignettes/flowWorkspace/inst/doc/flowWorkspace-Introduction.R, vignettes/flowWorkspace/inst/doc/HowToMergeGatingSet.R, vignettes/flowWorkspace/inst/doc/plotGate.R dependsOnMe: flowStats, ggcyto, openCyto importsMe: CytoML, flowDensity, ImmuneSpaceR suggestsMe: COMPASS, flowClust, flowCore Package: fmcsR Version: 1.24.0 Depends: R (>= 2.10.0), ChemmineR, methods Imports: RUnit, methods, ChemmineR, BiocGenerics, parallel Suggests: BiocStyle, knitr, knitcitations, knitrBootstrap License: Artistic-2.0 Archs: i386, x64 MD5sum: 62865bc0fa2c4ac4a6f437220ff05e8e NeedsCompilation: yes Title: Mismatch Tolerant Maximum Common Substructure Searching Description: The fmcsR package introduces an efficient maximum common substructure (MCS) algorithms combined with a novel matching strategy that allows for atom and/or bond mismatches in the substructures shared among two small molecules. The resulting flexible MCSs (FMCSs) are often larger than strict MCSs, resulting in the identification of more common features in their source structures, as well as a higher sensitivity in finding compounds with weak structural similarities. The fmcsR package provides several utilities to use the FMCS algorithm for pairwise compound comparisons, structure similarity searching and clustering. biocViews: Cheminformatics, BiomedicalInformatics, Pharmacogenetics, Pharmacogenomics, MicrotitrePlateAssay, CellBasedAssays, Visualization, Infrastructure, DataImport, Clustering, Proteomics, Metabolomics Author: Yan Wang, Tyler Backman, Kevin Horan, Thomas Girke Maintainer: Thomas Girke URL: https://github.com/girke-lab/fmcsR VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/fmcsR git_branch: RELEASE_3_8 git_last_commit: 0760b5f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/fmcsR_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/fmcsR_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/fmcsR_1.24.0.tgz vignettes: vignettes/fmcsR/inst/doc/fmcsR.html vignetteTitles: fmcsR hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/fmcsR/inst/doc/fmcsR.R importsMe: Rcpi suggestsMe: ChemmineR Package: focalCall Version: 1.16.0 Depends: R(>= 2.10.0), CGHcall Suggests: RUnit, BiocGenerics License: GPL-2 MD5sum: b19052a468311959ee34805929344404 NeedsCompilation: no Title: Detection of focal aberrations in DNA copy number data Description: Detection of genomic focal aberrations in high-resolution DNA copy number data biocViews: Microarray,Preprocessing,Visualization,Sequencing Author: Oscar Krijgsman Maintainer: Oscar Krijgsman URL: https://github.com/OscarKrijgsman/focalCall git_url: https://git.bioconductor.org/packages/focalCall git_branch: RELEASE_3_8 git_last_commit: d874a4c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/focalCall_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/focalCall_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/focalCall_1.16.0.tgz vignettes: vignettes/focalCall/inst/doc/focalCall.pdf vignetteTitles: focalCall hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/focalCall/inst/doc/focalCall.R Package: FoldGO Version: 1.0.2 Depends: R (>= 3.5) Imports: topGO (>= 2.30.1), ggplot2 (>= 2.2.1), tidyr (>= 0.8.0), stats, methods Suggests: knitr, rmarkdown, devtools, kableExtra License: GPL-3 MD5sum: 4be7f219652bc28ee4424f25d00461b8 NeedsCompilation: no Title: Package for Fold-specific GO Terms Recognition Description: FoldGO is a package designed to annotate gene sets derived from expression experiments and identify fold-change-specific GO terms. biocViews: DifferentialExpression, GeneExpression, GO, Software Author: Daniil Wiebe [aut, cre] Maintainer: Daniil Wiebe VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FoldGO git_branch: RELEASE_3_8 git_last_commit: bed1e14 git_last_commit_date: 2019-04-12 Date/Publication: 2019-04-12 source.ver: src/contrib/FoldGO_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/FoldGO_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FoldGO_1.0.2.tgz vignettes: vignettes/FoldGO/inst/doc/vignette.html vignetteTitles: FoldGO: a tool for fold-change-specific functional enrichment analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FoldGO/inst/doc/vignette.R Package: FourCSeq Version: 1.16.0 Depends: R (>= 3.0), GenomicRanges, ggplot2, DESeq2 (>= 1.9.11), splines, methods, LSD Imports: DESeq2, Biobase, Biostrings, GenomicRanges, SummarizedExperiment, Rsamtools, ggbio, reshape2, rtracklayer, fda, GenomicAlignments, gtools, Matrix Suggests: BiocStyle, knitr, TxDb.Dmelanogaster.UCSC.dm3.ensGene License: GPL (>= 3) MD5sum: 53c2a29adaf6ec73c43ccb06f633a330 NeedsCompilation: no Title: Package analyse 4C sequencing data Description: FourCSeq is an R package dedicated to the analysis of (multiplexed) 4C sequencing data. The package provides a pipeline to detect specific interactions between DNA elements and identify differential interactions between conditions. The statistical analysis in R starts with individual bam files for each sample as inputs. To obtain these files, the package contains a python script (extdata/python/demultiplex.py) to demultiplex libraries and trim off primer sequences. With a standard alignment software the required bam files can be then be generated. biocViews: Software, Preprocessing, Sequencing Author: Felix A. Klein, EMBL Heidelberg Maintainer: Felix A. Klein VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/FourCSeq git_branch: RELEASE_3_8 git_last_commit: 2484619 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FourCSeq_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FourCSeq_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FourCSeq_1.16.0.tgz vignettes: vignettes/FourCSeq/inst/doc/FourCSeq.pdf vignetteTitles: FourCSeq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FourCSeq/inst/doc/FourCSeq.R Package: FRGEpistasis Version: 1.18.0 Depends: R (>= 2.15), MASS, fda, methods, stats Imports: utils License: GPL-2 MD5sum: 69714b75285540f4339872f28b55ca84 NeedsCompilation: no Title: Epistasis Analysis for Quantitative Traits by Functional Regression Model Description: A Tool for Epistasis Analysis Based on Functional Regression Model biocViews: Genetics, NetworkInference, GeneticVariability, Software Author: Futao Zhang Maintainer: Futao Zhang git_url: https://git.bioconductor.org/packages/FRGEpistasis git_branch: RELEASE_3_8 git_last_commit: c71d0ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FRGEpistasis_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FRGEpistasis_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FRGEpistasis_1.18.0.tgz vignettes: vignettes/FRGEpistasis/inst/doc/FRGEpistasis.pdf vignetteTitles: FRGEpistasis: A Tool for Epistasis Analysis Based on Functional Regression Model hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FRGEpistasis/inst/doc/FRGEpistasis.R Package: frma Version: 1.34.0 Depends: R (>= 2.10.0), Biobase (>= 2.6.0) Imports: Biobase, MASS, DBI, affy, methods, oligo, oligoClasses, preprocessCore, utils, BiocGenerics Suggests: hgu133afrmavecs, frmaExampleData License: GPL (>= 2) MD5sum: b37d6b5a88ba58da47c33d6d7f09b93a NeedsCompilation: no Title: Frozen RMA and Barcode Description: Preprocessing and analysis for single microarrays and microarray batches. biocViews: Software, Microarray, Preprocessing Author: Matthew N. McCall , Rafael A. Irizarry , with contributions from Terry Therneau Maintainer: Matthew N. McCall URL: http://bioconductor.org git_url: https://git.bioconductor.org/packages/frma git_branch: RELEASE_3_8 git_last_commit: 2d39fc6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/frma_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/frma_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/frma_1.34.0.tgz vignettes: vignettes/frma/inst/doc/frma.pdf vignetteTitles: frma: Preprocessing for single arrays and array batches hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/frma/inst/doc/frma.R importsMe: ChIPXpress suggestsMe: frmaTools Package: frmaTools Version: 1.34.0 Depends: R (>= 2.10.0), affy Imports: Biobase, DBI, methods, preprocessCore, stats, utils Suggests: oligo, pd.huex.1.0.st.v2, pd.hugene.1.0.st.v1, frma, affyPLM, hgu133aprobe, hgu133atagprobe, hgu133plus2probe, hgu133acdf, hgu133atagcdf, hgu133plus2cdf, hgu133afrmavecs, frmaExampleData License: GPL (>= 2) MD5sum: a62d9d619c2495c994c3ef00f8d44708 NeedsCompilation: no Title: Frozen RMA Tools Description: Tools for advanced use of the frma package. biocViews: Software, Microarray, Preprocessing Author: Matthew N. McCall , Rafael A. Irizarry Maintainer: Matthew N. McCall URL: http://bioconductor.org git_url: https://git.bioconductor.org/packages/frmaTools git_branch: RELEASE_3_8 git_last_commit: 8a899f5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/frmaTools_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/frmaTools_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/frmaTools_1.34.0.tgz vignettes: vignettes/frmaTools/inst/doc/frmaTools.pdf vignetteTitles: frmaTools: Create packages containing the vectors used by frma. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/frmaTools/inst/doc/frmaTools.R Package: FunChIP Version: 1.8.0 Depends: R (>= 3.2), GenomicRanges Imports: shiny, fda, doParallel, GenomicAlignments, Rcpp, methods, foreach, parallel, GenomeInfoDb, Rsamtools, grDevices, graphics, stats, RColorBrewer LinkingTo: Rcpp License: Artistic-2.0 Archs: i386, x64 MD5sum: c8c104f2587cb6dad1645d758e3ef9f2 NeedsCompilation: yes Title: Clustering and Alignment of ChIP-Seq peaks based on their shapes Description: Preprocessing and smoothing of ChIP-Seq peaks and efficient implementation of the k-mean alignment algorithm to classify them. biocViews: StatisticalMethod, Clustering, ChIPSeq Author: Alice Parodi [aut, cre], Marco Morelli [aut, cre], Laura M. Sangalli [aut], Piercesare Secchi [aut], Simone Vantini [aut] Maintainer: Alice Parodi git_url: https://git.bioconductor.org/packages/FunChIP git_branch: RELEASE_3_8 git_last_commit: b48b714 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FunChIP_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FunChIP_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FunChIP_1.8.0.tgz vignettes: vignettes/FunChIP/inst/doc/FunChIP.pdf vignetteTitles: An introduction to FunChIP hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FunChIP/inst/doc/FunChIP.R Package: FunciSNP Version: 1.26.0 Depends: R (>= 2.14.0), ggplot2, TxDb.Hsapiens.UCSC.hg19.knownGene, FunciSNP.data Imports: methods, BiocGenerics, Biobase, S4Vectors, IRanges, GenomicRanges, Rsamtools (>= 1.6.1), rtracklayer (>= 1.14.1), ChIPpeakAnno (>= 2.2.0), VariantAnnotation, plyr, snpStats, ggplot2 (>= 0.9.0), reshape (>= 0.8.4), scales Suggests: org.Hs.eg.db Enhances: parallel License: GPL-3 MD5sum: e55399c304732cc26e706341e659018c NeedsCompilation: no Title: Integrating Functional Non-coding Datasets with Genetic Association Studies to Identify Candidate Regulatory SNPs Description: FunciSNP integrates information from GWAS, 1000genomes and chromatin feature to identify functional SNP in coding or non-coding regions. biocViews: Infrastructure, DataRepresentation, DataImport, SequenceMatching, Annotation Author: Simon G. Coetzee and Houtan Noushmehr, PhD Maintainer: Simon G. Coetzee URL: http://coetzeeseq.usc.edu/publication/Coetzee_SG_et_al_2012/ git_url: https://git.bioconductor.org/packages/FunciSNP git_branch: RELEASE_3_8 git_last_commit: 9589bf2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/FunciSNP_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/FunciSNP_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/FunciSNP_1.26.0.tgz vignettes: vignettes/FunciSNP/inst/doc/FunciSNP_vignette.pdf vignetteTitles: FunciSNP Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/FunciSNP/inst/doc/FunciSNP_vignette.R Package: funtooNorm Version: 1.6.0 Depends: R(>= 3.4) Imports: pls, matrixStats, minfi, methods, IlluminaHumanMethylation450kmanifest, IlluminaHumanMethylation450kanno.ilmn12.hg19, GenomeInfoDb, grDevices, graphics, stats Suggests: prettydoc, minfiData, knitr, rmarkdown License: GPL-3 MD5sum: c580cc3077ad762b790f4ccbc1ca9de8 NeedsCompilation: no Title: Normalization Procedure for Infinium HumanMethylation450 BeadChip Kit Description: Provides a function to normalize Illumina Infinium Human Methylation 450 BeadChip (Illumina 450K), correcting for tissue and/or cell type. biocViews: DNAMethylation, Preprocessing, Normalization Author: Celia Greenwood ,Stepan Grinek , Maxime Turgeon , Kathleen Klein Maintainer: Kathleen Klein VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/funtooNorm git_branch: RELEASE_3_8 git_last_commit: 9561443 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/funtooNorm_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/funtooNorm_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/funtooNorm_1.6.0.tgz vignettes: vignettes/funtooNorm/inst/doc/funtooNorm.pdf vignetteTitles: Normalizing Illumina Infinium Human Methylation 450k for multiple cell types with funtooNorm hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/funtooNorm/inst/doc/funtooNorm.R Package: GA4GHclient Version: 1.6.0 Depends: S4Vectors Imports: BiocGenerics, Biostrings, dplyr, GenomeInfoDb, GenomicRanges, httr, IRanges, jsonlite, methods, VariantAnnotation Suggests: AnnotationDbi, BiocStyle, DT, knitr, org.Hs.eg.db, rmarkdown, testthat, TxDb.Hsapiens.UCSC.hg19.knownGene License: GPL (>= 2) MD5sum: f69a308636d5abd8d6c3e071e0182437 NeedsCompilation: no Title: A Bioconductor package for accessing GA4GH API data servers Description: GA4GHclient provides an easy way to access public data servers through Global Alliance for Genomics and Health (GA4GH) genomics API. It provides low-level access to GA4GH API and translates response data into Bioconductor-based class objects. biocViews: DataRepresentation, ThirdPartyClient Author: Welliton Souza [aut, cre], Benilton Carvalho [ctb], Cristiane Rocha [ctb] Maintainer: Welliton Souza URL: https://github.com/labbcb/GA4GHclient VignetteBuilder: knitr BugReports: https://github.com/labbcb/GA4GHclient/issues git_url: https://git.bioconductor.org/packages/GA4GHclient git_branch: RELEASE_3_8 git_last_commit: a5da313 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GA4GHclient_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GA4GHclient_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GA4GHclient_1.6.0.tgz vignettes: vignettes/GA4GHclient/inst/doc/GA4GHclient.html vignetteTitles: GA4GHclient hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GA4GHclient/inst/doc/GA4GHclient.R dependsOnMe: GA4GHshiny Package: GA4GHshiny Version: 1.4.0 Depends: GA4GHclient Imports: AnnotationDbi, BiocGenerics, dplyr, DT, GenomeInfoDb, openxlsx, GenomicFeatures, methods, purrr, S4Vectors, shiny, shinyjs, tidyr, shinythemes Suggests: BiocStyle, org.Hs.eg.db, knitr, rmarkdown, testthat, TxDb.Hsapiens.UCSC.hg19.knownGene License: GPL-3 MD5sum: 5798bf389bc3818bb6508788039afce7 NeedsCompilation: no Title: Shiny application for interacting with GA4GH-based data servers Description: GA4GHshiny package provides an easy way to interact with data servers based on Global Alliance for Genomics and Health (GA4GH) genomics API through a Shiny application. It also integrates with Beacon Network. biocViews: GUI Author: Welliton Souza [aut, cre], Benilton Carvalho [ctb], Cristiane Rocha [ctb], Elizabeth Borgognoni [ctb] Maintainer: Welliton Souza URL: https://github.com/labbcb/GA4GHshiny VignetteBuilder: knitr BugReports: https://github.com/labbcb/GA4GHshiny/issues git_url: https://git.bioconductor.org/packages/GA4GHshiny git_branch: RELEASE_3_8 git_last_commit: d58def1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GA4GHshiny_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GA4GHshiny_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GA4GHshiny_1.4.0.tgz vignettes: vignettes/GA4GHshiny/inst/doc/GA4GHshiny.html vignetteTitles: GA4GHshiny hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GA4GHshiny/inst/doc/GA4GHshiny.R Package: gaga Version: 2.28.1 Depends: R (>= 2.8.0), Biobase, coda, EBarrays, mgcv Enhances: parallel License: GPL (>= 2) Archs: i386, x64 MD5sum: 7672c2b737019a0075a8989f3973b627 NeedsCompilation: yes Title: GaGa hierarchical model for high-throughput data analysis Description: Implements the GaGa model for high-throughput data analysis, including differential expression analysis, supervised gene clustering and classification. Additionally, it performs sequential sample size calculations using the GaGa and LNNGV models (the latter from EBarrays package). biocViews: ImmunoOncology, OneChannel, MassSpectrometry, MultipleComparison, DifferentialExpression, Classification Author: David Rossell . Maintainer: David Rossell git_url: https://git.bioconductor.org/packages/gaga git_branch: RELEASE_3_8 git_last_commit: 884f515 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/gaga_2.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gaga_2.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gaga_2.28.1.tgz vignettes: vignettes/gaga/inst/doc/gagamanual.pdf vignetteTitles: Manual for the gaga library hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gaga/inst/doc/gagamanual.R importsMe: casper Package: gage Version: 2.32.1 Depends: R (>= 2.10) Imports: graph, KEGGREST, AnnotationDbi Suggests: pathview, gageData, GO.db, org.Hs.eg.db, hgu133a.db, GSEABase, Rsamtools, GenomicAlignments, TxDb.Hsapiens.UCSC.hg19.knownGene, DESeq, DESeq2, edgeR, limma License: GPL (>=2.0) MD5sum: a2188515cb5331823906f0e26f06e939 NeedsCompilation: no Title: Generally Applicable Gene-set Enrichment for Pathway Analysis Description: GAGE is a published method for gene set (enrichment or GSEA) or pathway analysis. GAGE is generally applicable independent of microarray or RNA-Seq data attributes including sample sizes, experimental designs, assay platforms, and other types of heterogeneity, and consistently achieves superior performance over other frequently used methods. In gage package, we provide functions for basic GAGE analysis, result processing and presentation. We have also built pipeline routines for of multiple GAGE analyses in a batch, comparison between parallel analyses, and combined analysis of heterogeneous data from different sources/studies. In addition, we provide demo microarray data and commonly used gene set data based on KEGG pathways and GO terms. These funtions and data are also useful for gene set analysis using other methods. biocViews: ImmunoOncology, Pathways, GO, DifferentialExpression, Microarray, OneChannel, TwoChannel, RNASeq, Genetics, MultipleComparison, GeneSetEnrichment, GeneExpression, SystemsBiology, Sequencing Author: Weijun Luo Maintainer: Weijun Luo URL: http://www.biomedcentral.com/1471-2105/10/161 git_url: https://git.bioconductor.org/packages/gage git_branch: RELEASE_3_8 git_last_commit: 540898f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/gage_2.32.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gage_2.32.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gage_2.32.1.tgz vignettes: vignettes/gage/inst/doc/dataPrep.pdf, vignettes/gage/inst/doc/gage.pdf, vignettes/gage/inst/doc/RNA-seqWorkflow.pdf vignetteTitles: Gene set and data preparation, Generally Applicable Gene-set/Pathway Analysis, RNA-Seq Data Pathway and Gene-set Analysis Workflows hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gage/inst/doc/dataPrep.R, vignettes/gage/inst/doc/gage.R, vignettes/gage/inst/doc/RNA-seqWorkflow.R dependsOnMe: EGSEA importsMe: anamiR suggestsMe: FGNet, pathview Package: gaggle Version: 1.50.0 Depends: R (>= 2.3.0), rJava (>= 0.4), graph (>= 1.10.2), RUnit (>= 0.4.17) License: GPL version 2 or newer MD5sum: 0941a1c5621659082664ba61b3e33a61 NeedsCompilation: no Title: Broadcast data between R and Gaggle Description: This package contains functions enabling data exchange between R and Gaggle enabled bioinformatics software, including Cytoscape, Firegoose and Gaggle Genome Browser. biocViews: ThirdPartyClient, Visualization, Annotation, GraphAndNetwork, DataImport Author: Paul Shannon Maintainer: Christopher Bare URL: http://gaggle.systemsbiology.net/docs/geese/r/ git_url: https://git.bioconductor.org/packages/gaggle git_branch: RELEASE_3_8 git_last_commit: af6a1fe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gaggle_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gaggle_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gaggle_1.50.0.tgz vignettes: vignettes/gaggle/inst/doc/gaggle.pdf vignetteTitles: Gaggle Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gaggle/inst/doc/gaggle.R Package: gaia Version: 2.26.0 Depends: R (>= 2.10) License: GPL-2 MD5sum: e4d353ce4c66796d457f0a54189ed840 NeedsCompilation: no Title: GAIA: An R package for genomic analysis of significant chromosomal aberrations. Description: This package allows to assess the statistical significance of chromosomal aberrations. biocViews: aCGH, CopyNumberVariation Author: Sandro Morganella et al. Maintainer: S. Morganella git_url: https://git.bioconductor.org/packages/gaia git_branch: RELEASE_3_8 git_last_commit: da890c8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gaia_2.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gaia_2.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gaia_2.26.0.tgz vignettes: vignettes/gaia/inst/doc/gaia.pdf vignetteTitles: gaia hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gaia/inst/doc/gaia.R Package: GAprediction Version: 1.8.1 Depends: R (>= 3.3) Imports: glmnet, stats, utils, Matrix Suggests: knitr, rmarkdown License: GPL (>=2) MD5sum: 181fe65adf80c170982cfe2c8b21e273 NeedsCompilation: no Title: Prediction of gestational age with Illumina HumanMethylation450 data Description: [GAprediction] predicts gestational age using Illumina HumanMethylation450 CpG data. biocViews: ImmunoOncology, DNAMethylation, Epigenetics, Regression, BiomedicalInformatics Author: Jon Bohlin Maintainer: Jon Bohlin VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GAprediction git_branch: RELEASE_3_8 git_last_commit: 63d941f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GAprediction_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GAprediction_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GAprediction_1.8.1.tgz vignettes: vignettes/GAprediction/inst/doc/GAprediction.html vignetteTitles: GAprediction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GAprediction/inst/doc/GAprediction.R Package: garfield Version: 1.10.0 Suggests: knitr License: GPL-3 Archs: i386, x64 MD5sum: a32182358d9332b323393b06db079a20 NeedsCompilation: yes Title: GWAS Analysis of Regulatory or Functional Information Enrichment with LD correction Description: GARFIELD is a non-parametric functional enrichment analysis approach described in the paper GARFIELD: GWAS analysis of regulatory or functional information enrichment with LD correction. Briefly, it is a method that leverages GWAS findings with regulatory or functional annotations (primarily from ENCODE and Roadmap epigenomics data) to find features relevant to a phenotype of interest. It performs greedy pruning of GWAS SNPs (LD r2 > 0.1) and then annotates them based on functional information overlap. Next, it quantifies Fold Enrichment (FE) at various GWAS significance cutoffs and assesses them by permutation testing, while matching for minor allele frequency, distance to nearest transcription start site and number of LD proxies (r2 > 0.8). biocViews: Software, StatisticalMethod, Annotation, FunctionalPrediction, GenomeAnnotation Author: Sandro Morganella Maintainer: Valentina Iotchkova VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/garfield git_branch: RELEASE_3_8 git_last_commit: dd3cffe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/garfield_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/garfield_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/garfield_1.10.0.tgz vignettes: vignettes/garfield/inst/doc/vignette.pdf vignetteTitles: garfield Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: GARS Version: 1.2.0 Depends: R (>= 3.5), ggplot2, cluster Imports: DaMiRseq, MLSeq, stats, methods, SummarizedExperiment Suggests: BiocStyle, knitr, testthat License: GPL (>= 2) MD5sum: 682be28045f9dab362947bae60f43b76 NeedsCompilation: no Title: GARS: Genetic Algorithm for the identification of Robust Subsets of variables in high-dimensional and challenging datasets Description: Feature selection aims to identify and remove redundant, irrelevant and noisy variables from high-dimensional datasets. Selecting informative features affects the subsequent classification and regression analyses by improving their overall performances. Several methods have been proposed to perform feature selection: most of them relies on univariate statistics, correlation, entropy measurements or the usage of backward/forward regressions. Herein, we propose an efficient, robust and fast method that adopts stochastic optimization approaches for high-dimensional. GARS is an innovative implementation of a genetic algorithm that selects robust features in high-dimensional and challenging datasets. biocViews: Classification, FeatureExtraction, Clustering Author: Mattia Chiesa , Luca Piacentini Maintainer: Mattia Chiesa VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GARS git_branch: RELEASE_3_8 git_last_commit: 5f4198e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GARS_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GARS_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GARS_1.2.0.tgz vignettes: vignettes/GARS/inst/doc/GARS.pdf vignetteTitles: Titolo hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GARS/inst/doc/GARS.R Package: GateFinder Version: 1.2.1 Imports: splancs, mvoutlier, methods, stats, diptest, flowCore, flowFP, Suggests: RUnit, flowUtils, BiocGenerics License: Artistic-2.0 MD5sum: 68be7f15262768a1c57881a0f7c5eebf NeedsCompilation: no Title: Projection-based Gating Strategy Optimization for Flow and Mass Cytometry Description: Given a vector of cluster memberships for a cell population, identifies a sequence of gates (polygon filters on 2D scatter plots) for isolation of that cell type. biocViews: ImmunoOncology, FlowCytometry, CellBiology, Clustering Author: Nima Aghaeepour , Erin F. Simonds Maintainer: Nima Aghaeepour git_url: https://git.bioconductor.org/packages/GateFinder git_branch: RELEASE_3_8 git_last_commit: 23913cc git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GateFinder_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GateFinder_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GateFinder_1.2.1.tgz vignettes: vignettes/GateFinder/inst/doc/GateFinder.pdf vignetteTitles: GateFinder hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GateFinder/inst/doc/GateFinder.R Package: gcapc Version: 1.6.0 Depends: R (>= 3.4) Imports: BiocGenerics, GenomeInfoDb, S4Vectors, IRanges, Biostrings, BSgenome, GenomicRanges, Rsamtools, GenomicAlignments, matrixStats, MASS, splines, grDevices, graphics, stats, methods Suggests: BiocStyle, knitr, rmarkdown, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10 License: GPL-3 MD5sum: ac19d863951e0b659a1d4605aafeb1c6 NeedsCompilation: no Title: GC Aware Peak Caller Description: Peak calling for ChIP-seq data with consideration of potential GC bias in sequencing reads. GC bias is first estimated with generalized linear mixture models using effective GC strategy, then applied into peak significance estimation. biocViews: Sequencing, ChIPSeq, BatchEffect, PeakDetection Author: Mingxiang Teng and Rafael A. Irizarry Maintainer: Mingxiang Teng URL: https://github.com/tengmx/gcapc VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gcapc git_branch: RELEASE_3_8 git_last_commit: 7935a3f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gcapc_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gcapc_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gcapc_1.6.0.tgz vignettes: vignettes/gcapc/inst/doc/gcapc.html vignetteTitles: The gcapc user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gcapc/inst/doc/gcapc.R Package: gcatest Version: 1.12.0 Depends: R (>= 3.2) Imports: lfa Suggests: knitr, ggplot2 License: GPL-3 Archs: i386, x64 MD5sum: 4fdd3965d7db773c137fbd281f34d6e8 NeedsCompilation: yes Title: Genotype Conditional Association TEST Description: GCAT is an association test for genome wide association studies that controls for population structure under a general class of trait. models. biocViews: SNP, DimensionReduction, PrincipalComponent, GenomeWideAssociation Author: Wei Hao, Minsun Song, John D. Storey Maintainer: Wei Hao , John D. Storey URL: https://github.com/StoreyLab/gcatest VignetteBuilder: knitr BugReports: https://github.com/StoreyLab/gcatest/issues git_url: https://git.bioconductor.org/packages/gcatest git_branch: RELEASE_3_8 git_last_commit: c501596 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gcatest_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gcatest_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gcatest_1.12.0.tgz vignettes: vignettes/gcatest/inst/doc/gcatest.pdf vignetteTitles: gcat Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gcatest/inst/doc/gcatest.R Package: gCMAP Version: 1.26.0 Depends: GSEABase, limma (>= 3.20.0) Imports: Biobase, methods, GSEAlm, Category, Matrix (>= 1.0.9), parallel, annotate, genefilter, AnnotationDbi, DESeq, grDevices, graphics, stats, utils, bigmemory, bigmemoryExtras (>= 1.1.2) Suggests: BiocGenerics, KEGG.db, reactome.db, RUnit, GO.db, mgsa License: Artistic-2.0 OS_type: unix MD5sum: 3753b67183a2d0c21be53cf900eda12a NeedsCompilation: no Title: Tools for Connectivity Map-like analyses Description: The gCMAP package provides a toolkit for comparing differential gene expression profiles through gene set enrichment analysis. Starting from normalized microarray or RNA-seq gene expression values (stored in lists of ExpressionSet and CountDataSet objects) the package performs differential expression analysis using the limma or DESeq packages. Supplying a simple list of gene identifiers, global differential expression profiles or data from complete experiments as input, users can use a unified set of several well-known gene set enrichment analysis methods to retrieve experiments with similar changes in gene expression. To take into account the directionality of gene expression changes, gCMAPQuery introduces the SignedGeneSet class, directly extending GeneSet from the GSEABase package. To increase performance of large queries, multiple gene sets are stored as sparse incidence matrices within CMAPCollection eSets. gCMAP offers implementations of 1. Fisher's exact test (Fisher, J R Stat Soc, 1922) 2. The "connectivity map" method (Lamb et al, Science, 2006) 3. Parametric and non-parametric t-statistic summaries (Jiang & Gentleman, Bioinformatics, 2007) and 4. Wilcoxon / Mann-Whitney rank sum statistics (Wilcoxon, Biometrics Bulletin, 1945) as well as wrappers for the 5. camera (Wu & Smyth, Nucleic Acid Res, 2012) 6. mroast and romer (Wu et al, Bioinformatics, 2010) functions from the limma package and 7. wraps the gsea method from the mgsa package (Bauer et al, NAR, 2010). All methods return CMAPResult objects, an S4 class inheriting from AnnotatedDataFrame, containing enrichment statistics as well as annotation data and providing simple high-level summary plots. biocViews: Microarray, Software, Pathways, Annotation Author: Thomas Sandmann , Richard Bourgon and Sarah Kummerfeld Maintainer: Thomas Sandmann git_url: https://git.bioconductor.org/packages/gCMAP git_branch: RELEASE_3_8 git_last_commit: 0913280 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gCMAP_1.26.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gCMAP_1.26.0.tgz vignettes: vignettes/gCMAP/inst/doc/diffExprAnalysis.pdf, vignettes/gCMAP/inst/doc/gCMAP.pdf vignetteTitles: Creating reference datasets, gCMAP classes and methods hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gCMAP/inst/doc/diffExprAnalysis.R, vignettes/gCMAP/inst/doc/gCMAP.R dependsOnMe: gCMAPWeb Package: gCMAPWeb Version: 1.22.0 Depends: Biobase, gCMAP (>= 1.3.0), methods, R (>= 3.4), Rook Imports: brew, BiocGenerics, annotate, AnnotationDbi, graphics, grDevices, GSEABase, hwriter, parallel, stats, utils, yaml Suggests: affy, ArrayExpress, hgfocus.db, hgu133a.db, mgug4104a.db, org.Hs.eg.db, org.Mm.eg.db, RUnit Enhances: bigmemory, bigmemoryExtras License: Artistic-2.0 OS_type: unix MD5sum: 2d2b869ba468ba3932dc14580d96f88f NeedsCompilation: no Title: A web interface for gene-set enrichment analyses Description: The gCMAPWeb R package provides a graphical user interface for the gCMAP package. gCMAPWeb uses the Rook package and can be used either on a local machine, leveraging R's internal web server, or run on a dedicated rApache web server installation. gCMAPWeb allows users to search their own data sources and instructions to generate reference datasets from public repositories are included with the package. The package supports three common types of analyses, specifically queries with 1. one or two sets of query gene identifiers, whose members are expected to show changes in gene expression in a consistent direction. For example, an up-regulated gene set might contain genes activated by a transcription factor, a down-regulated geneset targets repressed by the same factor. 2. a single set of query gene identifiers, whose members are expected to show divergent differential expression (non-directional query). For example, members of a particular signaling pathway, some of which may be up- some down-regulated in response to a stimulus. 3. a query with the complete results of a differential expression profiling experiment. For example, gene identifiers and z-scores from a previous perturbation experiment. gCMAPWeb accepts three types of identifiers: EntreIds, gene Symbols and microarray probe ids and can be configured to work with any species supported by Bioconductor. For each query submission, significantly similar reference datasets will be identified and reported in graphical and tabular form. biocViews: GUI, GeneSetEnrichment, Visualization, GeneExpression, Transcription, Microarray, DifferentialExpression Author: Thomas Sandmann Maintainer: Thomas Sandmann git_url: https://git.bioconductor.org/packages/gCMAPWeb git_branch: RELEASE_3_8 git_last_commit: 2b0148b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gCMAPWeb_1.22.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gCMAPWeb_1.22.0.tgz vignettes: vignettes/gCMAPWeb/inst/doc/gCMAPWeb.pdf, vignettes/gCMAPWeb/inst/doc/referenceDatasets.pdf vignetteTitles: gCMAPWeb configuration, Recreating the Broad Connectivity Map v1 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gCMAPWeb/inst/doc/gCMAPWeb.R, vignettes/gCMAPWeb/inst/doc/referenceDatasets.R Package: gCrisprTools Version: 1.10.1 Depends: R (>= 3.3) Imports: Biobase, limma, RobustRankAggreg, ggplot2, PANTHER.db, rmarkdown, grDevices, graphics, stats, utils, parallel Suggests: edgeR, knitr, grid, AnnotationDbi, org.Mm.eg.db, org.Hs.eg.db, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: f135c06bdce869ccb792e504af360963 NeedsCompilation: no Title: Suite of Functions for Pooled Crispr Screen QC and Analysis Description: Set of tools for evaluating pooled high-throughput screening experiments, typically employing CRISPR/Cas9 or shRNA expression cassettes. Contains methods for interrogating library and cassette behavior within an experiment, identifying differentially abundant cassettes, aggregating signals to identify candidate targets for empirical validation, hypothesis testing, and comprehensive reporting. biocViews: ImmunoOncology, CRISPR, PooledScreens, ExperimentalDesign, BiomedicalInformatics, CellBiology, FunctionalGenomics, Pharmacogenomics, Pharmacogenetics, SystemsBiology, DifferentialExpression, GeneSetEnrichment, Genetics, MultipleComparison, Normalization, Preprocessing, QualityControl, RNASeq, Regression, Software, Visualization Author: Russell Bainer, Dariusz Ratman, Steve Lianoglou, Peter Haverty Maintainer: Peter Haverty VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gCrisprTools git_branch: RELEASE_3_8 git_last_commit: fe836ed git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/gCrisprTools_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gCrisprTools_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gCrisprTools_1.10.1.tgz vignettes: vignettes/gCrisprTools/inst/doc/Crispr_example_workflow.html, vignettes/gCrisprTools/inst/doc/gCrisprTools_Vignette.html vignetteTitles: Example_Workflow_gCrisprTools, gCrisprTools_Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gCrisprTools/inst/doc/Crispr_example_workflow.R, vignettes/gCrisprTools/inst/doc/gCrisprTools_Vignette.R Package: gcrma Version: 2.54.0 Depends: R (>= 2.6.0), affy (>= 1.23.2), graphics, methods, stats, utils Imports: Biobase, affy (>= 1.23.2), affyio (>= 1.13.3), XVector, Biostrings (>= 2.11.32), splines, BiocManager Suggests: affydata, tools, splines, hgu95av2cdf, hgu95av2probe License: LGPL Archs: i386, x64 MD5sum: 413897a1c3888e7ee57ee6c5f238934c NeedsCompilation: yes Title: Background Adjustment Using Sequence Information Description: Background adjustment using sequence information biocViews: Microarray, OneChannel, Preprocessing Author: Jean(ZHIJIN) Wu, Rafael Irizarry with contributions from James MacDonald Jeff Gentry Maintainer: Z. Wu git_url: https://git.bioconductor.org/packages/gcrma git_branch: RELEASE_3_8 git_last_commit: 9515fdb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gcrma_2.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gcrma_2.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gcrma_2.54.0.tgz vignettes: vignettes/gcrma/inst/doc/gcrma2.0.pdf vignetteTitles: gcrma1.2 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: affyILM, affyPLM, bgx, maskBAD, simpleaffy, webbioc importsMe: affycoretools, affylmGUI, simpleaffy suggestsMe: AffyExpress, ArrayTools, BiocCaseStudies, panp Package: GDCRNATools Version: 1.2.1 Depends: R (>= 3.5.0) Imports: shiny, jsonlite, rjson, XML, limma, edgeR, DESeq2, clusterProfiler, DOSE, org.Hs.eg.db, biomaRt, survival, survminer, pathview, ggplot2, gplots, DT, GenomicDataCommons, BiocParallel Suggests: knitr, testthat License: Artistic-2.0 MD5sum: 5e1632fd981aa03aa9714f1d847c64df NeedsCompilation: no Title: GDCRNATools: an R/Bioconductor package for integrative analysis of lncRNA, mRNA, and miRNA data in GDC Description: This is an easy-to-use package for downloading, organizing, and integrative analyzing RNA expression data in GDC with an emphasis on deciphering the lncRNA-mRNA related ceRNA regulatory network in cancer. Three databases of lncRNA-miRNA interactions including spongeScan, starBase, and miRcode, as well as three databases of mRNA-miRNA interactions including miRTarBase, starBase, and miRcode are incorporated into the package for ceRNAs network construction. limma, edgeR, and DESeq2 can be used to identify differentially expressed genes/miRNAs. Functional enrichment analyses including GO, KEGG, and DO can be performed based on the clusterProfiler and DO packages. Both univariate CoxPH and KM survival analyses of multiple genes can be implemented in the package. Besides some routine visualization functions such as volcano plot, bar plot, and KM plot, a few simply shiny apps are developed to facilitate visualization of results on a local webpage. biocViews: ImmunoOncology, GeneExpression, DifferentialExpression, GeneRegulation, GeneTarget, NetworkInference, Survival, Visualization, GeneSetEnrichment, NetworkEnrichment, Network, RNASeq, GO, KEGG Author: Ruidong Li, Han Qu, Shibo Wang, Julong Wei, Le Zhang, Renyuan Ma, Jianming Lu, Jianguo Zhu, Wei-De Zhong, Zhenyu Jia Maintainer: Ruidong Li , Han Qu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GDCRNATools git_branch: RELEASE_3_8 git_last_commit: 6d8e401 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GDCRNATools_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GDCRNATools_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GDCRNATools_1.2.1.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GDCRNATools/inst/doc/GDCRNATools.R Package: GDSArray Version: 1.2.0 Depends: R (>= 3.5), gdsfmt, methods, BiocGenerics, DelayedArray (>= 0.5.32) Imports: tools, S4Vectors (>= 0.17.34), SNPRelate, SeqArray Suggests: testthat, knitr, BiocStyle, BiocManager License: GPL-3 MD5sum: 6c3b4ae29009e0e1bf5c6cee249a25a5 NeedsCompilation: no Title: Representing GDS files as array-like objects Description: GDS files are widely used to represent genotyping or sequence data. The GDSArray package implements the `GDSArray` class to represent nodes in GDS files in a matrix-like representation that allows easy manipulation (e.g., subsetting, mathematical transformation) in _R_. The data remains on disk until needed, so that very large files can be processed. biocViews: Infrastructure, DataRepresentation, Sequencing, GenotypingArray Author: Qian Liu [aut, cre], Martin Morgan [aut], Hervé Pagès [aut] Maintainer: Qian Liu URL: https://github.com/Bioconductor/GDSArray VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/GDSArray/issues git_url: https://git.bioconductor.org/packages/GDSArray git_branch: RELEASE_3_8 git_last_commit: 0889e32 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GDSArray_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GDSArray_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GDSArray_1.2.0.tgz vignettes: vignettes/GDSArray/inst/doc/GDSArray.html vignetteTitles: GDSArray: Representing GDS files as array-like objects hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GDSArray/inst/doc/GDSArray.R Package: gdsfmt Version: 1.18.1 Depends: R (>= 2.15.0), methods Suggests: parallel, digest, crayon, RUnit, knitr, BiocGenerics License: LGPL-3 Archs: i386, x64 MD5sum: 7538626e88124c3fc733b67512f7179d NeedsCompilation: yes Title: R Interface to CoreArray Genomic Data Structure (GDS) Files Description: This package provides a high-level R interface to CoreArray Genomic Data Structure (GDS) data files, which are portable across platforms with hierarchical structure to store multiple scalable array-oriented data sets with metadata information. It is suited for large-scale datasets, especially for data which are much larger than the available random-access memory. The gdsfmt package offers the efficient operations specifically designed for integers of less than 8 bits, since a diploid genotype, like single-nucleotide polymorphism (SNP), usually occupies fewer bits than a byte. Data compression and decompression are available with relatively efficient random access. It is also allowed to read a GDS file in parallel with multiple R processes supported by the package parallel. biocViews: Infrastructure, DataImport Author: Xiuwen Zheng [aut, cre], Stephanie Gogarten [ctb], Jean-loup Gailly and Mark Adler [ctb] (for the included zlib sources), Yann Collet [ctb] (for the included LZ4 sources), xz contributors (for the included liblzma sources) Maintainer: Xiuwen Zheng URL: http://corearray.sourceforge.net/, http://github.com/zhengxwen/gdsfmt VignetteBuilder: knitr BugReports: http://github.com/zhengxwen/gdsfmt/issues git_url: https://git.bioconductor.org/packages/gdsfmt git_branch: RELEASE_3_8 git_last_commit: b911b95 git_last_commit_date: 2018-11-26 Date/Publication: 2018-11-27 source.ver: src/contrib/gdsfmt_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gdsfmt_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gdsfmt_1.18.1.tgz vignettes: vignettes/gdsfmt/inst/doc/gdsfmt_vignette.html vignetteTitles: Introduction to GDS Format hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gdsfmt/inst/doc/gdsfmt_vignette.R dependsOnMe: bigmelon, GDSArray, SeqArray, SNPRelate importsMe: GENESIS, GWASTools, SeqSQC, SeqVarTools suggestsMe: AnnotationHub, HIBAG linksToMe: SeqArray, SNPRelate Package: geecc Version: 1.16.1 Depends: R (>= 3.3.0), methods Imports: MASS, hypergea (>= 1.3.0), gplots, Rcpp (>= 0.11.3), graphics, stats, utils LinkingTo: Rcpp Suggests: hgu133plus2.db, GO.db, AnnotationDbi License: GPL (>= 2) Archs: i386, x64 MD5sum: 48ad185a3e1ba4bdf4b1bb868221b507 NeedsCompilation: yes Title: Gene Set Enrichment Analysis Extended to Contingency Cubes Description: Use log-linear models to perform hypergeometric and chi-squared tests for gene set enrichments for two (based on contingency tables) or three categories (contingency cubes). Categories can be differentially expressed genes, GO terms, sequence length, GC content, chromosomal position, phylostrata, divergence-strata, .... biocViews: ImmunoOncology, BiologicalQuestion, GeneSetEnrichment, WorkflowStep, GO, StatisticalMethod, GeneExpression, Transcription, RNASeq, Microarray Author: Markus Boenn Maintainer: Markus Boenn SystemRequirements: Rcpp git_url: https://git.bioconductor.org/packages/geecc git_branch: RELEASE_3_8 git_last_commit: 70356c9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/geecc_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/geecc_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geecc_1.16.1.tgz vignettes: vignettes/geecc/inst/doc/geecc.pdf vignetteTitles: geecc User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geecc/inst/doc/geecc.R Package: GEM Version: 1.8.0 Depends: R (>= 3.3) Imports: tcltk, ggplot2, methods, stats, grDevices, graphics, utils Suggests: knitr, RUnit, testthat, BiocGenerics License: Artistic-2.0 MD5sum: 06d08b08b90d67d3bfd976aef192dc52 NeedsCompilation: no Title: GEM: fast association study for the interplay of Gene, Environment and Methylation Description: Tools for analyzing EWAS, methQTL and GxE genome widely. biocViews: MethylSeq, MethylationArray, GenomeWideAssociation, Regression, DNAMethylation, SNP, GeneExpression, GUI Author: Hong Pan, Joanna D Holbrook, Neerja Karnani, Chee-Keong Kwoh Maintainer: Hong Pan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GEM git_branch: RELEASE_3_8 git_last_commit: 79d822c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GEM_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GEM_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GEM_1.8.0.tgz vignettes: vignettes/GEM/inst/doc/user_guide.html vignetteTitles: The GEM User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GEM/inst/doc/user_guide.R Package: genArise Version: 1.58.0 Depends: R (>= 1.7.1), locfit, tkrplot, methods Imports: graphics, grDevices, methods, stats, tcltk, utils, xtable License: file LICENSE License_restricts_use: yes MD5sum: 4b848ac87c655ce850a42af452508f99 NeedsCompilation: no Title: Microarray Analysis tool Description: genArise is an easy to use tool for dual color microarray data. Its GUI-Tk based environment let any non-experienced user performs a basic, but not simple, data analysis just following a wizard. In addition it provides some tools for the developer. biocViews: Microarray, TwoChannel, Preprocessing Author: Ana Patricia Gomez Mayen ,\\ Gustavo Corral Guille , \\ Lina Riego Ruiz ,\\ Gerardo Coello Coutino Maintainer: IFC Development Team URL: http://www.ifc.unam.mx/genarise git_url: https://git.bioconductor.org/packages/genArise git_branch: RELEASE_3_8 git_last_commit: 221709d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genArise_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genArise_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genArise_1.58.0.tgz vignettes: vignettes/genArise/inst/doc/genArise.pdf vignetteTitles: genAriseGUI Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/genArise/inst/doc/genArise.R Package: genbankr Version: 1.10.0 Depends: methods Imports: BiocGenerics, IRanges (>= 2.13.15), GenomicRanges (>= 1.31.10), GenomicFeatures (>= 1.31.5), Biostrings, VariantAnnotation, rtracklayer, S4Vectors (>= 0.17.28), GenomeInfoDb, Biobase Suggests: RUnit, rentrez, knitr, rmarkdown, BiocStyle License: Artistic-2.0 MD5sum: 3eb9b0da2de16e06cbf5adcf518b27ac NeedsCompilation: no Title: Parsing GenBank files into semantically useful objects Description: Reads Genbank files. biocViews: Infrastructure, DataImport Author: Gabriel Becker [aut, cre], Michael Lawrence [aut] Maintainer: Gabriel Becker VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/genbankr git_branch: RELEASE_3_8 git_last_commit: 359555b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genbankr_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genbankr_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genbankr_1.10.0.tgz vignettes: vignettes/genbankr/inst/doc/genbankr.html vignetteTitles: An introduction to genbankr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genbankr/inst/doc/genbankr.R Package: GeneAccord Version: 1.0.0 Depends: R (>= 3.5) Imports: biomaRt, caTools, dplyr, ggplot2, graphics, grDevices, gtools, ggpubr, magrittr, maxLik, RColorBrewer, reshape2, stats, tibble, utils Suggests: assertthat, BiocStyle, devtools, knitr, rmarkdown, testthat License: file LICENSE MD5sum: 20327d63683336b7ae0f47d9757727b3 NeedsCompilation: no Title: Detection of clonally exclusive gene or pathway pairs in a cohort of cancer patients Description: A statistical framework to examine the combinations of clones that co-exist in tumors. More precisely, the algorithm finds pairs of genes that are mutated in the same tumor but in different clones, i.e. their subclonal mutation profiles are mutually exclusive. We refer to this as clonally exclusive. It means that the mutations occurred in different branches of the tumor phylogeny, indicating parallel evolution of the clones. Our statistical framework assesses whether a pattern of clonal exclusivity occurs more often than expected by chance alone across a cohort of patients. The required input data are the mutated gene-to-clone assignments from a cohort of cancer patients, which were obtained by running phylogenetic tree inference methods. Reconstructing the evolutionary history of a tumor and detecting the clones is challenging. For nondeterministic algorithms, repeated tree inference runs may lead to slightly different mutation-to-clone assignments. Therefore, our algorithm was designed to allow the input of multiple gene-to-clone assignments per patient. They may have been generated by repeatedly performing the tree inference, or by sampling from the posterior distribution of trees. The tree inference methods designate the mutations to individual clones. The mutations can then be mapped to genes or pathways. Hence our statistical framework can be applied on the gene level, or on the pathway level to detect clonally exclusive pairs of pathways. If a pair is significantly clonally exclusive, it points towards the fact that this specific clone configuration confers a selective advantage, possibly through synergies between the clones with these mutations. biocViews: BiomedicalInformatics, GeneticVariability, GenomicVariation, SomaticMutation, FunctionalGenomics, Genetics, MathematicalBiology, SystemsBiology, FeatureExtraction, PatternLogic, Pathways Author: Ariane L. Moore, Jack Kuipers and Niko Beerenwinkel Maintainer: Ariane L. Moore URL: https://github.com/cbg-ethz/GeneAccord VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GeneAccord git_branch: RELEASE_3_8 git_last_commit: 21f4613 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneAccord_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneAccord_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneAccord_1.0.0.tgz vignettes: vignettes/GeneAccord/inst/doc/GeneAccord.html vignetteTitles: GeneAccord hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GeneAccord/inst/doc/GeneAccord.R Package: GeneAnswers Version: 2.24.0 Depends: R (>= 3.0.0), igraph, RCurl, annotate, Biobase (>= 1.12.0), methods, XML, RSQLite, MASS, Heatplus, RColorBrewer Imports: RBGL, annotate, downloader Suggests: GO.db, KEGG.db, reactome.db, biomaRt, AnnotationDbi, org.Hs.eg.db, org.Rn.eg.db, org.Mm.eg.db, org.Dm.eg.db, graph License: LGPL (>= 2) MD5sum: 0d3cf555819cf8b8d71029082abc33e1 NeedsCompilation: no Title: Integrated Interpretation of Genes Description: GeneAnswers provides an integrated tool for biological or medical interpretation of the given one or more groups of genes by means of statistical test. biocViews: Infrastructure, DataRepresentation, Visualization, GraphsAndNetworks Author: Lei Huang, Gang Feng, Pan Du, Tian Xia, Xishu Wang, Jing, Wen, Warren Kibbe and Simon Lin Maintainer: Lei Huang and Gang Feng git_url: https://git.bioconductor.org/packages/GeneAnswers git_branch: RELEASE_3_8 git_last_commit: 95cfd23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneAnswers_2.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneAnswers_2.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneAnswers_2.24.0.tgz vignettes: vignettes/GeneAnswers/inst/doc/geneAnswers.pdf, vignettes/GeneAnswers/inst/doc/getListGIF.pdf vignetteTitles: GeneAnswers, GeneAnswers web-based visualization module hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneAnswers/inst/doc/geneAnswers.R, vignettes/GeneAnswers/inst/doc/getListGIF.R suggestsMe: InterMineR Package: geneAttribution Version: 1.8.0 Imports: utils, GenomicRanges, org.Hs.eg.db, BiocGenerics, GenomeInfoDb, GenomicFeatures, IRanges, rtracklayer Suggests: TxDb.Hsapiens.UCSC.hg38.knownGene, TxDb.Hsapiens.UCSC.hg19.knownGene, knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: f789b0c41a0d5bcce055f113b718d583 NeedsCompilation: no Title: Identification of candidate genes associated with genetic variation Description: Identification of the most likely gene or genes through which variation at a given genomic locus in the human genome acts. The most basic functionality assumes that the closer gene is to the input locus, the more likely the gene is to be causative. Additionally, any empirical data that links genomic regions to genes (e.g. eQTL or genome conformation data) can be used if it is supplied in the UCSC .BED file format. biocViews: SNP, GenePrediction, GenomeWideAssociation, VariantAnnotation, GenomicVariation Author: Arthur Wuster Maintainer: Arthur Wuster VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/geneAttribution git_branch: RELEASE_3_8 git_last_commit: ea6e316 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneAttribution_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneAttribution_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneAttribution_1.8.0.tgz vignettes: vignettes/geneAttribution/inst/doc/geneAttribution.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: GeneBreak Version: 1.12.0 Depends: R(>= 3.2), QDNAseq, CGHcall, CGHbase, GenomicRanges Imports: graphics, methods License: GPL-2 MD5sum: 6210aae2a4a0e02205f7fcb10831f943 NeedsCompilation: no Title: Gene Break Detection Description: Recurrent breakpoint gene detection on copy number aberration profiles. biocViews: aCGH, CopyNumberVariation, DNASeq, Genetics, Sequencing, WholeGenome, Visualization Author: Evert van den Broek, Stef van Lieshout Maintainer: Evert van den Broek URL: https://github.com/stefvanlieshout/GeneBreak git_url: https://git.bioconductor.org/packages/GeneBreak git_branch: RELEASE_3_8 git_last_commit: 7437a2c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneBreak_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneBreak_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneBreak_1.12.0.tgz vignettes: vignettes/GeneBreak/inst/doc/GeneBreak.pdf vignetteTitles: GeneBreak hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneBreak/inst/doc/GeneBreak.R Package: geneClassifiers Version: 1.6.0 Depends: utils Imports: methods, stats, Biobase, BiocGenerics Suggests: testthat License: GPL-2 MD5sum: 2af1e841e8a184c21b9d0d1c6907d376 NeedsCompilation: no Title: Application of gene classifiers Description: This packages aims for easy accessible application of classifiers which have been published in literature using an ExpressionSet as input. biocViews: GeneExpression, BiomedicalInformatics, Classification, Survival, Microarray Author: R Kuiper Maintainer: R Kuiper git_url: https://git.bioconductor.org/packages/geneClassifiers git_branch: RELEASE_3_8 git_last_commit: edae1e5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneClassifiers_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneClassifiers_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneClassifiers_1.6.0.tgz vignettes: vignettes/geneClassifiers/inst/doc/geneClassifiers.pdf, vignettes/geneClassifiers/inst/doc/MissingCovariates.pdf vignetteTitles: geneClassifiers introduction, geneClassifiers and missing probesets hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geneClassifiers/inst/doc/geneClassifiers.R Package: GeneExpressionSignature Version: 1.28.0 Depends: R (>= 2.13), Biobase, PGSEA Suggests: apcluster,GEOquery License: GPL-2 MD5sum: 00e1e0a915a2a1455f65c1dd159427cc NeedsCompilation: no Title: Gene Expression Signature based Similarity Metric Description: This package gives the implementations of the gene expression signature and its distance to each. Gene expression signature is represented as a list of genes whose expression is correlated with a biological state of interest. And its distance is defined using a nonparametric, rank-based pattern-matching strategy based on the Kolmogorov-Smirnov statistic. Gene expression signature and its distance can be used to detect similarities among the signatures of drugs, diseases, and biological states of interest. biocViews: GeneExpression Author: Yang Cao Maintainer: Yang Cao , Fei Li ,Lu Han git_url: https://git.bioconductor.org/packages/GeneExpressionSignature git_branch: RELEASE_3_8 git_last_commit: f2ebf23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneExpressionSignature_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneExpressionSignature_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneExpressionSignature_1.28.0.tgz vignettes: vignettes/GeneExpressionSignature/inst/doc/GeneExpressionSignature.pdf vignetteTitles: GeneExpressionSignature hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneExpressionSignature/inst/doc/GeneExpressionSignature.R Package: genefilter Version: 1.64.0 Imports: S4Vectors (>= 0.9.42), AnnotationDbi, annotate, Biobase, graphics, methods, stats, survival Suggests: class, hgu95av2.db, tkWidgets, ALL, ROC, DESeq, pasilla, RColorBrewer, BiocStyle, knitr License: Artistic-2.0 Archs: i386, x64 MD5sum: 88bde15c167b64adeaeb6396a4adafed NeedsCompilation: yes Title: genefilter: methods for filtering genes from high-throughput experiments Description: Some basic functions for filtering genes. biocViews: Microarray Author: R. Gentleman, V. Carey, W. Huber, F. Hahne Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/genefilter git_branch: RELEASE_3_8 git_last_commit: 82e91b7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genefilter_1.64.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genefilter_1.64.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genefilter_1.64.0.tgz vignettes: vignettes/genefilter/inst/doc/howtogenefilter.pdf, vignettes/genefilter/inst/doc/howtogenefinder.pdf, vignettes/genefilter/inst/doc/independent_filtering_plots.pdf, vignettes/genefilter/inst/doc/independent_filtering.pdf vignetteTitles: Using the genefilter function to filter genes from a microarray dataset, How to find genes whose expression profile is similar to that of specified genes, Additional plots for: Independent filtering increases power for detecting differentially expressed genes,, Bourgon et al.,, PNAS (2010), Diagnostics for independent filtering hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genefilter/inst/doc/howtogenefilter.R, vignettes/genefilter/inst/doc/howtogenefinder.R, vignettes/genefilter/inst/doc/independent_filtering_plots.R, vignettes/genefilter/inst/doc/independent_filtering.R dependsOnMe: a4Base, cellHTS2, charm, CNTools, GeneMeta, simpleaffy, sva importsMe: affyQCReport, annmap, arrayQualityMetrics, Category, cbaf, countsimQC, covRNA, DESeq, DESeq2, DEXSeq, eisa, gCMAP, GGBase, GISPA, GSRI, JunctionSeq, methyAnalysis, methylumi, minfi, MLInterfaces, mogsa, pcaExplorer, PECA, phenoTest, Ringo, simpleaffy, TCGAbiolinks, tilingArray, XDE, zinbwave suggestsMe: AffyExpress, annotate, ArrayTools, BiocCaseStudies, BioNet, categoryCompare, ClassifyR, clusterStab, codelink, compcodeR, DelayedArray, EnrichedHeatmap, factDesign, ffpe, GenoGAM, GenomicFiles, GOstats, GSAR, GSEAlm, GSVA, logicFS, lumi, MCRestimate, npGSEA, oligo, phyloseq, pvac, qpgraph, rtracklayer, siggenes, SSPA, topGO Package: genefu Version: 2.14.0 Depends: survcomp, mclust, limma,biomaRt, iC10, AIMS, R (>= 2.10) Imports: amap Suggests: GeneMeta, breastCancerVDX, breastCancerMAINZ, breastCancerTRANSBIG, breastCancerUPP, breastCancerUNT, breastCancerNKI, rmeta, Biobase, xtable, knitr, caret, survival License: Artistic-2.0 MD5sum: 26fd028d750b137edebcdbf8966c0324 NeedsCompilation: no Title: Computation of Gene Expression-Based Signatures in Breast Cancer Description: Description: This package contains functions implementing various tasks usually required by gene expression analysis, especially in breast cancer studies: gene mapping between different microarray platforms, identification of molecular subtypes, implementation of published gene signatures, gene selection, and survival analysis. biocViews: DifferentialExpression, GeneExpression, Visualization, Clustering, Classification Author: Deena M.A. Gendoo, Natchar Ratanasirigulchai, Markus S. Schroder, Laia Pare, Joel S. Parker, Aleix Prat, and Benjamin Haibe-Kains Maintainer: Benjamin Haibe-Kains , Markus Schroeder URL: http://www.pmgenomics.ca/bhklab/software/genefu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/genefu git_branch: RELEASE_3_8 git_last_commit: 0825dec git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genefu_2.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genefu_2.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genefu_2.14.0.tgz vignettes: vignettes/genefu/inst/doc/genefu.pdf vignetteTitles: genefu An Introduction (HowTo) hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genefu/inst/doc/genefu.R importsMe: consensusOV Package: GeneGA Version: 1.32.0 Depends: seqinr, hash, methods License: GPL version 2 MD5sum: 4d664e7a6933501a3286da527d3f306c NeedsCompilation: no Title: Design gene based on both mRNA secondary structure and codon usage bias using Genetic algorithm Description: R based Genetic algorithm for gene expression optimization by considering both mRNA secondary structure and codon usage bias, GeneGA includes the information of highly expressed genes of almost 200 genomes. Meanwhile, Vienna RNA Package is needed to ensure GeneGA to function properly. biocViews: GeneExpression Author: Zhenpeng Li and Haixiu Huang Maintainer: Zhenpeng Li URL: http://www.tbi.univie.ac.at/~ivo/RNA/ git_url: https://git.bioconductor.org/packages/GeneGA git_branch: RELEASE_3_8 git_last_commit: af4f820 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneGA_1.32.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneGA_1.32.0.tgz vignettes: vignettes/GeneGA/inst/doc/GeneGA.pdf vignetteTitles: GeneGA hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneGA/inst/doc/GeneGA.R Package: GeneGeneInteR Version: 1.8.0 Depends: R (>= 3.3) Imports: snpStats, mvtnorm, GGtools, Rsamtools, igraph, kernlab, FactoMineR, plspm, IRanges, GenomicRanges, data.table,rioja,grDevices, graphics,stats,utils License: GPL (>= 2) MD5sum: aa36bdccea1e40711a5ed4b583c8e602 NeedsCompilation: no Title: Tools for Testing Gene-Gene Interaction at the Gene Level Description: The aim of this package is to propose several methods for testing gene-gene interaction in case-control association studies. Such a test can be done by aggregating SNP-SNP interaction tests performed at the SNP level (SSI) or by using gene-gene multidimensionnal methods (GGI) methods. The package also proposes tools for a graphic display of the results. biocViews: GenomeWideAssociation, SNP, Genetics, GeneticVariability Author: Mathieu Emily, Nicolas Sounac, Florian Kroell, Magalie Houee-Bigot Maintainer: Mathieu Emily , Magalie Houee-Bigot git_url: https://git.bioconductor.org/packages/GeneGeneInteR git_branch: RELEASE_3_8 git_last_commit: 08468c0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneGeneInteR_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneGeneInteR_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneGeneInteR_1.8.0.tgz vignettes: vignettes/GeneGeneInteR/inst/doc/GenePair.pdf, vignettes/GeneGeneInteR/inst/doc/VignetteGeneGeneInteR_Introduction.pdf vignetteTitles: Pairwise interaction tests, GeneGeneInteR Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneGeneInteR/inst/doc/GenePair.R, vignettes/GeneGeneInteR/inst/doc/VignetteGeneGeneInteR_Introduction.R Package: GeneMeta Version: 1.54.0 Depends: R (>= 2.10), methods, Biobase (>= 2.5.5), genefilter Imports: methods, Biobase (>= 2.5.5) Suggests: RColorBrewer License: Artistic-2.0 MD5sum: f6cc399bae052e2cbeb38d2bcbe3cd10 NeedsCompilation: no Title: MetaAnalysis for High Throughput Experiments Description: A collection of meta-analysis tools for analysing high throughput experimental data biocViews: Sequencing, GeneExpression, Microarray Author: Lara Lusa , R. Gentleman, M. Ruschhaupt Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/GeneMeta git_branch: RELEASE_3_8 git_last_commit: 932553c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneMeta_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneMeta_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneMeta_1.54.0.tgz vignettes: vignettes/GeneMeta/inst/doc/GeneMeta.pdf vignetteTitles: GeneMeta Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneMeta/inst/doc/GeneMeta.R importsMe: XDE suggestsMe: genefu Package: GeneNetworkBuilder Version: 1.24.1 Depends: R (>= 2.15.1), Rcpp (>= 0.9.13) Imports: plyr, graph, htmlwidgets, Rgraphviz, rjson, XML, methods, grDevices, stats, graphics LinkingTo: Rcpp Suggests: RUnit, BiocGenerics, RBGL, knitr, simpIntLists, shiny, STRINGdb License: GPL (>= 2) Archs: i386, x64 MD5sum: 78efd28f739cfac2789316471521961f NeedsCompilation: yes Title: Build Regulatory Network from ChIP-chip/ChIP-seq and Expression Data Description: Appliation for discovering direct or indirect targets of transcription factors using ChIP-chip or ChIP-seq, and microarray or RNA-seq gene expression data. Inputting a list of genes of potential targets of one TF from ChIP-chip or ChIP-seq, and the gene expression results, GeneNetworkBuilder generates a regulatory network of the TF. biocViews: Sequencing, Microarray, GraphAndNetwork Author: Jianhong Ou , Haibo Liu, Heidi A Tissenbaum and Lihua Julie Zhu Maintainer: Jianhong Ou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GeneNetworkBuilder git_branch: RELEASE_3_8 git_last_commit: c100f80 git_last_commit_date: 2019-04-08 Date/Publication: 2019-04-09 source.ver: src/contrib/GeneNetworkBuilder_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneNetworkBuilder_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneNetworkBuilder_1.24.1.tgz vignettes: vignettes/GeneNetworkBuilder/inst/doc/GeneNetworkBuilder_vignettes.html, vignettes/GeneNetworkBuilder/inst/doc/GeneNetworkFromGenes.html, vignettes/GeneNetworkBuilder/inst/doc/with.BioGRID.STRING.html vignetteTitles: GeneNetworkBuilder Vignette, Generate Network from a list of gene, Working with BioGRID,, STRING hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneNetworkBuilder/inst/doc/GeneNetworkBuilder_vignettes.R, vignettes/GeneNetworkBuilder/inst/doc/GeneNetworkFromGenes.R, vignettes/GeneNetworkBuilder/inst/doc/with.BioGRID.STRING.R Package: GeneOverlap Version: 1.18.0 Imports: stats, RColorBrewer, gplots, methods Suggests: RUnit, BiocGenerics, BiocStyle License: GPL-3 MD5sum: dd4b8465cdd86f717727612caef4f1af NeedsCompilation: no Title: Test and visualize gene overlaps Description: Test two sets of gene lists and visualize the results. biocViews: MultipleComparison, Visualization Author: Li Shen, Mount Sinai Maintainer: Li Shen, Mount Sinai URL: http://shenlab-sinai.github.io/shenlab-sinai/ git_url: https://git.bioconductor.org/packages/GeneOverlap git_branch: RELEASE_3_8 git_last_commit: 0750179 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneOverlap_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneOverlap_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneOverlap_1.18.0.tgz vignettes: vignettes/GeneOverlap/inst/doc/GeneOverlap.pdf vignetteTitles: Testing and visualizing gene overlaps with the "GeneOverlap" package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneOverlap/inst/doc/GeneOverlap.R importsMe: CEMiTool Package: geneplast Version: 1.8.0 Depends: R (>= 3.3), methods Imports: igraph, snow, ape, grDevices, graphics, stats, utils Suggests: RTN, RUnit, BiocGenerics, BiocStyle, knitr, rmarkdown License: GPL (>= 2) MD5sum: bcdbc3f90a41dc19ce54893cbc0cf1b5 NeedsCompilation: no Title: Evolutionary and plasticity analysis of orthologous groups Description: Geneplast is designed for evolutionary and plasticity analysis based on orthologous groups distribution in a given species tree. It uses Shannon information theory and orthologs abundance to estimate the Evolutionary Plasticity Index. Additionally, it implements the Bridge algorithm to determine the evolutionary root of a given gene based on its orthologs distribution. biocViews: Genetics, GeneRegulation, SystemsBiology Author: Rodrigo Dalmolin, Mauro Castro Maintainer: Mauro Castro VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/geneplast git_branch: RELEASE_3_8 git_last_commit: 4fde86d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneplast_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneplast_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneplast_1.8.0.tgz vignettes: vignettes/geneplast/inst/doc/geneplast.html vignetteTitles: "Geneplast: evolutionary rooting and plasticity analysis." hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geneplast/inst/doc/geneplast.R Package: geneplotter Version: 1.60.0 Depends: R (>= 2.10), methods, Biobase, BiocGenerics, lattice, annotate Imports: AnnotationDbi, graphics, grDevices, grid, RColorBrewer, stats, utils Suggests: Rgraphviz, fibroEset, hgu95av2.db, hu6800.db, hgu133a.db License: Artistic-2.0 MD5sum: 077d06670401f046e762f770a0815a25 NeedsCompilation: no Title: Graphics related functions for Bioconductor Description: Functions for plotting genomic data biocViews: Visualization Author: R. Gentleman, Biocore Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/geneplotter git_branch: RELEASE_3_8 git_last_commit: 6723a9f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneplotter_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneplotter_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneplotter_1.60.0.tgz vignettes: vignettes/geneplotter/inst/doc/byChroms.pdf, vignettes/geneplotter/inst/doc/visualize.pdf vignetteTitles: How to assemble a chromLocation object, Visualization of Microarray Data hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geneplotter/inst/doc/byChroms.R, vignettes/geneplotter/inst/doc/visualize.R dependsOnMe: HMMcopy importsMe: biocGraph, DESeq, DESeq2, DEXSeq, EnrichmentBrowser, GSVA, IsoGeneGUI, JunctionSeq, MethylSeekR, RNAinteract, RNAither suggestsMe: BiocCaseStudies, biocGraph, Category, chimera, GOstats Package: geneRecommender Version: 1.54.0 Depends: R (>= 1.8.0), Biobase (>= 1.4.22), methods Imports: Biobase, methods, stats License: GPL (>= 2) MD5sum: fa33e09ffa3ace8332c399d2d48728a8 NeedsCompilation: no Title: A gene recommender algorithm to identify genes coexpressed with a query set of genes Description: This package contains a targeted clustering algorithm for the analysis of microarray data. The algorithm can aid in the discovery of new genes with similar functions to a given list of genes already known to have closely related functions. biocViews: Microarray, Clustering Author: Gregory J. Hather , with contributions from Art B. Owen and Terence P. Speed Maintainer: Greg Hather git_url: https://git.bioconductor.org/packages/geneRecommender git_branch: RELEASE_3_8 git_last_commit: e0255d3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneRecommender_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneRecommender_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneRecommender_1.54.0.tgz vignettes: vignettes/geneRecommender/inst/doc/geneRecommender.pdf vignetteTitles: Using the geneRecommender Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geneRecommender/inst/doc/geneRecommender.R Package: GeneRegionScan Version: 1.38.0 Depends: methods, Biobase (>= 2.5.5), Biostrings Imports: S4Vectors (>= 0.9.25), Biobase (>= 2.5.5), affxparser, RColorBrewer, Biostrings Suggests: BSgenome, affy, AnnotationDbi License: GPL (>= 2) MD5sum: 2260cef9b94226c671ee7b49585b48c2 NeedsCompilation: no Title: GeneRegionScan Description: A package with focus on analysis of discrete regions of the genome. This package is useful for investigation of one or a few genes using Affymetrix data, since it will extract probe level data using the Affymetrix Power Tools application and wrap these data into a ProbeLevelSet. A ProbeLevelSet directly extends the expressionSet, but includes additional information about the sequence of each probe and the probe set it is derived from. The package includes a number of functions used for plotting these probe level data as a function of location along sequences of mRNA-strands. This can be used for analysis of variable splicing, and is especially well suited for use with exon-array data. biocViews: Microarray, DataImport, SNP, OneChannel, Visualization Author: Lasse Folkersen, Diego Diez Maintainer: Lasse Folkersen git_url: https://git.bioconductor.org/packages/GeneRegionScan git_branch: RELEASE_3_8 git_last_commit: f0438bb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneRegionScan_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneRegionScan_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneRegionScan_1.38.0.tgz vignettes: vignettes/GeneRegionScan/inst/doc/GeneRegionScan.pdf vignetteTitles: GeneRegionScan hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneRegionScan/inst/doc/GeneRegionScan.R Package: geneRxCluster Version: 1.18.0 Depends: GenomicRanges,IRanges Suggests: RUnit, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: 8d1ada8668cffaf687eb24c1313cf667 NeedsCompilation: yes Title: gRx Differential Clustering Description: Detect Differential Clustering of Genomic Sites such as gene therapy integrations. The package provides some functions for exploring genomic insertion sites originating from two different sources. Possibly, the two sources are two different gene therapy vectors. Vectors are preferred that target sensitive regions less frequently, motivating the search for localized clusters of insertions and comparison of the clusters formed by integration of different vectors. Scan statistics allow the discovery of spatial differences in clustering and calculation of False Discovery Rates (FDRs) providing statistical methods for comparing retroviral vectors. A scan statistic for comparing two vectors using multiple window widths to detect clustering differentials and compute FDRs is implemented here. biocViews: Sequencing, Clustering, Genetics Author: Charles Berry Maintainer: Charles Berry git_url: https://git.bioconductor.org/packages/geneRxCluster git_branch: RELEASE_3_8 git_last_commit: 8c75128 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneRxCluster_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneRxCluster_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneRxCluster_1.18.0.tgz vignettes: vignettes/geneRxCluster/inst/doc/tutorial.pdf vignetteTitles: Using geneRxCluster hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geneRxCluster/inst/doc/tutorial.R Package: GeneSelectMMD Version: 2.26.0 Depends: R (>= 2.13.2), Biobase Imports: Biobase, MASS, graphics, stats, survival, limma Suggests: ALL License: GPL (>= 2) Archs: i386, x64 MD5sum: d3e9c106d9ae273e16d315dc1e37f123 NeedsCompilation: yes Title: Gene selection based on the marginal distributions of gene profiles that characterized by a mixture of three-component multivariate distributions Description: Gene selection based on a mixture of marginal distributions biocViews: DifferentialExpression Author: Jarrett Morrow , Weiliang Qiu , Wenqing He , Xiaogang Wang , Ross Lazarus . Maintainer: Weiliang Qiu git_url: https://git.bioconductor.org/packages/GeneSelectMMD git_branch: RELEASE_3_8 git_last_commit: 6ea0097 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneSelectMMD_2.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneSelectMMD_2.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneSelectMMD_2.26.0.tgz vignettes: vignettes/GeneSelectMMD/inst/doc/gsMMD.pdf vignetteTitles: Gene Selection based on a mixture of marginal distributions hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneSelectMMD/inst/doc/gsMMD.R importsMe: iCheck Package: GeneSelector Version: 2.32.0 Depends: R (>= 2.5.1), methods, stats, Biobase Imports: multtest, siggenes, samr, limma Suggests: multtest, siggenes, samr, limma License: GPL (>= 2) Archs: i386, x64 MD5sum: d33abf828afc8bb90576ee93daf62701 NeedsCompilation: yes Title: Stability and Aggregation of ranked gene lists Description: The term 'GeneSelector' refers to a filter selecting those genes which are consistently identified as differentially expressed using various statistical procedures. 'Selected' genes are those present at the top of the list in various ranking methods (currently 14). In addition, the stability of the findings can be taken into account in the final ranking by examining perturbed versions of the original data set, e.g. by leaving samples, swapping class labels, generating bootstrap replicates or adding noise. Given multiple ranked lists, one can use aggregation methods in order to find a synthesis. biocViews: StatisticalMethod, DifferentialExpression Author: Martin Slawski , Anne-Laure Boulesteix . Maintainer: Martin Slawski PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/GeneSelector git_branch: RELEASE_3_8 git_last_commit: 72c2f53 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneSelector_2.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneSelector_2.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneSelector_2.32.0.tgz vignettes: vignettes/GeneSelector/inst/doc/GeneSelector.pdf vignetteTitles: GeneSelector.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneSelector/inst/doc/GeneSelector.R Package: GENESIS Version: 2.12.4 Imports: Biobase, BiocGenerics, GWASTools, gdsfmt, GenomicRanges, IRanges, S4Vectors, SeqArray, SeqVarTools, SNPRelate, data.table, dplyr, foreach, graphics, grDevices, igraph, Matrix, methods, reshape2, stats, utils Suggests: CompQuadForm, poibin, survey, testthat, knitr, rmarkdown, GWASdata, ggplot2, GGally, RColorBrewer, TxDb.Hsapiens.UCSC.hg19.knownGene License: GPL-3 MD5sum: f57b5829858e3f0b3477b310887df342 NeedsCompilation: no Title: GENetic EStimation and Inference in Structured samples (GENESIS): Statistical methods for analyzing genetic data from samples with population structure and/or relatedness Description: The GENESIS package provides methodology for estimating, inferring, and accounting for population and pedigree structure in genetic analyses. The current implementation provides functions to perform PC-AiR (Conomos et al., 2015, Gen Epi) and PC-Relate (Conomos et al., 2016, AJHG). PC-AiR performs a Principal Components Analysis on genome-wide SNP data for the detection of population structure in a sample that may contain known or cryptic relatedness. Unlike standard PCA, PC-AiR accounts for relatedness in the sample to provide accurate ancestry inference that is not confounded by family structure. PC-Relate uses ancestry representative principal components to adjust for population structure/ancestry and accurately estimate measures of recent genetic relatedness such as kinship coefficients, IBD sharing probabilities, and inbreeding coefficients. Additionally, functions are provided to perform efficient variance component estimation and mixed model association testing for both quantitative and binary phenotypes. biocViews: SNP, GeneticVariability, Genetics, StatisticalMethod, DimensionReduction, PrincipalComponent, GenomeWideAssociation, QualityControl, BiocViews Author: Matthew P. Conomos, Stephanie M. Gogarten, Lisa Brown, Han Chen, Ken Rice, Tamar Sofer, Timothy Thornton, Chaoyu Yu Maintainer: Stephanie M. Gogarten URL: https://github.com/UW-GAC/GENESIS VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GENESIS git_branch: RELEASE_3_8 git_last_commit: 0b4d36e git_last_commit_date: 2019-02-20 Date/Publication: 2019-02-20 source.ver: src/contrib/GENESIS_2.12.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/GENESIS_2.12.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GENESIS_2.12.4.tgz vignettes: vignettes/GENESIS/inst/doc/assoc_test_seq.html, vignettes/GENESIS/inst/doc/assoc_test.html, vignettes/GENESIS/inst/doc/pcair.html vignetteTitles: Analyzing Sequence Data using the GENESIS Package, Genetic Association Testing using the GENESIS Package, Population Structure and Relatedness Inference using the GENESIS Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GENESIS/inst/doc/assoc_test_seq.R, vignettes/GENESIS/inst/doc/assoc_test.R, vignettes/GENESIS/inst/doc/pcair.R Package: GeneStructureTools Version: 1.2.1 Imports: Biostrings,GenomicRanges,IRanges,data.table,plyr,stringdist,stringr,S4Vectors,BSgenome.Mmusculus.UCSC.mm10,stats,utils,Gviz,rtracklayer,methods Suggests: BiocStyle, knitr, rmarkdown License: BSD_3_clause + file LICENSE MD5sum: ec230df5a13d5672f139cd9a3f515b80 NeedsCompilation: no Title: Tools for spliced gene structure manipulation and analysis Description: GeneStructureTools can be used to create in silico alternative splicing events, and analyse potential effects this has on functional gene products. biocViews: ImmunoOncology, Software, DifferentialSplicing, FunctionalPrediction, Transcriptomics, AlternativeSplicing, RNASeq Author: Beth Signal Maintainer: Beth Signal VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GeneStructureTools git_branch: RELEASE_3_8 git_last_commit: 2a83f22 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GeneStructureTools_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneStructureTools_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneStructureTools_1.2.1.tgz vignettes: vignettes/GeneStructureTools/inst/doc/Vignette.html vignetteTitles: Introduction to GeneStructureTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GeneStructureTools/inst/doc/Vignette.R Package: geNetClassifier Version: 1.22.0 Depends: R (>= 2.10.1), Biobase (>= 2.5.5), EBarrays, minet, methods Imports: e1071, graphics Suggests: leukemiasEset, RUnit, BiocGenerics Enhances: RColorBrewer, igraph, infotheo License: GPL (>= 2) MD5sum: 7ed135e01c9a31922be170711651ed12 NeedsCompilation: no Title: Classify diseases and build associated gene networks using gene expression profiles Description: Comprehensive package to automatically train and validate a multi-class SVM classifier based on gene expression data. Provides transparent selection of gene markers, their coexpression networks, and an interface to query the classifier. biocViews: Classification, DifferentialExpression, Microarray Author: Sara Aibar, Celia Fontanillo and Javier De Las Rivas. Bioinformatics and Functional Genomics Group. Cancer Research Center (CiC-IBMCC, CSIC/USAL). Salamanca. Spain. Maintainer: Sara Aibar URL: http://www.cicancer.org git_url: https://git.bioconductor.org/packages/geNetClassifier git_branch: RELEASE_3_8 git_last_commit: 939288e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geNetClassifier_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geNetClassifier_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geNetClassifier_1.22.0.tgz vignettes: vignettes/geNetClassifier/inst/doc/geNetClassifier-vignette.pdf vignetteTitles: geNetClassifier-vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/geNetClassifier/inst/doc/geNetClassifier-vignette.R importsMe: bioCancer, canceR Package: GeneticsDesign Version: 1.50.0 Imports: gmodels, graphics, gtools (>= 2.4.0), mvtnorm, stats License: GPL-2 MD5sum: c1cc329cd3f43602ab706b0988a01ae7 NeedsCompilation: no Title: Functions for designing genetics studies Description: This package contains functions useful for designing genetics studies, including power and sample-size calculations. biocViews: Genetics Author: Gregory Warnes David Duffy , Michael Man Weiliang Qiu Ross Lazarus Maintainer: The R Genetics Project git_url: https://git.bioconductor.org/packages/GeneticsDesign git_branch: RELEASE_3_8 git_last_commit: d834298 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneticsDesign_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneticsDesign_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneticsDesign_1.50.0.tgz vignettes: vignettes/GeneticsDesign/inst/doc/GPC.pdf vignetteTitles: Power Calculation for Testing If Disease is Associated a Marker in a Case-Control Study Using the \Rpackage{GeneticsDesign} Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GeneticsDesign/inst/doc/GPC.R Package: GeneticsPed Version: 1.44.0 Depends: R (>= 2.4.0), MASS Imports: gdata, genetics Suggests: RUnit, gtools License: LGPL (>= 2.1) | file LICENSE Archs: i386, x64 MD5sum: 596538e0ee1818d212af9d5e61296166 NeedsCompilation: yes Title: Pedigree and genetic relationship functions Description: Classes and methods for handling pedigree data. It also includes functions to calculate genetic relationship measures as relationship and inbreeding coefficients and other utilities. Note that package is not yet stable. Use it with care! biocViews: Genetics Author: Gregor Gorjanc and David A. Henderson , with code contributions by Brian Kinghorn and Andrew Percy (see file COPYING) Maintainer: David Henderson URL: http://rgenetics.org git_url: https://git.bioconductor.org/packages/GeneticsPed git_branch: RELEASE_3_8 git_last_commit: 2af303a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GeneticsPed_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GeneticsPed_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GeneticsPed_1.44.0.tgz vignettes: vignettes/GeneticsPed/inst/doc/geneticRelatedness.pdf, vignettes/GeneticsPed/inst/doc/pedigreeHandling.pdf, vignettes/GeneticsPed/inst/doc/quanGenAnimalModel.pdf vignetteTitles: Calculation of genetic relatedness/relationship between individuals in the pedigree, Pedigree handling, Quantitative genetic (animal) model example in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GeneticsPed/inst/doc/geneticRelatedness.R, vignettes/GeneticsPed/inst/doc/pedigreeHandling.R, vignettes/GeneticsPed/inst/doc/quanGenAnimalModel.R Package: geneXtendeR Version: 1.8.0 Depends: rtracklayer, GO.db, R (>= 3.5.0) Imports: data.table, dplyr, graphics, networkD3, RColorBrewer, SnowballC, tm, utils, wordcloud, AnnotationDbi, BiocStyle, org.Rn.eg.db Suggests: knitr, rmarkdown, testthat, org.Ag.eg.db, org.Bt.eg.db, org.Ce.eg.db, org.Cf.eg.db, org.Dm.eg.db, org.Dr.eg.db, org.Gg.eg.db, org.Hs.eg.db, org.Mm.eg.db, org.Pt.eg.db, org.Sc.sgd.db, org.Ss.eg.db, org.Xl.eg.db, rtracklayer License: GPL (>= 3) Archs: i386, x64 MD5sum: 967c99eb692b4bff278ddd7d808b1806 NeedsCompilation: yes Title: Optimized Functional Annotation Of ChIP-seq Data Description: geneXtendeR optimizes the functional annotation of ChIP-seq peaks by exploring relative differences in annotating ChIP-seq peak sets to variable-length gene bodies. In contrast to prior techniques, geneXtendeR considers peak annotations beyond just the closest gene, allowing users to see peak summary statistics for the first-closest gene, second-closest gene, ..., n-closest gene whilst ranking the output according to biologically relevant events and iteratively comparing the fidelity of peak-to-gene overlap across a user-defined range of upstream and downstream extensions on the original boundaries of each gene's coordinates. Since different ChIP-seq peak callers produce different differentially enriched peaks with a large variance in peak length distribution and total peak count, annotating peak lists with their nearest genes can often be a noisy process. As such, the goal of geneXtendeR is to robustly link differentially enriched peaks with their respective genes, thereby aiding experimental follow-up and validation in designing primers for a set of prospective gene candidates during qPCR. biocViews: ChIPSeq, Genetics, Annotation, GenomeAnnotation, DifferentialPeakCalling, Coverage, PeakDetection, ChipOnChip, HistoneModification, DataImport, NaturalLanguageProcessing, Visualization, GO, Software Author: Bohdan Khomtchouk [aut, cre], William Koehler [aut] Maintainer: Bohdan Khomtchouk URL: https://github.com/Bohdan-Khomtchouk/geneXtendeR VignetteBuilder: knitr BugReports: https://github.com/Bohdan-Khomtchouk/geneXtendeR/issues git_url: https://git.bioconductor.org/packages/geneXtendeR git_branch: RELEASE_3_8 git_last_commit: ea67de7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/geneXtendeR_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/geneXtendeR_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/geneXtendeR_1.8.0.tgz vignettes: vignettes/geneXtendeR/inst/doc/geneXtendeR.pdf vignetteTitles: geneXtendeR.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: GENIE3 Version: 1.4.3 Imports: stats, reshape2 Suggests: knitr, rmarkdown, foreach, doRNG, doParallel, Biobase, SummarizedExperiment, testthat, methods License: GPL (>= 2) Archs: i386, x64 MD5sum: a6e39df7d3435c7a90fb3c2de78c284e NeedsCompilation: yes Title: GEne Network Inference with Ensemble of trees Description: This package implements the GENIE3 algorithm for inferring gene regulatory networks from expression data. biocViews: NetworkInference, SystemsBiology, DecisionTree, Regression, Network, GraphAndNetwork, GeneExpression Author: Van Anh Huynh-Thu, Sara Aibar, Pierre Geurts Maintainer: Van Anh Huynh-Thu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GENIE3 git_branch: RELEASE_3_8 git_last_commit: ae719c7 git_last_commit_date: 2019-01-31 Date/Publication: 2019-02-01 source.ver: src/contrib/GENIE3_1.4.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/GENIE3_1.4.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GENIE3_1.4.3.tgz vignettes: vignettes/GENIE3/inst/doc/GENIE3.html vignetteTitles: GENIE3 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GENIE3/inst/doc/GENIE3.R importsMe: netbenchmark Package: genoCN Version: 1.34.0 Imports: graphics, stats, utils License: GPL (>=2) Archs: i386, x64 MD5sum: 7b95b4cd827c5f41d1b35f5537be32f9 NeedsCompilation: yes Title: genotyping and copy number study tools Description: Simultaneous identification of copy number states and genotype calls for regions of either copy number variations or copy number aberrations biocViews: Microarray, Genetics Author: Wei Sun and ZhengZheng Tang Maintainer: Wei Sun git_url: https://git.bioconductor.org/packages/genoCN git_branch: RELEASE_3_8 git_last_commit: 98a342d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genoCN_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genoCN_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genoCN_1.34.0.tgz vignettes: vignettes/genoCN/inst/doc/genoCN.pdf vignetteTitles: add stuff hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genoCN/inst/doc/genoCN.R Package: GenoGAM Version: 2.0.3 Depends: R (>= 3.5), SummarizedExperiment (>= 1.1.19), HDF5Array (>= 1.8.0), rhdf5 (>= 2.21.6), S4Vectors (>= 0.9.34), Matrix (>= 1.2-8), data.table (>= 1.9.4) Imports: Rcpp (>= 0.12.14), sparseinv (>= 0.1.1), Rsamtools (>= 1.18.2), GenomicRanges (>= 1.23.16), BiocParallel (>= 1.5.17), DESeq2 (>= 1.11.23), futile.logger (>= 1.4.1), GenomeInfoDb (>= 1.7.6), GenomicAlignments (>= 1.7.17), IRanges (>= 2.5.30), Biostrings (>= 2.39.14), DelayedArray (>= 0.3.19), methods, stats LinkingTo: Rcpp, RcppArmadillo Suggests: BiocStyle, chipseq (>= 1.21.2), LSD (>= 3.0.0), genefilter (>= 1.54.2), ggplot2 (>= 2.1.0), testthat, knitr, rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 20b27bcfc6df98840cca2c698ab55b0f NeedsCompilation: yes Title: A GAM based framework for analysis of ChIP-Seq data Description: This package allows statistical analysis of genome-wide data with smooth functions using generalized additive models based on the implementation from the R-package 'mgcv'. It provides methods for the statistical analysis of ChIP-Seq data including inference of protein occupancy, and pointwise and region-wise differential analysis. Estimation of dispersion and smoothing parameters is performed by cross-validation. Scaling of generalized additive model fitting to whole chromosomes is achieved by parallelization over overlapping genomic intervals. biocViews: Regression, DifferentialPeakCalling, ChIPSeq, DifferentialExpression, Genetics, Epigenetics, WholeGenome, ChipOnChip, ImmunoOncology Author: Georg Stricker [aut, cre], Alexander Engelhardt [aut], Julien Gagneur [aut] Maintainer: Georg Stricker URL: https://github.com/gstricker/GenoGAM VignetteBuilder: knitr BugReports: https://github.com/gstricker/GenoGAM/issues git_url: https://git.bioconductor.org/packages/GenoGAM git_branch: RELEASE_3_8 git_last_commit: bb9cd4a git_last_commit_date: 2019-03-19 Date/Publication: 2019-03-20 source.ver: src/contrib/GenoGAM_2.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenoGAM_2.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenoGAM_2.0.3.tgz vignettes: vignettes/GenoGAM/inst/doc/GenoGAM.html vignetteTitles: "Modeling ChIP-Seq data with GenoGAM 2.0: A Genome-wide generalized additive model" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenoGAM/inst/doc/GenoGAM.R Package: genomation Version: 1.14.0 Depends: R (>= 3.0.0),grid Imports: Biostrings (>= 2.47.6), BSgenome (>= 1.47.3), data.table, GenomeInfoDb, GenomicRanges (>= 1.31.8), GenomicAlignments (>= 1.15.6), S4Vectors (>= 0.17.25), ggplot2, gridBase, impute, IRanges (>= 2.13.12), matrixStats, methods, parallel, plotrix, plyr, readr, reshape2, Rsamtools (>= 1.31.2), seqPattern, rtracklayer (>= 1.39.7), RUnit, Rcpp (>= 0.12.14) LinkingTo: Rcpp Suggests: BiocGenerics, genomationData, knitr, RColorBrewer, rmarkdown License: Artistic-2.0 Archs: i386, x64 MD5sum: b5adfde48396a2fd9ffd760e880690f8 NeedsCompilation: yes Title: Summary, annotation and visualization of genomic data Description: A package for summary and annotation of genomic intervals. Users can visualize and quantify genomic intervals over pre-defined functional regions, such as promoters, exons, introns, etc. The genomic intervals represent regions with a defined chromosome position, which may be associated with a score, such as aligned reads from HT-seq experiments, TF binding sites, methylation scores, etc. The package can use any tabular genomic feature data as long as it has minimal information on the locations of genomic intervals. In addition, It can use BAM or BigWig files as input. biocViews: Annotation, Sequencing, Visualization, CpGIsland Author: Altuna Akalin [aut, cre], Vedran Franke [aut, cre], Katarzyna Wreczycka [aut], Alexander Gosdschan [ctb], Liz Ing-Simmons [ctb], Bozena Mika-Gospodorz [ctb] Maintainer: Altuna Akalin , Vedran Franke , Katarzyna Wreczycka URL: http://bioinformatics.mdc-berlin.de/genomation/ VignetteBuilder: knitr BugReports: https://github.com/BIMSBbioinfo/genomation/issues git_url: https://git.bioconductor.org/packages/genomation git_branch: RELEASE_3_8 git_last_commit: 6b67490 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genomation_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genomation_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genomation_1.14.0.tgz vignettes: vignettes/genomation/inst/doc/GenomationManual.html vignetteTitles: genomation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genomation/inst/doc/GenomationManual.R importsMe: CexoR, fCCAC, RCAS suggestsMe: methylKit Package: GenomeGraphs Version: 1.42.0 Depends: R (>= 2.10), methods, biomaRt, grid License: Artistic-2.0 MD5sum: 7be8b00de248fe8b5b73d43d17c9ea7a NeedsCompilation: no Title: Plotting genomic information from Ensembl Description: Genomic data analyses requires integrated visualization of known genomic information and new experimental data. GenomeGraphs uses the biomaRt package to perform live annotation queries to Ensembl and translates this to e.g. gene/transcript structures in viewports of the grid graphics package. This results in genomic information plotted together with your data. Another strength of GenomeGraphs is to plot different data types such as array CGH, gene expression, sequencing and other data, together in one plot using the same genome coordinate system. biocViews: Visualization, Microarray Author: Steffen Durinck , James Bullard Maintainer: Steffen Durinck git_url: https://git.bioconductor.org/packages/GenomeGraphs git_branch: RELEASE_3_8 git_last_commit: c8c01b5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomeGraphs_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomeGraphs_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomeGraphs_1.42.0.tgz vignettes: vignettes/GenomeGraphs/inst/doc/GenomeGraphs.pdf vignetteTitles: The GenomeGraphs users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomeGraphs/inst/doc/GenomeGraphs.R dependsOnMe: Genominator, waveTiling suggestsMe: oligo, rMAT, triplex Package: GenomeInfoDb Version: 1.18.2 Depends: R (>= 3.1), methods, BiocGenerics (>= 0.13.8), S4Vectors (>= 0.17.25), IRanges (>= 2.13.12) Imports: stats, stats4, utils, RCurl, GenomeInfoDbData Suggests: GenomicRanges, Rsamtools, GenomicAlignments, BSgenome, GenomicFeatures, BSgenome.Scerevisiae.UCSC.sacCer2, BSgenome.Celegans.UCSC.ce2, BSgenome.Hsapiens.NCBI.GRCh38, TxDb.Dmelanogaster.UCSC.dm3.ensGene, RUnit, BiocStyle, knitr License: Artistic-2.0 MD5sum: 85a150381afdc6a02838db760a7e79e2 NeedsCompilation: no Title: Utilities for manipulating chromosome and other 'seqname' identifiers Description: Contains data and functions that define and allow translation between different chromosome sequence naming conventions (e.g., "chr1" versus "1"), including a function that attempts to place sequence names in their natural, rather than lexicographic, order. biocViews: Genetics, DataRepresentation, Annotation, GenomeAnnotation Author: Sonali Arora, Martin Morgan, Marc Carlson, H. Pagès Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr Video: http://youtu.be/wdEjCYSXa7w git_url: https://git.bioconductor.org/packages/GenomeInfoDb git_branch: RELEASE_3_8 git_last_commit: 557b75e git_last_commit_date: 2019-02-11 Date/Publication: 2019-02-12 source.ver: src/contrib/GenomeInfoDb_1.18.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomeInfoDb_1.18.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomeInfoDb_1.18.2.tgz vignettes: vignettes/GenomeInfoDb/inst/doc/Accept-organism-for-GenomeInfoDb.pdf, vignettes/GenomeInfoDb/inst/doc/GenomeInfoDb.pdf vignetteTitles: GenomeInfoDb: Submitting your organism to GenomeInfoDb, GenomeInfoDb: Introduction to GenomeInfoDb hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomeInfoDb/inst/doc/Accept-organism-for-GenomeInfoDb.R, vignettes/GenomeInfoDb/inst/doc/GenomeInfoDb.R dependsOnMe: BSgenome, bumphunter, CODEX, CSAR, GenomicAlignments, GenomicFeatures, GenomicRanges, GenomicTuples, gmapR, groHMM, HelloRanges, htSeqTools, methyAnalysis, MTseeker, Rsamtools, VariantAnnotation importsMe: AllelicImbalance, alpine, amplican, AneuFinder, AnnotationHubData, annotatr, ATACseqQC, BaalChIP, ballgown, biovizBase, BiSeq, bnbc, branchpointer, breakpointR, BSgenome, bsseq, CAGEfightR, CAGEr, casper, CexoR, chimeraviz, chipenrich, ChIPexoQual, ChIPpeakAnno, ChIPseeker, chromstaR, chromVAR, cn.mops, CNEr, CNPBayes, CNVPanelizer, compEpiTools, consensusSeekeR, conumee, CopywriteR, CrispRVariants, csaw, customProDB, DeepBlueR, derfinder, derfinderPlot, DEScan2, diffHic, diffloop, DMRScan, dmrseq, DominoEffect, easyRNASeq, ELMER, ensembldb, ensemblVEP, epigenomix, epivizrData, epivizrStandalone, erma, esATAC, EventPointer, exomeCopy, FunChIP, funtooNorm, GA4GHclient, GA4GHshiny, gcapc, genbankr, geneAttribution, GenoGAM, genomation, genomeIntervals, GenomicFiles, GenomicInteractions, GenomicScores, genoset, genotypeeval, GenVisR, ggbio, GGtools, GoogleGenomics, gQTLstats, GreyListChIP, GUIDEseq, Gviz, gwascat, h5vc, heatmaps, HiCBricks, HiTC, HTSeqGenie, IMAS, InPAS, InteractionSet, IsoformSwitchAnalyzeR, IVAS, karyoploteR, ldblock, MACPET, MADSEQ, maser, metagene, metavizr, methimpute, methInheritSim, methylKit, methylPipe, methylumi, methyvim, minfi, MinimumDistance, mosaics, motifbreakR, motifmatchr, msgbsR, multiHiCcompare, MutationalPatterns, myvariant, NADfinder, NarrowPeaks, normr, nucleR, OMICsPCA, ORFik, Organism.dplyr, panelcn.mops, Pi, plyranges, podkat, prebs, ProteomicsAnnotationHubData, PureCN, qpgraph, qsea, QuasR, R3CPET, r3Cseq, RaggedExperiment, RareVariantVis, Rariant, Rcade, RCAS, recount, regioneR, regionReport, Repitools, RiboProfiling, riboSeqR, RJMCMCNucleosomes, roar, RTCGAToolbox, rtracklayer, scmeth, scruff, segmentSeq, SeqArray, seqCAT, seqplots, seqsetvis, sevenC, SGSeq, ShortRead, SNPchip, SNPhood, soGGi, SomaticSignatures, SparseSignatures, SplicingGraphs, SPLINTER, srnadiff, STAN, strandCheckR, SummarizedExperiment, TarSeqQC, TCGAbiolinks, TCGAutils, TFBSTools, TitanCNA, TnT, trackViewer, transcriptR, tRNAscanImport, TSRchitect, TVTB, tximeta, TxRegInfra, Ularcirc, VanillaICE, VariantFiltering, VariantTools, wiggleplotr, YAPSA suggestsMe: AnnotationForge, AnnotationHub, BiocOncoTK, chromswitch, ExperimentHubData, gQTLBase, QDNAseq, recoup, TFutils Package: genomeIntervals Version: 1.38.0 Depends: R (>= 2.15.0), methods, intervals (>= 0.14.0), BiocGenerics (>= 0.15.2) Imports: GenomeInfoDb (>= 1.5.8), GenomicRanges (>= 1.21.16), IRanges(>= 2.3.14), S4Vectors (>= 0.7.10) License: Artistic-2.0 MD5sum: 4944f98e184cd5b015136453854d8bad NeedsCompilation: no Title: Operations on genomic intervals Description: This package defines classes for representing genomic intervals and provides functions and methods for working with these. Note: The package provides the basic infrastructure for and is enhanced by the package 'girafe'. biocViews: DataImport, Infrastructure, Genetics Author: Julien Gagneur , Joern Toedling, Richard Bourgon, Nicolas Delhomme Maintainer: Julien Gagneur git_url: https://git.bioconductor.org/packages/genomeIntervals git_branch: RELEASE_3_8 git_last_commit: 1acbdc9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genomeIntervals_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genomeIntervals_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genomeIntervals_1.38.0.tgz vignettes: vignettes/genomeIntervals/inst/doc/genomeIntervals.pdf vignetteTitles: Overview of the genomeIntervals package. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genomeIntervals/inst/doc/genomeIntervals.R dependsOnMe: girafe importsMe: easyRNASeq Package: genomes Version: 3.12.0 Depends: readr, curl License: GPL-3 MD5sum: 725ed613b762b70263f03f55a1792cd4 NeedsCompilation: no Title: Genome sequencing project metadata Description: Download genome and assembly reports from NCBI biocViews: Annotation, Genetics Author: Chris Stubben Maintainer: Chris Stubben git_url: https://git.bioconductor.org/packages/genomes git_branch: RELEASE_3_8 git_last_commit: 5f003ca git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genomes_3.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genomes_3.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genomes_3.12.0.tgz vignettes: vignettes/genomes/inst/doc/genomes.pdf vignetteTitles: Genome metadata hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genomes/inst/doc/genomes.R Package: GenomicAlignments Version: 1.18.1 Depends: R (>= 2.10), methods, BiocGenerics (>= 0.15.3), S4Vectors (>= 0.19.11), IRanges (>= 2.15.12), GenomeInfoDb (>= 1.13.1), GenomicRanges (>= 1.33.4), SummarizedExperiment (>= 1.9.13), Biostrings (>= 2.47.6), Rsamtools (>= 1.31.2) Imports: methods, utils, stats, BiocGenerics, S4Vectors, IRanges, GenomicRanges, Biostrings, Rsamtools, BiocParallel LinkingTo: S4Vectors, IRanges Suggests: ShortRead, rtracklayer, BSgenome, GenomicFeatures, RNAseqData.HNRNPC.bam.chr14, pasillaBamSubset, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene, BSgenome.Dmelanogaster.UCSC.dm3, BSgenome.Hsapiens.UCSC.hg19, DESeq2, edgeR, RUnit, BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: 0220afca94e1abcdb173b1df36f1cc60 NeedsCompilation: yes Title: Representation and manipulation of short genomic alignments Description: Provides efficient containers for storing and manipulating short genomic alignments (typically obtained by aligning short reads to a reference genome). This includes read counting, computing the coverage, junction detection, and working with the nucleotide content of the alignments. biocViews: ImmunoOncology, Genetics, Infrastructure, DataImport, Sequencing, RNASeq, SNP, Coverage, Alignment Author: Hervé Pagès, Valerie Obenchain, Martin Morgan Maintainer: Bioconductor Package Maintainer Video: https://www.youtube.com/watch?v=2KqBSbkfhRo , https://www.youtube.com/watch?v=3PK_jx44QTs git_url: https://git.bioconductor.org/packages/GenomicAlignments git_branch: RELEASE_3_8 git_last_commit: 8ac41e5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GenomicAlignments_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicAlignments_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicAlignments_1.18.1.tgz vignettes: vignettes/GenomicAlignments/inst/doc/GenomicAlignmentsIntroduction.pdf, vignettes/GenomicAlignments/inst/doc/OverlapEncodings.pdf, vignettes/GenomicAlignments/inst/doc/summarizeOverlaps.pdf, vignettes/GenomicAlignments/inst/doc/WorkingWithAlignedNucleotides.pdf vignetteTitles: An Introduction to the GenomicAlignments Package, Overlap encodings, Counting reads with summarizeOverlaps, Working with aligned nucleotides hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicAlignments/inst/doc/GenomicAlignmentsIntroduction.R, vignettes/GenomicAlignments/inst/doc/OverlapEncodings.R, vignettes/GenomicAlignments/inst/doc/summarizeOverlaps.R, vignettes/GenomicAlignments/inst/doc/WorkingWithAlignedNucleotides.R dependsOnMe: AllelicImbalance, Basic4Cseq, chimera, ChIPexoQual, exomePeak, GoogleGenomics, groHMM, Guitar, HelloRanges, hiReadsProcessor, MTseeker, ORFik, prebs, recoup, RIPSeeker, rnaSeqMap, ShortRead, SplicingGraphs importsMe: alpine, AneuFinder, ASpli, ATACseqQC, BaalChIP, biovizBase, breakpointR, CAGEr, chimeraviz, ChIPpeakAnno, ChIPQC, chromstaR, CNEr, consensusDE, contiBAIT, CopywriteR, CoverageView, CrispRVariants, customProDB, derfinder, DEScan2, DiffBind, easyRNASeq, FourCSeq, FunChIP, gcapc, GenoGAM, genomation, GenomicFiles, ggbio, gmapR, GreyListChIP, GUIDEseq, Gviz, HTSeqGenie, icetea, IMAS, INSPEcT, IntEREst, MACPET, MADSEQ, MDTS, metagene, methylPipe, mosaics, msgbsR, NADfinder, PICS, plyranges, QuasR, ramwas, Rcade, Repitools, RiboProfiling, RNAprobR, roar, Rqc, rtracklayer, scruff, seqplots, seqsetvis, SGSeq, soGGi, SplicingGraphs, SPLINTER, srnadiff, strandCheckR, TarSeqQC, TCseq, trackViewer, transcriptR, TSRchitect suggestsMe: amplican, BiocParallel, gage, GenomeInfoDb, GenomicDataCommons, GenomicFeatures, GenomicRanges, IRanges, Rsamtools, similaRpeak, Streamer Package: GenomicDataCommons Version: 1.6.0 Depends: R (>= 3.4.0), magrittr Imports: stats, httr, xml2, jsonlite, utils, lazyeval, readr, GenomicRanges, IRanges, dplyr, rappdirs, SummarizedExperiment, S4Vectors Suggests: BiocStyle, knitr, rmarkdown, DT, testthat, listviewer, ggplot2, GenomicAlignments, Rsamtools License: Artistic-2.0 MD5sum: 390615fd4999a0564cea10c4242c878e NeedsCompilation: no Title: NIH / NCI Genomic Data Commons Access Description: Programmatically access the NIH / NCI Genomic Data Commons RESTful service. biocViews: DataImport, Sequencing Author: Martin Morgan [aut], Sean Davis [aut, cre] Maintainer: Sean Davis URL: https://bioconductor.org/packages/GenomicDataCommons, http://github.com/Bioconductor/GenomicDataCommons VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/GenomicDataCommons/issues/new git_url: https://git.bioconductor.org/packages/GenomicDataCommons git_branch: RELEASE_3_8 git_last_commit: 7bdc2aa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomicDataCommons_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicDataCommons_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicDataCommons_1.6.0.tgz vignettes: vignettes/GenomicDataCommons/inst/doc/overview.html vignetteTitles: Introduction to Accessing the NCI Genomic Data Commons hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicDataCommons/inst/doc/overview.R importsMe: GDCRNATools, TCGAutils Package: GenomicFeatures Version: 1.34.8 Depends: BiocGenerics (>= 0.1.0), S4Vectors (>= 0.17.29), IRanges (>= 2.13.23), GenomeInfoDb (>= 1.15.4), GenomicRanges (>= 1.31.17), AnnotationDbi (>= 1.41.4) Imports: methods, utils, stats, tools, DBI, RSQLite (>= 2.0), RCurl, XVector (>= 0.19.7), Biostrings (>= 2.47.6), rtracklayer (>= 1.39.7), biomaRt (>= 2.17.1), Biobase (>= 2.15.1) Suggests: RMariaDB, org.Mm.eg.db, org.Hs.eg.db, BSgenome, BSgenome.Hsapiens.UCSC.hg19 (>= 1.3.17), BSgenome.Celegans.UCSC.ce2, BSgenome.Dmelanogaster.UCSC.dm3 (>= 1.3.17), mirbase.db, FDb.UCSC.tRNAs, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene (>= 2.7.1), TxDb.Mmusculus.UCSC.mm10.knownGene, TxDb.Hsapiens.UCSC.hg19.lincRNAsTranscripts, TxDb.Hsapiens.UCSC.hg38.knownGene, SNPlocs.Hsapiens.dbSNP144.GRCh38, Rsamtools, pasillaBamSubset (>= 0.0.5), GenomicAlignments (>= 1.15.7), ensembldb, RUnit, BiocStyle, knitr License: Artistic-2.0 MD5sum: 860a760f0f624a08396e87aa264df689 NeedsCompilation: no Title: Tools for making and manipulating transcript centric annotations Description: A set of tools and methods for making and manipulating transcript centric annotations. With these tools the user can easily download the genomic locations of the transcripts, exons and cds of a given organism, from either the UCSC Genome Browser or a BioMart database (more sources will be supported in the future). This information is then stored in a local database that keeps track of the relationship between transcripts, exons, cds and genes. Flexible methods are provided for extracting the desired features in a convenient format. biocViews: Genetics, Infrastructure, Annotation, Sequencing, GenomeAnnotation Author: M. Carlson, H. Pagès, P. Aboyoun, S. Falcon, M. Morgan, D. Sarkar, M. Lawrence, V. Obenchain Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GenomicFeatures git_branch: RELEASE_3_8 git_last_commit: c798b3b git_last_commit_date: 2019-04-09 Date/Publication: 2019-04-10 source.ver: src/contrib/GenomicFeatures_1.34.8.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicFeatures_1.34.8.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicFeatures_1.34.8.tgz vignettes: vignettes/GenomicFeatures/inst/doc/GenomicFeatures.pdf vignetteTitles: Making and Utilizing TxDb Objects hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicFeatures/inst/doc/GenomicFeatures.R dependsOnMe: cpvSNP, ensembldb, exomePeak, GSReg, Guitar, HelloRanges, InPAS, OrganismDbi, OUTRIDER, RareVariantVis, RNAprobR, SplicingGraphs importsMe: AllelicImbalance, alpine, AnnotationHubData, annotatr, appreci8R, ASpli, BiocOncoTK, biovizBase, bumphunter, CAGEfightR, casper, ChIPpeakAnno, ChIPQC, ChIPseeker, compEpiTools, CompGO, consensusDE, crisprseekplus, csaw, customProDB, derfinder, derfinderPlot, EDASeq, ELMER, epivizrData, epivizrStandalone, esATAC, EventPointer, GA4GHshiny, genbankr, geneAttribution, GenVisR, ggbio, gmapR, gQTLstats, Gviz, gwascat, HTSeqGenie, icetea, INSPEcT, IntEREst, karyoploteR, lumi, mCSEA, metagene, methyAnalysis, msgbsR, MTseeker, ORFik, Organism.dplyr, PGA, proBAMr, PureCN, qpgraph, QuasR, RCAS, RiboProfiling, scruff, SGSeq, SplicingGraphs, SPLINTER, srnadiff, systemPipeR, TCGAbiolinks, TCGAutils, TFEA.ChIP, trackViewer, transcriptR, tximeta, Ularcirc, VariantAnnotation, VariantFiltering, VariantTools, wavClusteR suggestsMe: AnnotationHub, biomvRCNS, Biostrings, chipseq, chromPlot, CrispRVariants, cummeRbund, DEXSeq, flipflop, GenomeInfoDb, GenomicAlignments, GenomicRanges, groHMM, IRanges, MiRaGE, recount, RIPSeeker, Rsamtools, rtracklayer, ShortRead, SummarizedExperiment, TFutils, TnT, wiggleplotr Package: GenomicFiles Version: 1.18.0 Depends: R (>= 3.1.0), methods, BiocGenerics (>= 0.11.2), GenomicRanges (>= 1.31.16), SummarizedExperiment, BiocParallel (>= 1.1.0), Rsamtools (>= 1.17.29), rtracklayer (>= 1.25.3) Imports: GenomicAlignments (>= 1.7.7), IRanges, S4Vectors (>= 0.9.25), VariantAnnotation (>= 1.27.9), GenomeInfoDb Suggests: BiocStyle, RUnit, genefilter, deepSNV, RNAseqData.HNRNPC.bam.chr14, Biostrings, Homo.sapiens License: Artistic-2.0 MD5sum: 2776040839b95869d3c9686fedb8144a NeedsCompilation: no Title: Distributed computing by file or by range Description: This package provides infrastructure for parallel computations distributed 'by file' or 'by range'. User defined MAPPER and REDUCER functions provide added flexibility for data combination and manipulation. biocViews: Genetics, Infrastructure, DataImport, Sequencing, Coverage Author: Bioconductor Package Maintainer [aut, cre], Valerie Obenchain [aut], Michael Love [aut], Lori Shepherd [aut], Martin Morgan [aut] Maintainer: Bioconductor Package Maintainer Video: https://www.youtube.com/watch?v=3PK_jx44QTs git_url: https://git.bioconductor.org/packages/GenomicFiles git_branch: RELEASE_3_8 git_last_commit: 506f52e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomicFiles_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicFiles_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicFiles_1.18.0.tgz vignettes: vignettes/GenomicFiles/inst/doc/GenomicFiles.pdf vignetteTitles: Introduction to GenomicFiles hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicFiles/inst/doc/GenomicFiles.R dependsOnMe: erma importsMe: CAGEfightR, contiBAIT, derfinder, gQTLBase, gQTLstats, ldblock, QuasR, Rqc suggestsMe: TFutils, TxRegInfra Package: GenomicInteractions Version: 1.16.0 Depends: R (>= 3.5), InteractionSet Imports: Rsamtools, rtracklayer, GenomicRanges (>= 1.29.6), IRanges, BiocGenerics (>= 0.15.3), data.table, stringr, GenomeInfoDb, ggplot2, grid, gridExtra, methods, igraph, S4Vectors (>= 0.13.13), dplyr, Gviz, Biobase, graphics, stats, utils, grDevices Suggests: knitr, BiocStyle, testthat License: GPL-3 MD5sum: c1beef4055b4d2e6cd2ccba99b7f331b NeedsCompilation: no Title: R package for handling genomic interaction data Description: R package for handling Genomic interaction data, such as ChIA-PET/Hi-C, annotating genomic features with interaction information and producing various plots / statistics. biocViews: Software,Infrastructure,DataImport,DataRepresentation,HiC Author: Harmston, N., Ing-Simmons, E., Perry, M., Baresic, A., Lenhard, B. Maintainer: Liz Ing-Simmons URL: https://github.com/ComputationalRegulatoryGenomicsICL/GenomicInteractions/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GenomicInteractions git_branch: RELEASE_3_8 git_last_commit: 12be4cc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomicInteractions_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicInteractions_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicInteractions_1.16.0.tgz vignettes: vignettes/GenomicInteractions/inst/doc/chiapet_vignette.html, vignettes/GenomicInteractions/inst/doc/hic_vignette.html vignetteTitles: chiapet_vignette.html, GenomicInteractions-HiC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicInteractions/inst/doc/chiapet_vignette.R, vignettes/GenomicInteractions/inst/doc/hic_vignette.R importsMe: CAGEfightR suggestsMe: Chicago, ELMER, sevenC Package: GenomicRanges Version: 1.34.0 Depends: R (>= 2.10), methods, stats4, BiocGenerics (>= 0.25.3), S4Vectors (>= 0.19.11), IRanges (>= 2.15.12), GenomeInfoDb (>= 1.15.2) Imports: utils, stats, XVector (>= 0.19.8) LinkingTo: S4Vectors, IRanges Suggests: Matrix, Biobase, AnnotationDbi, annotate, Biostrings (>= 2.25.3), SummarizedExperiment (>= 0.1.5), Rsamtools (>= 1.13.53), GenomicAlignments, rtracklayer, BSgenome, GenomicFeatures, Gviz, VariantAnnotation, AnnotationHub, DESeq2, DEXSeq, edgeR, KEGGgraph, RNAseqData.HNRNPC.bam.chr14, pasillaBamSubset, KEGG.db, hgu95av2.db, hgu95av2probe, BSgenome.Scerevisiae.UCSC.sacCer2, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10, TxDb.Athaliana.BioMart.plantsmart22, TxDb.Dmelanogaster.UCSC.dm3.ensGene, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Mmusculus.UCSC.mm10.knownGene, RUnit, digest, knitr, BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: efe660c341dcd0c0b07d2e9086b63434 NeedsCompilation: yes Title: Representation and manipulation of genomic intervals and variables defined along a genome Description: The ability to efficiently represent and manipulate genomic annotations and alignments is playing a central role when it comes to analyzing high-throughput sequencing data (a.k.a. NGS data). The GenomicRanges package defines general purpose containers for storing and manipulating genomic intervals and variables defined along a genome. More specialized containers for representing and manipulating short alignments against a reference genome, or a matrix-like summarization of an experiment, are defined in the GenomicAlignments and SummarizedExperiment packages, respectively. Both packages build on top of the GenomicRanges infrastructure. biocViews: Genetics, Infrastructure, Sequencing, Annotation, Coverage, GenomeAnnotation Author: P. Aboyoun, H. Pagès, and M. Lawrence Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GenomicRanges git_branch: RELEASE_3_8 git_last_commit: ebaad5c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomicRanges_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicRanges_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicRanges_1.34.0.tgz vignettes: vignettes/GenomicRanges/inst/doc/ExtendingGenomicRanges.pdf, vignettes/GenomicRanges/inst/doc/GenomicRangesHOWTOs.pdf, vignettes/GenomicRanges/inst/doc/GRanges_and_GRangesList_slides.pdf, vignettes/GenomicRanges/inst/doc/Ten_things_slides.pdf, vignettes/GenomicRanges/inst/doc/GenomicRangesIntroduction.html vignetteTitles: 5. Extending GenomicRanges, 2. GenomicRanges HOWTOs, 3. A quick introduction to GRanges and GRangesList objects (slides), 4. Ten Things You Didn't Know (slides from BioC 2016), 1. An Introduction to the GenomicRanges Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicRanges/inst/doc/ExtendingGenomicRanges.R, vignettes/GenomicRanges/inst/doc/GenomicRangesHOWTOs.R, vignettes/GenomicRanges/inst/doc/GenomicRangesIntroduction.R, vignettes/GenomicRanges/inst/doc/GRanges_and_GRangesList_slides.R, vignettes/GenomicRanges/inst/doc/Ten_things_slides.R dependsOnMe: AllelicImbalance, AneuFinder, annmap, AnnotationHubData, BaalChIP, Basic4Cseq, baySeq, biomvRCNS, BiSeq, bnbc, BPRMeth, breakpointR, BSgenome, bsseq, BubbleTree, bumphunter, CAFE, CAGEfightR, casper, CHARGE, chimera, chimeraviz, ChIPpeakAnno, ChIPQC, chipseq, chroGPS, chromPlot, chromstaR, chromswitch, CINdex, cleanUpdTSeq, cn.mops, CNPBayes, cnvGSA, CNVPanelizer, COCOA, compEpiTools, consensusSeekeR, CSAR, csaw, deepSNV, DEScan2, DESeq2, DEXSeq, DiffBind, diffHic, DMCHMM, DMRcaller, DMRforPairs, DNAshapeR, DOQTL, EnrichedHeatmap, ensembldb, ensemblVEP, 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alpine, amplican, AnnotationFilter, annotatr, apeglm, appreci8R, ArrayExpressHTS, ASpli, AssessORF, ATACseqQC, BadRegionFinder, ballgown, bamsignals, BBCAnalyzer, beadarray, BEAT, BiFET, BiocOncoTK, biovizBase, BiSeq, branchpointer, BSgenome, CAGEr, CexoR, chipenrich, ChIPexoQual, ChIPseeker, chipseq, ChIPseqR, ChIPSeqSpike, chromDraw, ChromHeatMap, chromVAR, cicero, CNEr, coMET, compartmap, contiBAIT, conumee, copynumber, CopywriteR, CoverageView, crisprseekplus, CrispRVariants, customProDB, DChIPRep, debrowser, DeepBlueR, DEFormats, derfinder, derfinderPlot, diffloop, DMRcate, dmrseq, DominoEffect, DRIMSeq, easyRNASeq, EDASeq, ELMER, epivizr, epivizrData, erma, EventPointer, flipflop, FourCSeq, FunciSNP, GA4GHclient, gcapc, genbankr, geneAttribution, GeneGeneInteR, GENESIS, GenoGAM, genomation, genomeIntervals, GenomicAlignments, GenomicDataCommons, GenomicInteractions, genotypeeval, GenVisR, GGBase, ggbio, GGtools, GOfuncR, GoogleGenomics, gpart, gQTLBase, gQTLstats, gwascat, h5vc, heatmaps, HiCBricks, HiCcompare, HilbertCurve, hiReadsProcessor, HTSeqGenie, icetea, ideal, IMAS, INSPEcT, InterMineR, ipdDb, IsoformSwitchAnalyzeR, isomiRs, iteremoval, IVAS, karyoploteR, loci2path, LOLA, LoomExperiment, lumi, M3D, MACPET, MADSEQ, mCSEA, MDTS, MEAL, MEDIPS, methInheritSim, methyAnalysis, methylInheritance, MethylSeekR, methylumi, MinimumDistance, MIRA, MMDiff2, mosaics, motifbreakR, motifmatchr, MTseeker, MultiAssayExperiment, MultiDataSet, multiHiCcompare, NarrowPeaks, normr, nucleR, oligoClasses, OmaDB, openPrimeR, Organism.dplyr, OrganismDbi, OUTRIDER, panelcn.mops, Pbase, pcaExplorer, pepStat, Pi, PICS, pqsfinder, prebs, primirTSS, proBAMr, PureCN, Pviz, pwOmics, QDNAseq, qpgraph, qPLEXanalyzer, qsea, R3CPET, R453Plus1Toolbox, RareVariantVis, RCAS, recount, regioneR, regionReport, REMP, Repitools, RGMQL, RiboProfiling, Rmmquant, RNAprobR, rnaSeqMap, roar, RTCGAToolbox, scmeth, scoreInvHap, scPipe, scruff, seq2pathway, SeqArray, seqPattern, seqplots, seqsetvis, SeqSQC, SeqVarTools, sesame, sevenC, ShortRead, signeR, simulatorZ, SNPchip, soGGi, SparseSignatures, SplicingGraphs, SPLINTER, srnadiff, STAN, strandCheckR, SVM2CRM, systemPipeR, TCGAbiolinks, TCGAutils, TCseq, TFARM, TFBSTools, TFEA.ChIP, TFHAZ, TitanCNA, tracktables, transcriptR, transite, trena, triplex, TSRchitect, TVTB, TxRegInfra, Uniquorn, VariantFiltering, waveTiling, wiggleplotr suggestsMe: AnnotationHub, biobroom, BiocGenerics, BiocParallel, Chicago, cummeRbund, epivizrChart, GenomeInfoDb, Glimma, GSReg, GWASTools, HDF5Array, interactiveDisplay, IRanges, metaseqR, MiRaGE, NarrowPeaks, NGScopy, omicsPrint, Onassis, RTCGA, S4Vectors, SeqGSEA, TFutils Package: GenomicScores Version: 1.6.0 Depends: R (>= 3.4), S4Vectors (>= 0.7.21), GenomicRanges, methods, BiocGenerics (>= 0.13.8) Imports: utils, XML, Biobase, IRanges (>= 2.3.23), Biostrings, BSgenome, GenomeInfoDb, AnnotationHub Suggests: BiocStyle, knitr, rmarkdown, BSgenome.Hsapiens.UCSC.hg19, phastCons100way.UCSC.hg19, MafDb.1Kgenomes.phase1.hs37d5, SNPlocs.Hsapiens.dbSNP144.GRCh37, VariantAnnotation, TxDb.Hsapiens.UCSC.hg19.knownGene, gwascat, RColorBrewer License: Artistic-2.0 MD5sum: 002dca8198727b7629cf69f5b17b6240 NeedsCompilation: no Title: Infrastructure to work with genomewide position-specific scores Description: Provide infrastructure to store and access genomewide position-specific scores within R and Bioconductor. biocViews: Infrastructure, Genetics, Annotation, Sequencing, Coverage Author: Robert Castelo [aut, cre], Pau Puigdevall [ctb] Maintainer: Robert Castelo URL: https://github.com/rcastelo/GenomicScores VignetteBuilder: knitr BugReports: https://github.com/rcastelo/GenomicScores/issues git_url: https://git.bioconductor.org/packages/GenomicScores git_branch: RELEASE_3_8 git_last_commit: 6644e90 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomicScores_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicScores_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicScores_1.6.0.tgz vignettes: vignettes/GenomicScores/inst/doc/GenomicScores.html vignetteTitles: An introduction to the GenomicScores package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicScores/inst/doc/GenomicScores.R importsMe: appreci8R, ATACseqQC, primirTSS, RareVariantVis, VariantFiltering Package: GenomicTuples Version: 1.16.0 Depends: R (>= 3.3.0), GenomicRanges (>= 1.31.8), GenomeInfoDb (>= 1.15.2), S4Vectors (>= 0.17.25) Imports: methods, BiocGenerics (>= 0.21.2), Rcpp (>= 0.11.2), IRanges (>= 2.13.13), data.table, stats4 LinkingTo: Rcpp Suggests: testthat, knitr, BiocStyle, rmarkdown License: Artistic-2.0 Archs: i386, x64 MD5sum: 9b7b5ed8d0fbd6a214f5556b2c38a4b0 NeedsCompilation: yes Title: Representation and Manipulation of Genomic Tuples Description: GenomicTuples defines general purpose containers for storing genomic tuples. It aims to provide functionality for tuples of genomic co-ordinates that are analogous to those available for genomic ranges in the GenomicRanges Bioconductor package. biocViews: Infrastructure, DataRepresentation, Sequencing Author: Peter Hickey , with contributions from Marcin Cieslik and Hervé Pagès. Maintainer: Peter Hickey URL: www.github.com/PeteHaitch/GenomicTuples VignetteBuilder: knitr BugReports: https://github.com/PeteHaitch/GenomicTuples/issues git_url: https://git.bioconductor.org/packages/GenomicTuples git_branch: RELEASE_3_8 git_last_commit: 3a2cd2b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenomicTuples_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenomicTuples_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenomicTuples_1.16.0.tgz vignettes: vignettes/GenomicTuples/inst/doc/GenomicTuplesIntroduction.html vignetteTitles: GenomicTuplesIntroduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenomicTuples/inst/doc/GenomicTuplesIntroduction.R Package: Genominator Version: 1.36.0 Depends: R (>= 2.10), methods, RSQLite, DBI (>= 0.2-5), BiocGenerics (>= 0.1.0), IRanges (>= 2.5.27), GenomeGraphs Imports: graphics, stats, utils Suggests: biomaRt, ShortRead, yeastRNASeq License: Artistic-2.0 MD5sum: a787b87c5fee3feaea76a0151ccdee50 NeedsCompilation: no Title: Analyze, manage and store genomic data Description: Tools for storing, accessing, analyzing and visualizing genomic data. biocViews: Infrastructure Author: James Bullard, Kasper Daniel Hansen Maintainer: James Bullard git_url: https://git.bioconductor.org/packages/Genominator git_branch: RELEASE_3_8 git_last_commit: d9658ef git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Genominator_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Genominator_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Genominator_1.36.0.tgz vignettes: vignettes/Genominator/inst/doc/Genominator.pdf, vignettes/Genominator/inst/doc/plotting.pdf, vignettes/Genominator/inst/doc/withShortRead.pdf vignetteTitles: The Genominator User Guide, Plotting with Genominator, Working with the ShortRead Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Genominator/inst/doc/Genominator.R, vignettes/Genominator/inst/doc/plotting.R, vignettes/Genominator/inst/doc/withShortRead.R Package: genoset Version: 1.38.0 Depends: R (>= 2.10), BiocGenerics (>= 0.11.3), GenomicRanges (>= 1.17.19), SummarizedExperiment (>= 1.1.6) Imports: S4Vectors (>= 0.13.13), GenomeInfoDb (>= 1.1.3), IRanges (>= 2.5.12), methods, graphics Suggests: testthat, knitr, BiocStyle, rmarkdown, DNAcopy, stats, BSgenome, Biostrings Enhances: parallel License: Artistic-2.0 Archs: i386, x64 MD5sum: 68336a575e2390f041edb49ed5b68477 NeedsCompilation: yes Title: A RangedSummarizedExperiment with methods for copy number analysis Description: GenoSet provides an extension of the RangedSummarizedExperiment class with additional API features. This class provides convenient and fast methods for working with segmented genomic data. Additionally, GenoSet provides the class RleDataFrame which stores runs of data along the genome for multiple samples and provides very fast summaries of arbitrary row sets (regions of the genome). biocViews: Infrastructure, DataRepresentation, Microarray, SNP, CopyNumberVariation Author: Peter M. Haverty Maintainer: Peter M. Haverty URL: https://github.com/phaverty/genoset VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/genoset git_branch: RELEASE_3_8 git_last_commit: a1f8bdc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genoset_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genoset_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genoset_1.38.0.tgz vignettes: vignettes/genoset/inst/doc/genoset.html vignetteTitles: genoset hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genoset/inst/doc/genoset.R importsMe: methyAnalysis, VegaMC Package: genotypeeval Version: 1.14.0 Depends: R (>= 3.4.0), VariantAnnotation Imports: ggplot2, rtracklayer, BiocGenerics, GenomicRanges, GenomeInfoDb, IRanges, methods, BiocParallel, graphics, stats Suggests: rmarkdown, testthat, SNPlocs.Hsapiens.dbSNP141.GRCh38, TxDb.Hsapiens.UCSC.hg38.knownGene License: file LICENSE MD5sum: d8c0444b34549730384bdad50312d814 NeedsCompilation: no Title: QA/QC of a gVCF or VCF file Description: Takes in a gVCF or VCF and reports metrics to assess quality of calls. biocViews: Genetics, BatchEffect, Sequencing, SNP, VariantAnnotation, DataImport Author: Jennifer Tom [aut, cre] Maintainer: Jennifer Tom VignetteBuilder: rmarkdown git_url: https://git.bioconductor.org/packages/genotypeeval git_branch: RELEASE_3_8 git_last_commit: 1a09286 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/genotypeeval_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/genotypeeval_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genotypeeval_1.14.0.tgz vignettes: vignettes/genotypeeval/inst/doc/genotypeeval_vignette.html vignetteTitles: genotypeeval_vignette.html hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Package: genphen Version: 1.10.3 Depends: R (>= 3.5.0), Rcpp (>= 0.12.17), methods, stats, graphics Imports: rstan (>= 2.17.3), rstantools (>= 1.5.0), ranger, parallel, foreach, doParallel, e1071, Biostrings LinkingTo: StanHeaders (>= 2.17.2), rstan (>= 2.17.3), BH (>= 1.66.0-1), Rcpp (>= 0.12.17), RcppEigen (>= 0.3.3.4.0) Suggests: testthat License: GPL (>= 2) Archs: i386, x64 MD5sum: 6c3e3183b08dd7577c4eb0bfc72aacc8 NeedsCompilation: yes Title: A tool for quantification of associations between genotypes and phenotypes in genome wide association studies (GWAS) with Bayesian inference and statistical learning Description: Genetic association studies are an essential tool for studying the relationship between genotypes and phenotypes. With genphen we can jointly study multiple phenotypes of different types, by quantifying the association between different genotypes and each phenotype using a hybrid method which uses statistical learning techniques such as random forest and support vector machines, and Bayesian inference using hierarchical models. biocViews: GenomeWideAssociation, Regression, Classification, SupportVectorMachine, Genetics, SequenceMatching, Bayesian, FeatureExtraction, Sequencing Author: Simo Kitanovski Maintainer: Simo Kitanovski SystemRequirements: GNU make git_url: https://git.bioconductor.org/packages/genphen git_branch: RELEASE_3_8 git_last_commit: 4224c97 git_last_commit_date: 2019-03-11 Date/Publication: 2019-03-11 source.ver: src/contrib/genphen_1.10.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/genphen_1.10.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/genphen_1.10.3.tgz vignettes: vignettes/genphen/inst/doc/genphenManual.pdf vignetteTitles: genphen overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/genphen/inst/doc/genphenManual.R Package: GenRank Version: 1.10.0 Depends: R (>= 3.2.3) Imports: matrixStats, reshape2, survcomp Suggests: knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: 68b7b5b4ad252221ec675ee9f40e0037 NeedsCompilation: no Title: Candidate gene prioritization based on convergent evidence Description: Methods for ranking genes based on convergent evidence obtained from multiple independent evidence layers. This package adapts three methods that are popular for meta-analysis. biocViews: GeneExpression, SNP, CopyNumberVariation, Microarray, Sequencing, Software, Genetics Author: Chakravarthi Kanduri Maintainer: Chakravarthi Kanduri URL: https://github.com/chakri9/GenRank VignetteBuilder: knitr BugReports: https://github.com/chakri9/GenRank/issues git_url: https://git.bioconductor.org/packages/GenRank git_branch: RELEASE_3_8 git_last_commit: 1eb7573 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GenRank_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenRank_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenRank_1.10.0.tgz vignettes: vignettes/GenRank/inst/doc/GenRank_Vignette.html vignetteTitles: Introduction to GenRank Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GenRank/inst/doc/GenRank_Vignette.R Package: GenVisR Version: 1.14.2 Depends: R (>= 3.3.0), methods Imports: AnnotationDbi, biomaRt, BiocGenerics, Biostrings, DBI, FField, GenomicFeatures, GenomicRanges (>= 1.25.4), ggplot2 (>= 2.1.0), grid, gridExtra (>= 2.0.0), gtable, gtools, IRanges (>= 2.7.5), plyr (>= 1.8.3), reshape2, Rsamtools, scales, stats, utils, viridis, data.table, BSgenome, grDevices, GenomeInfoDb, VariantAnnotation Suggests: BiocStyle, BSgenome.Hsapiens.UCSC.hg19, knitr, RMySQL, roxygen2, testthat, TxDb.Hsapiens.UCSC.hg19.knownGene, rmarkdown, vdiffr, formatR, TxDb.Hsapiens.UCSC.hg38.knownGene, BSgenome.Hsapiens.UCSC.hg38 License: GPL-3 + file LICENSE MD5sum: 970d7bdf968cc909da48746af4f61700 NeedsCompilation: no Title: Genomic Visualizations in R Description: Produce highly customizable publication quality graphics for genomic data primarily at the cohort level. biocViews: Infrastructure, DataRepresentation, Classification, DNASeq Author: Zachary Skidmore [aut, cre], Alex Wagner [aut], Robert Lesurf [aut], Katie Campbell [aut], Jason Kunisaki [aut], Obi Griffith [aut], Malachi Griffith [aut] Maintainer: Zachary Skidmore VignetteBuilder: knitr BugReports: https://github.com/griffithlab/GenVisR/issues git_url: https://git.bioconductor.org/packages/GenVisR git_branch: RELEASE_3_8 git_last_commit: 4b931cc git_last_commit_date: 2019-04-04 Date/Publication: 2019-04-04 source.ver: src/contrib/GenVisR_1.14.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/GenVisR_1.14.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GenVisR_1.14.2.tgz vignettes: vignettes/GenVisR/inst/doc/Intro.html, vignettes/GenVisR/inst/doc/Upcoming_Features.html, vignettes/GenVisR/inst/doc/waterfall_introduction.html vignetteTitles: GenVisR: An introduction, Visualizing Small Variants, waterfall: function introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GenVisR/inst/doc/Intro.R, vignettes/GenVisR/inst/doc/Upcoming_Features.R, vignettes/GenVisR/inst/doc/waterfall_introduction.R Package: GEOmetadb Version: 1.44.0 Depends: GEOquery,RSQLite Suggests: knitr, rmarkdown, dplyr, tm, wordcloud License: Artistic-2.0 MD5sum: 9c85e98fb9e4f41fa76e8bac68ff4d35 NeedsCompilation: no Title: A compilation of metadata from NCBI GEO Description: The NCBI Gene Expression Omnibus (GEO) represents the largest public repository of microarray data. However, finding data of interest can be challenging using current tools. GEOmetadb is an attempt to make access to the metadata associated with samples, platforms, and datasets much more feasible. This is accomplished by parsing all the NCBI GEO metadata into a SQLite database that can be stored and queried locally. GEOmetadb is simply a thin wrapper around the SQLite database along with associated documentation. Finally, the SQLite database is updated regularly as new data is added to GEO and can be downloaded at will for the most up-to-date metadata. GEOmetadb paper: http://bioinformatics.oxfordjournals.org/cgi/content/short/24/23/2798 . biocViews: Infrastructure Author: Jack Zhu and Sean Davis Maintainer: Jack Zhu URL: http://gbnci.abcc.ncifcrf.gov/geo/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GEOmetadb git_branch: RELEASE_3_8 git_last_commit: 72a4529 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GEOmetadb_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GEOmetadb_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GEOmetadb_1.44.0.tgz vignettes: vignettes/GEOmetadb/inst/doc/GEOmetadb.html vignetteTitles: GEOmetadb hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GEOmetadb/inst/doc/GEOmetadb.R importsMe: Onassis Package: GEOquery Version: 2.50.5 Depends: methods, Biobase Imports: httr, readr (>= 1.3.1), xml2, dplyr, tidyr, magrittr, limma Suggests: knitr, rmarkdown, BiocGenerics, testthat, covr License: GPL-2 MD5sum: 735b0cfac76e3ae465e8dfcc9d7f4ce5 NeedsCompilation: no Title: Get data from NCBI Gene Expression Omnibus (GEO) Description: The NCBI Gene Expression Omnibus (GEO) is a public repository of microarray data. Given the rich and varied nature of this resource, it is only natural to want to apply BioConductor tools to these data. GEOquery is the bridge between GEO and BioConductor. biocViews: Microarray, DataImport, OneChannel, TwoChannel, SAGE Author: Sean Davis Maintainer: Sean Davis URL: https://github.com/seandavi/GEOquery VignetteBuilder: knitr BugReports: https://github.com/seandavi/GEOquery/issues/new git_url: https://git.bioconductor.org/packages/GEOquery git_branch: RELEASE_3_8 git_last_commit: 135c17f git_last_commit_date: 2018-12-22 Date/Publication: 2018-12-22 source.ver: src/contrib/GEOquery_2.50.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/GEOquery_2.50.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GEOquery_2.50.5.tgz vignettes: vignettes/GEOquery/inst/doc/GEOquery.html vignetteTitles: Using GEOquery hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GEOquery/inst/doc/GEOquery.R dependsOnMe: DrugVsDisease, SCAN.UPC importsMe: bigmelon, ChIPXpress, coexnet, crossmeta, EGAD, GSEABenchmarkeR, MACPET, minfi, MoonlightR, phantasus, recount, SRAdb suggestsMe: AUCell, CAMTHC, ctsGE, diffcoexp, dyebias, ELBOW, EpiDISH, fgsea, multiClust, MultiDataSet, omicsPrint, pathprint, PGSEA, RGSEA, Rnits, runibic, skewr, TargetScore, zFPKM Package: GEOsubmission Version: 1.34.0 Imports: affy, Biobase, utils License: GPL (>= 2) MD5sum: 54b2359778553d53725c9974f1cda515 NeedsCompilation: no Title: Prepares microarray data for submission to GEO Description: Helps to easily submit a microarray dataset and the associated sample information to GEO by preparing a single file for upload (direct deposit). biocViews: Microarray Author: Alexandre Kuhn Maintainer: Alexandre Kuhn git_url: https://git.bioconductor.org/packages/GEOsubmission git_branch: RELEASE_3_8 git_last_commit: 5b61ea2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GEOsubmission_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GEOsubmission_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GEOsubmission_1.34.0.tgz vignettes: vignettes/GEOsubmission/inst/doc/GEOsubmission.pdf vignetteTitles: GEOsubmission Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GEOsubmission/inst/doc/GEOsubmission.R Package: gep2pep Version: 1.2.0 Imports: repo (>= 2.1.1), foreach, stats, utils, GSEABase, methods, Biobase, XML, rhdf5, digest, iterators Suggests: WriteXLS, testthat, knitr, rmarkdown License: GPL-3 MD5sum: fd48276c9acea753df8d96b68a5b5ab0 NeedsCompilation: no Title: Creation and Analysis of Pathway Expression Profiles (PEPs) Description: Pathway Expression Profiles (PEPs) are based on the expression of pathways (defined as sets of genes) as opposed to individual genes. This package converts gene expression profiles to PEPs and performs enrichment analysis of both pathways and experimental conditions, such as "drug set enrichment analysis" and "gene2drug" drug discovery analysis respectively. biocViews: GeneExpression, DifferentialExpression, GeneSetEnrichment, DimensionReduction, Pathways Author: Francesco Napolitano Maintainer: Francesco Napolitano VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gep2pep git_branch: RELEASE_3_8 git_last_commit: fb62d67 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gep2pep_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gep2pep_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gep2pep_1.2.0.tgz vignettes: vignettes/gep2pep/inst/doc/vignette.html vignetteTitles: Introduction to gep2pep hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gep2pep/inst/doc/vignette.R Package: gespeR Version: 1.14.1 Depends: methods, graphics, ggplot2, R(>= 2.10) Imports: Matrix, glmnet, cellHTS2, Biobase, biomaRt, doParallel, parallel, foreach, reshape2, dplyr Suggests: knitr License: GPL-3 MD5sum: 127a58bd025ef4bb29c6bfadc805dbd7 NeedsCompilation: no Title: Gene-Specific Phenotype EstimatoR Description: Estimates gene-specific phenotypes from off-target confounded RNAi screens. The phenotype of each siRNA is modeled based on on-targeted and off-targeted genes, using a regularized linear regression model. biocViews: ImmunoOncology, CellBasedAssays, Preprocessing, GeneTarget, Regression, Visualization Author: Fabian Schmich Maintainer: Fabian Schmich URL: http://www.cbg.ethz.ch/software/gespeR VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gespeR git_branch: RELEASE_3_8 git_last_commit: 3943779 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/gespeR_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gespeR_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gespeR_1.14.1.tgz vignettes: vignettes/gespeR/inst/doc/gespeR.pdf vignetteTitles: An R package for deconvoluting off-target confounded RNAi screens hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gespeR/inst/doc/gespeR.R Package: GEWIST Version: 1.26.0 Depends: R (>= 2.10), car License: GPL-2 MD5sum: d056905b8d6521e06a936955e8fdab08 NeedsCompilation: no Title: Gene Environment Wide Interaction Search Threshold Description: This 'GEWIST' package provides statistical tools to efficiently optimize SNP prioritization for gene-gene and gene-environment interactions. biocViews: MultipleComparison, Genetics Author: Wei Q. Deng, Guillaume Pare Maintainer: Wei Q. Deng git_url: https://git.bioconductor.org/packages/GEWIST git_branch: RELEASE_3_8 git_last_commit: b3773a7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GEWIST_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GEWIST_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GEWIST_1.26.0.tgz vignettes: vignettes/GEWIST/inst/doc/GEWIST.pdf vignetteTitles: GEWIST.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GEWIST/inst/doc/GEWIST.R Package: GGBase Version: 3.44.0 Depends: R (>= 2.14), methods, snpStats Imports: limma, genefilter, Biobase, BiocGenerics, S4Vectors, IRanges, Matrix, AnnotationDbi, digest, GenomicRanges, SummarizedExperiment Suggests: GGtools, illuminaHumanv1.db, knitr License: Artistic-2.0 MD5sum: 126306447c411a4c114df4a7f83fdce7 NeedsCompilation: no Title: GGBase infrastructure for genetics of gene expression package GGtools Description: infrastructure biocViews: Genetics, Infrastructure Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GGBase git_branch: RELEASE_3_8 git_last_commit: ceb1303 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GGBase_3.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GGBase_3.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GGBase_3.44.0.tgz vignettes: vignettes/GGBase/inst/doc/ggbase.pdf vignetteTitles: GGBase -- infrastructure for GGtools,, genetics of gene expression hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GGBase/inst/doc/ggbase.R dependsOnMe: GGtools Package: ggbio Version: 1.30.0 Depends: methods, BiocGenerics, ggplot2 (>= 1.0.0) Imports: grid, grDevices, graphics, stats, utils, gridExtra, scales, reshape2, gtable, Hmisc, biovizBase (>= 1.29.2), Biobase, S4Vectors (>= 0.13.13), IRanges (>= 2.11.16), GenomeInfoDb (>= 1.1.3), GenomicRanges (>= 1.29.14), SummarizedExperiment, Biostrings, Rsamtools (>= 1.17.28), GenomicAlignments (>= 1.1.16), BSgenome, VariantAnnotation (>= 1.11.4), rtracklayer (>= 1.25.16), GenomicFeatures (>= 1.29.11), OrganismDbi, GGally, ensembldb (>= 1.99.13), AnnotationDbi, AnnotationFilter, rlang Suggests: vsn, BSgenome.Hsapiens.UCSC.hg19, Homo.sapiens, TxDb.Hsapiens.UCSC.hg19.knownGene, chipseq, TxDb.Mmusculus.UCSC.mm9.knownGene, knitr, BiocStyle, testthat, EnsDb.Hsapiens.v75, tinytex License: Artistic-2.0 MD5sum: fff6ae2022a12bfc785903fa9f64e7a8 NeedsCompilation: no Title: Visualization tools for genomic data Description: The ggbio package extends and specializes the grammar of graphics for biological data. The graphics are designed to answer common scientific questions, in particular those often asked of high throughput genomics data. All core Bioconductor data structures are supported, where appropriate. The package supports detailed views of particular genomic regions, as well as genome-wide overviews. Supported overviews include ideograms and grand linear views. High-level plots include sequence fragment length, edge-linked interval to data view, mismatch pileup, and several splicing summaries. biocViews: Infrastructure, Visualization Author: Tengfei Yin [aut], Michael Lawrence [aut, ths, cre], Dianne Cook [aut, ths], Johannes Rainer [ctb] Maintainer: Michael Lawrence URL: http://tengfei.github.com/ggbio/ VignetteBuilder: knitr BugReports: https://github.com/tengfei/ggbio/issues git_url: https://git.bioconductor.org/packages/ggbio git_branch: RELEASE_3_8 git_last_commit: 8b05258 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ggbio_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ggbio_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ggbio_1.30.0.tgz vignettes: vignettes/ggbio/inst/doc/ggbio.pdf vignetteTitles: Part 0: Introduction and quick start hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: CAFE, intansv importsMe: derfinderPlot, FourCSeq, gwascat, msgbsR, Pi, R3CPET, Rariant, ReportingTools, RiboProfiling, scruff, SomaticSignatures suggestsMe: beadarray, ensembldb, GoogleGenomics, gQTLstats, interactiveDisplay, regionReport, RnBeads Package: ggcyto Version: 1.10.2 Depends: methods, ggplot2(>= 2.2.1.9000), flowCore(>= 1.41.5), ncdfFlow(>= 2.17.1), flowWorkspace(>= 3.17.24) Imports: plyr, scales, data.table, RColorBrewer, gridExtra, rlang Suggests: testthat, flowWorkspaceData, knitr, rmarkdown, flowStats, openCyto, flowViz, ggridges, vdiffr License: Artistic-2.0 MD5sum: e0920fe47092b142ac3e9e9207e05869 NeedsCompilation: no Title: Visualize Cytometry data with ggplot Description: With the dedicated fortify method implemented for flowSet, ncdfFlowSet and GatingSet classes, both raw and gated flow cytometry data can be plotted directly with ggplot. ggcyto wrapper and some customed layers also make it easy to add gates and population statistics to the plot. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays, Infrastructure, Visualization Author: Mike Jiang Maintainer: Mike Jiang URL: https://github.com/RGLab/ggcyto/issues VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ggcyto git_branch: RELEASE_3_8 git_last_commit: e3dd40f git_last_commit_date: 2019-01-14 Date/Publication: 2019-01-14 source.ver: src/contrib/ggcyto_1.10.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/ggcyto_1.10.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ggcyto_1.10.2.tgz vignettes: vignettes/ggcyto/inst/doc/autoplot.html, vignettes/ggcyto/inst/doc/ggcyto.flowSet.html, vignettes/ggcyto/inst/doc/ggcyto.GatingSet.html, vignettes/ggcyto/inst/doc/Top_features_of_ggcyto.html vignetteTitles: Quick plot for cytometry data, Visualize flowSet with ggcyto, Visualize GatingSet with ggcyto, Feature summary of ggcyto hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ggcyto/inst/doc/autoplot.R, vignettes/ggcyto/inst/doc/ggcyto.flowSet.R, vignettes/ggcyto/inst/doc/ggcyto.GatingSet.R, vignettes/ggcyto/inst/doc/Top_features_of_ggcyto.R importsMe: CytoML suggestsMe: flowCore, flowWorkspace, openCyto Package: GGtools Version: 5.18.0 Depends: R (>= 2.14), GGBase (>= 3.19.7), data.table, parallel, Homo.sapiens Imports: methods, utils, stats, BiocGenerics (>= 0.25.1), snpStats, ff, Rsamtools, AnnotationDbi, Biobase, bit, VariantAnnotation, hexbin, rtracklayer, Gviz, stats4, S4Vectors (>= 0.9.25), IRanges, GenomeInfoDb, GenomicRanges (>= 1.29.6), iterators, Biostrings, ROCR, biglm, ggplot2, reshape2 Suggests: GGdata, illuminaHumanv1.db, SNPlocs.Hsapiens.dbSNP144.GRCh37, multtest, aod, rmeta Enhances: MatrixEQTL, foreach, doParallel, gwascat License: Artistic-2.0 MD5sum: 7c5237419693c7989d912bd329dd982b NeedsCompilation: no Title: software and data for analyses in genetics of gene expression Description: software and data for analyses in genetics of gene expression and/or DNA methylation biocViews: Genetics, GeneExpression, GeneticVariability, SNP Author: VJ Carey Maintainer: VJ Carey git_url: https://git.bioconductor.org/packages/GGtools git_branch: RELEASE_3_8 git_last_commit: a112a77 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GGtools_5.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GGtools_5.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GGtools_5.18.0.tgz vignettes: vignettes/GGtools/inst/doc/GGtools.pdf vignetteTitles: GGtools: software for eQTL identification hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GGtools/inst/doc/GGtools.R importsMe: GeneGeneInteR suggestsMe: GGBase, gQTLBase Package: ggtree Version: 1.14.6 Depends: R (>= 3.4.0) Imports: ape, dplyr, ggplot2 (>= 3.0.0), grDevices, grid, magrittr, methods, purrr, rlang, rvcheck (>= 0.1.0), scales, tibble, tidyr, tidytree (>= 0.1.9), treeio (>= 1.3.14), utils Suggests: colorspace, cowplot, emojifont, ggimage, knitr, prettydoc, rmarkdown, testthat License: Artistic-2.0 MD5sum: 24ac81b25f9cf479493198f55b4468a1 NeedsCompilation: no Title: an R package for visualization and annotation of phylogenetic trees with their covariates and other associated data Description: 'ggtree' extends the 'ggplot2' plotting system which implemented the grammar of graphics. 'ggtree' is designed for visualization and annotation of phylogenetic trees with their covariates and other associated data. biocViews: Alignment, Annotation, Clustering, DataImport, MultipleSequenceAlignment, ReproducibleResearch, Software, Visualization Author: Guangchuang Yu [aut, cre, cph] (), Tommy Tsan-Yuk Lam [aut, ths], Justin Silverman [ctb], Bradley Jones [ctb], Watal M. Iwasaki [ctb] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/ggtree VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/ggtree/issues git_url: https://git.bioconductor.org/packages/ggtree git_branch: RELEASE_3_8 git_last_commit: 85a8780 git_last_commit_date: 2019-01-14 Date/Publication: 2019-01-14 source.ver: src/contrib/ggtree_1.14.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/ggtree_1.14.6.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ggtree_1.14.6.tgz vignettes: vignettes/ggtree/inst/doc/ggtree.html, vignettes/ggtree/inst/doc/treeAnnotation.html, vignettes/ggtree/inst/doc/treeManipulation.html, vignettes/ggtree/inst/doc/treeVisualization.html vignetteTitles: 01 ggtree Introduction, 04 Tree Annotation, 03 Tree Manipulation, 02 Tree Visualization hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ggtree/inst/doc/ggtree.R, vignettes/ggtree/inst/doc/treeAnnotation.R, vignettes/ggtree/inst/doc/treeManipulation.R, vignettes/ggtree/inst/doc/treeVisualization.R importsMe: LINC, LymphoSeq, philr, singleCellTK, universalmotif suggestsMe: metagenomeFeatures, treeio Package: GIGSEA Version: 1.0.0 Depends: R (>= 3.5), Matrix, MASS, locfdr, stats, utils Suggests: knitr, rmarkdown License: LGPL-3 MD5sum: b2a1158dd46f573307badd416a2c2206 NeedsCompilation: no Title: Genotype Imputed Gene Set Enrichment Analysis Description: We presented the Genotype-imputed Gene Set Enrichment Analysis (GIGSEA), a novel method that uses GWAS-and-eQTL-imputed trait-associated differential gene expression to interrogate gene set enrichment for the trait-associated SNPs. By incorporating eQTL from large gene expression studies, e.g. GTEx, GIGSEA appropriately addresses such challenges for SNP enrichment as gene size, gene boundary, SNP distal regulation, and multiple-marker regulation. The weighted linear regression model, taking as weights both imputation accuracy and model completeness, was used to perform the enrichment test, properly adjusting the bias due to redundancy in different gene sets. The permutation test, furthermore, is used to evaluate the significance of enrichment, whose efficiency can be largely elevated by expressing the computational intensive part in terms of large matrix operation. We have shown the appropriate type I error rates for GIGSEA (<5%), and the preliminary results also demonstrate its good performance to uncover the real signal. biocViews: GeneSetEnrichment,SNP,VariantAnnotation,GeneExpression,GeneRegulation,Regression,DifferentialExpression Author: Shijia Zhu Maintainer: Shijia Zhu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GIGSEA git_branch: RELEASE_3_8 git_last_commit: 945edad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GIGSEA_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GIGSEA_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GIGSEA_1.0.0.tgz vignettes: vignettes/GIGSEA/inst/doc/GIGSEA_tutorial.pdf vignetteTitles: GIGSEA: Genotype Imputed Gene Set Enrichment Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GIGSEA/inst/doc/GIGSEA_tutorial.R Package: girafe Version: 1.34.0 Depends: R (>= 2.10.0), methods, BiocGenerics (>= 0.13.8), S4Vectors (>= 0.17.25), Rsamtools (>= 1.31.2), intervals (>= 0.13.1), ShortRead (>= 1.37.1), genomeIntervals (>= 1.25.1), grid Imports: methods, Biobase, Biostrings (>= 2.47.6), graphics, grDevices, stats, utils, IRanges (>= 2.13.12) Suggests: MASS, org.Mm.eg.db, RColorBrewer Enhances: genomeIntervals License: Artistic-2.0 Archs: i386, x64 MD5sum: 18a9eabd7dba531cefb42bbd99372c25 NeedsCompilation: yes Title: Genome Intervals and Read Alignments for Functional Exploration Description: The package 'girafe' deals with the genome-level representation of aligned reads from next-generation sequencing data. It contains an object class for enabling a detailed description of genome intervals with aligned reads and functions for comparing, visualising, exporting and working with such intervals and the aligned reads. As such, the package interacts with and provides a link between the packages ShortRead, IRanges and genomeIntervals. biocViews: Sequencing Author: Joern Toedling, with contributions from Constance Ciaudo, Olivier Voinnet, Edith Heard, Emmanuel Barillot, and Wolfgang Huber Maintainer: J. Toedling git_url: https://git.bioconductor.org/packages/girafe git_branch: RELEASE_3_8 git_last_commit: d2764ce git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/girafe_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/girafe_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/girafe_1.34.0.tgz vignettes: vignettes/girafe/inst/doc/girafe.pdf vignetteTitles: Genome intervals and read alignments for functional exploration hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/girafe/inst/doc/girafe.R Package: GISPA Version: 1.6.0 Depends: R (>= 3.3.2) Imports: Biobase, changepoint, data.table, genefilter, graphics, GSEABase, HH, lattice, latticeExtra, plyr, scatterplot3d, stats Suggests: knitr License: GPL-2 MD5sum: 6f8b3bfbd6ddbb19055508854568fa4b NeedsCompilation: no Title: GISPA: Method for Gene Integrated Set Profile Analysis Description: GISPA is a method intended for the researchers who are interested in defining gene sets with similar, a priori specified molecular profile. GISPA method has been previously published in Nucleic Acid Research (Kowalski et al., 2016; PMID: 26826710). biocViews: StatisticalMethod,GeneSetEnrichment,GenomeWideAssociation Author: Bhakti Dwivedi and Jeanne Kowalski Maintainer: Bhakti Dwivedi VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GISPA git_branch: RELEASE_3_8 git_last_commit: 564ccf7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GISPA_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GISPA_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GISPA_1.6.0.tgz vignettes: vignettes/GISPA/inst/doc/GISPA_manual.html vignetteTitles: GISPA:Method for Gene Integrated Set Profile Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GISPA/inst/doc/GISPA_manual.R Package: GLAD Version: 2.46.0 Depends: R (>= 2.10) Imports: aws License: GPL-2 Archs: i386, x64 MD5sum: a27d757cf431fe1ca45706b90060d032 NeedsCompilation: yes Title: Gain and Loss Analysis of DNA Description: Analysis of array CGH data : detection of breakpoints in genomic profiles and assignment of a status (gain, normal or loss) to each chromosomal regions identified. biocViews: Microarray, CopyNumberVariation Author: Philippe Hupe Maintainer: Philippe Hupe URL: http://bioinfo.curie.fr SystemRequirements: gsl. Note: users should have GSL installed. Windows users: 'consult the README file available in the inst directory of the source distribution for necessary configuration instructions'. git_url: https://git.bioconductor.org/packages/GLAD git_branch: RELEASE_3_8 git_last_commit: 41a6cb7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GLAD_2.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GLAD_2.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GLAD_2.46.0.tgz vignettes: vignettes/GLAD/inst/doc/GLAD.pdf vignetteTitles: GLAD hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GLAD/inst/doc/GLAD.R dependsOnMe: ADaCGH2, ITALICS, MANOR, seqCNA importsMe: ITALICS, MANOR, snapCGH suggestsMe: RnBeads Package: Glimma Version: 1.10.1 Depends: R (>= 3.4.0) Imports: edgeR, grDevices, jsonlite, methods, stats, S4Vectors, utils Suggests: BiocStyle, IRanges, GenomicRanges, SummarizedExperiment, DESeq2, limma, testthat, knitr, rmarkdown, pryr License: GPL-3 | file LICENSE MD5sum: df85a720ef95a30e9f19ca7536a9bfe3 NeedsCompilation: no Title: Interactive HTML graphics Description: This package generates interactive visualisations for analysis of RNA-sequencing data using output from limma, edgeR or DESeq2 packages in an HTML page. The interactions are built on top of the popular static representations of analysis results in order to provide additional information. biocViews: ImmunoOncology, DifferentialExpression, GeneExpression, Microarray, ReportWriting, RNASeq, Sequencing, Visualization Author: Shian Su [aut, cre], Matthew Ritchie [aut], Charity Law [aut], Stuart Lee [ctb] Maintainer: Shian Su URL: https://github.com/Shians/Glimma VignetteBuilder: knitr BugReports: https://github.com/Shians/Glimma/issues git_url: https://git.bioconductor.org/packages/Glimma git_branch: RELEASE_3_8 git_last_commit: ffc7abc git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Glimma_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Glimma_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Glimma_1.10.1.tgz vignettes: vignettes/Glimma/inst/doc/Glimma.pdf vignetteTitles: Glimma Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Glimma/inst/doc/Glimma.R importsMe: EGSEA Package: glmSparseNet Version: 1.0.0 Depends: R (>= 3.5), Matrix, MultiAssayExperiment, glmnet Imports: SummarizedExperiment, STRINGdb, biomaRt, futile.logger, sparsebn, sparsebnUtils, forcats, dplyr, readr, ggplot2, survminer, reshape2, stats, stringr, rlang, parallel, methods, loose.rock Suggests: testthat, knitr, rmarkdown, survival, survcomp, pROC, VennDiagram, BiocStyle, curatedTCGAData, TCGAutils License: GPL (>=3) MD5sum: 9ed879fd69f8bd537dcefa694c561bce NeedsCompilation: no Title: Network Centrality Metrics for Elastic-Net Regularized Models Description: glmSparseNet is an R-package that generalizes sparse regression models when the features (e.g. genes) have a graph structure (e.g. protein-protein interactions), by including network-based regularizers. glmSparseNet uses the glmnet R-package, by including centrality measures of the network as penalty weights in the regularization. The current version implements regularization based on node degree, i.e. the strength and/or number of its associated edges, either by promoting hubs in the solution or orphan genes in the solution. All the glmnet distribution families are supported, namely "gaussian", "poisson", "binomial", "multinomial", "cox", and "mgaussian". biocViews: Software, StatisticalMethod, DimensionReduction, Regression, Classification, Survival, Network, GraphAndNetwork Author: André Veríssimo [aut, cre], Susana Vinga [aut], Eunice Carrasquinha [ctb], Marta Lopes [ctb] Maintainer: André Veríssimo URL: https://www.github.com/sysbiomed/glmSparseNet VignetteBuilder: knitr BugReports: https://www.github.com/sysbiomed/glmSparseNet/issues git_url: https://git.bioconductor.org/packages/glmSparseNet git_branch: RELEASE_3_8 git_last_commit: 3ddc9ef git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/glmSparseNet_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/glmSparseNet_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/glmSparseNet_1.0.0.tgz vignettes: vignettes/glmSparseNet/inst/doc/example_brca_logistic.html, vignettes/glmSparseNet/inst/doc/example_brca_protein-protein-interactions_survival.html, vignettes/glmSparseNet/inst/doc/example_brca_survival.html, vignettes/glmSparseNet/inst/doc/example_prad_survival.html, vignettes/glmSparseNet/inst/doc/example_skcm_survival.html vignetteTitles: Example for Classification -- Breast Invasive Carcinoma, Breast survival dataset using network from STRING DB, Example for Survival Data -- Breast Invasive Carcinoma, Example for Survival Data -- Prostate Adenocarcinoma, Example for Survival Data -- Skin Melanoma hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/glmSparseNet/inst/doc/example_brca_logistic.R, vignettes/glmSparseNet/inst/doc/example_brca_protein-protein-interactions_survival.R, vignettes/glmSparseNet/inst/doc/example_brca_survival.R, vignettes/glmSparseNet/inst/doc/example_prad_survival.R, vignettes/glmSparseNet/inst/doc/example_skcm_survival.R Package: GlobalAncova Version: 4.0.0 Depends: methods, corpcor, globaltest Imports: annotate, AnnotationDbi, Biobase, dendextend, GSEABase, VGAM Suggests: GO.db, KEGG.db, golubEsets, hu6800.db, vsn, Rgraphviz License: GPL (>= 2) Archs: i386, x64 MD5sum: 9f9fd66217449c73f94bf8bd70ba82bb NeedsCompilation: yes Title: Global test for groups of variables via model comparisons Description: The association between a variable of interest (e.g. two groups) and the global pattern of a group of variables (e.g. a gene set) is tested via a global F-test. We give the following arguments in support of the GlobalAncova approach: After appropriate normalisation, gene-expression-data appear rather symmetrical and outliers are no real problem, so least squares should be rather robust. ANCOVA with interaction yields saturated data modelling e.g. different means per group and gene. Covariate adjustment can help to correct for possible selection bias. Variance homogeneity and uncorrelated residuals cannot be expected. Application of ordinary least squares gives unbiased, but no longer optimal estimates (Gauss-Markov-Aitken). Therefore, using the classical F-test is inappropriate, due to correlation. The test statistic however mirrors deviations from the null hypothesis. In combination with a permutation approach, empirical significance levels can be approximated. Alternatively, an approximation yields asymptotic p-values. The framework is generalized to groups of categorical variables or even mixed data by a likelihood ratio approach. Closed and hierarchical testing procedures are supported. This work was supported by the NGFN grant 01 GR 0459, BMBF, Germany and BMBF grant 01ZX1309B, Germany. biocViews: Microarray, OneChannel, DifferentialExpression, Pathways, Regression Author: U. Mansmann, R. Meister, M. Hummel, R. Scheufele, with contributions from S. Knueppel Maintainer: Manuela Hummel git_url: https://git.bioconductor.org/packages/GlobalAncova git_branch: RELEASE_3_8 git_last_commit: ef226ba git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GlobalAncova_4.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GlobalAncova_4.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GlobalAncova_4.0.0.tgz vignettes: vignettes/GlobalAncova/inst/doc/GlobalAncova.pdf, vignettes/GlobalAncova/inst/doc/GlobalAncovaDecomp.pdf vignetteTitles: GlobalAncova.pdf, GlobalAncovaDecomp.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GlobalAncova/inst/doc/GlobalAncova.R, vignettes/GlobalAncova/inst/doc/GlobalAncovaDecomp.R Package: globalSeq Version: 1.10.1 Depends: R (>= 3.0.0) Suggests: knitr, testthat, SummarizedExperiment, S4Vectors License: GPL-3 MD5sum: b8378c9ceb14159be27fb3fcd47ee8fc NeedsCompilation: no Title: Global Test for Counts Description: The method may be conceptualised as a test of overall significance in regression analysis, where the response variable is overdispersed and the number of explanatory variables exceeds the sample size. Useful for testing for association between RNA-Seq and high-dimensional data. biocViews: ImmunoOncology, GeneExpression, ExonArray, DifferentialExpression, GenomeWideAssociation, Transcriptomics, DimensionReduction, Regression, Sequencing, WholeGenome, RNASeq, ExomeSeq, miRNA, MultipleComparison Author: Armin Rauschenberger [aut, cre] Maintainer: Armin Rauschenberger URL: https://github.com/rauschenberger/globalSeq VignetteBuilder: knitr BugReports: https://github.com/rauschenberger/globalSeq/issues git_url: https://git.bioconductor.org/packages/globalSeq git_branch: RELEASE_3_8 git_last_commit: ff16856 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/globalSeq_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/globalSeq_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/globalSeq_1.10.1.tgz vignettes: vignettes/globalSeq/inst/doc/globalSeq.pdf, vignettes/globalSeq/inst/doc/article.html, vignettes/globalSeq/inst/doc/vignette.html vignetteTitles: globalSeq, pkgdown, pkgdown hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/globalSeq/inst/doc/globalSeq.R Package: globaltest Version: 5.36.0 Depends: methods, survival Imports: Biobase, AnnotationDbi, annotate, graphics Suggests: vsn, golubEsets, KEGG.db, hu6800.db, Rgraphviz, GO.db, lungExpression, org.Hs.eg.db, GSEABase, penalized, gss, MASS, boot, rpart License: GPL (>= 2) MD5sum: 0c2d22bf1ee33788c7ab870b595e78b0 NeedsCompilation: no Title: Testing Groups of Covariates/Features for Association with a Response Variable, with Applications to Gene Set Testing Description: The global test tests groups of covariates (or features) for association with a response variable. This package implements the test with diagnostic plots and multiple testing utilities, along with several functions to facilitate the use of this test for gene set testing of GO and KEGG terms. biocViews: Microarray, OneChannel, Bioinformatics, DifferentialExpression, GO, Pathways Author: Jelle Goeman and Jan Oosting, with contributions by Livio Finos and Aldo Solari Maintainer: Jelle Goeman git_url: https://git.bioconductor.org/packages/globaltest git_branch: RELEASE_3_8 git_last_commit: a97475f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/globaltest_5.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/globaltest_5.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/globaltest_5.36.0.tgz vignettes: vignettes/globaltest/inst/doc/GlobalTest.pdf vignetteTitles: Global Test hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/globaltest/inst/doc/GlobalTest.R dependsOnMe: GlobalAncova importsMe: BiSeq, EGSEA, SIM suggestsMe: topGO Package: gmapR Version: 1.24.2 Depends: R (>= 2.15.0), methods, GenomeInfoDb (>= 1.1.3), GenomicRanges (>= 1.31.8), Rsamtools (>= 1.31.2) Imports: S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), BiocGenerics (>= 0.25.1), rtracklayer (>= 1.39.7), GenomicFeatures (>= 1.31.3), Biostrings, VariantAnnotation (>= 1.25.11), tools, Biobase, BSgenome, GenomicAlignments (>= 1.15.6), BiocParallel Suggests: RUnit, BSgenome.Dmelanogaster.UCSC.dm3, BSgenome.Scerevisiae.UCSC.sacCer3, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome.Hsapiens.UCSC.hg19, LungCancerLines License: Artistic-2.0 MD5sum: dd6df01657a3a6bb12f82d4607a6ecf0 NeedsCompilation: yes Title: An R interface to the GMAP/GSNAP/GSTRUCT suite Description: GSNAP and GMAP are a pair of tools to align short-read data written by Tom Wu. This package provides convenience methods to work with GMAP and GSNAP from within R. In addition, it provides methods to tally alignment results on a per-nucleotide basis using the bam_tally tool. biocViews: Alignment Author: Cory Barr, Thomas Wu, Michael Lawrence Maintainer: Michael Lawrence git_url: https://git.bioconductor.org/packages/gmapR git_branch: RELEASE_3_8 git_last_commit: 7bcf7c4 git_last_commit_date: 2019-02-05 Date/Publication: 2019-02-05 source.ver: src/contrib/gmapR_1.24.2.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gmapR_1.24.2.tgz vignettes: vignettes/gmapR/inst/doc/gmapR.pdf vignetteTitles: gmapR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gmapR/inst/doc/gmapR.R dependsOnMe: HTSeqGenie importsMe: MTseeker suggestsMe: VariantTools Package: GMRP Version: 1.10.1 Depends: R(>= 3.3.0),stats,utils,graphics, grDevices, diagram, plotrix, base,GenomicRanges Suggests: BiocStyle, BiocGenerics License: GPL (>= 2) MD5sum: 4103cc393e2719f8324e96f4fcc67c9c NeedsCompilation: no Title: GWAS-based Mendelian Randomization and Path Analyses Description: Perform Mendelian randomization analysis of multiple SNPs to determine risk factors causing disease of study and to exclude confounding variabels and perform path analysis to construct path of risk factors to the disease. biocViews: Sequencing, Regression, SNP Author: Yuan-De Tan Maintainer: Yuan-De Tan git_url: https://git.bioconductor.org/packages/GMRP git_branch: RELEASE_3_8 git_last_commit: 7516bfb git_last_commit_date: 2018-11-26 Date/Publication: 2018-11-26 source.ver: src/contrib/GMRP_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GMRP_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GMRP_1.10.1.tgz vignettes: vignettes/GMRP/inst/doc/GMRP-manual.pdf, vignettes/GMRP/inst/doc/GMRP.pdf vignetteTitles: GMRP-manual.pdf, Causal Effect Analysis of Risk Factors for Disease with the "GMRP" package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GMRP/inst/doc/GMRP.R Package: GOexpress Version: 1.16.1 Depends: R (>= 3.4), grid, stats, graphics, Biobase (>= 2.22.0) Imports: biomaRt (>= 2.18.0), stringr (>= 0.6.2), ggplot2 (>= 0.9.0), RColorBrewer (>= 1.0), gplots (>= 2.13.0), randomForest (>= 4.6), RCurl (>= 1.95) Suggests: BiocStyle License: GPL (>= 3) MD5sum: 57cdb880bcb1886070d784cdca9a148b NeedsCompilation: no Title: Visualise microarray and RNAseq data using gene ontology annotations Description: The package contains methods to visualise the expression profile of genes from a microarray or RNA-seq experiment, and offers a supervised clustering approach to identify GO terms containing genes with expression levels that best classify two or more predefined groups of samples. Annotations for the genes present in the expression dataset may be obtained from Ensembl through the biomaRt package, if not provided by the user. The default random forest framework is used to evaluate the capacity of each gene to cluster samples according to the factor of interest. Finally, GO terms are scored by averaging the rank (alternatively, score) of their respective gene sets to cluster the samples. P-values may be computed to assess the significance of GO term ranking. Visualisation function include gene expression profile, gene ontology-based heatmaps, and hierarchical clustering of experimental samples using gene expression data. biocViews: ImmunoOncology, Software, GeneExpression, Transcription, DifferentialExpression, GeneSetEnrichment, DataRepresentation, Clustering, TimeCourse, Microarray, Sequencing, RNASeq, Annotation, MultipleComparison, Pathways, GO, Visualization Author: Kevin Rue-Albrecht [aut, cre], Tharvesh M.L. Ali [ctb], Paul A. McGettigan [ctb], Belinda Hernandez [ctb], David A. Magee [ctb], Nicolas C. Nalpas [ctb], Andrew Parnell [ctb], Stephen V. Gordon [ths], David E. MacHugh [ths] Maintainer: Kevin Rue-Albrecht URL: https://github.com/kevinrue/GOexpress git_url: https://git.bioconductor.org/packages/GOexpress git_branch: RELEASE_3_8 git_last_commit: a9b01a7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GOexpress_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOexpress_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOexpress_1.16.1.tgz vignettes: vignettes/GOexpress/inst/doc/GOexpress-UsersGuide.pdf vignetteTitles: UsersGuide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOexpress/inst/doc/GOexpress-UsersGuide.R Package: GOfuncR Version: 1.2.0 Depends: R (>= 3.4), vioplot (>= 0.2), Imports: Rcpp (>= 0.11.5), mapplots (>= 1.5), gtools (>= 3.5.0), GenomicRanges (>= 1.28.4), IRanges, AnnotationDbi, utils, grDevices, graphics, stats, LinkingTo: Rcpp Suggests: Homo.sapiens, BiocStyle, knitr, testthat License: GPL (>= 2) Archs: i386, x64 MD5sum: 751400dc73371df5c86c87511fecdede NeedsCompilation: yes Title: Gene ontology enrichment using FUNC Description: GOfuncR performs a gene ontology enrichment analysis based on the ontology enrichment software FUNC. GO-annotations are obtained from OrganismDb or OrgDb packages ('Homo.sapiens' by default); the GO-graph is included in the package and updated regularly (11-Oct-2018). GOfuncR provides the standard candidate vs. background enrichment analysis using the hypergeometric test, as well as three additional tests: (i) the Wilcoxon rank-sum test that is used when genes are ranked, (ii) a binomial test that is used when genes are associated with two counts and (iii) a Chi-square or Fisher's exact test that is used in cases when genes are associated with four counts. To correct for multiple testing and interdependency of the tests, family-wise error rates are computed based on random permutations of the gene-associated variables. GOfuncR also provides tools for exploring the ontology graph and the annotations, and options to take gene-length or spatial clustering of genes into account. It is also possible to provide custom gene coordinates, annotations and ontologies. biocViews: GeneSetEnrichment, GO Author: Steffi Grote Maintainer: Steffi Grote VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GOfuncR git_branch: RELEASE_3_8 git_last_commit: 140a3ce git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOfuncR_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOfuncR_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOfuncR_1.2.0.tgz vignettes: vignettes/GOfuncR/inst/doc/GOfuncR.html vignetteTitles: Introduction to GOfuncR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOfuncR/inst/doc/GOfuncR.R importsMe: ABAEnrichment Package: GOFunction Version: 1.30.0 Depends: R (>= 2.11.0), methods, Biobase (>= 2.8.0), graph (>= 1.26.0), Rgraphviz (>= 1.26.0), GO.db (>= 2.4.1), AnnotationDbi (>= 1.10.2), SparseM (>= 0.85) Imports: methods, Biobase, graph, Rgraphviz, GO.db, AnnotationDbi, DBI, SparseM License: GPL (>= 2) MD5sum: 72307dd4950cad125f42856c1153729b NeedsCompilation: no Title: GO-function: deriving biologcially relevant functions from statistically significant functions Description: The GO-function package provides a tool to address the redundancy that result from the GO structure or multiple annotation genes and derive biologically relevant functions from the statistically significant functions based on some intuitive assumption and statistical testing. biocViews: GO, Pathways, Microarray, GeneSetEnrichment Author: Jing Wang Maintainer: Jing Wang git_url: https://git.bioconductor.org/packages/GOFunction git_branch: RELEASE_3_8 git_last_commit: 9891bd6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOFunction_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOFunction_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOFunction_1.30.0.tgz vignettes: vignettes/GOFunction/inst/doc/GOFunction.pdf vignetteTitles: GO-function hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOFunction/inst/doc/GOFunction.R Package: GoogleGenomics Version: 2.4.0 Depends: R (>= 3.1.0), GenomicAlignments (>= 1.0.1), VariantAnnotation Imports: Biostrings, GenomeInfoDb, GenomicRanges, IRanges, httr, rjson, Rsamtools, S4Vectors (>= 0.9.25), Biobase, methods, utils Suggests: BiocStyle, RProtoBuf, httpuv, knitr, rmarkdown, testthat, ggbio, ggplot2, BSgenome.Hsapiens.UCSC.hg19, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene License: Apache License (== 2.0) | file LICENSE Archs: i386, x64 MD5sum: 8617e932deeb38b5cb428ef2707b247e NeedsCompilation: yes Title: R Client for Google Genomics API Description: Provides an R package to interact with the Google Genomics API. biocViews: DataImport, ThirdPartyClient, Genetics Author: Cassie Doll, Nicole Deflaux Maintainer: Siddhartha Bagaria URL: https://cloud.google.com/genomics/ SystemRequirements: GNU make VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/GoogleGenomics/issues PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/GoogleGenomics git_branch: RELEASE_3_8 git_last_commit: a4b96ab git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GoogleGenomics_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GoogleGenomics_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GoogleGenomics_2.4.0.tgz vignettes: vignettes/GoogleGenomics/inst/doc/AnnotatingVariants.html, vignettes/GoogleGenomics/inst/doc/PlottingAlignments.html, vignettes/GoogleGenomics/inst/doc/VariantAnnotation-comparison-test.html vignetteTitles: Annotating Variants, Plotting Alignments, Reproducing Variant Annotation Results hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GoogleGenomics/inst/doc/AnnotatingVariants.R, vignettes/GoogleGenomics/inst/doc/PlottingAlignments.R, vignettes/GoogleGenomics/inst/doc/VariantAnnotation-comparison-test.R Package: GOpro Version: 1.8.0 Depends: R (>= 3.4) Imports: AnnotationDbi, dendextend, doParallel, foreach, parallel, org.Hs.eg.db, GO.db, Rcpp, stats, graphics, MultiAssayExperiment, IRanges, S4Vectors LinkingTo: Rcpp, BH Suggests: knitr, rmarkdown, RTCGA.PANCAN12, BiocStyle, testthat License: GPL-3 Archs: i386, x64 MD5sum: 5d1245837ea8262a04366bef11ae4cf7 NeedsCompilation: yes Title: Find the most characteristic gene ontology terms for groups of human genes Description: Find the most characteristic gene ontology terms for groups of human genes. This package was created as a part of the thesis which was developed under the auspices of MI^2 Group (http://mi2.mini.pw.edu.pl/, https://github.com/geneticsMiNIng). biocViews: Annotation, Clustering, GO, GeneExpression, GeneSetEnrichment, MultipleComparison Author: Lidia Chrabaszcz Maintainer: Lidia Chrabaszcz URL: https://github.com/mi2-warsaw/GOpro VignetteBuilder: knitr BugReports: https://github.com/mi2-warsaw/GOpro/issues git_url: https://git.bioconductor.org/packages/GOpro git_branch: RELEASE_3_8 git_last_commit: 2faa9b8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOpro_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOpro_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOpro_1.8.0.tgz vignettes: vignettes/GOpro/inst/doc/GOpro_vignette.html vignetteTitles: GOpro: Determine groups of genes and find their characteristic GO term hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOpro/inst/doc/GOpro_vignette.R Package: goProfiles Version: 1.44.0 Depends: Biobase, AnnotationDbi, GO.db, CompQuadForm, stringr Suggests: org.Hs.eg.db License: GPL-2 MD5sum: cee2739892a0f493ca62346297a00d42 NeedsCompilation: no Title: goProfiles: an R package for the statistical analysis of functional profiles Description: The package implements methods to compare lists of genes based on comparing the corresponding 'functional profiles'. biocViews: Annotation, GO, GeneExpression, GeneSetEnrichment, GraphAndNetwork, Microarray, MultipleComparison, Pathways, Software Author: Alex Sanchez, Jordi Ocana and Miquel Salicru Maintainer: Alex Sanchez git_url: https://git.bioconductor.org/packages/goProfiles git_branch: RELEASE_3_8 git_last_commit: 9306d2f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/goProfiles_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/goProfiles_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/goProfiles_1.44.0.tgz vignettes: vignettes/goProfiles/inst/doc/goProfiles-comparevisual.pdf, vignettes/goProfiles/inst/doc/goProfiles-plotProfileMF.pdf, vignettes/goProfiles/inst/doc/goProfiles.pdf vignetteTitles: goProfiles-comparevisual.pdf, goProfiles-plotProfileMF.pdf, goProfiles Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/goProfiles/inst/doc/goProfiles.R Package: GOSemSim Version: 2.8.0 Depends: R (>= 3.4.0) Imports: AnnotationDbi, GO.db, methods, utils LinkingTo: Rcpp Suggests: AnnotationHub, BiocManager, clusterProfiler, DOSE, knitr, org.Hs.eg.db, prettydoc, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: 8f4ba171e35070a482be6ea54d0cc814 NeedsCompilation: yes Title: GO-terms Semantic Similarity Measures Description: The semantic comparisons of Gene Ontology (GO) annotations provide quantitative ways to compute similarities between genes and gene groups, and have became important basis for many bioinformatics analysis approaches. GOSemSim is an R package for semantic similarity computation among GO terms, sets of GO terms, gene products and gene clusters. GOSemSim implemented five methods proposed by Resnik, Schlicker, Jiang, Lin and Wang respectively. biocViews: Annotation, GO, Clustering, Pathways, Network, Software Author: Guangchuang Yu [aut, cre], Alexey Stukalov [ctb], Chuanle Xiao [ctb], Lluís Revilla Sancho [ctb] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/GOSemSim VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/GOSemSim/issues git_url: https://git.bioconductor.org/packages/GOSemSim git_branch: RELEASE_3_8 git_last_commit: c8c985b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOSemSim_2.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOSemSim_2.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOSemSim_2.8.0.tgz vignettes: vignettes/GOSemSim/inst/doc/GOSemSim.html vignetteTitles: An introduction to GOSemSim hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOSemSim/inst/doc/GOSemSim.R dependsOnMe: tRanslatome importsMe: clusterProfiler, DOSE, enrichplot, meshes, Rcpi suggestsMe: BioCor, epiNEM, FELLA, SemDist Package: goseq Version: 1.34.1 Depends: R (>= 2.11.0), BiasedUrn, geneLenDataBase (>= 1.9.2) Imports: mgcv, graphics, stats, utils, AnnotationDbi, GO.db,BiocGenerics Suggests: edgeR, org.Hs.eg.db, rtracklayer License: LGPL (>= 2) MD5sum: f521a65052ddd286a3b0aa5a5f106f85 NeedsCompilation: no Title: Gene Ontology analyser for RNA-seq and other length biased data Description: Detects Gene Ontology and/or other user defined categories which are over/under represented in RNA-seq data biocViews: ImmunoOncology, Sequencing, GO, GeneExpression, Transcription, RNASeq Author: Matthew Young Maintainer: Nadia Davidson , Anthony Hawkins git_url: https://git.bioconductor.org/packages/goseq git_branch: RELEASE_3_8 git_last_commit: bad217b git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/goseq_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/goseq_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/goseq_1.34.1.tgz vignettes: vignettes/goseq/inst/doc/goseq.pdf vignetteTitles: goseq User's Guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/goseq/inst/doc/goseq.R dependsOnMe: rgsepd importsMe: ideal, PathwaySplice, SMITE Package: GOSim Version: 1.20.0 Depends: GO.db, annotate Imports: org.Hs.eg.db, AnnotationDbi, topGO, cluster, flexmix, RBGL, graph, Matrix, corpcor, Rcpp LinkingTo: Rcpp Enhances: igraph License: GPL (>= 2) Archs: i386, x64 MD5sum: 87d1eb1841be4fa7d9c2e145051806c5 NeedsCompilation: yes Title: Computation of functional similarities between GO terms and gene products; GO enrichment analysis Description: This package implements several functions useful for computing similarities between GO terms and gene products based on their GO annotation. Moreover it allows for computing a GO enrichment analysis biocViews: GO, Clustering, Software, Pathways Author: Holger Froehlich Maintainer: Holger Froehlich git_url: https://git.bioconductor.org/packages/GOSim git_branch: RELEASE_3_8 git_last_commit: b83ce5e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOSim_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOSim_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOSim_1.20.0.tgz vignettes: vignettes/GOSim/inst/doc/GOSim.pdf vignetteTitles: GOsim hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOSim/inst/doc/GOSim.R Package: goSTAG Version: 1.6.1 Depends: R (>= 3.4) Imports: AnnotationDbi, biomaRt, GO.db, graphics, memoise, stats, utils Suggests: BiocStyle, knitr, rmarkdown, testthat License: GPL-3 MD5sum: 7e6c56c3730f5b5601d6ca456d4a8922 NeedsCompilation: no Title: A tool to use GO Subtrees to Tag and Annotate Genes within a set Description: Gene lists derived from the results of genomic analyses are rich in biological information. For instance, differentially expressed genes (DEGs) from a microarray or RNA-Seq analysis are related functionally in terms of their response to a treatment or condition. Gene lists can vary in size, up to several thousand genes, depending on the robustness of the perturbations or how widely different the conditions are biologically. Having a way to associate biological relatedness between hundreds and thousands of genes systematically is impractical by manually curating the annotation and function of each gene. Over-representation analysis (ORA) of genes was developed to identify biological themes. Given a Gene Ontology (GO) and an annotation of genes that indicate the categories each one fits into, significance of the over-representation of the genes within the ontological categories is determined by a Fisher's exact test or modeling according to a hypergeometric distribution. Comparing a small number of enriched biological categories for a few samples is manageable using Venn diagrams or other means for assessing overlaps. However, with hundreds of enriched categories and many samples, the comparisons are laborious. Furthermore, if there are enriched categories that are shared between samples, trying to represent a common theme across them is highly subjective. goSTAG uses GO subtrees to tag and annotate genes within a set. goSTAG visualizes the similarities between the over-representation of DEGs by clustering the p-values from the enrichment statistical tests and labels clusters with the GO term that has the most paths to the root within the subtree generated from all the GO terms in the cluster. biocViews: GeneExpression, DifferentialExpression, GeneSetEnrichment, Clustering, Microarray, mRNAMicroarray, RNASeq, Visualization, GO, ImmunoOncology Author: Brian D. Bennett and Pierre R. Bushel Maintainer: Brian D. Bennett VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/goSTAG git_branch: RELEASE_3_8 git_last_commit: b36ec25 git_last_commit_date: 2018-11-29 Date/Publication: 2018-12-01 source.ver: src/contrib/goSTAG_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/goSTAG_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/goSTAG_1.6.1.tgz vignettes: vignettes/goSTAG/inst/doc/goSTAG.html vignetteTitles: The goSTAG User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/goSTAG/inst/doc/goSTAG.R Package: GOstats Version: 2.48.0 Depends: R (>= 2.10), Biobase (>= 1.15.29), Category (>= 2.43.2), graph Imports: methods, stats, stats4, AnnotationDbi (>= 0.0.89), GO.db (>= 1.13.0), RBGL, annotate (>= 1.13.2), AnnotationForge, Rgraphviz Suggests: hgu95av2.db (>= 1.13.0), ALL, multtest, genefilter, RColorBrewer, xtable, SparseM, GSEABase, geneplotter, org.Hs.eg.db, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: 5f5df1dbb7717f909a32a5ed83159006 NeedsCompilation: no Title: Tools for manipulating GO and microarrays Description: A set of tools for interacting with GO and microarray data. A variety of basic manipulation tools for graphs, hypothesis testing and other simple calculations. biocViews: Annotation, GO, MultipleComparison, GeneExpression, Microarray, Pathways, GeneSetEnrichment, GraphAndNetwork Author: Robert Gentleman [aut], Seth Falcon [ctb], Robert Castelo [ctb], Bioconductor Package Maintainer [cre] Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/GOstats git_branch: RELEASE_3_8 git_last_commit: 5db7020 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOstats_2.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOstats_2.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOstats_2.48.0.tgz vignettes: vignettes/GOstats/inst/doc/GOstatsForUnsupportedOrganisms.pdf, vignettes/GOstats/inst/doc/GOstatsHyperG.pdf, vignettes/GOstats/inst/doc/GOvis.pdf vignetteTitles: Hypergeometric tests for less common model organisms, Hypergeometric Tests Using GOstats, Visualizing Data Using GOstats hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOstats/inst/doc/GOstatsForUnsupportedOrganisms.R, vignettes/GOstats/inst/doc/GOstatsHyperG.R, vignettes/GOstats/inst/doc/GOvis.R dependsOnMe: MineICA, RDAVIDWebService importsMe: affycoretools, attract, categoryCompare, ideal, MIGSA, miRLAB, pcaExplorer, systemPipeR suggestsMe: BiocCaseStudies, Category, eisa, fastLiquidAssociation, GSEAlm, HTSanalyzeR, interactiveDisplay, MineICA, MLP, MmPalateMiRNA, qpgraph, RnBeads, safe Package: GOsummaries Version: 2.18.0 Depends: R (>= 2.15), Rcpp Imports: plyr, grid, gProfileR, reshape2, limma, ggplot2, gtable LinkingTo: Rcpp Suggests: vegan License: GPL (>= 2) Archs: i386, x64 MD5sum: ea44c2e32bb5f0d12f0aad1b5ffdcdce NeedsCompilation: yes Title: Word cloud summaries of GO enrichment analysis Description: A package to visualise Gene Ontology (GO) enrichment analysis results on gene lists arising from different analyses such clustering or PCA. The significant GO categories are visualised as word clouds that can be combined with different plots summarising the underlying data. biocViews: GeneExpression, Clustering, GO, Visualization Author: Raivo Kolde Maintainer: Raivo Kolde URL: https://github.com/raivokolde/GOsummaries git_url: https://git.bioconductor.org/packages/GOsummaries git_branch: RELEASE_3_8 git_last_commit: d2ab8c4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GOsummaries_2.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOsummaries_2.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOsummaries_2.18.0.tgz vignettes: vignettes/GOsummaries/inst/doc/GOsummaries-basics.pdf vignetteTitles: GOsummaries basics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOsummaries/inst/doc/GOsummaries-basics.R Package: GOTHiC Version: 1.18.1 Depends: R (>= 2.15.1), methods, utils, GenomicRanges, Biostrings, BSgenome, data.table Imports: BiocGenerics, S4Vectors (>= 0.9.38), IRanges, Rsamtools, ShortRead, rtracklayer, ggplot2 Suggests: HiCDataLymphoblast Enhances: parallel License: GPL-3 MD5sum: 75d75848bc836cfc3451497abfe41243 NeedsCompilation: no Title: Binomial test for Hi-C data analysis Description: This is a Hi-C analysis package using a cumulative binomial test to detect interactions between distal genomic loci that have significantly more reads than expected by chance in Hi-C experiments. It takes mapped paired NGS reads as input and gives back the list of significant interactions for a given bin size in the genome. biocViews: ImmunoOncology, Sequencing, Preprocessing, Epigenetics, HiC Author: Borbala Mifsud and Robert Sugar Maintainer: Borbala Mifsud git_url: https://git.bioconductor.org/packages/GOTHiC git_branch: RELEASE_3_8 git_last_commit: 7a8cdd4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GOTHiC_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GOTHiC_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GOTHiC_1.18.1.tgz vignettes: vignettes/GOTHiC/inst/doc/package_vignettes.pdf vignetteTitles: package_vignettes.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GOTHiC/inst/doc/package_vignettes.R Package: goTools Version: 1.56.0 Depends: GO.db Imports: AnnotationDbi, GO.db, graphics, grDevices Suggests: hgu133a.db License: GPL-2 MD5sum: 61fbb92f3f3abdcb58dfdf024fe10d84 NeedsCompilation: no Title: Functions for Gene Ontology database Description: Wraper functions for description/comparison of oligo ID list using Gene Ontology database biocViews: Microarray,GO,Visualization Author: Yee Hwa (Jean) Yang , Agnes Paquet Maintainer: Agnes Paquet git_url: https://git.bioconductor.org/packages/goTools git_branch: RELEASE_3_8 git_last_commit: c10fd9d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/goTools_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/goTools_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/goTools_1.56.0.tgz vignettes: vignettes/goTools/inst/doc/goTools.pdf vignetteTitles: goTools overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/goTools/inst/doc/goTools.R Package: gpart Version: 1.0.3 Depends: R (>= 3.5.0), grid, Homo.sapiens, TxDb.Hsapiens.UCSC.hg38.knownGene, Imports: igraph, biomaRt, Rcpp, data.table, OrganismDbi, AnnotationDbi, grDevices, stats, utils, GenomicRanges, IRanges LinkingTo: Rcpp Suggests: knitr, rmarkdown, BiocStyle, testthat License: MIT + file LICENSE Archs: i386, x64 MD5sum: fcf82ce2280f7bab3e4259ec627ed4dc NeedsCompilation: yes Title: Human genome partitioning of dense sequencing data by identifying haplotype blocks Description: we provide a new SNP sequence partitioning method which partitions the whole SNP sequence based on not only LD block structures but also gene location information. The LD block construction for GPART is performed using Big-LD algorithm, with additional improvement from previous version reported in Kim et al.(2017). We also add a visualization tool to show the LD heatmap with the information of LD block boundaries and gene locations in the package. biocViews: Software, Clustering Author: Sun Ah Kim [aut, cre, cph], Yun Joo Yoo [aut, cph] Maintainer: Sun Ah Kim VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gpart git_branch: RELEASE_3_8 git_last_commit: 7fdaae0 git_last_commit_date: 2019-03-31 Date/Publication: 2019-04-01 source.ver: src/contrib/gpart_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/gpart_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gpart_1.0.3.tgz vignettes: vignettes/gpart/inst/doc/gpart.html vignetteTitles: Your Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/gpart/inst/doc/gpart.R Package: gpls Version: 1.54.0 Imports: stats Suggests: MASS License: Artistic-2.0 MD5sum: 0ff76e002a0dcaa8da6bfb4435129896 NeedsCompilation: no Title: Classification using generalized partial least squares Description: Classification using generalized partial least squares for two-group and multi-group (more than 2 group) classification. biocViews: Classification, Microarray, Regression Author: Beiying Ding Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/gpls git_branch: RELEASE_3_8 git_last_commit: 6197171 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gpls_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gpls_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gpls_1.54.0.tgz vignettes: vignettes/gpls/inst/doc/gpls.pdf vignetteTitles: gpls Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gpls/inst/doc/gpls.R suggestsMe: MCRestimate, MLInterfaces Package: gprege Version: 1.26.0 Depends: R (>= 2.10), gptk Suggests: spam License: AGPL-3 MD5sum: 8c3464efa7978c37ba0203de3ae063ae NeedsCompilation: no Title: Gaussian Process Ranking and Estimation of Gene Expression time-series Description: The gprege package implements the methodology described in Kalaitzis & Lawrence (2011) "A simple approach to ranking differentially expressed gene expression time-courses through Gaussian process regression". The software fits two GPs with the an RBF (+ noise diagonal) kernel on each profile. One GP kernel is initialised wih a short lengthscale hyperparameter, signal variance as the observed variance and a zero noise variance. It is optimised via scaled conjugate gradients (netlab). A second GP has fixed hyperparameters: zero inverse-width, zero signal variance and noise variance as the observed variance. The log-ratio of marginal likelihoods of the two hypotheses acts as a score of differential expression for the profile. Comparison via ROC curves is performed against BATS (Angelini et.al, 2007). A detailed discussion of the ranking approach and dataset used can be found in the paper (http://www.biomedcentral.com/1471-2105/12/180). biocViews: Microarray, Preprocessing, Bioinformatics, DifferentialExpression, TimeCourse Author: Alfredo Kalaitzis Maintainer: Alfredo Kalaitzis BugReports: alkalait@gmail.com git_url: https://git.bioconductor.org/packages/gprege git_branch: RELEASE_3_8 git_last_commit: 634cc15 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gprege_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gprege_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gprege_1.26.0.tgz vignettes: vignettes/gprege/inst/doc/gprege_quick.pdf vignetteTitles: gprege Quick Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gprege/inst/doc/gprege_quick.R Package: gQTLBase Version: 1.14.0 Imports: GenomicRanges, methods, BatchJobs, BBmisc, S4Vectors, BiocGenerics, foreach, doParallel, bit, ff, rtracklayer, ffbase, GenomicFiles, SummarizedExperiment Suggests: geuvStore2, knitr, rmarkdown, BiocStyle, RUnit, GGtools, Homo.sapiens, IRanges, erma, GenomeInfoDb, gwascat, geuvPack License: Artistic-2.0 MD5sum: 0b4b30b4c1152b7f98e2c7a8f2f130d9 NeedsCompilation: no Title: gQTLBase: infrastructure for eQTL, mQTL and similar studies Description: Infrastructure for eQTL, mQTL and similar studies. Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gQTLBase git_branch: RELEASE_3_8 git_last_commit: ed26678 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gQTLBase_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gQTLBase_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gQTLBase_1.14.0.tgz vignettes: vignettes/gQTLBase/inst/doc/gQTLBase.html vignetteTitles: gQTLBase infrastructure for eQTL archives hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gQTLBase/inst/doc/gQTLBase.R importsMe: gQTLstats Package: gQTLstats Version: 1.14.1 Depends: R (>= 3.1.0), Homo.sapiens Imports: methods, snpStats, BiocGenerics, S4Vectors (>= 0.9.25), IRanges, GenomeInfoDb, GenomicFiles, GenomicRanges, SummarizedExperiment, VariantAnnotation, Biobase, BatchJobs, gQTLBase, limma, mgcv, dplyr, AnnotationDbi, GenomicFeatures, ggplot2, reshape2, doParallel, foreach, ffbase, BBmisc, beeswarm, HardyWeinberg, graphics, stats, utils, shiny, plotly, erma, ggbeeswarm Suggests: geuvPack, geuvStore2, Rsamtools, knitr, rmarkdown, ggbio, BiocStyle, RUnit, multtest, gwascat, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene, ldblock License: Artistic-2.0 MD5sum: ea1b9a23888994108a07fb9b092f9513 NeedsCompilation: no Title: gQTLstats: computationally efficient analysis for eQTL and allied studies Description: computationally efficient analysis of eQTL, mQTL, dsQTL, etc. Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gQTLstats git_branch: RELEASE_3_8 git_last_commit: 4c3ac12 git_last_commit_date: 2019-03-20 Date/Publication: 2019-03-20 source.ver: src/contrib/gQTLstats_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gQTLstats_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gQTLstats_1.14.1.tgz vignettes: vignettes/gQTLstats/inst/doc/gQTLstats.html vignetteTitles: gQTLstats: statistics for genetics of genomic features hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gQTLstats/inst/doc/gQTLstats.R importsMe: gwascat Package: graph Version: 1.60.0 Depends: R (>= 2.10), methods, BiocGenerics (>= 0.13.11) Imports: stats, stats4, utils Suggests: SparseM (>= 0.36), XML, RBGL, RUnit, cluster Enhances: Rgraphviz License: Artistic-2.0 Archs: i386, x64 MD5sum: ee2a677386e14496f7efcdb18b033bff NeedsCompilation: yes Title: graph: A package to handle graph data structures Description: A package that implements some simple graph handling capabilities. biocViews: GraphAndNetwork Author: R. Gentleman, Elizabeth Whalen, W. Huber, S. Falcon Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/graph git_branch: RELEASE_3_8 git_last_commit: e2aecb0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/graph_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/graph_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/graph_1.60.0.tgz vignettes: vignettes/graph/inst/doc/clusterGraph.pdf, vignettes/graph/inst/doc/graph.pdf, vignettes/graph/inst/doc/graphAttributes.pdf, vignettes/graph/inst/doc/GraphClass.pdf, vignettes/graph/inst/doc/MultiGraphClass.pdf vignetteTitles: clusterGraph and distGraph, Graph, Attributes for Graph Objects, Graph Design, graphBAM and MultiGraph classes hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/graph/inst/doc/clusterGraph.R, vignettes/graph/inst/doc/graph.R, vignettes/graph/inst/doc/graphAttributes.R, vignettes/graph/inst/doc/GraphClass.R, vignettes/graph/inst/doc/MultiGraphClass.R dependsOnMe: apComplex, biocGraph, BioMVCClass, BioNet, BLMA, CellNOptR, clipper, CNORfeeder, EnrichmentBrowser, gaggle, GOFunction, GOstats, GraphAT, GSEABase, hypergraph, maigesPack, MineICA, NetSAM, pathRender, Pigengene, pkgDepTools, RbcBook1, RBGL, RBioinf, RCyjs, RDAVIDWebService, Rgraphviz, ROntoTools, RpsiXML, SRAdb, topGO, vtpnet importsMe: alpine, AnalysisPageServer, BgeeDB, BiocCheck, biocGraph, biocViews, CAMERA, Category, categoryCompare, chimeraviz, ChIPpeakAnno, CHRONOS, CytoML, DAPAR, DEGraph, DEsubs, epiNEM, EventPointer, ExperimentHubData, FEM, flowCL, flowClust, flowCore, flowUtils, flowWorkspace, gage, GeneNetworkBuilder, GOFunction, GOSim, GraphAT, graphite, gwascat, HTSanalyzeR, hyperdraw, KEGGgraph, keggorthology, MIGSA, NCIgraph, NeighborNet, nem, netresponse, OncoSimulR, OrganismDbi, pathview, PCpheno, PhenStat, pkgDepTools, ppiStats, pwOmics, qpgraph, RchyOptimyx, RCy3, RGraph2js, rsbml, Rtreemix, signet, SplicingGraphs, Streamer, ToPASeq, trackViewer, VariantFiltering suggestsMe: AnnotationDbi, BiocCaseStudies, DEGraph, EBcoexpress, ecolitk, GeneAnswers, KEGGlincs, MmPalateMiRNA, netbenchmark, NetPathMiner, rBiopaxParser, rTRM, S4Vectors, SPIA, VariantTools Package: GraphAlignment Version: 1.46.0 License: file LICENSE License_restricts_use: yes Archs: i386, x64 MD5sum: bdea26bff023e6e73179fc7d34097a1a NeedsCompilation: yes Title: GraphAlignment Description: Graph alignment is an extension package for the R programming environment which provides functions for finding an alignment between two networks based on link and node similarity scores. (J. Berg and M. Laessig, "Cross-species analysis of biological networks by Bayesian alignment", PNAS 103 (29), 10967-10972 (2006)) biocViews: GraphAndNetwork, Network Author: Joern P. Meier , Michal Kolar, Ville Mustonen, Michael Laessig, and Johannes Berg. Maintainer: Joern P. Meier URL: http://www.thp.uni-koeln.de/~berg/GraphAlignment/ git_url: https://git.bioconductor.org/packages/GraphAlignment git_branch: RELEASE_3_8 git_last_commit: 3de4130 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GraphAlignment_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GraphAlignment_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GraphAlignment_1.46.0.tgz vignettes: vignettes/GraphAlignment/inst/doc/GraphAlignment.pdf vignetteTitles: GraphAlignment hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GraphAlignment/inst/doc/GraphAlignment.R Package: GraphAT Version: 1.54.0 Depends: R (>= 2.10), graph, methods Imports: graph, MCMCpack, methods, stats License: LGPL MD5sum: 01fbc5e58324e882d6885a62e4c037c5 NeedsCompilation: no Title: Graph Theoretic Association Tests Description: Functions and data used in Balasubramanian, et al. (2004) biocViews: Network, GraphAndNetwork Author: R. Balasubramanian, T. LaFramboise, D. Scholtens Maintainer: Thomas LaFramboise git_url: https://git.bioconductor.org/packages/GraphAT git_branch: RELEASE_3_8 git_last_commit: 3fb3491 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GraphAT_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GraphAT_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GraphAT_1.54.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: graphite Version: 1.28.2 Depends: R (>= 2.10), methods Imports: AnnotationDbi, checkmate, graph, httr, rappdirs, stats, utils Suggests: a4Preproc, ALL, BiocStyle, clipper, codetools, hgu133plus2.db, hgu95av2.db, impute, knitr, org.Hs.eg.db, parallel, R.rsp, RCy3, rmarkdown, SPIA (>= 2.2), testthat, topologyGSA (>= 1.4.0) License: AGPL-3 MD5sum: f0dc9917ebb03a2711270681bea60e6f NeedsCompilation: no Title: GRAPH Interaction from pathway Topological Environment Description: Graph objects from pathway topology derived from Biocarta, HumanCyc, KEGG, NCI, Panther, PathBank, PharmGKB, Reactome and SMPDB databases. biocViews: Pathways, ThirdPartyClient, GraphAndNetwork, Network, Reactome, KEGG, BioCarta, Metabolomics Author: Gabriele Sales , Enrica Calura , Chiara Romualdi Maintainer: Gabriele Sales VignetteBuilder: R.rsp git_url: https://git.bioconductor.org/packages/graphite git_branch: RELEASE_3_8 git_last_commit: 875f94b git_last_commit_date: 2019-01-15 Date/Publication: 2019-01-18 source.ver: src/contrib/graphite_1.28.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/graphite_1.28.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/graphite_1.28.2.tgz vignettes: vignettes/graphite/inst/doc/graphite.pdf, vignettes/graphite/inst/doc/metabolites.pdf vignetteTitles: GRAPH Interaction from pathway Topological Environment, metabolites.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/graphite/inst/doc/graphite.R dependsOnMe: ToPASeq importsMe: EnrichmentBrowser, mogsa, ReactomePA, StarBioTrek suggestsMe: clipper, signet Package: GraphPAC Version: 1.24.0 Depends: R(>= 2.15),iPAC, igraph, TSP, RMallow Suggests: RUnit, BiocGenerics License: GPL-2 MD5sum: a4ca5bc3f6a808a8fbdadf2da251e745 NeedsCompilation: no Title: Identification of Mutational Clusters in Proteins via a Graph Theoretical Approach. Description: Identifies mutational clusters of amino acids in a protein while utilizing the proteins tertiary structure via a graph theoretical model. biocViews: Clustering, Proteomics Author: Gregory Ryslik, Hongyu Zhao Maintainer: Gregory Ryslik git_url: https://git.bioconductor.org/packages/GraphPAC git_branch: RELEASE_3_8 git_last_commit: 02da345 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GraphPAC_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GraphPAC_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GraphPAC_1.24.0.tgz vignettes: vignettes/GraphPAC/inst/doc/GraphPAC.pdf vignetteTitles: iPAC: identification of Protein Amino acid Mutations hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GraphPAC/inst/doc/GraphPAC.R dependsOnMe: QuartPAC Package: GRENITS Version: 1.34.0 Depends: R (>= 2.12.0), Rcpp (>= 0.8.6), RcppArmadillo (>= 0.2.8), ggplot2 (>= 0.9.0) Imports: graphics, grDevices, reshape2, stats, utils LinkingTo: Rcpp, RcppArmadillo Suggests: network License: GPL (>= 2) Archs: i386, x64 MD5sum: 70f49c97897e351c99d0b6c2394f520b NeedsCompilation: yes Title: Gene Regulatory Network Inference Using Time Series Description: The package offers four network inference statistical models using Dynamic Bayesian Networks and Gibbs Variable Selection: a linear interaction model, two linear interaction models with added experimental noise (Gaussian and Student distributed) for the case where replicates are available and a non-linear interaction model. biocViews: NetworkInference, GeneRegulation, TimeCourse, GraphAndNetwork, GeneExpression, Network, Bayesian Author: Edward Morrissey Maintainer: Edward Morrissey git_url: https://git.bioconductor.org/packages/GRENITS git_branch: RELEASE_3_8 git_last_commit: cdbb850 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GRENITS_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GRENITS_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GRENITS_1.34.0.tgz vignettes: vignettes/GRENITS/inst/doc/GRENITS_package.pdf vignetteTitles: GRENITS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GRENITS/inst/doc/GRENITS_package.R Package: GreyListChIP Version: 1.14.0 Depends: R (>= 3.5), methods, GenomicRanges Imports: GenomicAlignments, BSgenome, Rsamtools, rtracklayer, MASS, parallel, GenomeInfoDb, SummarizedExperiment, stats, utils Suggests: BiocStyle, BiocGenerics, RUnit Enhances: BSgenome.Hsapiens.UCSC.hg19 License: Artistic-2.0 MD5sum: ff01f53cc4c0b6c6a42e908cc436bdb4 NeedsCompilation: no Title: Grey Lists -- Mask Artefact Regions Based on ChIP Inputs Description: Identify regions of ChIP experiments with high signal in the input, that lead to spurious peaks during peak calling. Remove reads aligning to these regions prior to peak calling, for cleaner ChIP analysis. biocViews: ChIPSeq, Alignment, Preprocessing, DifferentialPeakCalling, Sequencing, GenomeAnnotation, Coverage Author: Gord Brown Maintainer: Gordon Brown git_url: https://git.bioconductor.org/packages/GreyListChIP git_branch: RELEASE_3_8 git_last_commit: a269832 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GreyListChIP_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GreyListChIP_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GreyListChIP_1.14.0.tgz vignettes: vignettes/GreyListChIP/inst/doc/GreyList-demo.pdf vignetteTitles: Generating Grey Lists from Input Libraries hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GreyListChIP/inst/doc/GreyList-demo.R Package: GRmetrics Version: 1.8.1 Depends: R (>= 3.3), SummarizedExperiment Imports: drc, plotly, ggplot2, S4Vectors Suggests: knitr, rmarkdown, BiocStyle License: GPL-3 MD5sum: b8489f60afaf6fdd7a7d8607051bf841 NeedsCompilation: no Title: Calculate growth-rate inhibition (GR) metrics Description: Functions for calculating and visualizing growth-rate inhibition (GR) metrics. biocViews: ImmunoOncology, CellBasedAssays, CellBiology, Software, TimeCourse, Visualization Author: Nicholas Clark Maintainer: Nicholas Clark , Mario Medvedovic URL: https://github.com/uc-bd2k/GRmetrics VignetteBuilder: knitr BugReports: https://github.com/uc-bd2k/GRmetrics/issues git_url: https://git.bioconductor.org/packages/GRmetrics git_branch: RELEASE_3_8 git_last_commit: 23541ea git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GRmetrics_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GRmetrics_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GRmetrics_1.8.1.tgz vignettes: vignettes/GRmetrics/inst/doc/GRmetrics-vignette.html vignetteTitles: GRmetrics: an R package for calculation and visualization of dose-response metrics based on growth rate inhibition hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GRmetrics/inst/doc/GRmetrics-vignette.R Package: groHMM Version: 1.16.0 Depends: R (>= 3.0.2), MASS, parallel, S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), GenomeInfoDb, GenomicRanges (>= 1.31.8), GenomicAlignments (>= 1.15.6), rtracklayer (>= 1.39.7) Suggests: BiocStyle, GenomicFeatures, edgeR, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene License: GPL-3 Archs: i386, x64 MD5sum: 3d1cc353a06a4bc8d282f3712167ade0 NeedsCompilation: yes Title: GRO-seq Analysis Pipeline Description: A pipeline for the analysis of GRO-seq data. biocViews: Sequencing, Software Author: Charles G. Danko, Minho Chae, Andre Martins, W. Lee Kraus Maintainer: Anusha Nagari , Tulip Nandu , W. Lee Kraus URL: https://github.com/Kraus-Lab/groHMM BugReports: https://github.com/Kraus-Lab/groHMM/issues git_url: https://git.bioconductor.org/packages/groHMM git_branch: RELEASE_3_8 git_last_commit: 218ef0f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/groHMM_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/groHMM_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/groHMM_1.16.0.tgz vignettes: vignettes/groHMM/inst/doc/groHMM.pdf vignetteTitles: groHMM tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/groHMM/inst/doc/groHMM.R Package: GRridge Version: 1.6.0 Depends: R (>= 3.2), penalized, Iso, survival, methods, graph,stats,glmnet,mvtnorm Suggests: testthat License: GPL-3 MD5sum: d5da4e835e460089ca8be2f16538e44c NeedsCompilation: no Title: Better prediction by use of co-data: Adaptive group-regularized ridge regression Description: This package allows the use of multiple sources of co-data (e.g. external p-values, gene lists, annotation) to improve prediction of binary, continuous and survival response using (logistic, linear or Cox) group-regularized ridge regression. It also facilitates post-hoc variable selection and prediction diagnostics by cross-validation using ROC curves and AUC. biocViews: Classification, Regression, Survival, Bayesian, RNASeq, GenePrediction, GeneExpression, Pathways, GeneSetEnrichment, GO, KEGG, GraphAndNetwork Author: Mark A. van de Wiel , Putri W. Novianti Maintainer: Mark A. van de Wiel git_url: https://git.bioconductor.org/packages/GRridge git_branch: RELEASE_3_8 git_last_commit: 3670d28 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GRridge_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GRridge_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GRridge_1.6.0.tgz vignettes: vignettes/GRridge/inst/doc/GRridge.pdf vignetteTitles: GRridge hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GRridge/inst/doc/GRridge.R Package: GSALightning Version: 1.10.0 Depends: R (>= 3.3.0) Imports: Matrix, data.table, stats Suggests: knitr, rmarkdown License: GPL (>=2) MD5sum: 28383657aa63e5f8fe8140563135c3d0 NeedsCompilation: no Title: Fast Permutation-based Gene Set Analysis Description: GSALightning provides a fast implementation of permutation-based gene set analysis for two-sample problem. This package is particularly useful when testing simultaneously a large number of gene sets, or when a large number of permutations is necessary for more accurate p-values estimation. biocViews: Software, BiologicalQuestion, GeneSetEnrichment, DifferentialExpression, GeneExpression, Transcription Author: Billy Heung Wing Chang Maintainer: Billy Heung Wing Chang URL: https://github.com/billyhw/GSALightning VignetteBuilder: knitr BugReports: https://github.com/billyhw/GSALightning/issues git_url: https://git.bioconductor.org/packages/GSALightning git_branch: RELEASE_3_8 git_last_commit: 6f1b6cd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSALightning_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSALightning_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSALightning_1.10.0.tgz vignettes: vignettes/GSALightning/inst/doc/vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/GSALightning/inst/doc/vignette.R Package: GSAR Version: 1.16.0 Depends: R (>= 3.0.1), igraph (>= 0.7.1) Imports: stats, graphics Suggests: MASS, GSVAdata, ALL, tweeDEseqCountData, GSEABase, annotate, org.Hs.eg.db, Biobase, genefilter, hgu95av2.db, edgeR, BiocStyle License: GPL (>=2) MD5sum: dfc4fe251c7b1129b68af45dfb7a3d4d NeedsCompilation: no Title: Gene Set Analysis in R Description: Gene set analysis using specific alternative hypotheses. Tests for differential expression, scale and net correlation structure. biocViews: Software, StatisticalMethod, DifferentialExpression Author: Yasir Rahmatallah , Galina Glazko Maintainer: Yasir Rahmatallah , Galina Glazko git_url: https://git.bioconductor.org/packages/GSAR git_branch: RELEASE_3_8 git_last_commit: 0dca61b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSAR_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSAR_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSAR_1.16.0.tgz vignettes: vignettes/GSAR/inst/doc/GSAR.pdf vignetteTitles: Gene Set Analysis in R -- the GSAR Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSAR/inst/doc/GSAR.R Package: GSCA Version: 2.12.0 Depends: shiny, sp, gplots, ggplot2, reshape2, RColorBrewer, rhdf5, R(>= 2.10.0) Imports: graphics Suggests: Affyhgu133aExpr, Affymoe4302Expr, Affyhgu133A2Expr, Affyhgu133Plus2Expr License: GPL(>=2) MD5sum: 5c525cb073c7ab3b0d0d2db4e4dc2f9c NeedsCompilation: no Title: GSCA: Gene Set Context Analysis Description: GSCA takes as input several lists of activated and repressed genes. GSCA then searches through a compendium of publicly available gene expression profiles for biological contexts that are enriched with a specified pattern of gene expression. GSCA provides both traditional R functions and interactive, user-friendly user interface. biocViews: GeneExpression, Visualization, GUI Author: Zhicheng Ji, Hongkai Ji Maintainer: Zhicheng Ji git_url: https://git.bioconductor.org/packages/GSCA git_branch: RELEASE_3_8 git_last_commit: dc0593b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSCA_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSCA_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSCA_2.12.0.tgz vignettes: vignettes/GSCA/inst/doc/GSCA.pdf vignetteTitles: GSCA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSCA/inst/doc/GSCA.R Package: GSEABase Version: 1.44.0 Depends: R (>= 2.6.0), BiocGenerics (>= 0.13.8), Biobase (>= 2.17.8), annotate (>= 1.45.3), methods, graph (>= 1.37.2) Imports: AnnotationDbi, XML Suggests: hgu95av2.db, GO.db, org.Hs.eg.db, Rgraphviz, ReportingTools, testthat, BiocStyle, knitr License: Artistic-2.0 MD5sum: 5b59c4714c169230996c60cf235300bc NeedsCompilation: no Title: Gene set enrichment data structures and methods Description: This package provides classes and methods to support Gene Set Enrichment Analysis (GSEA). biocViews: GeneExpression, GeneSetEnrichment, GraphAndNetwork, GO, KEGG Author: Martin Morgan, Seth Falcon, Robert Gentleman Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GSEABase git_branch: RELEASE_3_8 git_last_commit: 7042ff6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSEABase_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSEABase_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSEABase_1.44.0.tgz vignettes: vignettes/GSEABase/inst/doc/GSEABase.pdf vignetteTitles: An introduction to GSEABase hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSEABase/inst/doc/GSEABase.R dependsOnMe: AGDEX, BicARE, CCPROMISE, cpvSNP, gCMAP, npGSEA, PROMISE, splineTimeR, TissueEnrich importsMe: AUCell, BioCor, canceR, Category, categoryCompare, cellHTS2, EnrichmentBrowser, gCMAPWeb, gep2pep, GISPA, GlobalAncova, GSRI, GSVA, HTSanalyzeR, MIGSA, miRSM, mogsa, oppar, PCpheno, phenoTest, POST, PROMISE, RcisTarget, ReportingTools, slalom suggestsMe: BiocCaseStudies, clusterProfiler, gage, globaltest, GOstats, GSAR, MAST, PGSEA, phenoTest, TFEA.ChIP, TFutils Package: GSEABenchmarkeR Version: 1.2.1 Depends: R(>= 3.5.0), Biobase, SummarizedExperiment Imports: AnnotationDbi, AnnotationHub, BiocFileCache, BiocParallel, edgeR, EnrichmentBrowser, ExperimentHub, GEOquery, grDevices, graphics, KEGGandMetacoreDzPathwaysGEO, KEGGdzPathwaysGEO, methods, rappdirs, S4Vectors, stats, utils Suggests: BiocStyle, knitr, rmarkdown License: Artistic-2.0 MD5sum: d02f8a00f4d953337503e68c1ce48c6a NeedsCompilation: no Title: Reproducible GSEA Benchmarking Description: The GSEABenchmarkeR package implements an extendable framework for reproducible evaluation of set- and network-based methods for enrichment analysis of gene expression data. This includes support for the efficient execution of these methods on comprehensive real data compendia (microarray and RNA-seq) using parallel computation on standard workstations and institutional computer grids. Methods can then be assessed with respect to runtime, statistical significance, and relevance of the results for the phenotypes investigated. biocViews: ImmunoOncology, Microarray, RNASeq, GeneExpression, DifferentialExpression, Pathways, GraphAndNetwork, Network, GeneSetEnrichment, NetworkEnrichment, Visualization, ReportWriting Author: Ludwig Geistlinger [aut, cre], Gergely Csaba [aut], Mara Santarelli [ctb], Lucas Schiffer [ctb], Marcel Ramos [ctb], Ralf Zimmer [aut], Levi Waldron [aut] Maintainer: Ludwig Geistlinger URL: https://github.com/waldronlab/GSEABenchmarkeR VignetteBuilder: knitr BugReports: https://github.com/waldronlab/GSEABenchmarkeR/issues git_url: https://git.bioconductor.org/packages/GSEABenchmarkeR git_branch: RELEASE_3_8 git_last_commit: fca0f42 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GSEABenchmarkeR_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSEABenchmarkeR_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSEABenchmarkeR_1.2.1.tgz vignettes: vignettes/GSEABenchmarkeR/inst/doc/GSEABenchmarkeR.html vignetteTitles: Reproducible GSEA Benchmarking hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSEABenchmarkeR/inst/doc/GSEABenchmarkeR.R Package: GSEAlm Version: 1.42.0 Depends: Biobase Suggests: GSEABase,Category, multtest, ALL, annotate, hgu95av2.db, genefilter, GOstats, RColorBrewer License: Artistic-2.0 MD5sum: 042abec16df906184e23c4677d4ab42d NeedsCompilation: no Title: Linear Model Toolset for Gene Set Enrichment Analysis Description: Models and methods for fitting linear models to gene expression data, together with tools for computing and using various regression diagnostics. biocViews: Microarray Author: Assaf Oron, Robert Gentleman (with contributions from S. Falcon and Z. Jiang) Maintainer: Assaf Oron git_url: https://git.bioconductor.org/packages/GSEAlm git_branch: RELEASE_3_8 git_last_commit: c3fe6a4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSEAlm_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSEAlm_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSEAlm_1.42.0.tgz vignettes: vignettes/GSEAlm/inst/doc/GSEAlm.pdf vignetteTitles: Linear models in GSEA hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSEAlm/inst/doc/GSEAlm.R importsMe: canceR, gCMAP Package: gsean Version: 1.2.1 Depends: R (>= 3.5), fgsea, PPInfer Suggests: SummarizedExperiment, knitr, plotly, RANKS, WGCNA License: Artistic-2.0 MD5sum: c0a9a40b1b16e5ebac1c83811c585cf6 NeedsCompilation: no Title: Gene Set Enrichment Analysis with Networks Description: Biological molecules in a living organism seldom work individually. They usually interact each other in a cooperative way. Biological process is too complicated to understand without considering such interactions. Thus, network-based procedures can be seen as powerful methods for studying complex process. However, many methods are devised for analyzing individual genes. It is said that techniques based on biological networks such as gene co-expression are more precise ways to represent information than those using lists of genes only. This package is aimed to integrate the gene expression and biological network. A biological network is constructed from gene expression data and it is used for Gene Set Enrichment Analysis. biocViews: Software, StatisticalMethod, Network, GraphAndNetwork, GeneSetEnrichment, GeneExpression, NetworkEnrichment, Pathways, DifferentialExpression Author: Dongmin Jung Maintainer: Dongmin Jung VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gsean git_branch: RELEASE_3_8 git_last_commit: ac6503e git_last_commit_date: 2019-02-11 Date/Publication: 2019-02-14 source.ver: src/contrib/gsean_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/gsean_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gsean_1.2.1.tgz vignettes: vignettes/gsean/inst/doc/gsean.html vignetteTitles: gsean hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gsean/inst/doc/gsean.R Package: GSReg Version: 1.16.0 Depends: R (>= 2.13.1), Homo.sapiens, org.Hs.eg.db, GenomicFeatures, AnnotationDbi Suggests: GenomicRanges, GSBenchMark License: GPL-2 Archs: i386, x64 MD5sum: 723ed94d28d5f414bde41f093c8409b9 NeedsCompilation: yes Title: Gene Set Regulation (GS-Reg) Description: A package for gene set analysis based on the variability of expressions as well as a method to detect Alternative Splicing Events . It implements DIfferential RAnk Conservation (DIRAC) and gene set Expression Variation Analysis (EVA) methods. For detecting Differentially Spliced genes, it provides an implementation of the Spliced-EVA (SEVA). biocViews: GeneRegulation, Pathways, GeneExpression, GeneticVariability, GeneSetEnrichment, AlternativeSplicing Author: Bahman Afsari , Elana J. Fertig Maintainer: Bahman Afsari , Elana J. Fertig git_url: https://git.bioconductor.org/packages/GSReg git_branch: RELEASE_3_8 git_last_commit: 1286f6e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSReg_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSReg_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSReg_1.16.0.tgz vignettes: vignettes/GSReg/inst/doc/GSReg.pdf vignetteTitles: Working with the GSReg package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSReg/inst/doc/GSReg.R Package: GSRI Version: 2.30.0 Depends: R (>= 2.14.2), fdrtool Imports: methods, graphics, stats, utils, genefilter, Biobase, GSEABase, les (>= 1.1.6) Suggests: limma, hgu95av2.db Enhances: parallel License: GPL-3 MD5sum: f57c37cdbe4fd009e96b330b0c6d4272 NeedsCompilation: no Title: Gene Set Regulation Index Description: The GSRI package estimates the number of differentially expressed genes in gene sets, utilizing the concept of the Gene Set Regulation Index (GSRI). biocViews: Microarray, Transcription, DifferentialExpression, GeneSetEnrichment, GeneRegulation Author: Julian Gehring, Kilian Bartholome, Clemens Kreutz, Jens Timmer Maintainer: Julian Gehring git_url: https://git.bioconductor.org/packages/GSRI git_branch: RELEASE_3_8 git_last_commit: d0a317c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSRI_2.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSRI_2.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSRI_2.30.0.tgz vignettes: vignettes/GSRI/inst/doc/gsri.pdf vignetteTitles: Introduction to the GSRI package: Estimating Regulatory Effects utilizing the Gene Set Regulation Index hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSRI/inst/doc/gsri.R Package: GSVA Version: 1.30.0 Depends: R (>= 3.0.0) Imports: methods, BiocGenerics, Biobase, GSEABase (>= 1.17.4), geneplotter, shiny, shinythemes Suggests: limma, RColorBrewer, genefilter, mclust, edgeR, snow, parallel, GSVAdata License: GPL (>= 2) Archs: i386, x64 MD5sum: eab560c63cf486e47723ab7d6292bc76 NeedsCompilation: yes Title: Gene Set Variation Analysis for microarray and RNA-seq data Description: Gene Set Variation Analysis (GSVA) is a non-parametric, unsupervised method for estimating variation of gene set enrichment through the samples of a expression data set. GSVA performs a change in coordinate systems, transforming the data from a gene by sample matrix to a gene-set by sample matrix, thereby allowing the evaluation of pathway enrichment for each sample. This new matrix of GSVA enrichment scores facilitates applying standard analytical methods like functional enrichment, survival analysis, clustering, CNV-pathway analysis or cross-tissue pathway analysis, in a pathway-centric manner. biocViews: Microarray, Pathways, GeneSetEnrichment Author: Justin Guinney [aut, cre], Robert Castelo [aut], Joan Fernandez [ctb] Maintainer: Justin Guinney URL: https://github.com/rcastelo/GSVA BugReports: https://github.com/rcastelo/GSVA/issues git_url: https://git.bioconductor.org/packages/GSVA git_branch: RELEASE_3_8 git_last_commit: 7296f48 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GSVA_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GSVA_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GSVA_1.30.0.tgz vignettes: vignettes/GSVA/inst/doc/GSVA.pdf vignetteTitles: Gene Set Variation Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GSVA/inst/doc/GSVA.R importsMe: consensusOV, EGSEA, oppar, singleCellTK suggestsMe: MCbiclust Package: gtrellis Version: 1.14.0 Depends: R (>= 3.1.2), grid, IRanges, GenomicRanges Imports: circlize (>= 0.3.3), GetoptLong, grDevices, utils Suggests: testthat (>= 1.0.0), knitr, RColorBrewer, markdown, ComplexHeatmap (>= 1.9.7), Cairo, png, jpeg, tiff License: MIT + file LICENSE MD5sum: 8fc5688a3249a05d5088b29ea8885535 NeedsCompilation: no Title: Genome Level Trellis Layout Description: Genome level Trellis graph visualizes genomic data conditioned by genomic categories (e.g. chromosomes). For each genomic category, multiple dimensional data which are represented as tracks describe different features from different aspects. This package provides high flexibility to arrange genomic categories and to add self-defined graphics in the plot. biocViews: Software, Visualization, Sequencing Author: Zuguang Gu Maintainer: Zuguang Gu URL: https://github.com/jokergoo/gtrellis VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gtrellis git_branch: RELEASE_3_8 git_last_commit: 93935fb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gtrellis_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gtrellis_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gtrellis_1.14.0.tgz vignettes: vignettes/gtrellis/inst/doc/gtrellis.html vignetteTitles: Make Genome-level Trellis Graph hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/gtrellis/inst/doc/gtrellis.R importsMe: YAPSA Package: GUIDEseq Version: 1.12.1 Depends: R (>= 3.2.0), GenomicRanges, BiocGenerics Imports: BiocParallel, Biostrings, CRISPRseek, ChIPpeakAnno, data.table, matrixStats, BSgenome, parallel, IRanges (>= 2.5.5), S4Vectors (>= 0.9.6), GenomicAlignments (>= 1.7.3), GenomeInfoDb, Rsamtools, hash, limma Suggests: knitr, RUnit, BiocStyle, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db License: GPL (>= 2) MD5sum: 6d589d9de284ad6efba4d43e6165e2a3 NeedsCompilation: no Title: GUIDE-seq analysis pipeline Description: The package implements GUIDE-seq analysis workflow including functions for obtaining unique insertion sites (proxy of cleavage sites), estimating the locations of the insertion sites, aka, peaks, merging estimated insertion sites from plus and minus strand, and performing off target search of the extended regions around insertion sites. biocViews: ImmunoOncology, GeneRegulation, Sequencing, WorkflowStep, CRISPR Author: Lihua Julie Zhu, Michael Lawrence, Ankit Gupta, Hervé Pagès , Alper Kucukural, Manuel Garber, Scot A. Wolfe Maintainer: Lihua Julie Zhu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/GUIDEseq git_branch: RELEASE_3_8 git_last_commit: e6c1cdf git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/GUIDEseq_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/GUIDEseq_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GUIDEseq_1.12.1.tgz vignettes: vignettes/GUIDEseq/inst/doc/GUIDEseq.pdf vignetteTitles: GUIDEseq Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GUIDEseq/inst/doc/GUIDEseq.R importsMe: crisprseekplus Package: Guitar Version: 1.20.1 Depends: Rsamtools, GenomicFeatures, rtracklayer, GenomicAlignments, GenomicRanges, ggplot2, grid, IRanges License: GPL-2 MD5sum: 2a40227682263aa6cd477bbcfc80c729 NeedsCompilation: no Title: Guitar Description: The package is designed for visualization of RNA-related genomic features with respect to the landmarks of RNA transcripts, i.e., transcription starting site, start codon, stop codon and transcription ending site. biocViews: ImmunoOncology, Sequencing, SplicedAlignment, Alignment, DataImport, RNASeq, MethylSeq, QualityControl, Transcription, Coverage Author: Jia Meng Maintainer: Jia Meng git_url: https://git.bioconductor.org/packages/Guitar git_branch: RELEASE_3_8 git_last_commit: a8093ea git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Guitar_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Guitar_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Guitar_1.20.1.tgz vignettes: vignettes/Guitar/inst/doc/Guitar-Overview.pdf vignetteTitles: Sample Guitar workflow hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Guitar/inst/doc/Guitar-Overview.R Package: Gviz Version: 1.26.5 Depends: R (>= 2.10.0), methods, S4Vectors (>= 0.9.25), IRanges (>= 1.99.18), GenomicRanges (>= 1.17.20), grid Imports: XVector (>= 0.5.7), rtracklayer (>= 1.25.13), lattice, RColorBrewer, biomaRt (>= 2.11.0), AnnotationDbi (>= 1.27.5), Biobase (>= 2.15.3), GenomicFeatures (>= 1.17.22), BSgenome (>= 1.33.1), Biostrings (>= 2.33.11), biovizBase (>= 1.13.8), Rsamtools (>= 1.17.28), latticeExtra (>= 0.6-26), matrixStats (>= 0.8.14), GenomicAlignments (>= 1.1.16), GenomeInfoDb (>= 1.1.3), BiocGenerics (>= 0.11.3), digest(>= 0.6.8) Suggests: xtable, BSgenome.Hsapiens.UCSC.hg19, BiocStyle License: Artistic-2.0 MD5sum: 5a602f40f5838e1f63766b74a2c7eb93 NeedsCompilation: no Title: Plotting data and annotation information along genomic coordinates Description: Genomic data analyses requires integrated visualization of known genomic information and new experimental data. Gviz uses the biomaRt and the rtracklayer packages to perform live annotation queries to Ensembl and UCSC and translates this to e.g. gene/transcript structures in viewports of the grid graphics package. This results in genomic information plotted together with your data. biocViews: Visualization, Microarray Author: Florian Hahne, Steffen Durinck, Robert Ivanek, Arne Mueller, Steve Lianoglou, Ge Tan , Lance Parsons , Shraddha Pai Maintainer: Robert Ivanek git_url: https://git.bioconductor.org/packages/Gviz git_branch: RELEASE_3_8 git_last_commit: 430310b git_last_commit_date: 2019-02-21 Date/Publication: 2019-02-21 source.ver: src/contrib/Gviz_1.26.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/Gviz_1.26.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Gviz_1.26.5.tgz vignettes: vignettes/Gviz/inst/doc/Gviz.pdf vignetteTitles: Gviz users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Gviz/inst/doc/Gviz.R dependsOnMe: biomvRCNS, chimeraviz, cicero, coMET, cummeRbund, DMRforPairs, Pbase, Pviz importsMe: AllelicImbalance, ASpli, CAGEfightR, DMRcate, ELMER, GenomicInteractions, GGtools, gwascat, InPAS, maser, mCSEA, MEAL, methyAnalysis, methylPipe, motifbreakR, Pi, PING, primirTSS, SPLINTER, STAN, trackViewer, TVTB, VariantFiltering suggestsMe: annmap, cellbaseR, CNEr, DeepBlueR, ensembldb, GenomicRanges, interactiveDisplay, InterMineR, pqsfinder, QuasR, RnBeads, SplicingGraphs, TFutils, TxRegInfra Package: gwascat Version: 2.14.0 Depends: R (>= 3.5.0), Homo.sapiens Imports: methods, BiocGenerics, S4Vectors (>= 0.9.25), IRanges, GenomeInfoDb, GenomicRanges (>= 1.29.6), snpStats, Biostrings, Rsamtools, rtracklayer, gQTLstats, Gviz, VariantAnnotation, AnnotationHub, AnnotationDbi, GenomicFeatures, graph, ggbio, ggplot2, SummarizedExperiment Suggests: DO.db, DT, utils, knitr, RBGL, RUnit Enhances: SNPlocs.Hsapiens.dbSNP144.GRCh37 License: Artistic-2.0 MD5sum: 4a30aafb9ce69767d6b21553fbba9607 NeedsCompilation: no Title: representing and modeling data in the EMBL-EBI GWAS catalog Description: Represent and model data in the EMBL-EBI GWAS catalog. biocViews: Genetics Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: utils, knitr git_url: https://git.bioconductor.org/packages/gwascat git_branch: RELEASE_3_8 git_last_commit: b44d2e0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gwascat_2.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gwascat_2.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gwascat_2.14.0.tgz vignettes: vignettes/gwascat/inst/doc/gwascat.pdf, vignettes/gwascat/inst/doc/gwascatOnt.html vignetteTitles: gwascat -- exploring NHGRI GWAS catalog, gwascat -- GRanges for GWAS hits in EBI catalog hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gwascat/inst/doc/gwascat.R, vignettes/gwascat/inst/doc/gwascatOnt.R dependsOnMe: vtpnet suggestsMe: GenomicScores, gQTLBase, gQTLstats, hmdbQuery, TFutils Package: GWASTools Version: 1.28.0 Depends: Biobase Imports: graphics, stats, utils, methods, gdsfmt, DBI, RSQLite, GWASExactHW, DNAcopy, survival, sandwich, lmtest, logistf, quantsmooth Suggests: ncdf4, GWASdata, BiocGenerics, RUnit, Biostrings, GenomicRanges, IRanges, SNPRelate, snpStats, S4Vectors, VariantAnnotation License: Artistic-2.0 MD5sum: e37216b340d24ffb378566279397852a NeedsCompilation: no Title: Tools for Genome Wide Association Studies Description: Classes for storing very large GWAS data sets and annotation, and functions for GWAS data cleaning and analysis. biocViews: SNP, GeneticVariability, QualityControl, Microarray Author: Stephanie M. Gogarten, Cathy Laurie, Tushar Bhangale, Matthew P. Conomos, Cecelia Laurie, Michael Lawrence, Caitlin McHugh, Ian Painter, Xiuwen Zheng, Jess Shen, Rohit Swarnkar, Adrienne Stilp, Sarah Nelson Maintainer: Stephanie M. Gogarten URL: https://github.com/smgogarten/GWASTools git_url: https://git.bioconductor.org/packages/GWASTools git_branch: RELEASE_3_8 git_last_commit: b1c2cf9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/GWASTools_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/GWASTools_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/GWASTools_1.28.0.tgz vignettes: vignettes/GWASTools/inst/doc/Affymetrix.pdf, vignettes/GWASTools/inst/doc/DataCleaning.pdf, vignettes/GWASTools/inst/doc/Formats.pdf vignetteTitles: Preparing Affymetrix Data, GWAS Data Cleaning, Data formats in GWASTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/GWASTools/inst/doc/Affymetrix.R, vignettes/GWASTools/inst/doc/DataCleaning.R, vignettes/GWASTools/inst/doc/Formats.R importsMe: GENESIS, gwasurvivr suggestsMe: podkat Package: gwasurvivr Version: 1.0.0 Depends: R (>= 3.4.0) Imports: GWASTools, survival, VariantAnnotation, parallel, matrixStats, SummarizedExperiment, stats, utils, SNPRelate Suggests: BiocStyle, knitr, rmarkdown License: Artistic-2.0 MD5sum: 0ac5d680b32b6c05cd5774b9691580bd NeedsCompilation: no Title: gwasurvivr: an R package for genome wide survival analysis Description: gwasurvivr is a package to perform survival analysis using Cox proportional hazard models on imputed genetic data. biocViews: GenomeWideAssociation, Survival, Regression, Genetics, SNP, GeneticVariability, Pharmacogenomics, BiomedicalInformatics Author: Abbas Rizvi, Ezgi Karaesmen, Martin Morgan, Lara Sucheston-Campbell Maintainer: Abbas Rizvi URL: https://github.com/suchestoncampbelllab/gwasurvivr VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/gwasurvivr git_branch: RELEASE_3_8 git_last_commit: 43c8762 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/gwasurvivr_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/gwasurvivr_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/gwasurvivr_1.0.0.tgz vignettes: vignettes/gwasurvivr/inst/doc/gwasurvivr_Introduction.html vignetteTitles: gwasurvivr Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/gwasurvivr/inst/doc/gwasurvivr_Introduction.R Package: h5vc Version: 2.16.0 Depends: grid, gridExtra, ggplot2 Imports: rhdf5, reshape, S4Vectors, IRanges, Biostrings, Rsamtools (>= 1.19.38), methods, GenomicRanges, abind, BiocParallel, BatchJobs, h5vcData, GenomeInfoDb LinkingTo: Rsamtools Suggests: knitr, locfit, BSgenome.Hsapiens.UCSC.hg19, biomaRt, BSgenome.Hsapiens.NCBI.GRCh38, RUnit, BiocGenerics License: GPL (>= 3) Archs: i386, x64 MD5sum: eb32bc8bba6b5a375da0738e0b28c392 NeedsCompilation: yes Title: Managing alignment tallies using a hdf5 backend Description: This package contains functions to interact with tally data from NGS experiments that is stored in HDF5 files. Author: Paul Theodor Pyl Maintainer: Paul Theodor Pyl VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/h5vc git_branch: RELEASE_3_8 git_last_commit: fd6bd12 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/h5vc_2.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/h5vc_2.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/h5vc_2.16.0.tgz vignettes: vignettes/h5vc/inst/doc/h5vc.simple.genome.browser.html, vignettes/h5vc/inst/doc/h5vc.tour.html vignetteTitles: Building a minimal genome browser with h5vc and shiny, h5vc -- Tour hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/h5vc/inst/doc/h5vc.simple.genome.browser.R, vignettes/h5vc/inst/doc/h5vc.tour.R Package: hapFabia Version: 1.24.0 Depends: R (>= 2.12.0), Biobase, fabia (>= 2.3.1) Imports: methods, graphics, grDevices, stats, utils License: LGPL (>= 2.1) Archs: i386, x64 MD5sum: acb38ecfda83a4ce592621b4fa13583c NeedsCompilation: yes Title: hapFabia: Identification of very short segments of identity by descent (IBD) characterized by rare variants in large sequencing data Description: A package to identify very short IBD segments in large sequencing data by FABIA biclustering. Two haplotypes are identical by descent (IBD) if they share a segment that both inherited from a common ancestor. Current IBD methods reliably detect long IBD segments because many minor alleles in the segment are concordant between the two haplotypes. However, many cohort studies contain unrelated individuals which share only short IBD segments. This package provides software to identify short IBD segments in sequencing data. Knowledge of short IBD segments are relevant for phasing of genotyping data, association studies, and for population genetics, where they shed light on the evolutionary history of humans. The package supports VCF formats, is based on sparse matrix operations, and provides visualization of haplotype clusters in different formats. biocViews: Genetics, GeneticVariability, SNP, Sequencing, Sequencing, Visualization, Clustering, SequenceMatching, Software Author: Sepp Hochreiter Maintainer: Sepp Hochreiter URL: http://www.bioinf.jku.at/software/hapFabia/hapFabia.html git_url: https://git.bioconductor.org/packages/hapFabia git_branch: RELEASE_3_8 git_last_commit: 8cce3d2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hapFabia_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hapFabia_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hapFabia_1.24.0.tgz vignettes: vignettes/hapFabia/inst/doc/hapfabia.pdf vignetteTitles: hapFabia: Manual for the R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hapFabia/inst/doc/hapfabia.R Package: Harman Version: 1.10.0 Depends: R (>= 3.5) Imports: Rcpp (>= 0.11.2), graphics, stats LinkingTo: Rcpp Suggests: HarmanData, BiocGenerics, BiocStyle, knitr, rmarkdown, RUnit, RColorBrewer, bladderbatch, limma, minfi, lumi, msmsEDA, affydata, minfiData, sva License: GPL-3 + file LICENCE Archs: i386, x64 MD5sum: d93baf47bf61f0f0fb45d0a06e0e797a NeedsCompilation: yes Title: The removal of batch effects from datasets using a PCA and constrained optimisation based technique Description: Harman is a PCA and constrained optimisation based technique that maximises the removal of batch effects from datasets, with the constraint that the probability of overcorrection (i.e. removing genuine biological signal along with batch noise) is kept to a fraction which is set by the end-user. biocViews: BatchEffect, Microarray, MultipleComparison, PrincipalComponent, Normalization, Preprocessing, DNAMethylation, Transcription, Software, StatisticalMethod Author: Josh Bowden [aut], Jason Ross [aut, cre], Yalchin Oytam [aut] Maintainer: Jason Ross URL: http://www.bioinformatics.csiro.au/harman/ VignetteBuilder: knitr BugReports: https://github.com/JasonR055/Harman/issues git_url: https://git.bioconductor.org/packages/Harman git_branch: RELEASE_3_8 git_last_commit: ec4882c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Harman_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Harman_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Harman_1.10.0.tgz vignettes: vignettes/Harman/inst/doc/IntroductionToHarman.html vignetteTitles: IntroductionToHarman hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Harman/inst/doc/IntroductionToHarman.R importsMe: debrowser Package: Harshlight Version: 1.54.0 Depends: R (>= 2.10) Imports: affy, altcdfenvs, Biobase, stats, utils License: GPL (>= 2) Archs: i386, x64 MD5sum: 001fce5a89c331b48513365b01adceb5 NeedsCompilation: yes Title: A "corrective make-up" program for microarray chips Description: The package is used to detect extended, diffuse and compact blemishes on microarray chips. Harshlight automatically marks the areas in a collection of chips (affybatch objects) and a corrected AffyBatch object is returned, in which the defected areas are substituted with NAs or the median of the values of the same probe in the other chips in the collection. The new version handle the substitute value as whole matrix to solve the memory problem. biocViews: Microarray, QualityControl, Preprocessing, OneChannel, ReportWriting Author: Mayte Suarez-Farinas, Maurizio Pellegrino, Knut M. Wittkowski, Marcelo O. Magnasco Maintainer: Maurizio Pellegrino URL: http://asterion.rockefeller.edu/Harshlight/ git_url: https://git.bioconductor.org/packages/Harshlight git_branch: RELEASE_3_8 git_last_commit: 277554c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Harshlight_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Harshlight_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Harshlight_1.54.0.tgz vignettes: vignettes/Harshlight/inst/doc/Harshlight.pdf vignetteTitles: Harshlight hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Harshlight/inst/doc/Harshlight.R Package: HDF5Array Version: 1.10.1 Depends: R (>= 3.4), methods, DelayedArray (>= 0.7.41), rhdf5 (>= 2.25.6) Imports: utils, tools, BiocGenerics (>= 0.25.1), S4Vectors, IRanges Suggests: h5vcData, SummarizedExperiment (>= 1.9.6), GenomicRanges, ExperimentHub, BiocParallel, BiocStyle License: Artistic-2.0 MD5sum: 8364b79376541c14faea8f90d97be4a4 NeedsCompilation: no Title: HDF5 backend for DelayedArray objects Description: Implements the HDF5Array and TENxMatrix classes, 2 convenient and memory-efficient array-like containers for on-disk representation of HDF5 datasets. HDF5Array is for datasets that use the conventional (i.e. dense) HDF5 representation. TENxMatrix is for datasets that use the HDF5-based sparse matrix representation from 10x Genomics (e.g. the 1.3 Million Brain Cell Dataset). Both containers being DelayedArray extensions, they support all operations supported by DelayedArray objects. These operations can be either delayed or block-processed. biocViews: Infrastructure, DataRepresentation, DataImport, Sequencing, RNASeq, Coverage, Annotation, GenomeAnnotation, SingleCell, ImmunoOncology Author: Hervé Pagès Maintainer: Hervé Pagès git_url: https://git.bioconductor.org/packages/HDF5Array git_branch: RELEASE_3_8 git_last_commit: 0b8ae1d git_last_commit_date: 2018-12-05 Date/Publication: 2018-12-05 source.ver: src/contrib/HDF5Array_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/HDF5Array_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HDF5Array_1.10.1.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: GenoGAM importsMe: beachmat, bsseq, clusterExperiment, DelayedMatrixStats, DropletUtils, LoomExperiment, minfi, scmeth suggestsMe: BiocSklearn, DelayedArray, MultiAssayExperiment, scran, SummarizedExperiment Package: HDTD Version: 1.16.0 Depends: R (>= 3.4) Imports: stats, Rcpp (>= 0.12.13) LinkingTo: Rcpp, RcppArmadillo Suggests: knitr, markdown License: GPL-3 Archs: i386, x64 MD5sum: e4763c7b65d7e166c2f1d04aece51437 NeedsCompilation: yes Title: Statistical Inference about the Mean Matrix and the Covariance Matrices in High-Dimensional Transposable Data (HDTD) Description: Characterization of intra-individual variability using physiologically relevant measurements provides important insights into fundamental biological questions ranging from cell type identity to tumor development. For each individual, the data measurements can be written as a matrix with the different subsamples of the individual recorded in the columns and the different phenotypic units recorded in the rows. Datasets of this type are called high-dimensional transposable data. The HDTD package provides functions for conducting statistical inference for the mean relationship between the row and column variables and for the covariance structure within and between the row and column variables. biocViews: DifferentialExpression, Genetics, GeneExpression, Microarray, Sequencing, StatisticalMethod, Software Author: Anestis Touloumis [cre, aut], John C. Marioni [aut], Simon Tavar\'{e} [aut] Maintainer: Anestis Touloumis URL: http://github.com/AnestisTouloumis/HDTD VignetteBuilder: knitr BugReports: http://github.com/AnestisTouloumis/HDTD/issues git_url: https://git.bioconductor.org/packages/HDTD git_branch: RELEASE_3_8 git_last_commit: 164489f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HDTD_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HDTD_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HDTD_1.16.0.tgz vignettes: vignettes/HDTD/inst/doc/HDTD.html vignetteTitles: HDTD to Analyze High-Dimensional Transposable Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HDTD/inst/doc/HDTD.R Package: heatmaps Version: 1.6.0 Depends: R (>= 3.4) Imports: methods, grDevices, graphics, stats, Biostrings, GenomicRanges, IRanges, KernSmooth, plotrix, Matrix, EBImage, RColorBrewer, BiocGenerics, GenomeInfoDb Suggests: BSgenome.Drerio.UCSC.danRer7, knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: fc9f322f10602a84bcea0fe147003763 NeedsCompilation: no Title: Flexible Heatmaps for Functional Genomics and Sequence Features Description: This package provides functions for plotting heatmaps of genome-wide data across genomic intervals, such as ChIP-seq signals at peaks or across promoters. Many functions are also provided for investigating sequence features. biocViews: Visualization, SequenceMatching, FunctionalGenomics Author: Malcolm Perry Maintainer: Malcolm Perry VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/heatmaps git_branch: RELEASE_3_8 git_last_commit: 73d7ccb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/heatmaps_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/heatmaps_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/heatmaps_1.6.0.tgz vignettes: vignettes/heatmaps/inst/doc/heatmaps.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/heatmaps/inst/doc/heatmaps.R Package: Heatplus Version: 2.28.0 Imports: graphics, grDevices, stats, RColorBrewer Suggests: Biobase, hgu95av2.db, limma License: GPL (>= 2) MD5sum: 20b3fb9d045f7ca40aa14fd4c9cef45c NeedsCompilation: no Title: Heatmaps with row and/or column covariates and colored clusters Description: Display a rectangular heatmap (intensity plot) of a data matrix. By default, both samples (columns) and features (row) of the matrix are sorted according to a hierarchical clustering, and the corresponding dendrogram is plotted. Optionally, panels with additional information about samples and features can be added to the plot. biocViews: Microarray, Visualization Author: Alexander Ploner Maintainer: Alexander Ploner URL: https://github.com/alexploner/Heatplus BugReports: https://github.com/alexploner/Heatplus/issues git_url: https://git.bioconductor.org/packages/Heatplus git_branch: RELEASE_3_8 git_last_commit: 4c45c7f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Heatplus_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Heatplus_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Heatplus_2.28.0.tgz vignettes: vignettes/Heatplus/inst/doc/annHeatmap.pdf, vignettes/Heatplus/inst/doc/annHeatmapCommentedSource.pdf, vignettes/Heatplus/inst/doc/oldHeatplus.pdf vignetteTitles: Annotated and regular heatmaps, Commented package source, Old functions (deprecated) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Heatplus/inst/doc/annHeatmap.R, vignettes/Heatplus/inst/doc/annHeatmapCommentedSource.R, vignettes/Heatplus/inst/doc/oldHeatplus.R dependsOnMe: GeneAnswers, phenoTest, tRanslatome Package: HelloRanges Version: 1.8.0 Depends: methods, BiocGenerics, S4Vectors (>= 0.17.39), IRanges (>= 2.13.12), GenomicRanges (>= 1.31.10), Biostrings (>= 2.41.3), BSgenome, GenomicFeatures (>= 1.31.5), VariantAnnotation (>= 1.19.3), Rsamtools, GenomicAlignments (>= 1.15.7), rtracklayer (>= 1.33.8), GenomeInfoDb, SummarizedExperiment Imports: docopt, stats, tools, utils Suggests: HelloRangesData, BiocStyle License: GPL (>= 2) MD5sum: ff03ab06cd4a7cf29704657f16a06fd8 NeedsCompilation: no Title: Introduce *Ranges to bedtools users Description: Translates bedtools command-line invocations to R code calling functions from the Bioconductor *Ranges infrastructure. This is intended to educate novice Bioconductor users and to compare the syntax and semantics of the two frameworks. biocViews: Sequencing, Annotation, Coverage, GenomeAnnotation, DataImport, SequenceMatching, VariantAnnotation Author: Michael Lawrence Maintainer: Michael Lawrence git_url: https://git.bioconductor.org/packages/HelloRanges git_branch: RELEASE_3_8 git_last_commit: 2cd7590 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HelloRanges_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HelloRanges_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HelloRanges_1.8.0.tgz vignettes: vignettes/HelloRanges/inst/doc/tutorial.pdf vignetteTitles: HelloRanges Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HelloRanges/inst/doc/tutorial.R importsMe: OMICsPCA suggestsMe: plyranges Package: HELP Version: 1.40.0 Depends: R (>= 2.8.0), stats, graphics, grDevices, Biobase, methods License: GPL (>= 2) MD5sum: e91bbeed8854a990d4c6ae520eed86df NeedsCompilation: no Title: Tools for HELP data analysis Description: The package contains a modular pipeline for analysis of HELP microarray data, and includes graphical and mathematical tools with more general applications. biocViews: CpGIsland, DNAMethylation, Microarray, TwoChannel, DataImport, QualityControl, Preprocessing, Visualization Author: Reid F. Thompson , John M. Greally , with contributions from Mark Reimers Maintainer: Reid F. Thompson git_url: https://git.bioconductor.org/packages/HELP git_branch: RELEASE_3_8 git_last_commit: 7e9ccc3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HELP_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HELP_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HELP_1.40.0.tgz vignettes: vignettes/HELP/inst/doc/HELP.pdf vignetteTitles: 1. Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HELP/inst/doc/HELP.R Package: HEM Version: 1.54.0 Depends: R (>= 2.1.0) Imports: Biobase, grDevices, stats, utils License: GPL (>= 2) Archs: i386, x64 MD5sum: d2d002ac97b8d515dc6b5676329209fa NeedsCompilation: yes Title: Heterogeneous error model for identification of differentially expressed genes under multiple conditions Description: This package fits heterogeneous error models for analysis of microarray data biocViews: Microarray, DifferentialExpression Author: HyungJun Cho and Jae K. Lee Maintainer: HyungJun Cho URL: http://www.healthsystem.virginia.edu/internet/hes/biostat/bioinformatics/ git_url: https://git.bioconductor.org/packages/HEM git_branch: RELEASE_3_8 git_last_commit: db5935a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HEM_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HEM_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HEM_1.54.0.tgz vignettes: vignettes/HEM/inst/doc/HEM.pdf vignetteTitles: HEM Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: hiAnnotator Version: 1.16.0 Depends: GenomicRanges, R (>= 2.10) Imports: foreach, iterators, rtracklayer, dplyr, BSgenome, ggplot2, scales, methods Suggests: knitr, doParallel, testthat, BiocGenerics License: GPL (>= 2) MD5sum: 708f87c006a43e2d4626012d67f9423b NeedsCompilation: no Title: Functions for annotating GRanges objects Description: hiAnnotator contains set of functions which allow users to annotate a GRanges object with custom set of annotations. The basic philosophy of this package is to take two GRanges objects (query & subject) with common set of seqnames (i.e. chromosomes) and return associated annotation per seqnames and rows from the query matching seqnames and rows from the subject (i.e. genes or cpg islands). The package comes with three types of annotation functions which calculates if a position from query is: within a feature, near a feature, or count features in defined window sizes. Moreover, each function is equipped with parallel backend to utilize the foreach package. In addition, the package is equipped with wrapper functions, which finds appropriate columns needed to make a GRanges object from a common data frame. biocViews: Software, Annotation Author: Nirav V Malani Maintainer: Nirav V Malani VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hiAnnotator git_branch: RELEASE_3_8 git_last_commit: f7b67a6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hiAnnotator_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hiAnnotator_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hiAnnotator_1.16.0.tgz vignettes: vignettes/hiAnnotator/inst/doc/Intro.html vignetteTitles: Using hiAnnotator hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hiAnnotator/inst/doc/Intro.R dependsOnMe: hiReadsProcessor Package: HIBAG Version: 1.18.1 Depends: R (>= 3.2.0) Imports: methods Suggests: parallel, knitr, gdsfmt (>= 1.2.2), SNPRelate (>= 1.1.6), ggplot2, reshape2 License: GPL-3 Archs: i386, x64 MD5sum: a1ba0ae738fdd4bac94f1e44b6710ce0 NeedsCompilation: yes Title: HLA Genotype Imputation with Attribute Bagging Description: It is a software package for imputing HLA types using SNP data, and relies on a training set of HLA and SNP genotypes. HIBAG can be used by researchers with published parameter estimates instead of requiring access to large training sample datasets. It combines the concepts of attribute bagging, an ensemble classifier method, with haplotype inference for SNPs and HLA types. Attribute bagging is a technique which improves the accuracy and stability of classifier ensembles using bootstrap aggregating and random variable selection. biocViews: Genetics, StatisticalMethod Author: Xiuwen Zheng [aut, cre, cph], Bruce Weir [ctb, ths] Maintainer: Xiuwen Zheng URL: http://github.com/zhengxwen/HIBAG, http://zhengxwen.github.io/HIBAG, http://www.biostat.washington.edu/~bsweir/HIBAG/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/HIBAG git_branch: RELEASE_3_8 git_last_commit: 5692a74 git_last_commit_date: 2018-11-15 Date/Publication: 2018-11-15 source.ver: src/contrib/HIBAG_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/HIBAG_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HIBAG_1.18.1.tgz vignettes: vignettes/HIBAG/inst/doc/HIBAG_Tutorial.html vignetteTitles: HIBAG vignette html hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HIBAG/inst/doc/HIBAG_Tutorial.R Package: HiCBricks Version: 1.0.0 Depends: R (>= 3.5), utils, curl, rhdf5, R6, grid Imports: ggplot2, viridis, RColorBrewer, scales, reshape2, stringr, data.table, GenomeInfoDb, GenomicRanges, stats, IRanges, grDevices, S4Vectors, digest, BiocFileCache, rappdirs License: MIT + file LICENSE MD5sum: 00c648457572e0c06e09e1abe2cc7c96 NeedsCompilation: no Title: Framework for Storing and Accessing Hi-C Data Through HDF Files Description: A flexible framework for storing and accessing high-resolution Hi-C data through HDF files. HiCBricks allows import of Hi-C data through various formats such as the 2D matrix format or a generalized n-column table formats. In terms of access, HiCBricks offers functions to retrieve values from genomic loci separated by a certain distance, or the ability to fetch matrix subsets using word alike terms. HiCBricks will at a later point offer the ability to fetch multiple matrix subsets using fewer calls. It offers the capacity to store GenomicRanges that may be associated to a particular Hi-C experiment, to do basic ranges overlap (any, within) with the Hi-C experiment associated Ranges object and also to store any metadata that users may think to be relevant for their Hi-C experiment. Finally, you can do TAD calls with LSD and create pretty heatmaps. biocViews: DataImport, Infrastructure, Software, Technology, Sequencing, HiC Author: Koustav Pal [aut, cre], Carmen Livi [ctb] Maintainer: Koustav Pal git_url: https://git.bioconductor.org/packages/HiCBricks git_branch: RELEASE_3_8 git_last_commit: f6d5887 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HiCBricks_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HiCBricks_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HiCBricks_1.0.0.tgz vignettes: vignettes/HiCBricks/inst/doc/HiCBricks-Vignette.pdf vignetteTitles: HiCBricks hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/HiCBricks/inst/doc/HiCBricks-Vignette.R Package: HiCcompare Version: 1.4.0 Depends: R (>= 3.4.0), dplyr Imports: data.table, ggplot2, gridExtra, mgcv, stats, InteractionSet, GenomicRanges, IRanges, S4Vectors, BiocParallel, QDNAseq, KernSmooth, methods, utils, graphics, pheatmap, gtools Suggests: knitr, rmarkdown, testthat, multiHiCcompare License: MIT + file LICENSE MD5sum: 76d89712dadfae982a63327c74a4a2d4 NeedsCompilation: no Title: HiCcompare: Joint normalization and comparative analysis of multiple Hi-C datasets Description: HiCcompare provides functions for joint normalization and difference detection in multiple Hi-C datasets. HiCcompare operates on processed Hi-C data in the form of chromosome-specific chromatin interaction matrices. It accepts three-column tab-separated text files storing chromatin interaction matrices in a sparse matrix format which are available from several sources. HiCcompare is designed to give the user the ability to perform a comparative analysis on the 3-Dimensional structure of the genomes of cells in different biological states.`HiCcompare` differs from other packages that attempt to compare Hi-C data in that it works on processed data in chromatin interaction matrix format instead of pre-processed sequencing data. In addition, `HiCcompare` provides a non-parametric method for the joint normalization and removal of biases between two Hi-C datasets for the purpose of comparative analysis. `HiCcompare` also provides a simple yet robust method for detecting differences between Hi-C datasets. biocViews: Software, HiC, Sequencing, Normalization Author: John Stansfield [aut, cre], Mikhail Dozmorov [aut] Maintainer: John Stansfield VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/HiCcompare git_branch: RELEASE_3_8 git_last_commit: cc74239 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HiCcompare_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HiCcompare_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HiCcompare_1.4.0.tgz vignettes: vignettes/HiCcompare/inst/doc/HiCcompare-vignette.html vignetteTitles: HiCcompare Usage Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/HiCcompare/inst/doc/HiCcompare-vignette.R importsMe: multiHiCcompare Package: hicrep Version: 1.6.0 Depends: R (>= 3.4) Imports: stats Suggests: knitr, rmarkdown, testthat License: GPL (>= 2.0) MD5sum: 451cb0aae520cb05dca1b5766b9a8bd6 NeedsCompilation: no Title: Measuring the reproducibility of Hi-C data Description: Hi-C is a powerful technology for studying genome-wide chromatin interactions. However, current methods for assessing Hi-C data reproducibility can produce misleading results because they ignore spatial features in Hi-C data, such as domain structure and distance-dependence. We present a novel reproducibility measure that systematically takes these features into consideration. This measure can assess pairwise differences between Hi-C matrices under a wide range of settings, and can be used to determine optimal sequencing depth. Compared to existing approaches, it consistently shows higher accuracy in distinguishing subtle differences in reproducibility and depicting interrelationships of cell lineages than existing approaches. This R package `hicrep` implements our approach. biocViews: Sequencing, HiC, QualityControl Author: Tao Yang [aut, cre] Maintainer: Tao Yang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hicrep git_branch: RELEASE_3_8 git_last_commit: 0df78b1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hicrep_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hicrep_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hicrep_1.6.0.tgz vignettes: vignettes/hicrep/inst/doc/hicrep-vigenette.html vignetteTitles: Evaluate reproducibility of Hi-C data with `hicrep` hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hicrep/inst/doc/hicrep-vigenette.R Package: hierGWAS Version: 1.12.0 Depends: R (>= 3.2.0) Imports: fastcluster,glmnet, fmsb Suggests: BiocGenerics, RUnit, MASS License: GPL-3 MD5sum: 161b52663e1b82379b6d2a876d74d33a NeedsCompilation: no Title: Asessing statistical significance in predictive GWA studies Description: Testing individual SNPs, as well as arbitrarily large groups of SNPs in GWA studies, using a joint model of all SNPs. The method controls the FWER, and provides an automatic, data-driven refinement of the SNP clusters to smaller groups or single markers. biocViews: SNP, LinkageDisequilibrium, Clustering Author: Laura Buzdugan Maintainer: Laura Buzdugan git_url: https://git.bioconductor.org/packages/hierGWAS git_branch: RELEASE_3_8 git_last_commit: 67b1222 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hierGWAS_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hierGWAS_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hierGWAS_1.12.0.tgz vignettes: vignettes/hierGWAS/inst/doc/hierGWAS.pdf vignetteTitles: User manual for R-Package hierGWAS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hierGWAS/inst/doc/hierGWAS.R Package: hierinf Version: 1.0.0 Depends: R (>= 3.5.0) Imports: fmsb, glmnet, methods, parallel, stats Suggests: knitr, MASS, testthat License: GPL-3 | file LICENSE MD5sum: f42529167e8ea2fd49e7290a6c4431d1 NeedsCompilation: no Title: Hierarchical Inference Description: Tools to perform hierarchical inference for one or multiple studies / data sets based on high-dimensional multivariate (generalised) linear models. A possible application is to perform hierarchical inference for GWA studies to find significant groups or single SNPs (if the signal is strong) in a data-driven and automated procedure. The method is based on an efficient hierarchical multiple testing correction and controls the FWER. The functions can easily be run in parallel. biocViews: Clustering, GenomeWideAssociation, LinkageDisequilibrium, Regression, SNP Author: Claude Renaux [aut, cre], Laura Buzdugan [aut], Markus Kalisch [aut], Peter Bühlmann [aut] Maintainer: Claude Renaux VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hierinf git_branch: RELEASE_3_8 git_last_commit: 5d4b24c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hierinf_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hierinf_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hierinf_1.0.0.tgz vignettes: vignettes/hierinf/inst/doc/vignette-hierinf.pdf vignetteTitles: vignette-hierinf.Rnw hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/hierinf/inst/doc/vignette-hierinf.R Package: HilbertCurve Version: 1.12.0 Depends: R (>= 3.1.2), grid Imports: methods, utils, HilbertVis, png, grDevices, circlize (>= 0.3.3), IRanges, GenomicRanges Suggests: knitr, testthat (>= 1.0.0), ComplexHeatmap (>= 1.13.2), markdown, RColorBrewer, RCurl, GetoptLong License: MIT + file LICENSE MD5sum: ba470369553e2da65efa8ca89a886146 NeedsCompilation: no Title: Making 2D Hilbert Curve Description: Hilbert curve is a type of space-filling curves that fold one dimensional axis into a two dimensional space, but with still preserves the locality. This package aims to provide an easy and flexible way to visualize data through Hilbert curve. biocViews: Software, Visualization, Sequencing, Coverage, GenomeAnnotation Author: Zuguang Gu Maintainer: Zuguang Gu URL: https://github.com/jokergoo/HilbertCurve VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/HilbertCurve git_branch: RELEASE_3_8 git_last_commit: 924a7b1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HilbertCurve_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HilbertCurve_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HilbertCurve_1.12.0.tgz vignettes: vignettes/HilbertCurve/inst/doc/HilbertCurve.html vignetteTitles: Making 2D Hilbert Curve hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/HilbertCurve/inst/doc/HilbertCurve.R suggestsMe: ComplexHeatmap Package: HilbertVis Version: 1.40.0 Depends: R (>= 2.6.0), grid, lattice Suggests: IRanges, EBImage License: GPL (>= 3) Archs: i386, x64 MD5sum: c7f99d6848ef995298d264b0e8996f1f NeedsCompilation: yes Title: Hilbert curve visualization Description: Functions to visualize long vectors of integer data by means of Hilbert curves biocViews: Visualization Author: Simon Anders Maintainer: Simon Anders URL: http://www.ebi.ac.uk/~anders/hilbert git_url: https://git.bioconductor.org/packages/HilbertVis git_branch: RELEASE_3_8 git_last_commit: 99e90cf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HilbertVis_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HilbertVis_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HilbertVis_1.40.0.tgz vignettes: vignettes/HilbertVis/inst/doc/HilbertVis.pdf vignetteTitles: Visualising very long data vectors with the Hilbert curve hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HilbertVis/inst/doc/HilbertVis.R dependsOnMe: HilbertVisGUI importsMe: ChIPseqR, HilbertCurve Package: HilbertVisGUI Version: 1.40.0 Depends: R (>= 2.6.0), HilbertVis (>= 1.1.6) Suggests: lattice, IRanges License: GPL (>= 3) Archs: x64 MD5sum: c57941da89777104f1818f25aefd8c5f NeedsCompilation: yes Title: HilbertVisGUI Description: An interactive tool to visualize long vectors of integer data by means of Hilbert curves biocViews: Visualization Author: Simon Anders Maintainer: Simon Anders URL: http://www.ebi.ac.uk/~anders/hilbert SystemRequirements: gtkmm-2.4, GNU make git_url: https://git.bioconductor.org/packages/HilbertVisGUI git_branch: RELEASE_3_8 git_last_commit: fb3f968 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HilbertVisGUI_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HilbertVisGUI_1.40.0.zip vignettes: vignettes/HilbertVisGUI/inst/doc/HilbertVisGUI.pdf vignetteTitles: See vignette in package HilbertVis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: TRUE hasLICENSE: FALSE Package: hipathia Version: 1.4.1 Depends: R (>= 3.5), igraph (>= 1.0.1), AnnotationHub(>= 2.6.5), MultiAssayExperiment(>= 1.4.9), SummarizedExperiment(>= 1.8.1) Imports: coin, stats, limma, grDevices, utils, graphics, preprocessCore, servr, DelayedArray, matrixStats, methods, S4Vectors Suggests: BiocStyle, knitr, rmarkdown, testthat License: GPL-2 MD5sum: e14a55dc818f1176ceeb7b2ed3d30356 NeedsCompilation: no Title: HiPathia: High-throughput Pathway Analysis Description: Hipathia is a method for the computation of signal transduction along signaling pathways from transcriptomic data. The method is based on an iterative algorithm which is able to compute the signal intensity passing through the nodes of a network by taking into account the level of expression of each gene and the intensity of the signal arriving to it. It also provides a new approach to functional analysis allowing to compute the signal arriving to the functions annotated to each pathway. biocViews: Pathways, GraphAndNetwork, GeneExpression, GeneSignaling, GO Author: Marta R. Hidalgo [aut, cre], José Carbonell-Caballero [ctb], Francisco Salavert [ctb], Alicia Amadoz [ctb], Çankut Cubuk [ctb], Joaquin Dopazo [ctb] Maintainer: Marta R. Hidalgo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hipathia git_branch: RELEASE_3_8 git_last_commit: de4ab53 git_last_commit_date: 2019-01-30 Date/Publication: 2019-01-31 source.ver: src/contrib/hipathia_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/hipathia_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hipathia_1.4.1.tgz vignettes: vignettes/hipathia/inst/doc/hipathia-vignette.pdf vignetteTitles: Hipathia Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hipathia/inst/doc/hipathia-vignette.R Package: hiReadsProcessor Version: 1.18.0 Depends: Biostrings, GenomicAlignments, BiocParallel, hiAnnotator, R (>= 3.0) Imports: sonicLength, dplyr, BiocGenerics, GenomicRanges, rSFFreader, readxl, methods Suggests: knitr, testthat License: GPL-3 MD5sum: 8dbd21ace9a68bf4f83bd337b8531f61 NeedsCompilation: no Title: Functions to process LM-PCR reads from 454/Illumina data Description: hiReadsProcessor contains set of functions which allow users to process LM-PCR products sequenced using any platform. Given an excel/txt file containing parameters for demultiplexing and sample metadata, the functions automate trimming of adaptors and identification of the genomic product. Genomic products are further processed for QC and abundance quantification. biocViews: Sequencing, Preprocessing Author: Nirav V Malani Maintainer: Nirav V Malani SystemRequirements: BLAT, UCSC hg18 in 2bit format for BLAT VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hiReadsProcessor git_branch: RELEASE_3_8 git_last_commit: c231665 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hiReadsProcessor_1.18.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hiReadsProcessor_1.18.0.tgz vignettes: vignettes/hiReadsProcessor/inst/doc/Tutorial.html vignetteTitles: Using hiReadsProcessor hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hiReadsProcessor/inst/doc/Tutorial.R Package: HIREewas Version: 1.0.2 Depends: R (>= 3.5.0) Imports: quadprog, gplots, grDevices, stats Suggests: BiocStyle, knitr, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: af011790e1dd234cbd7df579cb6f5fba NeedsCompilation: yes Title: Detection of cell-type-specific risk-CpG sites in epigenome-wide association studies Description: In epigenome-wide association studies, the measured signals for each sample are a mixture of methylation profiles from different cell types. The current approaches to the association detection only claim whether a cytosine-phosphate-guanine (CpG) site is associated with the phenotype or not, but they cannot determine the cell type in which the risk-CpG site is affected by the phenotype. We propose a solid statistical method, HIgh REsolution (HIRE), which not only substantially improves the power of association detection at the aggregated level as compared to the existing methods but also enables the detection of risk-CpG sites for individual cell types. The "HIREewas" R package is to implement HIRE model in R. biocViews: DNAMethylation, DifferentialMethylation, FeatureExtraction Author: Xiangyu Luo , Can Yang , Yingying Wei Maintainer: Xiangyu Luo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/HIREewas git_branch: RELEASE_3_8 git_last_commit: 6cd599f git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/HIREewas_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/HIREewas_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HIREewas_1.0.2.tgz vignettes: vignettes/HIREewas/inst/doc/HIREewas.pdf vignetteTitles: HIREewas hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HIREewas/inst/doc/HIREewas.R Package: HiTC Version: 1.26.0 Depends: R (>= 2.15.0), methods, IRanges, GenomicRanges Imports: Biostrings, graphics, grDevices, rtracklayer, RColorBrewer, Matrix, parallel, GenomeInfoDb Suggests: BiocStyle, HiCDataHumanIMR90 License: Artistic-2.0 MD5sum: eb493286bde0c875cc990d458b6b532d NeedsCompilation: no Title: High Throughput Chromosome Conformation Capture analysis Description: The HiTC package was developed to explore high-throughput 'C' data such as 5C or Hi-C. Dedicated R classes as well as standard methods for quality controls, normalization, visualization, and further analysis are also provided. biocViews: Sequencing, HighThroughputSequencing, HiC Author: Nicolas Servant Maintainer: Nicolas Servant git_url: https://git.bioconductor.org/packages/HiTC git_branch: RELEASE_3_8 git_last_commit: be108ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HiTC_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HiTC_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HiTC_1.26.0.tgz vignettes: vignettes/HiTC/inst/doc/HiC_analysis.pdf, vignettes/HiTC/inst/doc/HiTC.pdf vignetteTitles: Hi-C data analysis using HiTC, Introduction to HiTC package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HiTC/inst/doc/HiC_analysis.R, vignettes/HiTC/inst/doc/HiTC.R Package: hmdbQuery Version: 1.2.0 Depends: R (>= 3.5), XML Imports: S4Vectors, methods, utils Suggests: knitr, annotate, gwascat, testthat License: Artistic-2.0 MD5sum: 146f2e50a7a23ec70e559d88066f3615 NeedsCompilation: no Title: utilities for exploration of human metabolome database Description: Define utilities for exploration of human metabolome database, including functions to retrieve specific metabolite entries and data snapshots with pairwise associations (metabolite-gene,-protein,-disease). biocViews: Metabolomics, Infrastructure Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hmdbQuery git_branch: RELEASE_3_8 git_last_commit: 17208a6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hmdbQuery_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hmdbQuery_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hmdbQuery_1.2.0.tgz vignettes: vignettes/hmdbQuery/inst/doc/hmdbQuery.html vignetteTitles: hmdbQuery: working with Human Metabolome Database (hmdb.ca) hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hmdbQuery/inst/doc/hmdbQuery.R Package: HMMcopy Version: 1.24.0 Depends: R (>= 2.10.0), IRanges (>= 1.4.16), geneplotter (>= 1.24.0) License: GPL-3 Archs: i386, x64 MD5sum: b9a3c1f7f7ac714bacc10a09afaa9664 NeedsCompilation: yes Title: Copy number prediction with correction for GC and mappability bias for HTS data Description: Corrects GC and mappability biases for readcounts (i.e. coverage) in non-overlapping windows of fixed length for single whole genome samples, yielding a rough estimate of copy number for furthur analysis. Designed for rapid correction of high coverage whole genome tumour and normal samples. biocViews: Sequencing, Preprocessing, Visualization, CopyNumberVariation, Microarray Author: Daniel Lai, Gavin Ha, Sohrab Shah Maintainer: Daniel Lai , Sohrab Shah git_url: https://git.bioconductor.org/packages/HMMcopy git_branch: RELEASE_3_8 git_last_commit: 51f9790 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HMMcopy_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HMMcopy_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HMMcopy_1.24.0.tgz vignettes: vignettes/HMMcopy/inst/doc/HMMcopy.pdf vignetteTitles: HMMcopy hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HMMcopy/inst/doc/HMMcopy.R importsMe: qsea Package: hopach Version: 2.42.0 Depends: R (>= 2.11.0), cluster, Biobase, methods Imports: graphics, grDevices, stats, utils, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: 35465e16c6f9f85363b0e00701eb5e52 NeedsCompilation: yes Title: Hierarchical Ordered Partitioning and Collapsing Hybrid (HOPACH) Description: The HOPACH clustering algorithm builds a hierarchical tree of clusters by recursively partitioning a data set, while ordering and possibly collapsing clusters at each level. The algorithm uses the Mean/Median Split Silhouette (MSS) criteria to identify the level of the tree with maximally homogeneous clusters. It also runs the tree down to produce a final ordered list of the elements. The non-parametric bootstrap allows one to estimate the probability that each element belongs to each cluster (fuzzy clustering). biocViews: Clustering Author: Katherine S. Pollard, with Mark J. van der Laan and Greg Wall Maintainer: Katherine S. Pollard URL: http://www.stat.berkeley.edu/~laan/, http://docpollard.org/ git_url: https://git.bioconductor.org/packages/hopach git_branch: RELEASE_3_8 git_last_commit: 483b613 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hopach_2.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hopach_2.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hopach_2.42.0.tgz vignettes: vignettes/hopach/inst/doc/hopach.pdf vignetteTitles: hopach hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hopach/inst/doc/hopach.R importsMe: phenoTest suggestsMe: BiocCaseStudies Package: HPAanalyze Version: 1.0.0 Depends: R (>= 3.5.0) Imports: dplyr, XLConnect, ggplot2, readr, tibble, xml2, reshape2, tidyr, magrittr, stats, utils, hpar, cowplot Suggests: knitr, rmarkdown, devtools, BiocStyle License: GPL-3 + file LICENSE MD5sum: 211c3fa0f4c721603e9c913f2723bbf5 NeedsCompilation: no Title: Retrieve and analyze data from the Human Protein Atlas Description: Provide functions for retrieving, exploratory analyzing and visualizing the Human Protein Atlas data. biocViews: Proteomics, CellBiology, Visualization, Software Author: Anh Nhat Tran [aut, cre] Maintainer: Anh Nhat Tran VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/HPAanalyze git_branch: RELEASE_3_8 git_last_commit: 2d7785a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HPAanalyze_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HPAanalyze_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HPAanalyze_1.0.0.tgz vignettes: vignettes/HPAanalyze/inst/doc/HPAanalyze_basics.html vignetteTitles: "Working with HPAanalyze package" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/HPAanalyze/inst/doc/HPAanalyze_basics.R Package: hpar Version: 1.24.0 Depends: R (>= 2.15) Imports: utils Suggests: org.Hs.eg.db, GO.db, knitr, BiocStyle, testthat License: Artistic-2.0 MD5sum: d424723a0f21b8ad24e7280040c4cea7 NeedsCompilation: no Title: Human Protein Atlas in R Description: The hpar package provides a simple R interface to and data from the Human Protein Atlas project. biocViews: Proteomics, Homo_sapiens, CellBiology Author: Laurent Gatto Maintainer: Laurent Gatto VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/hpar git_branch: RELEASE_3_8 git_last_commit: f153015 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hpar_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hpar_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hpar_1.24.0.tgz vignettes: vignettes/hpar/inst/doc/hpar.html vignetteTitles: Human Protein Atlas in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hpar/inst/doc/hpar.R importsMe: HPAanalyze, MetaboSignal suggestsMe: pRoloc Package: HTqPCR Version: 1.36.0 Depends: Biobase, RColorBrewer, limma Imports: affy, Biobase, gplots, graphics, grDevices, limma, methods, RColorBrewer, stats, stats4, utils Suggests: statmod License: Artistic-2.0 MD5sum: 6b49cf2e293bb387f20845b568bfc20b NeedsCompilation: no Title: Automated analysis of high-throughput qPCR data Description: Analysis of Ct values from high throughput quantitative real-time PCR (qPCR) assays across multiple conditions or replicates. The input data can be from spatially-defined formats such ABI TaqMan Low Density Arrays or OpenArray; LightCycler from Roche Applied Science; the CFX plates from Bio-Rad Laboratories; conventional 96- or 384-well plates; or microfluidic devices such as the Dynamic Arrays from Fluidigm Corporation. HTqPCR handles data loading, quality assessment, normalization, visualization and parametric or non-parametric testing for statistical significance in Ct values between features (e.g. genes, microRNAs). biocViews: MicrotitrePlateAssay, DifferentialExpression, GeneExpression, DataImport, QualityControl, Preprocessing, Visualization, MultipleComparison, qPCR Author: Heidi Dvinge, Paul Bertone Maintainer: Heidi Dvinge URL: http://www.ebi.ac.uk/bertone/software git_url: https://git.bioconductor.org/packages/HTqPCR git_branch: RELEASE_3_8 git_last_commit: bb0a84e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HTqPCR_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HTqPCR_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HTqPCR_1.36.0.tgz vignettes: vignettes/HTqPCR/inst/doc/HTqPCR.pdf vignetteTitles: qPCR analysis in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HTqPCR/inst/doc/HTqPCR.R importsMe: nondetects, unifiedWMWqPCR Package: HTSanalyzeR Version: 2.34.1 Depends: R (>= 2.15), igraph, methods Imports: graph, igraph, GSEABase, BioNet, cellHTS2, AnnotationDbi, biomaRt, RankProd Suggests: KEGG.db, GO.db, org.Dm.eg.db, GOstats, org.Ce.eg.db, org.Mm.eg.db, org.Rn.eg.db, org.Hs.eg.db, snow License: Artistic-2.0 MD5sum: 9ed439c18d323f31118dd360e56dd500 NeedsCompilation: no Title: Gene set over-representation, enrichment and network analyses for high-throughput screens Description: This package provides classes and methods for gene set over-representation, enrichment and network analyses on high-throughput screens. The over-representation analysis is performed based on hypergeometric tests. The enrichment analysis is based on the GSEA algorithm (Subramanian et al. PNAS 2005). The network analysis identifies enriched subnetworks based on algorithms from the BioNet package (Beisser et al., Bioinformatics 2010). A pipeline is also specifically designed for cellHTS2 object to perform integrative network analyses of high-throughput RNA interference screens. The users can build their own analysis pipeline for their own data set based on this package. biocViews: ImmunoOncology, CellBasedAssays, MultipleComparison Author: Xin Wang , Camille Terfve , John C. Rose , Florian Markowetz Maintainer: Xin Wang git_url: https://git.bioconductor.org/packages/HTSanalyzeR git_branch: RELEASE_3_8 git_last_commit: 2e64a32 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/HTSanalyzeR_2.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/HTSanalyzeR_2.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HTSanalyzeR_2.34.1.tgz vignettes: vignettes/HTSanalyzeR/inst/doc/HTSanalyzeR-Vignette.pdf vignetteTitles: Main vignette:Gene set enrichment and network analysis of high-throughput RNAi screen data using HTSanalyzeR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HTSanalyzeR/inst/doc/HTSanalyzeR-Vignette.R importsMe: phenoTest Package: HTSeqGenie Version: 4.12.0 Depends: R (>= 3.0.0), gmapR (>= 1.8.0), ShortRead (>= 1.19.13), VariantAnnotation (>= 1.8.3) Imports: BiocGenerics (>= 0.2.0), S4Vectors (>= 0.9.25), IRanges (>= 1.21.39), GenomicRanges (>= 1.23.21), Rsamtools (>= 1.8.5), Biostrings (>= 2.24.1), chipseq (>= 1.6.1), hwriter (>= 1.3.0), Cairo (>= 1.5.5), GenomicFeatures (>= 1.9.31), BiocParallel, parallel, tools, rtracklayer (>= 1.17.19), GenomicAlignments, VariantTools (>= 1.7.7), GenomeInfoDb, SummarizedExperiment, methods Suggests: TxDb.Hsapiens.UCSC.hg19.knownGene, LungCancerLines, org.Hs.eg.db License: Artistic-2.0 MD5sum: 7e4ef25284d34c49ec0c01d8502f4622 NeedsCompilation: no Title: A NGS analysis pipeline. Description: Libraries to perform NGS analysis. Author: Gregoire Pau, Jens Reeder Maintainer: Jens Reeder git_url: https://git.bioconductor.org/packages/HTSeqGenie git_branch: RELEASE_3_8 git_last_commit: 56fca6c git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-01 source.ver: src/contrib/HTSeqGenie_4.12.0.tar.gz vignettes: vignettes/HTSeqGenie/inst/doc/HTSeqGenie.pdf vignetteTitles: HTSeqGenie hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HTSeqGenie/inst/doc/HTSeqGenie.R Package: htSeqTools Version: 1.30.0 Depends: R (>= 2.12.2), methods, BiocGenerics (>= 0.1.0), Biobase, S4Vectors, IRanges, methods, MASS, BSgenome, GenomeInfoDb (>= 1.1.3), GenomicRanges (>= 1.17.11) Enhances: parallel,multicore License: GPL (>=2) MD5sum: e62c9dd3fa250ff61a92ee38400b23b8 NeedsCompilation: no Title: Quality Control, Visualization and Processing for High-Throughput Sequencing data Description: We provide efficient, easy-to-use tools for High-Throughput Sequencing (ChIP-seq, RNAseq etc.). These include MDS plots (analogues to PCA), detecting inefficient immuno-precipitation or over-amplification artifacts, tools to identify and test for genomic regions with large accumulation of reads, and visualization of coverage profiles. biocViews: Sequencing, QualityControl Author: Evarist Planet, Camille Stephan-Otto, Oscar Reina, Oscar Flores, David Rossell Maintainer: Oscar Reina git_url: https://git.bioconductor.org/packages/htSeqTools git_branch: RELEASE_3_8 git_last_commit: 613ed18 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/htSeqTools_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/htSeqTools_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/htSeqTools_1.30.0.tgz vignettes: vignettes/htSeqTools/inst/doc/htSeqTools.pdf vignetteTitles: Manual for the htSeqTools library hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/htSeqTools/inst/doc/htSeqTools.R Package: HTSFilter Version: 1.22.1 Depends: R (>= 3.4) Imports: edgeR (>= 3.9.14), DESeq2 (>= 1.10.1), DESeq (>= 1.22.1), BiocParallel (>= 1.4.3), Biobase, utils, stats, grDevices, graphics, methods Suggests: EDASeq (>= 2.1.4), BiocStyle, testthat License: Artistic-2.0 MD5sum: 1a853603bd830413cee7db2f034d9148 NeedsCompilation: no Title: Filter replicated high-throughput transcriptome sequencing data Description: This package implements a filtering procedure for replicated transcriptome sequencing data based on a global Jaccard similarity index in order to identify genes with low, constant levels of expression across one or more experimental conditions. biocViews: ImmunoOncology, Sequencing, RNASeq, Preprocessing, DifferentialExpression, GeneExpression, Normalization Author: Andrea Rau, Melina Gallopin, Gilles Celeux, and Florence Jaffrezic Maintainer: Andrea Rau git_url: https://git.bioconductor.org/packages/HTSFilter git_branch: RELEASE_3_8 git_last_commit: f21f467 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/HTSFilter_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/HTSFilter_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HTSFilter_1.22.1.tgz vignettes: vignettes/HTSFilter/inst/doc/HTSFilter.pdf vignetteTitles: HTSFilter Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HTSFilter/inst/doc/HTSFilter.R importsMe: coseq Package: HybridMTest Version: 1.26.0 Depends: R (>= 2.9.0), Biobase, fdrtool, MASS, survival Imports: stats License: GPL Version 2 or later MD5sum: 37e8b32af15775b684fd95f27b08a29c NeedsCompilation: no Title: Hybrid Multiple Testing Description: Performs hybrid multiple testing that incorporates method selection and assumption evaluations into the analysis using empirical Bayes probability (EBP) estimates obtained by Grenander density estimation. For instance, for 3-group comparison analysis, Hybrid Multiple testing considers EBPs as weighted EBPs between F-test and H-test with EBPs from Shapiro Wilk test of normality as weigth. Instead of just using EBPs from F-test only or using H-test only, this methodology combines both types of EBPs through EBPs from Shapiro Wilk test of normality. This methodology uses then the law of total EBPs. biocViews: GeneExpression, Genetics, Microarray Author: Stan Pounds , Demba Fofana Maintainer: Demba Fofana git_url: https://git.bioconductor.org/packages/HybridMTest git_branch: RELEASE_3_8 git_last_commit: 3abf119 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/HybridMTest_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/HybridMTest_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/HybridMTest_1.26.0.tgz vignettes: vignettes/HybridMTest/inst/doc/HybridMTest.pdf vignetteTitles: Hybrid Multiple Testing hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/HybridMTest/inst/doc/HybridMTest.R Package: hyperdraw Version: 1.34.0 Depends: R (>= 2.9.0) Imports: methods, grid, graph, hypergraph, Rgraphviz, stats4 License: GPL (>= 2) MD5sum: 585067dc2db3c0ccf3d69733092811c8 NeedsCompilation: no Title: Visualizing Hypergaphs Description: Functions for visualizing hypergraphs. biocViews: Visualization, GraphAndNetwork Author: Paul Murrell Maintainer: Paul Murrell SystemRequirements: graphviz git_url: https://git.bioconductor.org/packages/hyperdraw git_branch: RELEASE_3_8 git_last_commit: 7722d5f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hyperdraw_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hyperdraw_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hyperdraw_1.34.0.tgz vignettes: vignettes/hyperdraw/inst/doc/hyperdraw.pdf vignetteTitles: Hyperdraw hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/hyperdraw/inst/doc/hyperdraw.R dependsOnMe: BiGGR Package: hypergraph Version: 1.54.0 Depends: R (>= 2.1.0), methods, utils, graph Suggests: BiocGenerics, RUnit License: Artistic-2.0 MD5sum: f26b3809c03897878b51a9f9e7fd11a1 NeedsCompilation: no Title: A package providing hypergraph data structures Description: A package that implements some simple capabilities for representing and manipulating hypergraphs. biocViews: GraphAndNetwork Author: Seth Falcon, Robert Gentleman Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/hypergraph git_branch: RELEASE_3_8 git_last_commit: cf134b9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/hypergraph_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/hypergraph_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/hypergraph_1.54.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: altcdfenvs, RpsiXML importsMe: BiGGR, hyperdraw Package: iASeq Version: 1.26.1 Depends: R (>= 2.14.1) Imports: graphics, grDevices License: GPL-2 MD5sum: 42f397bcc34329c812ef8d7c46cd774a NeedsCompilation: no Title: iASeq: integrating multiple sequencing datasets for detecting allele-specific events Description: It fits correlation motif model to multiple RNAseq or ChIPseq studies to improve detection of allele-specific events and describe correlation patterns across studies. biocViews: ImmunoOncology, SNP, RNASeq, ChIPSeq Author: Yingying Wei, Hongkai Ji Maintainer: Yingying Wei git_url: https://git.bioconductor.org/packages/iASeq git_branch: RELEASE_3_8 git_last_commit: 564a4e0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/iASeq_1.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/iASeq_1.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iASeq_1.26.1.tgz vignettes: vignettes/iASeq/inst/doc/iASeqVignette.pdf vignetteTitles: iASeq Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iASeq/inst/doc/iASeqVignette.R Package: iasva Version: 1.0.1 Depends: R (>= 3.5), Imports: irlba, stats, cluster, graphics, SummarizedExperiment, BiocParallel Suggests: knitr, testthat, rmarkdown, sva, Rtsne, pheatmap, corrplot, DescTools, RColorBrewer License: GPL-2 MD5sum: cacbbd2a06bd5897f1ef058d72f86823 NeedsCompilation: no Title: Iteratively Adjusted Surrogate Variable Analysis Description: Iteratively Adjusted Surrogate Variable Analysis (IA-SVA) is a statistical framework to uncover hidden sources of variation even when these sources are correlated. IA-SVA provides a flexible methodology to i) identify a hidden factor for unwanted heterogeneity while adjusting for all known factors; ii) test the significance of the putative hidden factor for explaining the unmodeled variation in the data; and iii), if significant, use the estimated factor as an additional known factor in the next iteration to uncover further hidden factors. biocViews: ImmunoOncology, Preprocessing, QualityControl, BatchEffect, RNASeq, Software, StatisticalMethod, FeatureExtraction Author: Donghyung Lee [aut, cre], Anthony Cheng [aut], Nathan Lawlor [aut], Duygu Ucar [aut] Maintainer: Donghyung Lee , Anthony Cheng VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/iasva git_branch: RELEASE_3_8 git_last_commit: 48bb686 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/iasva_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/iasva_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iasva_1.0.1.tgz vignettes: vignettes/iasva/inst/doc/detecting_hidden_heterogeneity_iasvaV0.95.html vignetteTitles: "Detecting hidden heterogeneity in single cell RNA-Seq data" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iasva/inst/doc/detecting_hidden_heterogeneity_iasvaV0.95.R Package: iBBiG Version: 1.26.0 Depends: biclust Imports: stats4,xtable,ade4 Suggests: methods License: Artistic-2.0 Archs: i386, x64 MD5sum: a8d9db691a24a412fd0e1bbbd10e635b NeedsCompilation: yes Title: Iterative Binary Biclustering of Genesets Description: iBBiG is a bi-clustering algorithm which is optimizes for binary data analysis. We apply it to meta-gene set analysis of large numbers of gene expression datasets. The iterative algorithm extracts groups of phenotypes from multiple studies that are associated with similar gene sets. iBBiG does not require prior knowledge of the number or scale of clusters and allows discovery of clusters with diverse sizes biocViews: Clustering, Annotation, GeneSetEnrichment Author: Daniel Gusenleitner, Aedin Culhane Maintainer: Aedin Culhane URL: http://bcb.dfci.harvard.edu/~aedin/publications/ git_url: https://git.bioconductor.org/packages/iBBiG git_branch: RELEASE_3_8 git_last_commit: 36376ef git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iBBiG_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iBBiG_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iBBiG_1.26.0.tgz vignettes: vignettes/iBBiG/inst/doc/tutorial.pdf vignetteTitles: iBBiG User Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iBBiG/inst/doc/tutorial.R importsMe: miRSM Package: ibh Version: 1.30.0 Depends: simpIntLists Suggests: yeastCC, stats License: GPL (>= 2) MD5sum: 2f9f043d554d46a1ce0146c3b59d556a NeedsCompilation: no Title: Interaction Based Homogeneity for Evaluating Gene Lists Description: This package contains methods for calculating Interaction Based Homogeneity to evaluate fitness of gene lists to an interaction network which is useful for evaluation of clustering results and gene list analysis. BioGRID interactions are used in the calculation. The user can also provide their own interactions. biocViews: QualityControl, DataImport, GraphAndNetwork, NetworkEnrichment Author: Kircicegi Korkmaz, Volkan Atalay, Rengul Cetin Atalay. Maintainer: Kircicegi Korkmaz git_url: https://git.bioconductor.org/packages/ibh git_branch: RELEASE_3_8 git_last_commit: 6168dc9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ibh_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ibh_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ibh_1.30.0.tgz vignettes: vignettes/ibh/inst/doc/ibh.pdf vignetteTitles: ibh hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ibh/inst/doc/ibh.R Package: iBMQ Version: 1.22.0 Depends: R(>= 2.15.0),Biobase (>= 2.16.0), ggplot2 (>= 0.9.2) License: Artistic-2.0 Archs: i386, x64 MD5sum: 18f8a0260516df35cf64a3dc6d8cf403 NeedsCompilation: yes Title: integrated Bayesian Modeling of eQTL data Description: integrated Bayesian Modeling of eQTL data biocViews: Microarray, Preprocessing, GeneExpression, SNP Author: Marie-Pier Scott-Boyer and Greg Imholte Maintainer: Greg Imholte URL: http://www.rglab.org SystemRequirements: GSL and OpenMP git_url: https://git.bioconductor.org/packages/iBMQ git_branch: RELEASE_3_8 git_last_commit: 53bdd28 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iBMQ_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iBMQ_1.22.0.zip vignettes: vignettes/iBMQ/inst/doc/iBMQ.pdf vignetteTitles: iBMQ: An Integrated Hierarchical Bayesian Model for Multivariate eQTL Mapping hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iBMQ/inst/doc/iBMQ.R Package: iCARE Version: 1.10.3 Depends: R (>= 3.3.0), plotrix, gtools, Hmisc Suggests: RUnit, BiocGenerics License: GPL-3 + file LICENSE Archs: i386, x64 MD5sum: 1c0bd342ec42f95b64b8ffe717abac8b NeedsCompilation: yes Title: A Tool for Individualized Coherent Absolute Risk Estimation (iCARE) Description: An R package to compute Individualized Coherent Absolute Risk Estimators. biocViews: Software, StatisticalMethod, GenomeWideAssociation Author: Paige Maas, Parichoy Pal Choudhury, Nilanjan Chatterjee and William Wheeler Maintainer: Bill Wheeler git_url: https://git.bioconductor.org/packages/iCARE git_branch: RELEASE_3_8 git_last_commit: ea396eb git_last_commit_date: 2018-12-10 Date/Publication: 2018-12-10 source.ver: src/contrib/iCARE_1.10.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/iCARE_1.10.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iCARE_1.10.3.tgz vignettes: vignettes/iCARE/inst/doc/vignette_model_validation.pdf, vignettes/iCARE/inst/doc/vignette.pdf vignetteTitles: iCARE Vignette, iCARE Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/iCARE/inst/doc/vignette_model_validation.R, vignettes/iCARE/inst/doc/vignette.R Package: Icens Version: 1.54.0 Depends: survival Imports: graphics License: Artistic-2.0 MD5sum: 6b85482eca0f13261be84bae8285c419 NeedsCompilation: no Title: NPMLE for Censored and Truncated Data Description: Many functions for computing the NPMLE for censored and truncated data. biocViews: Infrastructure Author: R. Gentleman and Alain Vandal Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/Icens git_branch: RELEASE_3_8 git_last_commit: dced3fe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Icens_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Icens_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Icens_1.54.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: PROcess importsMe: PROcess Package: icetea Version: 1.0.1 Depends: R (>= 3.5) Imports: stats, utils, methods, graphics, grDevices, ggplot2, GenomicFeatures, ShortRead, BiocParallel, Biostrings, S4Vectors, Rsamtools, BiocGenerics, IRanges, GenomicAlignments, GenomicRanges, rtracklayer, SummarizedExperiment, VariantAnnotation, limma, edgeR, csaw, TxDb.Dmelanogaster.UCSC.dm6.ensGene Suggests: knitr, rmarkdown, Rsubread (>= 1.29.0), testthat License: GPL-3 + file LICENSE MD5sum: e9f5e2354143ac9cce0a2ea79eb1ab00 NeedsCompilation: no Title: Integrating Cap Enrichment with Transcript Expression Analysis Description: icetea (Integrating Cap Enrichment with Transcript Expression Analysis) provides functions for end-to-end analysis of multiple 5'-profiling methods such as CAGE, RAMPAGE and MAPCap, beginning from raw reads to detection of transcription start sites using replicates. It also allows performing differential TSS detection between group of samples, therefore, integrating the mRNA cap enrichment information with transcript expression analysis. biocViews: ImmunoOncology, Transcription, GeneExpression, Sequencing, RNASeq, Transcriptomics, DifferentialExpression Author: Vivek Bhardwaj [aut, cre] Maintainer: Vivek Bhardwaj URL: https://github.com/vivekbhr/icetea VignetteBuilder: knitr BugReports: https://github.com/vivekbhr/icetea/issues git_url: https://git.bioconductor.org/packages/icetea git_branch: RELEASE_3_8 git_last_commit: b45586e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/icetea_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/icetea_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/icetea_1.0.1.tgz vignettes: vignettes/icetea/inst/doc/mapcap_analysis.html vignetteTitles: Analysing transcript 5'-profiling data using icetea hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/icetea/inst/doc/mapcap_analysis.R Package: iCheck Version: 1.12.0 Depends: R (>= 3.2.0), Biobase, lumi, gplots Imports: stats, graphics, preprocessCore, grDevices, randomForest, affy, limma, parallel, GeneSelectMMD, rgl, MASS, lmtest, scatterplot3d, utils License: GPL (>= 2) MD5sum: e13b3395b8c803eb0f0f12b16ef9c9f8 NeedsCompilation: no Title: QC Pipeline and Data Analysis Tools for High-Dimensional Illumina mRNA Expression Data Description: QC pipeline and data analysis tools for high-dimensional Illumina mRNA expression data. biocViews: GeneExpression, DifferentialExpression, Microarray, Preprocessing, DNAMethylation, OneChannel, TwoChannel, QualityControl Author: Weiliang Qiu [aut, cre], Brandon Guo [aut, ctb], Christopher Anderson [aut, ctb], Barbara Klanderman [aut, ctb], Vincent Carey [aut, ctb], Benjamin Raby [aut, ctb] Maintainer: Weiliang Qiu git_url: https://git.bioconductor.org/packages/iCheck git_branch: RELEASE_3_8 git_last_commit: 09c24e6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iCheck_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iCheck_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iCheck_1.12.0.tgz vignettes: vignettes/iCheck/inst/doc/iCheck.pdf vignetteTitles: iCheck hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iCheck/inst/doc/iCheck.R Package: iChip Version: 1.36.0 Depends: R (>= 2.10.0) Imports: limma License: GPL (>= 2) Archs: i386, x64 MD5sum: db251b763a1f7693401bcb60141bef87 NeedsCompilation: yes Title: Bayesian Modeling of ChIP-chip Data Through Hidden Ising Models Description: Hidden Ising models are implemented to identify enriched genomic regions in ChIP-chip data. They can be used to analyze the data from multiple platforms (e.g., Affymetrix, Agilent, and NimbleGen), and the data with single to multiple replicates. biocViews: ChIPchip, OneChannel, AgilentChip, Microarray Author: Qianxing Mo Maintainer: Qianxing Mo git_url: https://git.bioconductor.org/packages/iChip git_branch: RELEASE_3_8 git_last_commit: 873f708 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iChip_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iChip_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iChip_1.36.0.tgz vignettes: vignettes/iChip/inst/doc/iChip.pdf vignetteTitles: iChip hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iChip/inst/doc/iChip.R Package: iClusterPlus Version: 1.18.0 Depends: R (>= 3.3.0), parallel Suggests: RUnit, BiocGenerics License: GPL (>= 2) Archs: i386, x64 MD5sum: 651bb943711a5b111ac411d248784f84 NeedsCompilation: yes Title: Integrative clustering of multi-type genomic data Description: Integrative clustering of multiple genomic data using a joint latent variable model. biocViews: Microarray, Clustering Author: Qianxing Mo, Ronglai Shen Maintainer: Qianxing Mo , Ronglai Shen git_url: https://git.bioconductor.org/packages/iClusterPlus git_branch: RELEASE_3_8 git_last_commit: 3b2a748 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iClusterPlus_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iClusterPlus_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iClusterPlus_1.18.0.tgz vignettes: vignettes/iClusterPlus/inst/doc/iClusterPlus.pdf, vignettes/iClusterPlus/inst/doc/iManual.pdf vignetteTitles: iClusterPlus, iManual.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE suggestsMe: MultiDataSet Package: iCNV Version: 1.2.1 Depends: R (>= 3.3.1), CODEX Imports: fields, ggplot2, truncnorm, tidyr, data.table, dplyr, grDevices, graphics, stats, utils, rlang Suggests: knitr, rmarkdown, WES.1KG.WUGSC License: GPL-2 MD5sum: 8ac7190ed5a50ed053f107ea0a6d55e2 NeedsCompilation: no Title: Integrated Copy Number Variation detection Description: Integrative copy number variation (CNV) detection from multiple platform and experimental design. biocViews: ImmunoOncology, ExomeSeq, WholeGenome, SNP, CopyNumberVariation, HiddenMarkovModel Author: Zilu Zhou, Nancy Zhang Maintainer: Zilu Zhou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/iCNV git_branch: RELEASE_3_8 git_last_commit: 5f6a1c0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/iCNV_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/iCNV_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iCNV_1.2.1.tgz vignettes: vignettes/iCNV/inst/doc/iCNV-vignette.html vignetteTitles: iCNV Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iCNV/inst/doc/iCNV-vignette.R Package: iCOBRA Version: 1.10.0 Depends: R (>= 3.4) Imports: shiny (>= 0.9.1.9008), shinydashboard, shinyBS, reshape2, ggplot2 (>= 2.0.0), scales, ROCR, dplyr, DT, limma, methods, UpSetR Suggests: knitr, testthat License: GPL (>=2) MD5sum: 144995f01f0fd56500c6d211ae072a31 NeedsCompilation: no Title: Comparison and Visualization of Ranking and Assignment Methods Description: This package provides functions for calculation and visualization of performance metrics for evaluation of ranking and binary classification (assignment) methods. It also contains a shiny application for interactive exploration of results. biocViews: Classification Author: Charlotte Soneson [aut, cre] Maintainer: Charlotte Soneson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/iCOBRA git_branch: RELEASE_3_8 git_last_commit: 2f0af61 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iCOBRA_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iCOBRA_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iCOBRA_1.10.0.tgz vignettes: vignettes/iCOBRA/inst/doc/iCOBRA.html vignetteTitles: iCOBRA User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iCOBRA/inst/doc/iCOBRA.R suggestsMe: SummarizedBenchmark Package: ideal Version: 1.6.1 Depends: topGO Imports: DESeq2, SummarizedExperiment, GenomicRanges, IRanges, S4Vectors, ggplot2 (>= 2.0.0), d3heatmap, pheatmap, pcaExplorer, IHW, gplots, UpSetR, goseq, stringr, dplyr, limma, GOstats, GO.db, AnnotationDbi, shiny (>= 0.12.0), shinydashboard, shinyBS, DT, rentrez, rintrojs, knitr, rmarkdown, shinyAce, BiocParallel, grDevices, methods Suggests: testthat, BiocStyle, airway, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg38.knownGene, DEFormats, edgeR License: MIT + file LICENSE MD5sum: 58cd40764aac749155c99e0b330c7c36 NeedsCompilation: no Title: Interactive Differential Expression AnaLysis Description: This package provides functions for an Interactive Differential Expression AnaLysis of RNA-sequencing datasets, to extract quickly and effectively information downstream the step of differential expression. A Shiny application encapsulates the whole package. biocViews: ImmunoOncology, GeneExpression, DifferentialExpression, RNASeq, Sequencing, Visualization, QualityControl, GUI, GeneSetEnrichment, ReportWriting Author: Federico Marini [aut, cre] () Maintainer: Federico Marini URL: https://github.com/federicomarini/ideal, https://federicomarini.github.io/ideal/ VignetteBuilder: knitr BugReports: https://github.com/federicomarini/ideal/issues git_url: https://git.bioconductor.org/packages/ideal git_branch: RELEASE_3_8 git_last_commit: d202378 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ideal_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ideal_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ideal_1.6.1.tgz vignettes: vignettes/ideal/inst/doc/ideal-usersguide.html vignetteTitles: ideal User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ideal/inst/doc/ideal-usersguide.R Package: IdeoViz Version: 1.18.0 Depends: Biobase, IRanges, GenomicRanges, RColorBrewer, rtracklayer,graphics,GenomeInfoDb License: GPL-2 MD5sum: 9dc076de1e7d704ef8f359bc184c1b84 NeedsCompilation: no Title: Plots data (continuous/discrete) along chromosomal ideogram Description: Plots data associated with arbitrary genomic intervals along chromosomal ideogram. biocViews: Visualization,Microarray Author: Shraddha Pai , Jingliang Ren Maintainer: Shraddha Pai git_url: https://git.bioconductor.org/packages/IdeoViz git_branch: RELEASE_3_8 git_last_commit: 06d6ccc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IdeoViz_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IdeoViz_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IdeoViz_1.18.0.tgz vignettes: vignettes/IdeoViz/inst/doc/Vignette.pdf vignetteTitles: IdeoViz: a package for plotting simple data along ideograms hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/IdeoViz/inst/doc/Vignette.R Package: idiogram Version: 1.58.0 Depends: R (>= 2.10), methods, Biobase, annotate, plotrix Suggests: hu6800.db, hgu95av2.db, golubEsets License: GPL-2 MD5sum: d066bd7ee141691de135e4b6a5aebdda NeedsCompilation: no Title: idiogram Description: A package for plotting genomic data by chromosomal location biocViews: Visualization Author: Karl J. Dykema Maintainer: Karl J. Dykema git_url: https://git.bioconductor.org/packages/idiogram git_branch: RELEASE_3_8 git_last_commit: 6cf362b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/idiogram_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/idiogram_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/idiogram_1.58.0.tgz vignettes: vignettes/idiogram/inst/doc/idiogram.pdf vignetteTitles: HOWTO: idiogram hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/idiogram/inst/doc/idiogram.R dependsOnMe: reb Package: IdMappingAnalysis Version: 1.26.0 Depends: R (>= 2.14), R.oo (>= 1.13.0), rChoiceDialogs Imports: boot, mclust, RColorBrewer, Biobase License: GPL-2 MD5sum: 3c8890afd6e21106448dc0d3bc8b4d50 NeedsCompilation: no Title: ID Mapping Analysis Description: Identifier mapping performance analysis biocViews: Annotation, MultipleComparison Author: Alex Lisovich, Roger Day Maintainer: Alex Lisovich , Roger Day git_url: https://git.bioconductor.org/packages/IdMappingAnalysis git_branch: RELEASE_3_8 git_last_commit: 3e4929f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IdMappingAnalysis_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IdMappingAnalysis_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IdMappingAnalysis_1.26.0.tgz vignettes: vignettes/IdMappingAnalysis/inst/doc/IdMappingAnalysis.pdf vignetteTitles: Critically comparing identifier maps retrieved from bioinformatics annotation resources. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IdMappingAnalysis/inst/doc/IdMappingAnalysis.R Package: IdMappingRetrieval Version: 1.30.0 Depends: R.oo, XML, RCurl, rChoiceDialogs Imports: biomaRt, ENVISIONQuery, AffyCompatible, R.methodsS3, utils License: GPL-2 MD5sum: 7da2fe9ac3cf79adc91f06e3a343cf86 NeedsCompilation: no Title: ID Mapping Data Retrieval Description: Data retrieval for identifier mapping performance analysis biocViews: Annotation, MultipleComparison Author: Alex Lisovich, Roger Day Maintainer: Alex Lisovich , Roger Day git_url: https://git.bioconductor.org/packages/IdMappingRetrieval git_branch: RELEASE_3_8 git_last_commit: 54e25f2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IdMappingRetrieval_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IdMappingRetrieval_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IdMappingRetrieval_1.30.0.tgz vignettes: vignettes/IdMappingRetrieval/inst/doc/IdMappingRetrieval.pdf vignetteTitles: Collection and subsequent fast retrieval of identifier mapping related information from various online sources. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IdMappingRetrieval/inst/doc/IdMappingRetrieval.R Package: iGC Version: 1.12.0 Depends: R (>= 3.2.0) Imports: plyr, data.table Suggests: BiocStyle, knitr, rmarkdown Enhances: doMC License: GPL-2 MD5sum: 1914525e82325febd676e0700ec780e9 NeedsCompilation: no Title: An integrated analysis package of Gene expression and Copy number alteration Description: This package is intended to identify differentially expressed genes driven by Copy Number Alterations from samples with both gene expression and CNA data. biocViews: Software, Biological Question, DifferentialExpression, GenomicVariation, AssayDomain, CopyNumberVariation, GeneExpression, ResearchField, Genetics, Technology, Microarray, Sequencing, WorkflowStep, MultipleComparison Author: Yi-Pin Lai [aut], Liang-Bo Wang [aut, cre], Tzu-Pin Lu [aut], Eric Y. Chuang [aut] Maintainer: Liang-Bo Wang URL: http://github.com/ccwang002/iGC VignetteBuilder: knitr BugReports: http://github.com/ccwang002/iGC/issues git_url: https://git.bioconductor.org/packages/iGC git_branch: RELEASE_3_8 git_last_commit: 2cb99be git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iGC_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iGC_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iGC_1.12.0.tgz vignettes: vignettes/iGC/inst/doc/Introduction.html vignetteTitles: Introduction to iGC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iGC/inst/doc/Introduction.R Package: igvR Version: 1.2.0 Depends: R (>= 3.5.0), GenomicRanges, VariantAnnotation, rtracklayer, BrowserViz (>= 2.0) Imports: methods, BiocGenerics, httpuv, utils Suggests: RUnit, BiocStyle, knitr, rmarkdown License: MIT + file LICENSE MD5sum: 9e2eac0566ea2b2810e66375f24c9917 NeedsCompilation: no Title: igvR: integrative genomics viewer Description: Access to igv.js, the Integrative Genomics Viewer running in a web browser. biocViews: Visualization, ThirdPartyClient, GenomeBrowsers Author: Paul Shannon Maintainer: Paul Shannon VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/igvR git_branch: RELEASE_3_8 git_last_commit: ee4068f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/igvR_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/igvR_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/igvR_1.2.0.tgz vignettes: vignettes/igvR/inst/doc/igvR.html vignetteTitles: "igvR: programmatic access to igv.js,, a browser-based genome track viewer" hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/igvR/inst/doc/igvR.R Package: IHW Version: 1.10.1 Depends: R (>= 3.3.0) Imports: methods, slam, lpsymphony, fdrtool, BiocGenerics Suggests: ggplot2, dplyr, gridExtra, scales, DESeq2, airway, testthat, Matrix, BiocStyle, knitr, rmarkdown, devtools License: Artistic-2.0 MD5sum: 129c488c457edfc691d450a3a1d4860f NeedsCompilation: no Title: Independent Hypothesis Weighting Description: Independent hypothesis weighting (IHW) is a multiple testing procedure that increases power compared to the method of Benjamini and Hochberg by assigning data-driven weights to each hypothesis. The input to IHW is a two-column table of p-values and covariates. The covariate can be any continuous-valued or categorical variable that is thought to be informative on the statistical properties of each hypothesis test, while it is independent of the p-value under the null hypothesis. biocViews: ImmunoOncology, MultipleComparison, RNASeq Author: Nikos Ignatiadis [aut, cre], Wolfgang Huber [aut] Maintainer: Nikos Ignatiadis VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/IHW git_branch: RELEASE_3_8 git_last_commit: ecee111 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/IHW_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/IHW_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IHW_1.10.1.tgz vignettes: vignettes/IHW/inst/doc/introduction_to_ihw.html vignetteTitles: "Introduction to IHW" hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IHW/inst/doc/introduction_to_ihw.R importsMe: ideal suggestsMe: DESeq2, SummarizedBenchmark Package: illuminaio Version: 0.24.0 Imports: base64 Suggests: RUnit, BiocGenerics, IlluminaDataTestFiles (>= 1.0.2), BiocStyle License: GPL-2 Archs: i386, x64 MD5sum: 739638c3a278019ba705240fb8818a65 NeedsCompilation: yes Title: Parsing Illumina Microarray Output Files Description: Tools for parsing Illumina's microarray output files, including IDAT. biocViews: Infrastructure, DataImport, Microarray, ProprietaryPlatforms Author: Keith Baggerly [aut], Henrik Bengtsson [aut], Kasper Daniel Hansen [aut, cre], Matt Ritchie [aut], Mike L. Smith [aut], Tim Triche Jr. [ctb] Maintainer: Kasper Daniel Hansen URL: https://github.com/HenrikBengtsson/illuminaio BugReports: https://github.com/HenrikBengtsson/illuminaio/issues git_url: https://git.bioconductor.org/packages/illuminaio git_branch: RELEASE_3_8 git_last_commit: 47953c7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/illuminaio_0.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/illuminaio_0.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/illuminaio_0.24.0.tgz vignettes: vignettes/illuminaio/inst/doc/EncryptedFormat.pdf, vignettes/illuminaio/inst/doc/illuminaio.pdf vignetteTitles: Description of Encrypted IDAT Format, Introduction to illuminaio hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/illuminaio/inst/doc/illuminaio.R dependsOnMe: normalize450K, RnBeads, wateRmelon importsMe: beadarray, crlmm, methylumi, minfi, sesame suggestsMe: limma Package: imageHTS Version: 1.32.1 Depends: R (>= 2.9.0), EBImage (>= 4.3.12), cellHTS2 (>= 2.10.0) Imports: tools, Biobase, hwriter, methods, vsn, stats, utils, e1071 Suggests: BiocStyle, MASS License: LGPL-2.1 MD5sum: 653df3dba07dae97e77bccfae0c4f3a9 NeedsCompilation: no Title: Analysis of high-throughput microscopy-based screens Description: imageHTS is an R package dedicated to the analysis of high-throughput microscopy-based screens. The package provides a modular and extensible framework to segment cells, extract quantitative cell features, predict cell types and browse screen data through web interfaces. Designed to operate in distributed environments, imageHTS provides a standardized access to remote data and facilitates the dissemination of high-throughput microscopy-based datasets. biocViews: ImmunoOncology, Software, CellBasedAssays, Preprocessing, Visualization Author: Gregoire Pau, Xian Zhang, Michael Boutros, Wolfgang Huber Maintainer: Joseph Barry git_url: https://git.bioconductor.org/packages/imageHTS git_branch: RELEASE_3_8 git_last_commit: e914c11 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/imageHTS_1.32.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/imageHTS_1.32.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/imageHTS_1.32.1.tgz vignettes: vignettes/imageHTS/inst/doc/imageHTS-introduction.pdf vignetteTitles: Analysis of high-throughput microscopy-based screens with imageHTS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/imageHTS/inst/doc/imageHTS-introduction.R Package: IMAS Version: 1.6.1 Depends: R (> 3.0.0),GenomicFeatures, ggplot2, IVAS Imports: doParallel, lme4, BiocGenerics, GenomicRanges, IRanges, foreach, AnnotationDbi, S4Vectors, GenomeInfoDb, stats, ggfortify, grDevices, methods, Matrix, utils, graphics, gridExtra, grid, lattice, Rsamtools, survival, BiocParallel, GenomicAlignments, parallel Suggests: BiocStyle, RUnit License: GPL-2 MD5sum: c505d1d95a0b342aa38c92288341f853 NeedsCompilation: no Title: Integrative analysis of Multi-omics data for Alternative Splicing Description: Integrative analysis of Multi-omics data for Alternative splicing. biocViews: ImmunoOncology, AlternativeSplicing, DifferentialExpression, DifferentialSplicing, GeneExpression, GeneRegulation, Regression, RNASeq, Sequencing, SNP, Software, Transcription Author: Seonggyun Han, Younghee Lee Maintainer: Seonggyun Han git_url: https://git.bioconductor.org/packages/IMAS git_branch: RELEASE_3_8 git_last_commit: a03cea5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/IMAS_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/IMAS_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IMAS_1.6.1.tgz vignettes: vignettes/IMAS/inst/doc/IMAS.pdf vignetteTitles: IMAS : Integrative analysis of Multi-omics data for Alternative Splicing hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IMAS/inst/doc/IMAS.R Package: Imetagene Version: 1.12.0 Depends: R (>= 3.2.0), metagene, shiny Imports: d3heatmap, shinyBS, shinyFiles, shinythemes, ggplot2 Suggests: knitr, BiocStyle, rmarkdown License: Artistic-2.0 | file LICENSE MD5sum: 2e924c04928d481ee78f0fdf35f51eeb NeedsCompilation: no Title: A graphical interface for the metagene package Description: This package provide a graphical user interface to the metagene package. This will allow people with minimal R experience to easily complete metagene analysis. biocViews: ChIPSeq, Genetics, MultipleComparison, Coverage, Alignment, Sequencing Author: Audrey Lemacon , Charles Joly Beauparlant , Arnaud Droit Maintainer: Audrey Lemacon VignetteBuilder: knitr BugReports: https://github.com/andronekomimi/Imetagene/issues git_url: https://git.bioconductor.org/packages/Imetagene git_branch: RELEASE_3_8 git_last_commit: 88865e2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Imetagene_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Imetagene_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Imetagene_1.12.0.tgz vignettes: vignettes/Imetagene/inst/doc/imetagene.html vignetteTitles: Presentation of Imetagene hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Imetagene/inst/doc/imetagene.R Package: IMMAN Version: 1.2.0 Imports: STRINGdb, Biostrings, igraph, graphics, utils, seqinr, BiocFileCache Suggests: knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: cd457c7494ce1cb6339920531190bb73 NeedsCompilation: no Title: Interlog protein network reconstruction by Mapping and Mining ANalysis Description: Reconstructing Interlog Protein Network (IPN) integrated from several Protein protein Interaction Networks (PPINs). Using this package, overlaying different PPINs to mine conserved common networks between diverse species will be applicable. biocViews: SequenceMatching, Alignment, SystemsBiology, GraphAndNetwork, Network, Proteomics Author: Payman Nickchi, Abdollah Safari, Minoo Ashtiani, Mohieddin Jafari Maintainer: Minoo Ashtiani VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/IMMAN git_branch: RELEASE_3_8 git_last_commit: 77fbe7c git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/IMMAN_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IMMAN_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IMMAN_1.2.0.tgz vignettes: vignettes/IMMAN/inst/doc/IMMAN.html vignetteTitles: IMMAN hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IMMAN/inst/doc/IMMAN.R Package: ImmuneSpaceR Version: 1.10.5 Imports: utils, R6, data.table, curl, httr, Rlabkey (>= 2.1.136), Biobase, pheatmap, ggplot2, scales, stats, gtools, gplots, reshape2, plotly, heatmaply (>= 0.7.0), rjson, rmarkdown, preprocessCore, parallel, flowCore, flowWorkspace, digest Suggests: knitr, testthat License: GPL-2 MD5sum: 00ebc318cbc1ed66d7fd4712f8b8df32 NeedsCompilation: no Title: A Thin Wrapper around the ImmuneSpace Database Description: Provides a convenient API for accessing data sets within ImmuneSpace (www.immunespace.org), the data repository and analysis platform of the Human Immunology Project Consortium (HIPC). biocViews: DataImport, DataRepresentation, ThirdPartyClient Author: Greg Finak [aut], Renan Sauteraud [aut], Mike Jiang [aut], Gil Guday [aut], Leo Dashevskiy [aut], Evan Henrich [aut], Ju Yeong Kim [aut], Lauren Wolfe [aut], Raphael Gottardo [aut], ImmuneSpace Package Maintainer [cre, cph] Maintainer: ImmuneSpace Package Maintainer URL: https://github.com/RGLab/ImmuneSpaceR VignetteBuilder: knitr BugReports: https://github.com/RGLab/ImmuneSpaceR/issues git_url: https://git.bioconductor.org/packages/ImmuneSpaceR git_branch: RELEASE_3_8 git_last_commit: f275ebc git_last_commit_date: 2019-03-27 Date/Publication: 2019-03-27 source.ver: src/contrib/ImmuneSpaceR_1.10.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/ImmuneSpaceR_1.10.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ImmuneSpaceR_1.10.5.tgz vignettes: vignettes/ImmuneSpaceR/inst/doc/getDataset.html, vignettes/ImmuneSpaceR/inst/doc/getGEMatrix.html, vignettes/ImmuneSpaceR/inst/doc/interactiveNetrc.html, vignettes/ImmuneSpaceR/inst/doc/Intro_to_ImmuneSpaceR.html, vignettes/ImmuneSpaceR/inst/doc/report_SDY144.html, vignettes/ImmuneSpaceR/inst/doc/report_SDY180.html, vignettes/ImmuneSpaceR/inst/doc/report_SDY269.html vignetteTitles: Downloading Datasets with getDataset, Handling Expression Matrices with ImmuneSpaceR, interactive_netrc() Walkthrough, An Introduction to the ImmuneSpaceR Package, SDY144: Correlation of HAI/Virus Neutralizition Titer and Cell Counts, SDY180: Abundance of Plasmablasts Measured by Multiparameter Flow Cytometry, SDY269: Correlating HAI with Flow Cytometry and ELISPOT Results hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ImmuneSpaceR/inst/doc/getDataset.R, vignettes/ImmuneSpaceR/inst/doc/getGEMatrix.R, vignettes/ImmuneSpaceR/inst/doc/interactiveNetrc.R, vignettes/ImmuneSpaceR/inst/doc/Intro_to_ImmuneSpaceR.R, vignettes/ImmuneSpaceR/inst/doc/report_SDY144.R, vignettes/ImmuneSpaceR/inst/doc/report_SDY180.R, vignettes/ImmuneSpaceR/inst/doc/report_SDY269.R Package: immunoClust Version: 1.14.1 Depends: R(>= 3.3), methods, stats, graphics, grid, lattice, grDevices, flowCore Suggests: BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: de57ef8eaee13ab9a1c3dd9bbea5f857 NeedsCompilation: yes Title: immunoClust - Automated Pipeline for Population Detection in Flow Cytometry Description: Model based clustering and meta-clustering of Flow Cytometry Data biocViews: Clustering, FlowCytometry, CellBasedAssays, ImmunoOncology Author: Till Soerensen Maintainer: Till Soerensen git_url: https://git.bioconductor.org/packages/immunoClust git_branch: RELEASE_3_8 git_last_commit: c89a3c8 git_last_commit_date: 2018-12-01 Date/Publication: 2018-12-01 source.ver: src/contrib/immunoClust_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/immunoClust_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/immunoClust_1.14.1.tgz vignettes: vignettes/immunoClust/inst/doc/immunoClust.pdf vignetteTitles: immunoClust package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/immunoClust/inst/doc/immunoClust.R Package: IMPCdata Version: 1.18.0 Depends: R (>= 2.3.0) Imports: rjson License: file LICENSE MD5sum: 7a7078db25def7231965af0a6604b598 NeedsCompilation: no Title: Retrieves data from IMPC database Description: Package contains methods for data retrieval from IMPC Database. biocViews: ExperimentData Author: Natalja Kurbatova, Jeremy Mason Maintainer: Jeremy Mason git_url: https://git.bioconductor.org/packages/IMPCdata git_branch: RELEASE_3_8 git_last_commit: 16b3b95 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IMPCdata_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IMPCdata_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IMPCdata_1.18.0.tgz vignettes: vignettes/IMPCdata/inst/doc/IMPCdata.pdf vignetteTitles: IMPCdata Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/IMPCdata/inst/doc/IMPCdata.R Package: ImpulseDE Version: 1.8.0 Depends: graphics, grDevices, stats, utils, parallel, compiler, R (>= 3.2.3) Imports: amap, boot Suggests: longitudinal, knitr License: GPL-3 MD5sum: 99b95fd2df1ea360f4555129a1d845bb NeedsCompilation: no Title: Detection of DE genes in time series data using impulse models Description: ImpulseDE is suited to capture single impulse-like patterns in high throughput time series datasets. By fitting a representative impulse model to each gene, it reports differentially expressed genes whether across time points in a single experiment or between two time courses from two experiments. To optimize the running time, the code makes use of clustering steps and multi-threading. biocViews: Software, StatisticalMethod, TimeCourse Author: Jil Sander [aut, cre], Nir Yosef [aut] Maintainer: Jil Sander , Nir Yosef URL: https://github.com/YosefLab/ImpulseDE VignetteBuilder: knitr BugReports: https://github.com/YosefLab/ImpulseDE/issues git_url: https://git.bioconductor.org/packages/ImpulseDE git_branch: RELEASE_3_8 git_last_commit: 41a26ed git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ImpulseDE_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ImpulseDE_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ImpulseDE_1.8.0.tgz vignettes: vignettes/ImpulseDE/inst/doc/ImpulseDE.pdf vignetteTitles: ImpulseDE hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ImpulseDE/inst/doc/ImpulseDE.R Package: ImpulseDE2 Version: 1.6.1 Imports: Biobase, BiocParallel, ComplexHeatmap, circlize, compiler, cowplot, DESeq2, ggplot2, grDevices, knitr, Matrix, methods, S4Vectors, stats, SummarizedExperiment, utils License: Artistic-2.0 MD5sum: f96b8e442fa51bcfc48379cf4299de80 NeedsCompilation: no Title: Differential expression analysis of longitudinal count data sets Description: ImpulseDE2 is a differential expression algorithm for longitudinal count data sets which arise in sequencing experiments such as RNA-seq, ChIP-seq, ATAC-seq and DNaseI-seq. ImpulseDE2 is based on a negative binomial noise model with dispersion trend smoothing by DESeq2 and uses the impulse model to constrain the mean expression trajectory of each gene. The impulse model was empirically found to fit global expression changes in cells after environmental and developmental stimuli and is therefore appropriate in most cell biological scenarios. The constraint on the mean expression trajectory prevents overfitting to small expression fluctuations. Secondly, ImpulseDE2 has higher statistical testing power than generalized linear model-based differential expression algorithms which fit time as a categorial variable if more than six time points are sampled because of the fixed number of parameters. biocViews: ImmunoOncology, Software, StatisticalMethod, TimeCourse, Sequencing, DifferentialExpression, GeneExpression, CellBiology, CellBasedAssays Author: David S Fischer [aut, cre], Fabian J Theis [ctb], Nir Yosef [ctb] Maintainer: David S Fischer VignetteBuilder: knitr BugReports: https://github.com/YosefLab/ImpulseDE2/issues git_url: https://git.bioconductor.org/packages/ImpulseDE2 git_branch: RELEASE_3_8 git_last_commit: 06b8982 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ImpulseDE2_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ImpulseDE2_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ImpulseDE2_1.6.1.tgz vignettes: vignettes/ImpulseDE2/inst/doc/ImpulseDE2_Tutorial.html vignetteTitles: ImpulseDE2 Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ImpulseDE2/inst/doc/ImpulseDE2_Tutorial.R Package: impute Version: 1.56.0 Depends: R (>= 2.10) License: GPL-2 Archs: i386, x64 MD5sum: f9e8aa154a5e8069fe4cc12c61355e63 NeedsCompilation: yes Title: impute: Imputation for microarray data Description: Imputation for microarray data (currently KNN only) biocViews: Microarray Author: Trevor Hastie, Robert Tibshirani, Balasubramanian Narasimhan, Gilbert Chu Maintainer: Balasubramanian Narasimhan git_url: https://git.bioconductor.org/packages/impute git_branch: RELEASE_3_8 git_last_commit: 6c037ed git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/impute_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/impute_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/impute_1.56.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: CGHcall, TIN importsMe: CancerSubtypes, doppelgangR, EGAD, fastLiquidAssociation, genomation, MethylMix, miRLAB, MSnbase, Pigengene, REMP, Rnits suggestsMe: BioNet, graphite, MethPed, RnBeads, TCGAutils Package: INDEED Version: 1.0.1 Depends: R (>= 3.5), glasso (>= 1.8) Imports: utils (>= 3.3.1), stats (>= 3.3.1), graphics (>= 3.3.1), devtools (>= 1.13.0) Suggests: knitr (>= 1.19), rmarkdown (>= 1.8), testthat (>= 2.0.0) License: Artistic-2.0 MD5sum: d7292e9c864bf73b2f3c4ecad7b459aa NeedsCompilation: no Title: An Implementation of Integrated Differential Expression and Differential Network Analysis for Biomarker Candidate Selection Description: An Implementation of Integrated Differential Expression and Differential Network Analysis of Omic Data. The differential network is obtained based on partial correlation or correlation. biocViews: ImmunoOncology, Software, ResearchField, BiologicalQuestion, StatisticalMethod, DifferentialExpression, MassSpectrometry, Metabolomics Author: Zhenzhi Li Maintainer: Zhenzhi Li , Yiming Zuo URL: http://github.com/ressomlab/INDEED VignetteBuilder: knitr BugReports: http://github.com/ressomlab/INDEED/issues git_url: https://git.bioconductor.org/packages/INDEED git_branch: RELEASE_3_8 git_last_commit: d8c8869 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/INDEED_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/INDEED_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/INDEED_1.0.1.tgz vignettes: vignettes/INDEED/inst/doc/Introduction_to_INDEED.html vignetteTitles: INDEED R package for cancer biomarker candidate selection hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/INDEED/inst/doc/Introduction_to_INDEED.R Package: InPAS Version: 1.14.2 Depends: R (>= 3.1), methods, Biobase, GenomicRanges, GenomicFeatures, S4Vectors Imports: AnnotationDbi, BSgenome, cleanUpdTSeq, Gviz, seqinr, preprocessCore, IRanges, GenomeInfoDb, depmixS4, limma, BiocParallel Suggests: RUnit, BiocGenerics, BiocStyle, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10, org.Hs.eg.db, org.Mm.eg.db, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Mmusculus.UCSC.mm10.knownGene, rtracklayer, knitr License: GPL (>= 2) MD5sum: 2191bd7fa07c42f751d49ba206241ddd NeedsCompilation: no Title: Identification of Novel alternative PolyAdenylation Sites (PAS) Description: Alternative polyadenylation (APA) is one of the important post-transcriptional regulation mechanisms which occurs in most human genes. InPAS facilitates the discovery of novel APA sites from RNAseq data. It leverages cleanUpdTSeq to fine tune identified APA sites. biocViews: RNASeq, Sequencing, AlternativeSplicing, Coverage, DifferentialSplicing, GeneRegulation, Transcription, ImmunoOncology Author: Jianhong Ou, Sung Mi Park, Michael R. Green and Lihua Julie Zhu Maintainer: Jianhong Ou , Lihua Julie Zhu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/InPAS git_branch: RELEASE_3_8 git_last_commit: cad7f1f git_last_commit_date: 2019-04-09 Date/Publication: 2019-04-09 source.ver: src/contrib/InPAS_1.14.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/InPAS_1.14.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/InPAS_1.14.2.tgz vignettes: vignettes/InPAS/inst/doc/InPAS.html vignetteTitles: InPAS Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/InPAS/inst/doc/InPAS.R Package: INPower Version: 1.18.0 Depends: R (>= 3.1.0), mvtnorm Suggests: RUnit, BiocGenerics License: GPL-2 + file LICENSE MD5sum: be5f4b9a24bea8cb1b0942152d79f49c NeedsCompilation: no Title: An R package for computing the number of susceptibility SNPs Description: An R package for computing the number of susceptibility SNPs and power of future studies biocViews: SNP Author: Ju-Hyun Park Maintainer: Bill Wheeler git_url: https://git.bioconductor.org/packages/INPower git_branch: RELEASE_3_8 git_last_commit: b8886bc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/INPower_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/INPower_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/INPower_1.18.0.tgz vignettes: vignettes/INPower/inst/doc/vignette.pdf vignetteTitles: INPower Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/INPower/inst/doc/vignette.R Package: INSPEcT Version: 1.12.2 Depends: R (>= 3.2), methods, Biobase, BiocParallel Imports: pROC, deSolve, rootSolve, compiler, preprocessCore, GenomicFeatures, GenomicRanges, IRanges, BiocGenerics, GenomicAlignments, Rsamtools, S4Vectors, DESeq2, plgem, SummarizedExperiment, TxDb.Mmusculus.UCSC.mm9.knownGene, shiny Suggests: BiocStyle, knitr License: GPL-2 MD5sum: 063fc0c82b4549da99f42ae523ff3a10 NeedsCompilation: no Title: Analysis of 4sU-seq and RNA-seq time-course data Description: INSPEcT (INference of Synthesis, Processing and dEgradation rates from Transcriptomic data) RNA-seq data in time-course experiments or different conditions, with or without the support of nascent RNA data. biocViews: Sequencing, RNASeq, GeneRegulation, TimeCourse, SystemsBiology Author: Stefano de Pretis Maintainer: Stefano de Pretis VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/INSPEcT git_branch: RELEASE_3_8 git_last_commit: 4bd62ca git_last_commit_date: 2019-04-04 Date/Publication: 2019-04-04 source.ver: src/contrib/INSPEcT_1.12.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/INSPEcT_1.12.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/INSPEcT_1.12.2.tgz vignettes: vignettes/INSPEcT/inst/doc/INSPEcT.pdf, vignettes/INSPEcT/inst/doc/RNAdynamics.pdf vignetteTitles: INSPEcT, RNAdynamics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/INSPEcT/inst/doc/INSPEcT.R, vignettes/INSPEcT/inst/doc/RNAdynamics.R Package: InTAD Version: 1.2.3 Depends: R (>= 3.5), methods, S4Vectors, IRanges, GenomicRanges, MultiAssayExperiment, SummarizedExperiment,stats Imports: BiocGenerics,Biobase,rtracklayer,parallel,graphics,mclust,qvalue, ggplot2,utils,ggpubr Suggests: testthat, BiocStyle, knitr, rmarkdown License: GPL (>=2) MD5sum: 3d371b13e7c28938cad49e9d40d3557f NeedsCompilation: no Title: Search for correlation between epigenetic signals and gene expression in TADs Description: The package is focused on the detection of correlation between expressed genes and selected epigenomic signals i.e. enhancers obtained from ChIP-seq data within topologically associated domains (TADs). Various parameters can be controlled to investigate the influence of external factors and visualization plots are available for each analysis step. biocViews: Epigenetics, Sequencing, ChIPSeq, RNASeq, HiC, GeneExpression,ImmunoOncology Author: Konstantin Okonechnikov, Serap Erkek, Lukas Chavez Maintainer: Konstantin Okonechnikov VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/InTAD git_branch: RELEASE_3_8 git_last_commit: 31ed1ff git_last_commit_date: 2019-02-25 Date/Publication: 2019-02-27 source.ver: src/contrib/InTAD_1.2.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/InTAD_1.2.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/InTAD_1.2.3.tgz vignettes: vignettes/InTAD/inst/doc/InTAD.html vignetteTitles: Correlation of epigenetic signals and genes in TADs hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/InTAD/inst/doc/InTAD.R Package: intansv Version: 1.22.0 Depends: R (>= 2.14.0), plyr, ggbio, GenomicRanges Imports: BiocGenerics, IRanges License: Artistic-2.0 MD5sum: 1286b959d63fb61017de3f1244738a42 NeedsCompilation: no Title: Integrative analysis of structural variations Description: This package provides efficient tools to read and integrate structural variations predicted by popular softwares. Annotation and visulation of structural variations are also implemented in the package. biocViews: Genetics, Annotation, Sequencing, Software Author: Wen Yao Maintainer: Wen Yao git_url: https://git.bioconductor.org/packages/intansv git_branch: RELEASE_3_8 git_last_commit: e0d6813 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/intansv_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/intansv_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/intansv_1.22.0.tgz vignettes: vignettes/intansv/inst/doc/intansvOverview.pdf vignetteTitles: An Introduction to intansv hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/intansv/inst/doc/intansvOverview.R Package: InteractionSet Version: 1.10.0 Depends: R (>= 3.5), GenomicRanges, SummarizedExperiment Imports: IRanges, S4Vectors (>= 0.19.4), GenomeInfoDb, BiocGenerics, methods, Matrix, Rcpp LinkingTo: Rcpp Suggests: testthat, knitr, rmarkdown, BiocStyle License: GPL-3 Archs: i386, x64 MD5sum: 9aa7ddaaad56bef6685c95ae3950141a NeedsCompilation: yes Title: Base Classes for Storing Genomic Interaction Data Description: Provides the GInteractions, InteractionSet and ContactMatrix objects and associated methods for storing and manipulating genomic interaction data from Hi-C and ChIA-PET experiments. biocViews: Infrastructure, DataRepresentation, Software, HiC Author: Aaron Lun [aut, cre], Malcolm Perry [aut], Elizabeth Ing-Simmons [aut] Maintainer: Aaron Lun SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/InteractionSet git_branch: RELEASE_3_8 git_last_commit: fbbd09b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/InteractionSet_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/InteractionSet_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/InteractionSet_1.10.0.tgz vignettes: vignettes/InteractionSet/inst/doc/interactions.html vignetteTitles: Interacting with InteractionSet classes for genomic interaction data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/InteractionSet/inst/doc/interactions.R dependsOnMe: diffHic, GenomicInteractions, MACPET, sevenC importsMe: CAGEfightR, HiCcompare, trackViewer Package: interactiveDisplay Version: 1.20.0 Depends: R (>= 2.10), methods, BiocGenerics, grid Imports: interactiveDisplayBase (>= 1.7.3), shiny, RColorBrewer, ggplot2, reshape2, plyr, gridSVG, XML, Category, AnnotationDbi Suggests: RUnit, hgu95av2.db, knitr, GenomicRanges, SummarizedExperiment, GOstats, ggbio, GO.db, Gviz, rtracklayer, metagenomeSeq, gplots, vegan, Biobase Enhances: rstudio License: Artistic-2.0 MD5sum: 34c2b077ccf7ef2b8048e802cb499e32 NeedsCompilation: no Title: Package for enabling powerful shiny web displays of Bioconductor objects Description: The interactiveDisplay package contains the methods needed to generate interactive Shiny based display methods for Bioconductor objects. biocViews: GO, GeneExpression, Microarray, Sequencing, Classification, Network, QualityControl, Visualization, Visualization, Genetics, DataRepresentation, GUI, AnnotationData Author: Shawn Balcome, Marc Carlson Maintainer: Shawn Balcome VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/interactiveDisplay git_branch: RELEASE_3_8 git_last_commit: 0eec5d4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/interactiveDisplay_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/interactiveDisplay_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/interactiveDisplay_1.20.0.tgz vignettes: vignettes/interactiveDisplay/inst/doc/interactiveDisplay.pdf vignetteTitles: interactiveDisplay: A package for enabling interactive visualization of Bioconductor objects hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/interactiveDisplay/inst/doc/interactiveDisplay.R suggestsMe: metagenomeSeq Package: interactiveDisplayBase Version: 1.20.0 Depends: R (>= 2.10), methods, BiocGenerics Imports: shiny Suggests: knitr Enhances: rstudioapi License: Artistic-2.0 MD5sum: 9fde04ff11ca32a7c8d7a5e59e10efae NeedsCompilation: no Title: Base package for enabling powerful shiny web displays of Bioconductor objects Description: The interactiveDisplayBase package contains the the basic methods needed to generate interactive Shiny based display methods for Bioconductor objects. biocViews: GO, GeneExpression, Microarray, Sequencing, Classification, Network, QualityControl, Visualization, Visualization, Genetics, DataRepresentation, GUI, AnnotationData Author: Shawn Balcome, Marc Carlson Maintainer: Shawn Balcome VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/interactiveDisplayBase git_branch: RELEASE_3_8 git_last_commit: f40912c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/interactiveDisplayBase_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/interactiveDisplayBase_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/interactiveDisplayBase_1.20.0.tgz vignettes: vignettes/interactiveDisplayBase/inst/doc/interactiveDisplayBase.html vignetteTitles: Using interactiveDisplayBase for Bioconductor object visualization and modification hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/interactiveDisplayBase/inst/doc/interactiveDisplayBase.R importsMe: AnnotationHub, interactiveDisplay Package: IntEREst Version: 1.6.2 Depends: R (>= 3.4), GenomicRanges, Rsamtools, SummarizedExperiment, edgeR, S4Vectors Imports: seqLogo, Biostrings, GenomicFeatures, IRanges, seqinr, graphics, grDevices, stats, utils, grid, methods, DBI, RMySQL, GenomicAlignments, BiocParallel, BiocGenerics, DEXSeq, DESeq2 Suggests: clinfun, knitr, BSgenome.Hsapiens.UCSC.hg19 License: GPL-2 MD5sum: edf05a618b45a8de8a140ea064601d1a NeedsCompilation: no Title: Intron-Exon Retention Estimator Description: This package performs Intron-Exon Retention analysis on RNA-seq data (.bam files). biocViews: Software, AlternativeSplicing, Coverage, DifferentialSplicing, Sequencing, RNASeq, Alignment, Normalization, DifferentialExpression, ImmunoOncology Author: Ali Oghabian , Dario Greco , Mikko Frilander Maintainer: Ali Oghabian , Mikko Frilander VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/IntEREst git_branch: RELEASE_3_8 git_last_commit: 8b33290 git_last_commit_date: 2019-02-11 Date/Publication: 2019-02-11 source.ver: src/contrib/IntEREst_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/IntEREst_1.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IntEREst_1.6.2.tgz vignettes: vignettes/IntEREst/inst/doc/IntEREst.html vignetteTitles: IntEREst,, Intron Exon Retention Estimator hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IntEREst/inst/doc/IntEREst.R Package: InterMineR Version: 1.4.1 Depends: R (>= 3.4.1) Imports: Biostrings, RCurl, XML, xml2, RJSONIO, sqldf, igraph, httr, S4Vectors, IRanges, GenomicRanges, SummarizedExperiment, methods Suggests: BiocStyle, Gviz, knitr, rmarkdown, GeneAnswers, GO.db, org.Hs.eg.db License: LGPL MD5sum: 8b0b9de68ba80994ea1a0a7a6d90ee36 NeedsCompilation: no Title: R Interface with InterMine-Powered Databases Description: Databases based on the InterMine platform such as FlyMine, modMine (modENCODE), RatMine, YeastMine, HumanMine and TargetMine are integrated databases of genomic, expression and protein data for various organisms. Integrating data makes it possible to run sophisticated data mining queries that span domains of biological knowledge. This R package provides interfaces with these databases through webservices. It makes most from the correspondence of the data frame object in R and the table object in databases, while hiding the details of data exchange through XML or JSON. biocViews: GeneExpression, SNP, GeneSetEnrichment, DifferentialExpression, GeneRegulation, GenomeAnnotation, GenomeWideAssociation, FunctionalPrediction, AlternativeSplicing, ComparativeGenomics, FunctionalGenomics, Proteomics, SystemsBiology, Microarray, MultipleComparison, Pathways, GO, KEGG, Reactome, Visualization Author: Bing Wang, Julie Sullivan, Rachel Lyne, Konstantinos Kyritsis Maintainer: InterMine Team VignetteBuilder: knitr BugReports: https://github.com/intermine/intermineR/issues git_url: https://git.bioconductor.org/packages/InterMineR git_branch: RELEASE_3_8 git_last_commit: 1fdb15b git_last_commit_date: 2018-12-06 Date/Publication: 2018-12-06 source.ver: src/contrib/InterMineR_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/InterMineR_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/InterMineR_1.4.1.tgz vignettes: vignettes/InterMineR/inst/doc/Enrichment_Analysis_and_Visualization.html, vignettes/InterMineR/inst/doc/FlyMine_Genomic_Visualizations.html, vignettes/InterMineR/inst/doc/InterMineR.html vignetteTitles: Enrichment Analysis and Visualization, FlyMine Genomic Visualizations, InterMineR Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/InterMineR/inst/doc/Enrichment_Analysis_and_Visualization.R, vignettes/InterMineR/inst/doc/FlyMine_Genomic_Visualizations.R, vignettes/InterMineR/inst/doc/InterMineR.R Package: IntramiRExploreR Version: 1.4.0 Depends: R (>= 3.4) Imports: igraph (>= 1.0.1), FGNet (>= 3.0.7), knitr (>= 1.12.3), stats, utils, grDevices, graphics Suggests: RDAVIDWebService, gProfileR, topGO, KEGGprofile, org.Dm.eg.db, rmarkdown, testthat License: GPL-2 MD5sum: 9dacefac5bab443f1f1e9fb9327c02c0 NeedsCompilation: no Title: Predicting Targets for Drosophila Intragenic miRNAs Description: Intra-miR-ExploreR, an integrative miRNA target prediction bioinformatics tool, identifies targets combining expression and biophysical interactions of a given microRNA (miR). Using the tool, we have identified targets for 92 intragenic miRs in D. melanogaster, using available microarray expression data, from Affymetrix 1 and Affymetrix2 microarray array platforms, providing a global perspective of intragenic miR targets in Drosophila. Predicted targets are grouped according to biological functions using the DAVID Gene Ontology tool and are ranked based on a biologically relevant scoring system, enabling the user to identify functionally relevant targets for a given miR. biocViews: Software, Microarray, GeneTarget, StatisticalMethod, GeneExpression, GenePrediction Author: Surajit Bhattacharya and Daniel Cox Maintainer: Surajit Bhattacharya URL: https://github.com/sbhattacharya3/IntramiRExploreR/ VignetteBuilder: knitr BugReports: https://github.com/sbhattacharya3/IntramiRExploreR/issues git_url: https://git.bioconductor.org/packages/IntramiRExploreR git_branch: RELEASE_3_8 git_last_commit: 54a81cb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IntramiRExploreR_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IntramiRExploreR_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IntramiRExploreR_1.4.0.tgz vignettes: vignettes/IntramiRExploreR/inst/doc/IntramiRExploreR_vignettes.html vignetteTitles: IntramiRExploreR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IntramiRExploreR/inst/doc/IntramiRExploreR_vignettes.R Package: inveRsion Version: 1.30.0 Depends: methods, haplo.stats Imports: graphics, methods, utils License: GPL (>= 2) Archs: i386, x64 MD5sum: a412874157e3ce4f3c4ecea6fe37318f NeedsCompilation: yes Title: Inversions in genotype data Description: Package to find genetic inversions in genotype (SNP array) data. biocViews: Microarray, SNP Author: Alejandro Caceres Maintainer: Alejandro Caceres git_url: https://git.bioconductor.org/packages/inveRsion git_branch: RELEASE_3_8 git_last_commit: 348368f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/inveRsion_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/inveRsion_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/inveRsion_1.30.0.tgz vignettes: vignettes/inveRsion/inst/doc/inveRsion.pdf vignetteTitles: Quick start guide for inveRsion package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/inveRsion/inst/doc/inveRsion.R Package: IONiseR Version: 2.6.0 Depends: R (>= 3.4) Imports: rhdf5, dplyr, magrittr, tidyr, ShortRead, Biostrings, ggplot2, methods, BiocGenerics, XVector, tibble, stats, BiocParallel, bit64, stringr, utils Suggests: BiocStyle, knitr, rmarkdown, gridExtra, testthat, minionSummaryData License: MIT + file LICENSE MD5sum: 61e911d51f0caa89932208c837ab6342 NeedsCompilation: no Title: Quality Assessment Tools for Oxford Nanopore MinION data Description: IONiseR provides tools for the quality assessment of Oxford Nanopore MinION data. It extracts summary statistics from a set of fast5 files and can be used either before or after base calling. In addition to standard summaries of the read-types produced, it provides a number of plots for visualising metrics relative to experiment run time or spatially over the surface of a flowcell. biocViews: QualityControl, DataImport, Sequencing Author: Mike Smith [aut, cre] Maintainer: Mike Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/IONiseR git_branch: RELEASE_3_8 git_last_commit: 9690b6b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IONiseR_2.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IONiseR_2.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IONiseR_2.6.0.tgz vignettes: vignettes/IONiseR/inst/doc/IONiseR.html vignetteTitles: Quality assessment tools for nanopore data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/IONiseR/inst/doc/IONiseR.R Package: iPAC Version: 1.26.0 Depends: R(>= 2.15),gdata, scatterplot3d, Biostrings, multtest License: GPL-2 MD5sum: 11d1424c3e0f5f1d56e7a97e038d5c08 NeedsCompilation: no Title: Identification of Protein Amino acid Clustering Description: iPAC is a novel tool to identify somatic amino acid mutation clustering within proteins while taking into account protein structure. biocViews: Clustering, Proteomics Author: Gregory Ryslik, Hongyu Zhao Maintainer: Gregory Ryslik git_url: https://git.bioconductor.org/packages/iPAC git_branch: RELEASE_3_8 git_last_commit: bebe766 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iPAC_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iPAC_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iPAC_1.26.0.tgz vignettes: vignettes/iPAC/inst/doc/iPAC.pdf vignetteTitles: iPAC: identification of Protein Amino acid Mutations hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iPAC/inst/doc/iPAC.R dependsOnMe: QuartPAC Package: ipdDb Version: 1.0.0 Depends: R (>= 3.5.0), methods, AnnotationDbi (>= 1.43.1), AnnotationHub Imports: Biostrings, GenomicRanges, RSQLite, DBI, IRanges, stats, assertthat Suggests: knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: 2fb18bc886d7261c082f6aef486d862f NeedsCompilation: no Title: IPD IMGT/HLA and IPD KIR database for Homo sapiens Description: All alleles from the IPD IMGT/HLA and IPD KIR database for Homo sapiens. Reference: Robinson J, Maccari G, Marsh SGE, Walter L, Blokhuis J, Bimber B, Parham P, De Groot NG, Bontrop RE, Guethlein LA, and Hammond JA KIR Nomenclature in non-human species Immunogenetics (2018), in preparation. biocViews: GenomicVariation, SequenceMatching, VariantAnnotation, DataRepresentation Author: Steffen Klasberg Maintainer: Steffen Klasberg URL: https://github.com/DKMS-LSL/ipdDb organism: Homo sapiens VignetteBuilder: knitr BugReports: https://github.com/DKMS-LSL/ipdDb/issues/new git_url: https://git.bioconductor.org/packages/ipdDb git_branch: RELEASE_3_8 git_last_commit: 6169c71 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ipdDb_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ipdDb_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ipdDb_1.0.0.tgz vignettes: vignettes/ipdDb/inst/doc/Readme.html vignetteTitles: ipdDb hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ipdDb/inst/doc/Readme.R Package: IPO Version: 1.8.1 Depends: xcms (>= 1.50.0), rsm, CAMERA, grDevices, graphics, stats, utils Imports: BiocParallel Suggests: RUnit, BiocGenerics, msdata, mtbls2, faahKO, knitr Enhances: parallel License: GPL (>= 2) + file LICENSE MD5sum: 92f90da2968bdfe08a9683f1e032ebaa NeedsCompilation: no Title: Automated Optimization of XCMS Data Processing parameters Description: The outcome of XCMS data processing strongly depends on the parameter settings. IPO (`Isotopologue Parameter Optimization`) is a parameter optimization tool that is applicable for different kinds of samples and liquid chromatography coupled to high resolution mass spectrometry devices, fast and free of labeling steps. IPO uses natural, stable 13C isotopes to calculate a peak picking score. Retention time correction is optimized by minimizing the relative retention time differences within features and grouping parameters are optimized by maximizing the number of features showing exactly one peak from each injection of a pooled sample. The different parameter settings are achieved by design of experiment. The resulting scores are evaluated using response surface models. biocViews: ImmunoOncology, Metabolomics, MassSpectrometry Author: Gunnar Libiseller , Christoph Magnes , Thomas Riebenbauer Maintainer: Thomas Riebenbauer URL: https://github.com/rietho/IPO VignetteBuilder: knitr BugReports: https://github.com/rietho/IPO/issues/new git_url: https://git.bioconductor.org/packages/IPO git_branch: RELEASE_3_8 git_last_commit: 1ee8a65 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/IPO_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/IPO_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IPO_1.8.1.tgz vignettes: vignettes/IPO/inst/doc/IPO.html vignetteTitles: XCMS Parameter Optimization with IPO hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/IPO/inst/doc/IPO.R Package: IPPD Version: 1.30.0 Depends: R (>= 2.12.0), MASS, Matrix, XML, digest, bitops Imports: methods, stats, graphics License: GPL (version 2 or later) Archs: i386, x64 MD5sum: ae63fe883f60495d5f67784e28e11a6f NeedsCompilation: yes Title: Isotopic peak pattern deconvolution for Protein Mass Spectrometry by template matching Description: The package provides functionality to extract isotopic peak patterns from raw mass spectra. This is done by fitting a large set of template basis functions to the raw spectrum using either nonnegative least squares or least absolute deviation fittting. The package offers a flexible function which tries to estimate model parameters in a way tailored to the peak shapes in the data. The package also provides functionality to process LCMS runs. biocViews: Proteomics Author: Martin Slawski , Rene Hussong , Andreas Hildebrandt , Matthias Hein Maintainer: Martin Slawski git_url: https://git.bioconductor.org/packages/IPPD git_branch: RELEASE_3_8 git_last_commit: 6aea9f2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IPPD_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IPPD_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IPPD_1.30.0.tgz vignettes: vignettes/IPPD/inst/doc/IPPD.pdf vignetteTitles: IPPD Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IPPD/inst/doc/IPPD.R Package: IRanges Version: 2.16.0 Depends: R (>= 3.1.0), methods, utils, stats, BiocGenerics (>= 0.25.3), S4Vectors (>= 0.19.11) Imports: stats4 LinkingTo: S4Vectors Suggests: XVector, GenomicRanges, Rsamtools, GenomicAlignments, GenomicFeatures, BSgenome.Celegans.UCSC.ce2, pasillaBamSubset, RUnit, BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: f37fa0b9438adf9af358844bf1f87c02 NeedsCompilation: yes Title: Infrastructure for manipulating intervals on sequences Description: Provides efficient low-level and highly reusable S4 classes for storing, manipulating and aggregating over annotated ranges of integers. Implements an algebra of range operations, including efficient algorithms for finding overlaps and nearest neighbors. Defines efficient list-like classes for storing, transforming and aggregating large grouped data, i.e., collections of atomic vectors and DataFrames. biocViews: Infrastructure, DataRepresentation Author: H. Pagès, P. Aboyoun and M. Lawrence Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/IRanges git_branch: RELEASE_3_8 git_last_commit: 26834c6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IRanges_2.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IRanges_2.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IRanges_2.16.0.tgz vignettes: vignettes/IRanges/inst/doc/IRangesOverview.pdf vignetteTitles: An Overview of the IRanges package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IRanges/inst/doc/IRangesOverview.R dependsOnMe: AnnotationDbi, AnnotationHubData, BaalChIP, BayesPeak, biomvRCNS, Biostrings, BiSeq, BSgenome, BubbleTree, bumphunter, CAFE, casper, CexoR, chimeraviz, ChIPpeakAnno, chipseq, chroGPS, CNPBayes, CODEX, consensusSeekeR, CSAR, customProDB, deepSNV, DelayedArray, DESeq2, DEXSeq, DirichletMultinomial, DMCHMM, DMRcaller, epigenomix, ExCluster, exomeCopy, fCCAC, GenomeInfoDb, GenomicAlignments, GenomicFeatures, GenomicRanges, Genominator, groHMM, gtrellis, Guitar, Gviz, HelloRanges, HiTC, HMMcopy, htSeqTools, IdeoViz, InTAD, methyAnalysis, MotifDb, motifRG, NADfinder, ORFik, OTUbase, pepStat, PGA, PING, plyranges, proBAMr, PSICQUIC, RefNet, rfPred, rGADEM, rGREAT, RIPSeeker, RJMCMCNucleosomes, rMAT, Scale4C, scsR, SGSeq, SICtools, TEQC, triform, triplex, VariantTools, XVector importsMe: ALDEx2, AllelicImbalance, alpine, amplican, AneuFinder, annmap, annotatr, appreci8R, ArrayExpressHTS, ArrayTV, ASpli, AssessORF, ATACseqQC, ballgown, bamsignals, BayesPeak, BBCAnalyzer, beadarray, BiocOncoTK, biovizBase, BiSeq, BitSeq, bnbc, BPRMeth, branchpointer, breakpointR, BSgenome, bsseq, BUMHMM, CAGEfightR, CAGEr, CHARGE, charm, ChIC, ChIPanalyser, chipenrich, ChIPexoQual, ChIPQC, ChIPseeker, chipseq, ChIPseqR, ChIPSeqSpike, ChIPsim, ChromHeatMap, chromstaR, chromswitch, chromVAR, cicero, CINdex, cleaver, cn.mops, CNEr, CNVPanelizer, CNVrd2, cobindR, COCOA, coMET, compEpiTools, contiBAIT, conumee, copynumber, CopywriteR, CoverageView, CRISPRseek, CrispRVariants, csaw, dada2, debrowser, DECIPHER, DelayedMatrixStats, derfinder, derfinderHelper, derfinderPlot, DEScan2, DiffBind, diffHic, diffloop, DMRcate, DMRScan, dmrseq, DominoEffect, DOQTL, DRIMSeq, easyRNASeq, EDASeq, ELMER, EnrichedHeatmap, ensembldb, epivizr, epivizrData, erma, esATAC, EventPointer, FastqCleaner, fastseg, FindMyFriends, flipflop, FunciSNP, GA4GHclient, gcapc, genbankr, geneAttribution, GeneGeneInteR, GENESIS, GenoGAM, genomation, genomeIntervals, GenomicAlignments, GenomicDataCommons, GenomicFiles, GenomicInteractions, GenomicScores, GenomicTuples, genoset, genotypeeval, GenVisR, GGBase, ggbio, GGtools, girafe, gmapR, GOfuncR, GoogleGenomics, GOpro, GOTHiC, gpart, gQTLstats, GUIDEseq, gwascat, h5vc, HDF5Array, heatmaps, HiCBricks, HiCcompare, HilbertCurve, HTSeqGenie, icetea, ideal, IMAS, InPAS, INSPEcT, intansv, InteractionSet, IntEREst, InterMineR, ipdDb, IsoformSwitchAnalyzeR, isomiRs, IVAS, JunctionSeq, karyoploteR, LOLA, M3D, MACPET, MADSEQ, maser, MatrixRider, mCSEA, MDTS, MEAL, MEDIPS, metagene, methimpute, methInheritSim, methVisual, methyAnalysis, methylInheritance, methylKit, methylPipe, MethylSeekR, methylumi, methyvim, minfi, MinimumDistance, MIRA, mosaics, motifbreakR, motifmatchr, MotIV, msa, msgbsR, MSnbase, MTseeker, MultiAssayExperiment, MultiDataSet, MutationalPatterns, NarrowPeaks, normr, nucleoSim, nucleR, oligoClasses, OmaDB, OMICsPCA, openPrimeR, Organism.dplyr, OrganismDbi, OUTRIDER, panelcn.mops, Pbase, pcaExplorer, pdInfoBuilder, PICS, PING, plethy, podkat, polyester, pqsfinder, prebs, primirTSS, PureCN, Pviz, QDNAseq, qpgraph, qPLEXanalyzer, qsea, QuasR, R3CPET, r3Cseq, R453Plus1Toolbox, RaggedExperiment, RareVariantVis, Rariant, Rcade, recount, REDseq, regioneR, REMP, Repitools, ReportingTools, rGADEM, RiboProfiling, riboSeqR, rMAT, RNAprobR, rnaSeqMap, RnBeads, roar, Rqc, Rsamtools, rSFFreader, RSVSim, RTCGAToolbox, RTN, rtracklayer, SCAN.UPC, segmentSeq, SeqArray, seqCAT, seqPattern, seqplots, seqsetvis, SeqSQC, SeqVarTools, sesame, sevenC, ShortRead, SMITE, SNPchip, SNPhood, soGGi, SomaticSignatures, SparseSignatures, SplicingGraphs, SPLINTER, srnadiff, STAN, strandCheckR, SummarizedExperiment, SVM2CRM, TarSeqQC, TCGAbiolinks, TCGAutils, TCseq, TFBSTools, TFEA.ChIP, TFHAZ, TitanCNA, TnT, tracktables, trackViewer, transcriptR, TransView, triform, tRNA, tRNAdbImport, TSRchitect, TSSi, TVTB, TxRegInfra, Uniquorn, VanillaICE, VariantAnnotation, VariantFiltering, wavClusteR, waveTiling, wiggleplotr, XVector, yamss suggestsMe: annotate, AnnotationHub, BaseSpaceR, BiocGenerics, Chicago, ClassifyR, epivizrChart, Glimma, gQTLBase, GWASTools, HilbertVis, HilbertVisGUI, martini, MiRaGE, regionReport, RTCGA, S4Vectors, TFutils linksToMe: Biostrings, CNEr, DECIPHER, GenomicAlignments, GenomicRanges, kebabs, MatrixRider, Rsamtools, rSFFreader, rtracklayer, ShortRead, triplex, VariantAnnotation, VariantFiltering, XVector Package: iSEE Version: 1.2.4 Depends: R (>= 3.5), SummarizedExperiment, SingleCellExperiment Imports: methods, BiocGenerics, S4Vectors, utils, stats, shiny, shinydashboard, shinyAce, shinyjs, DT, rintrojs, ggplot2, colourpicker, igraph, vipor, mgcv, reshape2, rentrez, AnnotationDbi, graphics, grDevices, viridisLite, cowplot, scales, dplyr Suggests: testthat, BiocStyle, knitr, rmarkdown, scRNAseq, scater, DelayedArray (>= 0.7.44), Rtsne, irlba, RColorBrewer, viridis, org.Mm.eg.db, htmltools License: MIT + file LICENSE MD5sum: f77f982b91daf8f3612b397ceae5ce49 NeedsCompilation: no Title: Interactive SummarizedExperiment Explorer Description: Provides functions for creating an interactive Shiny-based graphical user interface for exploring data stored in SummarizedExperiment objects, including row- and column-level metadata. Particular attention is given to single-cell data in a SingleCellExperiment object with visualization of dimensionality reduction results. biocViews: ImmunoOncology, Visualization, GUI, DimensionReduction, FeatureExtraction, Clustering, Transcription, GeneExpression, Transcriptomics, SingleCell, CellBasedAssays Author: Kevin Rue-Albrecht [aut], Federico Marini [aut], Charlotte Soneson [aut, cre], Aaron Lun [aut] Maintainer: Charlotte Soneson URL: https://github.com/csoneson/iSEE VignetteBuilder: knitr BugReports: https://github.com/csoneson/iSEE/issues git_url: https://git.bioconductor.org/packages/iSEE git_branch: RELEASE_3_8 git_last_commit: a4018ef git_last_commit_date: 2019-04-09 Date/Publication: 2019-04-10 source.ver: src/contrib/iSEE_1.2.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/iSEE_1.2.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iSEE_1.2.4.tgz vignettes: vignettes/iSEE/inst/doc/basic.html, vignettes/iSEE/inst/doc/configure.html, vignettes/iSEE/inst/doc/custom.html, vignettes/iSEE/inst/doc/ecm.html vignetteTitles: 1. The iSEE User's Guide, 3. Configuring iSEE apps, 4. Deploying custom panels, 2. The ExperimentColorMap Class hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/iSEE/inst/doc/basic.R, vignettes/iSEE/inst/doc/configure.R, vignettes/iSEE/inst/doc/custom.R, vignettes/iSEE/inst/doc/ecm.R Package: iSeq Version: 1.34.0 Depends: R (>= 2.10.0) License: GPL (>= 2) Archs: i386, x64 MD5sum: 2059cc665dc0cd50aa204f216a64d332 NeedsCompilation: yes Title: Bayesian Hierarchical Modeling of ChIP-seq Data Through Hidden Ising Models Description: Bayesian hidden Ising models are implemented to identify IP-enriched genomic regions from ChIP-seq data. They can be used to analyze ChIP-seq data with and without controls and replicates. biocViews: ChIPSeq, Sequencing Author: Qianxing Mo Maintainer: Qianxing Mo git_url: https://git.bioconductor.org/packages/iSeq git_branch: RELEASE_3_8 git_last_commit: 6c28ee2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iSeq_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iSeq_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iSeq_1.34.0.tgz vignettes: vignettes/iSeq/inst/doc/iSeq.pdf vignetteTitles: iSeq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iSeq/inst/doc/iSeq.R Package: isobar Version: 1.28.1 Depends: R (>= 2.10.0), Biobase, stats, methods Imports: distr, plyr, biomaRt, ggplot2 Suggests: MSnbase, OrgMassSpecR, XML, RJSONIO, Hmisc, gplots, RColorBrewer, gridExtra, limma, boot, DBI, MASS License: LGPL-2 MD5sum: dc3151a6052b2661bfdfde74c5ae4b9f NeedsCompilation: no Title: Analysis and quantitation of isobarically tagged MSMS proteomics data Description: isobar provides methods for preprocessing, normalization, and report generation for the analysis of quantitative mass spectrometry proteomics data labeled with isobaric tags, such as iTRAQ and TMT. Features modules for integrating and validating PTM-centric datasets (isobar-PTM). More information on http://www.ms-isobar.org. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, Bioinformatics, MultipleComparisons, QualityControl Author: Florian P Breitwieser and Jacques Colinge , with contributions from Alexey Stukalov , Xavier Robin and Florent Gluck Maintainer: Florian P Breitwieser URL: https://github.com/fbreitwieser/isobar BugReports: https://github.com/fbreitwieser/isobar/issues git_url: https://git.bioconductor.org/packages/isobar git_branch: RELEASE_3_8 git_last_commit: 6763312 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/isobar_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/isobar_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/isobar_1.28.1.tgz vignettes: vignettes/isobar/inst/doc/isobar-devel.pdf, vignettes/isobar/inst/doc/isobar-ptm.pdf, vignettes/isobar/inst/doc/isobar-usecases.pdf, vignettes/isobar/inst/doc/isobar.pdf vignetteTitles: isobar for developers, isobar for quantification of PTM datasets, Usecases for isobar package, isobar package for iTRAQ and TMT protein quantification hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/isobar/inst/doc/isobar-devel.R, vignettes/isobar/inst/doc/isobar-ptm.R, vignettes/isobar/inst/doc/isobar-usecases.R, vignettes/isobar/inst/doc/isobar.R Package: IsoCorrectoR Version: 1.0.5 Depends: R (>= 3.5) Imports: dplyr, magrittr, methods, quadprog, readr, readxl, stringr, tibble, tools, utils, pracma, WriteXLS Suggests: knitr, rmarkdown, testthat License: GPL-3 MD5sum: 3f06be0cf58841751ea3031be9d33fe5 NeedsCompilation: no Title: Correction for natural isotope abundance and tracer purity in MS and MS/MS data from stable isotope labeling experiments Description: IsoCorrectoR performs the correction of mass spectrometry data from stable isotope labeling/tracing metabolomics experiments with regard to natural isotope abundance and tracer impurity. Data from both MS and MS/MS measurements can be corrected (with any tracer isotope: 13C, 15N, 18O...), as well as high resolution MS data from multiple-tracer experiments (e.g. 13C and 15N used simultaneously). See the Bioconductor package IsoCorrectoRGUI for a graphical user interface to IsoCorrectoR. IsoCorrectoRGUI is currently only available in the devel version of Bioconductor. biocViews: Software, Metabolomics, MassSpectrometry, Preprocessing, ImmunoOncology Author: Christian Kohler [cre, aut], Paul Heinrich [aut] Maintainer: Christian Kohler URL: https://genomics.ur.de/files/IsoCorrectoR/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/IsoCorrectoR git_branch: RELEASE_3_8 git_last_commit: 6b47de7 git_last_commit_date: 2018-12-07 Date/Publication: 2018-12-07 source.ver: src/contrib/IsoCorrectoR_1.0.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/IsoCorrectoR_1.0.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IsoCorrectoR_1.0.5.tgz vignettes: vignettes/IsoCorrectoR/inst/doc/IsoCorrectoR.html vignetteTitles: IsoCorrectoR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IsoCorrectoR/inst/doc/IsoCorrectoR.R Package: IsoformSwitchAnalyzeR Version: 1.4.0 Depends: R (>= 3.5), limma, DEXSeq, ggplot2 Imports: methods, BSgenome, plyr, reshape2, gridExtra, Biostrings, IRanges, GenomicRanges, DRIMSeq, RColorBrewer, rtracklayer, VennDiagram, DBI, grDevices, graphics, stats, utils, GenomeInfoDb, grid, tximport (>= 1.7.1), edgeR, futile.logger, limma, stringr, dplyr, magrittr, readr Suggests: knitr, BSgenome.Hsapiens.UCSC.hg19, cummeRbund License: GPL (>= 2) Archs: i386, x64 MD5sum: a4b45dc8dc2a54692d8a27ba67568d16 NeedsCompilation: yes Title: An R package to Identify, Annotate and Visualize Alternative Splicing and Isoform Switches with Functional Consequences (from RNA-seq data) Description: IsoformSwitchAnalyzeR enables identification and analysis of alternative splicing and isoform switches with predicted functional consequences (such as gain/loss of protein domains etc) from quantification by Kallisto, Salmon, Cufflinks/Cuffdiff, RSEM etc. biocViews: GeneExpression, Transcription, AlternativeSplicing, DifferentialExpression, DifferentialSplicing, Visualization, StatisticalMethod, TranscriptomeVariant, BiomedicalInformatics, FunctionalGenomics, SystemsBiology, Transcriptomics, RNASeq, Annotation, FunctionalPrediction, GenePrediction, DataImport, MultipleComparison, BatchEffect Author: Kristoffer Vitting-Seerup Maintainer: Kristoffer Vitting-Seerup URL: http://bioconductor.org/packages/IsoformSwitchAnalyzeR/ VignetteBuilder: knitr BugReports: https://github.com/kvittingseerup/IsoformSwitchAnalyzeR/issues git_url: https://git.bioconductor.org/packages/IsoformSwitchAnalyzeR git_branch: RELEASE_3_8 git_last_commit: d8e8d85 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IsoformSwitchAnalyzeR_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IsoformSwitchAnalyzeR_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IsoformSwitchAnalyzeR_1.4.0.tgz vignettes: vignettes/IsoformSwitchAnalyzeR/inst/doc/IsoformSwitchAnalyzeR.html vignetteTitles: IsoformSwitchAnalyzeR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IsoformSwitchAnalyzeR/inst/doc/IsoformSwitchAnalyzeR.R Package: IsoGeneGUI Version: 2.18.0 Depends: tcltk, xlsx Imports: Rcpp, tkrplot, multtest, relimp, geneplotter, RColorBrewer, Iso, IsoGene, ORCME, ORIClust, orQA, goric, ff, Biobase, jpeg Suggests: RUnit License: GPL-2 MD5sum: 872514812096a9484b45f0c86cd63911 NeedsCompilation: no Title: A graphical user interface to conduct a dose-response analysis of microarray data Description: The IsoGene Graphical User Interface (IsoGene-GUI) is a user friendly interface of the IsoGene package which is aimed to identify for genes with a monotonic trend in the expression levels with respect to the increasing doses. Additionally, GUI extension of original package contains various tools to perform clustering of dose-response profiles. Testing is addressed through several test statistics: global likelihood ratio test (E2), Bartholomew 1961, Barlow et al. 1972 and Robertson et al. 1988), Williams (1971, 1972), Marcus (1976), the M (Hu et al. 2005) and the modified M (Lin et al. 2007). The p-values of the global likelihood ratio test (E2) are obtained using the exact distribution and permutations. The other four test statistics are obtained using permutations. Several p-values adjustment are provided: Bonferroni, Holm (1979), Hochberg (1988), and Sidak procedures for controlling the family-wise Type I error rate (FWER), and BH (Benjamini and Hochberg 1995) and BY (Benjamini and Yekutieli 2001) procedures are used for controlling the FDR. The inference is based on resampling methods, which control the False Discovery Rate (FDR), for both permutations (Ge et al., 2003) and the Significance Analysis of Microarrays (SAM, Tusher et al., 2001). Clustering methods are outsourced from CRAN packages ORCME, ORIClust. The package ORCME is based on delta-clustering method (Cheng and Church, 2000) and ORIClust on Order Restricted Information Criterion (Liu et al., 2009), both perform same task but from different perspective and their outputs are clusters of genes. Additionally, profile selection for given gene based on Generalized ORIC (Kuiper et al., 2014) from package goric and permutation test for E2 based on package orQA are included in IsoGene-GUI. None of these four packages has GUI. biocViews: Microarray, DifferentialExpression, GUI Author: Setia Pramana, Dan Lin, Philippe Haldermans, Tobias Verbeke, Martin Otava Maintainer: Setia Pramana URL: http://ibiostat.be/online-resources/online-resources/isogenegui/isogenegui-package git_url: https://git.bioconductor.org/packages/IsoGeneGUI git_branch: RELEASE_3_8 git_last_commit: c2f9625 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IsoGeneGUI_2.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IsoGeneGUI_2.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IsoGeneGUI_2.18.0.tgz vignettes: vignettes/IsoGeneGUI/inst/doc/IsoGeneGUI.pdf vignetteTitles: IsoGeneGUI Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IsoGeneGUI/inst/doc/IsoGeneGUI.R Package: ISoLDE Version: 1.10.1 Depends: R (>= 3.3.0),graphics,grDevices,stats,utils License: GPL (>= 2.0) Archs: i386, x64 MD5sum: 415ea14c55b22b24737f4d7fba82e4c2 NeedsCompilation: yes Title: Integrative Statistics of alleLe Dependent Expression Description: This package provides ISoLDE a new method for identifying imprinted genes. This method is dedicated to data arising from RNA sequencing technologies. The ISoLDE package implements original statistical methodology described in the publication below. biocViews: ImmunoOncology, GeneExpression, Transcription, GeneSetEnrichment, Genetics, Sequencing, RNASeq, MultipleComparison, SNP, GeneticVariability, Epigenetics, MathematicalBiology, GeneRegulation Author: Christelle Reynès [aut, cre], Marine Rohmer [aut], Guilhem Kister [aut] Maintainer: Christelle Reynès URL: www.r-project.org git_url: https://git.bioconductor.org/packages/ISoLDE git_branch: RELEASE_3_8 git_last_commit: a65a412 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ISoLDE_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ISoLDE_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ISoLDE_1.10.1.tgz hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: isomiRs Version: 1.10.1 Depends: R (>= 3.5), DiscriMiner, SummarizedExperiment Imports: AnnotationDbi, assertive.sets, BiocGenerics, Biobase, cluster, cowplot, DEGreport, DESeq2, IRanges, dplyr, GenomicRanges, gplots, ggplot2, gtools, gridExtra, grid, grDevices, graphics, GGally, limma, methods, RColorBrewer, readr, reshape, rlang, stats, S4Vectors, tidyr, tibble Suggests: knitr, org.Mm.eg.db, targetscan.Hs.eg.db, pheatmap, BiocStyle, testthat License: MIT + file LICENSE MD5sum: bd0857ea13ce4f427d6eef0bcf147cc3 NeedsCompilation: no Title: Analyze isomiRs and miRNAs from small RNA-seq Description: Characterization of miRNAs and isomiRs, clustering and differential expression. biocViews: ImmunoOncology, miRNA, RNASeq, DifferentialExpression, Clustering Author: Lorena Pantano [aut, cre], Georgia Escaramis [aut] Maintainer: Lorena Pantano VignetteBuilder: knitr BugReports: https://github.com/lpantano/isomiRs/issues git_url: https://git.bioconductor.org/packages/isomiRs git_branch: RELEASE_3_8 git_last_commit: 92e8540 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/isomiRs_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/isomiRs_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/isomiRs_1.10.1.tgz vignettes: vignettes/isomiRs/inst/doc/isomiRs.html vignetteTitles: miRNA and isomiR analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/isomiRs/inst/doc/isomiRs.R Package: ITALICS Version: 2.42.0 Depends: R (>= 2.0.0), GLAD, ITALICSData, oligo, affxparser, pd.mapping50k.xba240 Imports: affxparser, DBI, GLAD, oligo, oligoClasses, stats Suggests: pd.mapping50k.hind240, pd.mapping250k.sty, pd.mapping250k.nsp License: GPL-2 MD5sum: ff61276d7d7957d1d43f81a3c44c143c NeedsCompilation: no Title: ITALICS Description: A Method to normalize of Affymetrix GeneChip Human Mapping 100K and 500K set biocViews: Microarray, CopyNumberVariation Author: Guillem Rigaill, Philippe Hupe Maintainer: Guillem Rigaill URL: http://bioinfo.curie.fr git_url: https://git.bioconductor.org/packages/ITALICS git_branch: RELEASE_3_8 git_last_commit: 46e8241 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ITALICS_2.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ITALICS_2.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ITALICS_2.42.0.tgz vignettes: vignettes/ITALICS/inst/doc/ITALICS.pdf vignetteTitles: ITALICS hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ITALICS/inst/doc/ITALICS.R Package: iterativeBMA Version: 1.40.0 Depends: BMA, leaps, Biobase (>= 2.5.5) License: GPL (>= 2) MD5sum: 7ceea6bdeb99f7b8ff5b46f8e938b860 NeedsCompilation: no Title: The Iterative Bayesian Model Averaging (BMA) algorithm Description: The iterative Bayesian Model Averaging (BMA) algorithm is a variable selection and classification algorithm with an application of classifying 2-class microarray samples, as described in Yeung, Bumgarner and Raftery (Bioinformatics 2005, 21: 2394-2402). biocViews: Microarray, Classification Author: Ka Yee Yeung, University of Washington, Seattle, WA, with contributions from Adrian Raftery and Ian Painter Maintainer: Ka Yee Yeung URL: http://faculty.washington.edu/kayee/research.html git_url: https://git.bioconductor.org/packages/iterativeBMA git_branch: RELEASE_3_8 git_last_commit: 4307c24 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iterativeBMA_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iterativeBMA_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iterativeBMA_1.40.0.tgz vignettes: vignettes/iterativeBMA/inst/doc/iterativeBMA.pdf vignetteTitles: The Iterative Bayesian Model Averaging Algorithm hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iterativeBMA/inst/doc/iterativeBMA.R Package: iterativeBMAsurv Version: 1.40.0 Depends: BMA, leaps, survival, splines Imports: graphics, grDevices, stats, survival, utils License: GPL (>= 2) MD5sum: 0260494ff7be19fe0716230c2162fb09 NeedsCompilation: no Title: The Iterative Bayesian Model Averaging (BMA) Algorithm For Survival Analysis Description: The iterative Bayesian Model Averaging (BMA) algorithm for survival analysis is a variable selection method for applying survival analysis to microarray data. biocViews: Microarray Author: Amalia Annest, University of Washington, Tacoma, WA Ka Yee Yeung, University of Washington, Seattle, WA Maintainer: Ka Yee Yeung URL: http://expression.washington.edu/ibmasurv/protected git_url: https://git.bioconductor.org/packages/iterativeBMAsurv git_branch: RELEASE_3_8 git_last_commit: 0958983 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iterativeBMAsurv_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iterativeBMAsurv_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iterativeBMAsurv_1.40.0.tgz vignettes: vignettes/iterativeBMAsurv/inst/doc/iterativeBMAsurv.pdf vignetteTitles: The Iterative Bayesian Model Averaging Algorithm For Survival Analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iterativeBMAsurv/inst/doc/iterativeBMAsurv.R Package: iterClust Version: 1.4.0 Depends: R (>= 3.4.1) Imports: Biobase, cluster, stats, methods Suggests: tsne, bcellViper License: file LICENSE MD5sum: 9d834de783d4ec4af9b9ead22236616b NeedsCompilation: no Title: Iterative Clustering Description: A framework for performing clustering analysis iteratively. biocViews: StatisticalMethod, Clustering Author: Hongxu Ding and Andrea Califano Maintainer: Hongxu Ding URL: https://github.com/hd2326/iterClust BugReports: https://github.com/hd2326/iterClust/issues git_url: https://git.bioconductor.org/packages/iterClust git_branch: RELEASE_3_8 git_last_commit: dcb47e9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iterClust_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iterClust_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iterClust_1.4.0.tgz vignettes: vignettes/iterClust/inst/doc/introduction.pdf vignetteTitles: introduction.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/iterClust/inst/doc/introduction.R Package: iteremoval Version: 1.2.0 Depends: R (>= 3.5.0), ggplot2 (>= 2.2.1) Imports: magrittr, graphics, utils, GenomicRanges, SummarizedExperiment Suggests: testthat, knitr License: GPL-2 MD5sum: eb105f0df6dd4e19a8683152705c6348 NeedsCompilation: no Title: Iteration removal method for feature selection Description: The package provides a flexible algorithm to screen features of two distinct groups in consideration of overfitting and overall performance. It was originally tailored for methylation locus screening of NGS data, and it can also be used as a generic method for feature selection. Each step of the algorithm provides a default method for simple implemention, and the method can be replaced by a user defined function. biocViews: StatisticalMethod Author: Jiacheng Chuan [aut, cre] Maintainer: Jiacheng Chuan URL: https://github.com/cihga39871/iteremoval VignetteBuilder: knitr BugReports: https://github.com/cihga39871/iteremoval/issues git_url: https://git.bioconductor.org/packages/iteremoval git_branch: RELEASE_3_8 git_last_commit: 9f039ae git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/iteremoval_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/iteremoval_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/iteremoval_1.2.0.tgz vignettes: vignettes/iteremoval/inst/doc/iteremoval.html vignetteTitles: An introduction to iteremoval hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/iteremoval/inst/doc/iteremoval.R Package: IVAS Version: 2.2.1 Depends: R (> 3.0.0),GenomicFeatures, ggplot2, Biobase Imports: doParallel, lme4, BiocGenerics, GenomicRanges, IRanges, foreach, AnnotationDbi, S4Vectors, GenomeInfoDb, ggfortify, grDevices, methods, Matrix, BiocParallel,utils, stats Suggests: BiocStyle License: GPL-2 MD5sum: 651a2e169eec4f8f2bff7bf085b68d76 NeedsCompilation: no Title: Identification of genetic Variants affecting Alternative Splicing Description: Identification of genetic variants affecting alternative splicing. biocViews: ImmunoOncology, AlternativeSplicing, DifferentialExpression, DifferentialSplicing, GeneExpression, GeneRegulation, Regression, RNASeq, Sequencing, SNP, Software, Transcription Author: Seonggyun Han, Sangsoo Kim Maintainer: Seonggyun Han git_url: https://git.bioconductor.org/packages/IVAS git_branch: RELEASE_3_8 git_last_commit: 5339eb3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/IVAS_2.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/IVAS_2.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IVAS_2.2.1.tgz vignettes: vignettes/IVAS/inst/doc/IVAS.pdf vignetteTitles: IVAS : Identification of genetic Variants affecting Alternative Splicing hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IVAS/inst/doc/IVAS.R dependsOnMe: IMAS Package: ivygapSE Version: 1.4.0 Depends: R (>= 3.5.0), SummarizedExperiment Imports: shiny, survival, survminer, hwriter, plotly, ggplot2, S4Vectors, graphics, stats, utils, UpSetR Suggests: knitr, png, limma, grid, DT, randomForest, digest, testthat License: Artistic-2.0 MD5sum: e40c121410d8cd59555a1860e69c7e02 NeedsCompilation: no Title: A SummarizedExperiment for Ivy-GAP data Description: Define a SummarizedExperiment and exploratory app for Ivy-GAP glioblastoma image, expression, and clinical data. biocViews: Transcription, Software, Visualization, Survival, GeneExpression, Sequencing Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ivygapSE git_branch: RELEASE_3_8 git_last_commit: 3a00343 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ivygapSE_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ivygapSE_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ivygapSE_1.4.0.tgz vignettes: vignettes/ivygapSE/inst/doc/ivygapSE.html vignetteTitles: ivygapSE -- SummarizedExperiment for Ivy-GAP hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ivygapSE/inst/doc/ivygapSE.R Package: IWTomics Version: 1.6.0 Depends: GenomicRanges Imports: parallel,gtable,grid,graphics,methods,IRanges,KernSmooth,fda,S4Vectors,grDevices,stats,utils,tools Suggests: knitr License: GPL (>=2) MD5sum: 41ae9142f344cc1b42205ffe20758cec NeedsCompilation: no Title: Interval-Wise Testing for Omics Data Description: Implementation of the Interval-Wise Testing (IWT) for omics data. This inferential procedure tests for differences in "Omics" data between two groups of genomic regions (or between a group of genomic regions and a reference center of symmetry), and does not require fixing location and scale at the outset. biocViews: StatisticalMethod, MultipleComparison, DifferentialExpression, DifferentialMethylation, DifferentialPeakCalling, GenomeAnnotation, DataImport Author: Marzia A Cremona, Alessia Pini, Francesca Chiaromonte, Simone Vantini Maintainer: Marzia A Cremona VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/IWTomics git_branch: RELEASE_3_8 git_last_commit: b4f7218 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/IWTomics_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/IWTomics_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/IWTomics_1.6.0.tgz vignettes: vignettes/IWTomics/inst/doc/IWTomics.pdf vignetteTitles: Introduction to IWTomics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/IWTomics/inst/doc/IWTomics.R Package: joda Version: 1.30.0 Depends: R (>= 2.0), bgmm, RBGL License: GPL (>= 2) MD5sum: 40973ebc5b8862fca57737b9a04128a6 NeedsCompilation: no Title: JODA algorithm for quantifying gene deregulation using knowledge Description: Package 'joda' implements three steps of an algorithm called JODA. The algorithm computes gene deregulation scores. For each gene, its deregulation score reflects how strongly an effect of a certain regulator's perturbation on this gene differs between two different cell populations. The algorithm utilizes regulator knockdown expression data as well as knowledge about signaling pathways in which the regulators are involved (formalized in a simple matrix model). biocViews: Microarray, Pathways, GraphAndNetwork, StatisticalMethod, NetworkInference Author: Ewa Szczurek Maintainer: Ewa Szczurek URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/joda git_branch: RELEASE_3_8 git_last_commit: b42b8ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/joda_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/joda_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/joda_1.30.0.tgz vignettes: vignettes/joda/inst/doc/JodaVignette.pdf vignetteTitles: Introduction to joda hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/joda/inst/doc/JodaVignette.R Package: JunctionSeq Version: 1.12.1 Depends: R (>= 3.2.2), methods, SummarizedExperiment (>= 0.2.0), Rcpp (>= 0.11.0), RcppArmadillo (>= 0.3.4.4) Imports: DESeq2 (>= 1.10.0), statmod, Hmisc, plotrix, stringr, Biobase (>= 2.30.0), locfit, BiocGenerics (>= 0.7.5), BiocParallel, genefilter, geneplotter, S4Vectors, IRanges, GenomicRanges, LinkingTo: Rcpp, RcppArmadillo Suggests: MASS, knitr, JctSeqData, BiocStyle Enhances: Cairo, pryr License: file LICENSE Archs: i386, x64 MD5sum: 4ea3d5ff90c42fccee17ca8949cb0b2e NeedsCompilation: yes Title: JunctionSeq: A Utility for Detection of Differential Exon and Splice-Junction Usage in RNA-Seq data Description: A Utility for Detection and Visualization of Differential Exon or Splice-Junction Usage in RNA-Seq data. biocViews: ImmunoOncology, Sequencing, RNASeq, DifferentialExpression Author: Stephen Hartley [aut, cre] (PhD), Simon Anders [cph], Alejandro Reyes [cph] Maintainer: Stephen Hartley URL: http://hartleys.github.io/JunctionSeq/index.html VignetteBuilder: knitr BugReports: https://github.com/hartleys/JunctionSeq/issues git_url: https://git.bioconductor.org/packages/JunctionSeq git_branch: RELEASE_3_8 git_last_commit: 8a1f6cf git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/JunctionSeq_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/JunctionSeq_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/JunctionSeq_1.12.1.tgz vignettes: vignettes/JunctionSeq/inst/doc/JunctionSeq.pdf vignetteTitles: JunctionSeq Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE importsMe: PathwaySplice Package: karyoploteR Version: 1.8.8 Depends: R (>= 3.4), regioneR, GenomicRanges, methods Imports: regioneR, GenomicRanges, IRanges, Rsamtools, stats, graphics, memoise, rtracklayer, GenomeInfoDb, S4Vectors, biovizBase, digest, bezier, GenomicFeatures, bamsignals Suggests: BiocStyle, knitr, testthat, magrittr, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, pasillaBamSubset License: Artistic-2.0 MD5sum: cf4ced2a1bebc254974adcb84e27b141 NeedsCompilation: no Title: Plot customizable linear genomes displaying arbitrary data Description: karyoploteR creates karyotype plots of arbitrary genomes and offers a complete set of functions to plot arbitrary data on them. It mimicks many R base graphics functions coupling them with a coordinate change function automatically mapping the chromosome and data coordinates into the plot coordinates. In addition to the provided data plotting functions, it is easy to add new ones. biocViews: Visualization, CopyNumberVariation, Sequencing, Coverage, DNASeq, ChIPSeq, MethylSeq, DataImport, OneChannel Author: Bernat Gel Maintainer: Bernat Gel URL: https://github.com/bernatgel/karyoploteR VignetteBuilder: knitr BugReports: https://github.com/bernatgel/karyoploteR/issues git_url: https://git.bioconductor.org/packages/karyoploteR git_branch: RELEASE_3_8 git_last_commit: be20832 git_last_commit_date: 2019-04-02 Date/Publication: 2019-04-02 source.ver: src/contrib/karyoploteR_1.8.8.tar.gz win.binary.ver: bin/windows/contrib/3.5/karyoploteR_1.8.8.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/karyoploteR_1.8.8.tgz vignettes: vignettes/karyoploteR/inst/doc/karyoploteR.html vignetteTitles: karyoploteR vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/karyoploteR/inst/doc/karyoploteR.R Package: KCsmart Version: 2.40.0 Depends: siggenes, multtest, KernSmooth Imports: methods, BiocGenerics Enhances: Biobase, CGHbase License: GPL-3 MD5sum: 8f57fd4003e5da98c7cd7749ac054e70 NeedsCompilation: no Title: Multi sample aCGH analysis package using kernel convolution Description: Multi sample aCGH analysis package using kernel convolution biocViews: CopyNumberVariation, Visualization, aCGH, Microarray Author: Jorma de Ronde, Christiaan Klijn, Arno Velds Maintainer: Jorma de Ronde git_url: https://git.bioconductor.org/packages/KCsmart git_branch: RELEASE_3_8 git_last_commit: 0a1c75e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/KCsmart_2.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/KCsmart_2.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/KCsmart_2.40.0.tgz vignettes: vignettes/KCsmart/inst/doc/KCS.pdf vignetteTitles: KCsmart example session hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/KCsmart/inst/doc/KCS.R Package: kebabs Version: 1.16.0 Depends: R (>= 3.2.0), Biostrings (>= 2.35.5), kernlab Imports: methods, stats, Rcpp (>= 0.11.2), Matrix, XVector (>= 0.7.3), S4Vectors (>= 0.5.11), e1071, LiblineaR, graphics, grDevices, utils, apcluster LinkingTo: IRanges, XVector, Biostrings, Rcpp, S4Vectors Suggests: SparseM, Biobase, BiocGenerics, knitr License: GPL (>= 2.1) Archs: i386, x64 MD5sum: 219c50a9e26b4adfd9e23c8fb3684bc6 NeedsCompilation: yes Title: Kernel-Based Analysis Of Biological Sequences Description: The package provides functionality for kernel-based analysis of DNA, RNA, and amino acid sequences via SVM-based methods. As core functionality, kebabs implements following sequence kernels: spectrum kernel, mismatch kernel, gappy pair kernel, and motif kernel. Apart from an efficient implementation of standard position-independent functionality, the kernels are extended in a novel way to take the position of patterns into account for the similarity measure. Because of the flexibility of the kernel formulation, other kernels like the weighted degree kernel or the shifted weighted degree kernel with constant weighting of positions are included as special cases. An annotation-specific variant of the kernels uses annotation information placed along the sequence together with the patterns in the sequence. The package allows for the generation of a kernel matrix or an explicit feature representation in dense or sparse format for all available kernels which can be used with methods implemented in other R packages. With focus on SVM-based methods, kebabs provides a framework which simplifies the usage of existing SVM implementations in kernlab, e1071, and LiblineaR. Binary and multi-class classification as well as regression tasks can be used in a unified way without having to deal with the different functions, parameters, and formats of the selected SVM. As support for choosing hyperparameters, the package provides cross validation - including grouped cross validation, grid search and model selection functions. For easier biological interpretation of the results, the package computes feature weights for all SVMs and prediction profiles which show the contribution of individual sequence positions to the prediction result and indicate the relevance of sequence sections for the learning result and the underlying biological functions. biocViews: SupportVectorMachine, Classification, Clustering, Regression Author: Johannes Palme Maintainer: Ulrich Bodenhofer URL: http://www.bioinf.jku.at/software/kebabs/ https://github.com/UBod/kebabs VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/kebabs git_branch: RELEASE_3_8 git_last_commit: 726b350 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/kebabs_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/kebabs_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/kebabs_1.16.0.tgz vignettes: vignettes/kebabs/inst/doc/kebabs.pdf vignetteTitles: KeBABS - An R Package for Kernel Based Analysis of Biological Sequences hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/kebabs/inst/doc/kebabs.R dependsOnMe: procoil importsMe: FindMyFriends, odseq Package: KEGGgraph Version: 1.42.0 Depends: R (>= 2.10.0) Imports: methods, XML (>= 2.3-0), graph, utils Suggests: Rgraphviz, RBGL, RUnit, RColorBrewer, KEGG.db, org.Hs.eg.db, hgu133plus2.db, SPIA License: GPL (>= 2) MD5sum: 6299732316aed3d57a74c3750b1ab43c NeedsCompilation: no Title: KEGGgraph: A graph approach to KEGG PATHWAY in R and Bioconductor Description: KEGGGraph is an interface between KEGG pathway and graph object as well as a collection of tools to analyze, dissect and visualize these graphs. It parses the regularly updated KGML (KEGG XML) files into graph models maintaining all essential pathway attributes. The package offers functionalities including parsing, graph operation, visualization and etc. biocViews: Pathways, GraphAndNetwork, Visualization, KEGG Author: Jitao David Zhang, with inputs from Paul Shannon Maintainer: Jitao David Zhang URL: http://www.nextbiomotif.com git_url: https://git.bioconductor.org/packages/KEGGgraph git_branch: RELEASE_3_8 git_last_commit: 7d907e2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/KEGGgraph_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/KEGGgraph_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/KEGGgraph_1.42.0.tgz vignettes: vignettes/KEGGgraph/inst/doc/KEGGgraph.pdf, vignettes/KEGGgraph/inst/doc/KEGGgraphApp.pdf vignetteTitles: KEGGgraph: graph approach to KEGG PATHWAY, KEGGgraph: Application Examples hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/KEGGgraph/inst/doc/KEGGgraph.R, vignettes/KEGGgraph/inst/doc/KEGGgraphApp.R dependsOnMe: ROntoTools, SPIA importsMe: clipper, DEGraph, EnrichmentBrowser, MetaboSignal, MWASTools, NCIgraph, pathview suggestsMe: DEGraph, GenomicRanges Package: KEGGlincs Version: 1.8.0 Depends: R (>= 3.3), KOdata, hgu133a.db, org.Hs.eg.db (>= 3.3.0) Imports: AnnotationDbi,KEGGgraph,igraph,plyr,gtools,httr,RJSONIO,KEGGREST, methods,graphics,stats,utils, XML, grDevices Suggests: BiocManager (>= 1.20.3), knitr, graph License: GPL-3 MD5sum: 563a47dca90ab2a1999f27257ad8a4bc NeedsCompilation: no Title: Visualize all edges within a KEGG pathway and overlay LINCS data [option] Description: See what is going on 'under the hood' of KEGG pathways by explicitly re-creating the pathway maps from information obtained from KGML files. biocViews: NetworkInference, GeneExpression, DataRepresentation, ThirdPartyClient,CellBiology,GraphAndNetwork,Pathways,KEGG,Network Author: Shana White Maintainer: Shana White , Mario Medvedovic SystemRequirements: Cytoscape (>= 3.3.0), Java (>= 8) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/KEGGlincs git_branch: RELEASE_3_8 git_last_commit: 4c5235e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/KEGGlincs_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/KEGGlincs_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/KEGGlincs_1.8.0.tgz vignettes: vignettes/KEGGlincs/inst/doc/Example-workflow.html vignetteTitles: KEGGlincs Workflows hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/KEGGlincs/inst/doc/Example-workflow.R Package: keggorthology Version: 2.34.0 Depends: R (>= 2.5.0),stats,graph,hgu95av2.db Imports: AnnotationDbi,graph,DBI, graph, grDevices, methods, stats, tools, utils Suggests: RBGL,ALL License: Artistic-2.0 MD5sum: 62ca96db218f39f0168b022ccf63fcce NeedsCompilation: no Title: graph support for KO, KEGG Orthology Description: graphical representation of the Feb 2010 KEGG Orthology. The KEGG orthology is a set of pathway IDs that are not to be confused with the KEGG ortholog IDs. biocViews: Pathways, GraphAndNetwork, Visualization, KEGG Author: VJ Carey Maintainer: VJ Carey git_url: https://git.bioconductor.org/packages/keggorthology git_branch: RELEASE_3_8 git_last_commit: 3c9f18b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/keggorthology_2.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/keggorthology_2.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/keggorthology_2.34.0.tgz vignettes: vignettes/keggorthology/inst/doc/keggorth.pdf vignetteTitles: keggorthology overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/keggorthology/inst/doc/keggorth.R suggestsMe: MLInterfaces Package: KEGGprofile Version: 1.24.0 Depends: RCurl Imports: AnnotationDbi,png,TeachingDemos,XML,KEGG.db,KEGGREST,biomaRt License: GPL (>= 2) MD5sum: 94f3b5f4687557760207e432fba9c2e9 NeedsCompilation: no Title: An annotation and visualization package for multi-types and multi-groups expression data in KEGG pathway Description: KEGGprofile is an annotation and visualization tool which integrated the expression profiles and the function annotation in KEGG pathway maps. The multi-types and multi-groups expression data can be visualized in one pathway map. KEGGprofile facilitated more detailed analysis about the specific function changes inner pathway or temporal correlations in different genes and samples. biocViews: Pathways, KEGG Author: Shilin Zhao, Yan Guo, Yu Shyr Maintainer: Shilin Zhao git_url: https://git.bioconductor.org/packages/KEGGprofile git_branch: RELEASE_3_8 git_last_commit: 77f95ff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/KEGGprofile_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/KEGGprofile_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/KEGGprofile_1.24.0.tgz vignettes: vignettes/KEGGprofile/inst/doc/KEGGprofile.pdf vignetteTitles: KEGGprofile: Application Examples hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/KEGGprofile/inst/doc/KEGGprofile.R suggestsMe: IntramiRExploreR Package: KEGGREST Version: 1.22.0 Imports: methods, httr, png, Biostrings Suggests: RUnit, BiocGenerics, knitr License: Artistic-2.0 MD5sum: a261af7eef51941349a3ff93d4b4e28b NeedsCompilation: no Title: Client-side REST access to KEGG Description: A package that provides a client interface to the KEGG REST server. Based on KEGGSOAP by J. Zhang, R. Gentleman, and Marc Carlson, and KEGG (python package) by Aurelien Mazurie. biocViews: Annotation, Pathways, ThirdPartyClient, KEGG Author: Dan Tenenbaum Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/KEGGREST git_branch: RELEASE_3_8 git_last_commit: 4374507 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/KEGGREST_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/KEGGREST_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/KEGGREST_1.22.0.tgz vignettes: vignettes/KEGGREST/inst/doc/KEGGREST-vignette.html vignetteTitles: Accessing the KEGG REST API hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/KEGGREST/inst/doc/KEGGREST-vignette.R dependsOnMe: PAPi, ROntoTools importsMe: attract, CNEr, EnrichmentBrowser, FELLA, gage, MetaboSignal, MWASTools, pathview, PathwaySplice, YAPSA Package: kimod Version: 1.10.0 Depends: R(>= 3.3),methods Imports: cluster, graphics, Biobase License: GPL (>=2) MD5sum: 3320975d680f42063eced2de930fe779 NeedsCompilation: no Title: A k-tables approach to integrate multiple Omics-Data Description: This package allows to work with mixed omics data (transcriptomics, proteomics, microarray-chips, rna-seq data), introducing the following improvements: distance options (for numeric and/or categorical variables) for each of the tables, bootstrap resampling techniques on the residuals matrices for all methods, that enable perform confidence ellipses for the projection of individuals, variables and biplot methodology to project variables (gene expression) on the compromise. Since the main purpose of the package is to use these techniques to omic data analysis, it includes an example data from four different microarray platforms (i.e.,Agilent, Affymetrix HGU 95, Affymetrix HGU 133 and Affymetrix HGU 133plus 2.0) on the NCI-60 cell lines.NCI60_4arrays is a list containing the NCI-60 microarray data with only few hundreds of genes randomly selected in each platform to keep the size of the package small. The data are the same that the package omicade4 used to implement the co-inertia analysis. The references in packages follow the style of the APA-6th norm. biocViews: Microarray, Visualization, GeneExpression, ExperimentData, Proteomics Author: Maria Laura Zingaretti, Johanna Altair Demey-Zambrano, Jose Luis Vicente-Villardon, Jhonny Rafael Demey Maintainer: M L Zingaretti git_url: https://git.bioconductor.org/packages/kimod git_branch: RELEASE_3_8 git_last_commit: 126c425 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/kimod_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/kimod_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/kimod_1.10.0.tgz vignettes: vignettes/kimod/inst/doc/kimod-vignette.pdf vignetteTitles: kimod A K-tables approach to integrate multiple Omics-Data in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/kimod/inst/doc/kimod-vignette.R Package: KinSwingR Version: 1.0.3 Depends: R (>= 3.5) Imports: data.table, BiocParallel, sqldf, stats, grid Suggests: knitr, rmarkdown License: GPL-3 MD5sum: 2fdf011f7c6e01a7283be53eadfec809 NeedsCompilation: no Title: KinSwingR: network-based kinase activity prediction Description: KinSwingR integrates phosphosite data derived from mass-spectrometry data and kinase-substrate predictions to predict kinase activity. Several functions allow the user to build PWM models of kinase-subtrates, statistically infer PWM:substrate matches, and integrate these data to infer kinase activity. biocViews: Proteomics, SequenceMatching, Network Author: Ashley J. Waardenberg [aut, cre] Maintainer: Ashley J. Waardenberg VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/KinSwingR git_branch: RELEASE_3_8 git_last_commit: d7df7ee git_last_commit_date: 2018-11-12 Date/Publication: 2018-11-12 source.ver: src/contrib/KinSwingR_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/KinSwingR_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/KinSwingR_1.0.3.tgz vignettes: vignettes/KinSwingR/inst/doc/KinSwingR.html vignetteTitles: KinSwingR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/KinSwingR/inst/doc/KinSwingR.R Package: kissDE Version: 1.2.0 Imports: aod, Biobase, DESeq2, DSS, ggplot2, gplots, graphics, grDevices, matrixStats, stats, utils, foreach, doParallel, parallel Suggests: BiocStyle, testthat License: GPL (>= 2) MD5sum: a68a4d0b79ff6681ae24ccd879f5caba NeedsCompilation: no Title: Retrieves Condition-Specific Variants in RNA-Seq Data Description: Retrieves condition-specific variants in RNA-seq data (SNVs, alternative-splicings, indels). It has been developed as a post-treatment of 'KisSplice' but can also be used with user's own data. biocViews: AlternativeSplicing, DifferentialSplicing, ExperimentalDesign, GenomicVariation, RNASeq, Transcriptomics Author: Clara Benoit-Pilven [aut], Camille Marchet [aut], Janice Kielbassa [aut], Lilia Brinza [aut], Audric Cologne [aut], Aurélie Siberchicot [aut, cre], Vincent Lacroix [aut], Frank Picard [ctb], Laurent Jacob [ctb], Vincent Miele [ctb] Maintainer: Aurélie Siberchicot git_url: https://git.bioconductor.org/packages/kissDE git_branch: RELEASE_3_8 git_last_commit: d9b3c63 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/kissDE_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/kissDE_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/kissDE_1.2.0.tgz vignettes: vignettes/kissDE/inst/doc/kissDE.pdf vignetteTitles: kissDE.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/kissDE/inst/doc/kissDE.R Package: lapmix Version: 1.48.0 Depends: R (>= 2.6.0),stats Imports: Biobase, graphics, grDevices, methods, stats, tools, utils License: GPL (>= 2) MD5sum: c923e2cecb461a0f5eda9c6c1e79b1f8 NeedsCompilation: no Title: Laplace Mixture Model in Microarray Experiments Description: Laplace mixture modelling of microarray experiments. A hierarchical Bayesian approach is used, and the hyperparameters are estimated using empirical Bayes. The main purpose is to identify differentially expressed genes. biocViews: Microarray, OneChannel, DifferentialExpression Author: Yann Ruffieux, contributions from Debjani Bhowmick, Anthony C. Davison, and Darlene R. Goldstein Maintainer: Yann Ruffieux URL: http://www.r-project.org, http://www.bioconductor.org, http://stat.epfl.ch git_url: https://git.bioconductor.org/packages/lapmix git_branch: RELEASE_3_8 git_last_commit: 3d5fea5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lapmix_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lapmix_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lapmix_1.48.0.tgz vignettes: vignettes/lapmix/inst/doc/lapmix-example.pdf vignetteTitles: lapmix example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/lapmix/inst/doc/lapmix-example.R Package: LBE Version: 1.50.0 Depends: stats Imports: graphics, grDevices, methods, stats, utils Suggests: qvalue License: GPL-2 MD5sum: fe7324956ca41278f4c97e74910242bd NeedsCompilation: no Title: Estimation of the false discovery rate. Description: LBE is an efficient procedure for estimating the proportion of true null hypotheses, the false discovery rate (and so the q-values) in the framework of estimating procedures based on the marginal distribution of the p-values without assumption for the alternative hypothesis. biocViews: MultipleComparison Author: Cyril Dalmasso Maintainer: Cyril Dalmasso git_url: https://git.bioconductor.org/packages/LBE git_branch: RELEASE_3_8 git_last_commit: bb5a5de git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LBE_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LBE_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LBE_1.50.0.tgz vignettes: vignettes/LBE/inst/doc/LBE.pdf vignetteTitles: LBE Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LBE/inst/doc/LBE.R Package: ldblock Version: 1.12.1 Depends: R (>= 3.1), methods, Homo.sapiens Imports: Matrix, snpStats, erma, VariantAnnotation, GenomeInfoDb, Rsamtools, GO.db, GenomicFiles (>= 1.13.6), BiocGenerics (>= 0.25.1) Suggests: RUnit, BiocGenerics, knitr License: Artistic-2.0 MD5sum: d9af44f526d370c52dea29671f0afc4e NeedsCompilation: no Title: data structures for linkage disequilibrium measures in populations Description: Define data structures for linkage disequilibrium measures in populations. Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ldblock git_branch: RELEASE_3_8 git_last_commit: 0d7c6a0 git_last_commit_date: 2019-04-03 Date/Publication: 2019-04-03 source.ver: src/contrib/ldblock_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ldblock_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ldblock_1.12.1.tgz vignettes: vignettes/ldblock/inst/doc/ldblock.pdf vignetteTitles: LD block import and manipulation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ldblock/inst/doc/ldblock.R suggestsMe: gQTLstats Package: LEA Version: 2.4.0 Depends: R (>= 3.3.0), methods, stats, utils, graphics Suggests: knitr License: GPL-3 Archs: i386, x64 MD5sum: 09abcae8ba7f52591c344deec4c62867 NeedsCompilation: yes Title: LEA: an R package for Landscape and Ecological Association Studies Description: LEA is an R package dedicated to landscape genomics and ecological association tests. LEA can run analyses of population structure and genomewide tests for local adaptation. The package includes statistical methods for estimating ancestry coefficients from large genotypic matrices and for evaluating the number of ancestral populations (snmf, pca). It performs statistical tests using latent factor mixed models for identifying genetic polymorphisms that exhibit association with environmental gradients or phenotypic traits (lfmm). LEA is mainly based on optimized C programs that can scale with the dimension of large data sets. biocViews: Software, StatisticalMethod, Clustering, Regression Author: Eric Frichot , Olivier Francois Maintainer: Eric Frichot , Olivier Francois URL: http://membres-timc.imag.fr/Olivier.Francois/lea.html VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/LEA git_branch: RELEASE_3_8 git_last_commit: b2000d6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LEA_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LEA_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LEA_2.4.0.tgz vignettes: vignettes/LEA/inst/doc/LEA.pdf vignetteTitles: LEA: An R Package for Landscape and Ecological Association Studies hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LEA/inst/doc/LEA.R Package: LedPred Version: 1.16.0 Depends: R (>= 3.2.0), e1071 (>= 1.6) Imports: akima, ggplot2, irr, jsonlite, parallel, plot3D, plyr, RCurl, ROCR, testthat License: MIT | file LICENSE MD5sum: 689b1b8c2a3248119bd8f8c4c6f16c77 NeedsCompilation: no Title: Learning from DNA to Predict Enhancers Description: This package aims at creating a predictive model of regulatory sequences used to score unknown sequences based on the content of DNA motifs, next-generation sequencing (NGS) peaks and signals and other numerical scores of the sequences using supervised classification. The package contains a workflow based on the support vector machine (SVM) algorithm that maps features to sequences, optimize SVM parameters and feature number and creates a model that can be stored and used to score the regulatory potential of unknown sequences. biocViews: SupportVectorMachine, Software, MotifAnnotation, ChIPSeq, Sequencing, Classification Author: Elodie Darbo, Denis Seyres, Aitor Gonzalez Maintainer: Aitor Gonzalez BugReports: https://github.com/aitgon/LedPred/issues git_url: https://git.bioconductor.org/packages/LedPred git_branch: RELEASE_3_8 git_last_commit: a980734 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LedPred_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LedPred_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LedPred_1.16.0.tgz vignettes: vignettes/LedPred/inst/doc/LedPred.pdf vignetteTitles: LedPred Example hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/LedPred/inst/doc/LedPred.R Package: les Version: 1.32.0 Depends: R (>= 2.13.2), methods, graphics, fdrtool Imports: boot, gplots, RColorBrewer Suggests: Biobase, limma Enhances: parallel License: GPL-3 MD5sum: d1f865bfb6b23e1d6dc272b84ca3c8d7 NeedsCompilation: no Title: Identifying Differential Effects in Tiling Microarray Data Description: The 'les' package estimates Loci of Enhanced Significance (LES) in tiling microarray data. These are regions of regulation such as found in differential transcription, CHiP-chip, or DNA modification analysis. The package provides a universal framework suitable for identifying differential effects in tiling microarray data sets, and is independent of the underlying statistics at the level of single probes. biocViews: Microarray, DifferentialExpression, ChIPchip, DNAMethylation, Transcription Author: Julian Gehring, Clemens Kreutz, Jens Timmer Maintainer: Julian Gehring git_url: https://git.bioconductor.org/packages/les git_branch: RELEASE_3_8 git_last_commit: fa5d10a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/les_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/les_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/les_1.32.0.tgz vignettes: vignettes/les/inst/doc/les.pdf vignetteTitles: Introduction to the les package: Identifying Differential Effects in Tiling Microarray Data with the Loci of Enhanced Significance Framework hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/les/inst/doc/les.R importsMe: GSRI Package: levi Version: 1.0.0 Depends: R(>= 3.5.0) Imports: DT(>= 0.4), RColorBrewer(>= 1.1-2), colorspace(>= 1.3-2), dplyr(>= 0.7.4), ggplot2(>= 2.2.1), httr(>= 1.3.1), igraph(>= 1.2.1), reshape2(>= 1.4.3), shiny(>= 1.0.5), shinydashboard(>= 0.7.0), shinyjs(>= 1.0), xml2(>= 1.2.0), knitr, Rcpp (>= 0.12.18), grid, grDevices, stats, utils, testthat LinkingTo: Rcpp License: GPL (>= 2) Archs: i386, x64 MD5sum: 816a51b096ed10aa182443879db1c581 NeedsCompilation: yes Title: Landscape Expression Visualization Interface Description: The tool integrates data from biological networks with transcriptomes, displaying a heatmap with surface curves to evidence the altered regions. biocViews: GeneExpression, Sequencing, Network Author: Jose Rafael Pilan , Agnes Alessandra Sekijima Takeda , Jose Luiz Rybarczyk Filho Maintainer: Jose Luiz Rybarczyk Filho VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/levi git_branch: RELEASE_3_8 git_last_commit: 0a68eb6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/levi_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/levi_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/levi_1.0.0.tgz vignettes: vignettes/levi/inst/doc/levi.html vignetteTitles: "Using levi" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/levi/inst/doc/levi.R Package: lfa Version: 1.12.0 Depends: R (>= 3.2) Imports: corpcor Suggests: knitr, ggplot2 License: GPL-3 Archs: i386, x64 MD5sum: 0d6d80f6ebb2ff5c3fc03d7255c2d4e5 NeedsCompilation: yes Title: Logistic Factor Analysis for Categorical Data Description: LFA is a method for a PCA analogue on Binomial data via estimation of latent structure in the natural parameter. biocViews: SNP, DimensionReduction, PrincipalComponent Author: Wei Hao, Minsun Song, John D. Storey Maintainer: Wei Hao , John D. Storey URL: https://github.com/StoreyLab/lfa VignetteBuilder: knitr BugReports: https://github.com/StoreyLab/lfa/issues git_url: https://git.bioconductor.org/packages/lfa git_branch: RELEASE_3_8 git_last_commit: 3fd0811 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lfa_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lfa_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lfa_1.12.0.tgz vignettes: vignettes/lfa/inst/doc/lfa.pdf vignetteTitles: lfa Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/lfa/inst/doc/lfa.R importsMe: gcatest Package: limma Version: 3.38.3 Depends: R (>= 2.3.0) Imports: grDevices, graphics, stats, utils, methods Suggests: affy, AnnotationDbi, BiasedUrn, Biobase, ellipse, GO.db, gplots, illuminaio, locfit, MASS, org.Hs.eg.db, splines, statmod (>= 1.2.2), vsn License: GPL (>=2) Archs: i386, x64 MD5sum: 71d46ed99a9c5267645c6ad5c6bec64b NeedsCompilation: yes Title: Linear Models for Microarray Data Description: Data analysis, linear models and differential expression for microarray data. biocViews: ExonArray, GeneExpression, Transcription, AlternativeSplicing, DifferentialExpression, DifferentialSplicing, GeneSetEnrichment, DataImport, Bayesian, Clustering, Regression, TimeCourse, Microarray, MicroRNAArray, mRNAMicroarray, OneChannel, ProprietaryPlatforms, TwoChannel, Sequencing, RNASeq, BatchEffect, MultipleComparison, Normalization, Preprocessing, QualityControl, BiomedicalInformatics, CellBiology, Cheminformatics, Epigenetics, FunctionalGenomics, Genetics, ImmunoOncology, Metabolomics, Proteomics, SystemsBiology, Transcriptomics Author: Gordon Smyth [cre,aut], Yifang Hu [ctb], Matthew Ritchie [ctb], Jeremy Silver [ctb], James Wettenhall [ctb], Davis McCarthy [ctb], Di Wu [ctb], Wei Shi [ctb], Belinda Phipson [ctb], Aaron Lun [ctb], Natalie Thorne [ctb], Alicia Oshlack [ctb], Carolyn de Graaf [ctb], Yunshun Chen [ctb], Mette Langaas [ctb], Egil Ferkingstad [ctb], Marcus Davy [ctb], Francois Pepin [ctb], Dongseok Choi [ctb] Maintainer: Gordon Smyth URL: http://bioinf.wehi.edu.au/limma git_url: https://git.bioconductor.org/packages/limma git_branch: RELEASE_3_8 git_last_commit: 77b292e git_last_commit_date: 2018-12-01 Date/Publication: 2018-12-02 source.ver: src/contrib/limma_3.38.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/limma_3.38.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/limma_3.38.3.tgz vignettes: vignettes/limma/inst/doc/intro.pdf, vignettes/limma/inst/doc/usersguide.pdf vignetteTitles: Limma One Page Introduction, usersguide.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4Base, AffyExpress, birta, BLMA, CALIB, cghMCR, codelink, convert, Cormotif, DrugVsDisease, edgeR, ExiMiR, ExpressionAtlas, gCMAP, HTqPCR, IsoformSwitchAnalyzeR, maigesPack, marray, metagenomeSeq, metaseqR, MmPalateMiRNA, mpra, qpcrNorm, qusage, RBM, Ringo, RnBeads, Rnits, snapCGH, splineTimeR, SRGnet, SSPA, tRanslatome, TurboNorm, variancePartition, wateRmelon importsMe: ABSSeq, affycoretools, affylmGUI, anamiR, ArrayExpress, arrayQuality, arrayQualityMetrics, ArrayTools, artMS, ATACseqQC, attract, ballgown, BatchQC, beadarray, biotmle, birte, bsseq, BubbleTree, bumphunter, CALIB, CancerMutationAnalysis, CancerSubtypes, casper, CATALYST, CEMiTool, charm, ChIPpeakAnno, clusterExperiment, coexnet, compcodeR, consensusDE, consensusOV, CountClust, crlmm, crossmeta, csaw, cTRAP, ctsGE, DaMiRseq, debrowser, DEP, derfinderPlot, DEsubs, DiffBind, diffcyt, diffHic, diffloop, DMRcate, Doscheda, DRIMSeq, EBSEA, eegc, EGAD, EGSEA, EnrichmentBrowser, erccdashboard, EventPointer, explorase, flowBin, gCrisprTools, GDCRNATools, GeneSelectMMD, GeneSelector, GEOquery, GGBase, GOsummaries, gQTLstats, GUIDEseq, hipathia, HTqPCR, icetea, iCheck, iChip, iCOBRA, ideal, InPAS, IsoformSwitchAnalyzeR, isomiRs, limmaGUI, Linnorm, lmdme, LVSmiRNA, mAPKL, mCSEA, MEAL, methylKit, MethylMix, methyvim, MIGSA, minfi, miRLAB, missMethyl, MLSeq, MmPalateMiRNA, monocle, MoonlightR, MSstats, MSstatsTMT, MultiDataSet, NADfinder, nem, nethet, nondetects, NormalyzerDE, OGSA, OLIN, omicRexposome, PAA, PADOG, PathoStat, pcaExplorer, PECA, pepStat, phantasus, phenoTest, polyester, psichomics, qPLEXanalyzer, qsea, regsplice, Ringo, RNAinteract, RNAither, RTCGAToolbox, RTN, RTopper, scone, scran, SEPIRA, seqsetvis, sigaR, SimBindProfiles, singleCellTK, snapCGH, STATegRa, SVAPLSseq, systemPipeR, TCGAbiolinks, timecourse, TimeSeriesExperiment, TPP, transcriptogramer, TVTB, tweeDEseq, vsn, Wrench, yamss, yarn suggestsMe: ABarray, ADaCGH2, beadarraySNP, biobroom, BiocCaseStudies, BioNet, Category, categoryCompare, celaref, ClassifyR, CMA, coGPS, cydar, DEGreport, derfinder, DEScan2, dyebias, ELBOW, fgsea, gage, GeneSelector, Glimma, GSRI, GSVA, Harman, Heatplus, isobar, ivygapSE, les, lumi, MAST, mdgsa, methylumi, MLP, npGSEA, oligo, oppar, paxtoolsr, PGSEA, piano, plw, PREDA, puma, Rcade, RTopper, rtracklayer, scater, stageR, subSeq, SummarizedBenchmark, tximport, zFPKM Package: limmaGUI Version: 1.58.0 Imports: methods, grDevices, graphics, limma, R2HTML, tcltk, tkrplot, xtable, utils License: GPL (>=2) MD5sum: 294967acdf8df9dfe9242d09ba53b527 NeedsCompilation: no Title: GUI for limma Package With Two Color Microarrays Description: A Graphical User Interface for differential expression analysis of two-color microarray data using the limma package. biocViews: GUI, GeneExpression, DifferentialExpression, DataImport, Bayesian, Regression, TimeCourse, Microarray, mRNAMicroarray, TwoChannel, BatchEffect, MultipleComparison, Normalization, Preprocessing, QualityControl Author: James Wettenhall [aut], Gordon Smyth [aut], Keith Satterley [ctb] Maintainer: Gordon Smyth URL: http://bioinf.wehi.edu.au/limmaGUI/ git_url: https://git.bioconductor.org/packages/limmaGUI git_branch: RELEASE_3_8 git_last_commit: c2dd15e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/limmaGUI_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/limmaGUI_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/limmaGUI_1.58.0.tgz vignettes: vignettes/limmaGUI/inst/doc/extract.pdf, vignettes/limmaGUI/inst/doc/limmaGUI.pdf, vignettes/limmaGUI/inst/doc/LinModIntro.pdf, vignettes/limmaGUI/inst/doc/about.html, vignettes/limmaGUI/inst/doc/CustMenu.html, vignettes/limmaGUI/inst/doc/import.html, vignettes/limmaGUI/inst/doc/index.html, vignettes/limmaGUI/inst/doc/InputFiles.html, vignettes/limmaGUI/inst/doc/lgDevel.html, vignettes/limmaGUI/inst/doc/windowsFocus.html vignetteTitles: Extracting limma objects from limmaGUI files, limmaGUI Vignette, LinModIntro.pdf, about.html, CustMenu.html, import.html, index.html, InputFiles.html, lgDevel.html, windowsFocus.html hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/limmaGUI/inst/doc/limmaGUI.R Package: LINC Version: 1.10.0 Depends: R (>= 3.3.1), methods, stats Imports: Rcpp (>= 0.11.0), DOSE, ggtree, gridExtra, ape, grid, png, Biobase, sva, reshape2, utils, grDevices, org.Hs.eg.db, clusterProfiler, ggplot2, ReactomePA LinkingTo: Rcpp Suggests: RUnit, BiocGenerics, knitr, biomaRt License: Artistic-2.0 Archs: i386, x64 MD5sum: 29086a9caad42adcd346b9efa078457e NeedsCompilation: yes Title: co-expression of lincRNAs and protein-coding genes Description: This package provides methods to compute co-expression networks of lincRNAs and protein-coding genes. Biological terms associated with the sets of protein-coding genes predict the biological contexts of lincRNAs according to the 'Guilty by Association' approach. biocViews: Software, BiologicalQuestion, GeneRegulation, GeneExpression Author: Manuel Goepferich, Carl Herrmann Maintainer: Manuel Goepferich VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/LINC git_branch: RELEASE_3_8 git_last_commit: 2d43a07 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LINC_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LINC_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LINC_1.10.0.tgz vignettes: vignettes/LINC/inst/doc/LINC.html vignetteTitles: "LINC - Co-Expression Analysis of lincRNAs" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LINC/inst/doc/LINC.R Package: LineagePulse Version: 1.2.1 Imports: BiocParallel, circlize, compiler, ComplexHeatmap, ggplot2, gplots, grDevices, grid, knitr, Matrix, methods, RColorBrewer, SingleCellExperiment, splines, stats, SummarizedExperiment, utils License: Artistic-2.0 MD5sum: 385ebc5c90bd6423aef96cd378c380d1 NeedsCompilation: no Title: Differential expression analysis and model fitting for single-cell RNA-seq data Description: LineagePulse is a differential expression and expression model fitting package tailored to single-cell RNA-seq data (scRNA-seq). LineagePulse accounts for batch effects, drop-out and variable sequencing depth. One can use LineagePulse to perform longitudinal differential expression analysis across pseudotime as a continuous coordinate or between discrete groups of cells (e.g. pre-defined clusters or experimental conditions). Expression model fits can be directly extracted from LineagePulse. biocViews: ImmunoOncology, Software, StatisticalMethod, TimeCourse, Sequencing, DifferentialExpression, GeneExpression, CellBiology, CellBasedAssays, SingleCell Author: David S Fischer [aut, cre], Fabian Theis [ctb], Nir Yosef [ctb] Maintainer: David S Fischer VignetteBuilder: knitr BugReports: https://github.com/YosefLab/LineagePulse/issues git_url: https://git.bioconductor.org/packages/LineagePulse git_branch: RELEASE_3_8 git_last_commit: 1ec2a20 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/LineagePulse_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/LineagePulse_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LineagePulse_1.2.1.tgz vignettes: vignettes/LineagePulse/inst/doc/LineagePulse_Tutorial.html vignetteTitles: LineagePulse hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LineagePulse/inst/doc/LineagePulse_Tutorial.R Package: Linnorm Version: 2.6.1 Depends: R(>= 3.4) Imports: Rcpp (>= 0.12.2), RcppArmadillo (>= 0.8.100.1.0), fpc, vegan, mclust, apcluster, ggplot2, ellipse, limma, utils, statmod, MASS, igraph, grDevices, graphics, fastcluster, ggdendro, zoo, stats, amap, Rtsne, gmodels LinkingTo: Rcpp, RcppArmadillo Suggests: BiocStyle, knitr, rmarkdown, gplots, RColorBrewer, moments, testthat License: MIT + file LICENSE Archs: i386, x64 MD5sum: f495a73301ba6e1d7de21dac647cc6fd NeedsCompilation: yes Title: Linear model and normality based transformation method (Linnorm) Description: Linnorm is an R package for the analysis of RNA-seq, scRNA-seq, ChIP-seq count data or any large scale count data. It transforms such datasets for parametric tests. In addition to the transformtion function (Linnorm), the following pipelines are implemented: 1. Library size/Batch effect normalization (Linnorm.Norm), 2. Cell subpopluation analysis and visualization using t-SNE or PCA K-means clustering or Hierarchical clustering (Linnorm.tSNE, Linnorm.PCA, Linnorm.HClust), 3. Differential expression analysis or differential peak detection using limma (Linnorm.limma), 4. Highly variable gene discovery and visualization (Linnorm.HVar), 5. Gene correlation network analysis and visualization (Linnorm.Cor), 6. Stable gene selection for scRNA-seq data; for users without or do not want to rely on spike-in genes (Linnorm.SGenes). 7. Data imputation. (under development) (Linnorm.DataImput). Linnorm can work with raw count, CPM, RPKM, FPKM and TPM. Additionally, the RnaXSim function is included for simulating RNA-seq data for the evaluation of DEG analysis methods. biocViews: ImmunoOncology, Sequencing, ChIPSeq, RNASeq, DifferentialExpression, GeneExpression, Genetics, Normalization, Software, Transcription, BatchEffect, PeakDetection, Clustering, Network, SingleCell Author: Shun Hang Yip , Panwen Wang , Jean-Pierre Kocher , Pak Chung Sham , Junwen Wang Maintainer: Ken Shun Hang Yip URL: http://www.jjwanglab.org/Linnorm/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Linnorm git_branch: RELEASE_3_8 git_last_commit: af8fd00 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Linnorm_2.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Linnorm_2.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Linnorm_2.6.1.tgz vignettes: vignettes/Linnorm/inst/doc/Linnorm_User_Manual.pdf vignetteTitles: Linnorm User Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Linnorm/inst/doc/Linnorm_User_Manual.R Package: LiquidAssociation Version: 1.36.0 Depends: geepack, methods, yeastCC, org.Sc.sgd.db Imports: Biobase, graphics, grDevices, methods, stats License: GPL (>=3) MD5sum: 0c5372f29db62136b3797b29b3debe18 NeedsCompilation: no Title: LiquidAssociation Description: The package contains functions for calculate direct and model-based estimators for liquid association. It also provides functions for testing the existence of liquid association given a gene triplet data. biocViews: Pathways, GeneExpression, CellBiology, Genetics, Network, TimeCourse Author: Yen-Yi Ho Maintainer: Yen-Yi Ho git_url: https://git.bioconductor.org/packages/LiquidAssociation git_branch: RELEASE_3_8 git_last_commit: ceead18 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LiquidAssociation_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LiquidAssociation_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LiquidAssociation_1.36.0.tgz vignettes: vignettes/LiquidAssociation/inst/doc/LiquidAssociation.pdf vignetteTitles: LiquidAssociation Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LiquidAssociation/inst/doc/LiquidAssociation.R dependsOnMe: fastLiquidAssociation Package: lmdme Version: 1.24.0 Depends: R (>= 2.14.1), pls, stemHypoxia Imports: stats, methods, limma Enhances: parallel License: GPL (>=2) MD5sum: d84c1a13e28adbb587d9006cff7938db NeedsCompilation: no Title: Linear Model decomposition for Designed Multivariate Experiments Description: linear ANOVA decomposition of Multivariate Designed Experiments implementation based on limma lmFit. Features: i)Flexible formula type interface, ii) Fast limma based implementation, iii) p-values for each estimated coefficient levels in each factor, iv) F values for factor effects and v) plotting functions for PCA and PLS. biocViews: Microarray, OneChannel, TwoChannel, Visualization, DifferentialExpression, ExperimentData, Cancer Author: Cristobal Fresno and Elmer A. Fernandez Maintainer: Cristobal Fresno URL: http://www.bdmg.com.ar/?page_id=38 git_url: https://git.bioconductor.org/packages/lmdme git_branch: RELEASE_3_8 git_last_commit: 4ded3a9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lmdme_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lmdme_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lmdme_1.24.0.tgz vignettes: vignettes/lmdme/inst/doc/lmdme-vignette.pdf vignetteTitles: lmdme: linear model framework for PCA/PLS analysis of ANOVA decomposition on Designed Multivariate Experiments in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/lmdme/inst/doc/lmdme-vignette.R Package: LMGene Version: 2.38.0 Depends: R (>= 2.10.0), Biobase (>= 2.5.5), multtest, survival, affy Suggests: affydata License: LGPL MD5sum: 1d5e6672bd23b4c523568b712545643c NeedsCompilation: no Title: LMGene Software for Data Transformation and Identification of Differentially Expressed Genes in Gene Expression Arrays Description: LMGene package for analysis of microarray data using a linear model and glog data transformation biocViews: Microarray, DifferentialExpression, Preprocessing Author: David Rocke, Geun Cheol Lee, John Tillinghast, Blythe Durbin-Johnson, and Shiquan Wu Maintainer: Blythe Durbin-Johnson URL: http://dmrocke.ucdavis.edu/software.html git_url: https://git.bioconductor.org/packages/LMGene git_branch: RELEASE_3_8 git_last_commit: f352587 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LMGene_2.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LMGene_2.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LMGene_2.38.0.tgz vignettes: vignettes/LMGene/inst/doc/LMGene.pdf vignetteTitles: LMGene User's Guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LMGene/inst/doc/LMGene.R Package: LOBSTAHS Version: 1.8.1 Depends: R (>= 3.4), xcms, CAMERA, methods Imports: utils Suggests: PtH2O2lipids, knitr, rmarkdown License: GPL (>= 3) + file LICENSE MD5sum: 1acf4da2bb8e0d50fc8c96bd9499b2f2 NeedsCompilation: no Title: Lipid and Oxylipin Biomarker Screening through Adduct Hierarchy Sequences Description: LOBSTAHS is a multifunction package for screening, annotation, and putative identification of mass spectral features in large, HPLC-MS lipid datasets. In silico data for a wide range of lipids, oxidized lipids, and oxylipins can be generated from user-supplied structural criteria with a database generation function. LOBSTAHS then applies these databases to assign putative compound identities to features in any high-mass accuracy dataset that has been processed using xcms and CAMERA. Users can then apply a series of orthogonal screening criteria based on adduct ion formation patterns, chromatographic retention time, and other properties, to evaluate and assign confidence scores to this list of preliminary assignments. During the screening routine, LOBSTAHS rejects assignments that do not meet the specified criteria, identifies potential isomers and isobars, and assigns a variety of annotation codes to assist the user in evaluating the accuracy of each assignment. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics, Lipidomics, DataImport Author: James Collins [aut, cre], Helen Fredricks [aut], Bethanie Edwards [aut], Benjamin Van Mooy [aut] Maintainer: James Collins URL: http://bioconductor.org/packages/LOBSTAHS VignetteBuilder: knitr BugReports: https://github.com/vanmooylipidomics/LOBSTAHS/issues/new git_url: https://git.bioconductor.org/packages/LOBSTAHS git_branch: RELEASE_3_8 git_last_commit: 8b1c0d4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/LOBSTAHS_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/LOBSTAHS_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LOBSTAHS_1.8.1.tgz vignettes: vignettes/LOBSTAHS/inst/doc/LOBSTAHS.html vignetteTitles: Discovery,, Identification,, and Screening of Lipids and Oxylipins in HPLC-MS Datasets Using LOBSTAHS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/LOBSTAHS/inst/doc/LOBSTAHS.R Package: loci2path Version: 1.2.0 Depends: R (>= 3.4) Imports: pheatmap, wordcloud, RColorBrewer, data.table, methods, grDevices, stats, graphics, GenomicRanges, BiocParallel, S4Vectors Suggests: BiocStyle, knitr, rmarkdown License: Artistic-2.0 MD5sum: 90e463d21339295ec91413e52911e733 NeedsCompilation: no Title: Loci2path: regulatory annotation of genomic intervals based on tissue-specific expression QTLs Description: loci2path performs statistics-rigorous enrichment analysis of eQTLs in genomic regions of interest. Using eQTL collections provided by the Genotype-Tissue Expression (GTEx) project and pathway collections from MSigDB. biocViews: FunctionalGenomics, Genetics, GeneSetEnrichment, Software, GeneExpression, Sequencing, Coverage, BioCarta Author: Tianlei Xu Maintainer: Tianlei Xu URL: https://github.com/StanleyXu/loci2path VignetteBuilder: knitr BugReports: https://github.com/StanleyXu/loci2path/issues git_url: https://git.bioconductor.org/packages/loci2path git_branch: RELEASE_3_8 git_last_commit: 582bc31 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/loci2path_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/loci2path_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/loci2path_1.2.0.tgz vignettes: vignettes/loci2path/inst/doc/loci2path-vignette.html vignetteTitles: loci2path hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/loci2path/inst/doc/loci2path-vignette.R Package: logicFS Version: 2.2.0 Depends: LogicReg, mcbiopi, survival Imports: graphics, methods, stats Suggests: genefilter, siggenes License: LGPL (>= 2) MD5sum: c938e0a3bb72e81baeb62791e8cbd6d9 NeedsCompilation: no Title: Identification of SNP Interactions Description: Identification of interactions between binary variables using Logic Regression. Can, e.g., be used to find interesting SNP interactions. Contains also a bagging version of logic regression for classification. biocViews: SNP, Classification, Genetics Author: Holger Schwender, Tobias Tietz Maintainer: Holger Schwender git_url: https://git.bioconductor.org/packages/logicFS git_branch: RELEASE_3_8 git_last_commit: f5b2a7f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/logicFS_2.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/logicFS_2.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/logicFS_2.2.0.tgz vignettes: vignettes/logicFS/inst/doc/logicFS.pdf vignetteTitles: logicFS Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/logicFS/inst/doc/logicFS.R suggestsMe: trio Package: logitT Version: 1.40.0 Depends: affy Suggests: SpikeInSubset License: GPL (>= 2) Archs: i386, x64 MD5sum: b84aee3b9e43a884c6119562b543a9f2 NeedsCompilation: yes Title: logit-t Package Description: The logitT library implements the Logit-t algorithm introduced in --A high performance test of differential gene expression for oligonucleotide arrays-- by William J Lemon, Sandya Liyanarachchi and Ming You for use with Affymetrix data stored in an AffyBatch object in R. biocViews: Microarray, DifferentialExpression Author: Tobias Guennel Maintainer: Tobias Guennel URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/logitT git_branch: RELEASE_3_8 git_last_commit: 1a00eeb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/logitT_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/logitT_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/logitT_1.40.0.tgz vignettes: vignettes/logitT/inst/doc/logitT.pdf vignetteTitles: logitT primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/logitT/inst/doc/logitT.R Package: Logolas Version: 1.6.0 Depends: R (>= 3.4) Imports: grid, SQUAREM, LaplacesDemon, stats, graphics, utils, ggplot2, gridBase, Biostrings Suggests: knitr, rmarkdown, BiocStyle, Biobase, devtools, xtable, gridExtra, RColorBrewer, seqLogo, ggseqlogo License: GPL (>= 2) MD5sum: 3aacdce238af176577fbf05161b54325 NeedsCompilation: no Title: EDLogo Plots Featuring String Logos and Adaptive Scaling of Position-Weight Matrices Description: Produces logo plots highlighting both enrichment and depletion of characters, allows for plotting of string symbols, and performs scaling of position-weights adaptively, along with several fun stylizations. biocViews: SequenceMatching, Alignment, Software, Visualization, Bayesian Author: Kushal Dey [aut, cre], Dongyue Xie [aut], Peter Carbonetto [ctb], Matthew Stephens [aut] Maintainer: Kushal Dey URL: https://github.com/kkdey/Logolas VignetteBuilder: knitr BugReports: http://github.com/kkdey/Logolas/issues git_url: https://git.bioconductor.org/packages/Logolas git_branch: RELEASE_3_8 git_last_commit: 67c730d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Logolas_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Logolas_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Logolas_1.6.0.tgz vignettes: vignettes/Logolas/inst/doc/Logolas.html vignetteTitles: Guided Logolas Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Logolas/inst/doc/Logolas.R suggestsMe: universalmotif Package: lol Version: 1.30.0 Depends: penalized, Matrix Imports: Matrix, penalized, graphics, grDevices, stats License: GPL-2 MD5sum: 9339f2a964b2d4470286d87eaaba88cb NeedsCompilation: no Title: Lots Of Lasso Description: Various optimization methods for Lasso inference with matrix warpper biocViews: StatisticalMethod Author: Yinyin Yuan Maintainer: Yinyin Yuan git_url: https://git.bioconductor.org/packages/lol git_branch: RELEASE_3_8 git_last_commit: 42cca13 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lol_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lol_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lol_1.30.0.tgz vignettes: vignettes/lol/inst/doc/lol.pdf vignetteTitles: An introduction to the lol package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/lol/inst/doc/lol.R Package: LOLA Version: 1.12.0 Depends: R (>= 2.10) Imports: BiocGenerics, S4Vectors, IRanges, GenomicRanges, data.table, reshape2, utils, stats, methods Suggests: parallel, testthat, knitr, BiocStyle, rmarkdown Enhances: simpleCache, qvalue, ggplot2 License: GPL-3 MD5sum: e57b955b1d44900a375fce04c3217d1f NeedsCompilation: no Title: Locus overlap analysis for enrichment of genomic ranges Description: Provides functions for testing overlap of sets of genomic regions with public and custom region set (genomic ranges) databases. This makes it possible to do automated enrichment analysis for genomic region sets, thus facilitating interpretation of functional genomics and epigenomics data. biocViews: GeneSetEnrichment, GeneRegulation, GenomeAnnotation, SystemsBiology, FunctionalGenomics, ChIPSeq, MethylSeq, Sequencing Author: Nathan Sheffield [aut, cre], Christoph Bock [ctb] Maintainer: Nathan Sheffield URL: http://code.databio.org/LOLA VignetteBuilder: knitr BugReports: http://github.com/nsheff/LOLA git_url: https://git.bioconductor.org/packages/LOLA git_branch: RELEASE_3_8 git_last_commit: 5841496 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LOLA_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LOLA_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LOLA_1.12.0.tgz vignettes: vignettes/LOLA/inst/doc/choosingUniverse.html, vignettes/LOLA/inst/doc/gettingStarted.html, vignettes/LOLA/inst/doc/usingLOLACore.html vignetteTitles: 3. Choosing a Universe, 1. Getting Started with LOLA, 2. Using LOLA Core hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LOLA/inst/doc/choosingUniverse.R, vignettes/LOLA/inst/doc/gettingStarted.R, vignettes/LOLA/inst/doc/usingLOLACore.R suggestsMe: COCOA, DeepBlueR, MIRA Package: LoomExperiment Version: 1.0.4 Depends: R (>= 3.5.0), S4Vectors, SingleCellExperiment, SummarizedExperiment, methods, rhdf5, rtracklayer Imports: DelayedArray, GenomicRanges, HDF5Array, stats, utils Suggests: testthat, BiocStyle, knitr License: Artistic-2.0 MD5sum: aaf1936c00e72169f18f818b5ef63fcb NeedsCompilation: no Title: LoomExperiment container Description: The LoomExperiment class provide a means to easily convert Bioconductor's "Experiment" classes to loom files and vice versa. biocViews: ImmunoOncology, DataRepresentation, DataImport, Infrastructure, SingleCell Author: Martin Morgan, Daniel Van Twisk Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/LoomExperiment git_branch: RELEASE_3_8 git_last_commit: 54aba44 git_last_commit_date: 2019-03-06 Date/Publication: 2019-03-06 source.ver: src/contrib/LoomExperiment_1.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/LoomExperiment_1.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LoomExperiment_1.0.4.tgz vignettes: vignettes/LoomExperiment/inst/doc/LoomExperiment.html vignetteTitles: An introduction to the LoomExperiment class hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LoomExperiment/inst/doc/LoomExperiment.R Package: LowMACA Version: 1.12.1 Depends: R (>= 2.10) Imports: cgdsr, parallel, stringr, reshape2, data.table, RColorBrewer, methods, LowMACAAnnotation, BiocParallel, motifStack, Biostrings, httr Suggests: BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: f07683636d6e2a5d756ebb83e95ea9b2 NeedsCompilation: no Title: LowMACA - Low frequency Mutation Analysis via Consensus Alignment Description: The LowMACA package is a simple suite of tools to investigate and analyze the mutation profile of several proteins or pfam domains via consensus alignment. You can conduct an hypothesis driven exploratory analysis using our package simply providing a set of genes or pfam domains of your interest. biocViews: SomaticMutation, SequenceMatching, WholeGenome, Sequencing, Alignment, DataImport, MultipleSequenceAlignment Author: Stefano de Pretis , Giorgio Melloni Maintainer: Stefano de Pretis , Giorgio Melloni SystemRequirements: clustalo, gs, perl VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/LowMACA git_branch: RELEASE_3_8 git_last_commit: c58adb1 git_last_commit_date: 2019-03-08 Date/Publication: 2019-03-09 source.ver: src/contrib/LowMACA_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/LowMACA_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LowMACA_1.12.1.tgz vignettes: vignettes/LowMACA/inst/doc/LowMACA.html vignetteTitles: Bioconductor style for HTML documents hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LowMACA/inst/doc/LowMACA.R Package: LPE Version: 1.56.0 Depends: R (>= 2.10) Imports: stats License: LGPL MD5sum: 7ddf8da425759856e5c6071ec4762b6a NeedsCompilation: no Title: Methods for analyzing microarray data using Local Pooled Error (LPE) method Description: This LPE library is used to do significance analysis of microarray data with small number of replicates. It uses resampling based FDR adjustment, and gives less conservative results than traditional 'BH' or 'BY' procedures. Data accepted is raw data in txt format from MAS4, MAS5 or dChip. Data can also be supplied after normalization. LPE library is primarily used for analyzing data between two conditions. To use it for paired data, see LPEP library. For using LPE in multiple conditions, use HEM library. biocViews: Microarray, DifferentialExpression Author: Nitin Jain , Michael O'Connell , Jae K. Lee . Includes R source code contributed by HyungJun Cho Maintainer: Nitin Jain URL: http://www.r-project.org, http://www.healthsystem.virginia.edu/internet/hes/biostat/bioinformatics/, http://sourceforge.net/projects/r-lpe/ git_url: https://git.bioconductor.org/packages/LPE git_branch: RELEASE_3_8 git_last_commit: 0892844 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LPE_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LPE_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LPE_1.56.0.tgz vignettes: vignettes/LPE/inst/doc/LPE.pdf vignetteTitles: LPE test for microarray data with small number of replicates hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LPE/inst/doc/LPE.R dependsOnMe: LPEadj, PLPE importsMe: LPEadj suggestsMe: ABarray Package: LPEadj Version: 1.42.0 Depends: LPE Imports: LPE, stats License: LGPL MD5sum: a50c028087f227ddee20391e296bc199 NeedsCompilation: no Title: A correction of the local pooled error (LPE) method to replace the asymptotic variance adjustment with an unbiased adjustment based on sample size. Description: Two options are added to the LPE algorithm. The original LPE method sets all variances below the max variance in the ordered distribution of variances to the maximum variance. in LPEadj this option is turned off by default. The second option is to use a variance adjustment based on sample size rather than pi/2. By default the LPEadj uses the sample size based variance adjustment. biocViews: Microarray, Proteomics Author: Carl Murie , Robert Nadon Maintainer: Carl Murie git_url: https://git.bioconductor.org/packages/LPEadj git_branch: RELEASE_3_8 git_last_commit: 76a1f5f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LPEadj_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LPEadj_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LPEadj_1.42.0.tgz vignettes: vignettes/LPEadj/inst/doc/LPEadj.pdf vignetteTitles: LPEadj test for microarray data with small number of replicates hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LPEadj/inst/doc/LPEadj.R Package: lpNet Version: 2.14.0 Depends: lpSolve, nem License: Artistic License 2.0 MD5sum: 80548ee68471e1474411ea5d691d205b NeedsCompilation: no Title: Linear Programming Model for Network Inference Description: lpNet aims at infering biological networks, in particular signaling and gene networks. For that it takes perturbation data, either steady-state or time-series, as input and generates an LP model which allows the inference of signaling networks. For parameter identification either leave-one-out cross-validation or stratified n-fold cross-validation can be used. biocViews: NetworkInference Author: Bettina Knapp, Marta R. A. Matos, Johanna Mazur, Lars Kaderali Maintainer: Lars Kaderali git_url: https://git.bioconductor.org/packages/lpNet git_branch: RELEASE_3_8 git_last_commit: 064f79f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lpNet_2.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lpNet_2.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lpNet_2.14.0.tgz vignettes: vignettes/lpNet/inst/doc/vignette_lpNet.pdf vignetteTitles: lpNet,, network inference with a linear optimization program. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/lpNet/inst/doc/vignette_lpNet.R Package: lpsymphony Version: 1.10.0 Depends: R (>= 3.0.0) Suggests: BiocStyle, knitr Enhances: slam License: EPL Archs: i386, x64 MD5sum: ef6e41c4c16fa4ba123f2095618eff4b NeedsCompilation: yes Title: Symphony integer linear programming solver in R Description: This package was derived from Rsymphony_0.1-17 from CRAN. These packages provide an R interface to SYMPHONY, an open-source linear programming solver written in C++. The main difference between this package and Rsymphony is that it includes the solver source code (SYMPHONY version 5.6), while Rsymphony expects to find header and library files on the users' system. Thus the intention of lpsymphony is to provide an easy to install interface to SYMPHONY. For Windows, precompiled DLLs are included in this package. biocViews: Infrastructure, ThirdPartyClient Author: Vladislav Kim [aut, cre], Ted Ralphs [ctb], Menal Guzelsoy [ctb], Ashutosh Mahajan [ctb], Reinhard Harter [ctb], Kurt Hornik [ctb], Cyrille Szymanski [ctb], Stefan Theussl [ctb] Maintainer: Vladislav Kim URL: http://R-Forge.R-project.org/projects/rsymphony, https://projects.coin-or.org/SYMPHONY, http://www.coin-or.org/download/source/SYMPHONY/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/lpsymphony git_branch: RELEASE_3_8 git_last_commit: eb74955 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lpsymphony_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lpsymphony_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lpsymphony_1.10.0.tgz vignettes: vignettes/lpsymphony/inst/doc/lpsymphony.pdf vignetteTitles: Introduction to lpsymphony hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/lpsymphony/inst/doc/lpsymphony.R importsMe: IHW Package: LRBaseDbi Version: 1.0.0 Depends: R (>= 3.5.0) Imports: methods, stats, utils, AnnotationDbi, RSQLite, DBI, Biobase Suggests: RUnit, BiocGenerics, BiocStyle License: Artistic-2.0 MD5sum: f983eacbbe7593cfae1996944d5f4710 NeedsCompilation: no Title: DBI to construct LRBase-related package Description: Interface to construct LRBase package (LRBase.XXX.eg.db). biocViews: Infrastructure Author: Koki Tsuyuzaki Maintainer: Koki Tsuyuzaki VignetteBuilder: utils git_url: https://git.bioconductor.org/packages/LRBaseDbi git_branch: RELEASE_3_8 git_last_commit: 1fe8cf4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LRBaseDbi_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LRBaseDbi_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LRBaseDbi_1.0.0.tgz vignettes: vignettes/LRBaseDbi/inst/doc/LRBaseDbi.pdf vignetteTitles: LRBaseDbi hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LRBaseDbi/inst/doc/LRBaseDbi.R Package: lumi Version: 2.34.0 Depends: R (>= 2.10), Biobase (>= 2.5.5) Imports: affy (>= 1.23.4), methylumi (>= 2.3.2), GenomicFeatures, GenomicRanges, annotate, lattice, mgcv (>= 1.4-0), nleqslv, KernSmooth, preprocessCore, RSQLite, DBI, AnnotationDbi, MASS, graphics, stats, stats4, methods Suggests: beadarray, limma, vsn, lumiBarnes, lumiHumanAll.db, lumiHumanIDMapping, genefilter, RColorBrewer License: LGPL (>= 2) MD5sum: 8d2ae23d6b7c8021a10020c0f42baa71 NeedsCompilation: no Title: BeadArray Specific Methods for Illumina Methylation and Expression Microarrays Description: The lumi package provides an integrated solution for the Illumina microarray data analysis. It includes functions of Illumina BeadStudio (GenomeStudio) data input, quality control, BeadArray-specific variance stabilization, normalization and gene annotation at the probe level. It also includes the functions of processing Illumina methylation microarrays, especially Illumina Infinium methylation microarrays. biocViews: Microarray, OneChannel, Preprocessing, DNAMethylation, QualityControl, TwoChannel Author: Pan Du, Richard Bourgon, Gang Feng, Simon Lin Maintainer: Pan Du , Lei Huang , Gang Feng git_url: https://git.bioconductor.org/packages/lumi git_branch: RELEASE_3_8 git_last_commit: ff60f7d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/lumi_2.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/lumi_2.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/lumi_2.34.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: arrayMvout, iCheck, wateRmelon importsMe: anamiR, ffpe, methyAnalysis, MineICA suggestsMe: beadarray, blima, Harman, methylumi, tigre Package: LVSmiRNA Version: 1.32.0 Depends: R (>= 3.1.0), methods, splines Imports: BiocGenerics, stats4, graphics, stats, utils, MASS, Biobase, quantreg, limma, affy, SparseM, vsn, zlibbioc Enhances: parallel,snow, Rmpi License: GPL-2 Archs: i386, x64 MD5sum: 970f3c4e6fb62c5d9dcf870a700288ae NeedsCompilation: yes Title: LVS normalization for Agilent miRNA data Description: Normalization of Agilent miRNA arrays. biocViews: Microarray,AgilentChip,OneChannel,Preprocessing Author: Stefano Calza, Suo Chen, Yudi Pawitan Maintainer: Stefano Calza git_url: https://git.bioconductor.org/packages/LVSmiRNA git_branch: RELEASE_3_8 git_last_commit: 1b5458e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LVSmiRNA_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LVSmiRNA_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LVSmiRNA_1.32.0.tgz vignettes: vignettes/LVSmiRNA/inst/doc/LVSmiRNA.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LVSmiRNA/inst/doc/LVSmiRNA.R Package: LymphoSeq Version: 1.10.0 Depends: R (>= 3.3), LymphoSeqDB Imports: data.table, plyr, dplyr, reshape, VennDiagram, ggplot2, ineq, RColorBrewer, circlize, grid, utils, stats, ggtree, msa, Biostrings, phangorn, stringdist, UpSetR Suggests: knitr, pheatmap, wordcloud, rmarkdown License: Artistic-2.0 MD5sum: 1b5c24b3df8523d37d12cae3fdfe4a33 NeedsCompilation: no Title: Analyze high-throughput sequencing of T and B cell receptors Description: This R package analyzes high-throughput sequencing of T and B cell receptor complementarity determining region 3 (CDR3) sequences generated by Adaptive Biotechnologies' ImmunoSEQ assay. Its input comes from tab-separated value (.tsv) files exported from the ImmunoSEQ analyzer. biocViews: Software, Technology, Sequencing, TargetedResequencing, Alignment, MultipleSequenceAlignment Author: David Coffey Maintainer: David Coffey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/LymphoSeq git_branch: RELEASE_3_8 git_last_commit: 255c541 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/LymphoSeq_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/LymphoSeq_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/LymphoSeq_1.10.0.tgz vignettes: vignettes/LymphoSeq/inst/doc/LymphoSeq.html vignetteTitles: Analysis of high-throughput sequencing of T and B cell receptors with LymphoSeq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/LymphoSeq/inst/doc/LymphoSeq.R Package: M3C Version: 1.4.1 Depends: R (>= 3.4.0) Imports: ggplot2, Matrix, doSNOW, NMF, RColorBrewer, cluster, parallel, foreach, doParallel, matrixcalc, dendextend, sigclust, Rtsne, survival Suggests: knitr, rmarkdown License: AGPL-3 MD5sum: 77c756f2e0df9460a72956e7f7b8b542 NeedsCompilation: no Title: Monte Carlo Reference-based Consensus Clustering Description: Genome-wide data is used to stratify large complex datasets into classes using class discovery algorithms. A widely applied technique is consensus clustering, however; the approach is prone to overfitting and false positives. These issues arise from not considering reference distributions while selecting the number of classes (K). As a solution, we developed Monte Carlo reference-based consensus clustering (M3C). M3C uses a multi-core enabled Monte Carlo simulation to generate null distributions along the range of K which are used to select its value. Using a reference, that maintains the correlation structure of the input features, eliminates the limitations of consensus clustering. M3C uses the Relative Cluster Stability Index (RCSI) and p values to decide on the value of K and reject the null hypothesis, K=1. M3C can also quantify structural relationships between clusters, and uses spectral clustering to deal with non-Gaussian and complex structures. M3C can automatically analyse biological or clinical data with respect to the discovered classes. biocViews: ImmunoOncology, Clustering, GeneExpression, Transcription, RNASeq, Sequencing Author: Christopher John [aut, cre] Maintainer: Christopher John VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/M3C git_branch: RELEASE_3_8 git_last_commit: 4b3f65a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/M3C_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/M3C_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/M3C_1.4.1.tgz vignettes: vignettes/M3C/inst/doc/M3Cvignette.html vignetteTitles: M3C hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/M3C/inst/doc/M3Cvignette.R Package: M3D Version: 1.16.0 Depends: R (>= 3.3.0) Imports: parallel, Rcpp, BiocGenerics, S4Vectors, IRanges, GenomicRanges, SummarizedExperiment, BiSeq LinkingTo: Rcpp Suggests: BiocStyle, knitr, testthat License: Artistic License 2.0 Archs: x64 MD5sum: 77b8592c2b95342c0d27f10277002627 NeedsCompilation: yes Title: Identifies differentially methylated regions across testing groups Description: This package identifies statistically significantly differentially methylated regions of CpGs. It uses kernel methods (the Maximum Mean Discrepancy) to measure differences in methylation profiles, and relates these to inter-replicate changes, whilst accounting for variation in coverage profiles. biocViews: DNAMethylation, DifferentialMethylation, Coverage, CpGIsland Author: Tom Mayo Maintainer: Tom Mayo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/M3D git_branch: RELEASE_3_8 git_last_commit: af1923f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/M3D_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/M3D_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/M3D_1.16.0.tgz vignettes: vignettes/M3D/inst/doc/M3D_vignette.pdf vignetteTitles: An Introduction to the M$^3$D method hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/M3D/inst/doc/M3D_vignette.R Package: M3Drop Version: 1.8.1 Depends: R (>= 3.3), numDeriv Imports: RColorBrewer, gplots, bbmle, statmod, grDevices, graphics, stats Suggests: ROCR, knitr, M3DExampleData License: GPL (>=2) MD5sum: 6dc5e92a9ab6f512b94d362d100c170f NeedsCompilation: no Title: Michaelis-Menten Modelling of Dropouts in single-cell RNASeq Description: This package fits a Michaelis-Menten model to the pattern of dropouts in single-cell RNASeq data. This model is used as a null to identify significantly variable (i.e. differentially expressed) genes for use in downstream analysis, such as clustering cells. biocViews: ImmunoOncology, RNASeq, Sequencing, Transcriptomics, GeneExpression, Software, DifferentialExpression, DimensionReduction, FeatureExtraction Author: Tallulah Andrews Maintainer: Tallulah Andrews URL: https://github.com/tallulandrews/M3Drop VignetteBuilder: knitr BugReports: https://github.com/tallulandrews/M3Drop/issues git_url: https://git.bioconductor.org/packages/M3Drop git_branch: RELEASE_3_8 git_last_commit: f88412f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/M3Drop_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/M3Drop_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/M3Drop_1.8.1.tgz vignettes: vignettes/M3Drop/inst/doc/M3Drop_Vignette.pdf vignetteTitles: Introduction to M3Drop hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/M3Drop/inst/doc/M3Drop_Vignette.R Package: maanova Version: 1.52.0 Depends: R (>= 2.10) Imports: Biobase, graphics, grDevices, methods, stats, utils Suggests: qvalue, snow Enhances: Rmpi License: GPL (>= 2) Archs: i386, x64 MD5sum: 98d914299500ad6464eabd0244389b4a NeedsCompilation: yes Title: Tools for analyzing Micro Array experiments Description: Analysis of N-dye Micro Array experiment using mixed model effect. Containing analysis of variance, permutation and bootstrap, cluster and consensus tree. biocViews: Microarray, DifferentialExpression, Clustering Author: Hao Wu, modified by Hyuna Yang and Keith Sheppard with ideas from Gary Churchill, Katie Kerr and Xiangqin Cui. Maintainer: Keith Sheppard URL: http://research.jax.org/faculty/churchill git_url: https://git.bioconductor.org/packages/maanova git_branch: RELEASE_3_8 git_last_commit: 58ea7e9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maanova_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maanova_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maanova_1.52.0.tgz vignettes: vignettes/maanova/inst/doc/maanova.pdf vignetteTitles: R/maanova HowTo hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: macat Version: 1.56.0 Depends: Biobase, annotate Suggests: hgu95av2.db, stjudem License: Artistic-2.0 MD5sum: de0e3159813ba422b6ad6ff8e24776f4 NeedsCompilation: no Title: MicroArray Chromosome Analysis Tool Description: This library contains functions to investigate links between differential gene expression and the chromosomal localization of the genes. MACAT is motivated by the common observation of phenomena involving large chromosomal regions in tumor cells. MACAT is the implementation of a statistical approach for identifying significantly differentially expressed chromosome regions. The functions have been tested on a publicly available data set about acute lymphoblastic leukemia (Yeoh et al.Cancer Cell 2002), which is provided in the library 'stjudem'. biocViews: Microarray, DifferentialExpression, Visualization Author: Benjamin Georgi, Matthias Heinig, Stefan Roepcke, Sebastian Schmeier, Joern Toedling Maintainer: Joern Toedling git_url: https://git.bioconductor.org/packages/macat git_branch: RELEASE_3_8 git_last_commit: 36a51df git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/macat_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/macat_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/macat_1.56.0.tgz vignettes: vignettes/macat/inst/doc/macat.pdf vignetteTitles: MicroArray Chromosome Analysis Tool hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/macat/inst/doc/macat.R Package: maCorrPlot Version: 1.52.0 Depends: lattice Imports: graphics, grDevices, lattice, stats License: GPL (>= 2) MD5sum: 2cdfe3ac5b1ab5504522a96ce8fab1b3 NeedsCompilation: no Title: Visualize artificial correlation in microarray data Description: Graphically displays correlation in microarray data that is due to insufficient normalization biocViews: Microarray, Preprocessing, Visualization Author: Alexander Ploner Maintainer: Alexander Ploner URL: http://www.pubmedcentral.gov/articlerender.fcgi?tool=pubmed&pubmedid=15799785 git_url: https://git.bioconductor.org/packages/maCorrPlot git_branch: RELEASE_3_8 git_last_commit: 2915c9e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maCorrPlot_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maCorrPlot_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maCorrPlot_1.52.0.tgz vignettes: vignettes/maCorrPlot/inst/doc/maCorrPlot.pdf vignetteTitles: maCorrPlot Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/maCorrPlot/inst/doc/maCorrPlot.R Package: MACPET Version: 1.2.0 Depends: R (>= 3.5), InteractionSet (>= 1.8.0), bigmemory (>= 4.5.33), BH (>= 1.66.0.1), Rcpp (>= 0.12.17) Imports: intervals (>= 0.15.1), plyr (>= 1.8.4), Rsamtools (>= 1.32.0), stats (>= 3.5.0), utils (>= 3.5.0), methods (>= 3.5.0), GenomicRanges (>= 1.32.3), S4Vectors (>= 0.18.3), IRanges (>= 2.14.10), GenomeInfoDb (>= 1.16.0), gtools (>= 3.8.1), GenomicAlignments (>= 1.16.0), knitr (>= 1.20), rtracklayer (>= 1.40.3), BiocParallel (>= 1.14.1), Rbowtie (>= 1.20.0), GEOquery (>= 2.48.0), Biostrings (>= 2.48.0), ShortRead (>= 1.38.0), rbamtools (>= 2.16.11), futile.logger (>= 1.4.3) LinkingTo: Rcpp, bigmemory, BH Suggests: ggplot2 (>= 3.0.0), igraph (>= 1.2.1), rmarkdown (>= 1.10), reshape2 (>= 1.4.3), BiocStyle (>= 2.8.2) License: GPL-3 Archs: i386, x64 MD5sum: 30f1bd24dfd02ee23e5b41c72147f57d NeedsCompilation: yes Title: Model based analysis for paired-end data Description: The MACPET package can be used for complete interaction analysis for ChIA-PET data. MACPET reads ChIA-PET data in BAM or SAM format and separates the data into Self-ligated, Intra- and Inter-chromosomal PETs. Furthermore, MACPET breaks the genome into regions and applies 2D mixture models for identifying candidate peaks/binding sites using skewed generalized students-t distributions (SGT). It then uses a local poisson model for finding significant binding sites. Finally it runs an additive interaction-analysis model for calling for significant interactions between those peaks. MACPET is mainly written in C++, and it also supports the BiocParallel package. biocViews: Software, DNA3DStructure, PeakDetection, StatisticalMethod, Clustering, Classification, HiC Author: Ioannis Vardaxis Maintainer: Ioannis Vardaxis SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MACPET git_branch: RELEASE_3_8 git_last_commit: 7c55f69 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MACPET_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MACPET_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MACPET_1.2.0.tgz vignettes: vignettes/MACPET/inst/doc/MACPET.pdf vignetteTitles: MACPET hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MACPET/inst/doc/MACPET.R Package: made4 Version: 1.56.0 Depends: ade4, RColorBrewer,gplots,scatterplot3d Suggests: affy License: Artistic-2.0 MD5sum: b93783edb8e0c0de6df719e01b79ebfe NeedsCompilation: no Title: Multivariate analysis of microarray data using ADE4 Description: Multivariate data analysis and graphical display of microarray data. Functions include between group analysis and coinertia analysis. It contains functions that require ADE4. biocViews: Clustering, Classification, MultipleComparison Author: Aedin Culhane Maintainer: Aedin Culhane URL: http://www.hsph.harvard.edu/aedin-culhane/ git_url: https://git.bioconductor.org/packages/made4 git_branch: RELEASE_3_8 git_last_commit: 175c6c9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/made4_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/made4_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/made4_1.56.0.tgz vignettes: vignettes/made4/inst/doc/introduction.pdf vignetteTitles: introduction.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/made4/inst/doc/introduction.R dependsOnMe: bgafun importsMe: omicade4 Package: MADSEQ Version: 1.8.0 Depends: R(>= 3.4), rjags(>= 4-6), Imports: VGAM, coda, BSgenome, BSgenome.Hsapiens.UCSC.hg19, S4Vectors, methods, preprocessCore, GenomicAlignments, Rsamtools, Biostrings, GenomicRanges, IRanges, VariantAnnotation, SummarizedExperiment, GenomeInfoDb, rtracklayer, graphics, stats, grDevices, utils, zlibbioc, vcfR Suggests: knitr License: GPL(>=2) MD5sum: 4ca89b5fc53ad2b4b6806b37991fa2ab NeedsCompilation: no Title: Mosaic Aneuploidy Detection and Quantification using Massive Parallel Sequencing Data Description: The MADSEQ package provides a group of hierarchical Bayeisan models for the detection of mosaic aneuploidy, the inference of the type of aneuploidy and also for the quantification of the fraction of aneuploid cells in the sample. biocViews: GenomicVariation, SomaticMutation, VariantDetection, Bayesian, CopyNumberVariation, Sequencing, Coverage Author: Yu Kong, Adam Auton, John Murray Greally Maintainer: Yu Kong URL: https://github.com/ykong2/MADSEQ VignetteBuilder: knitr BugReports: https://github.com/ykong2/MADSEQ/issues git_url: https://git.bioconductor.org/packages/MADSEQ git_branch: RELEASE_3_8 git_last_commit: df64e91 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MADSEQ_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MADSEQ_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MADSEQ_1.8.0.tgz vignettes: vignettes/MADSEQ/inst/doc/MADSEQ-vignette.html vignetteTitles: R Package MADSEQ hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MADSEQ/inst/doc/MADSEQ-vignette.R Package: maftools Version: 1.8.10 Depends: R (>= 3.3) Imports: data.table, ggplot2(>= 2.0), cowplot, cometExactTest, RColorBrewer, NMF, ggrepel, methods, ComplexHeatmap, mclust, Biostrings, rjson, grid, wordcloud, grDevices, gridExtra, survival, BSgenome Suggests: knitr, rmarkdown License: MIT + file LICENSE MD5sum: aa93bf940064fd7ab01513d2c2ca0741 NeedsCompilation: no Title: Summarize, Analyze and Visualize MAF Files Description: Analyze and visualize Mutation Annotation Format (MAF) files from large scale sequencing studies. This package provides various functions to perform most commonly used analyses in cancer genomics and to create feature rich customizable visualzations with minimal effort. biocViews: DataRepresentation, DNASeq, Visualization, DriverMutation, VariantAnnotation, FeatureExtraction, Classification, SomaticMutation, Sequencing, FunctionalGenomics, Survival Author: Anand Mayakonda Maintainer: Anand Mayakonda URL: https://github.com/PoisonAlien/maftools VignetteBuilder: knitr BugReports: https://github.com/PoisonAlien/maftools/issues git_url: https://git.bioconductor.org/packages/maftools git_branch: RELEASE_3_8 git_last_commit: 9fedc12 git_last_commit_date: 2019-04-14 Date/Publication: 2019-04-14 source.ver: src/contrib/maftools_1.8.10.tar.gz win.binary.ver: bin/windows/contrib/3.5/maftools_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maftools_1.8.10.tgz vignettes: vignettes/maftools/inst/doc/maftools.html vignetteTitles: Summarize,, Analyze and Visualize MAF Files hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/maftools/inst/doc/maftools.R importsMe: TCGAbiolinksGUI suggestsMe: TCGAbiolinks Package: MAGeCKFlute Version: 1.2.3 Depends: R (>= 3.5), ggplot2, stats, grDevices, utils, pathview, gridExtra Imports: ggExtra, ggsci, ggrepel, clusterProfiler, png, data.table, pheatmap, sva, DOSE, biomaRt, grid, bladderbatch Suggests: knitr, rmarkdown, BiocStyle, org.Mm.eg.db License: GPL (>=3) MD5sum: 783deb6c1ff79461eacbb9016488283f NeedsCompilation: no Title: Integrative analysis pipeline for pooled CRISPR functional genetic screens Description: MAGeCKFlute is designed to surporting downstream analysis, utilizing the gene summary data provided through MAGeCK or MAGeCK-VISPR. Quality control, normalization, and screen hit identification for CRISPR screen data are performed in pipeline. Identified hits within the pipeline are categorized based on experimental design, and are subsequently interpreted by functional enrichment analysis. biocViews: Software, FunctionalGenomics, CRISPR, ImmunoOncology, BatchEffect, QualityControl, Normalization, GeneSetEnrichment, Pathways, Visualization Author: Wubing Zhang, Feizhen Wu, Binbin Wang Maintainer: Wubing Zhang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MAGeCKFlute git_branch: RELEASE_3_8 git_last_commit: 0df39fe git_last_commit_date: 2019-02-21 Date/Publication: 2019-02-21 source.ver: src/contrib/MAGeCKFlute_1.2.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/MAGeCKFlute_1.2.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MAGeCKFlute_1.2.3.tgz vignettes: vignettes/MAGeCKFlute/inst/doc/MAGeCKFlute.html vignetteTitles: MAGeCKFlute.Rmd hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MAGeCKFlute/inst/doc/MAGeCKFlute.R Package: maigesPack Version: 1.46.0 Depends: R (>= 2.10), convert, graph, limma, marray, methods Suggests: amap, annotate, class, e1071, MASS, multtest, OLIN, R2HTML, rgl, som License: GPL (>= 2) Archs: i386, x64 MD5sum: 98e206be973a22e3f190a1a3fc044acc NeedsCompilation: yes Title: Functions to handle cDNA microarray data, including several methods of data analysis Description: This package uses functions of various other packages together with other functions in a coordinated way to handle and analyse cDNA microarray data biocViews: Microarray, TwoChannel, Preprocessing, ThirdPartyClient, DifferentialExpression, Clustering, Classification, GraphAndNetwork Author: Gustavo H. Esteves , with contributions from Roberto Hirata Jr , E. Jordao Neves , Elier B. Cristo , Ana C. Simoes and Lucas Fahham Maintainer: Gustavo H. Esteves URL: http://www.maiges.org/en/software/ git_url: https://git.bioconductor.org/packages/maigesPack git_branch: RELEASE_3_8 git_last_commit: 36d093a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maigesPack_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maigesPack_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maigesPack_1.46.0.tgz vignettes: vignettes/maigesPack/inst/doc/maigesPack_tutorial.pdf vignetteTitles: maigesPack Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/maigesPack/inst/doc/maigesPack_tutorial.R Package: MAIT Version: 1.16.1 Depends: R (>= 2.10), CAMERA, Rcpp, pls Imports: gplots,e1071,class,MASS,plsgenomics,agricolae,xcms,methods,caret Suggests: faahKO Enhances: rgl License: GPL-2 MD5sum: 1408eff274fb1b85fc403e9e27bfd785 NeedsCompilation: no Title: Statistical Analysis of Metabolomic Data Description: The MAIT package contains functions to perform end-to-end statistical analysis of LC/MS Metabolomic Data. Special emphasis is put on peak annotation and in modular function design of the functions. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics, Software Author: Francesc Fernandez-Albert, Rafael Llorach, Cristina Andres-LaCueva, Alexandre Perera Maintainer: Pol Sola-Santos git_url: https://git.bioconductor.org/packages/MAIT git_branch: RELEASE_3_8 git_last_commit: 5d28eeb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MAIT_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MAIT_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MAIT_1.16.1.tgz vignettes: vignettes/MAIT/inst/doc/MAIT_Vignette.pdf vignetteTitles: \maketitleMAIT Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MAIT/inst/doc/MAIT_Vignette.R Package: makecdfenv Version: 1.58.0 Depends: R (>= 2.6.0), affyio Imports: Biobase, affy, methods, stats, utils, zlibbioc License: GPL (>= 2) Archs: i386, x64 MD5sum: 4f1ba6b03964861e6553e52ff5c9cfb3 NeedsCompilation: yes Title: CDF Environment Maker Description: This package has two functions. One reads a Affymetrix chip description file (CDF) and creates a hash table environment containing the location/probe set membership mapping. The other creates a package that automatically loads that environment. biocViews: OneChannel, DataImport, Preprocessing Author: Rafael A. Irizarry , Laurent Gautier , Wolfgang Huber , Ben Bolstad Maintainer: James W. MacDonald git_url: https://git.bioconductor.org/packages/makecdfenv git_branch: RELEASE_3_8 git_last_commit: 6f513e3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/makecdfenv_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/makecdfenv_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/makecdfenv_1.58.0.tgz vignettes: vignettes/makecdfenv/inst/doc/makecdfenv.pdf vignetteTitles: makecdfenv primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/makecdfenv/inst/doc/makecdfenv.R dependsOnMe: altcdfenvs Package: MANOR Version: 1.54.0 Depends: R (>= 2.10), GLAD Imports: GLAD, graphics, grDevices, stats, utils License: GPL-2 Archs: i386, x64 MD5sum: f06fe382abee16e0de2e65e43419d59f NeedsCompilation: yes Title: CGH Micro-Array NORmalization Description: Importation, normalization, visualization, and quality control functions to correct identified sources of variability in array-CGH experiments. biocViews: Microarray, TwoChannel, DataImport, QualityControl, Preprocessing, CopyNumberVariation Author: Pierre Neuvial , Philippe Hupe Maintainer: Pierre Neuvial URL: http://bioinfo.curie.fr/projects/manor/index.html git_url: https://git.bioconductor.org/packages/MANOR git_branch: RELEASE_3_8 git_last_commit: 8031892 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MANOR_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MANOR_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MANOR_1.54.0.tgz vignettes: vignettes/MANOR/inst/doc/MANOR.pdf vignetteTitles: MANOR overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MANOR/inst/doc/MANOR.R Package: manta Version: 1.28.1 Depends: R (>= 1.8.0), methods, edgeR (>= 2.5.13) Imports: Hmisc, caroline(>= 0.6.6) Suggests: RSQLite, plotrix License: Artistic-2.0 MD5sum: e84c29f60182bc44512867406a8ddf97 NeedsCompilation: no Title: Microbial Assemblage Normalized Transcript Analysis Description: Tools for robust comparative metatranscriptomics. biocViews: ImmunoOncology, DifferentialExpression, RNASeq, Genetics, GeneExpression, Sequencing, QualityControl, DataImport, Visualization Author: Ginger Armbrust, Adrian Marchetti Maintainer: Chris Berthiaume , Adrian Marchetti URL: http://manta.ocean.washington.edu/ git_url: https://git.bioconductor.org/packages/manta git_branch: RELEASE_3_8 git_last_commit: 25a9cd8 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/manta_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/manta_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/manta_1.28.1.tgz vignettes: vignettes/manta/inst/doc/manta.pdf vignetteTitles: manta hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/manta/inst/doc/manta.R Package: MantelCorr Version: 1.52.0 Depends: R (>= 2.10) Imports: stats License: GPL (>= 2) MD5sum: 8de0637aa10324d7ff3d37ca1ec4f7d5 NeedsCompilation: no Title: Compute Mantel Cluster Correlations Description: Computes Mantel cluster correlations from a (p x n) numeric data matrix (e.g. microarray gene-expression data). biocViews: Clustering Author: Brian Steinmeyer and William Shannon Maintainer: Brian Steinmeyer git_url: https://git.bioconductor.org/packages/MantelCorr git_branch: RELEASE_3_8 git_last_commit: 250373e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MantelCorr_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MantelCorr_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MantelCorr_1.52.0.tgz vignettes: vignettes/MantelCorr/inst/doc/MantelCorrVignette.pdf vignetteTitles: MantelCorrVignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MantelCorr/inst/doc/MantelCorrVignette.R Package: mAPKL Version: 1.12.0 Depends: R (>= 3.2.0), Biobase Imports: multtest, clusterSim, apcluster, limma, e1071, AnnotationDbi, methods, parmigene,igraph,reactome.db Suggests: BiocStyle, knitr, mAPKLData, hgu133plus2.db, RUnit, BiocGenerics License: GPL (>= 2) MD5sum: 99d91da662512e0f50d49ccde0262e5f NeedsCompilation: no Title: A Hybrid Feature Selection method for gene expression data Description: We propose a hybrid FS method (mAP-KL), which combines multiple hypothesis testing and affinity propagation (AP)-clustering algorithm along with the Krzanowski & Lai cluster quality index, to select a small yet informative subset of genes. biocViews: FeatureExtraction, DifferentialExpression, Microarray, GeneExpression Author: Argiris Sakellariou Maintainer: Argiris Sakellariou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mAPKL git_branch: RELEASE_3_8 git_last_commit: dbedcd3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mAPKL_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mAPKL_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mAPKL_1.12.0.tgz vignettes: vignettes/mAPKL/inst/doc/mAPKL.pdf vignetteTitles: mAPKL Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mAPKL/inst/doc/mAPKL.R Package: maPredictDSC Version: 1.20.0 Depends: R (>= 2.15.0), MASS,affy,limma,gcrma,ROC,class,e1071,caret,hgu133plus2.db,ROCR,AnnotationDbi,LungCancerACvsSCCGEO Suggests: parallel License: GPL-2 MD5sum: 58b9e88d3fdbb667047c967923367f82 NeedsCompilation: no Title: Phenotype prediction using microarray data: approach of the best overall team in the IMPROVER Diagnostic Signature Challenge Description: This package implements the classification pipeline of the best overall team (Team221) in the IMPROVER Diagnostic Signature Challenge. Additional functionality is added to compare 27 combinations of data preprocessing, feature selection and classifier types. biocViews: Microarray, Classification Author: Adi Laurentiu Tarca Maintainer: Adi Laurentiu Tarca URL: http://bioinformaticsprb.med.wayne.edu/maPredictDSC git_url: https://git.bioconductor.org/packages/maPredictDSC git_branch: RELEASE_3_8 git_last_commit: 845445c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maPredictDSC_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maPredictDSC_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maPredictDSC_1.20.0.tgz vignettes: vignettes/maPredictDSC/inst/doc/maPredictDSC.pdf vignetteTitles: maPredictDSC hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/maPredictDSC/inst/doc/maPredictDSC.R Package: mapscape Version: 1.6.0 Depends: R (>= 3.3) Imports: htmlwidgets (>= 0.5), jsonlite (>= 0.9.19), base64enc (>= 0.1-3), stringr (>= 1.0.0) Suggests: knitr, rmarkdown License: GPL-3 MD5sum: b0155ab540b77d549bf9d403b384e24a NeedsCompilation: no Title: mapscape Description: MapScape integrates clonal prevalence, clonal hierarchy, anatomic and mutational information to provide interactive visualization of spatial clonal evolution. There are four inputs to MapScape: (i) the clonal phylogeny, (ii) clonal prevalences, (iii) an image reference, which may be a medical image or drawing and (iv) pixel locations for each sample on the referenced image. Optionally, MapScape can accept a data table of mutations for each clone and their variant allele frequencies in each sample. The output of MapScape consists of a cropped anatomical image surrounded by two representations of each tumour sample. The first, a cellular aggregate, visually displays the prevalence of each clone. The second shows a skeleton of the clonal phylogeny while highlighting only those clones present in the sample. Together, these representations enable the analyst to visualize the distribution of clones throughout anatomic space. biocViews: Visualization Author: Maia Smith [aut, cre] Maintainer: Maia Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mapscape git_branch: RELEASE_3_8 git_last_commit: 9a5630a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mapscape_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mapscape_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mapscape_1.6.0.tgz vignettes: vignettes/mapscape/inst/doc/mapscape_vignette.html vignetteTitles: MapScape vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mapscape/inst/doc/mapscape_vignette.R Package: marray Version: 1.60.0 Depends: R (>= 2.10.0), limma, methods Suggests: tkWidgets License: LGPL MD5sum: 9620bb609afca132e43100410100b934 NeedsCompilation: no Title: Exploratory analysis for two-color spotted microarray data Description: Class definitions for two-color spotted microarray data. Fuctions for data input, diagnostic plots, normalization and quality checking. biocViews: Microarray, TwoChannel, Preprocessing Author: Yee Hwa (Jean) Yang with contributions from Agnes Paquet and Sandrine Dudoit. Maintainer: Yee Hwa (Jean) Yang URL: http://www.maths.usyd.edu.au/u/jeany/ git_url: https://git.bioconductor.org/packages/marray git_branch: RELEASE_3_8 git_last_commit: 26eeb2b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/marray_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/marray_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/marray_1.60.0.tgz vignettes: vignettes/marray/inst/doc/marray.pdf, vignettes/marray/inst/doc/marrayClasses.pdf, vignettes/marray/inst/doc/marrayClassesShort.pdf, vignettes/marray/inst/doc/marrayInput.pdf, vignettes/marray/inst/doc/marrayNorm.pdf, vignettes/marray/inst/doc/marrayPlots.pdf vignetteTitles: marray Overview, marrayClasses Overview, marrayClasses Tutorial (short), marrayInput Introduction, marray Normalization, marrayPlots Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/marray/inst/doc/marray.R, vignettes/marray/inst/doc/marrayClasses.R, vignettes/marray/inst/doc/marrayClassesShort.R, vignettes/marray/inst/doc/marrayInput.R, vignettes/marray/inst/doc/marrayNorm.R, vignettes/marray/inst/doc/marrayPlots.R dependsOnMe: CGHbase, convert, dyebias, maigesPack, MineICA, nnNorm, OLIN, RBM, stepNorm, TurboNorm importsMe: arrayQuality, ChAMP, methylPipe, MSstats, nnNorm, OLIN, OLINgui, piano, plrs, sigaR, stepNorm, timecourse suggestsMe: DEGraph, Mfuzz Package: martini Version: 1.2.0 Depends: R (>= 3.5) Imports: igraph (>= 1.0.1), Matrix, methods (>= 3.3.2), Rcpp (>= 0.12.8), snpStats (>= 1.20.0), S4Vectors (>= 0.12.2), stats, utils LinkingTo: Rgin, Rcpp, RcppEigen (>= 0.3.3.3.0) Suggests: biomaRt (>= 2.34.1), httr (>= 1.2.1), IRanges (>= 2.8.2), knitr, testthat, tidyverse, rmarkdown License: MIT + file LICENSE Archs: i386, x64 MD5sum: a700575374a986a0013bff3b1e08a134 NeedsCompilation: yes Title: GWAS Incorporating Networks Description: martini deals with the low power inherent to GWAS studies by using prior knowledge represented as a network. SNPs are the vertices of the network, and the edges represent biological relationships between them (genomic adjacency, belonging to the same gene, physical interaction between protein products). The network is scanned using SConES, which looks for groups of SNPs maximally associated with the phenotype, that form a close subnetwork. biocViews: Software, GenomeWideAssociation, SNP, GeneticVariability, Genetics, FeatureExtraction, GraphAndNetwork, Network Author: Hector Climente-Gonzalez [aut, cre], Chloe-Agathe Azencott [aut] Maintainer: Hector Climente-Gonzalez VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/martini git_branch: RELEASE_3_8 git_last_commit: 803ac70 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/martini_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/martini_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/martini_1.2.0.tgz vignettes: vignettes/martini/inst/doc/scones_usage.html, vignettes/martini/inst/doc/simulate_phenotype.html vignetteTitles: Running SConES, Simulating SConES-based phenotypes hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/martini/inst/doc/scones_usage.R, vignettes/martini/inst/doc/simulate_phenotype.R Package: maser Version: 1.0.0 Depends: R (>= 3.5.0), ggplot2, GenomicRanges Imports: dplyr, rtracklayer, reshape2, Gviz, DT, GenomeInfoDb, stats, utils, IRanges, methods, BiocGenerics, parallel, data.table Suggests: testthat, knitr, rmarkdown, BiocStyle, AnnotationHub License: MIT + file LICENSE MD5sum: 3736c02b9c3b7db33c31da8fa9e72eea NeedsCompilation: no Title: Mapping Alternative Splicing Events to pRoteins Description: This package provides functionalities for analysis, annotation and visualizaton of alternative splicing events. biocViews: AlternativeSplicing, Transcriptomics, Visualization Author: Diogo Veiga [aut, cre] Maintainer: Diogo Veiga URL: https://github.com/DiogoVeiga/maser VignetteBuilder: knitr BugReports: https://github.com/DiogoVeiga/maser/issues git_url: https://git.bioconductor.org/packages/maser git_branch: RELEASE_3_8 git_last_commit: 2b676a6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maser_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maser_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maser_1.0.0.tgz vignettes: vignettes/maser/inst/doc/Introduction.html, vignettes/maser/inst/doc/Protein_mapping.html vignetteTitles: Introduction, Mapping protein features to splicing events hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/maser/inst/doc/Introduction.R, vignettes/maser/inst/doc/Protein_mapping.R Package: maSigPro Version: 1.54.0 Depends: R (>= 2.3.1) Imports: Biobase, graphics, grDevices, venn, mclust, stats, MASS License: GPL (>= 2) MD5sum: 4a642f18b31d99eee5b5d7dcd7b54b8e NeedsCompilation: no Title: Significant Gene Expression Profile Differences in Time Course Gene Expression Data Description: maSigPro is a regression based approach to find genes for which there are significant gene expression profile differences between experimental groups in time course microarray and RNA-Seq experiments. biocViews: Microarray, RNA-Seq, Differential Expression, TimeCourse Author: Ana Conesa , Maria Jose Nueda Maintainer: Maria Jose Nueda URL: http://bioinfo.cipf.es/ git_url: https://git.bioconductor.org/packages/maSigPro git_branch: RELEASE_3_8 git_last_commit: bd6dc6c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maSigPro_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maSigPro_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maSigPro_1.54.0.tgz vignettes: vignettes/maSigPro/inst/doc/maSigPro.pdf, vignettes/maSigPro/inst/doc/maSigProUsersGuide.pdf vignetteTitles: maSigPro Vignette, maSigProUsersGuide.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: maskBAD Version: 1.26.0 Depends: R (>= 2.10), gcrma (>= 2.27.1), affy Suggests: hgu95av2probe, hgu95av2cdf License: GPL (>= 2) MD5sum: f4729f51911770bb1448510b43e5e479 NeedsCompilation: no Title: Masking probes with binding affinity differences Description: Package includes functions to analyze and mask microarray expression data. biocViews: Microarray Author: Michael Dannemann Maintainer: Michael Dannemann git_url: https://git.bioconductor.org/packages/maskBAD git_branch: RELEASE_3_8 git_last_commit: a96538d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/maskBAD_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/maskBAD_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/maskBAD_1.26.0.tgz vignettes: vignettes/maskBAD/inst/doc/maskBAD.pdf vignetteTitles: Package maskBAD hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/maskBAD/inst/doc/maskBAD.R Package: MassArray Version: 1.34.1 Depends: R (>= 2.10.0), methods Imports: graphics, grDevices, methods, stats, utils License: GPL (>=2) MD5sum: 4285277c93fb350d5b9ad3c1afb551ec NeedsCompilation: no Title: Analytical Tools for MassArray Data Description: This package is designed for the import, quality control, analysis, and visualization of methylation data generated using Sequenom's MassArray platform. The tools herein contain a highly detailed amplicon prediction for optimal assay design. Also included are quality control measures of data, such as primer dimer and bisulfite conversion efficiency estimation. Methylation data are calculated using the same algorithms contained in the EpiTyper software package. Additionally, automatic SNP-detection can be used to flag potentially confounded data from specific CG sites. Visualization includes barplots of methylation data as well as UCSC Genome Browser-compatible BED tracks. Multiple assays can be positionally combined for integrated analysis. biocViews: ImmunoOncology, DNAMethylation, SNP, MassSpectrometry, Genetics, DataImport, Visualization Author: Reid F. Thompson , John M. Greally Maintainer: Reid F. Thompson git_url: https://git.bioconductor.org/packages/MassArray git_branch: RELEASE_3_8 git_last_commit: 89284ef git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MassArray_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MassArray_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MassArray_1.34.1.tgz vignettes: vignettes/MassArray/inst/doc/MassArray.pdf vignetteTitles: 1. Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MassArray/inst/doc/MassArray.R Package: massiR Version: 1.18.0 Depends: cluster, gplots, diptest, Biobase, R (>= 3.0.2) Suggests: biomaRt, RUnit, BiocGenerics License: GPL-3 MD5sum: 155d85624615ff8b2a8dfc5614a8cc78 NeedsCompilation: no Title: massiR: MicroArray Sample Sex Identifier Description: Predicts the sex of samples in gene expression microarray datasets biocViews: Software, Microarray, GeneExpression, Clustering, Classification, QualityControl Author: Sam Buckberry Maintainer: Sam Buckberry git_url: https://git.bioconductor.org/packages/massiR git_branch: RELEASE_3_8 git_last_commit: 643b551 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/massiR_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/massiR_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/massiR_1.18.0.tgz vignettes: vignettes/massiR/inst/doc/massiR_Vignette.pdf vignetteTitles: massiR_Example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/massiR/inst/doc/massiR_Vignette.R Package: MassSpecWavelet Version: 1.48.1 Depends: waveslim Suggests: xcms, caTools License: LGPL (>= 2) Archs: i386, x64 MD5sum: 8dab87e926a37478d0dafab02cf9acee NeedsCompilation: yes Title: Mass spectrum processing by wavelet-based algorithms Description: Processing Mass Spectrometry spectrum by using wavelet based algorithm biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Pan Du, Warren Kibbe, Simon Lin Maintainer: Pan Du git_url: https://git.bioconductor.org/packages/MassSpecWavelet git_branch: RELEASE_3_8 git_last_commit: 1c37232 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MassSpecWavelet_1.48.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MassSpecWavelet_1.48.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MassSpecWavelet_1.48.1.tgz vignettes: vignettes/MassSpecWavelet/inst/doc/MassSpecWavelet.pdf vignetteTitles: MassSpecWavelet hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MassSpecWavelet/inst/doc/MassSpecWavelet.R importsMe: cosmiq, xcms Package: MAST Version: 1.8.2 Depends: SingleCellExperiment (>= 1.2.0), R(>= 3.5) Imports: Biobase, BiocGenerics, S4Vectors, data.table, ggplot2, plyr, stringr, abind, methods, parallel, reshape2, stats, stats4, graphics, utils, SummarizedExperiment(>= 1.5.3), progress Suggests: knitr, rmarkdown, testthat, lme4(>= 1.0), roxygen2(> 4.0.0), numDeriv, car, gdata, lattice, GGally, GSEABase, NMF, TxDb.Hsapiens.UCSC.hg19.knownGene, rsvd, limma, RColorBrewer, BiocStyle, scater License: GPL(>= 2) MD5sum: 32d1ce344aea77e90e2a12588c9cda33 NeedsCompilation: no Title: Model-based Analysis of Single Cell Transcriptomics Description: Methods and models for handling zero-inflated single cell assay data. biocViews: GeneExpression, DifferentialExpression, GeneSetEnrichment, RNASeq, Transcriptomics, SingleCell Author: Andrew McDavid [aut, cre], Greg Finak [aut], Masanao Yajima [aut] Maintainer: Andrew McDavid URL: https://github.com/RGLab/MAST/ VignetteBuilder: knitr BugReports: https://github.com/RGLab/MAST/issues git_url: https://git.bioconductor.org/packages/MAST git_branch: RELEASE_3_8 git_last_commit: 7ae6306 git_last_commit_date: 2019-01-16 Date/Publication: 2019-01-16 source.ver: src/contrib/MAST_1.8.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/MAST_1.8.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MAST_1.8.2.tgz vignettes: vignettes/MAST/inst/doc/MAITAnalysis.html, vignettes/MAST/inst/doc/MAST-interoperability.html, vignettes/MAST/inst/doc/MAST-Intro.html vignetteTitles: Using MAST for filtering,, differential expression and gene set enrichment in MAIT cells, Interoptability between MAST and SingleCellExperiment-derived packages, An Introduction to MAST hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MAST/inst/doc/MAITAnalysis.R, vignettes/MAST/inst/doc/MAST-interoperability.R, vignettes/MAST/inst/doc/MAST-Intro.R importsMe: celaref, singleCellTK suggestsMe: clusterExperiment Package: matchBox Version: 1.24.0 Depends: R (>= 2.8.0) License: Artistic-2.0 MD5sum: 96cde96f3ff554796874b2a7cc27bdb9 NeedsCompilation: no Title: Utilities to compute, compare, and plot the agreement between ordered vectors of features (ie. distinct genomic experiments). The package includes Correspondence-At-the-TOP (CAT) analysis. Description: The matchBox package enables comparing ranked vectors of features, merging multiple datasets, removing redundant features, using CAT-plots and Venn diagrams, and computing statistical significance. biocViews: Software, Annotation, Microarray, MultipleComparison, Visualization Author: Luigi Marchionni , Anuj Gupta Maintainer: Luigi Marchionni , Anuj Gupta git_url: https://git.bioconductor.org/packages/matchBox git_branch: RELEASE_3_8 git_last_commit: d6c1fed git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/matchBox_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/matchBox_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/matchBox_1.24.0.tgz vignettes: vignettes/matchBox/inst/doc/matchBox.pdf vignetteTitles: Working with the matchBox package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/matchBox/inst/doc/matchBox.R Package: MatrixRider Version: 1.14.0 Depends: R (>= 3.1.2) Imports: methods, TFBSTools, IRanges, XVector, Biostrings LinkingTo: IRanges, XVector, Biostrings, S4Vectors Suggests: RUnit, BiocGenerics, BiocStyle, JASPAR2014 License: GPL-3 Archs: i386, x64 MD5sum: 96fe9ae1dd48d87fae7b56afd0c4808e NeedsCompilation: yes Title: Obtain total affinity and occupancies for binding site matrices on a given sequence Description: Calculates a single number for a whole sequence that reflects the propensity of a DNA binding protein to interact with it. The DNA binding protein has to be described with a PFM matrix, for example gotten from Jaspar. biocViews: GeneRegulation, Genetics, MotifAnnotation Author: Elena Grassi Maintainer: Elena Grassi git_url: https://git.bioconductor.org/packages/MatrixRider git_branch: RELEASE_3_8 git_last_commit: c3d0d7a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MatrixRider_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MatrixRider_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MatrixRider_1.14.0.tgz vignettes: vignettes/MatrixRider/inst/doc/MatrixRider.pdf vignetteTitles: Total affinity and occupancies hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MatrixRider/inst/doc/MatrixRider.R Package: matter Version: 1.8.3 Depends: R (>= 3.5), methods, stats, biglm Imports: BiocGenerics, digest, irlba, utils Suggests: BiocStyle, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: fa921adb06830b0fbe2950757c3ee341 NeedsCompilation: yes Title: A framework for rapid prototyping with binary data on disk Description: Memory-efficient reading, writing, and manipulation of structured binary data on disk as vectors, matrices, arrays, lists, and data frames. biocViews: Software, Infrastructure Author: Kylie A. Bemis Maintainer: Kylie A. Bemis URL: https://github.com/kuwisdelu/matter git_url: https://git.bioconductor.org/packages/matter git_branch: RELEASE_3_8 git_last_commit: 4687b83 git_last_commit_date: 2018-12-18 Date/Publication: 2018-12-18 source.ver: src/contrib/matter_1.8.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/matter_1.8.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/matter_1.8.3.tgz vignettes: vignettes/matter/inst/doc/matter-supp1.pdf, vignettes/matter/inst/doc/matter-supp2.pdf, vignettes/matter/inst/doc/matter.pdf vignetteTitles: matter: Supplementary 1 - Simulations and comparative benchmarks, matter: Supplementary 2 - 3D mass spectrometry imaging case study, matter: Rapid prototyping with data on disk hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/matter/inst/doc/matter-supp1.R, vignettes/matter/inst/doc/matter-supp2.R, vignettes/matter/inst/doc/matter.R importsMe: Cardinal Package: MaxContrastProjection Version: 1.6.1 Depends: R (>= 3.4) Imports: EBImage, stats, methods Suggests: knitr, BiocStyle, testthat License: Artistic-2.0 MD5sum: 096471f0614f8a356dc6d62b1bab5c5b NeedsCompilation: no Title: Perform a maximum contrast projection of 3D images along the z-dimension into 2D Description: A problem when recording 3D fluorescent microscopy images is how to properly present these results in 2D. Maximum intensity projections are a popular method to determine the focal plane of each pixel in the image. The problem with this approach, however, is that out-of-focus elements will still be visible, making edges and fine structures difficult to detect. This package aims to resolve this problem by using the contrast around a given pixel to determine the focal plane, allowing for a much cleaner structure detection than would be otherwise possible. For convenience, this package also contains functions to perform various other types of projections, including a maximum intensity projection. biocViews: ImmunoOncology, CellBasedAssays, Preprocessing, Software, Visualization Author: Jan Sauer, Bernd Fischer Maintainer: Jan Sauer SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MaxContrastProjection git_branch: RELEASE_3_8 git_last_commit: 3dad069 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MaxContrastProjection_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MaxContrastProjection_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MaxContrastProjection_1.6.1.tgz vignettes: vignettes/MaxContrastProjection/inst/doc/MaxContrastProjection.pdf vignetteTitles: MaxContrastProjection hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MaxContrastProjection/inst/doc/MaxContrastProjection.R Package: MBAmethyl Version: 1.16.0 Depends: R (>= 2.15) License: Artistic-2.0 MD5sum: 6299112309d19ef270d439e7a23ee3ae NeedsCompilation: no Title: Model-based analysis of DNA methylation data Description: This package provides a function for reconstructing DNA methylation values from raw measurements. It iteratively implements the group fused lars to smooth related-by-location methylation values and the constrained least squares to remove probe affinity effect across multiple sequences. biocViews: DNAMethylation, MethylationArray Author: Tao Wang, Mengjie Chen Maintainer: Tao Wang git_url: https://git.bioconductor.org/packages/MBAmethyl git_branch: RELEASE_3_8 git_last_commit: 30fe61e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MBAmethyl_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MBAmethyl_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MBAmethyl_1.16.0.tgz vignettes: vignettes/MBAmethyl/inst/doc/MBAmethyl.pdf vignetteTitles: MBAmethyl Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MBAmethyl/inst/doc/MBAmethyl.R Package: MBASED Version: 1.16.0 Depends: RUnit, BiocGenerics, BiocParallel, GenomicRanges, SummarizedExperiment Suggests: BiocStyle License: Artistic-2.0 MD5sum: 503273be8ad6f478d004d993d9f1c054 NeedsCompilation: no Title: Package containing functions for ASE analysis using Meta-analysis Based Allele-Specific Expression Detection Description: The package implements MBASED algorithm for detecting allele-specific gene expression from RNA count data, where allele counts at individual loci (SNVs) are integrated into a gene-specific measure of ASE, and utilizes simulations to appropriately assess the statistical significance of observed ASE. biocViews: Sequencing, GeneExpression, Transcription Author: Oleg Mayba, Houston Gilbert Maintainer: Oleg Mayba git_url: https://git.bioconductor.org/packages/MBASED git_branch: RELEASE_3_8 git_last_commit: 6613177 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MBASED_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MBASED_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MBASED_1.16.0.tgz vignettes: vignettes/MBASED/inst/doc/MBASED.pdf vignetteTitles: MBASED hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MBASED/inst/doc/MBASED.R Package: MBCB Version: 1.36.0 Depends: R (>= 2.9.0), tcltk, tcltk2 Imports: preprocessCore, stats, utils License: GPL (>= 2) MD5sum: 21bf4710d8291d63d7c6615b73000955 NeedsCompilation: no Title: MBCB (Model-based Background Correction for Beadarray) Description: This package provides a model-based background correction method, which incorporates the negative control beads to pre-process Illumina BeadArray data. biocViews: Microarray, Preprocessing Author: Yang Xie Maintainer: Jeff Allen URL: http://www.utsouthwestern.edu git_url: https://git.bioconductor.org/packages/MBCB git_branch: RELEASE_3_8 git_last_commit: 2b2cc36 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MBCB_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MBCB_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MBCB_1.36.0.tgz vignettes: vignettes/MBCB/inst/doc/MBCB.pdf vignetteTitles: MBCB hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MBCB/inst/doc/MBCB.R Package: mBPCR Version: 1.36.0 Depends: oligoClasses, SNPchip Imports: Biobase Suggests: xtable License: GPL (>= 2) MD5sum: b429a42900934745c81407e4116c9f54 NeedsCompilation: no Title: Bayesian Piecewise Constant Regression for DNA copy number estimation Description: Estimates the DNA copy number profile using mBPCR to detect regions with copy number changes biocViews: aCGH, SNP, Microarray, CopyNumberVariation Author: P.M.V. Rancoita , with contributions from M. Hutter Maintainer: P.M.V. Rancoita URL: http://www.idsia.ch/~paola/mBPCR git_url: https://git.bioconductor.org/packages/mBPCR git_branch: RELEASE_3_8 git_last_commit: 1ba2248 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mBPCR_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mBPCR_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mBPCR_1.36.0.tgz vignettes: vignettes/mBPCR/inst/doc/mBPCR.pdf vignetteTitles: mBPCR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mBPCR/inst/doc/mBPCR.R Package: MBttest Version: 1.10.0 Depends: R (>= 3.3.0), stats, gplots, gtools,graphics,base, utils,grDevices Suggests: BiocStyle, BiocGenerics License: GPL-3 MD5sum: e7f88536245d563302be0374bcdf8009 NeedsCompilation: no Title: Multiple Beta t-Tests Description: MBttest method was developed from beta t-test method of Baggerly et al(2003). Compared to baySeq (Hard castle and Kelly 2010), DESeq (Anders and Huber 2010) and exact test (Robinson and Smyth 2007, 2008) and the GLM of McCarthy et al(2012), MBttest is of high work efficiency,that is, it has high power, high conservativeness of FDR estimation and high stability. MBttest is suit- able to transcriptomic data, tag data, SAGE data (count data) from small samples or a few replicate libraries. It can be used to identify genes, mRNA isoforms or tags differentially expressed between two conditions. biocViews: Sequencing, DifferentialExpression, MultipleComparison, SAGE, GeneExpression, Transcription, AlternativeSplicing,Coverage, DifferentialSplicing Author: Yuan-De Tan Maintainer: Yuan-De Tan git_url: https://git.bioconductor.org/packages/MBttest git_branch: RELEASE_3_8 git_last_commit: bbe6a6c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MBttest_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MBttest_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MBttest_1.10.0.tgz vignettes: vignettes/MBttest/inst/doc/MBttest-manual.pdf, vignettes/MBttest/inst/doc/MBttest.pdf vignetteTitles: MBttest-manual.pdf, Analysing RNA-Seq count data with the "MBttest" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MBttest/inst/doc/MBttest.R Package: mcaGUI Version: 1.30.0 Depends: lattice, MASS, proto, foreign, gWidgets(>= 0.0-36), gWidgetsRGtk2(>= 0.0-53), OTUbase, vegan, bpca Enhances: iplots, reshape, ggplot2, cairoDevice, OTUbase License: GPL (>= 2) MD5sum: 8375e8dda6d5515700a95ab587d07c2f NeedsCompilation: no Title: Microbial Community Analysis GUI Description: Microbial community analysis GUI for R using gWidgets. biocViews: GUI, Visualization, Clustering, Sequencing Author: Wade K. Copeland, Vandhana Krishnan, Daniel Beck, Matt Settles, James Foster, Kyu-Chul Cho, Mitch Day, Roxana Hickey, Ursel M.E. Schutte, Xia Zhou, Chris Williams, Larry J. Forney, Zaid Abdo, Poor Man's GUI (PMG) base code by John Verzani with contributions by Yvonnick Noel Maintainer: Wade K. Copeland URL: http://www.ibest.uidaho.edu/ibest/index.php git_url: https://git.bioconductor.org/packages/mcaGUI git_branch: RELEASE_3_8 git_last_commit: 7a7f259 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mcaGUI_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mcaGUI_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mcaGUI_1.30.0.tgz hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: MCbiclust Version: 1.6.1 Depends: R (>= 3.4) Imports: BiocParallel, graphics, utils, stats, AnnotationDbi, GO.db, org.Hs.eg.db, GGally, ggplot2, scales, cluster, WGCNA Suggests: gplots, knitr, rmarkdown, BiocStyle, gProfileR, MASS, dplyr, pander, devtools, testthat, GSVA License: GPL-2 MD5sum: ad86a6b63ac7543c156e6459a18b5af9 NeedsCompilation: no Title: Massive correlating biclusters for gene expression data and associated methods Description: Custom made algorithm and associated methods for finding, visualising and analysing biclusters in large gene expression data sets. Algorithm is based on with a supplied gene set of size n, finding the maximum strength correlation matrix containing m samples from the data set. biocViews: ImmunoOncology, Clustering, Microarray, StatisticalMethod, Software, RNASeq, GeneExpression Author: Robert Bentham Maintainer: Robert Bentham VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MCbiclust git_branch: RELEASE_3_8 git_last_commit: 908d0ea git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MCbiclust_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MCbiclust_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MCbiclust_1.6.1.tgz vignettes: vignettes/MCbiclust/inst/doc/MCbiclust_vignette.html vignetteTitles: Introduction to MCbiclust hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MCbiclust/inst/doc/MCbiclust_vignette.R Package: MCRestimate Version: 2.38.0 Depends: R (>= 2.7.2), golubEsets (>= 1.4.6) Imports: e1071 (>= 1.5-12), pamr (>= 1.22), randomForest (>= 3.9-6), RColorBrewer (>= 0.1-3), Biobase (>= 2.5.5), graphics, grDevices, stats, utils Suggests: xtable (>= 1.2-1), ROC (>= 1.8.0), genefilter (>= 1.12.0), gpls (>= 1.6.0) License: GPL (>= 2) MD5sum: f72686ef3ef87989030a376fec562d0f NeedsCompilation: no Title: Misclassification error estimation with cross-validation Description: This package includes a function for combining preprocessing and classification methods to calculate misclassification errors biocViews: Classification Author: Marc Johannes, Markus Ruschhaupt, Holger Froehlich, Ulrich Mansmann, Andreas Buness, Patrick Warnat, Wolfgang Huber, Axel Benner, Tim Beissbarth Maintainer: Marc Johannes git_url: https://git.bioconductor.org/packages/MCRestimate git_branch: RELEASE_3_8 git_last_commit: c3ee789 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MCRestimate_2.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MCRestimate_2.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MCRestimate_2.38.0.tgz vignettes: vignettes/MCRestimate/inst/doc/UsingMCRestimate.pdf vignetteTitles: HOW TO use MCRestimate hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MCRestimate/inst/doc/UsingMCRestimate.R Package: mCSEA Version: 1.2.2 Depends: R (>= 3.5), mCSEAdata, Homo.sapiens Imports: fgsea, GenomicFeatures, GenomicRanges, ggplot2, graphics, grDevices, Gviz, IRanges, limma, parallel, S4Vectors, stats, SummarizedExperiment, utils Suggests: Biobase, BiocGenerics, BiocStyle, FlowSorted.Blood.450k, knitr, leukemiasEset, minfi, minfiData, rmarkdown, RUnit License: GPL-2 MD5sum: 82334952608d289e73fc07e099af6150 NeedsCompilation: no Title: Methylated CpGs Set Enrichment Analysis Description: Identification of diferentially methylated regions (DMRs) in predefined regions (promoters, CpG islands...) from the human genome using Illumina's 450K or EPIC microarray data. Provides methods to rank CpG probes based on linear models and includes plotting functions. biocViews: ImmunoOncology, DifferentialMethylation, DNAMethylation, Epigenetics, Genetics, GenomeAnnotation, MethylationArray, Microarray, MultipleComparison, TwoChannel Author: Jordi Martorell-Marugán and Pedro Carmona-Sáez Maintainer: Jordi Martorell-Marugán VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mCSEA git_branch: RELEASE_3_8 git_last_commit: 5c1c44d git_last_commit_date: 2019-02-13 Date/Publication: 2019-02-13 source.ver: src/contrib/mCSEA_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/mCSEA_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mCSEA_1.2.2.tgz vignettes: vignettes/mCSEA/inst/doc/mCSEA.pdf vignetteTitles: Predefined DMRs identification with mCSEA package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mCSEA/inst/doc/mCSEA.R Package: mdgsa Version: 1.14.0 Depends: R (>= 2.14) Imports: AnnotationDbi, DBI, GO.db, KEGG.db, cluster, Matrix Suggests: BiocStyle, knitr, rmarkdown, limma, ALL, hgu95av2.db, RUnit, BiocGenerics License: GPL MD5sum: 28668e2ddf14e96380fbe1961c10e357 NeedsCompilation: no Title: Multi Dimensional Gene Set Analysis. Description: Functions to preform a Gene Set Analysis in several genomic dimensions. Including methods for miRNAs. biocViews: GeneSetEnrichment, Annotation, Pathways, GO Author: David Montaner Maintainer: David Montaner URL: https://github.com/dmontaner/mdgsa, http://www.dmontaner.com VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mdgsa git_branch: RELEASE_3_8 git_last_commit: 93627c0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mdgsa_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mdgsa_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mdgsa_1.14.0.tgz vignettes: vignettes/mdgsa/inst/doc/mdgsa_vignette.pdf vignetteTitles: mdgsa_vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mdgsa/inst/doc/mdgsa_vignette.R Package: mdp Version: 1.2.1 Depends: R (>= 3.5) Imports: ggplot2, gridExtra, grid, stats, utils Suggests: testthat, knitr, rmarkdown, fgsea License: GPL-3 MD5sum: 41a083a9ade6f745d3fb3593792124a5 NeedsCompilation: no Title: Molecular Degree of Perturbation calculates scores for transcriptome data samples based on their perturbation from controls Description: The Molecular Degree of Perturbation webtool quantifies the heterogeneity of samples. It takes a data.frame of omic data that contains at least two classes (control and test) and assigns a score to all samples based on how perturbed they are compared to the controls. It is based on the Molecular Distance to Health (Pankla et al. 2009), and expands on this algorithm by adding the options to calculate the z-score using the modified z-score (using median absolute deviation), change the z-score zeroing threshold, and look at genes that are most perturbed in the test versus control classes. biocViews: BiomedicalInformatics, QualityControl, Transcriptomics, SystemsBiology, Microarray, QualityControl Author: Melissa Lever [aut], Pedro Russo [aut], Helder Nakaya [aut, cre] Maintainer: Helder Nakaya URL: https://mdp.sysbio.tools/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mdp git_branch: RELEASE_3_8 git_last_commit: 11f846f git_last_commit_date: 2019-01-14 Date/Publication: 2019-01-14 source.ver: src/contrib/mdp_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/mdp_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mdp_1.2.1.tgz vignettes: vignettes/mdp/inst/doc/my-vignette.html vignetteTitles: Running the mdp package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mdp/inst/doc/my-vignette.R Package: mdqc Version: 1.44.0 Depends: R (>= 2.2.1), cluster, MASS License: LGPL (>= 2) MD5sum: d82132337f2ad3520bf49b73cb29c6f8 NeedsCompilation: no Title: Mahalanobis Distance Quality Control for microarrays Description: MDQC is a multivariate quality assessment method for microarrays based on quality control (QC) reports. The Mahalanobis distance of an array's quality attributes is used to measure the similarity of the quality of that array against the quality of the other arrays. Then, arrays with unusually high distances can be flagged as potentially low-quality. biocViews: Microarray, QualityControl Author: Justin Harrington Maintainer: Gabriela Cohen-Freue git_url: https://git.bioconductor.org/packages/mdqc git_branch: RELEASE_3_8 git_last_commit: f4464a4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mdqc_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mdqc_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mdqc_1.44.0.tgz vignettes: vignettes/mdqc/inst/doc/mdqcvignette.pdf vignetteTitles: Introduction to MDQC hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mdqc/inst/doc/mdqcvignette.R importsMe: arrayMvout Package: MDTS Version: 1.2.0 Depends: R (>= 3.5.0) Imports: GenomicAlignments, GenomicRanges, IRanges, Biostrings, DNAcopy, Rsamtools, parallel, stringr Suggests: testthat, knitr License: Artistic-2.0 MD5sum: 509a06e8a0f6897ed1edb83f5687b479 NeedsCompilation: no Title: Detection of de novo deletion in targeted sequencing trios Description: A package for the detection of de novo copy number deletions in targeted sequencing of trios with high sensitivity and positive predictive value. biocViews: StatisticalMethod, Technology, Sequencing, TargetedResequencing, Coverage, DataImport Author: Jack M.. Fu [aut, cre] Maintainer: Jack M.. Fu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MDTS git_branch: RELEASE_3_8 git_last_commit: 5d78cee git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MDTS_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MDTS_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MDTS_1.2.0.tgz vignettes: vignettes/MDTS/inst/doc/mdts.html vignetteTitles: Title of your vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MDTS/inst/doc/mdts.R Package: MEAL Version: 1.12.0 Depends: R (>= 3.2.0), Biobase, MultiDataSet Imports: GenomicRanges, limma, DMRcate, vegan, BiocGenerics, minfi, IRanges, S4Vectors, methods, parallel, ggplot2 (>= 2.0.0), permute, Gviz, missMethyl, isva, SummarizedExperiment, SmartSVA, graphics, stats, utils, matrixStats Suggests: testthat, IlluminaHumanMethylationEPICanno.ilm10b2.hg19, IlluminaHumanMethylation450kanno.ilmn12.hg19, knitr, minfiData, BiocStyle, rmarkdown, brgedata License: Artistic-2.0 MD5sum: fa53c8e7918242e6fadea0f6c9894496 NeedsCompilation: no Title: Perform methylation analysis Description: Package to integrate methylation and expression data. It can also perform methylation or expression analysis alone. Several plotting functionalities are included as well as a new region analysis based on redundancy analysis. Effect of SNPs on a region can also be estimated. biocViews: DNAMethylation, Microarray, Software, WholeGenome Author: Carlos Ruiz-Arenas [aut, cre], Juan R. Gonzalez [aut] Maintainer: Carlos Ruiz-Arenas VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MEAL git_branch: RELEASE_3_8 git_last_commit: e663698 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MEAL_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MEAL_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MEAL_1.12.0.tgz vignettes: vignettes/MEAL/inst/doc/caseExample.html, vignettes/MEAL/inst/doc/MEAL.html vignetteTitles: Expression and Methylation Analysis with MEAL, Methylation Analysis with MEAL hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MEAL/inst/doc/caseExample.R, vignettes/MEAL/inst/doc/MEAL.R Package: MeasurementError.cor Version: 1.54.0 License: LGPL MD5sum: fca8d3daecf480356153659e0a0c1e74 NeedsCompilation: no Title: Measurement Error model estimate for correlation coefficient Description: Two-stage measurement error model for correlation estimation with smaller bias than the usual sample correlation biocViews: StatisticalMethod Author: Beiying Ding Maintainer: Beiying Ding git_url: https://git.bioconductor.org/packages/MeasurementError.cor git_branch: RELEASE_3_8 git_last_commit: 435286f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MeasurementError.cor_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MeasurementError.cor_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MeasurementError.cor_1.54.0.tgz vignettes: vignettes/MeasurementError.cor/inst/doc/MeasurementError.cor.pdf vignetteTitles: MeasurementError.cor Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MeasurementError.cor/inst/doc/MeasurementError.cor.R Package: MEDIPS Version: 1.34.0 Depends: R (>= 3.0), BSgenome, Rsamtools Imports: GenomicRanges, Biostrings, graphics, gtools, IRanges, methods, stats, utils, edgeR, DNAcopy, biomaRt, rtracklayer, preprocessCore Suggests: BSgenome.Hsapiens.UCSC.hg19, MEDIPSData, BiocStyle License: GPL (>=2) MD5sum: 20d8d11b858c8912edff6d11917faa5c NeedsCompilation: no Title: DNA IP-seq data analysis Description: MEDIPS was developed for analyzing data derived from methylated DNA immunoprecipitation (MeDIP) experiments followed by sequencing (MeDIP-seq). However, MEDIPS provides functionalities for the analysis of any kind of quantitative sequencing data (e.g. ChIP-seq, MBD-seq, CMS-seq and others) including calculation of differential coverage between groups of samples and saturation and correlation analysis. biocViews: DNAMethylation, CpGIsland, DifferentialExpression, Sequencing, ChIPSeq, Preprocessing, QualityControl, Visualization, Microarray, Genetics, Coverage, GenomeAnnotation, CopyNumberVariation, SequenceMatching Author: Lukas Chavez, Matthias Lienhard, Joern Dietrich, Isaac Lopez Moyado Maintainer: Lukas Chavez git_url: https://git.bioconductor.org/packages/MEDIPS git_branch: RELEASE_3_8 git_last_commit: f92a513 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MEDIPS_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MEDIPS_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MEDIPS_1.34.0.tgz vignettes: vignettes/MEDIPS/inst/doc/MEDIPS.pdf vignetteTitles: MEDIPS hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MEDIPS/inst/doc/MEDIPS.R Package: MEDME Version: 1.42.0 Depends: R (>= 2.15), grDevices, graphics, methods, stats, utils Imports: Biostrings, MASS, drc Suggests: BSgenome.Hsapiens.UCSC.hg18, BSgenome.Mmusculus.UCSC.mm9 License: GPL (>= 2) Archs: i386, x64 MD5sum: a77cb873abc5ef82394b847801debb3a NeedsCompilation: yes Title: Modelling Experimental Data from MeDIP Enrichment Description: Description: MEDME allows the prediction of absolute and relative methylation levels based on measures obtained by MeDIP-microarray experiments biocViews: Microarray, CpGIsland, DNAMethylation Author: Mattia Pelizzola and Annette Molinaro Maintainer: Mattia Pelizzola git_url: https://git.bioconductor.org/packages/MEDME git_branch: RELEASE_3_8 git_last_commit: 13a76f9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MEDME_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MEDME_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MEDME_1.42.0.tgz vignettes: vignettes/MEDME/inst/doc/MEDME.pdf vignetteTitles: MEDME.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MEDME/inst/doc/MEDME.R Package: MEIGOR Version: 1.16.0 Depends: Rsolnp, snowfall, CNORode, deSolve Suggests: CellNOptR License: GPL-3 MD5sum: 3ebe8603dbf28a32751dc0e048d0b2c1 NeedsCompilation: no Title: MEIGO - MEtaheuristics for bIoinformatics Global Optimization Description: Global Optimization biocViews: SystemsBiology Author: Jose Egea, David Henriques, Alexandre Fdez. Villaverde, Thomas Cokelaer Maintainer: Jose Egea git_url: https://git.bioconductor.org/packages/MEIGOR git_branch: RELEASE_3_8 git_last_commit: b1105f9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MEIGOR_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MEIGOR_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MEIGOR_1.16.0.tgz vignettes: vignettes/MEIGOR/inst/doc/MEIGOR-vignette.pdf vignetteTitles: Main vignette:Global Optimization for Bioinformatics and Systems Biology hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MEIGOR/inst/doc/MEIGOR-vignette.R Package: MergeMaid Version: 2.54.0 Depends: R (>= 2.10.0), survival, Biobase, MASS, methods License: GPL (>= 2) MD5sum: 11c316392b5fb033937ab626cc4a1054 NeedsCompilation: no Title: Merge Maid Description: The functions in this R extension are intended for cross-study comparison of gene expression array data. Required from the user is gene expression matrices, their corresponding gene-id vectors and other useful information, and they could be 'list','matrix', or 'ExpressionSet'. The main function is 'mergeExprs' which transforms the input objects into data in the merged format, such that common genes in different datasets can be easily found. And the function 'intcor' calculate the correlation coefficients. Other functions use the output from 'modelOutcome' to graphically display the results and cross-validate associations of gene expression data with survival. biocViews: Microarray, DifferentialExpression, Visualization Author: Xiaogang Zhong Leslie Cope Elizabeth Garrett Giovanni Parmigiani Maintainer: Xiaogang Zhong URL: http://astor.som.jhmi.edu/MergeMaid git_url: https://git.bioconductor.org/packages/MergeMaid git_branch: RELEASE_3_8 git_last_commit: 8e79bd2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MergeMaid_2.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MergeMaid_2.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MergeMaid_2.54.0.tgz vignettes: vignettes/MergeMaid/inst/doc/MergeMaid.pdf vignetteTitles: MergeMaid primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE importsMe: metaArray, XDE Package: Mergeomics Version: 1.10.0 Depends: R (>= 3.0.1) Suggests: RUnit, BiocGenerics License: GPL (>= 2) MD5sum: 042173c4efb0b75209df2bf35cbf70d6 NeedsCompilation: no Title: Integrative network analysis of omics data Description: The Mergeomics pipeline serves as a flexible framework for integrating multidimensional omics-disease associations, functional genomics, canonical pathways and gene-gene interaction networks to generate mechanistic hypotheses. It includes two main parts, 1) Marker set enrichment analysis (MSEA); 2) Weighted Key Driver Analysis (wKDA). biocViews: Software Author: Ville-Petteri Makinen, Le Shu, Yuqi Zhao, Zeyneb Kurt, Bin Zhang, Xia Yang Maintainer: Zeyneb Kurt git_url: https://git.bioconductor.org/packages/Mergeomics git_branch: RELEASE_3_8 git_last_commit: d46f485 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Mergeomics_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Mergeomics_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Mergeomics_1.10.0.tgz vignettes: vignettes/Mergeomics/inst/doc/Mergeomics.pdf vignetteTitles: Mergeomics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Mergeomics/inst/doc/Mergeomics.R Package: MeSHDbi Version: 1.18.0 Depends: R (>= 3.0.1), BiocGenerics (>= 0.15.10) Imports: methods, AnnotationDbi (>= 1.31.19), RSQLite, Biobase Suggests: RUnit License: Artistic-2.0 MD5sum: 0a8007f98154bf5d6dc7399938c4c143 NeedsCompilation: no Title: DBI to construct MeSH-related package from sqlite file Description: The package is unified implementation of MeSH.db, MeSH.AOR.db, and MeSH.PCR.db and also is interface to construct Gene-MeSH package (MeSH.XXX.eg.db). loadMeSHDbiPkg import sqlite file and generate MeSH.XXX.eg.db. biocViews: Annotation, AnnotationData, Infrastructure Author: Koki Tsuyuzaki Maintainer: Koki Tsuyuzaki git_url: https://git.bioconductor.org/packages/MeSHDbi git_branch: RELEASE_3_8 git_last_commit: 1514f10 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MeSHDbi_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MeSHDbi_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MeSHDbi_1.18.0.tgz vignettes: vignettes/MeSHDbi/inst/doc/MeSHDbi.pdf vignetteTitles: MeSH.db hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE importsMe: meshr Package: meshes Version: 1.8.0 Depends: R (>= 3.4.0) Imports: AnnotationDbi, DOSE (>= 3.5.1), enrichplot, GOSemSim (>= 1.99.3), MeSH.db, methods, rvcheck Suggests: knitr, MeSH.Cel.eg.db, MeSH.Hsa.eg.db, prettydoc License: Artistic-2.0 MD5sum: 82fde49d4067c7941020d0da49df8f1d NeedsCompilation: no Title: MeSH Enrichment and Semantic analyses Description: MeSH (Medical Subject Headings) is the NLM controlled vocabulary used to manually index articles for MEDLINE/PubMed. MeSH terms were associated by Entrez Gene ID by three methods, gendoo, gene2pubmed and RBBH. This association is fundamental for enrichment and semantic analyses. meshes supports enrichment analysis (over-representation and gene set enrichment analysis) of gene list or whole expression profile. The semantic comparisons of MeSH terms provide quantitative ways to compute similarities between genes and gene groups. meshes implemented five methods proposed by Resnik, Schlicker, Jiang, Lin and Wang respectively and supports more than 70 species. biocViews: Annotation, Clustering, MultipleComparison, Software Author: Guangchuang Yu [aut, cre] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/meshes VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/meshes/issues git_url: https://git.bioconductor.org/packages/meshes git_branch: RELEASE_3_8 git_last_commit: c84c001 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/meshes_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/meshes_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/meshes_1.8.0.tgz vignettes: vignettes/meshes/inst/doc/meshes.html vignetteTitles: An introduction to meshes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/meshes/inst/doc/meshes.R Package: meshr Version: 1.18.0 Depends: R (>= 3.0.1) Imports: methods, stats, utils, fdrtool, MeSH.db, MeSH.AOR.db, MeSH.PCR.db, MeSHDbi, MeSH.Hsa.eg.db, MeSH.Aca.eg.db, MeSH.Bsu.168.eg.db, MeSH.Syn.eg.db, cummeRbund, org.Hs.eg.db, Category, S4Vectors, BiocGenerics, RSQLite License: Artistic-2.0 MD5sum: 2949ce68968d8e93325b2e4081038246 NeedsCompilation: no Title: Tools for conducting enrichment analysis of MeSH Description: A set of annotation maps describing the entire MeSH assembled using data from MeSH. biocViews: AnnotationData, FunctionalAnnotation, Bioinformatics, Statistics, Annotation, MultipleComparisons, MeSHDb Author: Koki Tsuyuzaki, Itoshi Nikaido, Gota Morota Maintainer: Koki Tsuyuzaki git_url: https://git.bioconductor.org/packages/meshr git_branch: RELEASE_3_8 git_last_commit: b3bb9d7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/meshr_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/meshr_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/meshr_1.18.0.tgz vignettes: vignettes/meshr/inst/doc/MeSH.pdf vignetteTitles: MeSH.db hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/meshr/inst/doc/MeSH.R Package: messina Version: 1.18.0 Depends: R (>= 3.1.0), survival (>= 2.37-4), methods Imports: Rcpp (>= 0.11.1), plyr (>= 1.8), ggplot2 (>= 0.9.3.1), grid (>= 3.1.0), foreach (>= 1.4.1), graphics LinkingTo: Rcpp Suggests: knitr (>= 1.5), antiProfilesData (>= 0.99.2), Biobase (>= 2.22.0), BiocStyle Enhances: doMC (>= 1.3.3) License: EPL (>= 1.0) Archs: i386, x64 MD5sum: 9e461e240fdb0e98fb3eac38288e5014 NeedsCompilation: yes Title: Single-gene classifiers and outlier-resistant detection of differential expression for two-group and survival problems. Description: Messina is a collection of algorithms for constructing optimally robust single-gene classifiers, and for identifying differential expression in the presence of outliers or unknown sample subgroups. The methods have application in identifying lead features to develop into clinical tests (both diagnostic and prognostic), and in identifying differential expression when a fraction of samples show unusual patterns of expression. biocViews: GeneExpression, DifferentialExpression, BiomedicalInformatics, Classification, Survival Author: Mark Pinese [aut], Mark Pinese [cre], Mark Pinese [cph] Maintainer: Mark Pinese VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/messina git_branch: RELEASE_3_8 git_last_commit: e516792 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/messina_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/messina_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/messina_1.18.0.tgz vignettes: vignettes/messina/inst/doc/messina.pdf vignetteTitles: Using Messina hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/messina/inst/doc/messina.R Package: metaArray Version: 1.60.0 Imports: Biobase, MergeMaid, graphics, stats License: LGPL-2 Archs: i386, x64 MD5sum: e6157bb8e824426a8762f4b0779f3eb8 NeedsCompilation: yes Title: Integration of Microarray Data for Meta-analysis Description: 1) Data transformation for meta-analysis of microarray Data: Transformation of gene expression data to signed probability scale (MCMC/EM methods) 2) Combined differential expression on raw scale: Weighted Z-score after stabilizing mean-variance relation within platform biocViews: Microarray, DifferentialExpression Author: Debashis Ghosh Hyungwon Choi Maintainer: Hyungwon Choi git_url: https://git.bioconductor.org/packages/metaArray git_branch: RELEASE_3_8 git_last_commit: c3aea92 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/metaArray_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/metaArray_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metaArray_1.60.0.tgz vignettes: vignettes/metaArray/inst/doc/metaArray.pdf vignetteTitles: metaArray Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metaArray/inst/doc/metaArray.R Package: Metab Version: 1.16.1 Depends: xcms, R (>= 3.0.1), svDialogs Imports: pander Suggests: RUnit, BiocGenerics License: GPL (>=2) MD5sum: 96f5fdfd612c7a2c52e89ac3d3a7f0c0 NeedsCompilation: no Title: Metab: An R Package for a High-Throughput Analysis of Metabolomics Data Generated by GC-MS. Description: Metab is an R package for high-throughput processing of metabolomics data analysed by the Automated Mass Spectral Deconvolution and Identification System (AMDIS) (http://chemdata.nist.gov/mass-spc/amdis/downloads/). In addition, it performs statistical hypothesis test (t-test) and analysis of variance (ANOVA). Doing so, Metab considerably speed up the data mining process in metabolomics and produces better quality results. Metab was developed using interactive features, allowing users with lack of R knowledge to appreciate its functionalities. biocViews: ImmunoOncology, Metabolomics, MassSpectrometry, AMDIS, GCMS Author: Raphael Aggio Maintainer: Raphael Aggio git_url: https://git.bioconductor.org/packages/Metab git_branch: RELEASE_3_8 git_last_commit: 773f043 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Metab_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Metab_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Metab_1.16.1.tgz vignettes: vignettes/Metab/inst/doc/MetabPackage.pdf vignetteTitles: Applying Metab hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Metab/inst/doc/MetabPackage.R Package: metabomxtr Version: 1.16.1 Depends: methods,Biobase Imports: optimx, Formula, plyr, multtest, BiocParallel, ggplot2 Suggests: xtable, reshape2 License: GPL-2 MD5sum: fde8b060af83e6b4e213b0dbe11a3f12 NeedsCompilation: no Title: A package to run mixture models for truncated metabolomics data with normal or lognormal distributions Description: The functions in this package return optimized parameter estimates and log likelihoods for mixture models of truncated data with normal or lognormal distributions. biocViews: ImmunoOncology, Metabolomics, MassSpectrometry Author: Michael Nodzenski, Anna Reisetter, Denise Scholtens Maintainer: Michael Nodzenski git_url: https://git.bioconductor.org/packages/metabomxtr git_branch: RELEASE_3_8 git_last_commit: ad960fb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/metabomxtr_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/metabomxtr_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metabomxtr_1.16.1.tgz vignettes: vignettes/metabomxtr/inst/doc/Metabomxtr_Vignette.pdf, vignettes/metabomxtr/inst/doc/mixnorm_Vignette.pdf vignetteTitles: metabomxtr, mixnorm hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metabomxtr/inst/doc/Metabomxtr_Vignette.R, vignettes/metabomxtr/inst/doc/mixnorm_Vignette.R Package: MetaboSignal Version: 1.12.0 Depends: R(>= 3.3) Imports: KEGGgraph, hpar, igraph, RCurl, KEGGREST, EnsDb.Hsapiens.v75, stats, graphics, utils, org.Hs.eg.db, biomaRt, AnnotationDbi, MWASTools, mygene Suggests: RUnit, BiocGenerics, knitr, BiocStyle, rmarkdown License: GPL-3 MD5sum: cde3fdfabbe4271392c9c5a5b6b0827f NeedsCompilation: no Title: MetaboSignal: a network-based approach to overlay and explore metabolic and signaling KEGG pathways Description: MetaboSignal is an R package that allows merging, analyzing and customizing metabolic and signaling KEGG pathways. It is a network-based approach designed to explore the topological relationship between genes (signaling- or enzymatic-genes) and metabolites, representing a powerful tool to investigate the genetic landscape and regulatory networks of metabolic phenotypes. biocViews: GraphAndNetwork, GeneSignaling, GeneTarget, Network, Pathways, KEGG, Reactome, Software Author: Andrea Rodriguez-Martinez, Rafael Ayala, Joram M. Posma, Ana L. Neves, Maryam Anwar, Jeremy K. Nicholson, Marc-Emmanuel Dumas Maintainer: Andrea Rodriguez-Martinez , Rafael Ayala VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MetaboSignal git_branch: RELEASE_3_8 git_last_commit: 410652c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MetaboSignal_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MetaboSignal_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MetaboSignal_1.12.0.tgz vignettes: vignettes/MetaboSignal/inst/doc/MetaboSignal.html, vignettes/MetaboSignal/inst/doc/MetaboSignal2.html vignetteTitles: MetaboSignal, MetaboSignal 2: merging KEGG with additional interaction resources hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MetaboSignal/inst/doc/MetaboSignal.R, vignettes/MetaboSignal/inst/doc/MetaboSignal2.R Package: metaCCA Version: 1.10.0 Suggests: knitr License: MIT + file LICENSE MD5sum: 50c6cad7861b8a8c9d42e5ee6cba4a4f NeedsCompilation: no Title: Summary Statistics-Based Multivariate Meta-Analysis of Genome-Wide Association Studies Using Canonical Correlation Analysis Description: metaCCA performs multivariate analysis of a single or multiple GWAS based on univariate regression coefficients. It allows multivariate representation of both phenotype and genotype. metaCCA extends the statistical technique of canonical correlation analysis to the setting where original individual-level records are not available, and employs a covariance shrinkage algorithm to achieve robustness. biocViews: GenomeWideAssociation, SNP, Genetics, Regression, StatisticalMethod, Software Author: Anna Cichonska Maintainer: Anna Cichonska URL: http://biorxiv.org/content/early/2015/07/16/022665 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/metaCCA git_branch: RELEASE_3_8 git_last_commit: c3e7a56 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/metaCCA_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/metaCCA_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metaCCA_1.10.0.tgz vignettes: vignettes/metaCCA/inst/doc/metaCCA.pdf vignetteTitles: metaCCA hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/metaCCA/inst/doc/metaCCA.R Package: MetaCyto Version: 1.4.1 Depends: R (>= 3.4) Imports: flowCore (>= 1.4),tidyr (>= 0.7),fastcluster,ggplot2,metafor,cluster,FlowSOM, grDevices, graphics, stats, utils Suggests: knitr, dplyr License: GPL (>= 2) MD5sum: 72f59f04fc721b26517bc2968210f410 NeedsCompilation: no Title: MetaCyto: A package for meta-analysis of cytometry data Description: This package provides functions for preprocessing, automated gating and meta-analysis of cytometry data. It also provides functions that facilitate the collection of cytometry data from the ImmPort database. biocViews: ImmunoOncology, CellBiology, FlowCytometry, Clustering, StatisticalMethod, Software, CellBasedAssays, Preprocessing Author: Zicheng Hu, Chethan Jujjavarapu, Sanchita Bhattacharya, Atul J. Butte Maintainer: Zicheng Hu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MetaCyto git_branch: RELEASE_3_8 git_last_commit: cb601de git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MetaCyto_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MetaCyto_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MetaCyto_1.4.1.tgz vignettes: vignettes/MetaCyto/inst/doc/MetaCyto_Vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MetaCyto/inst/doc/MetaCyto_Vignette.R Package: metagene Version: 2.14.0 Depends: R (>= 3.4.0), R6 (>= 2.0), GenomicRanges, BiocParallel Imports: rtracklayer, gplots, tools, GenomicAlignments, GenomeInfoDb, GenomicFeatures, IRanges, ggplot2, muStat, Rsamtools, DBChIP, matrixStats, purrr, data.table, magrittr, methods, utils, ensembldb, EnsDb.Hsapiens.v86, stringr Suggests: BiocGenerics, similaRpeak, RUnit, knitr, BiocStyle, rmarkdown, similaRpeak License: Artistic-2.0 | file LICENSE MD5sum: 5a33016df96518252fa9483efbea65f8 NeedsCompilation: no Title: A package to produce metagene plots Description: This package produces metagene plots to compare the behavior of DNA-interacting proteins at selected groups of genes/features. Bam files are used to increase the resolution. Multiple combination of group of bam files and/or group of genomic regions can be compared in a single analysis. Bootstraping analysis is used to compare the groups and locate regions with statistically different enrichment profiles. biocViews: ChIPSeq, Genetics, MultipleComparison, Coverage, Alignment, Sequencing Author: Charles Joly Beauparlant , Fabien Claude Lamaze , Rawane Samb , Cedric Lippens , Astrid Louise Deschenes and Arnaud Droit . Maintainer: Charles Joly Beauparlant VignetteBuilder: knitr BugReports: https://github.com/CharlesJB/metagene/issues git_url: https://git.bioconductor.org/packages/metagene git_branch: RELEASE_3_8 git_last_commit: 9359e75 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/metagene_2.14.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metagene_2.14.0.tgz vignettes: vignettes/metagene/inst/doc/metagene_rnaseq.html, vignettes/metagene/inst/doc/metagene.html vignetteTitles: RNA-seq exp ext, Introduction to metagene hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/metagene/inst/doc/metagene_rnaseq.R, vignettes/metagene/inst/doc/metagene.R dependsOnMe: Imetagene Package: metagenomeFeatures Version: 2.2.3 Depends: R (>= 3.5), Biobase (>= 2.17.8) Imports: Biostrings (>= 2.36.4), S4Vectors (>= 0.14.7), dplyr (>= 0.7.0), dbplyr(>= 1.0.0), stringr (>= 1.0.0), lazyeval (>= 0.1.10), RSQLite (>= 1.0.0), magrittr (>= 1.5), methods (>= 3.3.1), lattice (>= 0.20.33), ape (>= 3.5), DECIPHER (>= 2.4.0) Suggests: knitr (>= 1.11), testthat (>= 0.10.0), rmarkdown (>= 1.3), devtools (>= 1.13.5), ggtree(>= 1.8.2), BiocStyle (>= 2.8.2), phyloseq (>= 1.24.2), forcats (>= 0.3.0), ggplot2 (>= 3.0.0) License: Artistic-2.0 MD5sum: 2399f72b1eb906e7dea851f499a544ff NeedsCompilation: no Title: Exploration of marker-gene sequence taxonomic annotations Description: metagenomeFeatures was developed for use in exploring the taxonomic annotations for a marker-gene metagenomic sequence dataset. The package can be used to explore the taxonomic composition of a marker-gene database or annotated sequences from a marker-gene metagenome experiment. biocViews: ImmunoOncology, Microbiome, Metagenomics, Annotation, Infrastructure, Sequencing, Software Author: Nathan D. Olson, Joseph Nathaniel Paulson, Hector Corrada Bravo Maintainer: Nathan D. Olson URL: https://github.com/HCBravoLab/metagenomeFeatures VignetteBuilder: knitr BugReports: https://github.com/HCBravoLab/metagenomeFeatures/issues git_url: https://git.bioconductor.org/packages/metagenomeFeatures git_branch: RELEASE_3_8 git_last_commit: b33bd6b git_last_commit_date: 2019-02-25 Date/Publication: 2019-02-27 source.ver: src/contrib/metagenomeFeatures_2.2.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/metagenomeFeatures_2.2.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metagenomeFeatures_2.2.3.tgz vignettes: vignettes/metagenomeFeatures/inst/doc/database-explore.html, vignettes/metagenomeFeatures/inst/doc/MgDb_and_mgFeatures_classes.html, vignettes/metagenomeFeatures/inst/doc/retrieve-feature-data.html vignetteTitles: Exploring sequence and phylogenetic diversity for a taxonomic group of interest., `metagenomeFeatures` classes and methods., Using metagenomeFeatures to Retrieve Feature Data. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metagenomeFeatures/inst/doc/database-explore.R, vignettes/metagenomeFeatures/inst/doc/MgDb_and_mgFeatures_classes.R, vignettes/metagenomeFeatures/inst/doc/retrieve-feature-data.R Package: metagenomeSeq Version: 1.24.1 Depends: R(>= 3.0), Biobase, limma, glmnet, methods, RColorBrewer Imports: parallel, matrixStats, foreach, Matrix, gplots Suggests: annotate, BiocGenerics, biomformat, knitr, gss, testthat (>= 0.8), vegan, interactiveDisplay License: Artistic-2.0 MD5sum: 5ba3012b5450b59682c4c48dc406ffe5 NeedsCompilation: no Title: Statistical analysis for sparse high-throughput sequencing Description: metagenomeSeq is designed to determine features (be it Operational Taxanomic Unit (OTU), species, etc.) that are differentially abundant between two or more groups of multiple samples. metagenomeSeq is designed to address the effects of both normalization and under-sampling of microbial communities on disease association detection and the testing of feature correlations. biocViews: ImmunoOncology, Classification, Clustering, GeneticVariability, DifferentialExpression, Microbiome, Metagenomics, Normalization, Visualization, MultipleComparison, Sequencing, Software Author: Joseph Nathaniel Paulson, Nathan D. Olson, Justin Wagner, Hisham Talukder, Mihai Pop, Hector Corrada Bravo Maintainer: Joseph N. Paulson URL: https://github.com/nosson/metagenomeSeq/ VignetteBuilder: knitr BugReports: https://github.com/nosson/metagenomeSeq/issues git_url: https://git.bioconductor.org/packages/metagenomeSeq git_branch: RELEASE_3_8 git_last_commit: ef8c1c5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/metagenomeSeq_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/metagenomeSeq_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metagenomeSeq_1.24.1.tgz vignettes: vignettes/metagenomeSeq/inst/doc/fitTimeSeries.pdf, vignettes/metagenomeSeq/inst/doc/metagenomeSeq.pdf vignetteTitles: fitTimeSeries: differential abundance analysis through time or location, metagenomeSeq: statistical analysis for sparse high-throughput sequencing hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metagenomeSeq/inst/doc/fitTimeSeries.R, vignettes/metagenomeSeq/inst/doc/metagenomeSeq.R dependsOnMe: metavizr suggestsMe: interactiveDisplay, phyloseq, Wrench Package: metahdep Version: 1.40.0 Depends: R (>= 2.10), methods Suggests: affyPLM License: GPL-3 Archs: i386, x64 MD5sum: 1ec5c00ecd70c4a2989f0ef02ae1e868 NeedsCompilation: yes Title: Hierarchical Dependence in Meta-Analysis Description: Tools for meta-analysis in the presence of hierarchical (and/or sampling) dependence, including with gene expression studies biocViews: Microarray, DifferentialExpression Author: John R. Stevens, Gabriel Nicholas Maintainer: John R. Stevens git_url: https://git.bioconductor.org/packages/metahdep git_branch: RELEASE_3_8 git_last_commit: 38f418c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/metahdep_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/metahdep_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metahdep_1.40.0.tgz vignettes: vignettes/metahdep/inst/doc/metahdep.pdf vignetteTitles: metahdep Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metahdep/inst/doc/metahdep.R Package: metaMS Version: 1.18.1 Depends: R (>= 2.10), methods, CAMERA, xcms (>= 1.35) Imports: Matrix, tools, robustbase, BiocGenerics Suggests: metaMSdata, RUnit License: GPL (>= 2) MD5sum: 01f703155939aae7470e303f6a722cee NeedsCompilation: no Title: MS-based metabolomics annotation pipeline Description: MS-based metabolomics data processing and compound annotation pipeline. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics Author: Ron Wehrens [aut, cre] (author of GC-MS part), Pietro Franceschi [aut] (author of LC-MS part), Nir Shahaf [ctb], Matthias Scholz [ctb], Georg Weingart [ctb] (development of GC-MS approach), Elisabete Carvalho [ctb] (testing and feedback of GC-MS pipeline) Maintainer: Ron Wehrens URL: https://github.com/rwehrens/metaMS git_url: https://git.bioconductor.org/packages/metaMS git_branch: RELEASE_3_8 git_last_commit: 8284c97 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/metaMS_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/metaMS_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metaMS_1.18.1.tgz vignettes: vignettes/metaMS/inst/doc/runGC.pdf, vignettes/metaMS/inst/doc/runLC.pdf vignetteTitles: runGC, runLC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metaMS/inst/doc/runGC.R, vignettes/metaMS/inst/doc/runLC.R Package: MetaNeighbor Version: 1.2.1 Depends: R(>= 3.5) Imports: beanplot (>= 1.2), gplots (>= 3.0.1), RColorBrewer (>= 1.1), stats (>= 3.4), SummarizedExperiment (>= 1.6.5), utils (>= 3.4) Suggests: knitr (>= 1.17), rmarkdown (>= 1.6), testthat (>= 1.0.2) License: MIT + file LICENSE MD5sum: 6d970d23720abbee24bdfa7815e0e8ca NeedsCompilation: no Title: Single cell replicability analysis Description: MetaNeighbor allows users to quantify cell type replicability across datasets using neighbor voting. biocViews: ImmunoOncology, GeneExpression, GO, MultipleComparison, SingleCell, Transcriptomics Author: Megan Crow [aut, cre], Sara Ballouz [ctb], Manthan Shah [ctb], Jesse Gillis [aut] Maintainer: Manthan Shah VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MetaNeighbor git_branch: RELEASE_3_8 git_last_commit: 5f69820 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MetaNeighbor_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MetaNeighbor_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MetaNeighbor_1.2.1.tgz vignettes: vignettes/MetaNeighbor/inst/doc/MetaNeighbor.pdf vignetteTitles: MetaNeighbor user guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MetaNeighbor/inst/doc/MetaNeighbor.R Package: metaSeq Version: 1.22.1 Depends: R (>= 2.13.0), NOISeq, snow, Rcpp License: Artistic-2.0 MD5sum: 524028c02437bc7f07237cf2a83f727f NeedsCompilation: no Title: Meta-analysis of RNA-Seq count data in multiple studies Description: The probabilities by one-sided NOISeq are combined by Fisher's method or Stouffer's method biocViews: RNASeq, DifferentialExpression, Sequencing, ImmunoOncology Author: Koki Tsuyuzaki, Itoshi Nikaido Maintainer: Koki Tsuyuzaki git_url: https://git.bioconductor.org/packages/metaSeq git_branch: RELEASE_3_8 git_last_commit: 832ef5e git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/metaSeq_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/metaSeq_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metaSeq_1.22.1.tgz vignettes: vignettes/metaSeq/inst/doc/metaSeq.pdf vignetteTitles: metaSeq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metaSeq/inst/doc/metaSeq.R Package: metaseqR Version: 1.22.1 Depends: R (>= 2.13.0), EDASeq, DESeq, limma, qvalue Imports: edgeR, NOISeq, baySeq, NBPSeq, biomaRt, utils, gplots, corrplot, vsn, brew, rjson, log4r Suggests: BiocGenerics, GenomicRanges, rtracklayer, Rsamtools, survcomp, VennDiagram, knitr, zoo, RUnit, BiocManager, BSgenome, RSQLite Enhances: parallel, TCC, RMySQL License: GPL (>= 3) MD5sum: 68442083a54f6e92703baa04477846de NeedsCompilation: no Title: An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms. Description: Provides an interface to several normalization and statistical testing packages for RNA-Seq gene expression data. Additionally, it creates several diagnostic plots, performs meta-analysis by combinining the results of several statistical tests and reports the results in an interactive way. biocViews: ImmunoOncology, Software, GeneExpression, DifferentialExpression, WorkflowStep, Preprocessing, QualityControl, Normalization, ReportWriting, RNASeq Author: Panagiotis Moulos Maintainer: Panagiotis Moulos URL: http://www.fleming.gr VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/metaseqR git_branch: RELEASE_3_8 git_last_commit: a9560c7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/metaseqR_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/metaseqR_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metaseqR_1.22.1.tgz vignettes: vignettes/metaseqR/inst/doc/metaseqr-pdf.pdf vignetteTitles: RNA-Seq data analysis using mulitple statistical algorithms with metaseqR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/metaseqR/inst/doc/metaseqr-pdf.R Package: metavizr Version: 1.6.2 Depends: R (>= 3.4), metagenomeSeq (>= 1.17.1), methods, data.table, Biobase, digest Imports: epivizr, epivizrData, epivizrServer, epivizrStandalone, vegan, GenomeInfoDb, phyloseq, httr Suggests: knitr, BiocStyle, matrixStats, msd16s (>= 0.109.1), etec16s, testthat, gss, curatedMetagenomicData License: MIT + file LICENSE MD5sum: b30c08a4eade5259fed200c9b169f4fe NeedsCompilation: no Title: R Interface to the metaviz web app for interactive metagenomics data analysis and visualization Description: This package provides Websocket communication to the metaviz web app (http://metaviz.cbcb.umd.edu) for interactive visualization of metagenomics data. Objects in R/bioc interactive sessions can be displayed in plots and data can be explored using a facetzoom visualization. Fundamental Bioconductor data structures are supported (e.g., MRexperiment objects), while providing an easy mechanism to support other data structures. Visualizations (using d3.js) can be easily added to the web app as well. biocViews: Visualization, Infrastructure, GUI, Metagenomics, ImmunoOncology Author: Hector Corrada Bravo [cre, aut], Florin Chelaru [aut], Justin Wagner [aut], Jayaram Kancherla [aut], Joseph Paulson [aut] Maintainer: Hector Corrada Bravo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/metavizr git_branch: RELEASE_3_8 git_last_commit: eefb8e2 git_last_commit_date: 2019-04-10 Date/Publication: 2019-04-10 source.ver: src/contrib/metavizr_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/metavizr_1.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/metavizr_1.6.2.tgz vignettes: vignettes/metavizr/inst/doc/IntroToMetavizr.html vignetteTitles: Introduction to metavizr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/metavizr/inst/doc/IntroToMetavizr.R Package: MetCirc Version: 1.12.1 Depends: R (>= 3.5), amap (>= 0.8), circlize (>= 0.3.9), graphics (>= 3.5), grDevices (>= 3.5), methods (>= 3.5), scales (>= 0.3.0), shiny (>= 1.0.0), stats (>= 3.5) Suggests: BiocGenerics, knitr (>= 1.11) License: GPL-2 MD5sum: 2bc0310c41d407d8d94188648f7e582a NeedsCompilation: no Title: Navigating mass spectral similarity in high-resolution MS/MS metabolomics data Description: MetCirc comprises a workflow to interactively explore high-resolution MS/MS metabolomics data: create an MSP object, a format for MS/MS library data, bin m/z values of precursors, calculate similarity between precursors based on the normalised dot product and visualise similarities in a circular layout. Within the interactive framework the user can annotate MS/MS features based on their similarity to (known) related MS/MS features. biocViews: ImmunoOncology, Metabolomics, MassSpectrometry, Visualization Author: Thomas Naake and Emmanuel Gaquerel Maintainer: Thomas Naake VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MetCirc git_branch: RELEASE_3_8 git_last_commit: 942d673 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MetCirc_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MetCirc_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MetCirc_1.12.1.tgz vignettes: vignettes/MetCirc/inst/doc/MetCirc.pdf vignetteTitles: Workflow for Metabolomics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MetCirc/inst/doc/MetCirc.R Package: methimpute Version: 1.4.1 Depends: R (>= 3.4.0), GenomicRanges, ggplot2 Imports: Rcpp (>= 0.12.4.5), methods, utils, grDevices, stats, GenomeInfoDb, IRanges, Biostrings, reshape2, minpack.lm, data.table LinkingTo: Rcpp Suggests: knitr, BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: c63f19357ed780b1cb2cc16eecf61524 NeedsCompilation: yes Title: Imputation-guided re-construction of complete methylomes from WGBS data Description: This package implements functions for calling methylation for all cytosines in the genome. biocViews: ImmunoOncology, Software, DNAMethylation, Epigenetics, HiddenMarkovModel, Sequencing, Coverage Author: Aaron Taudt Maintainer: Aaron Taudt VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/methimpute git_branch: RELEASE_3_8 git_last_commit: 5eb3531 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/methimpute_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/methimpute_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methimpute_1.4.1.tgz vignettes: vignettes/methimpute/inst/doc/methimpute.pdf vignetteTitles: Methylation status calling with METHimpute hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methimpute/inst/doc/methimpute.R Package: methInheritSim Version: 1.4.1 Depends: R (>= 3.4) Imports: methylKit, GenomicRanges, GenomeInfoDb, parallel, BiocGenerics, S4Vectors, methods, stats, IRanges, msm Suggests: BiocStyle, knitr, rmarkdown, RUnit, methylInheritance License: Artistic-2.0 MD5sum: 70da35403445ef588556718166474bc0 NeedsCompilation: no Title: Simulating Whole-Genome Inherited Bisulphite Sequencing Data Description: Simulate a multigeneration methylation case versus control experiment with inheritance relation using a real control dataset. biocViews: BiologicalQuestion, Epigenetics, DNAMethylation, DifferentialMethylation, MethylSeq, Software, ImmunoOncology, StatisticalMethod, WholeGenome, Sequencing Author: Pascal Belleau, Astrid Deschênes and Arnaud Droit Maintainer: Pascal Belleau URL: https://github.com/belleau/methInheritSim VignetteBuilder: knitr BugReports: https://github.com/belleau/methInheritSim/issues git_url: https://git.bioconductor.org/packages/methInheritSim git_branch: RELEASE_3_8 git_last_commit: d53a297 git_last_commit_date: 2018-12-05 Date/Publication: 2018-12-05 source.ver: src/contrib/methInheritSim_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/methInheritSim_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methInheritSim_1.4.1.tgz vignettes: vignettes/methInheritSim/inst/doc/methInheritSim.html vignetteTitles: Simulating Whole-Genome Inherited Bisulphite Sequencing Data hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methInheritSim/inst/doc/methInheritSim.R suggestsMe: methylInheritance Package: MethPed Version: 1.10.1 Depends: R (>= 3.0.0), Biobase Imports: randomForest, grDevices, graphics, stats Suggests: BiocStyle, knitr, markdown, impute License: GPL-2 MD5sum: 2c3ea7058ebee1a25978d1a4030d7f77 NeedsCompilation: no Title: A DNA methylation classifier tool for the identification of pediatric brain tumor subtypes Description: Classification of pediatric tumors into biologically defined subtypes is challenging and multifaceted approaches are needed. For this aim, we developed a diagnostic classifier based on DNA methylation profiles. We offer MethPed as an easy-to-use toolbox that allows researchers and clinical diagnosticians to test single samples as well as large cohorts for subclass prediction of pediatric brain tumors. The current version of MethPed can classify the following tumor diagnoses/subgroups: Diffuse Intrinsic Pontine Glioma (DIPG), Ependymoma, Embryonal tumors with multilayered rosettes (ETMR), Glioblastoma (GBM), Medulloblastoma (MB) - Group 3 (MB_Gr3), Group 4 (MB_Gr3), Group WNT (MB_WNT), Group SHH (MB_SHH) and Pilocytic Astrocytoma (PiloAstro). biocViews: ImmunoOncology, DNAMethylation, Classification, Epigenetics Author: Mohammad Tanvir Ahamed [aut, trl], Anna Danielsson [aut], Szilárd Nemes [aut, trl], Helena Carén [aut, cre, cph] Maintainer: Helena Carén VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MethPed git_branch: RELEASE_3_8 git_last_commit: 16a25d3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MethPed_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MethPed_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MethPed_1.10.1.tgz vignettes: vignettes/MethPed/inst/doc/MethPed-vignette.html vignetteTitles: MethPed User Guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MethPed/inst/doc/MethPed-vignette.R Package: MethTargetedNGS Version: 1.14.0 Depends: R (>= 3.1.2), stringr, seqinr, gplots, Biostrings License: Artistic-2.0 MD5sum: ade70d7cd180adfcc0cbb28eec6345ef NeedsCompilation: no Title: Perform Methylation Analysis on Next Generation Sequencing Data Description: Perform step by step methylation analysis of Next Generation Sequencing data. biocViews: ResearchField, Genetics, Sequencing, Alignment, SequenceMatching, DataImport Author: Muhammad Ahmer Jamil with Contribution of Prof. Holger Frohlich and Priv.-Doz. Dr. Osman El-Maarri Maintainer: Muhammad Ahmer Jamil SystemRequirements: HMMER3 git_url: https://git.bioconductor.org/packages/MethTargetedNGS git_branch: RELEASE_3_8 git_last_commit: 0dabdf3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MethTargetedNGS_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MethTargetedNGS_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MethTargetedNGS_1.14.0.tgz vignettes: vignettes/MethTargetedNGS/inst/doc/MethTargetedNGS.pdf vignetteTitles: Introduction to MethTargetedNGS hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MethTargetedNGS/inst/doc/MethTargetedNGS.R Package: methVisual Version: 1.34.0 Depends: R (>= 2.11.0), Biostrings(>= 2.4.8), plotrix,gsubfn, grid,sqldf Imports: Biostrings, ca, graphics, grDevices, grid, gridBase, IRanges, stats, utils License: GPL (>= 2) MD5sum: ec537978bc45ab9ada43c3b429825362 NeedsCompilation: no Title: Methods for visualization and statistics on DNA methylation data Description: The package 'methVisual' allows the visualization of DNA methylation data after bisulfite sequencing. biocViews: DNAMethylation, Clustering, Classification Author: A. Zackay, C. Steinhoff Maintainer: Arie Zackay git_url: https://git.bioconductor.org/packages/methVisual git_branch: RELEASE_3_8 git_last_commit: afc0c5c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/methVisual_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/methVisual_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methVisual_1.34.0.tgz vignettes: vignettes/methVisual/inst/doc/methVisual.pdf vignetteTitles: Introduction to methVisual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methVisual/inst/doc/methVisual.R Package: methyAnalysis Version: 1.24.0 Depends: R (>= 2.10), grid, BiocGenerics, IRanges, GenomeInfoDb, GenomicRanges, Biobase (>= 2.34.0), org.Hs.eg.db Imports: grDevices, stats, utils, lumi, methylumi, Gviz, genoset, SummarizedExperiment, IRanges, GenomicRanges, VariantAnnotation, rtracklayer, GenomicFeatures, annotate, Biobase (>= 2.5.5), AnnotationDbi, genefilter, biomaRt, methods, parallel Suggests: FDb.InfiniumMethylation.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene License: Artistic-2.0 MD5sum: 3075fef8d84c73154ba460e1390106af NeedsCompilation: no Title: DNA methylation data analysis and visualization Description: The methyAnalysis package aims for the DNA methylation data analysis and visualization. A MethyGenoSet class is defined to keep the chromosome location information together with the data. The package also includes functions of estimating the methylation levels from Methy-Seq data. biocViews: Microarray, DNAMethylation, Visualization Author: Pan Du, Richard Bourgon Maintainer: Pan Du , Lei Huang , Gang Feng git_url: https://git.bioconductor.org/packages/methyAnalysis git_branch: RELEASE_3_8 git_last_commit: 061d1d6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/methyAnalysis_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/methyAnalysis_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methyAnalysis_1.24.0.tgz vignettes: vignettes/methyAnalysis/inst/doc/methyAnalysis.pdf vignetteTitles: An Introduction to the methyAnalysis package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methyAnalysis/inst/doc/methyAnalysis.R suggestsMe: methylumi Package: MethylAid Version: 1.16.0 Depends: R (>= 3.4) Imports: Biobase, BiocParallel, BiocGenerics, ggplot2, grid, gridBase, grDevices, graphics, hexbin, matrixStats, minfi (>= 1.22.0), methods, RColorBrewer, shiny, stats, SummarizedExperiment, utils Suggests: BiocStyle, knitr, MethylAidData, minfiData, minfiDataEPIC, RUnit License: GPL (>= 2) MD5sum: c654109f11f3e32cf050cee84dbb956f NeedsCompilation: no Title: Visual and interactive quality control of large Illumina DNA Methylation array data sets Description: A visual and interactive web application using RStudio's shiny package. Bad quality samples are detected using sample-dependent and sample-independent controls present on the array and user adjustable thresholds. In depth exploration of bad quality samples can be performed using several interactive diagnostic plots of the quality control probes present on the array. Furthermore, the impact of any batch effect provided by the user can be explored. biocViews: DNAMethylation, MethylationArray, Microarray, TwoChannel, QualityControl, BatchEffect, Visualization, GUI Author: Maarten van Iterson [aut, cre], Elmar Tobi[ctb], Roderick Slieker[ctb], Wouter den Hollander[ctb], Rene Luijk[ctb] and Bas Heijmans[ctb] Maintainer: M. van Iterson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MethylAid git_branch: RELEASE_3_8 git_last_commit: f06a617 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MethylAid_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MethylAid_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MethylAid_1.16.0.tgz vignettes: vignettes/MethylAid/inst/doc/MethylAid.pdf vignetteTitles: MethylAid: Visual and Interactive quality control of Illumina Human DNA Methylation array data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MethylAid/inst/doc/MethylAid.R Package: methylGSA Version: 1.0.4 Depends: R (>= 3.5) Imports: RobustRankAggreg, ggplot2, stringr, stats, clusterProfiler, missMethyl, org.Hs.eg.db, reactome.db, GO.db, AnnotationDbi, IlluminaHumanMethylation450kanno.ilmn12.hg19, IlluminaHumanMethylationEPICanno.ilm10b2.hg19 Suggests: knitr, rmarkdown, testthat, enrichplot License: GPL-2 MD5sum: b7239a6e1c62e72338b0d4da2fb0e817 NeedsCompilation: no Title: Gene Set Analysis Using the Outcome of Differential Methylation Description: The main functions for methylGSA are methylglm and methylRRA. methylGSA implements logistic regression adjusting number of probes as a covariate. methylRRA adjusts multiple p-values of each gene by Robust Rank Aggregation. For more detailed help information, please see the vignette. biocViews: DNAMethylation,DifferentialMethylation,GeneSetEnrichment,Regression, GeneRegulation,Pathways Author: Xu Ren [aut, cre], Pei Fen Kuan [aut] Maintainer: Xu Ren URL: https://github.com/reese3928/methylGSA VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/methylGSA git_branch: RELEASE_3_8 git_last_commit: 4d6929d git_last_commit_date: 2019-04-11 Date/Publication: 2019-04-11 source.ver: src/contrib/methylGSA_1.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/methylGSA_1.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methylGSA_1.0.4.tgz vignettes: vignettes/methylGSA/inst/doc/methylGSA-vignette.html vignetteTitles: methylGSA: Gene Set Analysis for DNA Methylation Datasets hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methylGSA/inst/doc/methylGSA-vignette.R Package: methylInheritance Version: 1.6.1 Depends: R (>= 3.4) Imports: methylKit, BiocParallel, GenomicRanges, IRanges, S4Vectors, methods, parallel, ggplot2, gridExtra, rebus Suggests: BiocStyle, BiocGenerics, knitr, rmarkdown, RUnit, methInheritSim License: Artistic-2.0 MD5sum: 21df16eb1d54500c0e3b1f7de6405a1d NeedsCompilation: no Title: Permutation-Based Analysis associating Conserved Differentially Methylated Elements Across Multiple Generations to a Treatment Effect Description: Permutation analysis, based on Monte Carlo sampling, for testing the hypothesis that the number of conserved differentially methylated elements, between several generations, is associated to an effect inherited from a treatment and that stochastic effect can be dismissed. biocViews: BiologicalQuestion, Epigenetics, DNAMethylation, DifferentialMethylation, MethylSeq, Software, ImmunoOncology, StatisticalMethod, WholeGenome, Sequencing Author: Astrid Deschênes, Pascal Belleau and Arnaud Droit Maintainer: Astrid Deschenes URL: https://github.com/adeschen/methylInheritance VignetteBuilder: knitr BugReports: https://github.com/adeschen/methylInheritance/issues git_url: https://git.bioconductor.org/packages/methylInheritance git_branch: RELEASE_3_8 git_last_commit: 61ee108 git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-04 source.ver: src/contrib/methylInheritance_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/methylInheritance_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methylInheritance_1.6.1.tgz vignettes: vignettes/methylInheritance/inst/doc/methylInheritance.html vignetteTitles: Permutation-Based Analysis associating Conserved Differentially Methylated Elements Across Multiple Generations to a Treatment Effect hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methylInheritance/inst/doc/methylInheritance.R suggestsMe: methInheritSim Package: methylKit Version: 1.8.1 Depends: R (>= 3.3.0), GenomicRanges (>= 1.18.1), methods Imports: IRanges, data.table (>= 1.9.6), parallel, S4Vectors (>= 0.13.13), GenomeInfoDb, KernSmooth, qvalue, emdbook, Rsamtools, gtools, fastseg, rtracklayer, mclust, Rcpp, R.utils, limma, grDevices, graphics, stats, utils LinkingTo: Rcpp, Rhtslib (>= 1.13.1), zlibbioc Suggests: testthat,knitr, rmarkdown, genomation, BiocManager License: Artistic-2.0 Archs: i386, x64 MD5sum: ce147e59306bc117dffbeea24518e169 NeedsCompilation: yes Title: DNA methylation analysis from high-throughput bisulfite sequencing results Description: methylKit is an R package for DNA methylation analysis and annotation from high-throughput bisulfite sequencing. The package is designed to deal with sequencing data from RRBS and its variants, but also target-capture methods and whole genome bisulfite sequencing. It also has functions to analyze base-pair resolution 5hmC data from experimental protocols such as oxBS-Seq and TAB-Seq. Perl is needed to read SAM files only. biocViews: DNAMethylation, Sequencing, MethylSeq Author: Altuna Akalin [aut, cre], Matthias Kormaksson [aut], Sheng Li [aut], Arsene Wabo [ctb], Adrian Bierling [aut], Alexander Gosdschan [aut] Maintainer: Altuna Akalin , Alexander Gosdschan URL: http://code.google.com/p/methylkit/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/methylKit git_branch: RELEASE_3_8 git_last_commit: a1e00fc git_last_commit_date: 2018-12-11 Date/Publication: 2018-12-11 source.ver: src/contrib/methylKit_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/methylKit_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methylKit_1.8.1.tgz vignettes: vignettes/methylKit/inst/doc/methylKit.html vignetteTitles: methylKit: User Guide v`r packageVersion('methylKit')` hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methylKit/inst/doc/methylKit.R importsMe: methInheritSim, methylInheritance Package: MethylMix Version: 2.12.0 Depends: R (>= 3.2.0) Imports: foreach, RPMM, RColorBrewer, ggplot2, RCurl, impute, data.table, limma, R.matlab, digest Suggests: BiocStyle, doParallel, testthat, knitr, rmarkdown License: GPL-2 MD5sum: e894baa2827b774cc07acc38faa8d6d2 NeedsCompilation: no Title: MethylMix: Identifying methylation driven cancer genes Description: MethylMix is an algorithm implemented to identify hyper and hypomethylated genes for a disease. MethylMix is based on a beta mixture model to identify methylation states and compares them with the normal DNA methylation state. MethylMix uses a novel statistic, the Differential Methylation value or DM-value defined as the difference of a methylation state with the normal methylation state. Finally, matched gene expression data is used to identify, besides differential, functional methylation states by focusing on methylation changes that effect gene expression. References: Gevaert 0. MethylMix: an R package for identifying DNA methylation-driven genes. Bioinformatics (Oxford, England). 2015;31(11):1839-41. doi:10.1093/bioinformatics/btv020. Gevaert O, Tibshirani R, Plevritis SK. Pancancer analysis of DNA methylation-driven genes using MethylMix. Genome Biology. 2015;16(1):17. doi:10.1186/s13059-014-0579-8. biocViews: DNAMethylation,StatisticalMethod,DifferentialMethylation,GeneRegulation,GeneExpression,MethylationArray,DifferentialExpression,Pathways,Network Author: Olivier Gevaert Maintainer: Olivier Gevaert VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MethylMix git_branch: RELEASE_3_8 git_last_commit: 5ab5dec git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MethylMix_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MethylMix_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MethylMix_2.12.0.tgz vignettes: vignettes/MethylMix/inst/doc/vignettes.html vignetteTitles: MethylMix hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MethylMix/inst/doc/vignettes.R Package: methylMnM Version: 1.20.0 Depends: R (>= 2.12.1), edgeR, statmod License: GPL-3 Archs: i386, x64 MD5sum: 595ea0397f953ec93b06932e0e724dd4 NeedsCompilation: yes Title: detect different methylation level (DMR) Description: To give the exactly p-value and q-value of MeDIP-seq and MRE-seq data for different samples comparation. biocViews: Software, DNAMethylation, Sequencing Author: Yan Zhou, Bo Zhang, Nan Lin, BaoXue Zhang and Ting Wang Maintainer: Yan Zhou git_url: https://git.bioconductor.org/packages/methylMnM git_branch: RELEASE_3_8 git_last_commit: e159800 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/methylMnM_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/methylMnM_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methylMnM_1.20.0.tgz vignettes: vignettes/methylMnM/inst/doc/methylMnM.pdf vignetteTitles: methylMnM hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methylMnM/inst/doc/methylMnM.R importsMe: SIMD Package: methylPipe Version: 1.16.0 Depends: R (>= 3.2.0), methods, grDevices, graphics, stats, utils, GenomicRanges, SummarizedExperiment (>= 0.2.0), Rsamtools Imports: marray, gplots, IRanges, BiocGenerics, Gviz, GenomicAlignments, Biostrings, parallel, data.table, GenomeInfoDb, S4Vectors Suggests: BSgenome.Hsapiens.UCSC.hg18, TxDb.Hsapiens.UCSC.hg18.knownGene, knitr, MethylSeekR License: GPL(>=2) Archs: i386, x64 MD5sum: 0174e17c1fbcf664052973c8be3f5c79 NeedsCompilation: yes Title: Base resolution DNA methylation data analysis Description: Memory efficient analysis of base resolution DNA methylation data in both the CpG and non-CpG sequence context. Integration of DNA methylation data derived from any methodology providing base- or low-resolution data. biocViews: MethylSeq, DNAMethylation, Coverage, Sequencing Author: Kamal Kishore Maintainer: Kamal Kishore VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/methylPipe git_branch: RELEASE_3_8 git_last_commit: 0cc3f02 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/methylPipe_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/methylPipe_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methylPipe_1.16.0.tgz vignettes: vignettes/methylPipe/inst/doc/methylPipe.pdf vignetteTitles: methylPipe.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methylPipe/inst/doc/methylPipe.R importsMe: compEpiTools Package: MethylSeekR Version: 1.22.0 Depends: rtracklayer (>= 1.16.3), parallel (>= 2.15.1), mhsmm (>= 0.4.4) Imports: IRanges (>= 1.16.3), BSgenome (>= 1.26.1), GenomicRanges (>= 1.10.5), geneplotter (>= 1.34.0), graphics (>= 2.15.2), grDevices (>= 2.15.2), parallel (>= 2.15.2), stats (>= 2.15.2), utils (>= 2.15.2) Suggests: BSgenome.Hsapiens.UCSC.hg18 License: GPL (>=2) MD5sum: 19080118abe4bf6ba3aed35b2643764b NeedsCompilation: no Title: Segmentation of Bis-seq data Description: This is a package for the discovery of regulatory regions from Bis-seq data biocViews: Sequencing, MethylSeq, DNAMethylation Author: Lukas Burger, Dimos Gaidatzis, Dirk Schubeler and Michael Stadler Maintainer: Lukas Burger git_url: https://git.bioconductor.org/packages/MethylSeekR git_branch: RELEASE_3_8 git_last_commit: b1eb0e5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MethylSeekR_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MethylSeekR_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MethylSeekR_1.22.0.tgz vignettes: vignettes/MethylSeekR/inst/doc/MethylSeekR.pdf vignetteTitles: MethylSeekR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MethylSeekR/inst/doc/MethylSeekR.R suggestsMe: methylPipe Package: methylumi Version: 2.28.0 Depends: Biobase, methods, R (>= 2.13), scales, reshape2, ggplot2, matrixStats, FDb.InfiniumMethylation.hg19 (>= 2.2.0), minfi Imports: BiocGenerics, S4Vectors, IRanges, GenomeInfoDb, GenomicRanges, SummarizedExperiment, Biobase, graphics, lattice, annotate, genefilter, AnnotationDbi, minfi, stats4, illuminaio Suggests: lumi, lattice, limma, xtable, SQN, MASS, matrixStats, parallel, rtracklayer, Biostrings, methyAnalysis, TCGAMethylation450k, IlluminaHumanMethylation450kanno.ilmn12.hg19, FDb.InfiniumMethylation.hg18 (>= 2.2.0), Homo.sapiens, knitr License: GPL-2 MD5sum: f1a2ca6160d851c6db5797cf4636058e NeedsCompilation: no Title: Handle Illumina methylation data Description: This package provides classes for holding and manipulating Illumina methylation data. Based on eSet, it can contain MIAME information, sample information, feature information, and multiple matrices of data. An "intelligent" import function, methylumiR can read the Illumina text files and create a MethyLumiSet. methylumIDAT can directly read raw IDAT files from HumanMethylation27 and HumanMethylation450 microarrays. Normalization, background correction, and quality control features for GoldenGate, Infinium, and Infinium HD arrays are also included. biocViews: DNAMethylation, TwoChannel, Preprocessing, QualityControl, CpGIsland Author: Sean Davis, Pan Du, Sven Bilke, Tim Triche, Jr., Moiz Bootwalla Maintainer: Sean Davis VignetteBuilder: knitr BugReports: https://github.com/seandavi/methylumi/issues/new git_url: https://git.bioconductor.org/packages/methylumi git_branch: RELEASE_3_8 git_last_commit: f7609e8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/methylumi_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/methylumi_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methylumi_2.28.0.tgz vignettes: vignettes/methylumi/inst/doc/methylumi.pdf, vignettes/methylumi/inst/doc/methylumi450k.pdf vignetteTitles: An Introduction to the methylumi package, Working with Illumina 450k Arrays using methylumi hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/methylumi/inst/doc/methylumi.R, vignettes/methylumi/inst/doc/methylumi450k.R dependsOnMe: bigmelon, RnBeads, skewr, wateRmelon importsMe: ffpe, lumi, methyAnalysis, missMethyl Package: methyvim Version: 1.4.0 Depends: R (>= 3.4.0) Imports: stats, cluster, methods, ggplot2, ggsci, gridExtra, superheat, dplyr, gtools, tmle, future, doFuture, S4Vectors, BiocGenerics, BiocParallel, SummarizedExperiment, GenomeInfoDb, bumphunter, IRanges, limma, minfi Suggests: testthat, knitr, rmarkdown, BiocStyle, SuperLearner, earth, nnet, gam, arm, snow, parallel, BatchJobs, minfiData, methyvimData License: file LICENSE MD5sum: c8c7263ae8d200c1780273158bfda8fb NeedsCompilation: no Title: Targeted, Robust, and Model-free Differential Methylation Analysis Description: This package provides facilities for differential methylation analysis based on variable importance measures (VIMs), a class of statistical target parameters that arise in causal inference. The estimation and inference procedures provided are nonparametric, relying on ensemble machine learning to flexibly assess functional relationships among covariates and the outcome of interest. These tools can be applied to differential methylation at the level of CpG sites, to obtain valid statistical inference even after corrections for multiple hypothesis testing. biocViews: Clustering, DNAMethylation, DifferentialMethylation, MethylationArray, MethylSeq Author: Nima Hejazi [aut, cre, cph], Mark van der Laan [aut, ths], Alan Hubbard [ctb, ths], Rachael Phillips [ctb] Maintainer: Nima Hejazi URL: https://github.com/nhejazi/methyvim VignetteBuilder: knitr BugReports: https://github.com/nhejazi/methyvim/issues git_url: https://git.bioconductor.org/packages/methyvim git_branch: RELEASE_3_8 git_last_commit: 13eae51 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/methyvim_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/methyvim_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/methyvim_1.4.0.tgz vignettes: vignettes/methyvim/inst/doc/using_methyvim.html vignetteTitles: Targeted Data-Adaptive Estimation and Inference for Differential Methylation Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/methyvim/inst/doc/using_methyvim.R Package: MetID Version: 1.0.0 Depends: R (>= 3.5) Imports: utils (>= 3.3.1), stats (>= 3.4.2), devtools (>= 1.13.0), stringr (>= 1.3.0), Matrix (>= 1.2-12), igraph (>= 1.2.1), ChemmineR (>= 2.30.2) Suggests: knitr (>= 1.19), rmarkdown (>= 1.8) License: Artistic-2.0 MD5sum: c5b7dea163a632b9626c4b3db70334bf NeedsCompilation: no Title: Network-based prioritization of putative metabolite IDs Description: This package uses an innovative network-based approach that will enhance our ability to determine the identities of significant ions detected by LC-MS. biocViews: AssayDomain, BiologicalQuestion, Infrastructure, ResearchField, StatisticalMethod, Technology, WorkflowStep, Network, KEGG Author: Zhenzhi Li Maintainer: Zhenzhi Li URL: https://github.com/ressomlab/MetID VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MetID git_branch: RELEASE_3_8 git_last_commit: 7a460ff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MetID_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MetID_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MetID_1.0.0.tgz vignettes: vignettes/MetID/inst/doc/Introduction_to_MetID.html vignetteTitles: Introduction to MetID hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MetID/inst/doc/Introduction_to_MetID.R Package: MetNet Version: 1.0.1 Depends: R (>= 3.5), stats (>= 3.5) Imports: bnlearn (>= 4.3), BiocParallel (>= 1.12.0), methods (>= 3.5), mpmi (>= 0.42), parmigene (>= 1.0.2), ppcor (>= 1.1), rfPermute (>= 2.1.5), sna (>= 2.4), stabs (>= 0.6), WGCNA (>= 1.61) Suggests: BiocGenerics (>= 0.24.0), BiocStyle (>= 2.6.1), igraph (>= 1.1.2), knitr (>= 1.11) License: GPL-2 MD5sum: 5619367429a7b8f6223eec1182628b2e NeedsCompilation: no Title: Inferring metabolic networks from untargeted high-resolution mass spectrometry data Description: MetNet contains functionality to infer metabolic network topologies from quantitative data and high-resolution mass/charge information. Using statistical models (including correlation, mutual information, regression and Bayes statistics) and quantitative data (intensity values of features) adjacency matrices are inferred that can be combined to a consensus matrix. Mass differences calculated between mass/charge values of features will be matched against a data frame of supplied mass/charge differences referring to transformations of enzymatic activities. In a third step, the two matrices are combined to form a adjacency matrix inferred from both quantitative and structure information. biocViews: ImmunoOncology, Metabolomics, MassSpectrometry, Network, Regression Author: Thomas Naake [aut, cre] Maintainer: Thomas Naake VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MetNet git_branch: RELEASE_3_8 git_last_commit: 87f2f49 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MetNet_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MetNet_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MetNet_1.0.1.tgz vignettes: vignettes/MetNet/inst/doc/MetNet.pdf vignetteTitles: Workflow for Metabolomics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MetNet/inst/doc/MetNet.R Package: mfa Version: 1.4.1 Depends: R (>= 3.4.0) Imports: methods, stats, ggplot2, Rcpp, dplyr, ggmcmc, MCMCpack, MCMCglmm, coda, magrittr, tibble, Biobase LinkingTo: Rcpp Suggests: knitr, rmarkdown, BiocStyle, testthat License: GPL (>= 2) Archs: i386, x64 MD5sum: 1ee7bd04f47841e4f17edaab630db379 NeedsCompilation: yes Title: Bayesian hierarchical mixture of factor analyzers for modelling genomic bifurcations Description: MFA models genomic bifurcations using a Bayesian hierarchical mixture of factor analysers. biocViews: ImmunoOncology, RNASeq, GeneExpression, Bayesian, SingleCell Author: Kieran Campbell [aut, cre] Maintainer: Kieran Campbell VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mfa git_branch: RELEASE_3_8 git_last_commit: 0b6807a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/mfa_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/mfa_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mfa_1.4.1.tgz vignettes: vignettes/mfa/inst/doc/introduction_to_mfa.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mfa/inst/doc/introduction_to_mfa.R suggestsMe: splatter Package: Mfuzz Version: 2.42.0 Depends: R (>= 2.5.0), Biobase (>= 2.5.5), e1071 Imports: tcltk, tkWidgets Suggests: marray License: GPL-2 MD5sum: e994e57b660e1e59335de41f82762d58 NeedsCompilation: no Title: Soft clustering of time series gene expression data Description: Package for noise-robust soft clustering of gene expression time-series data (including a graphical user interface) biocViews: Microarray, Clustering, TimeCourse, Preprocessing, Visualization Author: Matthias Futschik Maintainer: Matthias Futschik URL: http://mfuzz.sysbiolab.eu/ git_url: https://git.bioconductor.org/packages/Mfuzz git_branch: RELEASE_3_8 git_last_commit: 234f902 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Mfuzz_2.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Mfuzz_2.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Mfuzz_2.42.0.tgz vignettes: vignettes/Mfuzz/inst/doc/Mfuzz.pdf vignetteTitles: Introduction to Mfuzz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Mfuzz/inst/doc/Mfuzz.R dependsOnMe: cycle suggestsMe: pwOmics Package: MGFM Version: 1.16.0 Depends: AnnotationDbi,annotate Suggests: hgu133a.db License: GPL-3 MD5sum: 4c546557bee46a59290c4900403f7edf NeedsCompilation: no Title: Marker Gene Finder in Microarray gene expression data Description: The package is designed to detect marker genes from Microarray gene expression data sets biocViews: Genetics, GeneExpression, Microarray Author: Khadija El Amrani Maintainer: Khadija El Amrani git_url: https://git.bioconductor.org/packages/MGFM git_branch: RELEASE_3_8 git_last_commit: 64ff78e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MGFM_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MGFM_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MGFM_1.16.0.tgz vignettes: vignettes/MGFM/inst/doc/MGFM.pdf vignetteTitles: Using MGFM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MGFM/inst/doc/MGFM.R dependsOnMe: sampleClassifier Package: MGFR Version: 1.8.1 Depends: R (>= 3.3) Imports: biomaRt, annotate License: GPL-3 MD5sum: f4763f8617c9a23dd62d3dccd703724b NeedsCompilation: no Title: Marker Gene Finder in RNA-seq data Description: The package is designed to detect marker genes from RNA-seq data. biocViews: ImmunoOncology, Genetics, GeneExpression, RNASeq Author: Khadija El Amrani Maintainer: Khadija El Amrani git_url: https://git.bioconductor.org/packages/MGFR git_branch: RELEASE_3_8 git_last_commit: 431e32d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MGFR_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MGFR_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MGFR_1.8.1.tgz vignettes: vignettes/MGFR/inst/doc/MGFR.pdf vignetteTitles: Using MGFR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MGFR/inst/doc/MGFR.R dependsOnMe: sampleClassifier Package: mgsa Version: 1.30.0 Depends: R (>= 2.14.0), methods, gplots Imports: graphics, stats, utils Suggests: DBI, RSQLite, GO.db, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: 273187423f0ea752f7d0e31aa3def023 NeedsCompilation: yes Title: Model-based gene set analysis Description: Model-based Gene Set Analysis (MGSA) is a Bayesian modeling approach for gene set enrichment. The package mgsa implements MGSA and tools to use MGSA together with the Gene Ontology. biocViews: Pathways, GO, GeneSetEnrichment Author: Sebastian Bauer , Julien Gagneur Maintainer: Sebastian Bauer URL: https://github.com/sba1/mgsa-bioc git_url: https://git.bioconductor.org/packages/mgsa git_branch: RELEASE_3_8 git_last_commit: c4aec95 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mgsa_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mgsa_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mgsa_1.30.0.tgz vignettes: vignettes/mgsa/inst/doc/mgsa.pdf vignetteTitles: Overview of the mgsa package. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mgsa/inst/doc/mgsa.R suggestsMe: gCMAP Package: MiChip Version: 1.36.0 Depends: R (>= 2.3.0), Biobase Imports: Biobase License: GPL (>= 2) MD5sum: b64b0ae539c74dcf5d71610ffce198a2 NeedsCompilation: no Title: MiChip Parsing and Summarizing Functions Description: This package takes the MiChip miRNA microarray .grp scanner output files and parses these out, providing summary and plotting functions to analyse MiChip hybridizations. A set of hybridizations is packaged into an ExpressionSet allowing it to be used by other BioConductor packages. biocViews: Microarray, Preprocessing Author: Jonathon Blake Maintainer: Jonathon Blake git_url: https://git.bioconductor.org/packages/MiChip git_branch: RELEASE_3_8 git_last_commit: bec77ef git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MiChip_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MiChip_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MiChip_1.36.0.tgz vignettes: vignettes/MiChip/inst/doc/MiChip.pdf vignetteTitles: MiChip miRNA Microarray Processing hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MiChip/inst/doc/MiChip.R Package: microbiome Version: 1.4.2 Depends: R (>= 3.4.0), phyloseq, ggplot2 Imports: dplyr, reshape2, stats, tidyr, utils, vegan Suggests: BiocGenerics, BiocStyle, Cairo, knitcitations, knitr, rmarkdown, testthat License: BSD_2_clause + file LICENSE MD5sum: faf9cbb6d7ae71b815ead3c8448cde2a NeedsCompilation: no Title: Microbiome Analytics Description: Utilities for microbiome analysis. biocViews: Clustering, Metagenomics, Microbiome, Sequencing, SystemsBiology, ImmunoOncology Author: Leo Lahti [aut, cre], Sudarshan Shetty [aut] Maintainer: Leo Lahti URL: http://microbiome.github.io/microbiome VignetteBuilder: knitr BugReports: https://github.com/microbiome/microbiome/issues git_url: https://git.bioconductor.org/packages/microbiome git_branch: RELEASE_3_8 git_last_commit: d4437ff git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/microbiome_1.4.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/microbiome_1.4.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/microbiome_1.4.2.tgz vignettes: vignettes/microbiome/inst/doc/vignette.html vignetteTitles: microbiome R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/microbiome/inst/doc/vignette.R Package: microRNA Version: 1.40.0 Depends: R (>= 2.10) Imports: Biostrings (>= 2.11.32) License: Artistic-2.0 Archs: i386, x64 MD5sum: 2ee23e69a38f498c578d6721d97dc985 NeedsCompilation: yes Title: Data and functions for dealing with microRNAs Description: Different data resources for microRNAs and some functions for manipulating them. biocViews: Infrastructure, GenomeAnnotation, SequenceMatching Author: R. Gentleman, S. Falcon Maintainer: "James F. Reid" git_url: https://git.bioconductor.org/packages/microRNA git_branch: RELEASE_3_8 git_last_commit: 2aedc5e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/microRNA_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/microRNA_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/microRNA_1.40.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: Roleswitch suggestsMe: MmPalateMiRNA, rtracklayer Package: MIGSA Version: 1.6.0 Depends: R (>= 3.4), methods, BiocGenerics Imports: AnnotationDbi, Biobase, BiocParallel, compiler, data.table, edgeR, futile.logger, ggdendro, ggplot2, GO.db, GOstats, graph, graphics, grDevices, grid, GSEABase, ismev, limma, matrixStats, org.Hs.eg.db, RBGL, reshape2, Rgraphviz, RJSONIO, stats, utils, vegan Suggests: breastCancerMAINZ, breastCancerNKI, breastCancerTRANSBIG, breastCancerUNT, breastCancerUPP, breastCancerVDX, mGSZ, pbcmc, MIGSAdata License: GPL (>= 2) MD5sum: 0db3f4f96d22c45fbc237fdeeb59aa5e NeedsCompilation: no Title: Massive and Integrative Gene Set Analysis Description: Massive and Integrative Gene Set Analysis. The MIGSA package allows to perform a massive and integrative gene set analysis over several expression and gene sets simultaneously. It provides a common gene expression analytic framework that grants a comprehensive and coherent analysis. Only a minimal user parameter setting is required to perform both singular and gene set enrichment analyses in an integrative manner by means of the best available methods, i.e. dEnricher and mGSZ respectively. The greatest strengths of this big omics data tool are the availability of several functions to explore, analyze and visualize its results in order to facilitate the data mining task over huge information sources. MIGSA package also provides several functions that allow to easily load the most updated gene sets from several repositories. biocViews: Software, GeneSetEnrichment, Visualization, GeneExpression, Microarray, RNASeq, KEGG Author: Juan C. Rodriguez, Cristobal Fresno, Andrea S. Llera and Elmer A. Fernandez Maintainer: Juan C. Rodriguez URL: http://www.bdmg.com.ar/ git_url: https://git.bioconductor.org/packages/MIGSA git_branch: RELEASE_3_8 git_last_commit: fecd5a6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MIGSA_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MIGSA_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MIGSA_1.6.0.tgz vignettes: vignettes/MIGSA/inst/doc/gettingPbcmcData.pdf, vignettes/MIGSA/inst/doc/gettingTcgaData.pdf, vignettes/MIGSA/inst/doc/MIGSA.pdf vignetteTitles: Getting pbcmc datasets, Getting TCGA datasets, Massive and Integrative Gene Set Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MIGSA/inst/doc/gettingPbcmcData.R, vignettes/MIGSA/inst/doc/gettingTcgaData.R, vignettes/MIGSA/inst/doc/MIGSA.R Package: mimager Version: 1.6.0 Depends: Biobase Imports: BiocGenerics, S4Vectors, preprocessCore, grDevices, methods, grid, gtable, scales, DBI, affy, affyPLM, oligo, oligoClasses Suggests: knitr, rmarkdown, BiocStyle, testthat, lintr, Matrix, abind, affydata, hgu95av2cdf, oligoData, pd.hugene.1.0.st.v1 License: MIT + file LICENSE MD5sum: 15abbaac41f80515ccbc4fda98e409a9 NeedsCompilation: no Title: mimager: The Microarray Imager Description: Easily visualize and inspect microarrays for spatial artifacts. biocViews: Infrastructure, Visualization, Microarray Author: Aaron Wolen [aut, cre, cph] Maintainer: Aaron Wolen URL: https://github.com/aaronwolen/mimager VignetteBuilder: knitr BugReports: https://github.com/aaronwolen/mimager/issues git_url: https://git.bioconductor.org/packages/mimager git_branch: RELEASE_3_8 git_last_commit: 78a682d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mimager_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mimager_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mimager_1.6.0.tgz vignettes: vignettes/mimager/inst/doc/introduction.html vignetteTitles: mimager overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/mimager/inst/doc/introduction.R Package: MIMOSA Version: 1.20.1 Depends: R (>= 3.0.2), MASS, plyr, reshape, Biobase, ggplot2 Imports: methods, Formula, data.table, pracma, MCMCpack, coda, modeest, testthat, Rcpp, scales, LinkingTo: Rcpp, RcppArmadillo Suggests: parallel, knitr License: Artistic-2.0 Archs: i386, x64 MD5sum: 1d92a6dd8cee028f10c198bd80692890 NeedsCompilation: yes Title: Mixture Models for Single-Cell Assays Description: Modeling count data using Dirichlet-multinomial and beta-binomial mixtures with applications to single-cell assays. biocViews: ImmunoOncology, FlowCytometry, CellBasedAssays Author: Greg Finak Maintainer: Greg Finak VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MIMOSA git_branch: RELEASE_3_8 git_last_commit: 6012f34 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MIMOSA_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MIMOSA_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MIMOSA_1.20.1.tgz vignettes: vignettes/MIMOSA/inst/doc/MIMOSA.pdf vignetteTitles: MIMOSA: Mixture Models For Single Cell Assays hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MIMOSA/inst/doc/MIMOSA.R Package: MineICA Version: 1.22.0 Depends: R (>= 2.10), methods, BiocGenerics (>= 0.13.8), Biobase, plyr, ggplot2, scales, foreach, xtable, biomaRt, gtools, GOstats, cluster, marray, mclust, RColorBrewer, colorspace, igraph, Rgraphviz, graph, annotate, Hmisc, fastICA, JADE Imports: AnnotationDbi, lumi, fpc, lumiHumanAll.db Suggests: biomaRt, GOstats, cluster, hgu133a.db, mclust, igraph, breastCancerMAINZ, breastCancerTRANSBIG, breastCancerUPP, breastCancerVDX Enhances: doMC License: GPL-2 MD5sum: 0580f82c0a418930e9246cacb625dc93 NeedsCompilation: no Title: Analysis of an ICA decomposition obtained on genomics data Description: The goal of MineICA is to perform Independent Component Analysis (ICA) on multiple transcriptome datasets, integrating additional data (e.g molecular, clinical and pathological). This Integrative ICA helps the biological interpretation of the components by studying their association with variables (e.g sample annotations) and gene sets, and enables the comparison of components from different datasets using correlation-based graph. biocViews: Visualization, MultipleComparison Author: Anne Biton Maintainer: Anne Biton git_url: https://git.bioconductor.org/packages/MineICA git_branch: RELEASE_3_8 git_last_commit: 7e79aff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MineICA_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MineICA_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MineICA_1.22.0.tgz vignettes: vignettes/MineICA/inst/doc/MineICA.pdf vignetteTitles: MineICA: Independent component analysis of genomic data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MineICA/inst/doc/MineICA.R Package: minet Version: 3.40.0 Imports: infotheo License: file LICENSE Archs: i386, x64 MD5sum: cfe31fbcec7dfc321436f468487dd842 NeedsCompilation: yes Title: Mutual Information NETworks Description: This package implements various algorithms for inferring mutual information networks from data. biocViews: Microarray, GraphAndNetwork, Network, NetworkInference Author: Patrick E. Meyer, Frederic Lafitte, Gianluca Bontempi Maintainer: Patrick E. Meyer URL: http://minet.meyerp.com git_url: https://git.bioconductor.org/packages/minet git_branch: RELEASE_3_8 git_last_commit: 92840bd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/minet_3.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/minet_3.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/minet_3.40.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE dependsOnMe: BUS, geNetClassifier, netresponse importsMe: coexnet, epiNEM, netbenchmark, RTN suggestsMe: CNORfeeder, predictionet, TCGAbiolinks Package: minfi Version: 1.28.4 Depends: methods, BiocGenerics (>= 0.15.3), GenomicRanges, SummarizedExperiment (>= 1.1.6), Biostrings, bumphunter (>= 1.1.9) Imports: S4Vectors, GenomeInfoDb, Biobase (>= 2.33.2), IRanges, beanplot, RColorBrewer, lattice, nor1mix, siggenes, limma, preprocessCore, illuminaio (>= 0.23.2), DelayedMatrixStats (>= 1.3.4), mclust, genefilter, nlme, reshape, MASS, quadprog, data.table, GEOquery, stats, grDevices, graphics, utils, DelayedArray (>= 0.7.38), HDF5Array, BiocParallel Suggests: IlluminaHumanMethylation450kmanifest (>= 0.2.0), IlluminaHumanMethylation450kanno.ilmn12.hg19 (>= 0.2.1), minfiData (>= 0.18.0), minfiDataEPIC, FlowSorted.Blood.450k (>= 1.0.1), RUnit, digest, BiocStyle, knitr, rmarkdown, tools License: Artistic-2.0 MD5sum: bfc565f65775349c769b8a96eccb2f8a NeedsCompilation: no Title: Analyze Illumina Infinium DNA methylation arrays Description: Tools to analyze & visualize Illumina Infinium methylation arrays. biocViews: ImmunoOncology, DNAMethylation, DifferentialMethylation, Epigenetics, Microarray, MethylationArray, MultiChannel, TwoChannel, DataImport, Normalization, Preprocessing, QualityControl Author: Kasper Daniel Hansen [cre, aut], Martin Aryee [aut], Rafael A. Irizarry [aut], Andrew E. Jaffe [ctb], Jovana Maksimovic [ctb], E. Andres Houseman [ctb], Jean-Philippe Fortin [ctb], Tim Triche [ctb], Shan V. Andrews [ctb], Peter F. Hickey [ctb] Maintainer: Kasper Daniel Hansen URL: https://github.com/hansenlab/minfi VignetteBuilder: knitr BugReports: https://github.com/hansenlab/minfi/issues git_url: https://git.bioconductor.org/packages/minfi git_branch: RELEASE_3_8 git_last_commit: b5125b2 git_last_commit_date: 2019-03-08 Date/Publication: 2019-03-08 source.ver: src/contrib/minfi_1.28.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/minfi_1.28.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/minfi_1.28.4.tgz vignettes: vignettes/minfi/inst/doc/minfi.html vignetteTitles: minfi User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/minfi/inst/doc/minfi.R dependsOnMe: bigmelon, ChAMP, compartmap, conumee, DMRcate, methylumi, REMP, shinyMethyl importsMe: funtooNorm, MEAL, MethylAid, methylumi, methyvim, missMethyl, quantro, skewr suggestsMe: epivizrChart, Harman, mCSEA, MultiDataSet, RnBeads, sesame Package: MinimumDistance Version: 1.26.0 Depends: R (>= 3.3), VanillaICE (>= 1.31.3) Imports: methods, BiocGenerics, Biobase, S4Vectors (>= 0.9.25), IRanges, GenomeInfoDb, GenomicRanges (>= 1.17.16), SummarizedExperiment (>= 0.2.0), oligoClasses, DNAcopy, ff, foreach, matrixStats, lattice, data.table, grid, stats, utils Suggests: human610quadv1bCrlmm (>= 1.0.3), BSgenome.Hsapiens.UCSC.hg18, BSgenome.Hsapiens.UCSC.hg19, SNPchip, RUnit Enhances: snow, doSNOW License: Artistic-2.0 MD5sum: 94c0e99960d55c5416e88f76a65bc021 NeedsCompilation: no Title: A Package for De Novo CNV Detection in Case-Parent Trios Description: Analysis of de novo copy number variants in trios from high-dimensional genotyping platforms. biocViews: Microarray, SNP, CopyNumberVariation Author: Robert B Scharpf and Ingo Ruczinski Maintainer: Robert B Scharpf git_url: https://git.bioconductor.org/packages/MinimumDistance git_branch: RELEASE_3_8 git_last_commit: a1f0e23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MinimumDistance_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MinimumDistance_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MinimumDistance_1.26.0.tgz vignettes: vignettes/MinimumDistance/inst/doc/MinimumDistance.pdf vignetteTitles: Detection of de novo copy number alterations in case-parent trios hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MinimumDistance/inst/doc/MinimumDistance.R Package: MiPP Version: 1.54.0 Depends: R (>= 2.4) Imports: Biobase, e1071, MASS, stats License: GPL (>= 2) MD5sum: 44dbca699e0c65714e8fa3c1375205c3 NeedsCompilation: no Title: Misclassification Penalized Posterior Classification Description: This package finds optimal sets of genes that seperate samples into two or more classes. biocViews: Microarray, Classification Author: HyungJun Cho , Sukwoo Kim , Mat Soukup , and Jae K. Lee Maintainer: Sukwoo Kim URL: http://www.healthsystem.virginia.edu/internet/hes/biostat/bioinformatics/ git_url: https://git.bioconductor.org/packages/MiPP git_branch: RELEASE_3_8 git_last_commit: 4f52b11 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MiPP_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MiPP_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MiPP_1.54.0.tgz vignettes: vignettes/MiPP/inst/doc/MiPP.pdf vignetteTitles: MiPP Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: MIRA Version: 1.4.1 Depends: R (>= 3.5) Imports: BiocGenerics, S4Vectors, IRanges, GenomicRanges, data.table, ggplot2, Biobase, stats, bsseq, methods Suggests: knitr, parallel, testthat, BiocStyle, rmarkdown, AnnotationHub, LOLA License: GPL-3 MD5sum: 7a0dadc84b811cc05367daaca7373600 NeedsCompilation: no Title: Methylation-Based Inference of Regulatory Activity Description: MIRA measures the degree of "dip" in methylation level surrounding a regulatory site of interest, such as a transcription factor binding site, for instances of that type of site across the genome which can then be used to infer regulatory activity. biocViews: ImmunoOncology, DNAMethylation, GeneRegulation, GenomeAnnotation, SystemsBiology, FunctionalGenomics, ChIPSeq, MethylSeq, Sequencing, Epigenetics, Coverage Author: Nathan Sheffield [aut], Christoph Bock [ctb], John Lawson [aut, cre] Maintainer: John Lawson URL: http://databio.org/mira VignetteBuilder: knitr BugReports: https://github.com/databio/MIRA git_url: https://git.bioconductor.org/packages/MIRA git_branch: RELEASE_3_8 git_last_commit: 1986619 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MIRA_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MIRA_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MIRA_1.4.1.tgz vignettes: vignettes/MIRA/inst/doc/BiologicalApplication.html, vignettes/MIRA/inst/doc/GettingStarted.html vignetteTitles: Applying MIRA to a Biological Question, Getting Started with Methylation-based Inference of Regulatory Activity hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MIRA/inst/doc/BiologicalApplication.R, vignettes/MIRA/inst/doc/GettingStarted.R importsMe: COCOA Package: MiRaGE Version: 1.24.1 Depends: R (>= 3.1.0), Biobase(>= 2.23.3) Imports: BiocGenerics, S4Vectors, AnnotationDbi, BiocManager Suggests: seqinr (>= 3.0.7), biomaRt (>= 2.19.1), GenomicFeatures (>= 1.15.4), Biostrings (>= 2.31.3), BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10, miRNATarget, humanStemCell, IRanges, GenomicRanges (>= 1.8.3), BSgenome, beadarrayExampleData License: GPL MD5sum: 57cf751feeeae25612659e7c98962007 NeedsCompilation: no Title: MiRNA Ranking by Gene Expression Description: The package contains functions for inferece of target gene regulation by miRNA, based on only target gene expression profile. biocViews: ImmunoOncology, Microarray, GeneExpression, RNASeq, Sequencing, SAGE Author: Y-h. Taguchi Maintainer: Y-h. Taguchi git_url: https://git.bioconductor.org/packages/MiRaGE git_branch: RELEASE_3_8 git_last_commit: 2fa16b0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MiRaGE_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MiRaGE_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MiRaGE_1.24.1.tgz vignettes: vignettes/MiRaGE/inst/doc/MiRaGE.pdf vignetteTitles: How to use MiRaGE Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MiRaGE/inst/doc/MiRaGE.R Package: miRBaseConverter Version: 1.6.0 Depends: R (>= 3.4) Imports: stats Suggests: BiocGenerics, RUnit, knitr, rtracklayer, utils License: GPL (>= 2) MD5sum: 4333ef90ec81266289f19a0857a614a5 NeedsCompilation: no Title: A comprehensive and high-efficiency tool for converting and retrieving the information of miRNAs in different miRBase versions Description: A comprehensive tool for converting and retrieving the miRNA Name, Accession, Sequence, Version, History and Family information in different miRBase versions. It can process a huge number of miRNAs in a short time without other depends. biocViews: Software, miRNA Author: Taosheng Xu, Thuc Le Maintainer: Taosheng Xu URL: https://github.com/taoshengxu/miRBaseConverter VignetteBuilder: knitr BugReports: https://github.com/taoshengxu/miRBaseConverter/issues git_url: https://git.bioconductor.org/packages/miRBaseConverter git_branch: RELEASE_3_8 git_last_commit: 5f78e03 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRBaseConverter_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRBaseConverter_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRBaseConverter_1.6.0.tgz vignettes: vignettes/miRBaseConverter/inst/doc/miRBaseConverter-vignette.html vignetteTitles: "miRBaseConverter: A comprehensive and high-efficiency tool for converting and retrieving the information of miRNAs in different miRBase versions" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRBaseConverter/inst/doc/miRBaseConverter-vignette.R Package: miRcomp Version: 1.12.0 Depends: R (>= 3.2), Biobase (>= 2.22.0), miRcompData Imports: utils, methods, graphics, KernSmooth, stats Suggests: BiocStyle, knitr, rmarkdown, RUnit, BiocGenerics, shiny License: GPL-3 | file LICENSE MD5sum: 776c9e34a4c9d963f2588068c8438170 NeedsCompilation: no Title: Tools to assess and compare miRNA expression estimatation methods Description: Based on a large miRNA dilution study, this package provides tools to read in the raw amplification data and use these data to assess the performance of methods that estimate expression from the amplification curves. biocViews: Software, qPCR, Preprocessing, QualityControl Author: Matthew N. McCall , Lauren Kemperman Maintainer: Matthew N. McCall VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/miRcomp git_branch: RELEASE_3_8 git_last_commit: 921c373 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRcomp_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRcomp_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRcomp_1.12.0.tgz vignettes: vignettes/miRcomp/inst/doc/miRcomp.html vignetteTitles: Assessment and comparison of miRNA expression estimation methods (miRcomp) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/miRcomp/inst/doc/miRcomp.R Package: mirIntegrator Version: 1.12.0 Depends: R (>= 3.3) Imports: graph,ROntoTools, ggplot2, org.Hs.eg.db, AnnotationDbi, Rgraphviz Suggests: RUnit, BiocGenerics License: GPL (>=3) MD5sum: c89d486120b4e814ee43c8268a64e7d8 NeedsCompilation: no Title: Integrating microRNA expression into signaling pathways for pathway analysis Description: Tools for augmenting signaling pathways to perform pathway analysis of microRNA and mRNA expression levels. biocViews: Network, Microarray, GraphAndNetwork, Pathways, KEGG Author: Diana Diaz Maintainer: Diana Diaz URL: http://datad.github.io/mirIntegrator/ git_url: https://git.bioconductor.org/packages/mirIntegrator git_branch: RELEASE_3_8 git_last_commit: 52bcdd9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mirIntegrator_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mirIntegrator_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mirIntegrator_1.12.0.tgz vignettes: vignettes/mirIntegrator/inst/doc/mirIntegrator.pdf vignetteTitles: mirIntegrator Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mirIntegrator/inst/doc/mirIntegrator.R Package: miRLAB Version: 1.12.0 Imports: methods, stats, utils, RCurl, httr, stringr, Hmisc, energy, entropy, Roleswitch, gplots, glmnet, impute, limma, pcalg,TCGAbiolinks,dplyr,SummarizedExperiment, ctc, heatmap.plus, InvariantCausalPrediction, Category, GOstats, org.Hs.eg.db Suggests: knitr,BiocGenerics, AnnotationDbi,RUnit License: GPL (>=2) MD5sum: 0ff8f05e5b21897eb8a29bf4f4b93ea9 NeedsCompilation: no Title: Dry lab for exploring miRNA-mRNA relationships Description: Provide tools exploring miRNA-mRNA relationships, including popular miRNA target prediction methods, ensemble methods that integrate individual methods, functions to get data from online resources, functions to validate the results, and functions to conduct enrichment analyses. biocViews: miRNA, GeneExpression, NetworkInference, Network Author: Thuc Duy Le, Junpeng Zhang, Mo Chen, Vu Viet Hoang Pham Maintainer: Thuc Duy Le URL: https://github.com/pvvhoang/miRLAB VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/miRLAB git_branch: RELEASE_3_8 git_last_commit: 662fedd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRLAB_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRLAB_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRLAB_1.12.0.tgz vignettes: vignettes/miRLAB/inst/doc/miRLAB-vignette.html vignetteTitles: miRLAB hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRLAB/inst/doc/miRLAB-vignette.R Package: miRmine Version: 1.4.0 Depends: R (>= 3.4), SummarizedExperiment Suggests: BiocStyle, knitr, rmarkdown, DESeq2 License: GPL (>= 3) MD5sum: 2936f1b79cedb5ec7b30eda3374a3b1a NeedsCompilation: no Title: Data package with miRNA-seq datasets from miRmine database as RangedSummarizedExperiment Description: miRmine database is a collection of expression profiles from different publicly available miRNA-seq datasets, Panwar et al (2017) miRmine: A Database of Human miRNA Expression, prepared with this data package as RangedSummarizedExperiment. biocViews: Homo_sapiens_Data, RNASeqData, SequencingData, ExpressionData Author: Dusan Randjelovic [aut, cre] Maintainer: Dusan Randjelovic VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/miRmine git_branch: RELEASE_3_8 git_last_commit: 2957972 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRmine_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRmine_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRmine_1.4.0.tgz vignettes: vignettes/miRmine/inst/doc/miRmine.html vignetteTitles: miRmine hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRmine/inst/doc/miRmine.R Package: miRNAmeConverter Version: 1.10.0 Depends: miRBaseVersions.db Imports: DBI, AnnotationDbi, reshape2 Suggests: methods, testthat, knitr, rmarkdown License: Artistic-2.0 MD5sum: fe9206b632ea3f12bd7d4d20e7d65db6 NeedsCompilation: no Title: Convert miRNA Names to Different miRBase Versions Description: Translating mature miRNA names to different miRBase versions, sequence retrieval, checking names for validity and detecting miRBase version of a given set of names (data from http://www.mirbase.org/). biocViews: Preprocessing, miRNA Author: Stefan Haunsberger [aut, cre] Maintainer: Stefan J. Haunsberger VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/miRNAmeConverter git_branch: RELEASE_3_8 git_last_commit: 6e2b787 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRNAmeConverter_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRNAmeConverter_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRNAmeConverter_1.10.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: miRNApath Version: 1.42.0 Depends: methods, R(>= 2.7.0) License: LGPL-2.1 MD5sum: a7abdc36034d7ef47f5946a42bf72ff6 NeedsCompilation: no Title: miRNApath: Pathway Enrichment for miRNA Expression Data Description: This package provides pathway enrichment techniques for miRNA expression data. Specifically, the set of methods handles the many-to-many relationship between miRNAs and the multiple genes they are predicted to target (and thus affect.) It also handles the gene-to-pathway relationships separately. Both steps are designed to preserve the additive effects of miRNAs on genes, many miRNAs affecting one gene, one miRNA affecting multiple genes, or many miRNAs affecting many genes. biocViews: Annotation, Pathways, DifferentialExpression, NetworkEnrichment, miRNA Author: James M. Ward with contributions from Yunling Shi, Cindy Richards, John P. Cogswell Maintainer: James M. Ward git_url: https://git.bioconductor.org/packages/miRNApath git_branch: RELEASE_3_8 git_last_commit: 717b31d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRNApath_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRNApath_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRNApath_1.42.0.tgz vignettes: vignettes/miRNApath/inst/doc/miRNApath.pdf vignetteTitles: miRNApath: Pathway Enrichment for miRNA Expression Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRNApath/inst/doc/miRNApath.R Package: miRNAtap Version: 1.16.0 Depends: R (>= 3.3.0), AnnotationDbi Imports: DBI, RSQLite, stringr, sqldf, plyr, methods Suggests: topGO, org.Hs.eg.db, miRNAtap.db, testthat License: GPL-2 MD5sum: a56e2fa7cabbdeba36042c08fab11890 NeedsCompilation: no Title: miRNAtap: microRNA Targets - Aggregated Predictions Description: The package facilitates implementation of workflows requiring miRNA predictions, it allows to integrate ranked miRNA target predictions from multiple sources available online and aggregate them with various methods which improves quality of predictions above any of the single sources. Currently predictions are available for Homo sapiens, Mus musculus and Rattus norvegicus (the last one through homology translation). biocViews: Software, Classification, Microarray, Sequencing, miRNA Author: Maciej Pajak, T. Ian Simpson Maintainer: Maciej Pajak git_url: https://git.bioconductor.org/packages/miRNAtap git_branch: RELEASE_3_8 git_last_commit: d608e02 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRNAtap_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRNAtap_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRNAtap_1.16.0.tgz vignettes: vignettes/miRNAtap/inst/doc/miRNAtap.pdf vignetteTitles: miRNAtap hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRNAtap/inst/doc/miRNAtap.R importsMe: SpidermiR Package: miRSM Version: 1.0.0 Depends: R (>= 3.5.0) Imports: WGCNA, flashClust, dynamicTreeCut, GFA, igraph, linkcomm, MCL, NMF, biclust, runibic, iBBiG, fabia, BicARE, isa2, s4vd, BiBitR, rqubic, Biobase, PMA, stats, miRsponge, Rcpp, utils, SummarizedExperiment, GSEABase Suggests: BiocStyle, knitr, rmarkdown, testthat, org.Hs.eg.db License: GPL-3 Archs: i386, x64 MD5sum: b3a0717a35ca8d1c1edde44aaee7a27c NeedsCompilation: yes Title: Inferring miRNA sponge modules by integrating expression data and miRNA-target binding information Description: The package aims to identify miRNA sponge modules by integrating expression data and miRNA-target binding information. It provides several functions to study miRNA sponge modules, including popular methods for inferring gene modules (candidate miRNA sponge modules), and a function to identify miRNA sponge modules, as well as a function to conduct functional analysis of miRNA sponge modules. biocViews: GeneExpression, BiomedicalInformatics, Clustering, GeneSetEnrichment, Microarray, Software, GeneRegulation, GeneTarget Author: Junpeng Zhang [aut, cre] Maintainer: Junpeng Zhang URL: https://github.com/zhangjunpeng411/miRSM VignetteBuilder: knitr BugReports: https://github.com/zhangjunpeng411/miRSM/issues git_url: https://git.bioconductor.org/packages/miRSM git_branch: RELEASE_3_8 git_last_commit: 54b5bd5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/miRSM_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRSM_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRSM_1.0.0.tgz vignettes: vignettes/miRSM/inst/doc/miRSM.html vignetteTitles: miRSM: inferring miRNA sponge modules by integrating expression data and miRNA-target binding information hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRSM/inst/doc/miRSM.R Package: miRsponge Version: 1.8.2 Depends: R (>= 3.5.0) Imports: corpcor, parallel, igraph, MCL, clusterProfiler, ReactomePA, DOSE, survival, grDevices, graphics, stats, varhandle, linkcomm, utils, org.Hs.eg.db, Rcpp Suggests: BiocStyle, knitr, rmarkdown, testthat License: GPL-3 Archs: i386, x64 MD5sum: 7d00beacf8c16c24bd91d45b017ba570 NeedsCompilation: yes Title: Identification and analysis of miRNA sponge interaction networks and modules Description: The name of the miRsponge package has been changed into "miRspongeR". Future updates will be seen in the miRspongeR package (http://bioconductor.org/packages/miRspongeR/). This package provides several functions to study miRNA sponge (also called ceRNA or miRNA decoy), including popular methods for identifying miRNA sponge interactions, and the integrative method to integrate miRNA sponge interactions from different methods, as well as the functions to validate miRNA sponge interactions, and infer miRNA sponge modules, conduct enrichment analysis of modules, and conduct survival analysis of modules. biocViews: GeneExpression, BiomedicalInformatics, NetworkEnrichment, Survival, Microarray, Software Author: Junpeng Zhang Maintainer: Junpeng Zhang URL: VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/miRsponge git_branch: RELEASE_3_8 git_last_commit: 7f424e3 git_last_commit_date: 2019-03-12 Date/Publication: 2019-03-14 source.ver: src/contrib/miRsponge_1.8.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/miRsponge_1.8.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/miRsponge_1.8.2.tgz vignettes: vignettes/miRsponge/inst/doc/miRsponge.html vignetteTitles: miRsponge: identification and analysis of miRNA sponge interaction networks and modules hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/miRsponge/inst/doc/miRsponge.R importsMe: miRSM Package: Mirsynergy Version: 1.18.0 Depends: R (>= 3.0.2), igraph, ggplot2 Imports: graphics, grDevices, gridExtra, Matrix, parallel, RColorBrewer, reshape, scales, utils Suggests: glmnet, RUnit, BiocGenerics, knitr License: GPL-2 MD5sum: 59cb823d731e6970bc39bbee925bb6f3 NeedsCompilation: no Title: Mirsynergy Description: Detect synergistic miRNA regulatory modules by overlapping neighbourhood expansion. biocViews: Clustering Author: Yue Li Maintainer: Yue Li URL: http://www.cs.utoronto.ca/~yueli/Mirsynergy.html VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Mirsynergy git_branch: RELEASE_3_8 git_last_commit: 2410e04 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Mirsynergy_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Mirsynergy_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Mirsynergy_1.18.0.tgz vignettes: vignettes/Mirsynergy/inst/doc/Mirsynergy.pdf vignetteTitles: Mirsynergy hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Mirsynergy/inst/doc/Mirsynergy.R Package: missMethyl Version: 1.16.0 Depends: R (>= 2.3.0) Imports: limma, minfi, methylumi, IlluminaHumanMethylation450kmanifest, statmod, ruv, stringr, IlluminaHumanMethylation450kanno.ilmn12.hg19, org.Hs.eg.db, AnnotationDbi, BiasedUrn, GO.db, IlluminaHumanMethylationEPICmanifest, IlluminaHumanMethylationEPICanno.ilm10b4.hg19 Suggests: minfiData, BiocStyle, knitr, rmarkdown, edgeR, tweeDEseqCountData License: GPL-2 MD5sum: d18a07d4783273dabcefecbb86ceee77 NeedsCompilation: no Title: Analysing Illumina HumanMethylation BeadChip Data Description: Normalisation and testing for differential variability and differential methylation for data from Illumina's Infinium HumanMethylation450 array. The normalisation procedure is subset-quantile within-array normalisation (SWAN), which allows Infinium I and II type probes on a single array to be normalised together. The test for differential variability is based on an empirical Bayes version of Levene's test. Differential methylation testing is performed using RUV, which can adjust for systematic errors of unknown origin in high-dimensional data by using negative control probes. Gene ontology analysis is performed by taking into account the number of probes per gene on the array. biocViews: Normalization, DNAMethylation, MethylationArray, GenomicVariation, GeneticVariability, DifferentialMethylation, GeneSetEnrichment Author: Belinda Phipson and Jovana Maksimovic Maintainer: Belinda Phipson , Jovana Maksimovic , Andrew Lonsdale VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/missMethyl git_branch: RELEASE_3_8 git_last_commit: de46e07 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/missMethyl_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/missMethyl_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/missMethyl_1.16.0.tgz vignettes: vignettes/missMethyl/inst/doc/missMethyl.html vignetteTitles: missMethyl: Analysing Illumina HumanMethylation BeadChip Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/missMethyl/inst/doc/missMethyl.R importsMe: DMRcate, MEAL, methylGSA suggestsMe: RnBeads Package: missRows Version: 1.2.0 Depends: R (>= 3.5), methods, ggplot2, grDevices, MultiAssayExperiment Imports: plyr, stats, gtools, S4Vectors Suggests: BiocStyle, knitr, testthat License: Artistic-2.0 MD5sum: ffdf5f3c103e7749bacded4b44aa7762 NeedsCompilation: no Title: Handling Missing Individuals in Multi-Omics Data Integration Description: The missRows package implements the MI-MFA method to deal with missing individuals ('biological units') in multi-omics data integration. The MI-MFA method generates multiple imputed datasets from a Multiple Factor Analysis model, then the yield results are combined in a single consensus solution. The package provides functions for estimating coordinates of individuals and variables, imputing missing individuals, and various diagnostic plots to inspect the pattern of missingness and visualize the uncertainty due to missing values. biocViews: Software, StatisticalMethod, DimensionReduction, PrincipalComponent, MathematicalBiology, Visualization Author: Ignacio Gonzalez and Valentin Voillet Maintainer: Gonzalez Ignacio VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/missRows git_branch: RELEASE_3_8 git_last_commit: eec8082 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/missRows_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/missRows_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/missRows_1.2.0.tgz vignettes: vignettes/missRows/inst/doc/missRows.pdf vignetteTitles: missRows hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/missRows/inst/doc/missRows.R Package: mitoODE Version: 1.20.1 Depends: R (>= 2.14.0), minpack.lm, MASS, parallel, mitoODEdata, KernSmooth License: LGPL Archs: i386, x64 MD5sum: bae4fa58550a6de1e57956d17cb69ffb NeedsCompilation: yes Title: Implementation of the differential equation model described in "Dynamical modelling of phenotypes in a genome-wide RNAi live-cell imaging assay" Description: The package contains the methods to fit a cell-cycle model on cell count data and the code to reproduce the results shown in our paper "Dynamical modelling of phenotypes in a genome-wide RNAi live-cell imaging assay" by Pau, G., Walter, T., Neumann, B., Heriche, J.-K., Ellenberg, J., & Huber, W., BMC Bioinformatics (2013), 14(1), 308. doi:10.1186/1471-2105-14-308 biocViews: ImmunoOncology, ExperimentData, TimeCourse, CellBasedAssays, Preprocessing Author: Gregoire Pau Maintainer: Gregoire Pau SystemRequirements: git_url: https://git.bioconductor.org/packages/mitoODE git_branch: RELEASE_3_8 git_last_commit: 60b8815 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/mitoODE_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/mitoODE_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mitoODE_1.20.1.tgz vignettes: vignettes/mitoODE/inst/doc/mitoODE-introduction.pdf vignetteTitles: mitoODE hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mitoODE/inst/doc/mitoODE-introduction.R Package: mixOmics Version: 6.6.2 Depends: R (>= 3.5.0), MASS, lattice, ggplot2 Imports: igraph, ellipse, corpcor, RColorBrewer, parallel, dplyr, tidyr, reshape2, methods, matrixStats, rARPACK, gridExtra, grDevices, graphics, stats, utils Suggests: BiocStyle, knitr, rmarkdown, testthat, rgl License: GPL (>= 2) MD5sum: c9f7b5e91dad9dba4d0dc39da5dea927 NeedsCompilation: no Title: Omics Data Integration Project Description: Multivariate methods are well suited to large omics data sets where the number of variables (e.g. genes, proteins, metabolites) is much larger than the number of samples (patients, cells, mice). They have the appealing properties of reducing the dimension of the data by using instrumental variables (components), which are defined as combinations of all variables. Those components are then used to produce useful graphical outputs that enable better understanding of the relationships and correlation structures between the different data sets that are integrated. mixOmics offers a wide range of multivariate methods for the exploration and integration of biological datasets with a particular focus on variable selection. The package proposes several sparse multivariate models we have developed to identify the key variables that are highly correlated, and/or explain the biological outcome of interest. The data that can be analysed with mixOmics may come from high throughput sequencing technologies, such as omics data (transcriptomics, metabolomics, proteomics, metagenomics etc) but also beyond the realm of omics (e.g. spectral imaging). The methods implemented in mixOmics can also handle missing values without having to delete entire rows with missing data. A non exhaustive list of methods include variants of generalised Canonical Correlation Analysis, sparse Partial Least Squares and sparse Discriminant Analysis. Recently we implemented integrative methods to combine multiple data sets: N-integration with variants of Generalised Canonical Correlation Analysis and P-integration with variants of multi-group Partial Least Squares. biocViews: ImmunoOncology, Microarray, Sequencing, Metabolomics, Metagenomics, Proteomics, GenePrediction, MultipleComparison, Classification, Regression Author: Kim-Anh Le Cao, Florian Rohart, Ignacio Gonzalez, Sebastien Dejean with key contributors Benoit Gautier, Francois Bartolo and contributions from Pierre Monget, Jeff Coquery, FangZou Yao, Benoit Liquet. Maintainer: Kim-Anh Le Cao URL: http://www.mixOmics.org VignetteBuilder: knitr BugReports: https://bitbucket.org/klecao/package-mixomics/issues git_url: https://git.bioconductor.org/packages/mixOmics git_branch: RELEASE_3_8 git_last_commit: 240e862 git_last_commit_date: 2019-02-28 Date/Publication: 2019-03-01 source.ver: src/contrib/mixOmics_6.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/mixOmics_6.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mixOmics_6.6.2.tgz vignettes: vignettes/mixOmics/inst/doc/vignette.html vignetteTitles: mixOmics hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mixOmics/inst/doc/vignette.R dependsOnMe: compartmap Package: MLInterfaces Version: 1.62.1 Depends: R (>= 3.5), methods, BiocGenerics (>= 0.13.11), Biobase, annotate, cluster Imports: gdata, pls, sfsmisc, MASS, rpart, rda, genefilter, fpc, ggvis, shiny, gbm, RColorBrewer, hwriter, threejs (>= 0.2.2), mlbench, stats4, tools, grDevices, graphics, stats Suggests: class, e1071, ipred, randomForest, gpls, pamr, nnet, ALL, hgu95av2.db, som, hu6800.db, lattice, caret (>= 5.07), golubEsets, ada, keggorthology, kernlab, mboost, party Enhances: parallel License: LGPL MD5sum: 751c752a35d08edb6bf44155cbb2e0b0 NeedsCompilation: no Title: Uniform interfaces to R machine learning procedures for data in Bioconductor containers Description: This package provides uniform interfaces to machine learning code for data in R and Bioconductor containers. biocViews: Classification, Clustering Author: Vince Carey , Robert Gentleman, Jess Mar, and contributions from Jason Vertrees and Laurent Gatto Maintainer: V. Carey git_url: https://git.bioconductor.org/packages/MLInterfaces git_branch: RELEASE_3_8 git_last_commit: 6cf59a9 git_last_commit_date: 2019-04-03 Date/Publication: 2019-04-03 source.ver: src/contrib/MLInterfaces_1.62.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MLInterfaces_1.62.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MLInterfaces_1.62.1.tgz vignettes: vignettes/MLInterfaces/inst/doc/MLint_devel.pdf, vignettes/MLInterfaces/inst/doc/MLInterfaces.pdf, vignettes/MLInterfaces/inst/doc/MLprac2_2.pdf, vignettes/MLInterfaces/inst/doc/xvalComputerClusters.pdf vignetteTitles: MLInterfaces devel for schema-based MLearn, MLInterfaces Primer, A machine learning tutorial: applications of the Bioconductor MLInterfaces package to expression and ChIP-Seq data, MLInterfaces Computer Cluster hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MLInterfaces/inst/doc/MLint_devel.R, vignettes/MLInterfaces/inst/doc/MLInterfaces.R, vignettes/MLInterfaces/inst/doc/MLprac2_2.R, vignettes/MLInterfaces/inst/doc/xvalComputerClusters.R dependsOnMe: a4Classif, pRoloc, SigCheck suggestsMe: BiocCaseStudies Package: MLP Version: 1.30.0 Depends: AnnotationDbi, affy, plotrix, gplots, gmodels, gdata, gtools Suggests: GO.db, org.Hs.eg.db, org.Mm.eg.db, org.Rn.eg.db, org.Cf.eg.db, KEGG.db, annotate, Rgraphviz, GOstats, limma, mouse4302.db, reactome.db License: GPL-3 Archs: i386, x64 MD5sum: aa60c8428853779c635788ea6e600255 NeedsCompilation: no Title: MLP Description: Mean Log P Analysis biocViews: Genetics, Reactome, KEGG Author: Nandini Raghavan, Tobias Verbeke, An De Bondt with contributions by Javier Cabrera, Dhammika Amaratunga, Tine Casneuf and Willem Ligtenberg Maintainer: Tobias Verbeke git_url: https://git.bioconductor.org/packages/MLP git_branch: RELEASE_3_8 git_last_commit: f48b881 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MLP_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MLP_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MLP_1.30.0.tgz vignettes: vignettes/MLP/inst/doc/UsingMLP.pdf vignetteTitles: UsingMLP hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MLP/inst/doc/UsingMLP.R importsMe: esetVis suggestsMe: a4 Package: MLSeq Version: 2.0.1 Depends: caret, ggplot2 Imports: methods, DESeq2, edgeR, limma, Biobase, SummarizedExperiment, plyr, foreach, utils, sSeq, xtable Suggests: knitr, testthat, BiocStyle, VennDiagram, pamr License: GPL(>=2) MD5sum: c2bf959b54354af9048166692b8522bd NeedsCompilation: no Title: Machine Learning Interface for RNA-Seq Data Description: This package applies several machine learning methods, including SVM, bagSVM, Random Forest and CART to RNA-Seq data. biocViews: ImmunoOncology, Sequencing, RNASeq, Classification, Clustering Author: Gokmen Zararsiz, Dincer Goksuluk, Selcuk Korkmaz, Vahap Eldem, Izzet Parug Duru, Ahmet Ozturk, Ahmet Ergun Karaagaoglu Maintainer: Gokmen Zararsiz VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MLSeq git_branch: RELEASE_3_8 git_last_commit: 2b99386 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MLSeq_2.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MLSeq_2.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MLSeq_2.0.1.tgz vignettes: vignettes/MLSeq/inst/doc/MLSeq.pdf vignetteTitles: Beginner's guide to the "MLSeq" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MLSeq/inst/doc/MLSeq.R importsMe: GARS Package: MMDiff2 Version: 1.10.0 Depends: R (>= 3.3), Rsamtools, Biobase, Imports: GenomicRanges, locfit, BSgenome, Biostrings, shiny, ggplot2, RColorBrewer, graphics, grDevices, parallel, S4Vectors, methods Suggests: MMDiffBamSubset, MotifDb, knitr, BiocStyle, BSgenome.Mmusculus.UCSC.mm9 License: Artistic-2.0 MD5sum: e13ca07c7dea4123eb3cb08be914edef NeedsCompilation: no Title: Statistical Testing for ChIP-Seq data sets Description: This package detects statistically significant differences between read enrichment profiles in different ChIP-Seq samples. To take advantage of shape differences it uses Kernel methods (Maximum Mean Discrepancy, MMD). biocViews: ChIPSeq, DifferentialPeakCalling, Sequencing, Software Author: Gabriele Schweikert [cre, aut], David Kuo [aut] Maintainer: Gabriele Schweikert VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MMDiff2 git_branch: RELEASE_3_8 git_last_commit: df22203 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MMDiff2_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MMDiff2_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MMDiff2_1.10.0.tgz vignettes: vignettes/MMDiff2/inst/doc/MMDiff2.pdf vignetteTitles: An Introduction to the MMDiff2 method hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MMDiff2/inst/doc/MMDiff2.R Package: MmPalateMiRNA Version: 1.32.0 Depends: R (>= 2.13.0), methods, Biobase, xtable, limma, statmod, lattice, vsn Imports: limma, lattice, Biobase Suggests: GOstats, graph, Category, org.Mm.eg.db, microRNA, targetscan.Mm.eg.db, RSQLite, DBI, AnnotationDbi, clValid, class, cluster, multtest, RColorBrewer, latticeExtra License: GPL-3 MD5sum: f4d32e709429b59908cea3fd1ef9e70b NeedsCompilation: no Title: Murine Palate miRNA Expression Analysis Description: R package compendium for the analysis of murine palate miRNA two-color expression data. biocViews: Microarray, TwoChannel, QualityControl, Preprocessing, DifferentialExpression, MultipleComparison, Clustering, GO, Pathways, ReportWriting, SequenceMatching Author: Guy Brock , Partha Mukhopadhyay , Vasyl Pihur , Robert M. Greene , and M. Michele Pisano Maintainer: Guy Brock git_url: https://git.bioconductor.org/packages/MmPalateMiRNA git_branch: RELEASE_3_8 git_last_commit: c7088b6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MmPalateMiRNA_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MmPalateMiRNA_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MmPalateMiRNA_1.32.0.tgz vignettes: vignettes/MmPalateMiRNA/inst/doc/MmPalateMiRNA.pdf vignetteTitles: Palate miRNA Analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MmPalateMiRNA/inst/doc/MmPalateMiRNA.R Package: MODA Version: 1.8.0 Depends: R (>= 3.3) Imports: grDevices, graphics, stats, utils, WGCNA, dynamicTreeCut, igraph, cluster, AMOUNTAIN, RColorBrewer Suggests: BiocStyle, knitr, rmarkdown License: GPL (>= 2) MD5sum: 50ed2605dabd7656e45804206fcafc6f NeedsCompilation: no Title: MODA: MOdule Differential Analysis for weighted gene co-expression network Description: MODA can be used to estimate and construct condition-specific gene co-expression networks, and identify differentially expressed subnetworks as conserved or condition specific modules which are potentially associated with relevant biological processes. biocViews: GeneExpression, Microarray, DifferentialExpression, Network Author: Dong Li, James B. Brown, Luisa Orsini, Zhisong Pan, Guyu Hu and Shan He Maintainer: Dong Li git_url: https://git.bioconductor.org/packages/MODA git_branch: RELEASE_3_8 git_last_commit: 61bf4fb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MODA_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MODA_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MODA_1.8.0.tgz vignettes: vignettes/MODA/inst/doc/MODA.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: mogsa Version: 1.16.0 Depends: R (>= 3.2.0) Imports: methods, graphite, genefilter, BiocGenerics, gplots, GSEABase, Biobase, parallel, corpcor, svd, cluster Suggests: BiocStyle, knitr License: GPL-2 MD5sum: 8cf09a49ac7d52e667f40ab2e5d2922c NeedsCompilation: no Title: Multiple omics data integrative clustering and gene set analysis Description: This package provide a method for doing gene set analysis based on multiple omics data. biocViews: GeneExpression, PrincipalComponent, StatisticalMethod, Clustering, Software Author: Chen Meng Maintainer: Chen Meng VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mogsa git_branch: RELEASE_3_8 git_last_commit: 322a78f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mogsa_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mogsa_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mogsa_1.16.0.tgz vignettes: vignettes/mogsa/inst/doc/moCluster-knitr.pdf, vignettes/mogsa/inst/doc/mogsa-knitr.pdf vignetteTitles: mogsa: gene set analysis on multiple omics data, mogsa: gene set analysis on multiple omics data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mogsa/inst/doc/moCluster-knitr.R, vignettes/mogsa/inst/doc/mogsa-knitr.R Package: monocle Version: 2.10.1 Depends: R (>= 2.10.0), methods, Matrix (>= 1.2-6), Biobase, ggplot2 (>= 1.0.0), VGAM (>= 1.0-6), DDRTree (>= 0.1.4), Imports: parallel, igraph (>= 1.0.1), BiocGenerics, HSMMSingleCell (>= 0.101.5), plyr, cluster, combinat, fastICA, grid, irlba (>= 2.0.0), matrixStats, densityClust (>= 0.3), Rtsne, MASS, reshape2, limma, tibble, dplyr, qlcMatrix, pheatmap, stringr, proxy, slam, viridis, stats, biocViews, RANN(>= 2.5), Rcpp (>= 0.12.0) LinkingTo: Rcpp Suggests: destiny, Hmisc, knitr, Seurat, scater, testthat License: Artistic-2.0 MD5sum: c3b731e246cf7458e056039f63424cfc NeedsCompilation: yes Title: Clustering, differential expression, and trajectory analysis for single- cell RNA-Seq Description: Monocle performs differential expression and time-series analysis for single-cell expression experiments. It orders individual cells according to progress through a biological process, without knowing ahead of time which genes define progress through that process. Monocle also performs differential expression analysis, clustering, visualization, and other useful tasks on single cell expression data. It is designed to work with RNA-Seq and qPCR data, but could be used with other types as well. biocViews: ImmunoOncology, Sequencing, RNASeq, GeneExpression, DifferentialExpression, Infrastructure, DataImport, DataRepresentation, Visualization, Clustering, MultipleComparison, QualityControl Author: Cole Trapnell Maintainer: Cole Trapnell VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/monocle git_branch: RELEASE_3_8 git_last_commit: 2a006cf git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/monocle_2.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/monocle_2.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/monocle_2.10.1.tgz vignettes: vignettes/monocle/inst/doc/monocle-vignette.pdf vignetteTitles: Monocle: Cell counting,, differential expression,, and trajectory analysis for single-cell RNA-Seq experiments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/monocle/inst/doc/monocle-vignette.R dependsOnMe: cicero importsMe: uSORT suggestsMe: condcomp, scater, scran, sincell Package: MoonlightR Version: 1.8.0 Depends: R (>= 3.3), doParallel, foreach Imports: parmigene, randomForest, SummarizedExperiment, gplots, circlize, RColorBrewer, HiveR, clusterProfiler, DOSE, Biobase, limma, grDevices, graphics, TCGAbiolinks, GEOquery, stats, RISmed, grid, utils Suggests: BiocStyle, knitr, rmarkdown, testthat, devtools, roxygen2, png License: GPL (>= 3) Archs: i386, x64 MD5sum: ee7e9a7914dd2f526db0f189785be525 NeedsCompilation: no Title: Identify oncogenes and tumor suppressor genes from omics data Description: Motivation: The understanding of cancer mechanism requires the identification of genes playing a role in the development of the pathology and the characterization of their role (notably oncogenes and tumor suppressors). Results: We present an R/bioconductor package called MoonlightR which returns a list of candidate driver genes for specific cancer types on the basis of TCGA expression data. The method first infers gene regulatory networks and then carries out a functional enrichment analysis (FEA) (implementing an upstream regulator analysis, URA) to score the importance of well-known biological processes with respect to the studied cancer type. Eventually, by means of random forests, MoonlightR predicts two specific roles for the candidate driver genes: i) tumor suppressor genes (TSGs) and ii) oncogenes (OCGs). As a consequence, this methodology does not only identify genes playing a dual role (e.g. TSG in one cancer type and OCG in another) but also helps in elucidating the biological processes underlying their specific roles. In particular, MoonlightR can be used to discover OCGs and TSGs in the same cancer type. This may help in answering the question whether some genes change role between early stages (I, II) and late stages (III, IV) in breast cancer. In the future, this analysis could be useful to determine the causes of different resistances to chemotherapeutic treatments. biocViews: DNAMethylation, DifferentialMethylation, GeneRegulation, GeneExpression, MethylationArray, DifferentialExpression, Pathways, Network, Survival, GeneSetEnrichment, NetworkEnrichment Author: Antonio Colaprico*, Catharina Olsen*, Claudia Cava, Thilde Terkelsen, Laura Cantini, Andre Olsen, Gloria Bertoli, Andrei Zinovyev, Emmanuel Barillot, Isabella Castiglioni, Elena Papaleo, Gianluca Bontempi Maintainer: Antonio Colaprico , Catharina Olsen URL: https://github.com/torongs82/Moonlight VignetteBuilder: knitr BugReports: https://github.com/torongs82/Moonlight/issues git_url: https://git.bioconductor.org/packages/MoonlightR git_branch: RELEASE_3_8 git_last_commit: 5a26351 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-09 source.ver: src/contrib/MoonlightR_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MoonlightR_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MoonlightR_1.8.0.tgz vignettes: vignettes/MoonlightR/inst/doc/Moonlight.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MoonlightR/inst/doc/Moonlight.R Package: MoPS Version: 1.16.0 Imports: Biobase License: GPL-3 MD5sum: 45c3777290bc95c462428fcc28aa18e0 NeedsCompilation: no Title: MoPS - Model-based Periodicity Screening Description: Identification and characterization of periodic fluctuations in time-series data. biocViews: GeneRegulation,Classification,TimeCourse,Regression Author: Philipp Eser, Achim Tresch Maintainer: Philipp Eser git_url: https://git.bioconductor.org/packages/MoPS git_branch: RELEASE_3_8 git_last_commit: e9c74ec git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MoPS_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MoPS_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MoPS_1.16.0.tgz vignettes: vignettes/MoPS/inst/doc/MoPS.pdf vignetteTitles: Model-based Periodicity Screening hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MoPS/inst/doc/MoPS.R Package: mosaics Version: 2.20.0 Depends: R (>= 3.0.0), methods, graphics, Rcpp Imports: MASS, splines, lattice, IRanges, GenomicRanges, GenomicAlignments, Rsamtools, GenomeInfoDb, S4Vectors LinkingTo: Rcpp Suggests: mosaicsExample Enhances: parallel License: GPL (>= 2) MD5sum: 9e40d17d91730001365219582cd223fc NeedsCompilation: yes Title: MOSAiCS (MOdel-based one and two Sample Analysis and Inference for ChIP-Seq) Description: This package provides functions for fitting MOSAiCS and MOSAiCS-HMM, a statistical framework to analyze one-sample or two-sample ChIP-seq data of transcription factor binding and histone modification. biocViews: ChIPseq, Sequencing, Transcription, Genetics, Bioinformatics Author: Dongjun Chung, Pei Fen Kuan, Rene Welch, Sunduz Keles Maintainer: Dongjun Chung URL: http://groups.google.com/group/mosaics_user_group SystemRequirements: Perl git_url: https://git.bioconductor.org/packages/mosaics git_branch: RELEASE_3_8 git_last_commit: 056f67c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mosaics_2.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mosaics_2.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mosaics_2.20.0.tgz vignettes: vignettes/mosaics/inst/doc/mosaics-example.pdf vignetteTitles: MOSAiCS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mosaics/inst/doc/mosaics-example.R Package: motifbreakR Version: 1.12.0 Depends: R (>= 3.2), grid, MotifDb Imports: methods, compiler, grDevices, grImport, stringr, BiocGenerics, S4Vectors (>= 0.9.25), IRanges, GenomeInfoDb, GenomicRanges, Biostrings, BSgenome, rtracklayer, VariantAnnotation, BiocParallel, motifStack, Gviz, matrixStats, TFMPvalue Suggests: BSgenome.Hsapiens.UCSC.hg19, SNPlocs.Hsapiens.dbSNP.20120608, SNPlocs.Hsapiens.dbSNP142.GRCh37, knitr, rmarkdown, BSgenome.Drerio.UCSC.danRer7, BiocStyle License: GPL-2 Archs: i386, x64 MD5sum: f4acb1d102a78b4ca2bb951366e5cace NeedsCompilation: no Title: A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites Description: We introduce motifbreakR, which allows the biologist to judge in the first place whether the sequence surrounding the polymorphism is a good match, and in the second place how much information is gained or lost in one allele of the polymorphism relative to another. MotifbreakR is both flexible and extensible over previous offerings; giving a choice of algorithms for interrogation of genomes with motifs from public sources that users can choose from; these are 1) a weighted-sum probability matrix, 2) log-probabilities, and 3) weighted by relative entropy. MotifbreakR can predict effects for novel or previously described variants in public databases, making it suitable for tasks beyond the scope of its original design. Lastly, it can be used to interrogate any genome curated within Bioconductor (currently there are 22). biocViews: ChIPSeq, Visualization, MotifAnnotation Author: Simon Gert Coetzee [aut, cre] Dennis J. Hazelett [aut] Maintainer: Simon Gert Coetzee VignetteBuilder: knitr BugReports: https://github.com/Simon-Coetzee/motifbreakR/issues git_url: https://git.bioconductor.org/packages/motifbreakR git_branch: RELEASE_3_8 git_last_commit: c35ebfb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/motifbreakR_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/motifbreakR_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/motifbreakR_1.12.0.tgz vignettes: vignettes/motifbreakR/inst/doc/motifbreakR-vignette.html vignetteTitles: motifbreakR: an Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/motifbreakR/inst/doc/motifbreakR-vignette.R suggestsMe: universalmotif Package: motifcounter Version: 1.6.0 Depends: R(>= 3.0) Imports: Biostrings, methods Suggests: knitr, rmarkdown, testthat, MotifDb, seqLogo, prettydoc License: GPL-2 MD5sum: 17980f892c118972ea93583cd449328d NeedsCompilation: yes Title: R package for analysing TFBSs in DNA sequences Description: 'motifcounter' provides motif matching, motif counting and motif enrichment functionality based on position frequency matrices. The main features of the packages include the utilization of higher-order background models and accounting for self-overlapping motif matches when determining motif enrichment. The background model allows to capture dinucleotide (or higher-order nucleotide) composition adequately which may reduced model biases and misleading results compared to using simple GC background models. When conducting a motif enrichment analysis based on the motif match count, the package relies on a compound Poisson distribution or alternatively a combinatorial model. These distribution account for self-overlapping motif structures as exemplified by repeat-like or palindromic motifs, and allow to determine the p-value and fold-enrichment for a set of observed motif matches. biocViews: Transcription,MotifAnnotation,SequenceMatching,Software Author: Wolfgang Kopp [aut, cre] Maintainer: Wolfgang Kopp VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/motifcounter git_branch: RELEASE_3_8 git_last_commit: a7d2a37 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/motifcounter_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/motifcounter_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/motifcounter_1.6.0.tgz vignettes: vignettes/motifcounter/inst/doc/motifcounter.html vignetteTitles: Introduction to the `motifcounter` package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/motifcounter/inst/doc/motifcounter.R suggestsMe: universalmotif Package: MotifDb Version: 1.24.1 Depends: R (>= 3.5.0), methods, BiocGenerics, S4Vectors, IRanges, Biostrings Imports: rtracklayer, splitstackshape Suggests: RUnit License: Artistic-2.0 | file LICENSE License_is_FOSS: no License_restricts_use: yes Archs: i386, x64 MD5sum: 0e4f0a765443f27fa97aa8c26ba18331 NeedsCompilation: no Title: An Annotated Collection of Protein-DNA Binding Sequence Motifs Description: More than 9900 annotated position frequency matrices from 14 public sources, for multiple organisms. biocViews: MotifAnnotation Author: Paul Shannon, Matt Richards Maintainer: Paul Shannon git_url: https://git.bioconductor.org/packages/MotifDb git_branch: RELEASE_3_8 git_last_commit: db0caa6 git_last_commit_date: 2018-11-06 Date/Publication: 2018-11-06 source.ver: src/contrib/MotifDb_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MotifDb_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MotifDb_1.24.1.tgz vignettes: vignettes/MotifDb/inst/doc/MotifDb.pdf vignetteTitles: %%MotifDb Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MotifDb/inst/doc/MotifDb.R dependsOnMe: motifbreakR, trena importsMe: rTRMui suggestsMe: ATACseqQC, DiffLogo, MMDiff2, motifcounter, motifStack, profileScoreDist, PWMEnrich, rTRM, universalmotif, vtpnet Package: motifmatchr Version: 1.4.0 Depends: R (>= 3.3) Imports: Matrix, Rcpp, methods, TFBSTools, Biostrings, BSgenome, S4Vectors, SummarizedExperiment, GenomicRanges, IRanges, Rsamtools, GenomeInfoDb LinkingTo: Rcpp, RcppArmadillo Suggests: testthat, knitr, rmarkdown, BSgenome.Hsapiens.UCSC.hg19 License: GPL-3 + file LICENSE MD5sum: 81b108d831a4e6084991dadd868f779a NeedsCompilation: yes Title: Fast Motif Matching in R Description: Quickly find motif matches for many motifs and many sequences. Wraps C++ code from the MOODS motif calling library, which was developed by Pasi Rastas, Janne Korhonen, and Petri Martinmäki. biocViews: MotifAnnotation Author: Alicia Schep [aut, cre], Stanford University [cph] Maintainer: Alicia Schep SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/motifmatchr git_branch: RELEASE_3_8 git_last_commit: 3761e63 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/motifmatchr_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/motifmatchr_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/motifmatchr_1.4.0.tgz vignettes: vignettes/motifmatchr/inst/doc/motifmatchr.html vignetteTitles: motifmatchr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/motifmatchr/inst/doc/motifmatchr.R importsMe: esATAC suggestsMe: chromVAR Package: motifRG Version: 1.26.0 Depends: R (>= 2.15), Biostrings (>= 2.26), IRanges, seqLogo, parallel, methods, grid, graphics, BSgenome, XVector, BSgenome.Hsapiens.UCSC.hg19 Imports: Biostrings,IRanges,seqLogo,parallel,methods,grid,graphics,XVector License: Artistic-2.0 Archs: i386, x64 MD5sum: 6e6636d8724438f812dd372a28196722 NeedsCompilation: no Title: A package for discriminative motif discovery, designed for high throughput sequencing dataset Description: Tools for discriminative motif discovery using regression methods biocViews: Transcription,MotifDiscovery Author: Zizhen Yao Maintainer: Zizhen Yao git_url: https://git.bioconductor.org/packages/motifRG git_branch: RELEASE_3_8 git_last_commit: d008089 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/motifRG_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/motifRG_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/motifRG_1.26.0.tgz vignettes: vignettes/motifRG/inst/doc/motifRG.pdf vignetteTitles: motifRG: regression-based discriminative motif discovery hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/motifRG/inst/doc/motifRG.R dependsOnMe: RCAS suggestsMe: universalmotif Package: motifStack Version: 1.26.0 Depends: R (>= 2.15.1), methods, grImport, grid, MotIV, ade4, Biostrings Imports: XML, scales, htmlwidgets,grDevices, stats, stats4, graphics, utils Suggests: RUnit, BiocGenerics, MotifDb, RColorBrewer, BiocStyle, knitr License: GPL (>= 2) MD5sum: 1ae29bba676e9d9f4d6c43430266946d NeedsCompilation: no Title: Plot stacked logos for single or multiple DNA, RNA and amino acid sequence Description: The motifStack package is designed for graphic representation of multiple motifs with different similarity scores. It works with both DNA/RNA sequence motif and amino acid sequence motif. In addition, it provides the flexibility for users to customize the graphic parameters such as the font type and symbol colors. biocViews: SequenceMatching, Visualization, Sequencing, Microarray, Alignment, ChIPchip, ChIPSeq, MotifAnnotation, DataImport Author: Jianhong Ou, Michael Brodsky, Scot Wolfe and Lihua Julie Zhu Maintainer: Jianhong Ou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/motifStack git_branch: RELEASE_3_8 git_last_commit: 04a10c3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/motifStack_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/motifStack_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/motifStack_1.26.0.tgz vignettes: vignettes/motifStack/inst/doc/motifStack_HTML.html vignetteTitles: motifStack Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/motifStack/inst/doc/motifStack_HTML.R dependsOnMe: dagLogo importsMe: ATACseqQC, LowMACA, motifbreakR suggestsMe: ChIPpeakAnno, universalmotif Package: MotIV Version: 1.38.0 Depends: R (>= 2.10), BiocGenerics (>= 0.1.0) Imports: graphics, grid, methods, S4Vectors, IRanges (>= 1.13.5), Biostrings (>= 1.24.0), lattice, rGADEM, utils Suggests: rtracklayer License: GPL-2 MD5sum: 513e9e6da9a911fc4d5b23c48b06c5d2 NeedsCompilation: yes Title: Motif Identification and Validation Description: This package makes use of STAMP for comparing a set of motifs to a given database (e.g. JASPAR). It can also be used to visualize motifs, motif distributions, modules and filter motifs. biocViews: Microarray, ChIPchip, ChIPSeq, GenomicSequence, MotifAnnotation Author: Eloi Mercier, Raphael Gottardo Maintainer: Eloi Mercier , Raphael Gottardo SystemRequirements: GNU Scientific Library >= 1.6 (http://www.gnu.org/software/gsl/) git_url: https://git.bioconductor.org/packages/MotIV git_branch: RELEASE_3_8 git_last_commit: f1c999d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MotIV_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MotIV_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MotIV_1.38.0.tgz vignettes: vignettes/MotIV/inst/doc/MotIV.pdf vignetteTitles: The MotIV users guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MotIV/inst/doc/MotIV.R dependsOnMe: motifStack suggestsMe: universalmotif Package: MPFE Version: 1.18.0 License: GPL (>= 3) Archs: i386, x64 MD5sum: 92ff1513ce4265b001b14cf66c945c7d NeedsCompilation: no Title: Estimation of the amplicon methylation pattern distribution from bisulphite sequencing data Description: Estimate distribution of methylation patterns from a table of counts from a bisulphite sequencing experiment given a non-conversion rate and read error rate. biocViews: HighThroughputSequencingData, DNAMethylation, MethylSeq Author: Peijie Lin, Sylvain Foret, Conrad Burden Maintainer: Conrad Burden git_url: https://git.bioconductor.org/packages/MPFE git_branch: RELEASE_3_8 git_last_commit: de27e95 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MPFE_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MPFE_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MPFE_1.18.0.tgz vignettes: vignettes/MPFE/inst/doc/MPFE.pdf vignetteTitles: MPFE hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MPFE/inst/doc/MPFE.R Package: mpra Version: 1.4.1 Depends: R (>= 3.4.0), methods, BiocGenerics, SummarizedExperiment, limma Imports: S4Vectors, scales, stats, graphics, statmod Suggests: BiocStyle, knitr, rmarkdown, RUnit License: Artistic-2.0 MD5sum: b0422b285ab02e09f2f90544ce57a1d9 NeedsCompilation: no Title: Analyze massively parallel reporter assays Description: Tools for data management, count preprocessing, and differential analysis in massively parallel report assays (MPRA). biocViews: Software, GeneRegulation, Sequencing, FunctionalGenomics Author: Leslie Myint [cre, aut], Kasper D. Hansen [aut] Maintainer: Leslie Myint URL: https://github.com/hansenlab/mpra VignetteBuilder: knitr BugReports: https://github.com/hansenlab/mpra/issues git_url: https://git.bioconductor.org/packages/mpra git_branch: RELEASE_3_8 git_last_commit: 7d1ed91 git_last_commit_date: 2018-12-01 Date/Publication: 2018-12-01 source.ver: src/contrib/mpra_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/mpra_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mpra_1.4.1.tgz vignettes: vignettes/mpra/inst/doc/mpra.html vignetteTitles: mpra User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mpra/inst/doc/mpra.R Package: MPRAnalyze Version: 1.0.1 Imports: BiocParallel, methods, progress, stats, SummarizedExperiment Suggests: knitr License: GPL-3 MD5sum: 379f2205268c9a7b501dcf6947b9297e NeedsCompilation: no Title: Statistical Analysis of MPRA data Description: MPRAnalyze provides statistical framework for the analysis of data generated by Massively Parallel Reporter Assays (MPRAs), used to directly measure enhancer activity. MPRAnalyze can be used for quantification of enhancer activity, classification of active enhancers and comparative analyses of enhancer activity between conditions. MPRAnalyze construct a nested pair of generalized linear models (GLMs) to relate the DNA and RNA observations, easily adjustable to various experimental designs and conditions, and provides a set of rigorous statistical testig schemes. biocViews: ImmunoOncology, Software, StatisticalMethod, Sequencing, GeneExpression, CellBiology, CellBasedAssays, DifferentialExpression Author: Tal Ashuach [aut, cre], David S Fischer [aut], Nir Yosef [ctb], Fabian J Theis [ctb], Maintainer: Tal Ashuach URL: https://github.com/YosefLab/MPRAnalyze VignetteBuilder: knitr BugReports: https://github.com/YosefLab/MPRAnalyze git_url: https://git.bioconductor.org/packages/MPRAnalyze git_branch: RELEASE_3_8 git_last_commit: ef30857 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MPRAnalyze_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MPRAnalyze_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MPRAnalyze_1.0.1.tgz vignettes: vignettes/MPRAnalyze/inst/doc/vignette.html vignetteTitles: Analyzing MPRA data with MPRAnalyze hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MPRAnalyze/inst/doc/vignette.R Package: msa Version: 1.14.0 Depends: R (>= 3.1.0), methods, Biostrings (>= 2.40.0) Imports: Rcpp (>= 0.11.1), BiocGenerics, IRanges (>= 1.20.0), S4Vectors, tools LinkingTo: Rcpp Suggests: Biobase, knitr, seqinr, ape, phangorn License: GPL (>= 2) MD5sum: 65b7ca9155681b6bb247565c249918e3 NeedsCompilation: yes Title: Multiple Sequence Alignment Description: The 'msa' package provides a unified R/Bioconductor interface to the multiple sequence alignment algorithms ClustalW, ClustalOmega, and Muscle. All three algorithms are integrated in the package, therefore, they do not depend on any external software tools and are available for all major platforms. The multiple sequence alignment algorithms are complemented by a function for pretty-printing multiple sequence alignments using the LaTeX package TeXshade. biocViews: MultipleSequenceAlignment, Alignment, MultipleComparison, Sequencing Author: Enrico Bonatesta, Christoph Horejs-Kainrath, Ulrich Bodenhofer Maintainer: Ulrich Bodenhofer URL: http://www.bioinf.jku.at/software/msa/ SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/msa git_branch: RELEASE_3_8 git_last_commit: b311929 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/msa_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/msa_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/msa_1.14.0.tgz vignettes: vignettes/msa/inst/doc/msa.pdf vignetteTitles: msa - An R Package for Multiple Sequence Alignment hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/msa/inst/doc/msa.R importsMe: LymphoSeq, odseq Package: msgbsR Version: 1.6.1 Depends: R (>= 3.4), GenomicRanges, methods Imports: BSgenome, easyRNASeq, edgeR, GenomicAlignments, GenomicFeatures, GenomeInfoDb, ggbio, ggplot2, IRanges, parallel, plyr, Rsamtools, R.utils, stats, SummarizedExperiment, S4Vectors, utils Suggests: roxygen2, BSgenome.Rnorvegicus.UCSC.rn6 License: GPL-2 Archs: i386, x64 MD5sum: e21e0f768ccb595db67031e859437c2d NeedsCompilation: no Title: msgbsR: methylation sensitive genotyping by sequencing (MS-GBS) R functions Description: Pipeline for the anaysis of a MS-GBS experiment. biocViews: ImmunoOncology, DifferentialMethylation, DataImport, Epigenetics, MethylSeq Author: Benjamin Mayne Maintainer: Benjamin Mayne git_url: https://git.bioconductor.org/packages/msgbsR git_branch: RELEASE_3_8 git_last_commit: 411f316 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/msgbsR_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/msgbsR_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/msgbsR_1.6.1.tgz vignettes: vignettes/msgbsR/inst/doc/msgbsR_Vignette.pdf vignetteTitles: msgbsR_Example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/msgbsR/inst/doc/msgbsR_Vignette.R Package: MSGFgui Version: 1.16.1 Depends: mzR, xlsx Imports: shiny, mzID (>= 1.2), MSGFplus, shinyFiles (>= 0.4.0), tools Suggests: knitr, testthat License: GPL (>= 2) MD5sum: 4f7ca4e38b57cdeb850d92769e9450df NeedsCompilation: no Title: A shiny GUI for MSGFplus Description: This package makes it possible to perform analyses using the MSGFplus package in a GUI environment. Furthermore it enables the user to investigate the results using interactive plots, summary statistics and filtering. Lastly it exposes the current results to another R session so the user can seamlessly integrate the gui into other workflows. biocViews: ImmunoOncology, MassSpectrometry, Proteomics, GUI, Visualization Author: Thomas Lin Pedersen Maintainer: Thomas Lin Pedersen VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MSGFgui git_branch: RELEASE_3_8 git_last_commit: f1646ed git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MSGFgui_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSGFgui_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSGFgui_1.16.1.tgz vignettes: vignettes/MSGFgui/inst/doc/Using_MSGFgui.html vignetteTitles: Using MSGFgui hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSGFgui/inst/doc/Using_MSGFgui.R Package: MSGFplus Version: 1.16.1 Depends: methods Imports: mzID, ProtGenerics Suggests: gWidgets, knitr, testthat License: GPL (>= 2) MD5sum: 7e4934f61b71a759f7c9dadfd3398990 NeedsCompilation: no Title: An interface between R and MS-GF+ Description: This package contains function to perform peptide identification using the MS-GF+ algorithm. The package contains functionality for building up a parameter set both in code and through a simple GUI, as well as running the algorithm in batches, potentially asynchronously. biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Thomas Lin Pedersen Maintainer: Thomas Lin Pedersen SystemRequirements: Java (>= 1.7) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MSGFplus git_branch: RELEASE_3_8 git_last_commit: 62a4a5d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MSGFplus_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSGFplus_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSGFplus_1.16.1.tgz vignettes: vignettes/MSGFplus/inst/doc/Using_MSGFplus.html vignetteTitles: Using MSGFgui hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSGFplus/inst/doc/Using_MSGFplus.R importsMe: MSGFgui Package: msmsEDA Version: 1.20.1 Depends: R (>= 3.0.1), MSnbase Imports: MASS, gplots, RColorBrewer License: GPL-2 MD5sum: 32478cf98f71e29b6016d14147cc7dca NeedsCompilation: no Title: Exploratory Data Analysis of LC-MS/MS data by spectral counts Description: Exploratory data analysis to assess the quality of a set of LC-MS/MS experiments, and visualize de influence of the involved factors. biocViews: ImmunoOncology, Software, MassSpectrometry, Proteomics Author: Josep Gregori, Alex Sanchez, and Josep Villanueva Maintainer: Josep Gregori git_url: https://git.bioconductor.org/packages/msmsEDA git_branch: RELEASE_3_8 git_last_commit: 60c71ef git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/msmsEDA_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/msmsEDA_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/msmsEDA_1.20.1.tgz vignettes: vignettes/msmsEDA/inst/doc/msmsData-Vignette.pdf vignetteTitles: msmsEDA: Batch effects detection in LC-MSMS experiments hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/msmsEDA/inst/doc/msmsData-Vignette.R dependsOnMe: msmsTests suggestsMe: Harman Package: msmsTests Version: 1.20.1 Depends: R (>= 3.0.1), MSnbase, msmsEDA Imports: edgeR, qvalue License: GPL-2 MD5sum: 2b38c323def13d0e97cc178d25ffa300 NeedsCompilation: no Title: LC-MS/MS Differential Expression Tests Description: Statistical tests for label-free LC-MS/MS data by spectral counts, to discover differentially expressed proteins between two biological conditions. Three tests are available: Poisson GLM regression, quasi-likelihood GLM regression, and the negative binomial of the edgeR package.The three models admit blocking factors to control for nuissance variables.To assure a good level of reproducibility a post-test filter is available, where we may set the minimum effect size considered biologicaly relevant, and the minimum expression of the most abundant condition. biocViews: ImmunoOncology, Software, MassSpectrometry, Proteomics Author: Josep Gregori, Alex Sanchez, and Josep Villanueva Maintainer: Josep Gregori i Font git_url: https://git.bioconductor.org/packages/msmsTests git_branch: RELEASE_3_8 git_last_commit: fd16b98 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/msmsTests_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/msmsTests_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/msmsTests_1.20.1.tgz vignettes: vignettes/msmsTests/inst/doc/msmsTests-Vignette.pdf, vignettes/msmsTests/inst/doc/msmsTests-Vignette2.pdf vignetteTitles: msmsTests: post test filters to improve reproducibility, msmsTests: controlling batch effects by blocking hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/msmsTests/inst/doc/msmsTests-Vignette.R, vignettes/msmsTests/inst/doc/msmsTests-Vignette2.R suggestsMe: MSnID Package: MSnbase Version: 2.8.3 Depends: R (>= 3.1), methods, BiocGenerics (>= 0.7.1), Biobase (>= 2.15.2), mzR (>= 2.15.1), S4Vectors, ProtGenerics (>= 1.9.1) Imports: BiocParallel, IRanges (>= 2.13.28), plyr, preprocessCore, vsn, grid, stats4, affy, impute, pcaMethods, MALDIquant (>= 1.16), mzID (>= 1.5.2), digest, lattice, ggplot2, XML, scales, MASS, Rcpp LinkingTo: Rcpp Suggests: testthat, pryr, gridExtra, microbenchmark, zoo, knitr (>= 1.1.0), rols, Rdisop, pRoloc, pRolocdata (>= 1.7.1), msdata (>= 0.19.3), roxygen2, rgl, rpx, AnnotationHub, BiocStyle (>= 2.5.19), rmarkdown, imputeLCMD, norm, gplots, shiny, magrittr, SummarizedExperiment License: Artistic-2.0 MD5sum: 5769f7ad9a7932db4559b9b179a9d64c NeedsCompilation: yes Title: Base Functions and Classes for Mass Spectrometry and Proteomics Description: MSnbase provides infrastructure for manipulation, processing and visualisation of mass spectrometry and proteomics data, ranging from raw to quantitative and annotated data. biocViews: ImmunoOncology, Infrastructure, Proteomics, MassSpectrometry, QualityControl, DataImport Author: Laurent Gatto, Johannes Rainer and Sebastian Gibb with contributions from Guangchuang Yu, Samuel Wieczorek, Vasile-Cosmin Lazar, Vladislav Petyuk, Thomas Naake, Richie Cotton, Arne Smits, Martina Fisher, Ludger Goeminne, Adriaan Sticker and Lieven Clement. Maintainer: Laurent Gatto URL: https://github.com/lgatto/MSnbase VignetteBuilder: knitr BugReports: https://github.com/lgatto/MSnbase/issues git_url: https://git.bioconductor.org/packages/MSnbase git_branch: RELEASE_3_8 git_last_commit: ef88375 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MSnbase_2.8.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSnbase_2.8.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSnbase_2.8.3.tgz vignettes: vignettes/MSnbase/inst/doc/v01-MSnbase-demo.html, vignettes/MSnbase/inst/doc/v02-MSnbase-io.html, vignettes/MSnbase/inst/doc/v03-MSnbase-centroiding.html, vignettes/MSnbase/inst/doc/v04-benchmarking.html, vignettes/MSnbase/inst/doc/v05-MSnbase-development.html vignetteTitles: Base Functions and Classes for MS-based Proteomics, MSnbase IO capabilities, MSnbase: centroiding of profile-mode MS data, MSnbase2 benchmarking, A short introduction to `MSnbase` development hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSnbase/inst/doc/v01-MSnbase-demo.R, vignettes/MSnbase/inst/doc/v02-MSnbase-io.R, vignettes/MSnbase/inst/doc/v03-MSnbase-centroiding.R, vignettes/MSnbase/inst/doc/v04-benchmarking.R, vignettes/MSnbase/inst/doc/v05-MSnbase-development.R dependsOnMe: msmsEDA, msmsTests, pRoloc, pRolocGUI, proteoQC, qPLEXanalyzer, synapter, xcms importsMe: DAPAR, DEP, MSnID, MSstatsQC, Pbase, ProteomicsAnnotationHubData, topdownr suggestsMe: AnnotationHub, biobroom, BiocGenerics, isobar, qcmetrics, readat, rpx Package: MSnID Version: 1.16.1 Depends: R (>= 2.10), Rcpp Imports: MSnbase (>= 1.12.1), mzID (>= 1.3.5), R.cache, foreach, doParallel, parallel, methods, iterators, data.table, Biobase, ProtGenerics, reshape2, dplyr, mzR Suggests: BiocStyle, msmsTests, ggplot2, RUnit, BiocGenerics License: Artistic-2.0 Archs: i386, x64 MD5sum: 6ed6ba769c2e517b3bda627fa3f759ee NeedsCompilation: no Title: Utilities for Exploration and Assessment of Confidence of LC-MSn Proteomics Identifications Description: Extracts MS/MS ID data from mzIdentML (leveraging mzID package) or text files. After collating the search results from multiple datasets it assesses their identification quality and optimize filtering criteria to achieve the maximum number of identifications while not exceeding a specified false discovery rate. Also contains a number of utilities to explore the MS/MS results and assess missed and irregular enzymatic cleavages, mass measurement accuracy, etc. biocViews: Proteomics, MassSpectrometry, ImmunoOncology Author: Vlad Petyuk with contributions from Laurent Gatto Maintainer: Vlad Petyuk git_url: https://git.bioconductor.org/packages/MSnID git_branch: RELEASE_3_8 git_last_commit: 98a3641 git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/MSnID_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSnID_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSnID_1.16.1.tgz vignettes: vignettes/MSnID/inst/doc/msnid_vignette.pdf vignetteTitles: MSnID Package for Handling MS/MS Identifications hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSnID/inst/doc/msnid_vignette.R Package: msPurity Version: 1.8.1 Depends: Rcpp Imports: plyr, foreach, parallel, doSNOW, stringr, mzR, reshape2, fastcluster, ggplot2, DBI, RSQLite Suggests: testthat, xcms, BiocStyle, knitr, rmarkdown, msPurityData, CAMERA License: GPL (>= 2) MD5sum: 00618e4243b241439c5b2c303d3b7b2a NeedsCompilation: no Title: Automated Evaluation of Precursor Ion Purity for Mass Spectrometry Based Fragmentation in Metabolomics Description: Assess the contribution of the targeted precursor in fragmentation acquired or anticipated isolation windows using a metric called "precursor purity". Also provides simple processing steps (averaging, filtering, blank subtraction, etc) for DI-MS data. Works for both LC-MS(/MS) and DI-MS(/MS) data. Spectral matching of fragmentation spectra can also be run against a SQLite database of library spectra. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics, Software Author: Thomas N. Lawson, Ralf Weber, Martin Jones, Mark Viant, Warwick Dunn Maintainer: Thomas N. Lawson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/msPurity git_branch: RELEASE_3_8 git_last_commit: 850ac0f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/msPurity_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/msPurity_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/msPurity_1.8.1.tgz vignettes: vignettes/msPurity/inst/doc/msPurity-spectral-matching-vignette.html, vignettes/msPurity/inst/doc/msPurity-vignette.html vignetteTitles: msPurity spectral matching, msPurity hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/msPurity/inst/doc/msPurity-spectral-matching-vignette.R, vignettes/msPurity/inst/doc/msPurity-vignette.R Package: MSstats Version: 3.14.1 Depends: R (>= 3.4) Imports: lme4, marray, limma, gplots, ggplot2, methods, grid, ggrepel, preprocessCore, reshape2, survival, minpack.lm, utils, grDevices, graphics, stats, doSNOW, snow, foreach, data.table, MASS, dplyr, tidyr, stringr, randomForest Suggests: BiocStyle, knitr, rmarkdown, MSstatsBioData License: Artistic-2.0 MD5sum: ea3ae8006b39aa5e0662ea6b270b9653 NeedsCompilation: no Title: Protein Significance Analysis in DDA, SRM and DIA for Label-free or Label-based Proteomics Experiments Description: A set of tools for statistical relative protein significance analysis in DDA, SRM and DIA experiments. biocViews: ImmunoOncology, MassSpectrometry, Proteomics, Software, Normalization, QualityControl, TimeCourse Author: Meena Choi [aut, cre], Cyril Galitzine [aut], Ting Huang [aut], Tsung-Heng Tsai [aut], Olga Vitek [aut] Maintainer: Meena Choi URL: http://msstats.org VignetteBuilder: knitr BugReports: https://groups.google.com/forum/#!forum/msstats git_url: https://git.bioconductor.org/packages/MSstats git_branch: RELEASE_3_8 git_last_commit: 3dfe3d7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MSstats_3.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSstats_3.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSstats_3.14.1.tgz vignettes: vignettes/MSstats/inst/doc/MSstats.html vignetteTitles: MSstats: Protein/Peptide significance analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSstats/inst/doc/MSstats.R importsMe: artMS, MSstatsTMT Package: MSstatsQC Version: 2.0.1 Imports: dplyr,plotly,RecordLinkage,ggplot2,ggExtra, stats,grid, MSnbase, qcmetrics Suggests: knitr,rmarkdown, testthat, RforProteomics License: Artistic License 2.0 MD5sum: d9b69e724760fafae32e00e8c0d544fb NeedsCompilation: no Title: Longitudinal system suitability monitoring and quality control for proteomic experiments Description: MSstatsQC is an R package which provides longitudinal system suitability monitoring and quality control tools for proteomic experiments. biocViews: ImmunoOncology, Software, QualityControl, Proteomics, MassSpectrometry Author: Eralp Dogu [aut, cre], Sara Taheri [aut], Olga Vitek [aut] Maintainer: Eralp Dogu URL: http://msstats.org/msstatsqc VignetteBuilder: knitr BugReports: https://groups.google.com/forum/#!forum/msstatsqc git_url: https://git.bioconductor.org/packages/MSstatsQC git_branch: RELEASE_3_8 git_last_commit: 29d5c22 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MSstatsQC_2.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSstatsQC_2.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSstatsQC_2.0.1.tgz vignettes: vignettes/MSstatsQC/inst/doc/MSstatsQC.html vignetteTitles: MSstatsQC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSstatsQC/inst/doc/MSstatsQC.R importsMe: MSstatsQCgui Package: MSstatsQCgui Version: 1.2.1 Imports: shiny, MSstatsQC, ggExtra, gridExtra, plotly, dplyr, RecordLinkage, grid Suggests: knitr License: Artistic License 2.0 MD5sum: d666317e4fc2bb1e71da65368d997f83 NeedsCompilation: no Title: A graphical user interface for MSstatsQC package Description: MSstatsQCgui is a Shiny app which provides longitudinal system suitability monitoring and quality control tools for proteomic experiments. biocViews: ImmunoOncology, Software, QualityControl, Proteomics, MassSpectrometry, GUI Author: Eralp Dogu [aut, cre], Sara Taheri [aut], Olga Vitek [aut] Maintainer: Eralp Dogu URL: http://msstats.org/msstatsqc VignetteBuilder: knitr BugReports: https://groups.google.com/forum/#!forum/msstatsqc git_url: https://git.bioconductor.org/packages/MSstatsQCgui git_branch: RELEASE_3_8 git_last_commit: 6048825 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/MSstatsQCgui_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSstatsQCgui_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSstatsQCgui_1.2.1.tgz vignettes: vignettes/MSstatsQCgui/inst/doc/MSstatsQCgui.html vignetteTitles: MSstatsQCgui hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSstatsQCgui/inst/doc/MSstatsQCgui.R Package: MSstatsTMT Version: 1.1.2 Depends: R (>= 3.5) Imports: limma, lme4, dplyr, tidyr, nlme, reshape2, data.table, matrixStats, stats, utils, ggplot2, grDevices, graphics, MSstats Suggests: BiocStyle, knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: f174eaa0550932431bc710aa5e17f849 NeedsCompilation: no Title: Protein Significance Analysis in shotgun mass spectrometry-based proteomic experiments with tandem mass tag (TMT) labeling Description: Tools for protein significance analysis in shotgun mass spectrometry-based proteomic experiments with tandem mass tag (TMT) labeling. biocViews: ImmunoOncology, MassSpectrometry, Proteomics, Software Author: Ting Huang [aut, cre], Meena Choi [aut], Sicheng Hao [aut] Maintainer: Ting Huang URL: http://msstats.org/msstatstmt/ VignetteBuilder: knitr BugReports: https://groups.google.com/forum/#!forum/msstats git_url: https://git.bioconductor.org/packages/MSstatsTMT git_branch: RELEASE_3_8 git_last_commit: ab269e6 git_last_commit_date: 2019-02-25 Date/Publication: 2019-02-27 source.ver: src/contrib/MSstatsTMT_1.1.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/MSstatsTMT_1.1.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MSstatsTMT_1.1.2.tgz vignettes: vignettes/MSstatsTMT/inst/doc/MSstatsTMT.html vignetteTitles: MSstatsTMT User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MSstatsTMT/inst/doc/MSstatsTMT.R Package: MTseeker Version: 1.0.6 Depends: viridis, S4Vectors, GenomeInfoDb, GenomicAlignments, VariantAnnotation Imports: xml2, utils, gmapR, methods, IRanges, Biobase, circlize, jsonlite, graphics, Rsamtools, grDevices, Biostrings, rtracklayer, VariantTools, Homo.sapiens, BiocGenerics, GenomicRanges, GenomicFeatures, SummarizedExperiment Suggests: MTseekerData, BiocStyle, rmarkdown, ggthemes, ggplot2, pkgdown, knitr, rsvg License: GPL-3 MD5sum: 32712fee3db29edecc7b398e555850f1 NeedsCompilation: no Title: Bioconductor Tools for Human Mitochondrial Variant Analysis Description: Variant analysis tools for mitochondrial genetics. biocViews: Genetics, Metabolomics, VariantAnnotation Author: Tim Triche [cre, aut], Noor Sohail [aut], Ben Johnson [aut], Tim Vickers [ctb], Azif Zubair [ctb] Maintainer: Tim Triche VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MTseeker git_branch: RELEASE_3_8 git_last_commit: f86bf47 git_last_commit_date: 2018-11-12 Date/Publication: 2018-11-12 source.ver: src/contrib/MTseeker_1.0.6.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MTseeker_1.0.6.tgz vignettes: vignettes/MTseeker/inst/doc/oncocytomas.html vignetteTitles: MTseeker example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MTseeker/inst/doc/oncocytomas.R Package: Mulcom Version: 1.32.0 Depends: R (>= 2.10), fields, Biobase Imports: graphics, grDevices, stats, methods License: GPL-2 MD5sum: 10bd7bcd1965c6f95c7d5a5c110d9c49 NeedsCompilation: yes Title: Calculates Mulcom test Description: Identification of differentially expressed genes and false discovery rate (FDR) calculation by Multiple Comparison test biocViews: StatisticalMethod, MultipleComparison, Microarray, DifferentialExpression, GeneExpression Author: Claudio Isella Maintainer: Claudio Isella git_url: https://git.bioconductor.org/packages/Mulcom git_branch: RELEASE_3_8 git_last_commit: 4f49fd6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Mulcom_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Mulcom_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Mulcom_1.32.0.tgz vignettes: vignettes/Mulcom/inst/doc/MulcomVignette.pdf vignetteTitles: Mulcom Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Mulcom/inst/doc/MulcomVignette.R Package: MultiAssayExperiment Version: 1.8.3 Depends: R (>= 3.5.0), SummarizedExperiment (>= 1.3.81) Imports: methods, GenomicRanges (>= 1.25.93), BiocGenerics, S4Vectors (>= 0.17.5), IRanges, Biobase, stats, tidyr, utils Suggests: BiocStyle, testthat, knitr, rmarkdown, R.rsp, HDF5Array, RaggedExperiment, UpSetR, survival, survminer License: Artistic-2.0 Archs: i386, x64 MD5sum: e8d046e690d369776ebc4a3d442848c2 NeedsCompilation: no Title: Software for the integration of multi-omics experiments in Bioconductor Description: MultiAssayExperiment harmonizes data management of multiple assays performed on an overlapping set of specimens. It provides a familiar Bioconductor user experience by extending concepts from SummarizedExperiment, supporting an open-ended mix of standard data classes for individual assays, and allowing subsetting by genomic ranges or rownames. biocViews: Infrastructure, DataRepresentation Author: Marcel Ramos [aut, cre], Levi Waldron [aut], MultiAssay SIG [ctb] Maintainer: Marcel Ramos URL: http://waldronlab.io/MultiAssayExperiment/ VignetteBuilder: knitr, R.rsp BugReports: https://github.com/waldronlab/MultiAssayExperiment/issues git_url: https://git.bioconductor.org/packages/MultiAssayExperiment git_branch: RELEASE_3_8 git_last_commit: 2bec785 git_last_commit_date: 2019-02-12 Date/Publication: 2019-02-13 source.ver: src/contrib/MultiAssayExperiment_1.8.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/MultiAssayExperiment_1.8.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MultiAssayExperiment_1.8.3.tgz vignettes: vignettes/MultiAssayExperiment/inst/doc/MultiAssayExperiment_cheatsheet.pdf, vignettes/MultiAssayExperiment/inst/doc/MultiAssayExperiment.html, vignettes/MultiAssayExperiment/inst/doc/QuickStartMultiAssay.html, vignettes/MultiAssayExperiment/inst/doc/UsingHDF5Array.html vignetteTitles: MultiAssayExperiment_cheatsheet.pdf, Coordinating Analysis of Multi-Assay Experiments, Quick-start Guide, HDF5Array and MultiAssayExperiment hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MultiAssayExperiment/inst/doc/MultiAssayExperiment.R, vignettes/MultiAssayExperiment/inst/doc/QuickStartMultiAssay.R, vignettes/MultiAssayExperiment/inst/doc/UsingHDF5Array.R dependsOnMe: ClassifyR, glmSparseNet, hipathia, InTAD, missRows importsMe: AffiXcan, CAGEr, ELMER, GOpro, OMICsPCA, omicsPrint, TCGAutils suggestsMe: BiocOncoTK, MultiDataSet, RaggedExperiment Package: multiClust Version: 1.12.0 Imports: mclust, ctc, survival, cluster, dendextend, amap, graphics, grDevices Suggests: knitr, gplots, RUnit, BiocGenerics, preprocessCore, Biobase, GEOquery License: GPL (>= 2) MD5sum: bd8c78d8df3588f2f1cce8b43d17bdcc NeedsCompilation: no Title: multiClust: An R-package for Identifying Biologically Relevant Clusters in Cancer Transcriptome Profiles Description: Clustering is carried out to identify patterns in transcriptomics profiles to determine clinically relevant subgroups of patients. Feature (gene) selection is a critical and an integral part of the process. Currently, there are many feature selection and clustering methods to identify the relevant genes and perform clustering of samples. However, choosing an appropriate methodology is difficult. In addition, extensive feature selection methods have not been supported by the available packages. Hence, we developed an integrative R-package called multiClust that allows researchers to experiment with the choice of combination of methods for gene selection and clustering with ease. Using multiClust, we identified the best performing clustering methodology in the context of clinical outcome. Our observations demonstrate that simple methods such as variance-based ranking perform well on the majority of data sets, provided that the appropriate number of genes is selected. However, different gene ranking and selection methods remain relevant as no methodology works for all studies. biocViews: FeatureExtraction, Clustering, GeneExpression, Survival Author: Nathan Lawlor [aut, cre], Peiyong Guan [aut], Alec Fabbri [aut], Krish Karuturi [aut], Joshy George [aut] Maintainer: Nathan Lawlor VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/multiClust git_branch: RELEASE_3_8 git_last_commit: 2a34aa1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/multiClust_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/multiClust_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/multiClust_1.12.0.tgz vignettes: vignettes/multiClust/inst/doc/multiClust.html vignetteTitles: "A Guide to multiClust" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/multiClust/inst/doc/multiClust.R Package: MultiDataSet Version: 1.10.0 Depends: R (>= 3.3), Biobase Imports: BiocGenerics, GenomicRanges, IRanges, S4Vectors, SummarizedExperiment, methods, utils, ggplot2, ggrepel, qqman, limma Suggests: brgedata, minfi, minfiData, knitr, rmarkdown, testthat, omicade4, iClusterPlus, GEOquery, MultiAssayExperiment, BiocStyle, RaggedExperiment License: file LICENSE MD5sum: c16950d938bd000b1ba441a751320ed4 NeedsCompilation: no Title: Implementation of MultiDataSet and ResultSet Description: Implementation of the BRGE's (Bioinformatic Research Group in Epidemiology from Center for Research in Environmental Epidemiology) MultiDataSet and ResultSet. MultiDataSet is designed for integrating multi omics data sets and ResultSet is a container for omics results. This package contains base classes for MEAL and rexposome packages. biocViews: Software, DataRepresentation Author: Carlos Ruiz-Arenas [aut, cre], Carles Hernandez-Ferrer [aut], Juan R. Gonzalez [aut] Maintainer: Carlos Ruiz-Arenas VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MultiDataSet git_branch: RELEASE_3_8 git_last_commit: f5a992b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MultiDataSet_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MultiDataSet_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MultiDataSet_1.10.0.tgz vignettes: vignettes/MultiDataSet/inst/doc/MultiDataSet_3party_Integration.html, vignettes/MultiDataSet/inst/doc/MultiDataSet_Extending_Proteome.html, vignettes/MultiDataSet/inst/doc/MultiDataSet.html vignetteTitles: Using MultiDataSet with third party R packages, Adding a new type of data to MultiDataSet objects, Introduction to MultiDataSet hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MultiDataSet/inst/doc/MultiDataSet_3party_Integration.R, vignettes/MultiDataSet/inst/doc/MultiDataSet_Extending_Proteome.R, vignettes/MultiDataSet/inst/doc/MultiDataSet.R dependsOnMe: MEAL importsMe: omicRexposome Package: multiHiCcompare Version: 1.0.0 Depends: R (>= 3.5.0) Imports: data.table, dplyr, HiCcompare, edgeR, BiocParallel, qqman, pheatmap, methods, metap, GenomicRanges, graphics, stats, utils, pbapply, GenomeInfoDbData, BLMA, GenomeInfoDb Suggests: knitr, rmarkdown, testthat, BiocStyle License: MIT + file LICENSE MD5sum: c33ece7658baba97e8012e67ab1495ae NeedsCompilation: no Title: Normalize and detect differences between Hi-C datasets when replicates of each experimental condition are available Description: multiHiCcompare provides functions for joint normalization and difference detection in multiple Hi-C datasets. This extension of the original HiCcompare package now allows for Hi-C experiments with more than 2 groups and multiple samples per group. multiHiCcompare operates on processed Hi-C data in the form of sparse upper triangular matrices. It accepts four column (chromosome, region1, region2, IF) tab-separated text files storing chromatin interaction matrices. multiHiCcompare provides cyclic loess and fast loess (fastlo) methods adapted to jointly normalizing Hi-C data. Additionally, it provides a general linear model (GLM) framework adapting the edgeR package to detect differences in Hi-C data in a distance dependent manner. biocViews: Software, HiC, Sequencing, Normalization Author: John Stansfield [aut, cre], Mikhail Dozmorov [aut] Maintainer: John Stansfield VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/multiHiCcompare git_branch: RELEASE_3_8 git_last_commit: e315dae git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/multiHiCcompare_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/multiHiCcompare_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/multiHiCcompare_1.0.0.tgz vignettes: vignettes/multiHiCcompare/inst/doc/multiHiCcompare.html vignetteTitles: multiHiCcompare Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/multiHiCcompare/inst/doc/multiHiCcompare.R suggestsMe: HiCcompare Package: MultiMed Version: 2.4.0 Depends: R (>= 3.1.0) Suggests: RUnit, BiocGenerics License: GPL (>= 2) + file LICENSE MD5sum: 53df4140afc3b479077ff254370b89af NeedsCompilation: no Title: Testing multiple biological mediators simultaneously Description: Implements methods for testing multiple mediators biocViews: MultipleComparison, StatisticalMethod, Software Author: Simina M. Boca, Ruth Heller, Joshua N. Sampson Maintainer: Simina M. Boca git_url: https://git.bioconductor.org/packages/MultiMed git_branch: RELEASE_3_8 git_last_commit: 089a3dd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MultiMed_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MultiMed_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MultiMed_2.4.0.tgz vignettes: vignettes/MultiMed/inst/doc/MultiMed.pdf vignetteTitles: MultiMedTutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MultiMed/inst/doc/MultiMed.R Package: multiMiR Version: 1.4.0 Depends: R (>= 3.4) Imports: stats, XML, RCurl, purrr (>= 0.2.2), tibble (>= 1.2), methods, BiocGenerics, AnnotationDbi, dplyr, Suggests: BiocStyle, edgeR, knitr, rmarkdown, testthat (>= 1.0.2) License: MIT + file LICENSE MD5sum: 26ca39b201e466a51cdf18d73d243930 NeedsCompilation: no Title: Integration of multiple microRNA-target databases with their disease and drug associations Description: A collection of microRNAs/targets from external resources, including validated microRNA-target databases (miRecords, miRTarBase and TarBase), predicted microRNA-target databases (DIANA-microT, ElMMo, MicroCosm, miRanda, miRDB, PicTar, PITA and TargetScan) and microRNA-disease/drug databases (miR2Disease, Pharmaco-miR VerSe and PhenomiR). biocViews: miRNAData, Homo_sapiens_Data, Mus_musculus_Data, Rattus_norvegicus_Data, OrganismData Author: Yuanbin Ru [aut], Matt Mulvahill [cre, aut], Spencer Mahaffey [aut], Katerina Kechris [aut, cph, ths] Maintainer: Matt Mulvahill URL: https://github.com/KechrisLab/multiMiR VignetteBuilder: knitr BugReports: https://github.com/KechrisLab/multiMiR/issues git_url: https://git.bioconductor.org/packages/multiMiR git_branch: RELEASE_3_8 git_last_commit: 0863142 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/multiMiR_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/multiMiR_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/multiMiR_1.4.0.tgz vignettes: vignettes/multiMiR/inst/doc/multiMiR.html vignetteTitles: The multiMiR user's guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/multiMiR/inst/doc/multiMiR.R Package: multiOmicsViz Version: 1.6.0 Depends: R (>= 3.3.2) Imports: methods, parallel, doParallel, foreach, grDevices, graphics, utils, SummarizedExperiment, stats Suggests: BiocGenerics License: LGPL MD5sum: 1fb971e30027eab84bb48dd7552a11a4 NeedsCompilation: no Title: Plot the effect of one omics data on other omics data along the chromosome Description: Calculate the spearman correlation between the source omics data and other target omics data, identify the significant correlations and plot the significant correlations on the heat map in which the x-axis and y-axis are ordered by the chromosomal location. biocViews: Software, Visualization, SystemsBiology Author: Jing Wang Maintainer: Jing Wang git_url: https://git.bioconductor.org/packages/multiOmicsViz git_branch: RELEASE_3_8 git_last_commit: 2ef8363 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/multiOmicsViz_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/multiOmicsViz_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/multiOmicsViz_1.6.0.tgz vignettes: vignettes/multiOmicsViz/inst/doc/multiOmicsViz.pdf vignetteTitles: multiOmicsViz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/multiOmicsViz/inst/doc/multiOmicsViz.R Package: multiscan Version: 1.42.0 Depends: R (>= 2.3.0) Imports: Biobase, utils License: GPL (>= 2) MD5sum: f30405ccb188b9d543f7e32c4c1c1b61 NeedsCompilation: yes Title: R package for combining multiple scans Description: Estimates gene expressions from several laser scans of the same microarray biocViews: Microarray, Preprocessing Author: Mizanur Khondoker , Chris Glasbey, Bruce Worton. Maintainer: Mizanur Khondoker git_url: https://git.bioconductor.org/packages/multiscan git_branch: RELEASE_3_8 git_last_commit: 9a68631 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/multiscan_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/multiscan_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/multiscan_1.42.0.tgz vignettes: vignettes/multiscan/inst/doc/multiscan.pdf vignetteTitles: An R Package for Estimating Gene Expressions using Multiple Scans hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/multiscan/inst/doc/multiscan.R Package: multtest Version: 2.38.0 Depends: R (>= 2.10), methods, BiocGenerics, Biobase Imports: survival, MASS, stats4 Suggests: snow License: LGPL Archs: i386, x64 MD5sum: 8d72610b6a4266100d65cb49fca11158 NeedsCompilation: yes Title: Resampling-based multiple hypothesis testing Description: Non-parametric bootstrap and permutation resampling-based multiple testing procedures (including empirical Bayes methods) for controlling the family-wise error rate (FWER), generalized family-wise error rate (gFWER), tail probability of the proportion of false positives (TPPFP), and false discovery rate (FDR). Several choices of bootstrap-based null distribution are implemented (centered, centered and scaled, quantile-transformed). Single-step and step-wise methods are available. Tests based on a variety of t- and F-statistics (including t-statistics based on regression parameters from linear and survival models as well as those based on correlation parameters) are included. When probing hypotheses with t-statistics, users may also select a potentially faster null distribution which is multivariate normal with mean zero and variance covariance matrix derived from the vector influence function. Results are reported in terms of adjusted p-values, confidence regions and test statistic cutoffs. The procedures are directly applicable to identifying differentially expressed genes in DNA microarray experiments. biocViews: Microarray, DifferentialExpression, MultipleComparison Author: Katherine S. Pollard, Houston N. Gilbert, Yongchao Ge, Sandra Taylor, Sandrine Dudoit Maintainer: Katherine S. Pollard git_url: https://git.bioconductor.org/packages/multtest git_branch: RELEASE_3_8 git_last_commit: 4dfe71c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/multtest_2.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/multtest_2.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/multtest_2.38.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: a4Base, aCGH, BicARE, iPAC, KCsmart, LMGene, PREDA, rain, REDseq, SAGx, siggenes, webbioc importsMe: ABarray, aCGH, adSplit, ALDEx2, anota, ChIPpeakAnno, GeneSelector, IsoGeneGUI, mAPKL, metabomxtr, nethet, OCplus, phyloseq, REDseq, RTopper, singleCellTK, synapter, webbioc, xcms suggestsMe: annaffy, BiocCaseStudies, ecolitk, factDesign, GeneSelector, GGtools, GOstats, gQTLstats, GSEAlm, maigesPack, MmPalateMiRNA, pcot2, ropls, topGO Package: muscle Version: 3.24.0 Depends: Biostrings License: Unlimited Archs: i386, x64 MD5sum: 3fe18a5e6501d11231663070b783e744 NeedsCompilation: yes Title: Multiple Sequence Alignment with MUSCLE Description: MUSCLE performs multiple sequence alignments of nucleotide or amino acid sequences. biocViews: MultipleSequenceAlignment, Alignment, Sequencing, Genetics, SequenceMatching, DataImport Author: Algorithm by Robert C. Edgar. R port by Alex T. Kalinka. Maintainer: Alex T. Kalinka URL: http://www.drive5.com/muscle/ git_url: https://git.bioconductor.org/packages/muscle git_branch: RELEASE_3_8 git_last_commit: da46a28 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/muscle_3.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/muscle_3.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/muscle_3.24.0.tgz vignettes: vignettes/muscle/inst/doc/muscle-vignette.pdf vignetteTitles: A guide to using muscle hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/muscle/inst/doc/muscle-vignette.R Package: MutationalPatterns Version: 1.8.0 Depends: R (>= 3.4.0), GenomicRanges (>= 1.24.0), NMF (>= 0.20.6) Imports: stats, parallel, S4Vectors, BiocGenerics (>= 0.18.0), VariantAnnotation (>= 1.18.1), reshape2 (>= 1.4.1), plyr (>= 1.8.3), ggplot2 (>= 2.1.0), pracma (>= 1.8.8), SummarizedExperiment (>= 1.2.2), IRanges (>= 2.6.0), GenomeInfoDb (>= 1.12.0), Biostrings (>= 2.40.0), ggdendro (>= 0.1-20), cowplot (>= 0.9.2) Suggests: BSgenome (>= 1.40.0), BSgenome.Hsapiens.1000genomes.hs37d5 (>= 0.99.1), BSgenome.Hsapiens.UCSC.hg19 (>= 1.4.0), BiocStyle (>= 2.0.3), TxDb.Hsapiens.UCSC.hg19.knownGene (>= 3.2.2), biomaRt (>= 2.28.0), gridExtra (>= 2.2.1), rtracklayer (>= 1.32.2), testthat License: MIT + file LICENSE Archs: i386, x64 MD5sum: 9ce25a78720c4904d5b951f9d37b901a NeedsCompilation: no Title: Comprehensive genome-wide analysis of mutational processes Description: An extensive toolset for the characterization and visualization of a wide range of mutational patterns in base substitution catalogs. biocViews: Genetics, SomaticMutation Author: Francis Blokzijl, Roel Janssen, Ruben van Boxtel, Edwin Cuppen Maintainer: Roel Janssen , Francis Blokzijl URL: https://doi.org/10.1186/s13073-018-0539-0 git_url: https://git.bioconductor.org/packages/MutationalPatterns git_branch: RELEASE_3_8 git_last_commit: 5aed391 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MutationalPatterns_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MutationalPatterns_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MutationalPatterns_1.8.0.tgz vignettes: vignettes/MutationalPatterns/inst/doc/Introduction_to_MutationalPatterns.pdf vignetteTitles: Introduction to MutationalPatterns hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/MutationalPatterns/inst/doc/Introduction_to_MutationalPatterns.R Package: MVCClass Version: 1.56.0 Depends: R (>= 2.1.0), methods License: LGPL MD5sum: 7bcceaf0251bfe3b06c2ff5bd6d95e80 NeedsCompilation: no Title: Model-View-Controller (MVC) Classes Description: Creates classes used in model-view-controller (MVC) design biocViews: Visualization, Infrastructure, GraphAndNetwork Author: Elizabeth Whalen Maintainer: Elizabeth Whalen git_url: https://git.bioconductor.org/packages/MVCClass git_branch: RELEASE_3_8 git_last_commit: a28de14 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MVCClass_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MVCClass_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MVCClass_1.56.0.tgz vignettes: vignettes/MVCClass/inst/doc/MVCClass.pdf vignetteTitles: MVCClass hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: BioMVCClass Package: MWASTools Version: 1.6.0 Depends: R(>= 3.4) Imports: glm2, ppcor, qvalue, car, boot, grid, ggplot2, gridExtra, igraph, SummarizedExperiment, KEGGgraph, RCurl, KEGGREST, ComplexHeatmap, stats, utils Suggests: RUnit, BiocGenerics, knitr, BiocStyle, rmarkdown License: CC BY-NC-ND 4.0 MD5sum: 9cc4188f3ca64ea0f6161c11876fe795 NeedsCompilation: no Title: MWASTools: an integrated pipeline to perform metabolome-wide association studies Description: MWASTools provides a complete pipeline to perform metabolome-wide association studies. Key functionalities of the package include: quality control analysis of metabonomic data; MWAS using different association models (partial correlations; generalized linear models); model validation using non-parametric bootstrapping; visualization of MWAS results; NMR metabolite identification using STOCSY; and biological interpretation of MWAS results. biocViews: Metabolomics, Lipidomics, Cheminformatics, SystemsBiology, QualityControl Author: Andrea Rodriguez-Martinez, Joram M. Posma, Rafael Ayala, Ana L. Neves, Maryam Anwar, Jeremy K. Nicholson, Marc-Emmanuel Dumas Maintainer: Andrea Rodriguez-Martinez , Rafael Ayala VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/MWASTools git_branch: RELEASE_3_8 git_last_commit: 9f15823 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/MWASTools_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/MWASTools_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/MWASTools_1.6.0.tgz vignettes: vignettes/MWASTools/inst/doc/MWASTools.html vignetteTitles: MWASTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/MWASTools/inst/doc/MWASTools.R importsMe: MetaboSignal Package: mygene Version: 1.18.0 Depends: R (>= 3.2.1), GenomicFeatures, Imports: httr (>= 0.3), jsonlite (>= 0.9.7), S4Vectors, Hmisc, sqldf, plyr Suggests: BiocStyle License: Artistic-2.0 MD5sum: 3a0f8aff0ef5eef0df7ed072ef98b771 NeedsCompilation: no Title: Access MyGene.Info_ services Description: MyGene.Info_ provides simple-to-use REST web services to query/retrieve gene annotation data. It's designed with simplicity and performance emphasized. *mygene*, is an easy-to-use R wrapper to access MyGene.Info_ services. biocViews: Annotation Author: Adam Mark, Ryan Thompson, Cyrus Afrasiabi, Chunlei Wu Maintainer: Adam Mark, Cyrus Afrasiabi, Chunlei Wu git_url: https://git.bioconductor.org/packages/mygene git_branch: RELEASE_3_8 git_last_commit: 247454a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/mygene_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/mygene_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mygene_1.18.0.tgz vignettes: vignettes/mygene/inst/doc/mygene.pdf vignetteTitles: Using mygene.R hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mygene/inst/doc/mygene.R importsMe: MetaboSignal Package: myvariant Version: 1.12.0 Depends: R (>= 3.2.1), VariantAnnotation Imports: httr, jsonlite, S4Vectors, Hmisc, plyr, magrittr, GenomeInfoDb Suggests: BiocStyle License: Artistic-2.0 MD5sum: 186efbf26d9009e544d8874bb3f5778e NeedsCompilation: no Title: Accesses MyVariant.info variant query and annotation services Description: MyVariant.info is a comprehensive aggregation of variant annotation resources. myvariant is a wrapper for querying MyVariant.info services biocViews: VariantAnnotation, Annotation, GenomicVariation Author: Adam Mark Maintainer: Adam Mark, Chunlei Wu git_url: https://git.bioconductor.org/packages/myvariant git_branch: RELEASE_3_8 git_last_commit: 96b02ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/myvariant_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/myvariant_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/myvariant_1.12.0.tgz vignettes: vignettes/myvariant/inst/doc/myvariant.pdf vignetteTitles: Using MyVariant.R hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/myvariant/inst/doc/myvariant.R Package: mzID Version: 1.20.1 Depends: methods Imports: XML, plyr, parallel, doParallel, foreach, iterators, ProtGenerics Suggests: knitr, testthat License: GPL (>= 2) MD5sum: 75f396a9dea9aedeab107d5bdd4197f0 NeedsCompilation: no Title: An mzIdentML parser for R Description: A parser for mzIdentML files implemented using the XML package. The parser tries to be general and able to handle all types of mzIdentML files with the drawback of having less 'pretty' output than a vendor specific parser. Please contact the maintainer with any problems and supply an mzIdentML file so the problems can be fixed quickly. biocViews: ImmunoOncology, DataImport, MassSpectrometry, Proteomics Author: Thomas Lin Pedersen, Vladislav A Petyuk with contributions from Laurent Gatto and Sebastian Gibb. Maintainer: Thomas Lin Pedersen VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mzID git_branch: RELEASE_3_8 git_last_commit: 8195826 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/mzID_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/mzID_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mzID_1.20.1.tgz vignettes: vignettes/mzID/inst/doc/HOWTO_mzID.pdf vignetteTitles: Using mzID hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mzID/inst/doc/HOWTO_mzID.R importsMe: MSGFgui, MSGFplus, MSnbase, MSnID, Pbase suggestsMe: mzR Package: mzR Version: 2.16.2 Depends: Rcpp (>= 0.10.1), methods, utils Imports: Biobase, BiocGenerics (>= 0.13.6), ProtGenerics (>= 1.9.1), ncdf4 LinkingTo: Rcpp, zlibbioc, Rhdf5lib (>= 1.1.4) Suggests: msdata (>= 0.15.1), RUnit, mzID, BiocStyle (>= 2.5.19), knitr, XML License: Artistic-2.0 MD5sum: dc196dda519440a8b1419c4e65da3748 NeedsCompilation: yes Title: parser for netCDF, mzXML, mzData and mzML and mzIdentML files (mass spectrometry data) Description: mzR provides a unified API to the common file formats and parsers available for mass spectrometry data. It comes with a wrapper for the ISB random access parser for mass spectrometry mzXML, mzData and mzML files. The package contains the original code written by the ISB, and a subset of the proteowizard library for mzML and mzIdentML. The netCDF reading code has previously been used in XCMS. biocViews: ImmunoOncology, Infrastructure, DataImport, Proteomics, Metabolomics, MassSpectrometry Author: Bernd Fischer, Steffen Neumann, Laurent Gatto, Qiang Kou, Johannes Rainer Maintainer: Steffen Neumann , Laurent Gatto , Qiang Kou URL: https://github.com/sneumann/mzR/ SystemRequirements: C++11, GNU make VignetteBuilder: knitr BugReports: https://github.com/sneumann/mzR/issues/ git_url: https://git.bioconductor.org/packages/mzR git_branch: RELEASE_3_8 git_last_commit: 22d7dad git_last_commit_date: 2019-03-05 Date/Publication: 2019-03-05 source.ver: src/contrib/mzR_2.16.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/mzR_2.16.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/mzR_2.16.2.tgz vignettes: vignettes/mzR/inst/doc/mzR.html vignetteTitles: Accessin raw mass spectrometry and identification data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/mzR/inst/doc/mzR.R dependsOnMe: MSGFgui, MSnbase importsMe: MSnID, msPurity, Pbase, ProteomicsAnnotationHubData, SIMAT, topdownr, xcms, yamss suggestsMe: AnnotationHub, qcmetrics Package: NADfinder Version: 1.6.1 Depends: R (>= 3.4), BiocGenerics, IRanges, GenomicRanges, S4Vectors, SummarizedExperiment Imports: graphics, methods, baseline, signal, GenomicAlignments, GenomeInfoDb, rtracklayer, limma, trackViewer, stats, utils, Rsamtools, metap, EmpiricalBrownsMethod,ATACseqQC, corrplot, csaw Suggests: RUnit, BiocStyle, knitr, BSgenome.Mmusculus.UCSC.mm10, testthat, BiocManager License: GPL (>= 2) Archs: i386, x64 MD5sum: c3819b44a837e7bc4cef948651513532 NeedsCompilation: no Title: Call wide peaks for sequencing data Description: Nucleolus is an important structure inside the nucleus in eukaryotic cells. It is the site for transcribing rDNA into rRNA and for assembling ribosomes, aka ribosome biogenesis. In addition, nucleoli are dynamic hubs through which numerous proteins shuttle and contact specific non-rDNA genomic loci. Deep sequencing analyses of DNA associated with isolated nucleoli (NAD- seq) have shown that specific loci, termed nucleolus- associated domains (NADs) form frequent three- dimensional associations with nucleoli. NAD-seq has been used to study the biological functions of NAD and the dynamics of NAD distribution during embryonic stem cell (ESC) differentiation. Here, we developed a Bioconductor package NADfinder for bioinformatic analysis of the NAD-seq data, including normalization, smoothing, peak calling, peak trimming and annotation. biocViews: Sequencing, DNASeq, GeneRegulation, PeakDetection Author: Jianhong Ou, Haibo Liu, Jun Yu, Hervé Pagès, Paul Kaufman, Lihua Julie Zhu Maintainer: Jianhong Ou , Lihua Julie Zhu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/NADfinder git_branch: RELEASE_3_8 git_last_commit: 52f5e15 git_last_commit_date: 2019-03-22 Date/Publication: 2019-03-22 source.ver: src/contrib/NADfinder_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/NADfinder_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NADfinder_1.6.1.tgz vignettes: vignettes/NADfinder/inst/doc/NADfinder.html hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NADfinder/inst/doc/NADfinder.R Package: NanoStringDiff Version: 1.12.0 Depends: Biobase Imports: matrixStats, methods, Rcpp LinkingTo: Rcpp Suggests: testthat, BiocStyle License: GPL MD5sum: a651308ff607d0b38673ad2849dcd81b NeedsCompilation: yes Title: Differential Expression Analysis of NanoString nCounter Data Description: This Package utilizes a generalized linear model(GLM) of the negative binomial family to characterize count data and allows for multi-factor design. NanoStrongDiff incorporate size factors, calculated from positive controls and housekeeping controls, and background level, obtained from negative controls, in the model framework so that all the normalization information provided by NanoString nCounter Analyzer is fully utilized. biocViews: DifferentialExpression, Normalization Author: hong wang , tingting zhai , chi wang Maintainer: tingting zhai ,hong wang git_url: https://git.bioconductor.org/packages/NanoStringDiff git_branch: RELEASE_3_8 git_last_commit: 38531e3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NanoStringDiff_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NanoStringDiff_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NanoStringDiff_1.12.0.tgz vignettes: vignettes/NanoStringDiff/inst/doc/NanoStringDiff.pdf vignetteTitles: NanoStringDiff Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NanoStringDiff/inst/doc/NanoStringDiff.R Package: NanoStringQCPro Version: 1.14.0 Depends: R (>= 3.2), methods Imports: AnnotationDbi (>= 1.26.0), org.Hs.eg.db (>= 2.14.0), Biobase (>= 2.24.0), knitr (>= 1.12), NMF (>= 0.20.5), RColorBrewer (>= 1.0-5), png (>= 0.1-7) Suggests: roxygen2 (>= 4.0.1), testthat, BiocStyle, knitr, rmarkdown License: Artistic-2.0 Archs: i386, x64 MD5sum: 40009524e65ceb0fca927bfbda64acd0 NeedsCompilation: no Title: Quality metrics and data processing methods for NanoString mRNA gene expression data Description: NanoStringQCPro provides a set of quality metrics that can be used to assess the quality of NanoString mRNA gene expression data -- i.e. to identify outlier probes and outlier samples. It also provides different background subtraction and normalization approaches for this data. It outputs suggestions for flagging samples/probes and an easily sharable html quality control output. biocViews: Microarray, mRNAMicroarray, Preprocessing, Normalization, QualityControl, ReportWriting Author: Dorothee Nickles , Thomas Sandmann , Robert Ziman , Richard Bourgon Maintainer: Robert Ziman VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/NanoStringQCPro git_branch: RELEASE_3_8 git_last_commit: 44f77ca git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NanoStringQCPro_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NanoStringQCPro_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NanoStringQCPro_1.14.0.tgz vignettes: vignettes/NanoStringQCPro/inst/doc/vignetteNanoStringQCPro.pdf vignetteTitles: vignetteNanoStringQCPro.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: NarrowPeaks Version: 1.26.0 Depends: R (>= 2.10.0), splines Imports: BiocGenerics, S4Vectors, IRanges, GenomicRanges, GenomeInfoDb, fda, CSAR, ICSNP Suggests: rtracklayer, BiocStyle, GenomicRanges, CSAR License: Artistic-2.0 MD5sum: 31857409c4a4c04e695e58839670127e NeedsCompilation: yes Title: Shape-based Analysis of Variation in ChIP-seq using Functional PCA Description: The package applies a functional version of principal component analysis (FPCA) to: (1) Postprocess data in wiggle track format, commonly produced by generic ChIP-seq peak callers, by applying FPCA over a set of read-enriched regions (ChIP-seq peaks). This is done to study variability of the the peaks, or to shorten their genomic locations accounting for a given proportion of variation among the enrichment-score profiles. (2) Analyse differential variation between multiple ChIP-seq samples with replicates. The function 'narrowpeaksDiff' quantifies differences between the shapes, and uses Hotelling's T2 tests on the functional principal component scores to identify significant differences across conditions. An application of the package for Arabidopsis datasets is described in Mateos, Madrigal, et al. (2015) Genome Biology: 16:31. biocViews: Visualization, ChIPSeq, Transcription, Genetics, Sequencing, Sequencing Author: Pedro Madrigal , Pawel Krajewski Maintainer: Pedro Madrigal git_url: https://git.bioconductor.org/packages/NarrowPeaks git_branch: RELEASE_3_8 git_last_commit: 0d04471 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NarrowPeaks_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NarrowPeaks_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NarrowPeaks_1.26.0.tgz vignettes: vignettes/NarrowPeaks/inst/doc/NarrowPeaks.pdf vignetteTitles: NarrowPeaks Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NarrowPeaks/inst/doc/NarrowPeaks.R Package: NBSplice Version: 1.0.6 Depends: R (>= 3.5), methods Imports: edgeR, stats, MASS, car, mppa, BiocParallel, ggplot2, reshape2 Suggests: knitr, RUnit, BiocGenerics License: GPL (>=2) Archs: i386, x64 MD5sum: d0626bec690db0fab077ef81445d7edf NeedsCompilation: no Title: Negative Binomial Models to detect Differential Splicing Description: The package proposes a differential splicing evaluation method based on isoform quantification. It applies generalized linear models with negative binomial distribution to infer changes in isoform relative expression. biocViews: Software, StatisticalMethod, AlternativeSplicing, Regression, DifferentialExpression, DifferentialSplicing, RNASeq, ImmunoOncology Author: Gabriela A. Merino and Elmer A. Fernandez Maintainer: Gabriela Merino URL: http://www.bdmg.com.ar VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/NBSplice git_branch: RELEASE_3_8 git_last_commit: d87fa56 git_last_commit_date: 2019-04-02 Date/Publication: 2019-04-02 source.ver: src/contrib/NBSplice_1.0.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/NBSplice_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NBSplice_1.0.6.tgz vignettes: vignettes/NBSplice/inst/doc/NBSplice-vignette.html vignetteTitles: NBSplice-vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NBSplice/inst/doc/NBSplice-vignette.R Package: ncdfFlow Version: 2.28.1 Depends: R (>= 2.14.0), flowCore(>= 1.45.11), RcppArmadillo, methods, BH Imports: Biobase,BiocGenerics,flowCore,flowViz,zlibbioc LinkingTo: Rcpp,RcppArmadillo,BH, Rhdf5lib Suggests: testthat,parallel License: Artistic-2.0 MD5sum: fd2d7cc97af24e9ea30e17c5e4d0ab3b NeedsCompilation: yes Title: ncdfFlow: A package that provides HDF5 based storage for flow cytometry data. Description: Provides HDF5 storage based methods and functions for manipulation of flow cytometry data. biocViews: ImmunoOncology, FlowCytometry Author: Mike Jiang,Greg Finak,N. Gopalakrishnan Maintainer: Mike Jiang git_url: https://git.bioconductor.org/packages/ncdfFlow git_branch: RELEASE_3_8 git_last_commit: 5c7f7de git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ncdfFlow_2.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ncdfFlow_2.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ncdfFlow_2.28.1.tgz vignettes: vignettes/ncdfFlow/inst/doc/ncdfFlow.pdf vignetteTitles: Basic Functions for Flow Cytometry Data hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ncdfFlow/inst/doc/ncdfFlow.R dependsOnMe: flowStats, ggcyto importsMe: CytoML suggestsMe: COMPASS, cydar Package: NCIgraph Version: 1.30.0 Depends: R (>= 2.10.0) Imports: graph, KEGGgraph, methods, RBGL, RCy3, R.methodsS3 Suggests: Rgraphviz Enhances: DEGraph License: GPL-3 MD5sum: d43797d5c080c69cfd2ac24545dec3a1 NeedsCompilation: no Title: Pathways from the NCI Pathways Database Description: Provides various methods to load the pathways from the NCI Pathways Database in R graph objects and to re-format them. biocViews: Pathways, GraphAndNetwork Author: Laurent Jacob Maintainer: Laurent Jacob git_url: https://git.bioconductor.org/packages/NCIgraph git_branch: RELEASE_3_8 git_last_commit: cd841c9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NCIgraph_1.30.0.tar.gz vignettes: vignettes/NCIgraph/inst/doc/NCIgraph.pdf vignetteTitles: NCIgraph: networks from the NCI pathway integrated database as graphNEL objects. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NCIgraph/inst/doc/NCIgraph.R importsMe: DEGraph suggestsMe: DEGraph Package: ndexr Version: 1.4.1 Depends: igraph Imports: httr, jsonlite, plyr, tidyr Suggests: BiocStyle, testthat, knitr, rmarkdown License: BSD Archs: i386, x64 MD5sum: 59c656a9120eec6b187c4d44cca12cea NeedsCompilation: no Title: NDEx R client library Description: This package offers an interface to NDEx servers, e.g. the public server at http://ndexbio.org/. It can retrieve and save networks via the API. Networks are offered as RCX object and as igraph representation. biocViews: Pathways, DataImport, Network Author: Florian Auer , Frank Kramer , Alex Ishkin , Dexter Pratt Maintainer: Florian Auer URL: https://github.com/frankkramer-lab/ndexr VignetteBuilder: knitr BugReports: https://github.com/frankkramer-lab/ndexr/issues git_url: https://git.bioconductor.org/packages/ndexr git_branch: RELEASE_3_8 git_last_commit: 23412f7 git_last_commit_date: 2019-01-09 Date/Publication: 2019-01-11 source.ver: src/contrib/ndexr_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ndexr_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ndexr_1.4.1.tgz vignettes: vignettes/ndexr/inst/doc/ndexr-vignette.html vignetteTitles: NDExR Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ndexr/inst/doc/ndexr-vignette.R Package: NeighborNet Version: 1.0.0 Depends: methods Imports: graph, stats License: CC BY-NC-ND 4.0 MD5sum: a3341ae47afcce8284786132a3bdf393 NeedsCompilation: no Title: Neighbor_net analysis Description: Identify the putative mechanism explaining the active interactions between genes in the investigated phenotype. biocViews: Software, GeneExpression, StatisticalMethod, GraphAndNetwork Author: Sahar Ansari and Sorin Draghici Maintainer: Sahar Ansari git_url: https://git.bioconductor.org/packages/NeighborNet git_branch: RELEASE_3_8 git_last_commit: d526e45 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NeighborNet_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NeighborNet_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NeighborNet_1.0.0.tgz vignettes: vignettes/NeighborNet/inst/doc/neighborNet.pdf vignetteTitles: NeighborNet hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NeighborNet/inst/doc/neighborNet.R Package: nem Version: 2.56.0 Depends: R (>= 3.0) Imports: boot, e1071, graph, graphics, grDevices, methods, RBGL (>= 1.8.1), RColorBrewer, stats, utils, Rgraphviz, statmod, plotrix, limma Suggests: Biobase (>= 1.10) Enhances: doMC, snow, parallel License: GPL (>= 2) MD5sum: 0f3029446be3426d2e2ea986073e0122 NeedsCompilation: yes Title: (Dynamic) Nested Effects Models and Deterministic Effects Propagation Networks to reconstruct phenotypic hierarchies Description: The package 'nem' allows to reconstruct features of pathways from the nested structure of perturbation effects. It takes as input (1.) a set of pathway components, which were perturbed, and (2.) phenotypic readout of these perturbations (e.g. gene expression, protein expression). The output is a directed graph representing the phenotypic hierarchy. biocViews: Microarray, Bioinformatics, GraphsAndNetworks, Pathways, SystemsBiology, NetworkInference Author: Holger Froehlich, Florian Markowetz, Achim Tresch, Theresa Niederberger, Christian Bender, Matthias Maneck, Claudio Lottaz, Tim Beissbarth Maintainer: Holger Froehlich URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/nem git_branch: RELEASE_3_8 git_last_commit: d6f277a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/nem_2.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/nem_2.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nem_2.56.0.tgz vignettes: vignettes/nem/inst/doc/markowetz-thesis-2006.pdf, vignettes/nem/inst/doc/nem.pdf vignetteTitles: markowetz-thesis-2006.pdf, Nested Effects Models - An example in Drosophila immune response hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/nem/inst/doc/nem.R dependsOnMe: lpNet importsMe: birte, epiNEM, OncoSimulR suggestsMe: rBiopaxParser Package: netbenchmark Version: 1.14.0 Depends: grndata (>= 0.99.3) Imports: Rcpp (>= 0.11.0), minet, GENIE3, c3net, PCIT, GeneNet, tools, pracma, Matrix, corpcor, fdrtool LinkingTo: Rcpp Suggests: RUnit, BiocGenerics, knitr, graph License: CC BY-NC-SA 4.0 Archs: i386, x64 MD5sum: 3d0c34121a30be63e0fc2837c021f253 NeedsCompilation: yes Title: Benchmarking of several gene network inference methods Description: This package implements a benchmarking of several gene network inference algorithms from gene expression data. biocViews: Microarray, GraphAndNetwork, Network, NetworkInference, GeneExpression Author: Pau Bellot, Catharina Olsen, Patrick Meyer Maintainer: Pau Bellot URL: https://imatge.upc.edu/netbenchmark/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/netbenchmark git_branch: RELEASE_3_8 git_last_commit: cd81c69 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/netbenchmark_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/netbenchmark_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/netbenchmark_1.14.0.tgz vignettes: vignettes/netbenchmark/inst/doc/netbenchmark.html vignetteTitles: Netbenchmark hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/netbenchmark/inst/doc/netbenchmark.R Package: netbiov Version: 1.16.0 Depends: R (>= 3.1.0), igraph (>= 0.7.1) Suggests: BiocStyle,RUnit,BiocGenerics,Matrix License: GPL (>= 2) Archs: i386, x64 MD5sum: 41e9eece65723f5328ca9f15ffce01b9 NeedsCompilation: no Title: A package for visualizing complex biological network Description: A package that provides an effective visualization of large biological networks biocViews: GraphAndNetwork, Network, Software, Visualization Author: Shailesh tripathi and Frank Emmert-Streib Maintainer: Shailesh tripathi URL: http://www.bio-complexity.com git_url: https://git.bioconductor.org/packages/netbiov git_branch: RELEASE_3_8 git_last_commit: 4fb470e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/netbiov_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/netbiov_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/netbiov_1.16.0.tgz vignettes: vignettes/netbiov/inst/doc/netbiov-intro.pdf vignetteTitles: netbiov: An R package for visualizing biological networks hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/netbiov/inst/doc/netbiov-intro.R Package: nethet Version: 1.14.0 Imports: glasso, mvtnorm, parcor, GeneNet, huge, CompQuadForm, ggm, mclust, parallel, GSA, limma, multtest, ICSNP, glmnet, network, ggplot2 Suggests: knitr, xtable, BiocStyle License: GPL-2 MD5sum: de7f46b2f5c400fde16c3954ebc9ff1b NeedsCompilation: yes Title: A bioconductor package for high-dimensional exploration of biological network heterogeneity Description: Package nethet is an implementation of statistical solid methodology enabling the analysis of network heterogeneity from high-dimensional data. It combines several implementations of recent statistical innovations useful for estimation and comparison of networks in a heterogeneous, high-dimensional setting. In particular, we provide code for formal two-sample testing in Gaussian graphical models (differential network and GGM-GSA; Stadler and Mukherjee, 2013, 2014) and make a novel network-based clustering algorithm available (mixed graphical lasso, Stadler and Mukherjee, 2013). biocViews: Clustering, GraphAndNetwork Author: Nicolas Staedler, Frank Dondelinger Maintainer: Nicolas Staedler , Frank Dondelinger VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/nethet git_branch: RELEASE_3_8 git_last_commit: c4fd0d9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/nethet_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/nethet_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nethet_1.14.0.tgz vignettes: vignettes/nethet/inst/doc/nethet.pdf vignetteTitles: nethet hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/nethet/inst/doc/nethet.R Package: NetPathMiner Version: 1.18.0 Depends: R (>= 3.0.2), igraph (>= 1.0) Suggests: rBiopaxParser (>= 2.1), RCurl, graph License: GPL (>= 2) Archs: i386, x64 MD5sum: a7126fcb4431a1f78cb8e4742ae70635 NeedsCompilation: yes Title: NetPathMiner for Biological Network Construction, Path Mining and Visualization Description: NetPathMiner is a general framework for network path mining using genome-scale networks. It constructs networks from KGML, SBML and BioPAX files, providing three network representations, metabolic, reaction and gene representations. NetPathMiner finds active paths and applies machine learning methods to summarize found paths for easy interpretation. It also provides static and interactive visualizations of networks and paths to aid manual investigation. biocViews: GraphAndNetwork, Pathways, Network, Clustering, Classification Author: Ahmed Mohamed , Tim Hancock , Ichigaku Takigawa , Nicolas Wicker Maintainer: Ahmed Mohamed URL: https://github.com/ahmohamed/NetPathMiner SystemRequirements: libxml2, libSBML (>= 5.5) git_url: https://git.bioconductor.org/packages/NetPathMiner git_branch: RELEASE_3_8 git_last_commit: 8afb807 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NetPathMiner_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NetPathMiner_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NetPathMiner_1.18.0.tgz vignettes: vignettes/NetPathMiner/inst/doc/NPMVignette.pdf vignetteTitles: NetPathMiner Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NetPathMiner/inst/doc/NPMVignette.R Package: netprioR Version: 1.8.1 Depends: methods, graphics, R(>= 3.3) Imports: stats, Matrix, dplyr, doParallel, foreach, parallel, sparseMVN, ggplot2, gridExtra, pROC Suggests: knitr, BiocStyle, pander License: GPL-3 Archs: i386, x64 MD5sum: 3078ae2243153e998aabc88e6ac119aa NeedsCompilation: no Title: A model for network-based prioritisation of genes Description: A model for semi-supervised prioritisation of genes integrating network data, phenotypes and additional prior knowledge about TP and TN gene labels from the literature or experts. biocViews: ImmunoOncology, CellBasedAssays, Preprocessing, Network Author: Fabian Schmich Maintainer: Fabian Schmich URL: http://bioconductor.org/packages/netprioR VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/netprioR git_branch: RELEASE_3_8 git_last_commit: 23916ad git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/netprioR_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/netprioR_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/netprioR_1.8.1.tgz vignettes: vignettes/netprioR/inst/doc/netprioR.html vignetteTitles: netprioR Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/netprioR/inst/doc/netprioR.R Package: netReg Version: 1.6.0 Depends: R(>= 3.4) Imports: Rcpp, stats LinkingTo: Rcpp, RcppArmadillo Suggests: testthat, knitr, rmarkdown, BiocStyle, lintr, lassoshooting License: GPL-3 | BSL-1.0 + file LICENSE MD5sum: 8f3db56ff84e07615627658da1c40bff NeedsCompilation: yes Title: Network-Regularized Regression Models Description: netReg fits linear regression models using network-penalization. Graph prior knowledge, in the form of biological networks, is being incorporated into the loss function of the linear model. The networks describe biological relationships such as co-regulation or dependency of the same transcription factors/metabolites/etc. yielding a part sparse and part smooth solution for coefficient profiles. biocViews: Software, StatisticalMethod, Regression, FeatureExtraction, Network, GraphAndNetwork Author: Simon Dirmeier [aut, cre] Maintainer: Simon Dirmeier URL: https://github.com/dirmeier/netReg SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/dirmeier/netReg/issues git_url: https://git.bioconductor.org/packages/netReg git_branch: RELEASE_3_8 git_last_commit: 5019b18 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/netReg_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/netReg_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/netReg_1.6.0.tgz vignettes: vignettes/netReg/inst/doc/netReg.html vignetteTitles: netReg hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/netReg/inst/doc/netReg.R Package: netresponse Version: 1.42.0 Depends: R (>= 2.15.1), Rgraphviz, methods, minet, mclust, reshape2 Imports: dmt, ggplot2, graph, igraph, parallel, plyr, qvalue, RColorBrewer License: GPL (>=2) Archs: i386, x64 MD5sum: 6f7b9e38c87012015f0bb9ba8f53b718 NeedsCompilation: yes Title: Functional Network Analysis Description: Algorithms for functional network analysis. Includes an implementation of a variational Dirichlet process Gaussian mixture model for nonparametric mixture modeling. biocViews: CellBiology, Clustering, GeneExpression, Genetics, Network, GraphAndNetwork, DifferentialExpression, Microarray, Transcription Author: Leo Lahti, Olli-Pekka Huovilainen, Antonio Gusmao and Juuso Parkkinen Maintainer: Leo Lahti URL: https://github.com/antagomir/netresponse BugReports: https://github.com/antagomir/netresponse/issues git_url: https://git.bioconductor.org/packages/netresponse git_branch: RELEASE_3_8 git_last_commit: e9b9422 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/netresponse_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/netresponse_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/netresponse_1.42.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: NetSAM Version: 1.22.0 Depends: R (>= 2.15.1), methods, igraph (>= 0.6-1), seriation (>= 1.0-6), graph (>= 1.34.0) Imports: methods Suggests: RUnit, BiocGenerics License: LGPL Archs: i386, x64 MD5sum: 38f4ae15c77a17e4b2774fc0b6ce9e8d NeedsCompilation: no Title: Network Seriation And Modularization Description: The NetSAM (Network Seriation and Modularization) package takes an edge-list representation of a network as an input, performs network seriation and modularization analysis, and generates as files that can be used as an input for the one-dimensional network visualization tool NetGestalt (http://www.netgestalt.org) or other network analysis. biocViews: Visualization, Network Author: Jing Wang Maintainer: Bing Zhang git_url: https://git.bioconductor.org/packages/NetSAM git_branch: RELEASE_3_8 git_last_commit: 2a8f3cb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NetSAM_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NetSAM_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NetSAM_1.22.0.tgz vignettes: vignettes/NetSAM/inst/doc/NetSAM.pdf vignetteTitles: NetSAM hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NetSAM/inst/doc/NetSAM.R Package: netSmooth Version: 1.2.0 Depends: R (>= 3.5), scater (>= 1.7.11), clusterExperiment (>= 1.99.1) Imports: entropy, SummarizedExperiment, SingleCellExperiment, Matrix, cluster, data.table, stats, methods Suggests: knitr, testthat, Rtsne, biomaRt, igraph, STRINGdb, NMI, pheatmap, ggplot2, BiocStyle, rmarkdown, BiocParallel License: GPL-3 MD5sum: 30774513e8fa21902cc5d68b92e4ca54 NeedsCompilation: no Title: Network smoothing for scRNAseq Description: netSmooth is an R package for network smoothing of single cell RNA sequencing data. Using bio networks such as protein-protein interactions as priors for gene co-expression, netsmooth improves cell type identification from noisy, sparse scRNAseq data. biocViews: Network, GraphAndNetwork, SingleCell, RNASeq, GeneExpression, Sequencing, Transcriptomics, Normalization, Preprocessing, Clustering, DimensionReduction Author: Jonathan Ronen [aut, cre], Altuna Akalin [aut] Maintainer: Jonathan Ronen URL: https://github.com/BIMSBbioinfo/netSmooth VignetteBuilder: knitr BugReports: https://github.com/BIMSBbioinfo/netSmooth/issues git_url: https://git.bioconductor.org/packages/netSmooth git_branch: RELEASE_3_8 git_last_commit: 03b5acc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/netSmooth_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/netSmooth_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/netSmooth_1.2.0.tgz vignettes: vignettes/netSmooth/inst/doc/buildingPPIsFromStringDB.html, vignettes/netSmooth/inst/doc/netSmoothIntro.html vignetteTitles: netSmooth example, netSmooth example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/netSmooth/inst/doc/buildingPPIsFromStringDB.R, vignettes/netSmooth/inst/doc/netSmoothIntro.R Package: networkBMA Version: 2.22.0 Depends: R (>= 2.15.0), stats, utils, BMA, Rcpp (>= 0.10.3), RcppArmadillo (>= 0.3.810.2), RcppEigen (>= 0.3.1.2.1), leaps LinkingTo: Rcpp, RcppArmadillo, RcppEigen, BH License: GPL (>= 2) MD5sum: 44c5d02a7bd54f626209644786f8a5d4 NeedsCompilation: yes Title: Regression-based network inference using Bayesian Model Averaging Description: An extension of Bayesian Model Averaging (BMA) for network construction using time series gene expression data. Includes assessment functions and sample test data. biocViews: GraphsAndNetwork, NetworkInference, GeneExpression, GeneTarget, Network, Bayesian Author: Chris Fraley, Wm. Chad Young, Ling-Hong Hung, Kaiyuan Shi, Ka Yee Yeung, Adrian Raftery (with contributions from Kenneth Lo) Maintainer: Ka Yee Yeung SystemRequirements: liblapack-dev git_url: https://git.bioconductor.org/packages/networkBMA git_branch: RELEASE_3_8 git_last_commit: 3e29256 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/networkBMA_2.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/networkBMA_2.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/networkBMA_2.22.0.tgz vignettes: vignettes/networkBMA/inst/doc/networkBMA.pdf vignetteTitles: networkBMA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/networkBMA/inst/doc/networkBMA.R Package: NGScopy Version: 1.16.1 Depends: R (>= 3.1.0) Imports: methods, parallel, Xmisc (>= 0.2.1), rbamtools (>= 2.6.0), changepoint (>= 2.1.1) Suggests: RUnit, NGScopyData, GenomicRanges License: GPL (>=2) Archs: i386, x64 MD5sum: 031942d8487ccaa4d6144a4f721c9035 NeedsCompilation: no Title: NGScopy: Detection of Copy Number Variations in Next Generation Sequencing sequencing Description: NGScopy provides a quantitative caller for detecting copy number variations in next generation sequencing (NGS), including whole genome sequencing (WGS), whole exome sequencing (WES) and targeted panel sequencing (TPS). The caller can be parallelized by chromosomes to use multiple processors/cores on one computer. biocViews: ImmunoOncology, CopyNumberVariation, DNASeq, TargetedResequencing, ExomeSeq, WholeGenome, Sequencing Author: Xiaobei Zhao [aut, cre, cph] Maintainer: Xiaobei Zhao git_url: https://git.bioconductor.org/packages/NGScopy git_branch: RELEASE_3_8 git_last_commit: 61b4b5f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/NGScopy_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/NGScopy_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NGScopy_1.16.1.tgz vignettes: vignettes/NGScopy/inst/doc/NGScopy-vignette.pdf vignetteTitles: NGScopy: Detection of copy number variations in next generation sequencing (User's Guide) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NGScopy/inst/doc/NGScopy-vignette.R Package: nnNorm Version: 2.46.0 Depends: R(>= 2.2.0), marray Imports: graphics, grDevices, marray, methods, nnet, stats License: LGPL MD5sum: f9f516d28deb61db8d90266ed1adce97 NeedsCompilation: no Title: Spatial and intensity based normalization of cDNA microarray data based on robust neural nets Description: This package allows to detect and correct for spatial and intensity biases with two-channel microarray data. The normalization method implemented in this package is based on robust neural networks fitting. biocViews: Microarray, TwoChannel, Preprocessing Author: Adi Laurentiu Tarca Maintainer: Adi Laurentiu Tarca URL: http://bioinformaticsprb.med.wayne.edu/tarca/ git_url: https://git.bioconductor.org/packages/nnNorm git_branch: RELEASE_3_8 git_last_commit: 6d7248d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/nnNorm_2.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/nnNorm_2.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nnNorm_2.46.0.tgz vignettes: vignettes/nnNorm/inst/doc/nnNorm.pdf vignetteTitles: nnNorm Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/nnNorm/inst/doc/nnNorm.R Package: NOISeq Version: 2.26.1 Depends: R (>= 2.13.0), methods, Biobase (>= 2.13.11), splines (>= 3.0.1), Matrix (>= 1.2) License: Artistic-2.0 MD5sum: 2028db280d6562765567bc659dd1b7b6 NeedsCompilation: no Title: Exploratory analysis and differential expression for RNA-seq data Description: Analysis of RNA-seq expression data or other similar kind of data. Exploratory plots to evualuate saturation, count distribution, expression per chromosome, type of detected features, features length, etc. Differential expression between two experimental conditions with no parametric assumptions. biocViews: ImmunoOncology, RNASeq, DifferentialExpression, Visualization, Sequencing Author: Sonia Tarazona, Pedro Furio-Tari, Maria Jose Nueda, Alberto Ferrer and Ana Conesa Maintainer: Sonia Tarazona git_url: https://git.bioconductor.org/packages/NOISeq git_branch: RELEASE_3_8 git_last_commit: 95b9b71 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/NOISeq_2.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/NOISeq_2.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NOISeq_2.26.1.tgz vignettes: vignettes/NOISeq/inst/doc/NOISeq.pdf, vignettes/NOISeq/inst/doc/QCreport.pdf vignetteTitles: NOISeq User's Guide, QCreport.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NOISeq/inst/doc/NOISeq.R dependsOnMe: metaSeq importsMe: CNVPanelizer, metaseqR suggestsMe: compcodeR Package: nondetects Version: 2.12.0 Depends: R (>= 3.2), Biobase (>= 2.22.0) Imports: limma, mvtnorm, utils, methods, arm, HTqPCR (>= 1.16.0) Suggests: knitr, rmarkdown, BiocStyle (>= 1.0.0), RUnit, BiocGenerics (>= 0.8.0) License: GPL-3 MD5sum: 38eb1814c20ef744c713f59b42707d47 NeedsCompilation: no Title: Non-detects in qPCR data Description: Methods to model and impute non-detects in the results of qPCR experiments. biocViews: Software, AssayDomain, GeneExpression, Technology, qPCR, WorkflowStep, Preprocessing Author: Matthew N. McCall , Valeriia Sherina Maintainer: Valeriia Sherina VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/nondetects git_branch: RELEASE_3_8 git_last_commit: 69b725e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/nondetects_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/nondetects_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nondetects_2.12.0.tgz vignettes: vignettes/nondetects/inst/doc/nondetects.html vignetteTitles: Title of your vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/nondetects/inst/doc/nondetects.R Package: normalize450K Version: 1.10.0 Depends: R (>= 3.3), Biobase, illuminaio, quadprog Imports: utils License: BSD_2_clause + file LICENSE MD5sum: 0a46946dedab5b5e7ae7f269aedd7664 NeedsCompilation: no Title: Preprocessing of Illumina Infinium 450K data Description: Precise measurements are important for epigenome-wide studies investigating DNA methylation in whole blood samples, where effect sizes are expected to be small in magnitude. The 450K platform is often affected by batch effects and proper preprocessing is recommended. This package provides functions to read and normalize 450K '.idat' files. The normalization corrects for dye bias and biases related to signal intensity and methylation of probes using local regression. No adjustment for probe type bias is performed to avoid the trade-off of precision for accuracy of beta-values. biocViews: Normalization, DNAMethylation, Microarray, TwoChannel, Preprocessing, MethylationArray Author: Jonathan Alexander Heiss Maintainer: Jonathan Alexander Heiss git_url: https://git.bioconductor.org/packages/normalize450K git_branch: RELEASE_3_8 git_last_commit: 0e77ff5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/normalize450K_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/normalize450K_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/normalize450K_1.10.0.tgz vignettes: vignettes/normalize450K/inst/doc/read_and_normalize450K.pdf vignetteTitles: Normalization of 450K data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/normalize450K/inst/doc/read_and_normalize450K.R Package: NormalyzerDE Version: 1.0.0 Depends: R (>= 3.5) Imports: vsn, preprocessCore, limma, MASS, ape, car, ggplot2, methods, Biobase, RcmdrMisc, raster, utils, stats, SummarizedExperiment, matrixStats Suggests: knitr, testthat, rmarkdown, roxygen2, hexbin License: Artistic-2.0 MD5sum: e1ce8d162271f6aa58b181ea8135dfd8 NeedsCompilation: no Title: Evaluation of normalization methods and calculation of differential expression analysis statistics Description: NormalyzerDE provides screening of normalization methods for LC-MS based expression data. It calculates a range of normalized matrices using both existing approaches and a novel time-segmented approach, calculates performance measures and generates an evaluation report. Furthermore, it provides an easy utility for Limma- or ANOVA- based differential expression analysis. biocViews: Normalization, MultipleComparison, Visualization, Bayesian, Proteomics, Metabolomics, DifferentialExpression Author: Jakob Willforss Maintainer: Jakob Willforss URL: https://github.com/ComputationalProteomics/NormalyzerDE VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/NormalyzerDE git_branch: RELEASE_3_8 git_last_commit: 34d92b0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NormalyzerDE_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NormalyzerDE_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NormalyzerDE_1.0.0.tgz vignettes: vignettes/NormalyzerDE/inst/doc/vignette.pdf vignetteTitles: Differential expression and countering technical biases using NormalyzerDE hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NormalyzerDE/inst/doc/vignette.R Package: NormqPCR Version: 1.28.0 Depends: R(>= 2.14.0), stats, RColorBrewer, Biobase, methods, ReadqPCR, qpcR License: LGPL-3 MD5sum: b1753d4e090d39b0d490eb14ff5d47c3 NeedsCompilation: no Title: Functions for normalisation of RT-qPCR data Description: Functions for the selection of optimal reference genes and the normalisation of real-time quantitative PCR data. biocViews: MicrotitrePlateAssay, GeneExpression, qPCR Author: Matthias Kohl, James Perkins, Nor Izayu Abdul Rahman Maintainer: James Perkins URL: www.bioconductor.org/packages/release/bioc/html/NormqPCR.html git_url: https://git.bioconductor.org/packages/NormqPCR git_branch: RELEASE_3_8 git_last_commit: 562ece9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NormqPCR_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NormqPCR_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NormqPCR_1.28.0.tgz vignettes: vignettes/NormqPCR/inst/doc/NormqPCR.pdf vignetteTitles: NormqPCR: Functions for normalisation of RT-qPCR data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NormqPCR/inst/doc/NormqPCR.R Package: normr Version: 1.8.0 Depends: R (>= 3.3.0) Imports: methods, stats, utils, grDevices, parallel, GenomeInfoDb, GenomicRanges, IRanges, Rcpp (>= 0.11), qvalue (>= 2.2), bamsignals (>= 1.4), rtracklayer (>= 1.32) LinkingTo: Rcpp Suggests: BiocStyle, testthat (>= 1.0), knitr, rmarkdown Enhances: BiocParallel License: GPL-2 MD5sum: b809094a96f2751f7562dfa70759b690 NeedsCompilation: yes Title: Normalization and difference calling in ChIP-seq data Description: Robust normalization and difference calling procedures for ChIP-seq and alike data. Read counts are modeled jointly as a binomial mixture model with a user-specified number of components. A fitted background estimate accounts for the effect of enrichment in certain regions and, therefore, represents an appropriate null hypothesis. This robust background is used to identify significantly enriched or depleted regions. biocViews: Bayesian, DifferentialPeakCalling, Classification, DataImport, ChIPSeq, RIPSeq, FunctionalGenomics, Genetics, MultipleComparison, Normalization, PeakDetection, Preprocessing, Alignment Author: Johannes Helmuth [aut, cre], Ho-Ryun Chung [aut] Maintainer: Johannes Helmuth URL: https://github.com/your-highness/normR SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://github.com/your-highness/normR/issues git_url: https://git.bioconductor.org/packages/normr git_branch: RELEASE_3_8 git_last_commit: 63325d9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/normr_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/normr_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/normr_1.8.0.tgz vignettes: vignettes/normr/inst/doc/normr.html vignetteTitles: Introduction to the normR package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/normr/inst/doc/normr.R Package: npGSEA Version: 1.18.0 Depends: GSEABase (>= 1.24.0) Imports: Biobase, methods, BiocGenerics, graphics, stats Suggests: ALL, genefilter, limma, hgu95av2.db, ReportingTools, BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: 6cb8b32d6c6c22ce37e259a411912495 NeedsCompilation: no Title: Permutation approximation methods for gene set enrichment analysis (non-permutation GSEA) Description: Current gene set enrichment methods rely upon permutations for inference. These approaches are computationally expensive and have minimum achievable p-values based on the number of permutations, not on the actual observed statistics. We have derived three parametric approximations to the permutation distributions of two gene set enrichment test statistics. We are able to reduce the computational burden and granularity issues of permutation testing with our method, which is implemented in this package. npGSEA calculates gene set enrichment statistics and p-values without the computational cost of permutations. It is applicable in settings where one or many gene sets are of interest. There are also built-in plotting functions to help users visualize results. biocViews: GeneSetEnrichment, Microarray, StatisticalMethod, Pathways Author: Jessica Larson and Art Owen Maintainer: Jessica Larson git_url: https://git.bioconductor.org/packages/npGSEA git_branch: RELEASE_3_8 git_last_commit: f94564c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/npGSEA_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/npGSEA_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/npGSEA_1.18.0.tgz vignettes: vignettes/npGSEA/inst/doc/npGSEA.pdf vignetteTitles: Running gene set enrichment analysis with the "npGSEA" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/npGSEA/inst/doc/npGSEA.R Package: NTW Version: 1.32.0 Depends: R (>= 2.3.0) Imports: mvtnorm, stats, utils License: GPL-2 MD5sum: 68f21a43a4f188db6c040831e7385b10 NeedsCompilation: no Title: Predict gene network using an Ordinary Differential Equation (ODE) based method Description: This package predicts the gene-gene interaction network and identifies the direct transcriptional targets of the perturbation using an ODE (Ordinary Differential Equation) based method. biocViews: Preprocessing Author: Wei Xiao, Yin Jin, Darong Lai, Xinyi Yang, Yuanhua Liu, Christine Nardini Maintainer: Yuanhua Liu git_url: https://git.bioconductor.org/packages/NTW git_branch: RELEASE_3_8 git_last_commit: f4baa68 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NTW_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NTW_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NTW_1.32.0.tgz vignettes: vignettes/NTW/inst/doc/NTW.pdf vignetteTitles: NTW vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NTW/inst/doc/NTW.R Package: nucleoSim Version: 1.10.0 Imports: stats, IRanges, S4Vectors, graphics, methods Suggests: BiocStyle, BiocGenerics, knitr, rmarkdown, RUnit License: Artistic-2.0 MD5sum: 29ba1741cbd3ec9feee1a274523abc2f NeedsCompilation: no Title: Generate synthetic nucleosome maps Description: This package can generate a synthetic map with reads covering the nucleosome regions as well as a synthetic map with forward and reverse reads emulating next-generation sequencing. The user has choice between three different distributions for the read positioning: Normal, Student and Uniform. biocViews: Genetics, Sequencing, Software, StatisticalMethod, Alignment Author: Rawane Samb [aut], Astrid Deschênes [cre, aut], Pascal Belleau [aut], Arnaud Droit [aut] Maintainer: Astrid Deschenes URL: https://github.com/arnauddroitlab/nucleoSim VignetteBuilder: knitr BugReports: https://github.com/arnauddroitlab/nucleoSim/issues git_url: https://git.bioconductor.org/packages/nucleoSim git_branch: RELEASE_3_8 git_last_commit: 3890364 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/nucleoSim_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/nucleoSim_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nucleoSim_1.10.0.tgz vignettes: vignettes/nucleoSim/inst/doc/nucleoSim.html vignetteTitles: Generate synthetic nucleosome maps hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/nucleoSim/inst/doc/nucleoSim.R suggestsMe: RJMCMCNucleosomes Package: nucleR Version: 2.14.0 Depends: methods Imports: Biobase, BiocGenerics, Biostrings, GenomeInfoDb, GenomicRanges, IRanges, Rsamtools, S4Vectors, ShortRead, dplyr, ggplot2, magrittr, parallel, stats, utils Suggests: Starr, BiocStyle, knitr, rmarkdown, testthat License: LGPL (>= 3) MD5sum: 076a8f41e0d540563418f0874b2f3590 NeedsCompilation: no Title: Nucleosome positioning package for R Description: Nucleosome positioning for Tiling Arrays and NGS experiments. biocViews: NucleosomePositioning, Coverage, ChIPSeq, Microarray, Sequencing, Genetics, QualityControl, DataImport Author: Oscar Flores, Ricard Illa Maintainer: Ricard Illa VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/nucleR git_branch: RELEASE_3_8 git_last_commit: 28d33d4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/nucleR_2.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/nucleR_2.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nucleR_2.14.0.tgz vignettes: vignettes/nucleR/inst/doc/nucleR.pdf vignetteTitles: Vignette Title hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/nucleR/inst/doc/nucleR.R Package: nuCpos Version: 1.0.1 Depends: R (>= 3.5.1) Imports: graphics, methods Suggests: NuPoP, Biostrings, testthat License: GPL-2 MD5sum: 6ccdb6f4d22329dcde145b703cc56974 NeedsCompilation: yes Title: An R package for prediction of nucleosome positions Description: nuCpos, a derivative of NuPoP, is an R package for prediction of nucleosome positions. In nuCpos, a duration hidden Markov model is trained with a chemical map of nucleosomes either from budding yeast, fission yeast, or mouse embryonic stem cells. nuCpos outputs the Viterbi (most probable) path of nucleosome-linker states, predicted nucleosome occupancy scores and histone binding affinity (HBA) scores as NuPoP does. nuCpos can also calculate local and whole nucleosomal HBA scores for a given 147-bp sequence. Furthermore, effect of genetic alterations on nucleosome occupancy can be predicted with this package. The parental package NuPoP, which is based on an MNase-seq-based map of budding yeast nucleosomes, was developed by Ji-Ping Wang and Liqun Xi, licensed under GPL-2. biocViews: ImmunoOncology, Genetics, Epigenetics, NucleosomePositioning, HiddenMarkovModel Author: Hiroaki Kato, Takeshi Urano Maintainer: Hiroaki Kato git_url: https://git.bioconductor.org/packages/nuCpos git_branch: RELEASE_3_8 git_last_commit: 3451088 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/nuCpos_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/nuCpos_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/nuCpos_1.0.1.tgz vignettes: vignettes/nuCpos/inst/doc/nuCpos-intro.pdf vignetteTitles: An R package for prediction of nucleosome positioning hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/nuCpos/inst/doc/nuCpos-intro.R Package: NuPoP Version: 1.32.0 Depends: R (>= 2.10) License: GPL-2 Archs: i386, x64 MD5sum: 4770138a010896a75cfedbde935bc816 NeedsCompilation: yes Title: An R package for nucleosome positioning prediction Description: NuPoP is an R package for Nucleosome Positioning Prediction.This package is built upon a duration hidden Markov model proposed in Xi et al, 2010; Wang et al, 2008. The core of the package was written in Fotran. In addition to the R package, a stand-alone Fortran software tool is also available at http://nucleosome.stats.northwestern.edu. biocViews: Genetics,Visualization,Classification Author: Ji-Ping Wang ; Liqun Xi Maintainer: Ji-Ping Wang git_url: https://git.bioconductor.org/packages/NuPoP git_branch: RELEASE_3_8 git_last_commit: c2669a9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/NuPoP_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/NuPoP_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/NuPoP_1.32.0.tgz vignettes: vignettes/NuPoP/inst/doc/NuPoP-intro.pdf vignetteTitles: An R package for Nucleosome positioning prediction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/NuPoP/inst/doc/NuPoP-intro.R suggestsMe: nuCpos Package: occugene Version: 1.42.0 Depends: R (>= 2.0.0) License: GPL (>= 2) Archs: i386, x64 MD5sum: c294febad5ded94b6e0f1223beac3b78 NeedsCompilation: no Title: Functions for Multinomial Occupancy Distribution Description: Statistical tools for building random mutagenesis libraries for prokaryotes. The package has functions for handling the occupancy distribution for a multinomial and for estimating the number of essential genes in random transposon mutagenesis libraries. biocViews: Annotation, Pathways Author: Oliver Will Maintainer: Oliver Will git_url: https://git.bioconductor.org/packages/occugene git_branch: RELEASE_3_8 git_last_commit: c19ea72 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/occugene_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/occugene_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/occugene_1.42.0.tgz vignettes: vignettes/occugene/inst/doc/occugene.pdf vignetteTitles: occugene hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/occugene/inst/doc/occugene.R Package: OCplus Version: 1.56.0 Depends: R (>= 2.1.0) Imports: multtest (>= 1.7.3), graphics, grDevices, stats, akima License: LGPL MD5sum: 318784b120a74c9a49abecfdeb6d0891 NeedsCompilation: no Title: Operating characteristics plus sample size and local fdr for microarray experiments Description: This package allows to characterize the operating characteristics of a microarray experiment, i.e. the trade-off between false discovery rate and the power to detect truly regulated genes. The package includes tools both for planned experiments (for sample size assessment) and for already collected data (identification of differentially expressed genes). biocViews: Microarray, DifferentialExpression, MultipleComparison Author: Yudi Pawitan and Alexander Ploner Maintainer: Alexander Ploner git_url: https://git.bioconductor.org/packages/OCplus git_branch: RELEASE_3_8 git_last_commit: 122a7f3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OCplus_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OCplus_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OCplus_1.56.0.tgz vignettes: vignettes/OCplus/inst/doc/OCplus.pdf vignetteTitles: OCplus Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OCplus/inst/doc/OCplus.R Package: odseq Version: 1.10.0 Depends: R (>= 3.2.3) Imports: msa (>= 1.2.1), kebabs (>= 1.4.1), mclust (>= 5.1) Suggests: knitr(>= 1.11) License: MIT + file LICENSE MD5sum: 18974dd1cc6085e325565b9a4f01e635 NeedsCompilation: no Title: Outlier detection in multiple sequence alignments Description: Performs outlier detection of sequences in a multiple sequence alignment using bootstrap of predefined distance metrics. Outlier sequences can make downstream analyses unreliable or make the alignments less accurate while they are being constructed. This package implements the OD-seq algorithm proposed by Jehl et al (doi 10.1186/s12859-015-0702-1) for aligned sequences and a variant using string kernels for unaligned sequences. biocViews: Alignment, MultipleSequenceAlignment Author: José Jiménez Maintainer: José Jiménez VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/odseq git_branch: RELEASE_3_8 git_last_commit: 5c17c94 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/odseq_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/odseq_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/odseq_1.10.0.tgz vignettes: vignettes/odseq/inst/doc/vignette.pdf vignetteTitles: A quick tutorial to outlier detection in MSAs hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/odseq/inst/doc/vignette.R Package: OGSA Version: 1.12.0 Depends: R (>= 3.2.0) Imports: gplots(>= 2.8.0), limma(>= 3.18.13), Biobase License: GPL (== 2) MD5sum: 3e46b50f76f97e0da3c912e661bd5e12 NeedsCompilation: no Title: Outlier Gene Set Analysis Description: OGSA provides a global estimate of pathway deregulation in cancer subtypes by integrating the estimates of significance for individual pathway members that have been identified by outlier analysis. biocViews: GeneExpression, Microarray, CopyNumberVariation Author: Michael F. Ochs Maintainer: Michael F. Ochs git_url: https://git.bioconductor.org/packages/OGSA git_branch: RELEASE_3_8 git_last_commit: 502f31c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OGSA_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OGSA_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OGSA_1.12.0.tgz vignettes: vignettes/OGSA/inst/doc/OGSAUsersManual.pdf vignetteTitles: OGSA Users Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OGSA/inst/doc/OGSAUsersManual.R Package: oligo Version: 1.46.0 Depends: R (>= 3.2.0), BiocGenerics (>= 0.13.11), oligoClasses (>= 1.29.6), Biobase (>= 2.27.3), Biostrings (>= 2.35.12) Imports: affyio (>= 1.35.0), affxparser (>= 1.39.4), DBI (>= 0.3.1), ff, graphics, methods, preprocessCore (>= 1.29.0), RSQLite (>= 1.0.0), splines, stats, stats4, utils, zlibbioc LinkingTo: preprocessCore Suggests: BSgenome.Hsapiens.UCSC.hg18, hapmap100kxba, pd.hg.u95av2, pd.mapping50k.xba240, pd.huex.1.0.st.v2, pd.hg18.60mer.expr, pd.hugene.1.0.st.v1, maqcExpression4plex, genefilter, limma, RColorBrewer, oligoData, BiocStyle, knitr, RUnit, biomaRt, AnnotationDbi, GenomeGraphs, RCurl, ACME, biomaRt, AnnotationDbi, GenomeGraphs, RCurl Enhances: ff, doMC, doMPI License: LGPL (>= 2) MD5sum: a3ecdc244b8f0b20408c7251c13cc0ca NeedsCompilation: yes Title: Preprocessing tools for oligonucleotide arrays Description: A package to analyze oligonucleotide arrays (expression/SNP/tiling/exon) at probe-level. It currently supports Affymetrix (CEL files) and NimbleGen arrays (XYS files). biocViews: Microarray, OneChannel, TwoChannel, Preprocessing, SNP, DifferentialExpression, ExonArray, GeneExpression, DataImport Author: Benilton Carvalho and Rafael Irizarry Maintainer: Benilton Carvalho VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/oligo git_branch: RELEASE_3_8 git_last_commit: 42f2441 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/oligo_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/oligo_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/oligo_1.46.0.tgz vignettes: vignettes/oligo/inst/doc/oug.pdf vignetteTitles: oligo User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: ITALICS, pdInfoBuilder, puma, SCAN.UPC, waveTiling importsMe: ArrayExpress, charm, cn.farms, crossmeta, frma, ITALICS, mimager suggestsMe: BiocGenerics, fastseg, frmaTools Package: oligoClasses Version: 1.44.0 Depends: R (>= 2.14) Imports: BiocGenerics (>= 0.27.1), Biobase (>= 2.17.8), methods, graphics, IRanges (>= 2.5.17), GenomicRanges (>= 1.23.7), SummarizedExperiment, Biostrings (>= 2.23.6), affyio (>= 1.23.2), ff, foreach, BiocManager, utils, S4Vectors (>= 0.9.25), RSQLite, DBI Suggests: hapmapsnp5, hapmapsnp6, pd.genomewidesnp.6, pd.genomewidesnp.5, pd.mapping50k.hind240, pd.mapping50k.xba240, pd.mapping250k.sty, pd.mapping250k.nsp, genomewidesnp6Crlmm (>= 1.0.7), genomewidesnp5Crlmm (>= 1.0.6), RUnit, human370v1cCrlmm, SNPchip, VanillaICE, crlmm Enhances: doMC, doMPI, doSNOW, doParallel, doRedis License: GPL (>= 2) Archs: i386, x64 MD5sum: c58277928932218857e89afeeffc7aa9 NeedsCompilation: no Title: Classes for high-throughput arrays supported by oligo and crlmm Description: This package contains class definitions, validity checks, and initialization methods for classes used by the oligo and crlmm packages. biocViews: Infrastructure Author: Benilton Carvalho and Robert Scharpf Maintainer: Benilton Carvalho and Robert Scharpf git_url: https://git.bioconductor.org/packages/oligoClasses git_branch: RELEASE_3_8 git_last_commit: d3e1134 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/oligoClasses_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/oligoClasses_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/oligoClasses_1.44.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: cn.farms, crlmm, mBPCR, oligo, puma, waveTiling importsMe: affycoretools, ArrayTV, charm, frma, ITALICS, mimager, MinimumDistance, pdInfoBuilder, puma, SNPchip, VanillaICE suggestsMe: BiocGenerics Package: OLIN Version: 1.60.0 Depends: R (>= 2.10), methods, locfit, marray Imports: graphics, grDevices, limma, marray, methods, stats Suggests: convert License: GPL-2 MD5sum: 8c56f4b27a4c0fd7d3554d7153ba260b NeedsCompilation: no Title: Optimized local intensity-dependent normalisation of two-color microarrays Description: Functions for normalisation of two-color microarrays by optimised local regression and for detection of artefacts in microarray data biocViews: Microarray, TwoChannel, QualityControl, Preprocessing, Visualization Author: Matthias Futschik Maintainer: Matthias Futschik URL: http://olin.sysbiolab.eu git_url: https://git.bioconductor.org/packages/OLIN git_branch: RELEASE_3_8 git_last_commit: 0b37a98 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OLIN_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OLIN_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OLIN_1.60.0.tgz vignettes: vignettes/OLIN/inst/doc/OLIN.pdf vignetteTitles: Introduction to OLIN hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OLIN/inst/doc/OLIN.R dependsOnMe: OLINgui importsMe: OLINgui suggestsMe: maigesPack Package: OLINgui Version: 1.56.0 Depends: R (>= 2.0.0), OLIN (>= 1.4.0) Imports: graphics, marray, OLIN, tcltk, tkWidgets, widgetTools License: GPL-2 MD5sum: d80fde109f35a28abd65089848537969 NeedsCompilation: no Title: Graphical user interface for OLIN Description: Graphical user interface for the OLIN package biocViews: Microarray, TwoChannel, QualityControl, Preprocessing, Visualization Author: Matthias Futschik Maintainer: Matthias Futschik URL: http://olin.sysbiolab.eu git_url: https://git.bioconductor.org/packages/OLINgui git_branch: RELEASE_3_8 git_last_commit: f2272b9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OLINgui_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OLINgui_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OLINgui_1.56.0.tgz vignettes: vignettes/OLINgui/inst/doc/OLINgui.pdf vignetteTitles: Introduction to OLINgui hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OLINgui/inst/doc/OLINgui.R Package: OmaDB Version: 1.2.2 Depends: R (>= 3.5), httr (>= 1.2.1), plyr(>= 1.8.4) Imports: utils, ape, Biostrings, GenomicRanges, IRanges, methods, topGO, jsonlite Suggests: knitr, rmarkdown, testthat License: GPL-2 MD5sum: 1e4377b8324001afc3dbd38a7e5156a6 NeedsCompilation: no Title: R wrapper for the OMA REST API Description: A package for the orthology prediction data download from OMA database. biocViews: Software, ComparativeGenomics, FunctionalGenomics, Genetics, Annotation, GO, FunctionalPrediction Author: Klara Kaleb Maintainer: Klara Kaleb , Adrian Altenhoff VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/OmaDB git_branch: RELEASE_3_8 git_last_commit: 3696142 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/OmaDB_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/OmaDB_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OmaDB_1.2.2.tgz vignettes: vignettes/OmaDB/inst/doc/exploring_hogs.html, vignettes/OmaDB/inst/doc/OmaDB.html, vignettes/OmaDB/inst/doc/sequence_mapping.html, vignettes/OmaDB/inst/doc/tree_visualisation.html vignetteTitles: Exploring Hierarchical orthologous groups with OmaDB, Get started with OmaDB, Sequence Mapping with OmaDB, Exploring Taxonomic trees with OmaDB hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OmaDB/inst/doc/exploring_hogs.R, vignettes/OmaDB/inst/doc/OmaDB.R, vignettes/OmaDB/inst/doc/sequence_mapping.R, vignettes/OmaDB/inst/doc/tree_visualisation.R Package: omicade4 Version: 1.22.0 Depends: R (>= 3.0.0), ade4 Imports: made4 Suggests: BiocStyle License: GPL-2 MD5sum: 5a5e6def3842ea64955d6f4004c01ca0 NeedsCompilation: no Title: Multiple co-inertia analysis of omics datasets Description: Multiple co-inertia analysis of omics datasets biocViews: Software, Clustering, Classification, MultipleComparison Author: Chen Meng, Aedin Culhane, Amin M. Gholami. Maintainer: Chen Meng git_url: https://git.bioconductor.org/packages/omicade4 git_branch: RELEASE_3_8 git_last_commit: 28235a5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/omicade4_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/omicade4_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/omicade4_1.22.0.tgz vignettes: vignettes/omicade4/inst/doc/omicade4.pdf vignetteTitles: Using omicade4 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/omicade4/inst/doc/omicade4.R importsMe: omicRexposome suggestsMe: MultiDataSet Package: OmicCircos Version: 1.20.0 Depends: R (>= 2.14.0), methods,GenomicRanges License: GPL-2 MD5sum: 6f138f977152b3f86101ae451fc9368d NeedsCompilation: no Title: High-quality circular visualization of omics data Description: OmicCircos is an R application and package for generating high-quality circular plots for omics data. biocViews: Visualization,Statistics,Annotation Author: Ying Hu Chunhua Yan Maintainer: Ying Hu git_url: https://git.bioconductor.org/packages/OmicCircos git_branch: RELEASE_3_8 git_last_commit: 757204b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OmicCircos_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OmicCircos_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OmicCircos_1.20.0.tgz vignettes: vignettes/OmicCircos/inst/doc/OmicCircos_vignette.pdf vignetteTitles: OmicCircos vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OmicCircos/inst/doc/OmicCircos_vignette.R Package: omicplotR Version: 1.2.1 Depends: R (>= 3.5) Imports: ALDEx2 (>= 1.8.0), compositions, grDevices, knitr, matrixStats, rmarkdown, shiny, stats, vegan, zCompositions License: MIT + file LICENSE MD5sum: a5c76dfa4cdeb09e49897a0bcae31019 NeedsCompilation: no Title: Visual Exploration of Omic Datasets Using a Shiny App Description: A Shiny app for visual exploration of omic datasets as compositions, and differential abundance analysis using ALDEx2. Useful for exploring RNA-seq, meta-RNA-seq, 16s rRNA gene sequencing with visualizations such as principal component analysis biplots (coloured using metadata for visualizing each variable), dendrograms and stacked bar plots, and effect plots (ALDEx2). Input is a table of counts and metadata file (if metadata exists), with options to filter data by count or by metadata to remove low counts, or to visualize select samples according to selected metadata. biocViews: ImmunoOncology, Software, DifferentialExpression, GeneExpression, GUI, RNASeq, DNASeq, Metagenomics, Transcriptomics, Bayesian, Microbiome, Visualization, Sequencing Author: Daniel Giguere [aut, cre], Jean Macklaim [aut], Greg Gloor [aut] Maintainer: Daniel Giguere VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/omicplotR git_branch: RELEASE_3_8 git_last_commit: 3e141f1 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/omicplotR_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/omicplotR_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/omicplotR_1.2.1.tgz vignettes: vignettes/omicplotR/inst/doc/omicplotR.html vignetteTitles: omicplotR: A tool for visualization of omic datasets as compositions hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/omicplotR/inst/doc/omicplotR.R Package: omicRexposome Version: 1.4.1 Depends: R (>= 3.4), Biobase Imports: stats, utils, grDevices, graphics, methods, rexposome, limma, sva, ggplot2, ggrepel, PMA, omicade4, gridExtra, MultiDataSet, SmartSVA, isva, parallel, SummarizedExperiment, stringr Suggests: BiocStyle, knitr, rmarkdown, snpStats, brgedata License: MIT + file LICENSE MD5sum: a0c29f19039212edc03e4db5a5c1cf2c NeedsCompilation: no Title: Exposome and omic data associatin and integration analysis Description: omicRexposome systematizes the association evaluation between exposures and omic data, taking advantage of MultiDataSet for coordinated data management, rexposome for exposome data definition and limma for association testing. Also to perform data integration mixing exposome and omic data using multi co-inherent analysis (omicade4) and multi-canonical correlation analysis (PMA). biocViews: ImmunoOncology, WorkflowStep, MultipleComparison, Visualization, GeneExpression, DifferentialExpression, DifferentialMethylation, GeneRegulation, Epigenetics, Proteomics, Transcriptomics, StatisticalMethod, Regression Author: Carles Hernandez-Ferrer [aut, cre], Juan R. González [aut] Maintainer: Carles Hernandez-Ferrer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/omicRexposome git_branch: RELEASE_3_8 git_last_commit: 57fcb11 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/omicRexposome_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/omicRexposome_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/omicRexposome_1.4.1.tgz vignettes: vignettes/omicRexposome/inst/doc/exposome_omic_integration.html vignetteTitles: Exposome Data Integration with Omic Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/omicRexposome/inst/doc/exposome_omic_integration.R Package: OmicsMarkeR Version: 1.14.0 Depends: R (>= 3.2.0) Imports: graphics, stats, utils, plyr (>= 1.8), data.table (>= 1.9.4), caret (>= 6.0-37), DiscriMiner (>= 0.1-29), e1071 (>= 1.6-1), randomForest (>= 4.6-10), gbm (>= 2.1), pamr (>= 1.54.1), glmnet (>= 1.9-5), caTools (>= 1.14), foreach (>= 1.4.1), permute (>= 0.7-0), assertive (>= 0.3-0), assertive.base (>= 0.0-1) Suggests: testthat, BiocStyle, knitr License: GPL-3 MD5sum: 10593af3dcc1bdf37ac363bf3956af43 NeedsCompilation: no Title: Classification and Feature Selection for 'Omics' Datasets Description: Tools for classification and feature selection for 'omics' level datasets. It is a tool to provide multiple multivariate classification and feature selection techniques complete with multiple stability metrics and aggregation techniques. It is primarily designed for analysis of metabolomics datasets but potentially extendable to proteomics and transcriptomics applications. biocViews: Metabolomics, Classification, FeatureExtraction Author: Charles E. Determan Jr. Maintainer: Charles E. Determan Jr. URL: http://github.com/cdeterman/OmicsMarkeR VignetteBuilder: knitr BugReports: http://github.com/cdeterman/OmicsMarkeR/issues/new git_url: https://git.bioconductor.org/packages/OmicsMarkeR git_branch: RELEASE_3_8 git_last_commit: 8b71dd1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OmicsMarkeR_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OmicsMarkeR_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OmicsMarkeR_1.14.0.tgz vignettes: vignettes/OmicsMarkeR/inst/doc/OmicsMarkeR.pdf vignetteTitles: A Short Introduction to the OmicMarkeR Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OmicsMarkeR/inst/doc/OmicsMarkeR.R Package: OMICsPCA Version: 1.0.1 Depends: R (>= 3.5.0), OMICsPCAdata Imports: HelloRanges, fpc, stats, MultiAssayExperiment, pdftools, methods, grDevices, utils,clValid, NbClust, cowplot, rmarkdown, kableExtra, rtracklayer, IRanges, GenomeInfoDb, reshape2, ggplot2, factoextra, rgl, corrplot, MASS, graphics, FactoMineR, PerformanceAnalytics, tidyr, data.table, cluster, magick Suggests: knitr, RUnit, BiocGenerics License: GPL-3 MD5sum: fe7ca779103cbd3414d8d5b6bd4ad022 NeedsCompilation: no Title: An R package for quantitative integration and analysis of multiple omics assays from heterogeneous samples Description: OMICsPCA is an analysis pipeline designed to integrate multi OMICs experiments done on various subjects (e.g. Cell lines, individuals), treatments (e.g. disease/control) or time points and to analyse such integrated data from various various angles and perspectives. In it's core OMICsPCA uses Principal Component Analysis (PCA) to integrate multiomics experiments from various sources and thus has ability to over data insufficiency issues by using the ingegrated data as representatives. OMICsPCA can be used in various application including analysis of overall distribution of OMICs assays across various samples /individuals /time points; grouping assays by user-defined conditions; identification of source of variation, similarity/dissimilarity between assays, variables or individuals. biocViews: ImmunoOncology, MultipleComparison, PrincipalComponent, DataRepresentation, Workflow, Visualization, DimensionReduction, Clustering, BiologicalQuestion, EpigeneticsWorkflow, Transcription, GeneticVariability, GUI, BiomedicalInformatics, Epigenetics, FunctionalGenomics, SingleCell Author: Subhadeep Das [aut, cre], Dr. Sucheta Tripathy [ctb] Maintainer: Subhadeep Das VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/OMICsPCA git_branch: RELEASE_3_8 git_last_commit: f1cf3f0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/OMICsPCA_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/OMICsPCA_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OMICsPCA_1.0.1.tgz vignettes: vignettes/OMICsPCA/inst/doc/vignettes.html vignetteTitles: OMICsPCA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OMICsPCA/inst/doc/vignettes.R Package: omicsPrint Version: 1.2.1 Depends: R (>= 3.5), MASS Imports: methods, matrixStats, graphics, stats, SummarizedExperiment, MultiAssayExperiment, RaggedExperiment Suggests: BiocStyle, knitr, rmarkdown, testthat, GEOquery, VariantAnnotation, Rsamtools, BiocParallel, GenomicRanges, FDb.InfiniumMethylation.hg19, snpStats License: GPL (>= 2) MD5sum: 50236bbbb3b86de54afb81de6ea0aee5 NeedsCompilation: no Title: Cross omic genetic fingerprinting Description: omicsPrint provides functionality for cross omic genetic fingerprinting, for example, to verify sample relationships between multiple omics data types, i.e. genomic, transcriptomic and epigenetic (DNA methylation). biocViews: ImmunoOncology, QualityControl, Genetics, Epigenetics, Transcriptomics, DNAMethylation, Transcription, GeneticVariability Author: Maarten van Iterson [aut], Davy Cats [cre] Maintainer: Davy Cats VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/omicsPrint git_branch: RELEASE_3_8 git_last_commit: 1c34804 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/omicsPrint_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/omicsPrint_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/omicsPrint_1.2.1.tgz vignettes: vignettes/omicsPrint/inst/doc/omicsPrint.html vignetteTitles: omicsPrint: detection of data linkage errors in multiple omics studies hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/omicsPrint/inst/doc/omicsPrint.R Package: Onassis Version: 1.4.5 Depends: R (>= 3.5), rJava, OnassisJavaLibs Imports: GEOmetadb, RSQLite, data.table, methods, tools, utils, AnnotationDbi, RCurl, stats, DT, data.table, knitr Suggests: BiocStyle, rmarkdown, htmltools, org.Hs.eg.db, gplots, GenomicRanges, kableExtra License: GPL-2 MD5sum: 89a0e8751411bc21806a3159112bc2b8 NeedsCompilation: no Title: OnASSIs Ontology Annotation and Semantic SImilarity software Description: A package that allows the annotation of text with ontology terms (mainly from OBO ontologies) and the computation of semantic similarity measures based on the structure of the ontology between different annotated samples. biocViews: Annotation, DataImport, Clustering, Network, Software, GeneTarget Author: Eugenia Galeota Maintainer: Eugenia Galeota SystemRequirements: Java (>= 1.8) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Onassis git_branch: RELEASE_3_8 git_last_commit: da9876b git_last_commit_date: 2018-11-28 Date/Publication: 2018-11-28 source.ver: src/contrib/Onassis_1.4.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/Onassis_1.4.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Onassis_1.4.5.tgz vignettes: vignettes/Onassis/inst/doc/Onassis.html vignetteTitles: Onassis: Ontology Annotation and Semantic Similarity software hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Onassis/inst/doc/Onassis.R Package: oncomix Version: 1.4.0 Depends: R (>= 3.4.0) Imports: ggplot2, ggrepel, RColorBrewer, mclust, stats, SummarizedExperiment Suggests: knitr, rmarkdown, testthat, RMySQL License: GPL-3 MD5sum: 24f731f87764297454ff5a4a9357f994 NeedsCompilation: no Title: Identifying Genes Overexpressed in Subsets of Tumors from Tumor-Normal mRNA Expression Data Description: This package helps identify mRNAs that are overexpressed in subsets of tumors relative to normal tissue. Ideal inputs would be paired tumor-normal data from the same tissue from many patients (>15 pairs). This unsupervised approach relies on the observation that oncogenes are characteristically overexpressed in only a subset of tumors in the population, and may help identify oncogene candidates purely based on differences in mRNA expression between previously unknown subtypes. biocViews: GeneExpression, Sequencing Author: Daniel Pique, John Greally, Jessica Mar Maintainer: Daniel Pique VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/oncomix git_branch: RELEASE_3_8 git_last_commit: 0d85d2f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/oncomix_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/oncomix_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/oncomix_1.4.0.tgz vignettes: vignettes/oncomix/inst/doc/oncomix.html vignetteTitles: OncoMix Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/oncomix/inst/doc/oncomix.R Package: OncoScore Version: 1.10.0 Depends: R (>= 3.5), Imports: biomaRt, grDevices, graphics, utils, methods, Suggests: BiocGenerics, BiocStyle, knitr, testthat, License: file LICENSE MD5sum: 2037b880068e7ce59e92d799f28a9c4d NeedsCompilation: no Title: A tool to identify potentially oncogenic genes Description: OncoScore is a tool to measure the association of genes to cancer based on citation frequencies in biomedical literature. The score is evaluated from PubMed literature by dynamically updatable web queries. biocViews: BiomedicalInformatics Author: Luca De Sano [aut], Carlo Gambacorti Passerini [ctb], Rocco Piazza [ctb], Daniele Ramazzotti [aut, cre], Roberta Spinelli [ctb] Maintainer: Luca De Sano URL: https://github.com/danro9685/OncoScore VignetteBuilder: knitr BugReports: https://github.com/danro9685/OncoScore git_url: https://git.bioconductor.org/packages/OncoScore git_branch: RELEASE_3_8 git_last_commit: 8f1517b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OncoScore_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OncoScore_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OncoScore_1.10.0.tgz vignettes: vignettes/OncoScore/inst/doc/vignette.pdf vignetteTitles: OncoScore hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/OncoScore/inst/doc/vignette.R Package: OncoSimulR Version: 2.12.0 Depends: R (>= 3.3.0) Imports: Rcpp (>= 0.12.4), parallel, data.table, graph, Rgraphviz, gtools, igraph, methods, RColorBrewer, grDevices, car, dplyr, smatr, ggplot2, ggrepel, nem LinkingTo: Rcpp Suggests: BiocStyle, knitr, Oncotree, testthat (>= 1.0.0), rmarkdown, bookdown, pander License: GPL (>= 3) MD5sum: 44f9be22a9965fe0389aad902c2d08d0 NeedsCompilation: yes Title: Forward Genetic Simulation of Cancer Progression with Epistasis Description: Functions for forward population genetic simulation in asexual populations, with special focus on cancer progression. Fitness can be an arbitrary function of genetic interactions between multiple genes or modules of genes, including epistasis, order restrictions in mutation accumulation, and order effects. Mutation rates can differ between genes, and we can include mutator/antimutator genes (to model mutator phenotypes). Simulations use continuous-time models and can include driver and passenger genes and modules. Also included are functions for: simulating random DAGs of the type found in Oncogenetic Tress, Conjunctive Bayesian Networks, and other tumor progression models; plotting and sampling from single or multiple realizations of the simulations, including single-cell sampling; plotting the parent-child relationships of the clones; generating random fitness landscapes (Rough Mount Fuji, House of Cards, and additive models) and plotting them. biocViews: BiologicalQuestion, SomaticMutation Author: Ramon Diaz-Uriarte [aut, cre], Mark Taylor [ctb] Maintainer: Ramon Diaz-Uriarte URL: https://github.com/rdiaz02/OncoSimul, https://popmodels.cancercontrol.cancer.gov/gsr/packages/oncosimulr/ VignetteBuilder: knitr BugReports: https://github.com/rdiaz02/OncoSimul/issues git_url: https://git.bioconductor.org/packages/OncoSimulR git_branch: RELEASE_3_8 git_last_commit: 10d3d45 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OncoSimulR_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OncoSimulR_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OncoSimulR_2.12.0.tgz vignettes: vignettes/OncoSimulR/inst/doc/OncoSimulR.html vignetteTitles: OncoSimulR: forward genetic simulation in asexual populations with arbitrary epistatic interactions and a focus on modeling tumor progression. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OncoSimulR/inst/doc/OncoSimulR.R Package: oneSENSE Version: 1.4.1 Depends: R (>= 3.4), webshot, shiny, shinyFiles, scatterplot3d Imports: Rtsne, plotly, gplots, grDevices, graphics, stats, utils, methods, flowCore Suggests: knitr, rmarkdown License: GPL (>=3) Archs: i386, x64 MD5sum: e7058bb849855138a7ce8139c707d5a1 NeedsCompilation: no Title: One-Dimensional Soli-Expression by Nonlinear Stochastic Embedding (OneSENSE) Description: A graphical user interface that facilitates the dimensional reduction method based on the t-distributed stochastic neighbor embedding (t-SNE) algorithm, for categorical analysis of mass cytometry data. With One-SENSE, measured parameters are grouped into predefined categories, and cells are projected onto a space composed of one dimension for each category. Each dimension is informative and can be annotated through the use of heatplots aligned in parallel to each axis, allowing for simultaneous visualization of two catergories across a two-dimensional plot. The cellular occupancy of the resulting plots alllows for direct assessment of the relationships between the categories. biocViews: ImmunoOncology, Software, FlowCytometry, GUI, DimensionReduction Author: Cheng Yang, Evan Newell, Yong Kee Tan Maintainer: Yong Kee Tan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/oneSENSE git_branch: RELEASE_3_8 git_last_commit: 468b0db git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/oneSENSE_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/oneSENSE_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/oneSENSE_1.4.1.tgz vignettes: vignettes/oneSENSE/inst/doc/quickstart.html vignetteTitles: Introduction to oneSENSE GUI hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/oneSENSE/inst/doc/quickstart.R Package: onlineFDR Version: 1.0.0 Imports: stats Suggests: knitr, rmarkdown, testthat License: GPL-3 MD5sum: 0f6c5c4dc344739ada4dc4be60aea0a5 NeedsCompilation: no Title: Online FDR control Description: This package allows users to control the false discovery rate for online hypothesis testing, where hypotheses arrive sequentially in a stream, as presented by Javanmard and Montanari (2015, 2018). In this framework, a null hypothesis is rejected based only on the previous decisions, as the future p-values and the number of hypotheses to be tested are unknown. biocViews: MultipleComparison, Software, StatisticalMethod Author: David Robertson [aut, cre], Adel Javanmard [aut], Andrea Montanari [aut], Natasha Karp [aut] Maintainer: David Robertson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/onlineFDR git_branch: RELEASE_3_8 git_last_commit: fabda91 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/onlineFDR_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/onlineFDR_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/onlineFDR_1.0.0.tgz vignettes: vignettes/onlineFDR/inst/doc/onlineFDR-vignette.html vignetteTitles: Using the onlineFDR package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/onlineFDR/inst/doc/onlineFDR-vignette.R Package: ontoProc Version: 1.4.0 Depends: R (>= 3.5), ontologyIndex Imports: Biobase, S4Vectors, methods, AnnotationDbi, stats, utils, shiny Suggests: knitr, org.Hs.eg.db, org.Mm.eg.db, testthat, BiocStyle License: Artistic-2.0 MD5sum: 6c923d964ffaa80eff31fb0049e554ef NeedsCompilation: no Title: processing of ontologies of anatomy, cell lines, and so on Description: Support harvesting of diverse bioinformatic ontologies, making particular use of the ontologyIndex package on CRAN. We provide snapshots of key ontologies for terms about cells, cell lines, chemical compounds, and anatomy, to help analyze genome-scale experiments, particularly cell x compound screens. Another purpose is to strengthen development of compelling use cases for richer interfaces to emerging ontologies. biocViews: Infrastructure, GO Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ontoProc git_branch: RELEASE_3_8 git_last_commit: 1ae33ab git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ontoProc_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ontoProc_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ontoProc_1.4.0.tgz vignettes: vignettes/ontoProc/inst/doc/ontoProc.pdf vignetteTitles: ontoProc: RDF ontology processing hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ontoProc/inst/doc/ontoProc.R importsMe: pogos, tenXplore suggestsMe: BiocOncoTK Package: openCyto Version: 1.20.2 Depends: flowWorkspace(>= 3.17.43) Imports: methods,Biobase,BiocGenerics,gtools,flowCore(>= 1.31.17),flowViz,ncdfFlow(>= 2.11.34),flowWorkspace,flowStats(>= 3.29.1),flowClust(>= 3.11.4),MASS,clue,plyr,RBGL,graph,data.table,ks,RColorBrewer,lattice,rrcov,R.utils LinkingTo: Rcpp Suggests: flowWorkspaceData, knitr, testthat, utils, tools, parallel, ggcyto License: Artistic-2.0 MD5sum: 899e0cd6fc3e586b24579ae387f48d0a NeedsCompilation: yes Title: Hierarchical Gating Pipeline for flow cytometry data Description: This package is designed to facilitate the automated gating methods in sequential way to mimic the manual gating strategy. biocViews: ImmunoOncology, FlowCytometry, DataImport, Preprocessing, DataRepresentation Author: Mike Jiang, John Ramey, Greg Finak, Raphael Gottardo Maintainer: Mike Jiang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/openCyto git_branch: RELEASE_3_8 git_last_commit: cf01d58 git_last_commit_date: 2019-01-22 Date/Publication: 2019-01-22 source.ver: src/contrib/openCyto_1.20.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/openCyto_1.20.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/openCyto_1.20.2.tgz vignettes: vignettes/openCyto/inst/doc/HowToAutoGating.html, vignettes/openCyto/inst/doc/HowToWriteCSVTemplate.html, vignettes/openCyto/inst/doc/openCytoVignette.html vignetteTitles: How to use different auto gating functions, How to write a csv gating template, An Introduction to the openCyto package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/openCyto/inst/doc/HowToAutoGating.R, vignettes/openCyto/inst/doc/HowToWriteCSVTemplate.R, vignettes/openCyto/inst/doc/openCytoVignette.R importsMe: CytoML suggestsMe: flowCore, ggcyto Package: openPrimeR Version: 1.4.1 Depends: R (>= 3.4.0) Imports: Biostrings (>= 2.38.4), XML (>= 3.98-1.4), scales (>= 0.4.0), reshape2 (>= 1.4.1), seqinr (>= 3.3-3), IRanges (>= 2.4.8), GenomicRanges (>= 1.22.4), ggplot2 (>= 2.1.0), plyr (>= 1.8.4), dplyr (>= 0.5.0), stringdist (>= 0.9.4.1), stringr (>= 1.0.0), RColorBrewer (>= 1.1-2), DECIPHER (>= 1.16.1), lpSolveAPI (>= 5.5.2.0-17), digest (>= 0.6.9), Hmisc (>= 3.17-4), ape (>= 3.5), BiocGenerics (>= 0.16.1), S4Vectors (>= 0.8.11), foreach (>= 1.4.3), magrittr (>= 1.5), distr (>= 2.6), distrEx (>= 2.6), fitdistrplus (>= 1.0-7), uniqtag (>= 1.0), openxlsx (>= 4.0.17), grid (>= 3.1.0), grDevices (>= 3.1.0), stats (>= 3.1.0), utils (>= 3.1.0), methods (>= 3.1.0), tinytex (>= 0.5) Suggests: testthat (>= 1.0.2), knitr (>= 1.13), rmarkdown (>= 1.0), devtools (>= 1.12.0), doParallel (>= 1.0.10), pander (>= 0.6.0), learnr (>= 0.9) License: GPL-2 Archs: i386, x64 MD5sum: a1bc7c07f1486703b09f7f291737fe84 NeedsCompilation: no Title: Multiplex PCR Primer Design and Analysis Description: An implementation of methods for designing, evaluating, and comparing primer sets for multiplex PCR. Primers are designed by solving a set cover problem such that the number of covered template sequences is maximized with the smallest possible set of primers. To guarantee that high-quality primers are generated, only primers fulfilling constraints on their physicochemical properties are selected. A Shiny app providing a user interface for the functionalities of this package is provided by the 'openPrimeRui' package. biocViews: Software, Technology Author: Matthias Döring [aut, cre], Nico Pfeifer [aut] Maintainer: Matthias Döring SystemRequirements: MAFFT (>= 7.305), OligoArrayAux (>= 3.8), ViennaRNA (>= 2.4.1), MELTING (>= 5.1.1), Pandoc (>= 1.12.3) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/openPrimeR git_branch: RELEASE_3_8 git_last_commit: fb39229 git_last_commit_date: 2018-11-10 Date/Publication: 2018-11-10 source.ver: src/contrib/openPrimeR_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/openPrimeR_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/openPrimeR_1.4.1.tgz vignettes: vignettes/openPrimeR/inst/doc/openPrimeR_vignette.html vignetteTitles: openPrimeR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/openPrimeR/inst/doc/openPrimeR_vignette.R dependsOnMe: openPrimeRui Package: openPrimeRui Version: 1.4.1 Depends: R (>= 3.4.0), openPrimeR (>= 0.99.0) Imports: shiny (>= 1.0.2), shinyjs (>= 0.9), shinyBS (>= 0.61), DT (>= 0.2), rmarkdown (>= 1.0) Suggests: knitr (>= 1.13) License: GPL-2 MD5sum: 9c68b6e58d4425b89b2e45289a83878d NeedsCompilation: no Title: Shiny Application for Multiplex PCR Primer Design and Analysis Description: A Shiny application providing methods for designing, evaluating, and comparing primer sets for multiplex polymerase chain reaction. Primers are designed by solving a set cover problem such that the number of covered template sequences is maximized with the smallest possible set of primers. To guarantee that high-quality primers are generated, only primers fulfilling constraints on their physicochemical properties are selected. biocViews: Software, Technology Author: Matthias Döring [aut, cre], Nico Pfeifer [aut] Maintainer: Matthias Döring VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/openPrimeRui git_branch: RELEASE_3_8 git_last_commit: 12e61b5 git_last_commit_date: 2018-11-10 Date/Publication: 2018-11-10 source.ver: src/contrib/openPrimeRui_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/openPrimeRui_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/openPrimeRui_1.4.1.tgz vignettes: vignettes/openPrimeRui/inst/doc/openPrimeRui_vignette.html vignetteTitles: openPrimeRui hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/openPrimeRui/inst/doc/openPrimeRui_vignette.R Package: oposSOM Version: 2.0.0 Depends: R (>= 3.0), igraph (>= 1.0.0) Imports: fastICA, tsne, scatterplot3d, pixmap, fdrtool, ape, biomaRt, Biobase, RcppParallel, Rcpp LinkingTo: RcppParallel, Rcpp License: GPL (>=2) MD5sum: b313fe4f7305c8e1c1bcc5738e6924ff NeedsCompilation: yes Title: Comprehensive analysis of transciptome data Description: This package translates microarray expression data into metadata of reduced dimension. It provides various sample-centered and group-centered visualizations, sample similarity analyses and functional enrichment analyses. The underlying SOM algorithm combines feature clustering, multidimensional scaling and dimension reduction, along with strong visualization capabilities. It enables extraction and description of functional expression modules inherent in the data. biocViews: GeneExpression, DifferentialExpression, GeneSetEnrichment, DataRepresentation, Visualization Author: Henry Loeffler-Wirth , Hoang Thanh Le and Martin Kalcher Maintainer: Henry Loeffler-Wirth URL: http://som.izbi.uni-leipzig.de git_url: https://git.bioconductor.org/packages/oposSOM git_branch: RELEASE_3_8 git_last_commit: 1c15a85 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/oposSOM_2.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/oposSOM_2.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/oposSOM_2.0.0.tgz vignettes: vignettes/oposSOM/inst/doc/Vignette.pdf vignetteTitles: The oposSOM users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/oposSOM/inst/doc/Vignette.R Package: oppar Version: 1.10.0 Depends: R (>= 3.3) Imports: Biobase, methods, GSEABase, GSVA Suggests: knitr, rmarkdown, limma, org.Hs.eg.db, GO.db, snow, parallel License: GPL-2 Archs: i386, x64 MD5sum: 03de1726e43965f7622a81ccfc411f4d NeedsCompilation: yes Title: Outlier profile and pathway analysis in R Description: The R implementation of mCOPA package published by Wang et al. (2012). Oppar provides methods for Cancer Outlier profile Analysis. Although initially developed to detect outlier genes in cancer studies, methods presented in oppar can be used for outlier profile analysis in general. In addition, tools are provided for gene set enrichment and pathway analysis. biocViews: Pathways, GeneSetEnrichment, SystemsBiology, GeneExpression, Software Author: Chenwei Wang [aut], Alperen Taciroglu [aut], Stefan R Maetschke [aut], Colleen C Nelson [aut], Mark Ragan [aut], Melissa Davis [aut], Soroor Hediyeh zadeh [cre], Momeneh Foroutan [ctr] Maintainer: Soroor Hediyeh zadeh VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/oppar git_branch: RELEASE_3_8 git_last_commit: 4cc3e13 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/oppar_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/oppar_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/oppar_1.10.0.tgz vignettes: vignettes/oppar/inst/doc/oppar.html vignetteTitles: OPPAR: Outlier Profile and Pathway Analysis in R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/oppar/inst/doc/oppar.R Package: OPWeight Version: 1.4.1 Depends: R (>= 3.4.0), Imports: graphics, qvalue, MASS, tibble, stats, Suggests: airway, BiocStyle, cowplot, DESeq2, devtools, ggplot2, gridExtra, knitr, Matrix, rmarkdown, scales, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: ab80059bdb6f0f6e7af2168b8d05a074 NeedsCompilation: no Title: Optimal p-value weighting with independent information Description: This package perform weighted-pvalue based multiple hypothesis test and provides corresponding information such as ranking probability, weight, significant tests, etc . To conduct this testing procedure, the testing method apply a probabilistic relationship between the test rank and the corresponding test effect size. biocViews: ImmunoOncology, BiomedicalInformatics, MultipleComparison, Regression, RNASeq, SNP Author: Mohamad Hasan [aut, cre], Paul Schliekelman [aut] Maintainer: Mohamad Hasan URL: https://github.com/mshasan/OPWeight VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/OPWeight git_branch: RELEASE_3_8 git_last_commit: 7cb503a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/OPWeight_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/OPWeight_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OPWeight_1.4.1.tgz vignettes: vignettes/OPWeight/inst/doc/OPWeight.html vignetteTitles: "Introduction to OPWeight" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OPWeight/inst/doc/OPWeight.R Package: OrderedList Version: 1.54.0 Depends: R (>= 2.1.0), Biobase (>= 1.5.12), twilight (>= 1.9.2), methods Imports: Biobase, graphics, methods, stats, twilight License: GPL (>= 2) MD5sum: 6bd1c5786a4c4d6aec16c91f6c481984 NeedsCompilation: no Title: Similarities of Ordered Gene Lists Description: Detection of similarities between ordered lists of genes. Thereby, either simple lists can be compared or gene expression data can be used to deduce the lists. Significance of similarities is evaluated by shuffling lists or by resampling in microarray data, respectively. biocViews: Microarray, DifferentialExpression, MultipleComparison Author: Xinan Yang, Stefanie Scheid, Claudio Lottaz Maintainer: Claudio Lottaz URL: http://compdiag.molgen.mpg.de/software/index.shtml git_url: https://git.bioconductor.org/packages/OrderedList git_branch: RELEASE_3_8 git_last_commit: a32cd0c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OrderedList_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OrderedList_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OrderedList_1.54.0.tgz vignettes: vignettes/OrderedList/inst/doc/tr_2006_01.pdf vignetteTitles: Similarities of Ordered Gene Lists hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OrderedList/inst/doc/tr_2006_01.R Package: ORFik Version: 1.2.1 Depends: R (>= 3.5.0), IRanges (>= 2.13.28), GenomicRanges (>= 1.31.23), GenomicAlignments (>= 1.15.13) Imports: S4Vectors (>= 0.17.39), GenomeInfoDb (>= 1.15.5), GenomicFeatures (>= 1.31.10), rtracklayer (>= 1.39.9), Rcpp (>= 0.12.16), data.table (>= 1.10.4-3), Biostrings (>= 2.47.12), stats, tools, Rsamtools (>= 1.31.3), BiocGenerics (>= 0.25.3) LinkingTo: Rcpp Suggests: testthat, rmarkdown, knitr, BiocStyle, BSgenome, BSgenome.Hsapiens.UCSC.hg19, ggplot2 (>= 2.2.1) License: MIT + file LICENSE MD5sum: d551e6d9f9465235ec475ab30be11dc2 NeedsCompilation: yes Title: Open Reading Frames in Genomics Description: Tools for manipulation of RiboSeq, RNASeq and CageSeq data. ORFik is extremely fast through use of C, data.table and GenomicRanges. Package allows to reassign starts of the transcripts with the use of CageSeq data, automatic shifting of RiboSeq reads, finding of Open Reading Frames for the whole genomes and many more. biocViews: ImmunoOncology, Software, Sequencing, RiboSeq, RNASeq, FunctionalGenomics, Coverage, Alignment, DataImport Author: Kornel Labun [aut, cre, cph], Haakon Tjeldnes [aut, dtc], Katarzyna Chyzynska [ctb, dtc], Evind Valen [ths, fnd] Maintainer: Kornel Labun URL: https://github.com/JokingHero/ORFik VignetteBuilder: knitr BugReports: https://github.com/JokingHero/ORFik/issues git_url: https://git.bioconductor.org/packages/ORFik git_branch: RELEASE_3_8 git_last_commit: 2e3a8c6 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ORFik_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ORFik_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ORFik_1.2.1.tgz vignettes: vignettes/ORFik/inst/doc/ORFikOverview.html vignetteTitles: ORFik Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ORFik/inst/doc/ORFikOverview.R Package: Organism.dplyr Version: 1.10.0 Depends: R (>= 3.4), dplyr (>= 0.7.0), AnnotationFilter (>= 1.1.3) Imports: RSQLite, S4Vectors, GenomeInfoDb, IRanges, GenomicRanges, GenomicFeatures, AnnotationDbi, methods, tools, utils, BiocFileCache, DBI, dbplyr Suggests: org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg38.knownGene, org.Mm.eg.db, TxDb.Mmusculus.UCSC.mm10.ensGene, testthat, knitr, rmarkdown, BiocStyle, ggplot2 License: Artistic-2.0 Archs: i386, x64 MD5sum: 2852cd417e6f66dea89e0c4dbb7cd9d4 NeedsCompilation: no Title: dplyr-based Access to Bioconductor Annotation Resources Description: This package provides an alternative interface to Bioconductor 'annotation' resources, in particular the gene identifier mapping functionality of the 'org' packages (e.g., org.Hs.eg.db) and the genome coordinate functionality of the 'TxDb' packages (e.g., TxDb.Hsapiens.UCSC.hg38.knownGene). biocViews: Annotation, Sequencing, GenomeAnnotation Author: Martin Morgan [aut, cre], Yubo Cheng [ctb] Maintainer: Martin Morgan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Organism.dplyr git_branch: RELEASE_3_8 git_last_commit: 80f36e6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Organism.dplyr_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Organism.dplyr_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Organism.dplyr_1.10.0.tgz vignettes: vignettes/Organism.dplyr/inst/doc/Organism.dplyr.html vignetteTitles: Organism.dplyr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Organism.dplyr/inst/doc/Organism.dplyr.R Package: OrganismDbi Version: 1.24.0 Depends: R (>= 2.14.0), methods, BiocGenerics (>= 0.15.10), AnnotationDbi (>= 1.33.15), GenomicFeatures (>= 1.23.31) Imports: Biobase, BiocManager, GenomicRanges (>= 1.31.13), graph, IRanges, RBGL, DBI, S4Vectors (>= 0.9.25), stats Suggests: Homo.sapiens, Rattus.norvegicus, BSgenome.Hsapiens.UCSC.hg19, AnnotationHub, FDb.UCSC.tRNAs, rtracklayer, biomaRt, RUnit, RMariaDB License: Artistic-2.0 MD5sum: 5b61c03153b43c626fbdbbd1780e7652 NeedsCompilation: no Title: Software to enable the smooth interfacing of different database packages Description: The package enables a simple unified interface to several annotation packages each of which has its own schema by taking advantage of the fact that each of these packages implements a select methods. biocViews: Annotation, Infrastructure Author: Marc Carlson, Hervé Pagès, Martin Morgan, Valerie Obenchain Maintainer: Biocore Data Team git_url: https://git.bioconductor.org/packages/OrganismDbi git_branch: RELEASE_3_8 git_last_commit: 3428952 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/OrganismDbi_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OrganismDbi_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OrganismDbi_1.24.0.tgz vignettes: vignettes/OrganismDbi/inst/doc/OrganismDbi.pdf vignetteTitles: OrganismDbi: A meta framework for Annotation Packages hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OrganismDbi/inst/doc/OrganismDbi.R importsMe: AnnotationHubData, epivizrData, ggbio, gpart suggestsMe: ChIPpeakAnno, epivizrStandalone Package: OSAT Version: 1.30.0 Depends: methods,stats Suggests: xtable, Biobase License: Artistic-2.0 MD5sum: 25da0a3ebe891d2149a22612d0e2884e NeedsCompilation: no Title: OSAT: Optimal Sample Assignment Tool Description: A sizable genomics study such as microarray often involves the use of multiple batches (groups) of experiment due to practical complication. To minimize batch effects, a careful experiment design should ensure the even distribution of biological groups and confounding factors across batches. OSAT (Optimal Sample Assignment Tool) is developed to facilitate the allocation of collected samples to different batches. With minimum steps, it produces setup that optimizes the even distribution of samples in groups of biological interest into different batches, reducing the confounding or correlation between batches and the biological variables of interest. It can also optimize the even distribution of confounding factors across batches. Our tool can handle challenging instances where incomplete and unbalanced sample collections are involved as well as ideal balanced RCBD. OSAT provides a number of predefined layout for some of the most commonly used genomics platform. Related paper can be find at http://www.biomedcentral.com/1471-2164/13/689 . biocViews: DataRepresentation, Visualization, ExperimentalDesign, QualityControl Author: Li Yan Maintainer: Li Yan URL: http://www.biomedcentral.com/1471-2164/13/689 git_url: https://git.bioconductor.org/packages/OSAT git_branch: RELEASE_3_8 git_last_commit: dc662ac git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OSAT_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OSAT_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OSAT_1.30.0.tgz vignettes: vignettes/OSAT/inst/doc/OSAT.pdf vignetteTitles: An introduction to OSAT hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OSAT/inst/doc/OSAT.R Package: Oscope Version: 1.12.1 Depends: EBSeq, cluster, testthat, BiocParallel Suggests: BiocStyle License: Artistic-2.0 MD5sum: 4b517c5cae6be7f3f74636b817b7ad98 NeedsCompilation: no Title: Oscope - A statistical pipeline for identifying oscillatory genes in unsynchronized single cell RNA-seq Description: Oscope is a statistical pipeline developed to identifying and recovering the base cycle profiles of oscillating genes in an unsynchronized single cell RNA-seq experiment. The Oscope pipeline includes three modules: a sine model module to search for candidate oscillator pairs; a K-medoids clustering module to cluster candidate oscillators into groups; and an extended nearest insertion module to recover the base cycle order for each oscillator group. biocViews: ImmunoOncology, StatisticalMethod,RNASeq, Sequencing, GeneExpression Author: Ning Leng Maintainer: Ning Leng git_url: https://git.bioconductor.org/packages/Oscope git_branch: RELEASE_3_8 git_last_commit: 34d9912 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Oscope_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Oscope_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Oscope_1.12.1.tgz vignettes: vignettes/Oscope/inst/doc/Oscope_vignette.pdf vignetteTitles: Oscope_vigette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Oscope/inst/doc/Oscope_vignette.R Package: OTUbase Version: 1.32.0 Depends: R (>= 2.9.0), methods, S4Vectors, IRanges, ShortRead (>= 1.23.15), Biobase, vegan Imports: Biostrings License: Artistic-2.0 MD5sum: 1d7602393bcbe0d127f647249cf9a0e9 NeedsCompilation: no Title: Provides structure and functions for the analysis of OTU data Description: Provides a platform for Operational Taxonomic Unit based analysis biocViews: Sequencing, DataImport Author: Daniel Beck, Matt Settles, and James A. Foster Maintainer: Daniel Beck git_url: https://git.bioconductor.org/packages/OTUbase git_branch: RELEASE_3_8 git_last_commit: f1d9419 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OTUbase_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OTUbase_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OTUbase_1.32.0.tgz vignettes: vignettes/OTUbase/inst/doc/Introduction_to_OTUbase.pdf vignetteTitles: An introduction to OTUbase hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OTUbase/inst/doc/Introduction_to_OTUbase.R dependsOnMe: mcaGUI Package: OutlierD Version: 1.46.0 Depends: R (>= 2.3.0), Biobase, quantreg License: GPL (>= 2) MD5sum: faccbb13610392cf250252e1d03498f5 NeedsCompilation: no Title: Outlier detection using quantile regression on the M-A scatterplots of high-throughput data Description: This package detects outliers using quantile regression on the M-A scatterplots of high-throughput data. biocViews: Microarray Author: HyungJun Cho Maintainer: Sukwoo Kim URL: http://www.korea.ac.kr/~stat2242/ git_url: https://git.bioconductor.org/packages/OutlierD git_branch: RELEASE_3_8 git_last_commit: 01f3ca3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/OutlierD_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/OutlierD_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OutlierD_1.46.0.tgz vignettes: vignettes/OutlierD/inst/doc/OutlierD.pdf vignetteTitles: Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/OutlierD/inst/doc/OutlierD.R Package: OUTRIDER Version: 1.0.4 Depends: R (>= 3.5), BiocParallel, GenomicFeatures, SummarizedExperiment, data.table, methods Imports: BBmisc, Biobase, BiocGenerics, compiler, DESeq2 (>= 1.16.1), GenomicRanges, ggplot2, ggpubr, gplots, graphics, IRanges, matrixStats, plotly, plyr, pcaMethods, PRROC, RColorBrewer, Rcpp, reticulate, S4Vectors, scales, splines, stats, utils LinkingTo: Rcpp, RcppArmadillo Suggests: testthat, knitr, rmarkdown, BiocStyle, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db, RMySQL, AnnotationDbi, beeswarm, covr License: MIT + file LICENSE MD5sum: 6539a7eefb7f0db7da92788e5a8857e2 NeedsCompilation: yes Title: OUTRIDER - OUTlier in RNA-Seq fInDER Description: Identification of aberrant gene expression in RNA-seq data. Read count expectations are modeled by an autoencoder to control for confounders in the data. Given these expectations, the RNA-seq read counts are assumed to follow a negative binomial distribution with a gene-specific dispersion. Outliers are then identified as read counts that significantly deviate from this distribution. Furthermore, OUTRIDER provides useful plotting functions to analyze and visualize the results. biocViews: ImmunoOncology, RNASeq, Transcriptomics, Alignment, Sequencing, GeneExpression, Genetics Author: Felix Brechtmann [aut, cre], Christian Mertes [aut, cre], Ange Matuseviciute [aut, cre], Vicente Yepez [aut], Julien Gagneur [aut] Maintainer: Christian Mertes URL: https://github.com/gagneurlab/OUTRIDER VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/OUTRIDER git_branch: RELEASE_3_8 git_last_commit: 18fcd8e git_last_commit_date: 2019-03-18 Date/Publication: 2019-03-19 source.ver: src/contrib/OUTRIDER_1.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/OUTRIDER_1.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/OUTRIDER_1.0.4.tgz vignettes: vignettes/OUTRIDER/inst/doc/OUTRIDER.pdf vignetteTitles: OUTRIDER: OUTlier in RNA-seq fInDER hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/OUTRIDER/inst/doc/OUTRIDER.R Package: PAA Version: 1.16.0 Depends: R (>= 3.2.0), Rcpp (>= 0.11.6) Imports: e1071, gplots, gtools, limma, MASS, mRMRe, randomForest, ROCR, sva LinkingTo: Rcpp Suggests: BiocStyle, RUnit, BiocGenerics, vsn License: BSD_3_clause + file LICENSE Archs: i386, x64 MD5sum: 0452cfe09ff503b2cde95e81feafe9d5 NeedsCompilation: yes Title: PAA (Protein Array Analyzer) Description: PAA imports single color (protein) microarray data that has been saved in gpr file format - esp. ProtoArray data. After preprocessing (background correction, batch filtering, normalization) univariate feature preselection is performed (e.g., using the "minimum M statistic" approach - hereinafter referred to as "mMs"). Subsequently, a multivariate feature selection is conducted to discover biomarker candidates. Therefore, either a frequency-based backwards elimination aproach or ensemble feature selection can be used. PAA provides a complete toolbox of analysis tools including several different plots for results examination and evaluation. biocViews: Classification, Microarray, OneChannel, Proteomics Author: Michael Turewicz [aut, cre], Martin Eisenacher [ctb, cre] Maintainer: Michael Turewicz , Martin Eisenacher URL: http://www.ruhr-uni-bochum.de/mpc/software/PAA/ SystemRequirements: C++ software package Random Jungle git_url: https://git.bioconductor.org/packages/PAA git_branch: RELEASE_3_8 git_last_commit: 783aae5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PAA_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PAA_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PAA_1.16.0.tgz vignettes: vignettes/PAA/inst/doc/PAA_1.7.1.pdf, vignettes/PAA/inst/doc/PAA_vignette.pdf vignetteTitles: PAA_1.7.1.pdf, PAA tutorial hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/PAA/inst/doc/PAA_vignette.R Package: PADOG Version: 1.24.0 Depends: R (>= 3.0.0), KEGGdzPathwaysGEO, methods,Biobase Imports: limma, AnnotationDbi, GSA, foreach, doRNG, hgu133plus2.db, hgu133a.db, KEGG.db, nlme Suggests: doParallel, parallel License: GPL (>= 2) Archs: i386, x64 MD5sum: 56431caee5cc198ddfdd7f93646d72d9 NeedsCompilation: no Title: Pathway Analysis with Down-weighting of Overlapping Genes (PADOG) Description: This package implements a general purpose gene set analysis method called PADOG that downplays the importance of genes that apear often accross the sets of genes to be analyzed. The package provides also a benchmark for gene set analysis methods in terms of sensitivity and ranking using 24 public datasets from KEGGdzPathwaysGEO package. biocViews: Microarray, OneChannel, TwoChannel Author: Adi Laurentiu Tarca ; Zhonghui Xu Maintainer: Adi Laurentiu Tarca git_url: https://git.bioconductor.org/packages/PADOG git_branch: RELEASE_3_8 git_last_commit: ed3f896 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PADOG_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PADOG_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PADOG_1.24.0.tgz vignettes: vignettes/PADOG/inst/doc/PADOG.pdf vignetteTitles: PADOG hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PADOG/inst/doc/PADOG.R dependsOnMe: BLMA importsMe: EGSEA Package: paircompviz Version: 1.20.0 Depends: R (>= 2.10), Rgraphviz Imports: Rgraphviz Suggests: multcomp, reshape, rpart, plyr, xtable License: GPL (>=3.0) MD5sum: c2b68b9feed3ae0a7b15ad87e72465d6 NeedsCompilation: no Title: Multiple comparison test visualization Description: This package provides visualization of the results from the multiple (i.e. pairwise) comparison tests such as pairwise.t.test, pairwise.prop.test or pairwise.wilcox.test. The groups being compared are visualized as nodes in Hasse diagram. Such approach enables very clear and vivid depiction of which group is significantly greater than which others, especially if comparing a large number of groups. biocViews: GraphAndNetwork Author: Michal Burda Maintainer: Michal Burda git_url: https://git.bioconductor.org/packages/paircompviz git_branch: RELEASE_3_8 git_last_commit: da73f60 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/paircompviz_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/paircompviz_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/paircompviz_1.20.0.tgz vignettes: vignettes/paircompviz/inst/doc/vignette.pdf vignetteTitles: Using paircompviz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/paircompviz/inst/doc/vignette.R Package: pandaR Version: 1.14.0 Depends: R (>= 3.0.0), methods, Biobase, BiocGenerics, Imports: matrixStats, igraph, ggplot2, grid, reshape, plyr, RUnit, hexbin Suggests: knitr License: GPL-2 MD5sum: adba12e16232b6d5443a2877e53ad90b NeedsCompilation: no Title: PANDA Algorithm Description: Runs PANDA, an algorithm for discovering novel network structure by combining information from multiple complementary data sources. biocViews: StatisticalMethod, GraphAndNetwork, Microarray, GeneRegulation, NetworkInference, GeneExpression, Transcription, Network Author: Dan Schlauch, Joseph N. Paulson, Albert Young, John Quackenbush, Kimberly Glass Maintainer: Joseph N. Paulson , Dan Schlauch VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/pandaR git_branch: RELEASE_3_8 git_last_commit: 97367cc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pandaR_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pandaR_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pandaR_1.14.0.tgz vignettes: vignettes/pandaR/inst/doc/pandaR.html vignetteTitles: pandaR Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pandaR/inst/doc/pandaR.R Package: panelcn.mops Version: 1.4.0 Depends: R (>= 3.4), cn.mops, methods, utils, stats, graphics Imports: GenomicRanges, Rsamtools, IRanges, S4Vectors, GenomeInfoDb, grDevices Suggests: knitr, rmarkdown, RUnit, BiocGenerics License: LGPL (>= 2.0) MD5sum: 974ec0d14c6d3a3d8bca8c3f5140e718 NeedsCompilation: no Title: CNV detection tool for targeted NGS panel data Description: CNV detection tool for targeted NGS panel data. Extension of the cn.mops package. biocViews: Sequencing, CopyNumberVariation, CellBiology, GenomicVariation, VariantDetection, Genetics Author: Verena Haunschmid, Gundula Povysil Maintainer: Gundula Povysil VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/panelcn.mops git_branch: RELEASE_3_8 git_last_commit: 3a0b380 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/panelcn.mops_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/panelcn.mops_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/panelcn.mops_1.4.0.tgz vignettes: vignettes/panelcn.mops/inst/doc/panelcn.mops.pdf vignetteTitles: panelcn.mops: Manual for the R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/panelcn.mops/inst/doc/panelcn.mops.R Package: panp Version: 1.52.0 Depends: R (>= 2.10), affy (>= 1.23.4), Biobase (>= 2.5.5) Imports: Biobase, methods, stats, utils Suggests: gcrma License: GPL (>= 2) MD5sum: ce35790cd1d330942a3266e4c391d380 NeedsCompilation: no Title: Presence-Absence Calls from Negative Strand Matching Probesets Description: A function to make gene presence/absence calls based on distance from negative strand matching probesets (NSMP) which are derived from Affymetrix annotation. PANP is applied after gene expression values are created, and therefore can be used after any preprocessing method such as MAS5 or GCRMA, or PM-only methods like RMA. NSMP sets have been established for the HGU133A and HGU133-Plus-2.0 chipsets to date. biocViews: Infrastructure Author: Peter Warren Maintainer: Peter Warren git_url: https://git.bioconductor.org/packages/panp git_branch: RELEASE_3_8 git_last_commit: 0c0b523 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/panp_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/panp_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/panp_1.52.0.tgz vignettes: vignettes/panp/inst/doc/panp.pdf vignetteTitles: gene presence/absence calls hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/panp/inst/doc/panp.R Package: PANR Version: 1.28.1 Depends: R (>= 2.14), igraph Imports: graphics, grDevices, MASS, methods, pvclust, stats, utils, RedeR Suggests: snow License: Artistic-2.0 MD5sum: eeb904229161bcf7adf5cf5fbf7e482d NeedsCompilation: no Title: Posterior association networks and functional modules inferred from rich phenotypes of gene perturbations Description: This package provides S4 classes and methods for inferring functional gene networks with edges encoding posterior beliefs of gene association types and nodes encoding perturbation effects. biocViews: ImmunoOncology, NetworkInference, Visualization, GraphAndNetwork, Clustering, CellBasedAssays Author: Xin Wang Maintainer: Xin Wang git_url: https://git.bioconductor.org/packages/PANR git_branch: RELEASE_3_8 git_last_commit: 81b5a65 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PANR_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PANR_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PANR_1.28.1.tgz vignettes: vignettes/PANR/inst/doc/PANR-Vignette.pdf vignetteTitles: Main vignette:Posterior association network and enriched functional gene modules inferred from rich phenotypes of gene perturbations hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PANR/inst/doc/PANR-Vignette.R Package: PanVizGenerator Version: 1.10.0 Depends: methods Imports: shiny, tools, jsonlite, pcaMethods, FindMyFriends, igraph, stats, utils Suggests: BiocStyle, knitr, rmarkdown, testthat, digest License: GPL (>= 2) MD5sum: d4415d9cb3e2e6c4e46abfe7e5cf601e NeedsCompilation: no Title: Generate PanViz visualisations from your pangenome Description: PanViz is a JavaScript based visualisation tool for functionaly annotated pangenomes. PanVizGenerator is a companion for PanViz that facilitates the necessary data preprocessing step necessary to create a working PanViz visualization. The output is fully self-contained so the recipient of the visualization does not need R or PanVizGenerator installed. biocViews: ComparativeGenomics, GUI, Visualization Author: Thomas Lin Pedersen Maintainer: Thomas Lin Pedersen URL: https://github.com/thomasp85/PanVizGenerator VignetteBuilder: knitr BugReports: https://github.com/thomasp85/PanVizGenerator/issues git_url: https://git.bioconductor.org/packages/PanVizGenerator git_branch: RELEASE_3_8 git_last_commit: 789b930 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PanVizGenerator_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PanVizGenerator_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PanVizGenerator_1.10.0.tgz vignettes: vignettes/PanVizGenerator/inst/doc/panviz_howto.html vignetteTitles: Creating PanViz visualizations with PanVizGenerator hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PanVizGenerator/inst/doc/panviz_howto.R Package: PAPi Version: 1.22.1 Depends: R (>= 2.15.2), svDialogs, KEGGREST License: GPL(>= 2) MD5sum: 307adc3cc09bc79751f9a1787889cb26 NeedsCompilation: no Title: Predict metabolic pathway activity based on metabolomics data Description: The Pathway Activity Profiling - PAPi - is an R package for predicting the activity of metabolic pathways based solely on a metabolomics data set containing a list of metabolites identified and their respective abundances in different biological samples. PAPi generates hypothesis that improves the final biological interpretation. See Aggio, R.B.M; Ruggiero, K. and Villas-Boas, S.G. (2010) - Pathway Activity Profiling (PAPi): from metabolite profile to metabolic pathway activity. Bioinformatics. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics Author: Raphael Aggio Maintainer: Raphael Aggio git_url: https://git.bioconductor.org/packages/PAPi git_branch: RELEASE_3_8 git_last_commit: 6dcfa73 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PAPi_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PAPi_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PAPi_1.22.1.tgz vignettes: vignettes/PAPi/inst/doc/PAPi.pdf, vignettes/PAPi/inst/doc/PAPiPackage.pdf vignetteTitles: PAPi.pdf, Applying PAPi hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PAPi/inst/doc/PAPiPackage.R Package: parglms Version: 1.14.0 Depends: methods Imports: BiocGenerics, BatchJobs, foreach, doParallel Suggests: RUnit, sandwich, MASS, knitr License: Artistic-2.0 MD5sum: 61af77bc2927d500ecba6c0427cd8d68 NeedsCompilation: no Title: support for parallelized estimation of GLMs/GEEs Description: support for parallelized estimation of GLMs/GEEs, catering for dispersed data Author: VJ Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/parglms git_branch: RELEASE_3_8 git_last_commit: e6ac868 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/parglms_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/parglms_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/parglms_1.14.0.tgz vignettes: vignettes/parglms/inst/doc/parglms.pdf vignetteTitles: parglms: parallelized GLM hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/parglms/inst/doc/parglms.R Package: parody Version: 1.40.0 Depends: R (>= 2.5.0), methods, tools, utils License: Artistic-2.0 MD5sum: 7fed47b92aa3019bc677948bcd13cde6 NeedsCompilation: no Title: Parametric And Resistant Outlier DYtection Description: routines for univariate and multivariate outlier detection with a focus on parametric methods, but support for some methods based on resistant statistics biocViews: MultipleComparison Author: VJ Carey Maintainer: VJ Carey git_url: https://git.bioconductor.org/packages/parody git_branch: RELEASE_3_8 git_last_commit: 72c42dc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/parody_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/parody_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/parody_1.40.0.tgz vignettes: vignettes/parody/inst/doc/parody.pdf vignetteTitles: parody: parametric and resistant outlier detection hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/parody/inst/doc/parody.R dependsOnMe: arrayMvout Package: Path2PPI Version: 1.12.0 Depends: R (>= 3.2.1), igraph (>= 1.0.1), methods Suggests: knitr, rmarkdown, RUnit, BiocGenerics, BiocStyle License: GPL (>= 2) MD5sum: fa0f1aa93584b7a1d724309e6f8b60c4 NeedsCompilation: no Title: Prediction of pathway-related protein-protein interaction networks Description: Package to predict protein-protein interaction (PPI) networks in target organisms for which only a view information about PPIs is available. Path2PPI predicts PPI networks based on sets of proteins which can belong to a certain pathway from well-established model organisms. It helps to combine and transfer information of a certain pathway or biological process from several reference organisms to one target organism. Path2PPI only depends on the sequence similarity of the involved proteins. biocViews: NetworkInference, SystemsBiology, Network, Proteomics, Pathways Author: Oliver Philipp [aut, cre], Ina Koch [ctb] Maintainer: Oliver Philipp URL: http://www.bioinformatik.uni-frankfurt.de/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Path2PPI git_branch: RELEASE_3_8 git_last_commit: 1099cfc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Path2PPI_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Path2PPI_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Path2PPI_1.12.0.tgz vignettes: vignettes/Path2PPI/inst/doc/Path2PPI-tutorial.html vignetteTitles: Path2PPI - A brief tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Path2PPI/inst/doc/Path2PPI-tutorial.R Package: pathifier Version: 1.20.0 Imports: R.oo, princurve (>= 2.0.4) License: Artistic-1.0 MD5sum: a3c03fc2a9686179902658a4e3d02946 NeedsCompilation: no Title: Quantify deregulation of pathways in cancer Description: Pathifier is an algorithm that infers pathway deregulation scores for each tumor sample on the basis of expression data. This score is determined, in a context-specific manner, for every particular dataset and type of cancer that is being investigated. The algorithm transforms gene-level information into pathway-level information, generating a compact and biologically relevant representation of each sample. biocViews: Network Author: Yotam Drier Maintainer: Assif Yitzhaky git_url: https://git.bioconductor.org/packages/pathifier git_branch: RELEASE_3_8 git_last_commit: 2aed7d2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pathifier_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pathifier_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pathifier_1.20.0.tgz vignettes: vignettes/pathifier/inst/doc/Overview.pdf vignetteTitles: Quantify deregulation of pathways in cancer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pathifier/inst/doc/Overview.R Package: PathNet Version: 1.22.0 Depends: R (>= 1.14.0) Suggests: PathNetData, RUnit, BiocGenerics License: GPL-3 MD5sum: b7ba6c5f1e0cec5a3b1d5c820345b02a NeedsCompilation: no Title: An R package for pathway analysis using topological information Description: PathNet uses topological information present in pathways and differential expression levels of genes (obtained from microarray experiment) to identify pathways that are 1) significantly enriched and 2) associated with each other in the context of differential expression. The algorithm is described in: PathNet: A tool for pathway analysis using topological information. Dutta B, Wallqvist A, and Reifman J. Source Code for Biology and Medicine 2012 Sep 24;7(1):10. biocViews: Pathways, DifferentialExpression, MultipleComparison, KEGG, NetworkEnrichment, Network Author: Bhaskar Dutta , Anders Wallqvist , and Jaques Reifman Maintainer: Jason B. Smith git_url: https://git.bioconductor.org/packages/PathNet git_branch: RELEASE_3_8 git_last_commit: 80cf6f3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PathNet_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PathNet_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PathNet_1.22.0.tgz vignettes: vignettes/PathNet/inst/doc/PathNet.pdf vignetteTitles: PathNet hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PathNet/inst/doc/PathNet.R Package: PathoStat Version: 1.8.4 Depends: R (>= 3.5) Imports: limma, corpcor,matrixStats, reshape2, scales, ggplot2, rentrez, DT, tidyr, plyr, dplyr, phyloseq, shiny, stats, methods, XML, graphics, utils, BiocStyle, edgeR, DESeq2, ComplexHeatmap, plotly, webshot, vegan, shinyjs, glmnet, gmodels, ROCR, RColorBrewer, knitr, devtools, ape Suggests: rmarkdown, testthat License: GPL (>= 2) MD5sum: 385833d81ba649fab612821f5f0fad55 NeedsCompilation: no Title: PathoStat Statistical Microbiome Analysis Package Description: The purpose of this package is to perform Statistical Microbiome Analysis on metagenomics results from sequencing data samples. In particular, it supports analyses on the PathoScope generated report files. PathoStat provides various functionalities including Relative Abundance charts, Diversity estimates and plots, tests of Differential Abundance, Time Series visualization, and Core OTU analysis. biocViews: Microbiome, Metagenomics, GraphAndNetwork, Microarray, PatternLogic, PrincipalComponent, Sequencing, Software, Visualization, RNASeq, ImmunoOncology Author: Solaiappan Manimaran , Matthew Bendall , Sandro Valenzuela Diaz , Eduardo Castro , Tyler Faits , Yue Zhao , Anthony Nicholas Federico , W. Evan Johnson Maintainer: Solaiappan Manimaran , Yue Zhao URL: https://github.com/mani2012/PathoStat VignetteBuilder: knitr BugReports: https://github.com/mani2012/PathoStat/issues git_url: https://git.bioconductor.org/packages/PathoStat git_branch: RELEASE_3_8 git_last_commit: e2b4a5c git_last_commit_date: 2018-12-01 Date/Publication: 2018-12-02 source.ver: src/contrib/PathoStat_1.8.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/PathoStat_1.8.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PathoStat_1.8.4.tgz vignettes: vignettes/PathoStat/inst/doc/PathoStat-vignette.html vignetteTitles: PathoStat intro hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PathoStat/inst/doc/PathoStat-vignette.R Package: pathprint Version: 1.12.0 Depends: R (>= 3.4) Imports: stats, utils Suggests: ALL, GEOquery, pathprintGEOData, SummarizedExperiment License: GPL MD5sum: 4fa4f3fecafee2af2d62766f6affa9fa NeedsCompilation: no Title: Pathway fingerprinting for analysis of gene expression arrays Description: Algorithms to convert a gene expression array provided as an expression table or a GEO reference to a 'pathway fingerprint', a vector of discrete ternary scores representing high (1), low(-1) or insignificant (0) expression in a suite of pathways. biocViews: Transcription, GeneExpression, KEGG, Reactome Author: Gabriel Altschuler, Sokratis Kariotis Maintainer: Sokratis Kariotis git_url: https://git.bioconductor.org/packages/pathprint git_branch: RELEASE_3_8 git_last_commit: fbeb22a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pathprint_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pathprint_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pathprint_1.12.0.tgz vignettes: vignettes/pathprint/inst/doc/exampleFingerprint.pdf vignetteTitles: pathprint hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pathprint/inst/doc/exampleFingerprint.R Package: pathRender Version: 1.50.0 Depends: graph, Rgraphviz, RColorBrewer, cMAP, AnnotationDbi, methods, stats4 Suggests: ALL, hgu95av2.db License: LGPL MD5sum: 91a194d410a75cfcd81136ccce3496e7 NeedsCompilation: no Title: Render molecular pathways Description: build graphs from pathway databases, render them by Rgraphviz. biocViews: GraphAndNetwork, Pathways, Visualization Author: Li Long Maintainer: Vince Carey URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/pathRender git_branch: RELEASE_3_8 git_last_commit: d48cad5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pathRender_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pathRender_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pathRender_1.50.0.tgz vignettes: vignettes/pathRender/inst/doc/pathRender.pdf, vignettes/pathRender/inst/doc/plotExG.pdf vignetteTitles: pathRender overview, pathway graphs colored by expression map hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pathRender/inst/doc/pathRender.R, vignettes/pathRender/inst/doc/plotExG.R Package: pathVar Version: 1.12.0 Depends: R (>= 3.3.0), methods, ggplot2, gridExtra Imports: EMT, mclust, Matching, data.table, stats, grDevices, graphics, utils License: LGPL (>= 2.0) MD5sum: 6a0e4fc15f3b005a5d188b3242149420 NeedsCompilation: no Title: Methods to Find Pathways with Significantly Different Variability Description: This package contains the functions to find the pathways that have significantly different variability than a reference gene set. It also finds the categories from this pathway that are significant where each category is a cluster of genes. The genes are separated into clusters by their level of variability. biocViews: GeneticVariability, GeneSetEnrichment, Pathways Author: Laurence de Torrente, Samuel Zimmerman, Jessica Mar Maintainer: Samuel Zimmerman git_url: https://git.bioconductor.org/packages/pathVar git_branch: RELEASE_3_8 git_last_commit: 368f103 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pathVar_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pathVar_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pathVar_1.12.0.tgz vignettes: vignettes/pathVar/inst/doc/pathVar.pdf vignetteTitles: Tutorial on How to Use the Functions in the \texttt{PathVar} Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pathVar/inst/doc/pathVar.R Package: pathview Version: 1.22.3 Depends: R (>= 2.10), org.Hs.eg.db Imports: KEGGgraph, XML, Rgraphviz, graph, png, AnnotationDbi, KEGGREST, methods, utils Suggests: gage, org.Mm.eg.db, RUnit, BiocGenerics License: GPL (>=3.0) MD5sum: cce5e8272213de8ae7cbaa7531f81d67 NeedsCompilation: no Title: a tool set for pathway based data integration and visualization Description: Pathview is a tool set for pathway based data integration and visualization. It maps and renders a wide variety of biological data on relevant pathway graphs. All users need is to supply their data and specify the target pathway. Pathview automatically downloads the pathway graph data, parses the data file, maps user data to the pathway, and render pathway graph with the mapped data. In addition, Pathview also seamlessly integrates with pathway and gene set (enrichment) analysis tools for large-scale and fully automated analysis. biocViews: Pathways, GraphAndNetwork, Visualization, GeneSetEnrichment, DifferentialExpression, GeneExpression, Microarray, RNASeq, Genetics, Metabolomics, Proteomics, SystemsBiology, Sequencing Author: Weijun Luo Maintainer: Weijun Luo URL: https://pathview.uncc.edu/ git_url: https://git.bioconductor.org/packages/pathview git_branch: RELEASE_3_8 git_last_commit: ff86f9e git_last_commit_date: 2019-02-11 Date/Publication: 2019-02-12 source.ver: src/contrib/pathview_1.22.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/pathview_1.22.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pathview_1.22.3.tgz vignettes: vignettes/pathview/inst/doc/pathview.pdf vignetteTitles: Pathview: pathway based data integration and visualization hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pathview/inst/doc/pathview.R dependsOnMe: BioNetStat, EGSEA, MAGeCKFlute, RNASeqR importsMe: CompGO, debrowser, EnrichmentBrowser, GDCRNATools, TCGAbiolinksGUI suggestsMe: clusterProfiler, gage, Pi, TCGAbiolinks Package: PathwaySplice Version: 1.6.1 Depends: R (>= 3.5.0) Imports: goseq, Biobase, DOSE, reshape2, igraph, org.Hs.eg.db, org.Mm.eg.db, BiocGenerics, AnnotationDbi, JunctionSeq, BiasedUrn, GO.db,gdata, geneLenDataBase, grDevices, graphics, stats, utils, VennDiagram, RColorBrewer, ensembldb, AnnotationHub, S4Vectors, dplyr, plotly, webshot, htmlwidgets , mgcv ,gridExtra, grid ,gplots, tibble , EnrichmentBrowser, annotate , KEGGREST Suggests: testthat, knitr, rmarkdown License: LGPL(>=2) MD5sum: 460ce4880d1841ad53e424c63f229284 NeedsCompilation: no Title: An R Package for Unbiased Splicing Pathway Analysis Description: Pathway analysis of alternative splicing would be biased without accounting for the different number of exons associated with each gene, because genes with higher number of exons are more likely to be included in the 'significant' gene list in alternative splicing. PathwaySplice is an R package that: (1) performs pathway analysis that explicitly adjusts for the number of exons associated with each gene (2) visualizes selection bias due to different number of exons for each gene (3) formally tests for presence of bias using logistic regression (4) supports gene sets based on the Gene Ontology terms, as well as more broadly defined gene sets (e.g. MSigDB) or user defined gene sets (5) identifies the significant genes driving pathway significance (6) organizes significant pathways with an enrichment map, where pathways with large number of overlapping genes are grouped together in a network graph biocViews: ImmunoOncology, AlternativeSplicing, DifferentialSplicing, GeneSetEnrichment, GO, RNASeq, Sequencing, Software, Visualization, NetworkEnrichment, Network, Pathways, GraphAndNetwork, Regression Author: Aimin Yan, Xi Chen, Lily Wang Maintainer: Aimin Yan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PathwaySplice git_branch: RELEASE_3_8 git_last_commit: 9488b1f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PathwaySplice_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PathwaySplice_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PathwaySplice_1.6.1.tgz vignettes: vignettes/PathwaySplice/inst/doc/tutorial.html vignetteTitles: PathwaySplice hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PathwaySplice/inst/doc/tutorial.R Package: paxtoolsr Version: 1.16.0 Depends: R (>= 3.2), rJava (>= 0.9-8), XML Imports: utils, httr, igraph, plyr, rjson, R.utils, jsonlite, readr Suggests: testthat, knitr, BiocStyle, rmarkdown, RColorBrewer, biomaRt, estrogen, affy, hgu95av2, hgu95av2cdf, limma, foreach, doSNOW, parallel, org.Hs.eg.db License: LGPL-3 MD5sum: 8394eb60eeaee13886d8934e67581e7d NeedsCompilation: no Title: PaxtoolsR: Access Pathways from Multiple Databases through BioPAX and Pathway Commons Description: The package provides a set of R functions for interacting with BioPAX OWL files using Paxtools and the querying Pathway Commons (PC) molecular interaction database that are hosted by the Computational Biology Center at Memorial Sloan-Kettering Cancer Center (MSKCC). Pathway Commons databases include: BIND, BioGRID, CORUM, CTD, DIP, DrugBank, HPRD, HumanCyc, IntAct, KEGG, MirTarBase, Panther, PhosphoSitePlus, Reactome, RECON, TRANSFAC. biocViews: GeneSetEnrichment, GraphAndNetwork, Pathways, Software, SystemsBiology, NetworkEnrichment, Network, Reactome, KEGG Author: Augustin Luna Maintainer: Augustin Luna URL: https://github.com/BioPAX/paxtoolsr SystemRequirements: Java (>= 1.6) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/paxtoolsr git_branch: RELEASE_3_8 git_last_commit: b009b3d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/paxtoolsr_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/paxtoolsr_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/paxtoolsr_1.16.0.tgz vignettes: vignettes/paxtoolsr/inst/doc/using_paxtoolsr.html vignetteTitles: Using PaxtoolsR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/paxtoolsr/inst/doc/using_paxtoolsr.R Package: Pbase Version: 0.22.1 Depends: R (>= 2.10), methods, BiocGenerics, Rcpp, Gviz Imports: cleaver (>= 1.3.6), Biobase, Biostrings (>= 2.47.5), IRanges (>= 2.13.11), S4Vectors (>= 0.17.24), mzID, mzR (>= 1.99.1), MSnbase (>= 1.15.5), Pviz, biomaRt, GenomicRanges (>= 1.31.7), rtracklayer (>= 1.39.6), ensembldb (>= 1.99.13), BiocParallel, AnnotationFilter Suggests: testthat (>= 0.8), ggplot2, BSgenome.Hsapiens.NCBI.GRCh38, TxDb.Hsapiens.UCSC.hg38.knownGene, AnnotationHub, knitr, rmarkdown, BiocStyle, EnsDb.Hsapiens.v86 (>= 2.0.0) License: GPL-3 MD5sum: d4af30b3cf547b82b29d5b6853745661 NeedsCompilation: no Title: Manipulating and exploring protein and proteomics data Description: A set of classes and functions to investigate and understand protein sequence data in the context of a proteomics experiment. biocViews: ImmunoOncology, Infrastructure, Proteomics, MassSpectrometry, Visualization, DataImport, DataRepresentation Author: Laurent Gatto [aut], Sebastian Gibb [aut, cre] Maintainer: Sebastian Gibb , Laurent Gatto URL: https://github.com/ComputationalProteomicsUnit/Pbase VignetteBuilder: knitr BugReports: https://github.com/ComputationalProteomicsUnit/Pbase/issues git_url: https://git.bioconductor.org/packages/Pbase git_branch: RELEASE_3_8 git_last_commit: 6ef1b9f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Pbase_0.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Pbase_0.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Pbase_0.22.1.tgz vignettes: vignettes/Pbase/inst/doc/Pbase-data.html vignetteTitles: Pbase data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Pbase/inst/doc/Pbase-data.R Package: pcaExplorer Version: 2.8.1 Imports: DESeq2, SummarizedExperiment, GenomicRanges, IRanges, S4Vectors, genefilter, ggplot2 (>= 2.0.0), d3heatmap, scales, NMF, plyr, topGO, limma, GOstats, GO.db, AnnotationDbi, shiny (>= 0.12.0), shinydashboard, shinyBS, ggrepel, DT, shinyAce, threejs, biomaRt, pheatmap, knitr, rmarkdown, tidyr, grDevices, methods Suggests: testthat, BiocStyle, airway, org.Hs.eg.db License: MIT + file LICENSE MD5sum: e585314bacf69c921734b8f3e94f591c NeedsCompilation: no Title: Interactive Visualization of RNA-seq Data Using a Principal Components Approach Description: This package provides functionality for interactive visualization of RNA-seq datasets based on Principal Components Analysis. The methods provided allow for quick information extraction and effective data exploration. A Shiny application encapsulates the whole analysis. biocViews: ImmunoOncology, Visualization, RNASeq, DimensionReduction, PrincipalComponent, QualityControl, GUI, ReportWriting Author: Federico Marini [aut, cre] Maintainer: Federico Marini URL: https://github.com/federicomarini/pcaExplorer, https://federicomarini.github.io/pcaExplorer/ VignetteBuilder: knitr BugReports: https://github.com/federicomarini/pcaExplorer/issues git_url: https://git.bioconductor.org/packages/pcaExplorer git_branch: RELEASE_3_8 git_last_commit: 7d38a3c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/pcaExplorer_2.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/pcaExplorer_2.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pcaExplorer_2.8.1.tgz vignettes: vignettes/pcaExplorer/inst/doc/pcaExplorer.html vignetteTitles: pcaExplorer User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/pcaExplorer/inst/doc/pcaExplorer.R importsMe: ideal Package: pcaGoPromoter Version: 1.26.0 Depends: R (>= 2.14.0), ellipse, Biostrings Imports: AnnotationDbi Suggests: Rgraphviz, GO.db, hgu133plus2.db, mouse4302.db, rat2302.db, hugene10sttranscriptcluster.db, mogene10sttranscriptcluster.db, pcaGoPromoter.Hs.hg19, pcaGoPromoter.Mm.mm9, pcaGoPromoter.Rn.rn4, serumStimulation, parallel License: GPL (>= 2) MD5sum: 4e977c7652ab79cdbc1f34bb9f2e69e0 NeedsCompilation: no Title: pcaGoPromoter is used to analyze DNA micro array data Description: This package contains functions to ease the analyses of DNA micro arrays. It utilizes principal component analysis as the initial multivariate analysis, followed by functional interpretation of the principal component dimensions with overrepresentation analysis for GO terms and regulatory interpretations using overrepresentation analysis of predicted transcription factor binding sites with the primo algorithm. biocViews: GeneExpression, Microarray, GO , Visualization Author: Morten Hansen, Jorgen Olsen Maintainer: Morten Hansen git_url: https://git.bioconductor.org/packages/pcaGoPromoter git_branch: RELEASE_3_8 git_last_commit: 89221ea git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pcaGoPromoter_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pcaGoPromoter_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pcaGoPromoter_1.26.0.tgz vignettes: vignettes/pcaGoPromoter/inst/doc/pcaGoPromoter.pdf vignetteTitles: pcaGoPromoter hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pcaGoPromoter/inst/doc/pcaGoPromoter.R Package: pcaMethods Version: 1.74.0 Depends: Biobase, methods Imports: BiocGenerics, Rcpp (>= 0.11.3), MASS LinkingTo: Rcpp Suggests: matrixStats, lattice, ggplot2 License: GPL (>= 3) MD5sum: 6a9c216fb47845695f034c5a8d76a804 NeedsCompilation: yes Title: A collection of PCA methods Description: Provides Bayesian PCA, Probabilistic PCA, Nipals PCA, Inverse Non-Linear PCA and the conventional SVD PCA. A cluster based method for missing value estimation is included for comparison. BPCA, PPCA and NipalsPCA may be used to perform PCA on incomplete data as well as for accurate missing value estimation. A set of methods for printing and plotting the results is also provided. All PCA methods make use of the same data structure (pcaRes) to provide a common interface to the PCA results. Initiated at the Max-Planck Institute for Molecular Plant Physiology, Golm, Germany. biocViews: Bayesian Author: Wolfram Stacklies, Henning Redestig, Kevin Wright Maintainer: Henning Redestig URL: https://github.com/hredestig/pcamethods SystemRequirements: Rcpp BugReports: https://github.com/hredestig/pcamethods/issues git_url: https://git.bioconductor.org/packages/pcaMethods git_branch: RELEASE_3_8 git_last_commit: 1b8f0a5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pcaMethods_1.74.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pcaMethods_1.74.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pcaMethods_1.74.0.tgz vignettes: vignettes/pcaMethods/inst/doc/missingValues.pdf, vignettes/pcaMethods/inst/doc/outliers.pdf, vignettes/pcaMethods/inst/doc/pcaMethods.pdf vignetteTitles: Missing value imputation, Data with outliers, Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pcaMethods/inst/doc/missingValues.R, vignettes/pcaMethods/inst/doc/outliers.R, vignettes/pcaMethods/inst/doc/pcaMethods.R dependsOnMe: DeconRNASeq importsMe: CompGO, consensusDE, MSnbase, OUTRIDER, PanVizGenerator, scde, SomaticSignatures Package: PCAN Version: 1.10.0 Depends: R (>= 3.3), BiocParallel Imports: grDevices, stats Suggests: BiocStyle, knitr, rmarkdown, reactome.db, STRINGdb License: CC BY-NC-ND 4.0 Archs: i386, x64 MD5sum: 07f2255c8748a0a112ff3870d63e63ed NeedsCompilation: no Title: Phenotype Consensus ANalysis (PCAN) Description: Phenotypes comparison based on a pathway consensus approach. Assess the relationship between candidate genes and a set of phenotypes based on additional genes related to the candidate (e.g. Pathways or network neighbors). biocViews: Annotation, Sequencing, Genetics, FunctionalPrediction, VariantAnnotation, Pathways, Network Author: Matthew Page and Patrice Godard Maintainer: Matthew Page and Patrice Godard VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PCAN git_branch: RELEASE_3_8 git_last_commit: f18fc3e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PCAN_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PCAN_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PCAN_1.10.0.tgz vignettes: vignettes/PCAN/inst/doc/PCAN.html vignetteTitles: Assessing gene relevance for a set of phenotypes hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PCAN/inst/doc/PCAN.R Package: pcot2 Version: 1.50.0 Depends: R (>= 2.0.0), grDevices, Biobase, amap Suggests: multtest, hu6800.db, KEGG.db, mvtnorm License: GPL (>= 2) MD5sum: aa57791e2f80a012910aba04f449bf80 NeedsCompilation: no Title: Principal Coordinates and Hotelling's T-Square method Description: PCOT2 is a permutation-based method for investigating changes in the activity of multi-gene networks. It utilizes inter-gene correlation information to detect significant alterations in gene network activities. Currently it can be applied to two-sample comparisons. biocViews: Microarray, DifferentialExpression, KEGG, GeneExpression, Network Author: Sarah Song, Mik Black Maintainer: Sarah Song git_url: https://git.bioconductor.org/packages/pcot2 git_branch: RELEASE_3_8 git_last_commit: f5e8242 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pcot2_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pcot2_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pcot2_1.50.0.tgz vignettes: vignettes/pcot2/inst/doc/pcot2.pdf vignetteTitles: PCOT2 Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pcot2/inst/doc/pcot2.R Package: PCpheno Version: 1.44.0 Depends: R (>= 2.10), Category, ScISI (>= 1.3.0), SLGI, ppiStats, ppiData, annotate (>= 1.17.4) Imports: AnnotationDbi, Biobase, Category, GO.db, graph, graphics, GSEABase, KEGG.db, methods, ScISI, stats, stats4 Suggests: KEGG.db, GO.db, org.Sc.sgd.db License: Artistic-2.0 MD5sum: 145f9f7d83b7405cb42e5949fae540e2 NeedsCompilation: no Title: Phenotypes and cellular organizational units Description: Tools to integrate, annotate, and link phenotypes to cellular organizational units such as protein complexes and pathways. biocViews: GraphAndNetwork, Proteomics, Network Author: Nolwenn Le Meur and Robert Gentleman Maintainer: Nolwenn Le Meur git_url: https://git.bioconductor.org/packages/PCpheno git_branch: RELEASE_3_8 git_last_commit: ccb30ab git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PCpheno_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PCpheno_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PCpheno_1.44.0.tgz vignettes: vignettes/PCpheno/inst/doc/PCpheno.pdf vignetteTitles: PCpheno Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PCpheno/inst/doc/PCpheno.R Package: pcxn Version: 2.4.0 Depends: R (>= 3.4), pcxnData Imports: methods, grDevices, utils, pheatmap Suggests: igraph, annotate, org.Hs.eg.db License: MIT + file LICENSE MD5sum: 3945e77826c7917f07557d39f5d7af19 NeedsCompilation: no Title: Exploring, analyzing and visualizing functions utilizing the pcxnData package Description: Discover the correlated pathways/gene sets of a single pathway/gene set or discover correlation relationships among multiple pathways/gene sets. Draw a heatmap or create a network of your query and extract members of each pathway/gene set found in the available collections (MSigDB H hallmark, MSigDB C2 Canonical pathways, MSigDB C5 GO BP and Pathprint). biocViews: ExperimentData, ExpressionData, MicroarrayData, GEO, Homo_sapiens_Data, OneChannelData, PathwayInteractionDatabase Author: Sokratis Kariotis, Yered Pita-Juarez, Winston Hide, Wenbin Wei Maintainer: Sokratis Kariotis git_url: https://git.bioconductor.org/packages/pcxn git_branch: RELEASE_3_8 git_last_commit: 82d05f7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pcxn_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pcxn_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pcxn_2.4.0.tgz vignettes: vignettes/pcxn/inst/doc/using_pcxn.pdf vignetteTitles: pcxn hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/pcxn/inst/doc/using_pcxn.R Package: pdInfoBuilder Version: 1.46.0 Depends: R (>= 3.2.0), methods, Biobase (>= 2.27.3), RSQLite (>= 1.0.0), affxparser (>= 1.39.4), oligo (>= 1.31.5) Imports: Biostrings (>= 2.35.12), BiocGenerics (>= 0.13.11), DBI (>= 0.3.1), IRanges (>= 2.1.43), oligoClasses (>= 1.29.6), S4Vectors (>= 0.5.22) License: Artistic-2.0 MD5sum: 11f99f8aa61c41052f80979136449ca7 NeedsCompilation: yes Title: Platform Design Information Package Builder Description: Builds platform design information packages. These consist of a SQLite database containing feature-level data such as x, y position on chip and featureSet ID. The database also incorporates featureSet-level annotation data. The products of this packages are used by the oligo pkg. biocViews: Annotation, Infrastructure Author: Seth Falcon, Vince Carey, Matt Settles, Kristof de Beuf, Benilton Carvalho Maintainer: Benilton Carvalho git_url: https://git.bioconductor.org/packages/pdInfoBuilder git_branch: RELEASE_3_8 git_last_commit: 8073a8b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pdInfoBuilder_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pdInfoBuilder_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pdInfoBuilder_1.46.0.tgz vignettes: vignettes/pdInfoBuilder/inst/doc/BuildingPDInfoPkgs.pdf, vignettes/pdInfoBuilder/inst/doc/howto-AffymetrixMapping.pdf vignetteTitles: Building Annotation Packages with pdInfoBuilder for Use with the oligo Package, PDInfo Package Building Affymetrix Mapping Chips hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pdInfoBuilder/inst/doc/howto-AffymetrixMapping.R Package: PECA Version: 1.18.0 Depends: R (>= 3.3) Imports: ROTS, limma, affy, genefilter, preprocessCore, aroma.affymetrix, aroma.core Suggests: SpikeIn License: GPL (>= 2) Archs: i386, x64 MD5sum: 0403c0ac60f05fb12d20f3c186e0c140 NeedsCompilation: no Title: Probe-level Expression Change Averaging Description: Calculates Probe-level Expression Change Averages (PECA) to identify differential expression in Affymetrix gene expression microarray studies or in proteomic studies using peptide-level mesurements respectively. biocViews: Software, Proteomics, Microarray, DifferentialExpression, GeneExpression, ExonArray, DifferentialSplicing Author: Tomi Suomi, Jukka Hiissa, Laura L. Elo Maintainer: Tomi Suomi git_url: https://git.bioconductor.org/packages/PECA git_branch: RELEASE_3_8 git_last_commit: aaf72de git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PECA_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PECA_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PECA_1.18.0.tgz vignettes: vignettes/PECA/inst/doc/PECA.pdf vignetteTitles: PECA: Probe-level Expression Change Averaging hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PECA/inst/doc/PECA.R suggestsMe: SWATH2stats Package: PepsNMR Version: 1.0.2 Depends: R (>= 3.5) Imports: Matrix, ptw, ggplot2, gridExtra, matrixStats, reshape2, methods, graphics, stats Suggests: knitr, markdown, rmarkdown, BiocStyle, PepsNMRData License: GPL-2 | file LICENSE MD5sum: 864f6205711a82f4db94a2f1930237a6 NeedsCompilation: no Title: Pre-process 1H-NMR FID signals Description: This package provides R functions for common pre-procssing steps that are applied on 1H-NMR data. It also provides a function to read the FID signals directly in the Bruker format. biocViews: Software, Preprocessing, Visualization, Metabolomics, DataImport Author: Manon Martin [aut, cre], Bernadette Govaerts [aut, ths], Benoît Legat [aut], Pascal de Tullio [dtc], Bruno Boulanger [ctb], Paul H.C. Eilers [ctb], Julien Vanwinsberghe [ctb] Maintainer: Manon Martin URL: https://github.com/ManonMartin/PepsNMR VignetteBuilder: knitr BugReports: https://github.com/ManonMartin/PepsNMR/issues git_url: https://git.bioconductor.org/packages/PepsNMR git_branch: RELEASE_3_8 git_last_commit: aebf0b2 git_last_commit_date: 2019-03-08 Date/Publication: 2019-03-08 source.ver: src/contrib/PepsNMR_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/PepsNMR_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PepsNMR_1.0.2.tgz vignettes: vignettes/PepsNMR/inst/doc/PepsNMR_minimal_example.html vignetteTitles: Application of PepsNMR on the Human Serum dataset hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/PepsNMR/inst/doc/PepsNMR_minimal_example.R Package: pepStat Version: 1.16.0 Depends: R (>= 3.0.0), Biobase, IRanges Imports: limma, fields, GenomicRanges, ggplot2, plyr, tools, methods, data.table Suggests: pepDat, Pviz, knitr, shiny License: Artistic-2.0 MD5sum: c232a1a342e9683a99da75bc419d5f71 NeedsCompilation: no Title: Statistical analysis of peptide microarrays Description: Statistical analysis of peptide microarrays biocViews: Microarray, Preprocessing Author: Raphael Gottardo, Gregory C Imholte, Renan Sauteraud, Mike Jiang Maintainer: Gregory C Imholte URL: https://github.com/RGLab/pepStat VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/pepStat git_branch: RELEASE_3_8 git_last_commit: 3e2b046 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pepStat_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pepStat_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pepStat_1.16.0.tgz vignettes: vignettes/pepStat/inst/doc/pepStat.pdf vignetteTitles: Full peptide microarray analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pepStat/inst/doc/pepStat.R Package: pepXMLTab Version: 1.16.1 Depends: R (>= 3.0.1) Imports: XML(>= 3.98-1.1) Suggests: RUnit, BiocGenerics License: Artistic-2.0 MD5sum: c8a8a4e4efb1434b03f3f10eb0f47821 NeedsCompilation: no Title: Parsing pepXML files and filter based on peptide FDR. Description: Parsing pepXML files based one XML package. The package tries to handle pepXML files generated from different softwares. The output will be a peptide-spectrum-matching tabular file. The package also provide function to filter the PSMs based on FDR. biocViews: ImmunoOncology, Proteomics, MassSpectrometry Author: Xiaojing Wang Maintainer: Xiaojing Wang git_url: https://git.bioconductor.org/packages/pepXMLTab git_branch: RELEASE_3_8 git_last_commit: f58263f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/pepXMLTab_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/pepXMLTab_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pepXMLTab_1.16.1.tgz vignettes: vignettes/pepXMLTab/inst/doc/pepXMLTab.pdf vignetteTitles: Introduction to pepXMLTab hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pepXMLTab/inst/doc/pepXMLTab.R Package: perturbatr Version: 1.2.1 Depends: R (>= 3.5), methods, stats Imports: dplyr, ggplot2, tidyr, assertthat, lme4, splines, igraph, foreach, parallel, doParallel, diffusr, lazyeval, tibble, grid, utils, graphics, scales, magrittr, formula.tools, rlang Suggests: testthat, lintr, knitr, rmarkdown, BiocStyle License: GPL-3 MD5sum: fa76f0549fd75d023d2c5c231453cdee NeedsCompilation: no Title: Statistical Analysis of High-Throughput Genetic Perturbation Screens Description: perturbatr does stage-wise analysis of large-scale genetic perturbation screens for integrated data sets consisting of multiple screens. For multiple integrated perturbation screens a hierarchical model that considers the variance between different biological conditions is fitted. The resulting list of gene effects is then further extended using a network propagation algorithm to correct for false negatives. biocViews: ImmunoOncology, Regression, CellBasedAssays, Network Author: Simon Dirmeier [aut, cre] Maintainer: Simon Dirmeier URL: https://github.com/cbg-ethz/perturbatr VignetteBuilder: knitr BugReports: https://github.com/cbg-ethz/perturbatr/issues git_url: https://git.bioconductor.org/packages/perturbatr git_branch: RELEASE_3_8 git_last_commit: dca80de git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/perturbatr_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/perturbatr_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/perturbatr_1.2.1.tgz vignettes: vignettes/perturbatr/inst/doc/perturbatr.html vignetteTitles: perturbatr cookbook hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/perturbatr/inst/doc/perturbatr.R Package: PGA Version: 1.12.1 Depends: R (>= 3.5.0), IRanges, GenomicRanges, Biostrings (>= 2.26.3), data.table, rTANDEM Imports: S4Vectors (>= 0.9.25), Rsamtools (>= 1.10.2), GenomicFeatures (>= 1.19.8), biomaRt (>= 2.17.1), stringr, RCurl, Nozzle.R1, VariantAnnotation (>= 1.7.28), rtracklayer, RSQLite, ggplot2, AnnotationDbi, customProDB (>= 1.21.5), pheatmap Suggests: RMariaDB, BSgenome.Hsapiens.UCSC.hg19, RUnit, BiocGenerics, BiocStyle, knitr, R.utils License: GPL-2 MD5sum: 9d81a4174770180665ff1d6e06fc45ae NeedsCompilation: no Title: An package for identification of novel peptides by customized database derived from RNA-Seq Description: This package provides functions for construction of customized protein databases based on RNA-Seq data with/without genome guided, database searching, post-processing and report generation. This kind of customized protein database includes both the reference database (such as Refseq or ENSEMBL) and the novel peptide sequences form RNA-Seq data. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, Software, ReportWriting, RNASeq, Sequencing Author: Shaohang Xu, Bo Wen Maintainer: Bo Wen , Shaohang Xu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PGA git_branch: RELEASE_3_8 git_last_commit: 6d3c4b8 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PGA_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PGA_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PGA_1.12.1.tgz vignettes: vignettes/PGA/inst/doc/PGA.pdf vignetteTitles: PGA tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PGA/inst/doc/PGA.R Package: pgca Version: 1.6.1 Imports: utils, stats Suggests: knitr, testthat License: GPL (>= 2) MD5sum: 6d8bbcb59439c8d9294610f678d070bf NeedsCompilation: no Title: PGCA: An Algorithm to Link Protein Groups Created from MS/MS Data Description: Protein Group Code Algorithm (PGCA) is a computationally inexpensive algorithm to merge protein summaries from multiple experimental quantitative proteomics data. The algorithm connects two or more groups with overlapping accession numbers. In some cases, pairwise groups are mutually exclusive but they may still be connected by another group (or set of groups) with overlapping accession numbers. Thus, groups created by PGCA from multiple experimental runs (i.e., global groups) are called "connected" groups. These identified global protein groups enable the analysis of quantitative data available for protein groups instead of unique protein identifiers. biocViews: ImmunoOncology, WorkflowStep,AssayDomain,Proteomics,MassSpectrometry Author: Gabriela Cohen-Freue Maintainer: Gabriela Cohen-Freue VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/pgca git_branch: RELEASE_3_8 git_last_commit: 96b7ad9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/pgca_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/pgca_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pgca_1.6.1.tgz vignettes: vignettes/pgca/inst/doc/intro.html vignetteTitles: Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pgca/inst/doc/intro.R Package: PGSEA Version: 1.56.0 Depends: R (>= 2.10), GO.db, KEGG.db, AnnotationDbi, annaffy, methods, Biobase (>= 2.5.5) Suggests: GSEABase, GEOquery, org.Hs.eg.db, hgu95av2.db, limma License: GPL-2 MD5sum: 59661093e4e69ad9cb79b2f1243da19e NeedsCompilation: no Title: Parametric Gene Set Enrichment Analysis Description: Parametric Analysis of Gene Set Enrichment biocViews: Microarray Author: Kyle Furge and Karl Dykema Maintainer: Karl Dykema git_url: https://git.bioconductor.org/packages/PGSEA git_branch: RELEASE_3_8 git_last_commit: 1ee369f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PGSEA_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PGSEA_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PGSEA_1.56.0.tgz vignettes: vignettes/PGSEA/inst/doc/PGSEA.pdf, vignettes/PGSEA/inst/doc/PGSEA2.pdf vignetteTitles: HOWTO: PGSEA, HOWTO: PGSEA Example Workflow hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PGSEA/inst/doc/PGSEA.R, vignettes/PGSEA/inst/doc/PGSEA2.R dependsOnMe: GeneExpressionSignature Package: phantasus Version: 1.2.1 Depends: R (>= 3.5) Imports: ggplot2, protolite, Biobase, GEOquery, Rook, htmltools, httpuv, jsonlite, limma, opencpu, assertthat, methods, httr, rhdf5, utils, parallel, stringr, fgsea, svglite, gtable, stats, Matrix, Matrix.utils, pheatmap, scales, ccaPP, grid, grDevices Suggests: testthat, BiocStyle, knitr, rmarkdown, data.table License: MIT + file LICENSE MD5sum: 990d22722534910c8d036c0d78ba4692 NeedsCompilation: no Title: Visual and interactive gene expression analysis Description: Phantasus is a web-application for visual and interactive gene expression analysis. Phantasus is based on Morpheus – a web-based software for heatmap visualisation and analysis, which was integrated with an R environment via OpenCPU API. Aside from basic visualization and filtering methods, R-based methods such as k-means clustering, principal component analysis or differential expression analysis with limma package are supported. biocViews: GeneExpression, GUI, Visualization, DataRepresentation, Transcriptomics, RNASeq, Microarray, Normalization, Clustering, DifferentialExpression, PrincipalComponent, ImmunoOncology Author: Daria Zenkova [aut], Vladislav Kamenev [aut], Rita Sablina [ctb], Maxim Artyomov [aut], Alexey Sergushichev [aut, cre] Maintainer: Alexey Sergushichev URL: https://genome.ifmo.ru/phantasus, https://artyomovlab.wustl.edu/phantasus VignetteBuilder: knitr BugReports: https://github.com/ctlab/phantasus/issues git_url: https://git.bioconductor.org/packages/phantasus git_branch: RELEASE_3_8 git_last_commit: 05217c4 git_last_commit_date: 2018-12-11 Date/Publication: 2018-12-21 source.ver: src/contrib/phantasus_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/phantasus_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/phantasus_1.2.1.tgz vignettes: vignettes/phantasus/inst/doc/developer-tutorial.html, vignettes/phantasus/inst/doc/phantasus-tutorial.html vignetteTitles: Developing new tools, Using phantasus application hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/phantasus/inst/doc/developer-tutorial.R, vignettes/phantasus/inst/doc/phantasus-tutorial.R Package: PharmacoGx Version: 1.12.0 Depends: R (>= 3.4) Imports: Biobase, piano, magicaxis, RColorBrewer, parallel, caTools, methods, downloader, stats, utils, graphics, grDevices, lsa, reshape2 Suggests: xtable, testthat License: Artistic-2.0 MD5sum: bd3a5c92c8622f561b3c1cd6fe35e21b NeedsCompilation: no Title: Analysis of Large-Scale Pharmacogenomic Data Description: Contains a set of functions to perform large-scale analysis of pharmacogenomic data. biocViews: GeneExpression, Pharmacogenetics, Pharmacogenomics, Software, Classification Author: Petr Smirnov, Zhaleh Safikhani, Mark Freeman, Benjamin Haibe-Kains Maintainer: Benjamin Haibe-Kains BugReports: https://github.com/bhklab/PharmacoGx/issues git_url: https://git.bioconductor.org/packages/PharmacoGx git_branch: RELEASE_3_8 git_last_commit: 4bee043 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PharmacoGx_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PharmacoGx_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PharmacoGx_1.12.0.tgz vignettes: vignettes/PharmacoGx/inst/doc/CreatingPharmacoSet.pdf, vignettes/PharmacoGx/inst/doc/PharmacoGx.pdf vignetteTitles: Creating a PharmacoSet object, PharmacoGx: an R package for analysis of large pharmacogenomic datasets hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PharmacoGx/inst/doc/CreatingPharmacoSet.R, vignettes/PharmacoGx/inst/doc/PharmacoGx.R Package: phenopath Version: 1.6.7 Imports: Rcpp (>= 0.12.8), SummarizedExperiment, methods, stats, dplyr, tibble, ggplot2, tidyr LinkingTo: Rcpp Suggests: knitr, rmarkdown, forcats, testthat, BiocStyle, SingleCellExperiment License: Apache License (== 2.0) MD5sum: fa1c6dd217749433a1486affbf371ed2 NeedsCompilation: yes Title: Genomic trajectories with heterogeneous genetic and environmental backgrounds Description: PhenoPath infers genomic trajectories (pseudotimes) in the presence of heterogeneous genetic and environmental backgrounds and tests for interactions between them. biocViews: ImmunoOncology, RNASeq, GeneExpression, Bayesian, SingleCell, PrincipalComponent Author: Kieran Campbell Maintainer: Kieran Campbell VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/phenopath git_branch: RELEASE_3_8 git_last_commit: 181cbf9 git_last_commit_date: 2019-03-21 Date/Publication: 2019-03-21 source.ver: src/contrib/phenopath_1.6.7.tar.gz win.binary.ver: bin/windows/contrib/3.5/phenopath_1.6.7.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/phenopath_1.6.7.tgz vignettes: vignettes/phenopath/inst/doc/introduction_to_phenopath.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/phenopath/inst/doc/introduction_to_phenopath.R suggestsMe: splatter Package: phenoTest Version: 1.30.0 Depends: R (>= 2.12.0), Biobase, methods, annotate, Heatplus, BMA, ggplot2 Imports: survival, limma, Hmisc, gplots, Category, AnnotationDbi, hopach, biomaRt, GSEABase, genefilter, xtable, annotate, mgcv, SNPchip, hgu133a.db, HTSanalyzeR, ellipse Suggests: GSEABase, KEGG.db, GO.db Enhances: parallel, org.Ce.eg.db, org.Mm.eg.db, org.Rn.eg.db, org.Hs.eg.db, org.Dm.eg.db License: GPL (>=2) Archs: i386, x64 MD5sum: 448ca78e9eca883a0f9801e31a0e4336 NeedsCompilation: no Title: Tools to test association between gene expression and phenotype in a way that is efficient, structured, fast and scalable. We also provide tools to do GSEA (Gene set enrichment analysis) and copy number variation. Description: Tools to test correlation between gene expression and phenotype in a way that is efficient, structured, fast and scalable. GSEA is also provided. biocViews: Microarray, DifferentialExpression, MultipleComparison, Clustering, Classification Author: Evarist Planet Maintainer: Evarist Planet git_url: https://git.bioconductor.org/packages/phenoTest git_branch: RELEASE_3_8 git_last_commit: 25038fb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/phenoTest_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/phenoTest_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/phenoTest_1.30.0.tgz vignettes: vignettes/phenoTest/inst/doc/phenoTest.pdf vignetteTitles: Manual for the phenoTest library hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/phenoTest/inst/doc/phenoTest.R importsMe: canceR Package: PhenStat Version: 2.18.1 Depends: R (>= 3.5.0) Imports: SmoothWin, methods, car, nlme, nortest, MASS, msgps, logistf, knitr, tools, pingr, ggplot2, reshape, corrplot, graph, lme4, graphics, grDevices, utils, stats Suggests: RUnit, BiocGenerics License: file LICENSE MD5sum: dfee7c6bd38e48858051a2715bc2750f NeedsCompilation: no Title: Statistical analysis of phenotypic data Description: Package contains methods for statistical analysis of phenotypic data. biocViews: StatisticalMethod Author: Natalja Kurbatova, Natasha Karp, Jeremy Mason, Hamed Haselimashhadi Maintainer: Hamed Haselimashhadi git_url: https://git.bioconductor.org/packages/PhenStat git_branch: RELEASE_3_8 git_last_commit: 30a1e0e git_last_commit_date: 2019-04-15 Date/Publication: 2019-04-15 source.ver: src/contrib/PhenStat_2.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PhenStat_2.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PhenStat_2.18.1.tgz vignettes: vignettes/PhenStat/inst/doc/PhenStat.pdf, vignettes/PhenStat/inst/doc/PhenStatUsersGuide.pdf vignetteTitles: PhenStat Vignette, PhenStatUsersGuide.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/PhenStat/inst/doc/PhenStat.R Package: philr Version: 1.8.1 Imports: ape, phangorn, tidyr, ggplot2, ggtree Suggests: testthat, knitr, rmarkdown, BiocStyle, phyloseq, glmnet, dplyr License: GPL-3 MD5sum: bd10f494d79b06f27cdca4388feafbb5 NeedsCompilation: no Title: Phylogenetic partitioning based ILR transform for metagenomics data Description: PhILR is short for Phylogenetic Isometric Log-Ratio Transform. This package provides functions for the analysis of compositional data (e.g., data representing proportions of different variables/parts). Specifically this package allows analysis of compositional data where the parts can be related through a phylogenetic tree (as is common in microbiota survey data) and makes available the Isometric Log Ratio transform built from the phylogenetic tree and utilizing a weighted reference measure. biocViews: ImmunoOncology, Sequencing, Microbiome, Metagenomics, Software Author: Justin Silverman Maintainer: Justin Silverman URL: https://github.com/jsilve24/philr VignetteBuilder: knitr BugReports: https://github.com/jsilve24/philr/issues git_url: https://git.bioconductor.org/packages/philr git_branch: RELEASE_3_8 git_last_commit: 0102369 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/philr_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/philr_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/philr_1.8.1.tgz vignettes: vignettes/philr/inst/doc/philr-intro.html vignetteTitles: Introduction to PhILR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/philr/inst/doc/philr-intro.R Package: phosphonormalizer Version: 1.6.0 Depends: R (>= 3.4.0) Imports: plyr, stats, graphics, matrixStats Suggests: knitr, rmarkdown, testthat Enhances: MSnbase License: GPL (>= 2) MD5sum: c2476b36059d282f900701bc4982e9fb NeedsCompilation: no Title: Compensates for the bias introduced by median normalization in phosphoproteomics Description: It uses the overlap between enriched and non-enriched datasets to compensate for the bias introduced in global phosphorylation after applying median normalization. biocViews: Software, StatisticalMethod, WorkflowStep, Normalization, Proteomics Author: Sohrab Saraei, Tomi Suomi, Otto Kauko, Laura L. Elo Maintainer: Sohrab Saraei VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/phosphonormalizer git_branch: RELEASE_3_8 git_last_commit: 978bac7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/phosphonormalizer_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/phosphonormalizer_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/phosphonormalizer_1.6.0.tgz vignettes: vignettes/phosphonormalizer/inst/doc/phosphonormalizer.pdf, vignettes/phosphonormalizer/inst/doc/vignette.html vignetteTitles: phosphonormalizer: Phosphoproteomics Normalization, Pairwise normalization of phosphoproteomics data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/phosphonormalizer/inst/doc/phosphonormalizer.R, vignettes/phosphonormalizer/inst/doc/vignette.R Package: phyloseq Version: 1.26.1 Depends: R (>= 3.3.0) Imports: ade4 (>= 1.7.4), ape (>= 5.0), Biobase (>= 2.36.2), BiocGenerics (>= 0.22.0), biomformat (>= 1.0.0), Biostrings (>= 2.40.0), cluster (>= 2.0.4), data.table (>= 1.10.4), foreach (>= 1.4.3), ggplot2 (>= 2.1.0), igraph (>= 1.0.1), methods (>= 3.3.0), multtest (>= 2.28.0), plyr (>= 1.8.3), reshape2 (>= 1.4.1), scales (>= 0.4.0), vegan (>= 2.5) Suggests: BiocStyle (>= 2.4), DESeq2 (>= 1.16.1), genefilter (>= 1.58), knitr (>= 1.16), metagenomeSeq (>= 1.14), rmarkdown (>= 1.6), testthat (>= 1.0.2) Enhances: doParallel (>= 1.0.10) License: AGPL-3 MD5sum: 36ab5ccb3104cab595f84de6dd92944f NeedsCompilation: no Title: Handling and analysis of high-throughput microbiome census data Description: phyloseq provides a set of classes and tools to facilitate the import, storage, analysis, and graphical display of microbiome census data. biocViews: ImmunoOncology, Sequencing, Microbiome, Metagenomics, Clustering, Classification, MultipleComparison, GeneticVariability Author: Paul J. McMurdie , Susan Holmes , with contributions from Gregory Jordan and Scott Chamberlain Maintainer: Paul J. McMurdie URL: http://dx.plos.org/10.1371/journal.pone.0061217 VignetteBuilder: knitr BugReports: https://github.com/joey711/phyloseq/issues git_url: https://git.bioconductor.org/packages/phyloseq git_branch: RELEASE_3_8 git_last_commit: a084072 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/phyloseq_1.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/phyloseq_1.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/phyloseq_1.26.1.tgz vignettes: vignettes/phyloseq/inst/doc/phyloseq-analysis.html, vignettes/phyloseq/inst/doc/phyloseq-basics.html, vignettes/phyloseq/inst/doc/phyloseq-FAQ.html, vignettes/phyloseq/inst/doc/phyloseq-mixture-models.html vignetteTitles: analysis vignette, phyloseq basics vignette, phyloseq Frequently Asked Questions (FAQ), phyloseq and DESeq2 on Colorectal Cancer Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/phyloseq/inst/doc/phyloseq-analysis.R, vignettes/phyloseq/inst/doc/phyloseq-basics.R, vignettes/phyloseq/inst/doc/phyloseq-FAQ.R, vignettes/phyloseq/inst/doc/phyloseq-mixture-models.R dependsOnMe: microbiome, SIAMCAT importsMe: metavizr, PathoStat, RPA suggestsMe: decontam, metagenomeFeatures, philr Package: Pi Version: 1.10.0 Depends: XGR, igraph, dnet, ggplot2, graphics Imports: Matrix, MASS, ggbio, GenomicRanges, GenomeInfoDb, supraHex, scales, grDevices, ggrepel, ROCR, randomForest, glmnet, Gviz, lattice, caret, plot3D, stats Suggests: foreach, doParallel, BiocStyle, knitr, rmarkdown, png, GGally, gridExtra, ExpressionAtlas, ggforce, fgsea, pathview, tidyr License: GPL-3 MD5sum: 2fc7306e9555e44f153cf1b2b48802e2 NeedsCompilation: no Title: Leveraging Genetic Evidence to Prioritise Drug Targets at the Gene and Pathway Level Description: Priority index or Pi is developed as a genomic-led target prioritisation system, with the focus on leveraging human genetic data to prioritise potential drug targets at the gene, pathway and network level. The long term goal is to use such information to enhance early-stage target validation. Based on evidence of disease association from genome-wide association studies (GWAS), this prioritisation system is able to generate evidence to support identification of the specific modulated genes (seed genes) that are responsible for the genetic association signal by utilising knowledge of linkage disequilibrium (co-inherited genetic variants), distance of associated variants from the gene, evidence of independent genetic association with gene expression in disease-relevant tissues, cell types and states, and evidence of physical interactions between disease-associated genetic variants and gene promoters based on genome-wide capture HiC-generated promoter interactomes in primary blood cell types. Seed genes are scored in an integrative way, quantifying the genetic influence. Scored seed genes are subsequently used as baits to rank seed genes plus additional (non-seed) genes; this is achieved by iteratively exploring the global connectivity of a gene interaction network. Genes with the highest priority are further used to identify/prioritise pathways that are significantly enriched with highly prioritised genes. Prioritised genes are also used to identify a gene network interconnecting highly prioritised genes and a minimal number of less prioritised genes (which act as linkers bringing together highly prioritised genes). biocViews: Software, Genetics, GraphAndNetwork, Pathways, GeneExpression, GeneTarget, GenomeWideAssociation, LinkageDisequilibrium, Network, HiC Author: Hai Fang, the ULTRA-DD Consortium, Julian C Knight Maintainer: Hai Fang URL: http://pi314.r-forge.r-project.org VignetteBuilder: knitr BugReports: https://github.com/hfang-bristol/Pi/issues git_url: https://git.bioconductor.org/packages/Pi git_branch: RELEASE_3_8 git_last_commit: 4801867 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Pi_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Pi_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Pi_1.10.0.tgz vignettes: vignettes/Pi/inst/doc/Pi_vignettes.html vignetteTitles: Pi User Manual (R/Bioconductor package) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Pi/inst/doc/Pi_vignettes.R Package: piano Version: 1.22.0 Depends: R (>= 2.14.0) Imports: BiocGenerics, Biobase, gplots, igraph, relations, marray, fgsea Suggests: yeast2.db, rsbml, plotrix, limma, affy, plier, affyPLM, gtools, biomaRt, snowfall, AnnotationDbi License: GPL (>=2) MD5sum: ddf4cefb13b149cbac5ee9ecec0ffbc8 NeedsCompilation: no Title: Platform for integrative analysis of omics data Description: Piano performs gene set analysis using various statistical methods, from different gene level statistics and a wide range of gene-set collections. Furthermore, the Piano package contains functions for combining the results of multiple runs of gene set analyses. biocViews: Microarray, Preprocessing, QualityControl, DifferentialExpression, Visualization, GeneExpression, GeneSetEnrichment, Pathways Author: Leif Varemo and Intawat Nookaew Maintainer: Leif Varemo URL: http://www.sysbio.se/piano BugReports: https://github.com/varemo/piano/issues git_url: https://git.bioconductor.org/packages/piano git_branch: RELEASE_3_8 git_last_commit: 5041f48 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/piano_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/piano_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/piano_1.22.0.tgz vignettes: vignettes/piano/inst/doc/piano-vignette.pdf vignetteTitles: Piano - Platform for Integrative Analysis of Omics data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/piano/inst/doc/piano-vignette.R importsMe: cTRAP, PharmacoGx Package: pickgene Version: 1.54.0 Imports: graphics, grDevices, MASS, stats, utils License: GPL (>= 2) MD5sum: 8c766281cb3b997e869fb2afe3ab0a03 NeedsCompilation: no Title: Adaptive Gene Picking for Microarray Expression Data Analysis Description: Functions to Analyze Microarray (Gene Expression) Data. biocViews: Microarray, DifferentialExpression Author: Brian S. Yandell Maintainer: Brian S. Yandell URL: http://www.stat.wisc.edu/~yandell/statgen git_url: https://git.bioconductor.org/packages/pickgene git_branch: RELEASE_3_8 git_last_commit: d4ef3ca git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pickgene_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pickgene_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pickgene_1.54.0.tgz vignettes: vignettes/pickgene/inst/doc/pickgene.pdf vignetteTitles: Adaptive Gene Picking for Microarray Expression Data Analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: PICS Version: 2.26.0 Depends: R (>= 2.14.0), BiocGenerics (>= 0.1.3) Imports: methods, stats4, IRanges, GenomicRanges, graphics, grDevices, stats, Rsamtools, GenomicAlignments, S4Vectors Suggests: ShortRead, rtracklayer, parallel License: Artistic-2.0 MD5sum: 37aad6428e79e861d9e42d519aa133e5 NeedsCompilation: yes Title: Probabilistic inference of ChIP-seq Description: Probabilistic inference of ChIP-Seq using an empirical Bayes mixture model approach. biocViews: Clustering, Visualization, Sequencing, ChIPSeq Author: Xuekui Zhang , Raphael Gottardo Maintainer: Renan Sauteraud SystemRequirements: GSL (GNU Scientific Library) git_url: https://git.bioconductor.org/packages/PICS git_branch: RELEASE_3_8 git_last_commit: e7aafbe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PICS_2.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PICS_2.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PICS_2.26.0.tgz vignettes: vignettes/PICS/inst/doc/PICS.pdf vignetteTitles: The PICS users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PICS/inst/doc/PICS.R importsMe: PING Package: Pigengene Version: 1.8.1 Depends: R (>= 3.3.0), graph Imports: bnlearn, C50 (>= 0.1.2), MASS, matrixStats, partykit, Rgraphviz, WGCNA, GO.db, impute, preprocessCore, grDevices, graphics, stats, utils, parallel, pheatmap (>= 1.0.8) Suggests: org.Hs.eg.db, org.Mm.eg.db, biomaRt (>= 2.30.0), knitr, BiocStyle, AnnotationDbi, energy License: GPL (>=2) Archs: i386, x64 MD5sum: b3bf9c05943dbbeb9b265ae274105c07 NeedsCompilation: no Title: Infers biological signatures from gene expression data Description: Pigengene package provides an efficient way to infer biological signatures from gene expression profiles. The signatures are independent from the underlying platform, e.g., the input can be microarray or RNA Seq data. It can even infer the signatures using data from one platform, and evaluate them on the other. Pigengene identifies the modules (clusters) of highly coexpressed genes using coexpression network analysis, summarizes the biological information of each module in an eigengene, learns a Bayesian network that models the probabilistic dependencies between modules, and builds a decision tree based on the expression of eigengenes. biocViews: ImmunoOncology, GeneExpression, RNASeq, NetworkInference, Network, GraphAndNetwork, BiomedicalInformatics, SystemsBiology, Transcriptomics, Classification, Clustering, DecisionTree, DimensionReduction, PrincipalComponent, Microarray, Normalization Author: Habil Zare, Amir Foroushani, and Rupesh Agrahari Maintainer: Habil Zare VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Pigengene git_branch: RELEASE_3_8 git_last_commit: 59ee84d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Pigengene_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Pigengene_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Pigengene_1.8.1.tgz vignettes: vignettes/Pigengene/inst/doc/Pigengene_inference.pdf vignetteTitles: Pigengene: Computing and using eigengenes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Pigengene/inst/doc/Pigengene_inference.R Package: PING Version: 2.26.0 Depends: R(>= 2.15.0), chipseq, IRanges, GenomicRanges Imports: methods, PICS, graphics, grDevices, stats, Gviz, fda, BSgenome, stats4, BiocGenerics, IRanges, S4Vectors Suggests: parallel, ShortRead, rtracklayer License: Artistic-2.0 MD5sum: d7d3a4467e3c8ea97ff0099a4e31285c NeedsCompilation: yes Title: Probabilistic inference for Nucleosome Positioning with MNase-based or Sonicated Short-read Data Description: Probabilistic inference of ChIP-Seq using an empirical Bayes mixture model approach. biocViews: Clustering, StatisticalMethod, Visualization, Sequencing Author: Xuekui Zhang , Raphael Gottardo , Sangsoon Woo Maintainer: Renan Sauteraud git_url: https://git.bioconductor.org/packages/PING git_branch: RELEASE_3_8 git_last_commit: 5b0be17 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PING_2.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PING_2.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PING_2.26.0.tgz vignettes: vignettes/PING/inst/doc/PING-PE.pdf, vignettes/PING/inst/doc/PING.pdf vignetteTitles: Using PING with paired-end sequencing data, The PING users guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PING/inst/doc/PING-PE.R, vignettes/PING/inst/doc/PING.R Package: pint Version: 1.32.0 Depends: mvtnorm, methods, graphics, Matrix, dmt License: BSD_2_clause + file LICENSE Archs: i386, x64 MD5sum: 52094d95be76e9b7eb15f0c1f826f4fe NeedsCompilation: no Title: Pairwise INTegration of functional genomics data Description: Pairwise data integration for functional genomics, including tools for DNA/RNA/miRNA dependency screens. biocViews: aCGH, GeneExpression, Genetics, DifferentialExpression, Microarray Author: Olli-Pekka Huovilainen and Leo Lahti Maintainer: Olli-Pekka Huovilainen URL: https://github.com/antagomir/pint BugReports: https://github.com/antagomir/pint/issues git_url: https://git.bioconductor.org/packages/pint git_branch: RELEASE_3_8 git_last_commit: 84f300f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pint_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pint_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pint_1.32.0.tgz vignettes: vignettes/pint/inst/doc/depsearch.pdf vignetteTitles: pint hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/pint/inst/doc/depsearch.R Package: pkgDepTools Version: 1.48.0 Depends: methods, graph, RBGL Imports: graph, RBGL Suggests: Biobase, Rgraphviz, RCurl, BiocManager License: GPL-2 MD5sum: 9b7ac81bcf76d15218c6044b6620a931 NeedsCompilation: no Title: Package Dependency Tools Description: This package provides tools for computing and analyzing dependency relationships among R packages. It provides tools for building a graph-based representation of the dependencies among all packages in a list of CRAN-style package repositories. There are also utilities for computing installation order of a given package. If the RCurl package is available, an estimate of the download size required to install a given package and its dependencies can be obtained. biocViews: Infrastructure, GraphAndNetwork Author: Seth Falcon [aut], Bioconductor Package Maintainer [cre] Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/pkgDepTools git_branch: RELEASE_3_8 git_last_commit: 4b6228b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pkgDepTools_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pkgDepTools_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pkgDepTools_1.48.0.tgz vignettes: vignettes/pkgDepTools/inst/doc/pkgDepTools.pdf vignetteTitles: How to Use pkgDepTools hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pkgDepTools/inst/doc/pkgDepTools.R Package: plateCore Version: 1.40.1 Depends: R (>= 2.10), flowCore, flowViz, lattice, latticeExtra Imports: Biobase, flowCore, graphics, grDevices, lattice, MASS, methods, robustbase, stats, utils, flowStats Suggests: gplots License: Artistic-2.0 MD5sum: 59e976ddf32e8638605cf80e898752d7 NeedsCompilation: no Title: Statistical tools and data structures for plate-based flow cytometry Description: Provides basic S4 data structures and routines for analyzing plate based flow cytometry data. biocViews: ImmunoOncology, FlowCytometry, Infrastructure, CellBasedAssays Author: Errol Strain, Florian Hahne, and Perry Haaland Maintainer: Errol Strain URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/plateCore git_branch: RELEASE_3_8 git_last_commit: 625f4a9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/plateCore_1.40.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/plateCore_1.40.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plateCore_1.40.1.tgz vignettes: vignettes/plateCore/inst/doc/plateCoreVig.pdf vignetteTitles: An R Package for Analysis of High Throughput Flow Cytometry Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plateCore/inst/doc/plateCoreVig.R Package: plethy Version: 1.20.0 Depends: R (>= 3.1.0), methods, DBI (>= 0.5-1), RSQLite (>= 1.1), BiocGenerics, S4Vectors Imports: Streamer, IRanges, reshape2, plyr, RColorBrewer,ggplot2, Biobase Suggests: RUnit, BiocStyle License: GPL-3 MD5sum: cfaa49593a30cf99fe842236a8b34583 NeedsCompilation: no Title: R framework for exploration and analysis of respirometry data Description: This package provides the infrastructure and tools to import, query and perform basic analysis of whole body plethysmography and metabolism data. Currently support is limited to data derived from Buxco respirometry instruments as exported by their FinePointe software. biocViews: DataImport, biocViews, Infastructure, DataRepresentation,TimeCourse Author: Daniel Bottomly [aut, cre], Marty Ferris [ctb], Beth Wilmot [aut], Shannon McWeeney [aut] Maintainer: Daniel Bottomly git_url: https://git.bioconductor.org/packages/plethy git_branch: RELEASE_3_8 git_last_commit: 2a1bcbd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/plethy_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/plethy_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plethy_1.20.0.tgz vignettes: vignettes/plethy/inst/doc/plethy.pdf vignetteTitles: plethy hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plethy/inst/doc/plethy.R Package: plgem Version: 1.54.1 Depends: R (>= 2.10) Imports: utils, Biobase (>= 2.5.5), MASS License: GPL-2 MD5sum: 50972ec41ffdce6515857aac4e40fd7f NeedsCompilation: no Title: Detect differential expression in microarray and proteomics datasets with the Power Law Global Error Model (PLGEM) Description: The Power Law Global Error Model (PLGEM) has been shown to faithfully model the variance-versus-mean dependence that exists in a variety of genome-wide datasets, including microarray and proteomics data. The use of PLGEM has been shown to improve the detection of differentially expressed genes or proteins in these datasets. biocViews: ImmunoOncology, Microarray, DifferentialExpression, Proteomics, GeneExpression, MassSpectrometry Author: Mattia Pelizzola and Norman Pavelka Maintainer: Norman Pavelka URL: http://www.genopolis.it git_url: https://git.bioconductor.org/packages/plgem git_branch: RELEASE_3_8 git_last_commit: 7c5b73c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/plgem_1.54.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/plgem_1.54.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plgem_1.54.1.tgz vignettes: vignettes/plgem/inst/doc/plgem.pdf vignetteTitles: An introduction to PLGEM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plgem/inst/doc/plgem.R importsMe: INSPEcT Package: plier Version: 1.52.0 Depends: R (>= 2.0), methods Imports: affy, Biobase, methods License: GPL (>= 2) MD5sum: 878f9d104165863bb2779f78af70f559 NeedsCompilation: yes Title: Implements the Affymetrix PLIER algorithm Description: The PLIER (Probe Logarithmic Error Intensity Estimate) method produces an improved signal by accounting for experimentally observed patterns in probe behavior and handling error at the appropriately at low and high signal values. biocViews: Software Author: Affymetrix Inc., Crispin J Miller, PICR Maintainer: Crispin Miller git_url: https://git.bioconductor.org/packages/plier git_branch: RELEASE_3_8 git_last_commit: 2802101 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/plier_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/plier_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plier_1.52.0.tgz hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE suggestsMe: piano Package: plotGrouper Version: 1.0.1 Depends: R (>= 3.5) Imports: ggplot2 (>= 3.0.0), dplyr (>= 0.7.6), tidyr (>= 0.2.0), tibble (>= 1.4.2), stringr (>= 1.3.1), readr (>= 1.1.1), readxl (>= 1.1.0), scales (>= 1.0.0), stats, grid, gridExtra (>= 2.3), egg (>= 0.4.0), gtable (>= 0.2.0), ggpubr (>= 0.1.8), shiny (>= 1.1.0), shinythemes (>= 1.1.1), colourpicker (>= 1.0), magrittr (>= 1.5), Hmisc (>= 4.1.1), rlang (>= 0.2.2) Suggests: knitr, htmltools, BiocStyle, rmarkdown, testthat License: GPL-3 Archs: i386, x64 MD5sum: acacc62ceda98794cedee778f8c6a416 NeedsCompilation: no Title: Shiny app GUI wrapper for ggplot with built-in statistical analysis Description: A shiny app-based GUI wrapper for ggplot with built-in statistical analysis. Import data from file and use dropdown menus and checkboxes to specify the plotting variables, graph type, and look of your plots. Once created, plots can be saved independently or stored in a report that can be saved as a pdf. If new data are added to the file, the report can be refreshed to include new data. Statistical tests can be selected and added to the graphs. Analysis of flow cytometry data is especially integrated with plotGrouper. Count data can be transformed to return the absolute number of cells in a sample (this feature requires inclusion of the number of beads per sample and information about any dilution performed). biocViews: ImmunoOncology, FlowCytometry, GraphAndNetwork, StatisticalMethod, DataImport, GUI, MultipleComparison Author: John D. Gagnon [aut, cre] Maintainer: John D. Gagnon URL: https://jdgagnon.github.io/plotGrouper/ VignetteBuilder: knitr BugReports: https://github.com/jdgagnon/plotGrouper/issues git_url: https://git.bioconductor.org/packages/plotGrouper git_branch: RELEASE_3_8 git_last_commit: 20ce3cd git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/plotGrouper_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/plotGrouper_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plotGrouper_1.0.1.tgz vignettes: vignettes/plotGrouper/inst/doc/plotGrouper-vignette.html vignetteTitles: plotGrouper hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plotGrouper/inst/doc/plotGrouper-vignette.R Package: PLPE Version: 1.42.0 Depends: R (>= 2.6.2), Biobase (>= 2.5.5), LPE, MASS, methods License: GPL (>= 2) MD5sum: e14a72c1493694cf9270d6b3f8c7888c NeedsCompilation: no Title: Local Pooled Error Test for Differential Expression with Paired High-throughput Data Description: This package performs tests for paired high-throughput data. biocViews: Proteomics, Microarray, DifferentialExpression Author: HyungJun Cho and Jae K. Lee Maintainer: Soo-heang Eo URL: http://www.korea.ac.kr/~stat2242/ git_url: https://git.bioconductor.org/packages/PLPE git_branch: RELEASE_3_8 git_last_commit: 6ad37e1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PLPE_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PLPE_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PLPE_1.42.0.tgz vignettes: vignettes/PLPE/inst/doc/PLPE.pdf vignetteTitles: PLPE Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PLPE/inst/doc/PLPE.R Package: plrs Version: 1.22.0 Depends: R (>= 2.10), Biobase Imports: BiocGenerics, CGHbase, graphics, grDevices, ic.infer, marray, methods, quadprog, Rcsdp, stats, stats4, utils Suggests: mvtnorm, methods License: GPL (>=2.0) MD5sum: 41bf5ad9dc49a153c0fcb4ddfa4b5e44 NeedsCompilation: no Title: Piecewise Linear Regression Splines (PLRS) for the association between DNA copy number and gene expression Description: The present package implements a flexible framework for modeling the relationship between DNA copy number and gene expression data using Piecewise Linear Regression Splines (PLRS). biocViews: Regression Author: Gwenael G.R. Leday Maintainer: Gwenael G.R. Leday to git_url: https://git.bioconductor.org/packages/plrs git_branch: RELEASE_3_8 git_last_commit: 8a760ff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/plrs_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/plrs_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plrs_1.22.0.tgz vignettes: vignettes/plrs/inst/doc/plrs_vignette.pdf vignetteTitles: plrs hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plrs/inst/doc/plrs_vignette.R Package: plw Version: 1.42.0 Depends: R (>= 2.10), affy (>= 1.23.4) Imports: MASS, affy, graphics, splines, stats Suggests: limma License: GPL-2 MD5sum: dc4109cd98ee3817f3ab6b5308f13680 NeedsCompilation: yes Title: Probe level Locally moderated Weighted t-tests. Description: Probe level Locally moderated Weighted median-t (PLW) and Locally Moderated Weighted-t (LMW). biocViews: Microarray, OneChannel, TwoChannel, DifferentialExpression Author: Magnus Astrand Maintainer: Magnus Astrand git_url: https://git.bioconductor.org/packages/plw git_branch: RELEASE_3_8 git_last_commit: f3f1fcd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/plw_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/plw_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plw_1.42.0.tgz vignettes: vignettes/plw/inst/doc/HowToPLW.pdf vignetteTitles: HowTo plw hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plw/inst/doc/HowToPLW.R Package: plyranges Version: 1.2.0 Depends: R (>= 3.5), methods, BiocGenerics, IRanges (>= 2.12.0), GenomicRanges (>= 1.28.4) Imports: dplyr, rlang (>= 0.2.0), magrittr, tidyr, tidyselect, rtracklayer, GenomicAlignments, GenomeInfoDb, Rsamtools, S4Vectors (>= 0.17.41), utils Suggests: knitr, BiocStyle, rmarkdown, testthat, ggplot2, HelloRanges, HelloRangesData, BSgenome.Hsapiens.UCSC.hg19, pasillaBamSubset, covr License: Artistic-2.0 Archs: i386, x64 MD5sum: 7f6a2b20360203ca9fb94f75e10e0c17 NeedsCompilation: no Title: A fluent interface for manipulating GenomicRanges Description: A dplyr-like interface for interacting with the common Bioconductor classes Ranges and GenomicRanges. By providing a grammatical and consistent way of manipulating these classes their accessiblity for new Bioconductor users is hopefully increased. biocViews: Infrastructure, DataRepresentation, WorkflowStep, Coverage Author: Stuart Lee [aut, cre], Michael Lawrence [aut, ctb], Dianne Cook [aut, ctb] Maintainer: Stuart Lee VignetteBuilder: knitr BugReports: https://github.com/sa-lee/plyranges git_url: https://git.bioconductor.org/packages/plyranges git_branch: RELEASE_3_8 git_last_commit: 0e8d924 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/plyranges_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/plyranges_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/plyranges_1.2.0.tgz vignettes: vignettes/plyranges/inst/doc/an-introduction.html vignetteTitles: Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/plyranges/inst/doc/an-introduction.R Package: pmm Version: 1.14.0 Depends: R (>= 2.10) Imports: lme4, splines License: GPL-3 MD5sum: 62c7a8f094a67345c7f968665c5da863 NeedsCompilation: no Title: Parallel Mixed Model Description: The Parallel Mixed Model (PMM) approach is suitable for hit selection and cross-comparison of RNAi screens generated in experiments that are performed in parallel under several conditions. For example, we could think of the measurements or readouts from cells under RNAi knock-down, which are infected with several pathogens or which are grown from different cell lines. biocViews: SystemsBiology, Regression Author: Anna Drewek Maintainer: Anna Drewek git_url: https://git.bioconductor.org/packages/pmm git_branch: RELEASE_3_8 git_last_commit: e799069 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pmm_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pmm_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pmm_1.14.0.tgz vignettes: vignettes/pmm/inst/doc/pmm-package.pdf vignetteTitles: User manual for R-Package PMM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pmm/inst/doc/pmm-package.R Package: podkat Version: 1.14.0 Depends: R (>= 3.2.0), methods, Rsamtools, GenomicRanges Imports: Rcpp (>= 0.11.1), parallel, stats, graphics, grDevices, utils, Biobase, BiocGenerics, Matrix, GenomeInfoDb, IRanges, Biostrings, BSgenome (>= 1.32.0) LinkingTo: Rcpp, Rsamtools Suggests: BSgenome.Hsapiens.UCSC.hg38.masked, TxDb.Hsapiens.UCSC.hg38.knownGene, BSgenome.Mmusculus.UCSC.mm10.masked, GWASTools (>= 1.13.24), VariantAnnotation, SummarizedExperiment, knitr License: GPL (>= 2) MD5sum: bf4f038d282695aaab44b9f08dd840ed NeedsCompilation: yes Title: Position-Dependent Kernel Association Test Description: This package provides an association test that is capable of dealing with very rare and even private variants. This is accomplished by a kernel-based approach that takes the positions of the variants into account. The test can be used for pre-processed matrix data, but also directly for variant data stored in VCF files. Association testing can be performed whole-genome, whole-exome, or restricted to pre-defined regions of interest. The test is complemented by tools for analyzing and visualizing the results. biocViews: Genetics, WholeGenome, Annotation, VariantAnnotation, Sequencing, DataImport Author: Ulrich Bodenhofer Maintainer: Ulrich Bodenhofer URL: http://www.bioinf.jku.at/software/podkat/ https://github.com/UBod/podkat VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/podkat git_branch: RELEASE_3_8 git_last_commit: 5166924 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/podkat_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/podkat_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/podkat_1.14.0.tgz vignettes: vignettes/podkat/inst/doc/podkat.pdf vignetteTitles: PODKAT - An R Package for Association Testing Involving Rare and Private Variants hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/podkat/inst/doc/podkat.R Package: pogos Version: 1.2.1 Depends: R (>= 3.5.0), rjson (>= 0.2.15), httr (>= 1.3.1) Imports: methods, S4Vectors, utils, shiny, ontoProc, ggplot2, graphics Suggests: knitr, DT, ontologyPlot, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: 78a32cdb6179880f017f2b58923c6252 NeedsCompilation: no Title: PharmacOGenomics Ontology Support Description: Provide simple utilities for querying bhklab PharmacoDB, modeling API outputs, and integrating to cell and compound ontologies. biocViews: ImmunoOncology, Pharmacogenomics, PooledScreens Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/pogos git_branch: RELEASE_3_8 git_last_commit: 05b5c71 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/pogos_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/pogos_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pogos_1.2.1.tgz vignettes: vignettes/pogos/inst/doc/pogos.html vignetteTitles: pogos -- simple interface to bhklab PharmacoDB with emphasis on ontology hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pogos/inst/doc/pogos.R suggestsMe: BiocOncoTK Package: polyester Version: 1.18.0 Depends: R (>= 3.0.0) Imports: Biostrings (>= 2.32.0), IRanges, S4Vectors, logspline, limma, zlibbioc Suggests: knitr, ballgown License: Artistic-2.0 MD5sum: c7a2bb655890a4fa6f80eae248d10d94 NeedsCompilation: no Title: Simulate RNA-seq reads Description: This package can be used to simulate RNA-seq reads from differential expression experiments with replicates. The reads can then be aligned and used to perform comparisons of methods for differential expression. biocViews: Sequencing, DifferentialExpression Author: Alyssa C. Frazee, Andrew E. Jaffe, Rory Kirchner, Jeffrey T. Leek Maintainer: Jack Fu , Jeff Leek VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/polyester git_branch: RELEASE_3_8 git_last_commit: 86b9fc2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/polyester_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/polyester_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/polyester_1.18.0.tgz vignettes: vignettes/polyester/inst/doc/polyester.html vignetteTitles: The Polyester package for simulating RNA-seq reads hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/polyester/inst/doc/polyester.R Package: Polyfit Version: 1.16.1 Depends: DESeq Suggests: BiocStyle License: GPL (>= 3) MD5sum: 3bf6fc9eb02104686f15f1360a05d43b NeedsCompilation: no Title: Add-on to DESeq to improve p-values and q-values Description: Polyfit is an add-on to the packages DESeq which ensures the p-value distribution is uniform over the interval [0, 1] for data satisfying the null hypothesis of no differential expression, and uses an adpated Storey-Tibshiran method to calculate q-values. biocViews: ImmunoOncology, DifferentialExpression, Sequencing, RNASeq, GeneExpression Author: Conrad Burden Maintainer: Conrad Burden git_url: https://git.bioconductor.org/packages/Polyfit git_branch: RELEASE_3_8 git_last_commit: e9c53bc git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Polyfit_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Polyfit_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Polyfit_1.16.1.tgz vignettes: vignettes/Polyfit/inst/doc/polyfit.pdf vignetteTitles: Polyfit hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Polyfit/inst/doc/polyfit.R Package: POST Version: 1.6.0 Depends: R (>= 3.4.0) Imports: stats, CompQuadForm, Matrix, survival, Biobase, GSEABase License: GPL (>= 2) MD5sum: 53dc1ab5813de6f37505e96d2dd29c5c NeedsCompilation: no Title: Projection onto Orthogonal Space Testing for High Dimensional Data Description: Perform orthogonal projection of high dimensional data of a set, and statistical modeling of phenotye with projected vectors as predictor. biocViews: Microarray, GeneExpression Author: Xueyuan Cao and Stanley.pounds Maintainer: Xueyuan Cao git_url: https://git.bioconductor.org/packages/POST git_branch: RELEASE_3_8 git_last_commit: 81b9084 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/POST_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/POST_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/POST_1.6.0.tgz vignettes: vignettes/POST/inst/doc/POST.pdf vignetteTitles: An introduction to POST hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/POST/inst/doc/POST.R Package: PowerExplorer Version: 1.2.2 Depends: R (>= 3.5.0), SummarizedExperiment Imports: DESeq2, ROTS, vsn, stats, utils, methods, gridExtra, MASS, data.table, ggplot2, Biobase, S4Vectors, BiocParallel Suggests: knitr, rmarkdown License: Artistic-2.0 MD5sum: 8de67e18b225337478a5bde3e510a4b4 NeedsCompilation: no Title: Power Estimation Tool for RNA-Seq and proteomics data Description: Estimate and predict power among groups and multiple sample sizes with simulated data, the simulations are operated based on distribution parameters estimated from the provided input dataset. biocViews: ImmunoOncology, RNASeq, Proteomics, DifferentialExpression, MultipleComparison, Sequencing, Coverage, ChIPSeq Author: Xu Qiao [aut, cre], Laura Elo [cph] Maintainer: Xu Qiao URL: https://gitlab.utu.fi/CompBioMedNGSTools/PowerExplorer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PowerExplorer git_branch: RELEASE_3_8 git_last_commit: d2cb645 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PowerExplorer_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/PowerExplorer_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PowerExplorer_1.2.2.tgz vignettes: vignettes/PowerExplorer/inst/doc/PowerExplore_vignette.pdf vignetteTitles: PowerExplorer Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PowerExplorer/inst/doc/PowerExplore_vignette.R Package: powerTCR Version: 1.2.0 Imports: cubature, doParallel, evmix, foreach, magrittr, methods, parallel, purrr, stats, tcR, truncdist, vegan, VGAM Suggests: BiocStyle, knitr, rmarkdown, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: e355b3691f1b481999f271edce674a87 NeedsCompilation: no Title: Model-Based Comparative Analysis of the TCR Repertoire Description: This package provides a model for the clone size distribution of the TCR repertoire. Further, it permits comparative analysis of TCR repertoire libraries based on theoretical model fits. biocViews: Software, Clustering, BiomedicalInformatics Author: Hillary Koch Maintainer: Hillary Koch VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/powerTCR git_branch: RELEASE_3_8 git_last_commit: 9895403 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/powerTCR_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/powerTCR_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/powerTCR_1.2.0.tgz vignettes: vignettes/powerTCR/inst/doc/powerTCR.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/powerTCR/inst/doc/powerTCR.R Package: PPInfer Version: 1.8.1 Depends: biomaRt, fgsea, kernlab, ggplot2, igraph, STRINGdb, yeastExpData License: Artistic-2.0 MD5sum: 3f431c624b08318fd0ef332a6ae63e1a NeedsCompilation: no Title: Inferring functionally related proteins using protein interaction networks Description: Interactions between proteins occur in many, if not most, biological processes. Most proteins perform their functions in networks associated with other proteins and other biomolecules. This fact has motivated the development of a variety of experimental methods for the identification of protein interactions. This variety has in turn ushered in the development of numerous different computational approaches for modeling and predicting protein interactions. Sometimes an experiment is aimed at identifying proteins closely related to some interesting proteins. A network based statistical learning method is used to infer the putative functions of proteins from the known functions of its neighboring proteins on a PPI network. This package identifies such proteins often involved in the same or similar biological functions. biocViews: Software, StatisticalMethod, Network, GraphAndNetwork, GeneSetEnrichment, NetworkEnrichment, Pathways Author: Dongmin Jung, Xijin Ge Maintainer: Dongmin Jung git_url: https://git.bioconductor.org/packages/PPInfer git_branch: RELEASE_3_8 git_last_commit: 221064e git_last_commit_date: 2018-12-18 Date/Publication: 2018-12-19 source.ver: src/contrib/PPInfer_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PPInfer_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PPInfer_1.8.1.tgz vignettes: vignettes/PPInfer/inst/doc/PPInfer.pdf vignetteTitles: User manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PPInfer/inst/doc/PPInfer.R dependsOnMe: gsean Package: ppiStats Version: 1.48.0 Depends: ScISI (>= 1.13.2), lattice, ppiData (>= 0.1.19) Imports: Biobase, Category, graph, graphics, grDevices, lattice, methods, RColorBrewer, stats Suggests: yeastExpData, xtable License: Artistic-2.0 MD5sum: 143b0f3a760c921de1444f04cea91c98 NeedsCompilation: no Title: Protein-Protein Interaction Statistical Package Description: Tools for the analysis of protein interaction data. biocViews: Proteomics, GraphAndNetwork, Network, NetworkInference Author: T. Chiang and D. Scholtens with contributions from W. Huber and L. Wang Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/ppiStats git_branch: RELEASE_3_8 git_last_commit: 97d2b47 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ppiStats_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ppiStats_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ppiStats_1.48.0.tgz vignettes: vignettes/ppiStats/inst/doc/ppiStats.pdf vignetteTitles: ppiStats hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ppiStats/inst/doc/ppiStats.R dependsOnMe: PCpheno suggestsMe: BiocCaseStudies, RpsiXML Package: pqsfinder Version: 1.10.1 Depends: Biostrings Imports: Rcpp (>= 0.12.3), GenomicRanges, IRanges, S4Vectors, methods LinkingTo: Rcpp, BH (>= 1.66.0) Suggests: BiocStyle, knitr, Gviz, rtracklayer, ggplot2, BSgenome.Hsapiens.UCSC.hg38, testthat, stringr License: BSD_2_clause + file LICENSE MD5sum: c3993c918d5a16ae2198b8f9064ee1ae NeedsCompilation: yes Title: Identification of potential quadruplex forming sequences Description: The main functionality of this package is to detect DNA sequence patterns that are likely to fold into an intramolecular G-quadruplex (G4). Unlike many other approaches, this package is able to detect sequences responsible for G4s folded from imperfect G-runs containing bulges or mismatches and as such is more sensitive than competing algorithms. biocViews: MotifDiscovery, SequenceMatching, GeneRegulation Author: Jiri Hon, Matej Lexa and Tomas Martinek Maintainer: Jiri Hon SystemRequirements: GNU make, C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/pqsfinder git_branch: RELEASE_3_8 git_last_commit: 84e32c7 git_last_commit_date: 2019-04-04 Date/Publication: 2019-04-04 source.ver: src/contrib/pqsfinder_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/pqsfinder_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pqsfinder_1.10.1.tgz vignettes: vignettes/pqsfinder/inst/doc/pqsfinder.html vignetteTitles: pqsfinder: User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/pqsfinder/inst/doc/pqsfinder.R Package: prada Version: 1.58.1 Depends: R (>= 2.10), Biobase, RColorBrewer, grid, methods, rrcov Imports: Biobase, BiocGenerics, graphics, grDevices, grid, MASS, methods, RColorBrewer, rrcov, stats4, utils Suggests: cellHTS2, tcltk License: LGPL Archs: i386, x64 MD5sum: 49e2b7a57b55cfc61efcdff2cc960a20 NeedsCompilation: yes Title: Data analysis for cell-based functional assays Description: Tools for analysing and navigating data from high-throughput phenotyping experiments based on cellular assays and fluorescent detection (flow cytometry (FACS), high-content screening microscopy). biocViews: ImmunoOncology, CellBasedAssays, Visualization Author: Florian Hahne , Wolfgang Huber , Markus Ruschhaupt, Joern Toedling , Joseph Barry Maintainer: Florian Hahne git_url: https://git.bioconductor.org/packages/prada git_branch: RELEASE_3_8 git_last_commit: 4d57031 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/prada_1.58.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/prada_1.58.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/prada_1.58.1.tgz vignettes: vignettes/prada/inst/doc/norm2.pdf, vignettes/prada/inst/doc/prada2cellHTS.pdf vignetteTitles: Removal of contaminants from FACS data, Combining prada output and cellHTS2 hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/prada/inst/doc/norm2.R, vignettes/prada/inst/doc/prada2cellHTS.R dependsOnMe: RNAither importsMe: cellHTS2 Package: prebs Version: 1.22.1 Depends: R (>= 2.14.0), GenomicAlignments, affy, RPA Imports: parallel, methods, stats, GenomicRanges (>= 1.13.3), IRanges, Biobase, GenomeInfoDb, S4Vectors Suggests: prebsdata, hgu133plus2cdf, hgu133plus2probe License: Artistic-2.0 Archs: i386, x64 MD5sum: 1846e9ecb83fc78139bd5bfa9d899c9a NeedsCompilation: no Title: Probe region expression estimation for RNA-seq data for improved microarray comparability Description: The prebs package aims at making RNA-sequencing (RNA-seq) data more comparable to microarray data. The comparability is achieved by summarizing sequencing-based expressions of probe regions using a modified version of RMA algorithm. The pipeline takes mapped reads in BAM format as an input and produces either gene expressions or original microarray probe set expressions as an output. biocViews: ImmunoOncology, Microarray, RNASeq, Sequencing, GeneExpression, Preprocessing Author: Karolis Uziela and Antti Honkela Maintainer: Karolis Uziela git_url: https://git.bioconductor.org/packages/prebs git_branch: RELEASE_3_8 git_last_commit: d7c63e9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/prebs_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/prebs_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/prebs_1.22.1.tgz vignettes: vignettes/prebs/inst/doc/prebs.pdf vignetteTitles: prebs User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/prebs/inst/doc/prebs.R Package: PREDA Version: 1.28.0 Depends: R (>= 2.9.0), Biobase, lokern (>= 1.0.9), multtest, stats, methods, annotate Suggests: quantsmooth, qvalue, limma, caTools, affy, PREDAsampledata Enhances: Rmpi, rsprng License: GPL-2 MD5sum: 4bb593ea42c1bf03653cadffd9202aa4 NeedsCompilation: no Title: Position Related Data Analysis Description: Package for the position related analysis of quantitative functional genomics data. biocViews: Software, CopyNumberVariation, GeneExpression, Genetics Author: Francesco Ferrari Maintainer: Francesco Ferrari git_url: https://git.bioconductor.org/packages/PREDA git_branch: RELEASE_3_8 git_last_commit: 1fffe97 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PREDA_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PREDA_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PREDA_1.28.0.tgz vignettes: vignettes/PREDA/inst/doc/PREDAclasses.pdf, vignettes/PREDA/inst/doc/PREDAtutorial.pdf vignetteTitles: PREDA S4-classes, PREDA tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PREDA/inst/doc/PREDAtutorial.R Package: predictionet Version: 1.28.0 Depends: igraph, catnet Imports: penalized, RBGL, MASS Suggests: network, minet, knitr License: Artistic-2.0 MD5sum: d95f178dcf079e1c8c9d0a2462fba591 NeedsCompilation: yes Title: Inference for predictive networks designed for (but not limited to) genomic data Description: This package contains a set of functions related to network inference combining genomic data and prior information extracted from biomedical literature and structured biological databases. The main function is able to generate networks using Bayesian or regression-based inference methods; while the former is limited to < 100 of variables, the latter may infer networks with hundreds of variables. Several statistics at the edge and node levels have been implemented (edge stability, predictive ability of each node, ...) in order to help the user to focus on high quality subnetworks. Ultimately, this package is used in the 'Predictive Networks' web application developed by the Dana-Farber Cancer Institute in collaboration with Entagen. biocViews: GraphAndNetwork, NetworkInference Author: Benjamin Haibe-Kains, Catharina Olsen, Gianluca Bontempi, John Quackenbush Maintainer: Benjamin Haibe-Kains , Catharina Olsen URL: http://compbio.dfci.harvard.edu, http://www.ulb.ac.be/di/mlg git_url: https://git.bioconductor.org/packages/predictionet git_branch: RELEASE_3_8 git_last_commit: a4aa3bd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/predictionet_1.28.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/predictionet_1.28.0.tgz vignettes: vignettes/predictionet/inst/doc/predictionet.pdf vignetteTitles: predictionet hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/predictionet/inst/doc/predictionet.R Package: preprocessCore Version: 1.44.0 Imports: stats License: LGPL (>= 2) MD5sum: 973ffdd342f2443573ca0fe558fb0cdc NeedsCompilation: yes Title: A collection of pre-processing functions Description: A library of core preprocessing routines. biocViews: Infrastructure Author: Ben Bolstad Maintainer: Ben Bolstad URL: https://github.com/bmbolstad/preprocessCore git_url: https://git.bioconductor.org/packages/preprocessCore git_branch: RELEASE_3_8 git_last_commit: dc1dc61 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/preprocessCore_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/preprocessCore_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/preprocessCore_1.44.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: affyPLM, cqn, crlmm, RefPlus importsMe: affy, bnbc, charm, cn.farms, EMDomics, ExiMiR, fastLiquidAssociation, frma, frmaTools, hipathia, iCheck, ImmuneSpaceR, InPAS, INSPEcT, lumi, MADSEQ, MBCB, MEDIPS, mimager, minfi, MSnbase, MSstats, NormalyzerDE, oligo, PECA, Pigengene, qPLEXanalyzer, sesame, soGGi, waveTiling, yarn suggestsMe: multiClust linksToMe: affy, affyPLM, crlmm, oligo Package: primirTSS Version: 1.0.1 Depends: R (>= 3.5.0) Imports: GenomicRanges (>= 1.32.2), S4Vectors (>= 0.18.2), rtracklayer (>= 1.40.3), dplyr (>= 0.7.6), stringr (>= 1.3.1), tidyr (>= 0.8.1), Biostrings (>= 2.48.0), purrr (>= 0.2.5), BSgenome.Hsapiens.UCSC.hg38 (>= 1.4.1), phastCons100way.UCSC.hg38 (>= 3.7.1), GenomicScores (>= 1.4.1), shiny (>= 1.0.5), Gviz (>= 1.24.0), BiocGenerics (>= 0.26.0), IRanges (>= 2.14.10), TFBSTools (>= 1.18.0), JASPAR2018 (>= 1.1.1), tibble (>= 1.4.2), R.utils (>= 2.6.0), stats, utils Suggests: knitr, rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 766668da1afd9328500d67924f8f8522 NeedsCompilation: no Title: Prediction of pri-miRNA Transcription Start Site Description: A fast, convenient tool to identify the TSSs of miRNAs by integrating the data of H3K4me3 and Pol II as well as combining the conservation level and sequence feature, provided within both command-line and graphical interfaces, which achieves a better performance than the previous non-cell-specific methods on miRNA TSSs. biocViews: ImmunoOncology, Sequencing, RNASeq, Genetics, Preprocessing, Transcription, GeneRegulation Author: Pumin Li [aut, cre], Qi Xu [aut] Maintainer: Pumin Li URL: https://github.com/ipumin/primirTSS VignetteBuilder: knitr BugReports: http://github.com/ipumin/primirTSS/issues git_url: https://git.bioconductor.org/packages/primirTSS git_branch: RELEASE_3_8 git_last_commit: 3be26c7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/primirTSS_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/primirTSS_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/primirTSS_1.0.1.tgz vignettes: vignettes/primirTSS/inst/doc/primirTSS.html vignetteTitles: primirTSS hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/primirTSS/inst/doc/primirTSS.R Package: Prize Version: 1.12.1 Imports: diagram, stringr, ggplot2, reshape2, grDevices, matrixcalc, stats, gplots, methods, utils, graphics Suggests: RUnit, BiocGenerics License: Artistic-2.0 MD5sum: 06e1d7184b6e71370bb2784b9c94e615 NeedsCompilation: no Title: Prize: an R package for prioritization estimation based on analytic hierarchy process Description: The high throughput studies often produce large amounts of numerous genes and proteins of interest. While it is difficult to study and validate all of them. Analytic Hierarchy Process (AHP) offers a novel approach to narrowing down long lists of candidates by prioritizing them based on how well they meet the research goal. AHP is a mathematical technique for organizing and analyzing complex decisions where multiple criteria are involved. The technique structures problems into a hierarchy of elements, and helps to specify numerical weights representing the relative importance of each element. Numerical weight or priority derived from each element allows users to find alternatives that best suit their goal and their understanding of the problem. biocViews: ImmunoOncology, Software, MultipleComparison, GeneExpression, CellBiology, RNASeq Author: Daryanaz Dargahi Maintainer: Daryanaz Dargahi git_url: https://git.bioconductor.org/packages/Prize git_branch: RELEASE_3_8 git_last_commit: 489f702 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Prize_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Prize_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Prize_1.12.1.tgz vignettes: vignettes/Prize/inst/doc/Prize.pdf vignetteTitles: Prize: an R package for prioritization estimation based on analytic hierarchy process hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Prize/inst/doc/Prize.R Package: proBAMr Version: 1.16.1 Depends: R (>= 3.0.1), IRanges, AnnotationDbi Imports: GenomicRanges, Biostrings, GenomicFeatures, rtracklayer Suggests: RUnit, BiocGenerics License: Artistic-2.0 MD5sum: 36b0ffa9036fe83a0b7b85152bb178f4 NeedsCompilation: no Title: Generating SAM file for PSMs in shotgun proteomics data Description: Mapping PSMs back to genome. The package builds SAM file from shotgun proteomics data The package also provides function to prepare annotation from GTF file. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, Software, Visualization Author: Xiaojing Wang Maintainer: Xiaojing Wang git_url: https://git.bioconductor.org/packages/proBAMr git_branch: RELEASE_3_8 git_last_commit: 4252f31 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/proBAMr_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/proBAMr_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/proBAMr_1.16.1.tgz vignettes: vignettes/proBAMr/inst/doc/proBAMr.pdf vignetteTitles: Introduction to proBAMr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/proBAMr/inst/doc/proBAMr.R Package: PROcess Version: 1.58.1 Depends: Icens Imports: graphics, grDevices, Icens, stats, utils License: Artistic-2.0 MD5sum: a5b428d7ac389fb7f808711e6012b880 NeedsCompilation: no Title: Ciphergen SELDI-TOF Processing Description: A package for processing protein mass spectrometry data. biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Xiaochun Li Maintainer: Xiaochun Li git_url: https://git.bioconductor.org/packages/PROcess git_branch: RELEASE_3_8 git_last_commit: 1cbdcd5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PROcess_1.58.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PROcess_1.58.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PROcess_1.58.1.tgz vignettes: vignettes/PROcess/inst/doc/howtoprocess.pdf vignetteTitles: HOWTO PROcess hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PROcess/inst/doc/howtoprocess.R Package: procoil Version: 2.10.0 Depends: R (>= 3.3.0), kebabs Imports: methods, stats, graphics, S4Vectors, Biostrings, utils Suggests: knitr License: GPL (>= 2) MD5sum: 270f49603fd44f3062e45a3af865959a NeedsCompilation: no Title: Prediction of Oligomerization of Coiled Coil Proteins Description: The package allows for predicting whether a coiled coil sequence (amino acid sequence plus heptad register) is more likely to form a dimer or more likely to form a trimer. Additionally to the prediction itself, a prediction profile is computed which allows for determining the strengths to which the individual residues are indicative for either class. Prediction profiles can also be visualized as curves or heatmaps. biocViews: Proteomics, Classification, SupportVectorMachine Author: Ulrich Bodenhofer Maintainer: Ulrich Bodenhofer URL: http://www.bioinf.jku.at/software/procoil/ https://github.com/UBod/procoil VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/procoil git_branch: RELEASE_3_8 git_last_commit: 4269a33 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/procoil_2.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/procoil_2.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/procoil_2.10.0.tgz vignettes: vignettes/procoil/inst/doc/procoil.pdf vignetteTitles: PrOCoil - A Web Service and an R Package for Predicting the Oligomerization of Coiled-Coil Proteins hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/procoil/inst/doc/procoil.R Package: proFIA Version: 1.8.1 Depends: R (>= 2.5.0), xcms Imports: stats, graphics, utils, grDevices, methods, pracma, Biobase, minpack.lm, BiocParallel, missForest, ropls Suggests: BiocGenerics, plasFIA, knitr, License: CeCILL MD5sum: 1b956906a15daabb5dee28cc520d1aa4 NeedsCompilation: yes Title: Preprocessing of FIA-HRMS data Description: Flow Injection Analysis coupled to High-Resolution Mass Spectrometry is a promising approach for high-throughput metabolomics. FIA- HRMS data, however, cannot be pre-processed with current software tools which rely on liquid chromatography separation, or handle low resolution data only. Here we present the proFIA package, which implements a new methodology to pre-process FIA-HRMS raw data (netCDF, mzData, mzXML, and mzML) including noise modelling and injection peak reconstruction, and generate the peak table. The workflow includes noise modelling, band detection and filtering then signal matching and missing value imputation. The peak table can then be exported as a .tsv file for further analysis. Visualisations to assess the quality of the data and of the signal made are easely produced. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics, Lipidomics, Preprocessing, PeakDetection, Proteomics Author: Alexis Delabriere and Etienne Thevenot. Maintainer: Alexis Delabriere VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/proFIA git_branch: RELEASE_3_8 git_last_commit: aac9283 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/proFIA_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/proFIA_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/proFIA_1.8.1.tgz vignettes: vignettes/proFIA/inst/doc/proFIA-vignette.html vignetteTitles: processing FIA-HRMS data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/proFIA/inst/doc/proFIA-vignette.R Package: profileScoreDist Version: 1.10.0 Depends: R(>= 3.3) Imports: Rcpp, BiocGenerics, methods, graphics LinkingTo: Rcpp Suggests: BiocStyle, knitr, MotifDb License: MIT + file LICENSE Archs: i386, x64 MD5sum: c1043816d33dad80676d2e4b4b675a82 NeedsCompilation: yes Title: Profile score distributions Description: Regularization and score distributions for position count matrices. biocViews: Software, GeneRegulation, StatisticalMethod Author: Paal O. Westermark Maintainer: Paal O. Westermark VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/profileScoreDist git_branch: RELEASE_3_8 git_last_commit: 9656b28 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/profileScoreDist_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/profileScoreDist_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/profileScoreDist_1.10.0.tgz vignettes: vignettes/profileScoreDist/inst/doc/profileScoreDist-vignette.pdf vignetteTitles: Using profileScoreDist hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/profileScoreDist/inst/doc/profileScoreDist-vignette.R Package: progeny Version: 1.4.1 Depends: R (>= 3.4.0) Imports: Biobase Suggests: airway, biomaRt, BiocFileCache, broom, DESeq2, dplyr, knitr, readr, readxl License: Apache License (== 2.0) | file LICENSE Archs: i386, x64 MD5sum: 365223027856c35908a5d91a3d3846f5 NeedsCompilation: no Title: Pathway RespOnsive GENes for activity inference from gene expression Description: This package provides a function to infer pathway activity from gene expression using PROGENy. It contains the linear model we inferred in the publication "Perturbation-response genes reveal signaling footprints in cancer gene expression". biocViews: SystemsBiology, GeneExpression, FunctionalPrediction, GeneRegulation Author: Michael Schubert Maintainer: Michael Schubert URL: https://github.com/saezlab/progeny VignetteBuilder: knitr BugReports: https://github.com/saezlab/progeny/issues git_url: https://git.bioconductor.org/packages/progeny git_branch: RELEASE_3_8 git_last_commit: 8315610 git_last_commit_date: 2019-01-22 Date/Publication: 2019-01-22 source.ver: src/contrib/progeny_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/progeny_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/progeny_1.4.1.tgz vignettes: vignettes/progeny/inst/doc/progeny.html vignetteTitles: narray Usage Examples hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/progeny/inst/doc/progeny.R Package: pRoloc Version: 1.22.2 Depends: R (>= 2.15), MSnbase (>= 1.19.20), MLInterfaces (>= 1.37.1), methods, Rcpp (>= 0.10.3), BiocParallel Imports: Biobase, mclust (>= 4.3), caret, e1071, sampling, class, kernlab, lattice, nnet, randomForest, proxy, FNN, hexbin, BiocGenerics, stats, dendextend, RColorBrewer, scales, MASS, knitr, mvtnorm, LaplacesDemon, coda, mixtools, gtools, plyr, ggplot2, biomaRt, utils, grDevices, graphics LinkingTo: Rcpp, RcppArmadillo Suggests: testthat, rmarkdown, pRolocdata (>= 1.9.4), roxygen2, synapter, xtable, rgl, BiocStyle (>= 2.5.19), hpar (>= 1.15.3), dplyr, GO.db, AnnotationDbi, Rtsne (>= 0.13), nipals, reshape License: GPL-2 MD5sum: a03892c89c55e0beeddc202f661976ab NeedsCompilation: yes Title: A unifying bioinformatics framework for spatial proteomics Description: The pRoloc package implements machine learning and visualisation methods for the analysis and interogation of quantitiative mass spectrometry data to reliably infer protein sub-cellular localisation. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, Classification, Clustering, QualityControl Author: Laurent Gatto, Oliver Crook and Lisa M. Breckels with contributions from Thomas Burger and Samuel Wieczorek Maintainer: Laurent Gatto URL: https://github.com/lgatto/pRoloc VignetteBuilder: knitr Video: https://www.youtube.com/playlist?list=PLvIXxpatSLA2loV5Srs2VBpJIYUlVJ4ow BugReports: https://github.com/lgatto/pRoloc/issues git_url: https://git.bioconductor.org/packages/pRoloc git_branch: RELEASE_3_8 git_last_commit: 1098398 git_last_commit_date: 2019-03-15 Date/Publication: 2019-03-16 source.ver: src/contrib/pRoloc_1.22.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/pRoloc_1.22.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pRoloc_1.22.2.tgz vignettes: vignettes/pRoloc/inst/doc/v01-pRoloc-tutorial.html, vignettes/pRoloc/inst/doc/v02-pRoloc-ml.html, vignettes/pRoloc/inst/doc/v03-pRoloc-bayesian.html, vignettes/pRoloc/inst/doc/v04-pRoloc-goannotations.html, vignettes/pRoloc/inst/doc/v05-pRoloc-transfer-learning.html vignetteTitles: Using pRoloc for spatial proteomics data analysis, Machine learning techniques available in pRoloc, Bayesian spatial proteomics with pRoloc, Annotating spatial proteomics data, A transfer learning algorithm for spatial proteomics hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pRoloc/inst/doc/v01-pRoloc-tutorial.R, vignettes/pRoloc/inst/doc/v02-pRoloc-ml.R, vignettes/pRoloc/inst/doc/v03-pRoloc-bayesian.R, vignettes/pRoloc/inst/doc/v04-pRoloc-goannotations.R, vignettes/pRoloc/inst/doc/v05-pRoloc-transfer-learning.R dependsOnMe: pRolocGUI suggestsMe: MSnbase Package: pRolocGUI Version: 1.16.0 Depends: methods, R (>= 3.1.0), pRoloc (>= 1.11.1), Biobase, MSnbase (>= 2.1.11) Imports: shiny (>= 0.9.1), scales, dplyr, DT (>= 0.1.40), graphics, utils, ggplot2 Suggests: pRolocdata, knitr, BiocStyle (>= 2.5.19), rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 00b70d7e6c984f287bfbff80c165e87f NeedsCompilation: no Title: Interactive visualisation of spatial proteomics data Description: The package pRolocGUI comprises functions to interactively visualise organelle (spatial) proteomics data on the basis of pRoloc, pRolocdata and shiny. biocViews: Proteomics, Visualization, GUI Author: Lisa M Breckels, Thomas Naake and Laurent Gatto Maintainer: Laurent Gatto , Lisa M Breckels URL: http://ComputationalProteomicsUnit.github.io/pRolocGUI/ VignetteBuilder: knitr Video: https://www.youtube.com/playlist?list=PLvIXxpatSLA2loV5Srs2VBpJIYUlVJ4ow BugReports: https://github.com/ComputationalProteomicsUnit/pRolocGUI/issues git_url: https://git.bioconductor.org/packages/pRolocGUI git_branch: RELEASE_3_8 git_last_commit: 1c374e0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pRolocGUI_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pRolocGUI_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pRolocGUI_1.16.0.tgz vignettes: vignettes/pRolocGUI/inst/doc/pRolocGUI.html vignetteTitles: pRolocGUI - Interactive visualisation of spatial proteomics data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pRolocGUI/inst/doc/pRolocGUI.R Package: PROMISE Version: 1.34.0 Depends: R (>= 3.1.0), Biobase, GSEABase Imports: Biobase, GSEABase, stats License: GPL (>= 2) MD5sum: 1551860b6a6c1cb1e2e1c2eca0188269 NeedsCompilation: no Title: PRojection Onto the Most Interesting Statistical Evidence Description: A general tool to identify genomic features with a specific biologically interesting pattern of associations with multiple endpoint variables as described in Pounds et. al. (2009) Bioinformatics 25: 2013-2019 biocViews: Microarray, OneChannel, MultipleComparison, GeneExpression Author: Stan Pounds , Xueyuan Cao Maintainer: Stan Pounds , Xueyuan Cao git_url: https://git.bioconductor.org/packages/PROMISE git_branch: RELEASE_3_8 git_last_commit: e0fa09a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PROMISE_1.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PROMISE_1.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PROMISE_1.34.0.tgz vignettes: vignettes/PROMISE/inst/doc/PROMISE.pdf vignetteTitles: An introduction to PROMISE hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PROMISE/inst/doc/PROMISE.R dependsOnMe: CCPROMISE Package: PROPER Version: 1.14.1 Depends: R (>= 3.3) Imports: edgeR Suggests: BiocStyle,DESeq,DSS,knitr License: GPL MD5sum: 0c319501b8950f1968169b99f843db64 NeedsCompilation: no Title: PROspective Power Evaluation for RNAseq Description: This package provide simulation based methods for evaluating the statistical power in differential expression analysis from RNA-seq data. biocViews: ImmunoOncology, Sequencing, RNASeq, DifferentialExpression Author: Hao Wu Maintainer: Hao Wu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PROPER git_branch: RELEASE_3_8 git_last_commit: 09c1c89 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PROPER_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/PROPER_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PROPER_1.14.1.tgz vignettes: vignettes/PROPER/inst/doc/PROPER.pdf vignetteTitles: Power and Sample size analysis for gene expression from RNA-seq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PROPER/inst/doc/PROPER.R Package: PROPS Version: 1.4.0 Imports: bnlearn, reshape2, sva, stats, utils, Biobase Suggests: knitr, rmarkdown License: GPL-2 MD5sum: e52f805ee22719f72202aa8768657455 NeedsCompilation: no Title: PRObabilistic Pathway Score (PROPS) Description: This package calculates probabilistic pathway scores using gene expression data. Gene expression values are aggregated into pathway-based scores using Bayesian network representations of biological pathways. biocViews: Classification, Bayesian, GeneExpression Author: Lichy Han Maintainer: Lichy Han VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PROPS git_branch: RELEASE_3_8 git_last_commit: f4ca190 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PROPS_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PROPS_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PROPS_1.4.0.tgz vignettes: vignettes/PROPS/inst/doc/props.html vignetteTitles: PRObabilistic Pathway Scores (PROPS) hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PROPS/inst/doc/props.R Package: Prostar Version: 1.14.12 Depends: R (>= 3.5) Imports: DAPAR (>= 1.13.15), DAPARdata (>= 1.11.2), rhandsontable, data.table, shinyjs, DT, shiny, shinyBS, shinyAce, highcharter, htmlwidgets, webshot, R.utils, shinythemes, XML,later, rclipboard, shinycssloaders, future, promises, colourpicker, BiocManager, shinyjqui,shinyTree, shinyWidgets Suggests: BiocStyle, testthat License: Artistic-2.0 MD5sum: 34580bf16018a606bb064b4ce2b96aba NeedsCompilation: no Title: Provides a GUI for DAPAR Description: This package provides a GUI interface for DAPAR. biocViews: ImmunoOncology, MassSpectrometry, Normalization, Preprocessing, R.utils Proteomics,GO, GUI Author: Samuel Wieczorek [cre,aut], Florence Combes [aut], Thomas Burger [aut] Maintainer: Samuel Wieczorek git_url: https://git.bioconductor.org/packages/Prostar git_branch: RELEASE_3_8 git_last_commit: 2bae2f2 git_last_commit_date: 2019-03-06 Date/Publication: 2019-03-06 source.ver: src/contrib/Prostar_1.14.12.tar.gz win.binary.ver: bin/windows/contrib/3.5/Prostar_1.14.12.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Prostar_1.14.12.tgz vignettes: vignettes/Prostar/inst/doc/Prostar_UserManual.pdf vignetteTitles: Prostar user manual hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Prostar/inst/doc/Prostar_UserManual.R Package: prot2D Version: 1.20.0 Depends: R (>= 2.15),fdrtool,st,samr,Biobase,limma,Mulcom,impute,MASS,qvalue Suggests: made4,affy License: GPL (>= 2) MD5sum: 886c3086c4e35f8966e19c0c22facbfc NeedsCompilation: no Title: Statistical Tools for volume data from 2D Gel Electrophoresis Description: The purpose of this package is to analyze (i.e. Normalize and select significant spots) data issued from 2D GEl experiments biocViews: DifferentialExpression, MultipleComparison, Proteomics Author: Sebastien Artigaud Maintainer: Sebastien Artigaud PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/prot2D git_branch: RELEASE_3_8 git_last_commit: 4740d53 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/prot2D_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/prot2D_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/prot2D_1.20.0.tgz vignettes: vignettes/prot2D/inst/doc/prot2D.pdf vignetteTitles: prot2D hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/prot2D/inst/doc/prot2D.R Package: proteinProfiles Version: 1.22.0 Depends: R (>= 2.15.2) Imports: graphics, stats Suggests: testthat License: GPL-3 MD5sum: b6351027c4dfef576a396a03a053c864 NeedsCompilation: no Title: Protein Profiling Description: Significance assessment for distance measures of time-course protein profiles Author: Julian Gehring Maintainer: Julian Gehring git_url: https://git.bioconductor.org/packages/proteinProfiles git_branch: RELEASE_3_8 git_last_commit: 3afb962 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/proteinProfiles_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/proteinProfiles_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/proteinProfiles_1.22.0.tgz vignettes: vignettes/proteinProfiles/inst/doc/proteinProfiles.pdf vignetteTitles: The proteinProfiles package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/proteinProfiles/inst/doc/proteinProfiles.R Package: ProteomicsAnnotationHubData Version: 1.12.0 Depends: AnnotationHub (>= 2.1.45), AnnotationHubData, Imports: mzR (>= 2.3.2), MSnbase, Biostrings, GenomeInfoDb, utils, Biobase, BiocManager, RCurl Suggests: knitr, BiocStyle, rmarkdown, testthat License: Artistic-2.0 MD5sum: afbe09761bee9c27606041a3bef95f08 NeedsCompilation: no Title: Transform public proteomics data resources into Bioconductor Data Structures Description: These recipes convert a variety and a growing number of public proteomics data sets into easily-used standard Bioconductor data structures. biocViews: DataImport, Proteomics Author: Gatto Laurent [aut, cre], Sonali Arora [aut] Maintainer: Laurent Gatto URL: https://github.com/lgatto/ProteomicsAnnotationHubData VignetteBuilder: knitr BugReports: https://github.com/lgatto/ProteomicsAnnotationHubData/issues git_url: https://git.bioconductor.org/packages/ProteomicsAnnotationHubData git_branch: RELEASE_3_8 git_last_commit: 4b3e033 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ProteomicsAnnotationHubData_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ProteomicsAnnotationHubData_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ProteomicsAnnotationHubData_1.12.0.tgz vignettes: vignettes/ProteomicsAnnotationHubData/inst/doc/ProteomicsAnnotationHubData.html vignetteTitles: Proteomics Data in Annotation Hub hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ProteomicsAnnotationHubData/inst/doc/ProteomicsAnnotationHubData.R Package: ProteoMM Version: 1.0.1 Depends: R (>= 3.5) Imports: gdata, biomaRt, ggplot2, ggrepel, gtools, stats, matrixStats, graphics Suggests: BiocStyle, knitr, rmarkdown License: MIT MD5sum: 866dc078cf89001988f7fa74e118ef0d NeedsCompilation: no Title: Multi-Dataset Model-based Differential Expression Proteomics Analysis Platform Description: ProteoMM is a statistical method to perform model-based peptide-level differential expression analysis of single or multiple datasets. For multiple datasets ProteoMM produces a single fold change and p-value for each protein across multiple datasets. ProteoMM provides functionality for normalization, missing value imputation and differential expression. Model-based peptide-level imputation and differential expression analysis component of package follows the analysis described in “A statistical framework for protein quantitation in bottom-up MS based proteomics" (Karpievitch et al. Bioinformatics 2009). EigenMS normalisation is implemented as described in "Normalization of peak intensities in bottom-up MS-based proteomics using singular value decomposition." (Karpievitch et al. Bioinformatics 2009). biocViews: ImmunoOncology, MassSpectrometry, Proteomics, Normalization, DifferentialExpression Author: Yuliya V Karpievitch, Tim Stuart and Sufyaan Mohamed Maintainer: Yuliya V Karpievitch VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ProteoMM git_branch: RELEASE_3_8 git_last_commit: a295c86 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ProteoMM_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ProteoMM_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ProteoMM_1.0.1.tgz vignettes: vignettes/ProteoMM/inst/doc/ProteoMM_vignette.html vignetteTitles: Multi-Dataset Model-based Differential Expression Proteomics Platform hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ProteoMM/inst/doc/ProteoMM_vignette.R Package: proteoQC Version: 1.18.1 Depends: R (>= 3.0.0), XML, VennDiagram, MSnbase Imports: rTANDEM, plyr, seqinr, Nozzle.R1, ggplot2, reshape2, parallel, rpx, tidyr, dplyr, plotly, rmarkdown, Suggests: RforProteomics, knitr, BiocStyle, R.utils, RUnit,BiocGenerics License: LGPL-2 MD5sum: d8b9baf4fbe7c1615a3afc90c4dfbce5 NeedsCompilation: no Title: An R package for proteomics data quality control Description: This package creates an HTML format QC report for MS/MS-based proteomics data. The report is intended to allow the user to quickly assess the quality of proteomics data. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, QualityControl, Visualization, ReportWriting Author: Bo Wen , Laurent Gatto Maintainer: Bo Wen URL: https://github.com/wenbostar/proteoQC VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/proteoQC git_branch: RELEASE_3_8 git_last_commit: bb59619 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/proteoQC_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/proteoQC_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/proteoQC_1.18.1.tgz vignettes: vignettes/proteoQC/inst/doc/proteoQC.html vignetteTitles: 00 proteoQC introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/proteoQC/inst/doc/proteoQC.R Package: ProtGenerics Version: 1.14.0 Depends: methods License: Artistic-2.0 MD5sum: 837d899bc08e3518bf11a892f6b95e50 NeedsCompilation: no Title: S4 generic functions for Bioconductor proteomics infrastructure Description: S4 generic functions needed by Bioconductor proteomics packages. biocViews: Infrastructure, Proteomics, MassSpectrometry Author: Laurent Gatto Maintainer: Laurent Gatto URL: https://github.com/lgatto/ProtGenerics git_url: https://git.bioconductor.org/packages/ProtGenerics git_branch: RELEASE_3_8 git_last_commit: c85940b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ProtGenerics_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ProtGenerics_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ProtGenerics_1.14.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: Cardinal, MSnbase, tofsims, topdownr importsMe: ensembldb, MSGFplus, MSnID, mzID, mzR, xcms Package: PSEA Version: 1.16.0 Imports: Biobase, MASS Suggests: BiocStyle License: Artistic-2.0 MD5sum: 70a53aecf51323ffa3ed319f0983e175 NeedsCompilation: no Title: Population-Specific Expression Analysis. Description: Deconvolution of gene expression data by Population-Specific Expression Analysis (PSEA). biocViews: Software Author: Alexandre Kuhn Maintainer: Alexandre Kuhn git_url: https://git.bioconductor.org/packages/PSEA git_branch: RELEASE_3_8 git_last_commit: c41ec7e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PSEA_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PSEA_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PSEA_1.16.0.tgz vignettes: vignettes/PSEA/inst/doc/PSEA_RNAmixtures.pdf, vignettes/PSEA/inst/doc/PSEA.pdf vignetteTitles: PSEA: Deconvolution of RNA mixtures in Nature Methods paper, PSEA: Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PSEA/inst/doc/PSEA_RNAmixtures.R, vignettes/PSEA/inst/doc/PSEA.R Package: psichomics Version: 1.8.2 Depends: R (>= 3.5), shiny (>= 1.0.3), shinyBS Imports: AnnotationDbi, AnnotationHub, cluster, colourpicker, data.table, digest, dplyr, DT (>= 0.2), edgeR, fastICA, fastmatch, ggplot2, ggrepel, graphics, grDevices, highcharter (>= 0.5.0), htmltools, httr, jsonlite, limma, miscTools, pairsD3, plyr, Rcpp (>= 0.12.14), recount, R.utils, reshape2, shinyjs, stringr, stats, SummarizedExperiment, survival, tools, utils, XML, xtable, methods, org.Hs.eg.db LinkingTo: Rcpp Suggests: testthat, knitr, parallel, devtools, rmarkdown, gplots, covr, car, rstudioapi License: MIT + file LICENSE MD5sum: 3db39c92cc279bd625945359418ccde9 NeedsCompilation: yes Title: Graphical Interface for Alternative Splicing Quantification, Analysis and Visualisation Description: Interactive R package with an intuitive Shiny-based graphical interface for alternative splicing quantification and integrative analyses of alternative splicing and gene expression based on The Cancer Genome Atlas (TCGA), the Genotype-Tissue Expression project (GTEx), Sequence Read Archive (SRA) and user-provided data. The tool interactively performs survival, dimensionality reduction and median- and variance-based differential splicing and gene expression analyses that benefit from the incorporation of clinical and molecular sample-associated features (such as tumour stage or survival). Interactive visual access to genomic mapping and functional annotation of selected alternative splicing events is also included. biocViews: Sequencing, RNASeq, AlternativeSplicing, DifferentialSplicing, Transcription, GUI, PrincipalComponent, Survival, BiomedicalInformatics, Transcriptomics, ImmunoOncology, Visualization, MultipleComparison, GeneExpression, DifferentialExpression Author: Nuno Saraiva-Agostinho [aut, cre], Nuno Luís Barbosa-Morais [aut, led, ths], André Falcão [ths], Lina Gallego Paez [ctb], Marie Bordone [ctb], Teresa Maia [ctb], Mariana Ferreira [ctb], Ana Carolina Leote [ctb], Bernardo de Almeida [ctb] Maintainer: Nuno Saraiva-Agostinho URL: https://github.com/nuno-agostinho/psichomics VignetteBuilder: knitr BugReports: https://github.com/nuno-agostinho/psichomics/issues git_url: https://git.bioconductor.org/packages/psichomics git_branch: RELEASE_3_8 git_last_commit: 5490eef git_last_commit_date: 2019-03-27 Date/Publication: 2019-03-27 source.ver: src/contrib/psichomics_1.8.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/psichomics_1.8.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/psichomics_1.8.2.tgz vignettes: vignettes/psichomics/inst/doc/AS_events_preparation.html, vignettes/psichomics/inst/doc/CLI_tutorial.html, vignettes/psichomics/inst/doc/custom_data.html, vignettes/psichomics/inst/doc/GUI_tutorial.html vignetteTitles: Preparing alternative splicing annotations, Case study: command-line interface (CLI), SRA and user-provided RNA-seq data analysis, Case study: visual interface hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/psichomics/inst/doc/AS_events_preparation.R, vignettes/psichomics/inst/doc/CLI_tutorial.R, vignettes/psichomics/inst/doc/custom_data.R, vignettes/psichomics/inst/doc/GUI_tutorial.R Package: PSICQUIC Version: 1.20.0 Depends: R (>= 3.2.2), methods, IRanges, biomaRt (>= 2.34.1), BiocGenerics, httr, plyr Imports: RCurl Suggests: org.Hs.eg.db License: Apache License 2.0 Archs: i386, x64 MD5sum: 019a4417247c16e5ebcdf22ffac1c77b NeedsCompilation: no Title: Proteomics Standard Initiative Common QUery InterfaCe Description: PSICQUIC is a project within the HUPO Proteomics Standard Initiative (HUPO-PSI). It standardises programmatic access to molecular interaction databases. biocViews: DataImport, GraphAndNetwork, ThirdPartyClient Author: Paul Shannon Maintainer: Paul Shannon git_url: https://git.bioconductor.org/packages/PSICQUIC git_branch: RELEASE_3_8 git_last_commit: 0019202 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-31 source.ver: src/contrib/PSICQUIC_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PSICQUIC_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PSICQUIC_1.20.0.tgz vignettes: vignettes/PSICQUIC/inst/doc/PSICQUIC.pdf vignetteTitles: PSICQUIC hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PSICQUIC/inst/doc/PSICQUIC.R dependsOnMe: RefNet Package: psygenet2r Version: 1.14.0 Depends: R (>= 3.4) Imports: stringr, RCurl, igraph, ggplot2, reshape2, grid, parallel, biomaRt, BgeeDB, topGO, BiocManager, Biobase, labeling, GO.db Suggests: testthat, knitr License: MIT + file LICENSE MD5sum: ad685186daa974d0b5e6b91e0cc7d0b8 NeedsCompilation: no Title: psygenet2r - An R package for querying PsyGeNET and to perform comorbidity studies in psychiatric disorders Description: Package to retrieve data from PsyGeNET database (www.psygenet.org) and to perform comorbidity studies with PsyGeNET's and user's data. biocViews: Software, BiomedicalInformatics, Genetics, Infrastructure, DataImport, DataRepresentation Author: Alba Gutierrez-Sacristan [aut, cre], Carles Hernandez-Ferrer [aut], Jaun R. Gonzalez [aut], Laura I. Furlong [aut] Maintainer: Alba Gutierrez-Sacristan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/psygenet2r git_branch: RELEASE_3_8 git_last_commit: ff765b2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/psygenet2r_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/psygenet2r_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/psygenet2r_1.14.0.tgz vignettes: vignettes/psygenet2r/inst/doc/case_study.html, vignettes/psygenet2r/inst/doc/general_overview.html vignetteTitles: psygenet2r: Case study on GWAS on bipolar disorder, psygenet2r: An R package for querying PsyGeNET and to perform comorbidity studies in psychiatric disorders hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/psygenet2r/inst/doc/case_study.R, vignettes/psygenet2r/inst/doc/general_overview.R Package: puma Version: 3.24.0 Depends: R (>= 3.2.0), oligo (>= 1.32.0),graphics,grDevices, methods, stats, utils, mclust, oligoClasses Imports: Biobase (>= 2.5.5), affy (>= 1.46.0), affyio, oligoClasses Suggests: pumadata, affydata, snow, limma, ROCR,annotate License: LGPL MD5sum: c27be11118a5db7432f6b9cde9f06d5b NeedsCompilation: yes Title: Propagating Uncertainty in Microarray Analysis(including Affymetrix tranditional 3' arrays and exon arrays and Human Transcriptome Array 2.0) Description: Most analyses of Affymetrix GeneChip data (including tranditional 3' arrays and exon arrays and Human Transcriptome Array 2.0) are based on point estimates of expression levels and ignore the uncertainty of such estimates. By propagating uncertainty to downstream analyses we can improve results from microarray analyses. For the first time, the puma package makes a suite of uncertainty propagation methods available to a general audience. In additon to calculte gene expression from Affymetrix 3' arrays, puma also provides methods to process exon arrays and produces gene and isoform expression for alternative splicing study. puma also offers improvements in terms of scope and speed of execution over previously available uncertainty propagation methods. Included are summarisation, differential expression detection, clustering and PCA methods, together with useful plotting functions. biocViews: Microarray, OneChannel, Preprocessing, DifferentialExpression, Clustering, ExonArray, GeneExpression, mRNAMicroarray, ChipOnChip, AlternativeSplicing, DifferentialSplicing, Bayesian, TwoChannel, DataImport, HTA2.0 Author: Richard D. Pearson, Xuejun Liu, Magnus Rattray, Marta Milo, Neil D. Lawrence, Guido Sanguinetti, Li Zhang Maintainer: Xuejun Liu URL: http://umber.sbs.man.ac.uk/resources/puma git_url: https://git.bioconductor.org/packages/puma git_branch: RELEASE_3_8 git_last_commit: aeac592 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/puma_3.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/puma_3.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/puma_3.24.0.tgz vignettes: vignettes/puma/inst/doc/puma.pdf vignetteTitles: puma User Guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/puma/inst/doc/puma.R suggestsMe: tigre Package: PureCN Version: 1.12.2 Depends: R (>= 3.3), DNAcopy, VariantAnnotation (>= 1.14.1) Imports: GenomicRanges (>= 1.20.3), IRanges (>= 2.2.1), RColorBrewer, S4Vectors, data.table, grDevices, graphics, stats, utils, SummarizedExperiment, GenomeInfoDb, GenomicFeatures, Rsamtools, Biostrings, BiocGenerics, rtracklayer, ggplot2, gridExtra, futile.logger, VGAM, tools, rhdf5, Matrix Suggests: PSCBS, BiocStyle, BiocParallel, knitr, optparse, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db, covr, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: 23a314e7e4b704ba5ebb1178ac978ae9 NeedsCompilation: no Title: Copy number calling and SNV classification using targeted short read sequencing Description: This package estimates tumor purity, copy number, and loss of heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by somatic status and clonality. PureCN is designed for targeted short read sequencing data, integrates well with standard somatic variant detection and copy number pipelines, and has support for tumor samples without matching normal samples. biocViews: ImmunoOncology, CopyNumberVariation, Software, Sequencing, VariantAnnotation, VariantDetection, Coverage Author: Markus Riester [aut, cre], Angad P. Singh [aut] Maintainer: Markus Riester URL: https://github.com/lima1/PureCN VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PureCN git_branch: RELEASE_3_8 git_last_commit: 08de7f8 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/PureCN_1.12.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/PureCN_1.12.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PureCN_1.12.2.tgz vignettes: vignettes/PureCN/inst/doc/PureCN.pdf, vignettes/PureCN/inst/doc/Quick.pdf vignetteTitles: PureCN overview, Quick start and command line usage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PureCN/inst/doc/PureCN.R, vignettes/PureCN/inst/doc/Quick.R Package: pvac Version: 1.30.0 Depends: R (>= 2.8.0) Imports: affy (>= 1.20.0), stats, Biobase Suggests: pbapply, affydata, ALLMLL, genefilter License: LGPL (>= 2.0) MD5sum: 2d1c05d44125333ae877c99001bcfa6b NeedsCompilation: no Title: PCA-based gene filtering for Affymetrix arrays Description: The package contains the function for filtering genes by the proportion of variation accounted for by the first principal component (PVAC). biocViews: Microarray, OneChannel, QualityControl Author: Jun Lu and Pierre R. Bushel Maintainer: Jun Lu , Pierre R. Bushel git_url: https://git.bioconductor.org/packages/pvac git_branch: RELEASE_3_8 git_last_commit: 58b4e6e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pvac_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pvac_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pvac_1.30.0.tgz vignettes: vignettes/pvac/inst/doc/pvac.pdf vignetteTitles: PCA-based gene filtering for Affymetrix GeneChips hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pvac/inst/doc/pvac.R Package: pvca Version: 1.22.0 Depends: R (>= 2.15.1) Imports: Matrix, Biobase, vsn, stats, lme4 Suggests: golubEsets License: LGPL (>= 2.0) MD5sum: d138f4edb7fa0c055c6f0abad5dac160 NeedsCompilation: no Title: Principal Variance Component Analysis (PVCA) Description: This package contains the function to assess the batch sourcs by fitting all "sources" as random effects including two-way interaction terms in the Mixed Model(depends on lme4 package) to selected principal components, which were obtained from the original data correlation matrix. This package accompanies the book "Batch Effects and Noise in Microarray Experiements, chapter 12. biocViews: Microarray, BatchEffect Author: Pierre Bushel Maintainer: Jianying LI git_url: https://git.bioconductor.org/packages/pvca git_branch: RELEASE_3_8 git_last_commit: 8459d79 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pvca_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pvca_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pvca_1.22.0.tgz vignettes: vignettes/pvca/inst/doc/pvca.pdf vignetteTitles: Batch effect estimation in Microarray data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/pvca/inst/doc/pvca.R Package: Pviz Version: 1.16.0 Depends: R(>= 3.0.0), Gviz(>= 1.7.10) Imports: biovizBase, Biostrings, GenomicRanges, IRanges, data.table, methods Suggests: knitr, pepDat License: Artistic-2.0 MD5sum: f5bd670dee87e666b06e6e506d39c2e0 NeedsCompilation: no Title: Peptide Annotation and Data Visualization using Gviz Description: Pviz adapts the Gviz package for protein sequences and data. biocViews: Visualization, Proteomics, Microarray Author: Renan Sauteraud, Mike Jiang, Raphael Gottardo Maintainer: Renan Sauteraud VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Pviz git_branch: RELEASE_3_8 git_last_commit: c6a6fbc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Pviz_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Pviz_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Pviz_1.16.0.tgz vignettes: vignettes/Pviz/inst/doc/Pviz.pdf vignetteTitles: The Pviz users guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Pviz/inst/doc/Pviz.R importsMe: Pbase suggestsMe: pepStat Package: PWMEnrich Version: 4.18.0 Depends: methods, grid, BiocGenerics, Biostrings, Imports: seqLogo, gdata, evd Suggests: MotifDb, BSgenome.Dmelanogaster.UCSC.dm3, PWMEnrich.Dmelanogaster.background, testthat, gtools, parallel, PWMEnrich.Hsapiens.background, PWMEnrich.Mmusculus.background, BiocStyle, knitr License: LGPL (>= 2) MD5sum: b04f4faa148db904e60269da8b987bd6 NeedsCompilation: no Title: PWM enrichment analysis Description: A toolkit of high-level functions for DNA motif scanning and enrichment analysis built upon Biostrings. The main functionality is PWM enrichment analysis of already known PWMs (e.g. from databases such as MotifDb), but the package also implements high-level functions for PWM scanning and visualisation. The package does not perform "de novo" motif discovery, but is instead focused on using motifs that are either experimentally derived or computationally constructed by other tools. biocViews: MotifAnnotation, SequenceMatching, Software Author: Robert Stojnic, Diego Diez Maintainer: Robert Stojnic VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/PWMEnrich git_branch: RELEASE_3_8 git_last_commit: 62031bb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/PWMEnrich_4.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/PWMEnrich_4.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/PWMEnrich_4.18.0.tgz vignettes: vignettes/PWMEnrich/inst/doc/PWMEnrich.pdf vignetteTitles: Overview of the 'PWMEnrich' package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/PWMEnrich/inst/doc/PWMEnrich.R suggestsMe: rTRM, universalmotif Package: pwOmics Version: 1.14.0 Depends: R (>= 3.2) Imports: data.table, rBiopaxParser, igraph, STRINGdb, graphics, gplots, Biobase, BiocGenerics, AnnotationDbi, biomaRt, AnnotationHub, GenomicRanges, graph, grDevices, stats, utils Suggests: ebdbNet, longitudinal, Mfuzz License: GPL (>= 2) MD5sum: e762db025a30377ad4908bb3191d20e8 NeedsCompilation: no Title: Pathway-based data integration of omics data Description: pwOmics performs pathway-based level-specific data comparison of matching omics data sets based on pre-analysed user-specified lists of differential genes/transcripts and phosphoproteins. A separate downstream analysis of phosphoproteomic data including pathway identification, transcription factor identification and target gene identification is opposed to the upstream analysis starting with gene or transcript information as basis for identification of upstream transcription factors and potential proteomic regulators. The cross-platform comparative analysis allows for comprehensive analysis of single time point experiments and time-series experiments by providing static and dynamic analysis tools for data integration. In addition, it provides functions to identify individual signaling axes based on data integration. biocViews: SystemsBiology, Transcription, GeneTarget, GeneSignaling Author: Astrid Wachter Maintainer: Maren Sitte git_url: https://git.bioconductor.org/packages/pwOmics git_branch: RELEASE_3_8 git_last_commit: 1af1abe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/pwOmics_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/pwOmics_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/pwOmics_1.14.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: qcmetrics Version: 1.20.1 Depends: R (>= 3.3) Imports: Biobase, methods, knitr, tools, Nozzle.R1, xtable, pander, S4Vectors Suggests: affy, MSnbase, ggplot2, lattice, yaqcaffy, MAQCsubsetAFX, RforProteomics, AnnotationDbi, mzR, hgu133plus2cdf, BiocStyle License: GPL-2 MD5sum: d0608a6075048a6619562bb3c26ff9bf NeedsCompilation: no Title: A Framework for Quality Control Description: The package provides a framework for generic quality control of data. It permits to create, manage and visualise individual or sets of quality control metrics and generate quality control reports in various formats. biocViews: ImmunoOncology, Software, QualityControl, Proteomics, Microarray, MassSpectrometry, Visualization, ReportWriting Author: Laurent Gatto [aut, cre] Maintainer: Laurent Gatto URL: https://github.com/lgatto/qcmetrics VignetteBuilder: knitr BugReports: https://github.com/lgatto/qcmetrics/issues git_url: https://git.bioconductor.org/packages/qcmetrics git_branch: RELEASE_3_8 git_last_commit: b404c75 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/qcmetrics_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/qcmetrics_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qcmetrics_1.20.1.tgz vignettes: vignettes/qcmetrics/inst/doc/qcmetrics.pdf, vignettes/qcmetrics/inst/doc/vig-index.html vignetteTitles: The 'qcmetrics' infrastructure for quality control and reporting, Index file for the qcmetrics package vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qcmetrics/inst/doc/qcmetrics.R, vignettes/qcmetrics/inst/doc/vig-index.R importsMe: MSstatsQC Package: QDNAseq Version: 1.18.0 Depends: R (>= 3.1.0) Imports: graphics, methods, stats, utils, Biobase (>= 2.18.0), CGHbase (>= 1.18.0), CGHcall (>= 2.18.0), DNAcopy (>= 1.32.0), GenomicRanges (>= 1.20), IRanges (>= 2.2), matrixStats (>= 0.50.2), R.utils (>= 2.3.0), Rsamtools (>= 1.20), BiocParallel (>= 1.6.6), Suggests: BiocStyle (>= 1.8.0), BSgenome (>= 1.38.0), digest (>= 0.6.8), GenomeInfoDb (>= 1.6.0), future (>= 0.14.0), R.cache (>= 0.12.0) License: GPL MD5sum: d25872be8df20f65786d1df51d79181b NeedsCompilation: no Title: Quantitative DNA sequencing for chromosomal aberrations Description: Quantitative DNA sequencing for chromosomal aberrations. The genome is divided into non-overlapping fixed-sized bins, number of sequence reads in each counted, adjusted with a simultaneous two-dimensional loess correction for sequence mappability and GC content, and filtered to remove spurious regions in the genome. Downstream steps of segmentation and calling are also implemented via packages DNAcopy and CGHcall, respectively. biocViews: CopyNumberVariation, DNASeq, Genetics, GenomeAnnotation, Preprocessing, QualityControl, Sequencing Author: Ilari Scheinin [aut], Daoud Sie [aut, cre], Henrik Bengtsson [aut] Maintainer: Daoud Sie URL: https://github.com/ccagc/QDNAseq BugReports: https://github.com/ccagc/QDNAseq/issues git_url: https://git.bioconductor.org/packages/QDNAseq git_branch: RELEASE_3_8 git_last_commit: e78591d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/QDNAseq_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/QDNAseq_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QDNAseq_1.18.0.tgz vignettes: vignettes/QDNAseq/inst/doc/QDNAseq.pdf vignetteTitles: Introduction to QDNAseq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/QDNAseq/inst/doc/QDNAseq.R dependsOnMe: GeneBreak importsMe: ACE, HiCcompare Package: qpcrNorm Version: 1.40.0 Depends: methods, Biobase, limma, affy License: LGPL (>= 2) MD5sum: 16a79fad66a1af84d66805d099ba0c58 NeedsCompilation: no Title: Data-driven normalization strategies for high-throughput qPCR data. Description: The package contains functions to perform normalization of high-throughput qPCR data. Basic functions for processing raw Ct data plus functions to generate diagnostic plots are also available. biocViews: Preprocessing, GeneExpression Author: Jessica Mar Maintainer: Jessica Mar git_url: https://git.bioconductor.org/packages/qpcrNorm git_branch: RELEASE_3_8 git_last_commit: 54cc773 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/qpcrNorm_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/qpcrNorm_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qpcrNorm_1.40.0.tgz vignettes: vignettes/qpcrNorm/inst/doc/qpcrNorm.pdf vignetteTitles: qPCR Normalization Example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qpcrNorm/inst/doc/qpcrNorm.R suggestsMe: EasyqpcR Package: qpgraph Version: 2.16.0 Depends: R (>= 3.4) Imports: methods, parallel, Matrix (>= 1.0), grid, annotate, graph (>= 1.45.1), Biobase, S4Vectors, BiocParallel, AnnotationDbi, IRanges, GenomeInfoDb, GenomicRanges, GenomicFeatures, mvtnorm, qtl, Rgraphviz Suggests: RUnit, BiocGenerics, BiocStyle, genefilter, org.EcK12.eg.db, rlecuyer, snow, Category, GOstats License: GPL (>= 2) MD5sum: c31410ede77ec4bde909a2755488d2af NeedsCompilation: yes Title: Estimation of genetic and molecular regulatory networks from high-throughput genomics data Description: Estimate gene and eQTL networks from high-throughput expression and genotyping assays. biocViews: Microarray, GeneExpression, Transcription, Pathways, NetworkInference, GraphAndNetwork, GeneRegulation, Genetics, GeneticVariability, SNP, Software Author: Robert Castelo [aut, cre], Alberto Roverato [aut] Maintainer: Robert Castelo URL: https://github.com/rcastelo/qpgraph BugReports: https://github.com/rcastelo/rcastelo/issues git_url: https://git.bioconductor.org/packages/qpgraph git_branch: RELEASE_3_8 git_last_commit: c128a5f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/qpgraph_2.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/qpgraph_2.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qpgraph_2.16.0.tgz vignettes: vignettes/qpgraph/inst/doc/BasicUsersGuide.pdf, vignettes/qpgraph/inst/doc/eQTLnetworks.pdf, vignettes/qpgraph/inst/doc/qpgraphSimulate.pdf, vignettes/qpgraph/inst/doc/qpTxRegNet.pdf vignetteTitles: BasicUsersGuide.pdf, Estimate eQTL networks using qpgraph, Simulating molecular regulatory networks using qpgraph, Reverse-engineer transcriptional regulatory networks using qpgraph hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qpgraph/inst/doc/eQTLnetworks.R, vignettes/qpgraph/inst/doc/qpgraphSimulate.R, vignettes/qpgraph/inst/doc/qpTxRegNet.R importsMe: clipper Package: qPLEXanalyzer Version: 1.0.4 Depends: R (>= 3.5), Biobase, statmod, MSnbase Imports: tidyr, preprocessCore, limma, ggplot2, RColorBrewer, stats, utils, Biostrings, GenomicRanges, IRanges, graphics, BiocGenerics, stringr, purrr, tibble, ggdendro, grDevices, dplyr, magrittr, assertthat Suggests: UniProt.ws, knitr, qPLEXdata License: GPL-2 Archs: i386, x64 MD5sum: 8d736d0978292b9f5fad663b89a2c5c5 NeedsCompilation: no Title: Tools for qPLEX-RIME data analysis Description: Tools for quantitative proteomics data analysis generated from qPLEX-RIME method. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, Normalization, Preprocessing, QualityControl, DataImport Author: Matthew Eldridge [aut], Kamal Kishore [aut], Ashley Sawle [aut, cre] Maintainer: Ashley Sawle VignetteBuilder: knitr BugReports: https://github.com/crukci-bioinformatics/qPLEXanalyzer/issues git_url: https://git.bioconductor.org/packages/qPLEXanalyzer git_branch: RELEASE_3_8 git_last_commit: 06e9dd2 git_last_commit_date: 2019-04-09 Date/Publication: 2019-04-09 source.ver: src/contrib/qPLEXanalyzer_1.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/qPLEXanalyzer_1.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qPLEXanalyzer_1.0.4.tgz vignettes: vignettes/qPLEXanalyzer/inst/doc/qPLEXanalyzer.pdf vignetteTitles: qPLEXanalyzer.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qPLEXanalyzer/inst/doc/qPLEXanalyzer.R Package: qrqc Version: 1.36.0 Depends: reshape, ggplot2, Biostrings, biovizBase, brew, xtable, Rsamtools (>= 1.19.38), testthat Imports: reshape, ggplot2, Biostrings, biovizBase, graphics, methods, plyr, stats LinkingTo: Rsamtools License: GPL (>=2) MD5sum: f6cafce11da089f3c97ce564659f07a4 NeedsCompilation: yes Title: Quick Read Quality Control Description: Quickly scans reads and gathers statistics on base and quality frequencies, read length, k-mers by position, and frequent sequences. Produces graphical output of statistics for use in quality control pipelines, and an optional HTML quality report. S4 SequenceSummary objects allow specific tests and functionality to be written around the data collected. biocViews: Sequencing, QualityControl, DataImport, Preprocessing, Visualization Author: Vince Buffalo Maintainer: Vince Buffalo URL: http://github.com/vsbuffalo/qrqc git_url: https://git.bioconductor.org/packages/qrqc git_branch: RELEASE_3_8 git_last_commit: fb80b84 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/qrqc_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/qrqc_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qrqc_1.36.0.tgz vignettes: vignettes/qrqc/inst/doc/qrqc.pdf vignetteTitles: Using the qrqc package to gather information about sequence qualities hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qrqc/inst/doc/qrqc.R Package: qsea Version: 1.8.0 Depends: R (>= 3.5) Imports: Biostrings, graphics, gtools, methods, stats, utils, HMMcopy, rtracklayer, BSgenome, GenomicRanges, Rsamtools, IRanges, limma, GenomeInfoDb, BiocGenerics, grDevices, zoo, BiocParallel Suggests: BSgenome.Hsapiens.UCSC.hg19, MEDIPSData, testthat, BiocStyle, knitr, rmarkdown, BiocManager License: GPL (>=2) Archs: i386, x64 MD5sum: c2a094a5f1c9135228c41eef8ac4f639 NeedsCompilation: yes Title: IP-seq data analysis and vizualization Description: qsea (quantitative sequencing enrichment analysis) was developed as the successor of the MEDIPS package for analyzing data derived from methylated DNA immunoprecipitation (MeDIP) experiments followed by sequencing (MeDIP-seq). However, qsea provides several functionalities for the analysis of other kinds of quantitative sequencing data (e.g. ChIP-seq, MBD-seq, CMS-seq and others) including calculation of differential enrichment between groups of samples. biocViews: Sequencing, DNAMethylation, CpGIsland, ChIPSeq, Preprocessing, Normalization, QualityControl, Visualization, CopyNumberVariation, ChipOnChip, DifferentialMethylation Author: Matthias Lienhard, Lukas Chavez, Ralf Herwig Maintainer: Matthias Lienhard VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/qsea git_branch: RELEASE_3_8 git_last_commit: 7e31008 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/qsea_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/qsea_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qsea_1.8.0.tgz vignettes: vignettes/qsea/inst/doc/qsea_tutorial.html vignetteTitles: qsea hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qsea/inst/doc/qsea_tutorial.R Package: QSutils Version: 1.0.0 Depends: R (>= 3.5), Biostrings, BiocGenerics,methods Imports: ape, stats, psych Suggests: BiocStyle, knitr, rmarkdown, ggplot2 License: file LICENSE Archs: i386, x64 MD5sum: 1dcee86cb9a096cdc552fb279ce8f094 NeedsCompilation: no Title: Quasispecies Diversity Description: Set of utility functions for viral quasispecies analysis with NGS data. Most functions are equally useful for metagenomic studies. There are three main types: (1) data manipulation and exploration—functions useful for converting reads to haplotypes and frequencies, repairing reads, intersecting strand haplotypes, and visualizing haplotype alignments. (2) diversity indices—functions to compute diversity and entropy, in which incidence, abundance, and functional indices are considered. (3) data simulation—functions useful for generating random viral quasispecies data. biocViews: Software, Genetics, DNASeq, GeneticVariability, Sequencing, Alignment, SequenceMatching, DataImport Author: Mercedes Guerrero-Murillo and Josep Gregori i Font Maintainer: Mercedes Guerrero-Murillo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/QSutils git_branch: RELEASE_3_8 git_last_commit: 85827df git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/QSutils_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/QSutils_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QSutils_1.0.0.tgz vignettes: vignettes/QSutils/inst/doc/QSUtils-Alignment.html, vignettes/QSutils/inst/doc/QSutils-Diversity.html, vignettes/QSutils/inst/doc/QSutils-Simulation.html vignetteTitles: QSUtils-Alignment, QSutils-Diversity, QSutils-Simulation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/QSutils/inst/doc/QSUtils-Alignment.R, vignettes/QSutils/inst/doc/QSutils-Diversity.R, vignettes/QSutils/inst/doc/QSutils-Simulation.R Package: QUALIFIER Version: 1.26.1 Depends: R (>= 2.14.0),flowCore,flowViz,ncdfFlow,flowWorkspace, data.table,reshape Imports: MASS,hwriter,lattice,stats4,flowCore,flowViz,methods,flowWorkspace,latticeExtra,grDevices,tools, Biobase,XML,grid Suggests: RSVGTipsDevice, knitr License: Artistic-2.0 MD5sum: acc83dad5c3de23398ef292f3c78cb1b NeedsCompilation: no Title: Quality Control of Gated Flow Cytometry Experiments Description: Provides quality control and quality assessment tools for gated flow cytometry data. biocViews: ImmunoOncology, Infrastructure, FlowCytometry, CellBasedAssays Author: Mike Jiang,Greg Finak,Raphael Gottardo Maintainer: Mike Jiang VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/QUALIFIER git_branch: RELEASE_3_8 git_last_commit: 3c4dd17 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/QUALIFIER_1.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/QUALIFIER_1.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QUALIFIER_1.26.1.tgz vignettes: vignettes/QUALIFIER/inst/doc/QUALIFIER.html vignetteTitles: Quick plot for cytometry data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/QUALIFIER/inst/doc/QUALIFIER.R Package: quantro Version: 1.16.0 Depends: R (>= 3.1.3) Imports: Biobase, minfi, doParallel, foreach, iterators, ggplot2, methods, RColorBrewer Suggests: knitr, RUnit, BiocGenerics, BiocStyle License: GPL (>=3) MD5sum: f7d79a596f7a2e9c965a1e341aeca26c NeedsCompilation: no Title: A test for when to use quantile normalization Description: A data-driven test for the assumptions of quantile normalization using raw data such as objects that inherit eSets (e.g. ExpressionSet, MethylSet). Group level information about each sample (such as Tumor / Normal status) must also be provided because the test assesses if there are global differences in the distributions between the user-defined groups. biocViews: Normalization, Preprocessing, MultipleComparison, Microarray, Sequencing Author: Stephanie Hicks and Rafael Irizarry Maintainer: Stephanie Hicks VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/quantro git_branch: RELEASE_3_8 git_last_commit: cfc2e85 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/quantro_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/quantro_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/quantro_1.16.0.tgz vignettes: vignettes/quantro/inst/doc/quantro-vignette.pdf vignetteTitles: The quantro user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/quantro/inst/doc/quantro-vignette.R importsMe: yarn Package: quantsmooth Version: 1.48.0 Depends: R(>= 2.10.0), quantreg, grid License: GPL-2 MD5sum: 6617f7e9ad5b4d7f66a5eb214d6b7cee NeedsCompilation: no Title: Quantile smoothing and genomic visualization of array data Description: Implements quantile smoothing as introduced in: Quantile smoothing of array CGH data; Eilers PH, de Menezes RX; Bioinformatics. 2005 Apr 1;21(7):1146-53. biocViews: Visualization, CopyNumberVariation Author: Jan Oosting, Paul Eilers, Renee Menezes Maintainer: Jan Oosting git_url: https://git.bioconductor.org/packages/quantsmooth git_branch: RELEASE_3_8 git_last_commit: 693fc29 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/quantsmooth_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/quantsmooth_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/quantsmooth_1.48.0.tgz vignettes: vignettes/quantsmooth/inst/doc/quantsmooth.pdf vignetteTitles: quantsmooth hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/quantsmooth/inst/doc/quantsmooth.R dependsOnMe: beadarraySNP importsMe: GWASTools, SIM suggestsMe: PREDA Package: QuartPAC Version: 1.14.0 Depends: iPAC, GraphPAC, SpacePAC, data.table Suggests: RUnit, BiocGenerics, rgl License: GPL-2 MD5sum: f423fa2cb29443befb977c06700a8dcf NeedsCompilation: no Title: Identification of mutational clusters in protein quaternary structures. Description: Identifies clustering of somatic mutations in proteins over the entire quaternary structure. biocViews: Clustering, Proteomics, SomaticMutation Author: Gregory Ryslik, Yuwei Cheng, Hongyu Zhao Maintainer: Gregory Ryslik git_url: https://git.bioconductor.org/packages/QuartPAC git_branch: RELEASE_3_8 git_last_commit: 9b77264 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/QuartPAC_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/QuartPAC_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QuartPAC_1.14.0.tgz vignettes: vignettes/QuartPAC/inst/doc/QuartPAC.pdf vignetteTitles: SpacePAC: Identifying mutational clusters in 3D protein space using simulation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/QuartPAC/inst/doc/QuartPAC.R Package: QuasR Version: 1.22.1 Depends: parallel, GenomicRanges (>= 1.13.3), Rbowtie Imports: methods, grDevices, graphics, utils, zlibbioc, BiocGenerics, S4Vectors (>= 0.9.25), IRanges, BiocManager, Biobase, Biostrings, BSgenome, Rsamtools (>= 1.19.38), GenomicFeatures (>= 1.17.13), ShortRead (>= 1.19.1), GenomicAlignments, BiocParallel, GenomeInfoDb, rtracklayer, GenomicFiles LinkingTo: Rsamtools Suggests: Gviz, RUnit, BiocStyle, knitr, rmarkdown License: GPL-2 MD5sum: 4add73c5e114233621711ace6c8d1e35 NeedsCompilation: yes Title: Quantify and Annotate Short Reads in R Description: This package provides a framework for the quantification and analysis of Short Reads. It covers a complete workflow starting from raw sequence reads, over creation of alignments and quality control plots, to the quantification of genomic regions of interest. biocViews: Genetics, Preprocessing, Sequencing, ChIPSeq, RNASeq, MethylSeq, Coverage, Alignment, QualityControl, ImmunoOncology Author: Anita Lerch, Dimos Gaiditzis and Michael Stadler Maintainer: Michael Stadler VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/QuasR git_branch: RELEASE_3_8 git_last_commit: cd9cf74 git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/QuasR_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/QuasR_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QuasR_1.22.1.tgz vignettes: vignettes/QuasR/inst/doc/QuasR.html vignetteTitles: An introduction to QuasR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/QuasR/inst/doc/QuasR.R Package: QuaternaryProd Version: 1.16.0 Depends: R (>= 3.2.0), Rcpp (>= 0.11.3), dplyr, yaml (>= 2.1.18) LinkingTo: Rcpp Suggests: knitr License: GPL (>=3) Archs: x64 MD5sum: 47be657148eb3d8caa9db8d007f65c25 NeedsCompilation: yes Title: Computes the Quaternary Dot Product Scoring Statistic for Signed and Unsigned Causal Graphs Description: QuaternaryProd is an R package that performs causal reasoning on biological networks, including publicly available networks such as STRINGdb. QuaternaryProd is an open-source alternative to commercial products such as Inginuity Pathway Analysis. For a given a set of differentially expressed genes, QuaternaryProd computes the significance of upstream regulators in the network by performing causal reasoning using the Quaternary Dot Product Scoring Statistic (Quaternary Statistic), Ternary Dot product Scoring Statistic (Ternary Statistic) and Fisher's exact test (Enrichment test). The Quaternary Statistic handles signed, unsigned and ambiguous edges in the network. Ambiguity arises when the direction of causality is unknown, or when the source node (e.g., a protein) has edges with conflicting signs for the same target gene. On the other hand, the Ternary Statistic provides causal reasoning using the signed and unambiguous edges only. The Vignette provides more details on the Quaternary Statistic and illustrates an example of how to perform causal reasoning using STRINGdb. biocViews: GraphAndNetwork, GeneExpression, Transcription Author: Carl Tony Fakhry [cre, aut], Ping Chen [ths], Kourosh Zarringhalam [aut, ths] Maintainer: Carl Tony Fakhry VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/QuaternaryProd git_branch: RELEASE_3_8 git_last_commit: 5efb791 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/QuaternaryProd_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/QuaternaryProd_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QuaternaryProd_1.16.0.tgz vignettes: vignettes/QuaternaryProd/inst/doc/QuaternaryProdVignette.pdf vignetteTitles: QuaternaryProdVignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/QuaternaryProd/inst/doc/QuaternaryProdVignette.R Package: QUBIC Version: 1.10.0 Depends: R (>= 3.1), biclust Imports: Rcpp (>= 0.11.0), methods, Matrix LinkingTo: Rcpp, RcppArmadillo Suggests: QUBICdata, qgraph, fields, knitr, rmarkdown Enhances: RColorBrewer License: CC BY-NC-ND 4.0 + file LICENSE Archs: i386, x64 MD5sum: ab39857fee893ea726e3d3d1392ee190 NeedsCompilation: yes Title: An R package for qualitative biclustering in support of gene co-expression analyses Description: The core function of this R package is to provide the implementation of the well-cited and well-reviewed QUBIC algorithm, aiming to deliver an effective and efficient biclustering capability. This package also includes the following related functions: (i) a qualitative representation of the input gene expression data, through a well-designed discretization way considering the underlying data property, which can be directly used in other biclustering programs; (ii) visualization of identified biclusters using heatmap in support of overall expression pattern analysis; (iii) bicluster-based co-expression network elucidation and visualization, where different correlation coefficient scores between a pair of genes are provided; and (iv) a generalize output format of biclusters and corresponding network can be freely downloaded so that a user can easily do following comprehensive functional enrichment analysis (e.g. DAVID) and advanced network visualization (e.g. Cytoscape). biocViews: StatisticalMethod, Microarray, DifferentialExpression, MultipleComparison, Clustering, Visualization, GeneExpression, Network Author: Yu Zhang [aut, cre], Qin Ma [aut] Maintainer: Yu Zhang URL: http://github.com/zy26/QUBIC SystemRequirements: C++11, Rtools (>= 3.1) VignetteBuilder: knitr BugReports: http://github.com/zy26/QUBIC/issues git_url: https://git.bioconductor.org/packages/QUBIC git_branch: RELEASE_3_8 git_last_commit: c9a0816 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/QUBIC_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/QUBIC_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/QUBIC_1.10.0.tgz vignettes: vignettes/QUBIC/inst/doc/qubic_vignette.pdf vignetteTitles: QUBIC Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/QUBIC/inst/doc/qubic_vignette.R suggestsMe: runibic Package: qusage Version: 2.16.1 Depends: R (>= 2.10), limma (>= 3.14), methods Imports: utils, Biobase, nlme, lsmeans License: GPL (>= 2) Archs: i386, x64 MD5sum: ee3c63243de1348e2961fdaac0b02fe0 NeedsCompilation: no Title: qusage: Quantitative Set Analysis for Gene Expression Description: This package is an implementation the Quantitative Set Analysis for Gene Expression (QuSAGE) method described in (Yaari G. et al, Nucl Acids Res, 2013). This is a novel Gene Set Enrichment-type test, which is designed to provide a faster, more accurate, and easier to understand test for gene expression studies. qusage accounts for inter-gene correlations using the Variance Inflation Factor technique proposed by Wu et al. (Nucleic Acids Res, 2012). In addition, rather than simply evaluating the deviation from a null hypothesis with a single number (a P value), qusage quantifies gene set activity with a complete probability density function (PDF). From this PDF, P values and confidence intervals can be easily extracted. Preserving the PDF also allows for post-hoc analysis (e.g., pair-wise comparisons of gene set activity) while maintaining statistical traceability. Finally, while qusage is compatible with individual gene statistics from existing methods (e.g., LIMMA), a Welch-based method is implemented that is shown to improve specificity. For questions, contact Chris Bolen (cbolen1@gmail.com) or Steven Kleinstein (steven.kleinstein@yale.edu) biocViews: ImmunoOncology, GeneSetEnrichment, Microarray, RNASeq, Software Author: Christopher Bolen and Gur Yaari, with contributions from Juilee Thakar, Hailong Meng, Jacob Turner, Derek Blankenship, and Steven Kleinstein Maintainer: Christopher Bolen URL: http://clip.med.yale.edu/qusage git_url: https://git.bioconductor.org/packages/qusage git_branch: RELEASE_3_8 git_last_commit: 54c9f34 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/qusage_2.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/qusage_2.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qusage_2.16.1.tgz vignettes: vignettes/qusage/inst/doc/qusage.pdf vignetteTitles: Running qusage hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qusage/inst/doc/qusage.R suggestsMe: SigCheck Package: qvalue Version: 2.14.1 Depends: R(>= 2.10) Imports: splines, ggplot2, grid, reshape2 Suggests: knitr License: LGPL MD5sum: f1101a501c24d4090d67f9fc764bd3ab NeedsCompilation: no Title: Q-value estimation for false discovery rate control Description: This package takes a list of p-values resulting from the simultaneous testing of many hypotheses and estimates their q-values and local FDR values. The q-value of a test measures the proportion of false positives incurred (called the false discovery rate) when that particular test is called significant. The local FDR measures the posterior probability the null hypothesis is true given the test's p-value. Various plots are automatically generated, allowing one to make sensible significance cut-offs. Several mathematical results have recently been shown on the conservative accuracy of the estimated q-values from this software. The software can be applied to problems in genomics, brain imaging, astrophysics, and data mining. biocViews: MultipleComparisons Author: John D. Storey [aut, cre], Andrew J. Bass [aut], Alan Dabney [aut], David Robinson [aut], Gregory Warnes [ctb] Maintainer: John D. Storey , Andrew J. Bass URL: http://github.com/jdstorey/qvalue VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/qvalue git_branch: RELEASE_3_8 git_last_commit: b694e4b git_last_commit_date: 2019-01-10 Date/Publication: 2019-01-10 source.ver: src/contrib/qvalue_2.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/qvalue_2.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/qvalue_2.14.1.tgz vignettes: vignettes/qvalue/inst/doc/qvalue.pdf vignetteTitles: qvalue Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/qvalue/inst/doc/qvalue.R dependsOnMe: anota, CancerMutationAnalysis, DEGseq, DrugVsDisease, metaseqR, r3Cseq, SSPA, webbioc importsMe: Anaquin, anota, clusterProfiler, derfinder, DOSE, edge, erccdashboard, EventPointer, methylKit, msmsTests, MWASTools, netresponse, normr, OPWeight, Rnits, SDAMS, sights, sRAP, subSeq, synapter, trigger, webbioc suggestsMe: biobroom, LBE, maanova, PREDA, RnBeads, SummarizedBenchmark Package: R3CPET Version: 1.14.0 Depends: R (>= 3.2), Rcpp (>= 0.10.4), methods Imports: methods, parallel, clues, ggplot2, pheatmap, clValid, igraph, data.table, reshape2, Hmisc, RCurl, BiocGenerics, S4Vectors, IRanges (>= 2.13.12), GenomeInfoDb, GenomicRanges (>= 1.31.8), ggbio LinkingTo: Rcpp Suggests: BiocStyle, knitr, TxDb.Hsapiens.UCSC.hg19.knownGene, biovizBase, biomaRt, AnnotationDbi, org.Hs.eg.db, shiny, ChIPpeakAnno License: GPL (>=2) MD5sum: de75b6f33919464203ed7042c9fc5f6e NeedsCompilation: yes Title: 3CPET: Finding Co-factor Complexes in Chia-PET experiment using a Hierarchical Dirichlet Process Description: The package provides a method to infer the set of proteins that are more probably to work together to maintain chormatin interaction given a ChIA-PET experiment results. biocViews: NetworkInference, GenePrediction, Bayesian, GraphAndNetwork, Network, GeneExpression, HiC Author: Djekidel MN, Yang Chen et al. Maintainer: Mohamed Nadhir Djekidel VignetteBuilder: knitr BugReports: https://github.com/sirusb/R3CPET/issues git_url: https://git.bioconductor.org/packages/R3CPET git_branch: RELEASE_3_8 git_last_commit: 78d0702 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/R3CPET_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/R3CPET_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/R3CPET_1.14.0.tgz vignettes: vignettes/R3CPET/inst/doc/R3CPET.pdf vignetteTitles: 3CPET: Finding Co-factor Complexes maintaining Chia-PET interactions hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/R3CPET/inst/doc/R3CPET.R Package: r3Cseq Version: 1.28.0 Depends: GenomicRanges, Rsamtools, rtracklayer, VGAM, qvalue Imports: methods, GenomeInfoDb, IRanges, Biostrings, data.table, sqldf, RColorBrewer Suggests: BSgenome.Mmusculus.UCSC.mm9.masked, BSgenome.Mmusculus.UCSC.mm10.masked, BSgenome.Hsapiens.UCSC.hg18.masked, BSgenome.Hsapiens.UCSC.hg19.masked, BSgenome.Rnorvegicus.UCSC.rn5.masked License: GPL-3 Archs: i386, x64 MD5sum: e900fcaf098fd698650694cf4f2b3dad NeedsCompilation: no Title: Analysis of Chromosome Conformation Capture and Next-generation Sequencing (3C-seq) Description: This package is an implementation of data analysis for the long-range interactions from 3C-seq assay. biocViews: Preprocessing, Sequencing Author: Supat Thongjuea, MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, UK Maintainer: Supat Thongjuea URL: http://r3cseq.genereg.net git_url: https://git.bioconductor.org/packages/r3Cseq git_branch: RELEASE_3_8 git_last_commit: 321df82 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/r3Cseq_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/r3Cseq_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/r3Cseq_1.28.0.tgz vignettes: vignettes/r3Cseq/inst/doc/r3Cseq.pdf vignetteTitles: r3Cseq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/r3Cseq/inst/doc/r3Cseq.R Package: R453Plus1Toolbox Version: 1.32.0 Depends: R (>= 2.12.0), methods, VariantAnnotation (>= 1.25.11), Biostrings (>= 2.47.6), Biobase Imports: utils, grDevices, graphics, stats, tools, xtable, R2HTML, TeachingDemos, BiocGenerics, S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), XVector, GenomicRanges (>= 1.31.8), SummarizedExperiment, biomaRt, BSgenome (>= 1.47.3), Rsamtools, ShortRead (>= 1.37.1) Suggests: rtracklayer, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Scerevisiae.UCSC.sacCer2 License: LGPL-3 MD5sum: 4a5bb4fe4d331ca8c30ca120a0d8ea17 NeedsCompilation: yes Title: A package for importing and analyzing data from Roche's Genome Sequencer System Description: The R453Plus1 Toolbox comprises useful functions for the analysis of data generated by Roche's 454 sequencing platform. It adds functions for quality assurance as well as for annotation and visualization of detected variants, complementing the software tools shipped by Roche with their product. Further, a pipeline for the detection of structural variants is provided. biocViews: Sequencing, Infrastructure, DataImport, DataRepresentation, Visualization, QualityControl, ReportWriting Author: Hans-Ulrich Klein, Christoph Bartenhagen, Christian Ruckert Maintainer: Hans-Ulrich Klein git_url: https://git.bioconductor.org/packages/R453Plus1Toolbox git_branch: RELEASE_3_8 git_last_commit: c3e31d8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/R453Plus1Toolbox_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/R453Plus1Toolbox_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/R453Plus1Toolbox_1.32.0.tgz vignettes: vignettes/R453Plus1Toolbox/inst/doc/vignette.pdf vignetteTitles: A package for importing and analyzing data from Roche's Genome Sequencer System hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/R453Plus1Toolbox/inst/doc/vignette.R Package: R4RNA Version: 1.10.0 Depends: R (>= 3.2.0), Biostrings (>= 2.38.0) License: GPL-3 Archs: i386, x64 MD5sum: e6c4cca4a785471fb80fbf9f3d66358e NeedsCompilation: no Title: An R package for RNA visualization and analysis Description: A package for RNA basepair analysis, including the visualization of basepairs as arc diagrams for easy comparison and annotation of sequence and structure. Arc diagrams can additionally be projected onto multiple sequence alignments to assess basepair conservation and covariation, with numerical methods for computing statistics for each. biocViews: Alignment, MultipleSequenceAlignment, Preprocessing, Visualization, DataImport, DataRepresentation, MultipleComparison Author: Daniel Lai, Irmtraud Meyer Maintainer: Daniel Lai URL: http://www.e-rna.org/r-chie/ git_url: https://git.bioconductor.org/packages/R4RNA git_branch: RELEASE_3_8 git_last_commit: ba27cc1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/R4RNA_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/R4RNA_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/R4RNA_1.10.0.tgz vignettes: vignettes/R4RNA/inst/doc/R4RNA.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/R4RNA/inst/doc/R4RNA.R Package: RaggedExperiment Version: 1.6.0 Depends: R (>= 3.5.0), GenomicRanges Imports: BiocGenerics, GenomeInfoDb, IRanges, methods, S4Vectors, stats, SummarizedExperiment Suggests: BiocStyle, knitr, testthat, MultiAssayExperiment License: Artistic-2.0 MD5sum: a07596ff746251104b6c1ce3ddd933e2 NeedsCompilation: no Title: Representation of Sparse Experiments and Assays Across Samples Description: This package provides a flexible representation of copy number, mutation, and other data that fit into the ragged array schema for genomic location data. The basic representation of such data provides a rectangular flat table interface to the user with range information in the rows and samples/specimen in the columns. biocViews: Infrastructure, DataRepresentation Author: Martin Morgan [aut, cre], Marcel Ramos [aut] Maintainer: Martin Morgan VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/RaggedExperiment/issues git_url: https://git.bioconductor.org/packages/RaggedExperiment git_branch: RELEASE_3_8 git_last_commit: dec7201 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RaggedExperiment_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RaggedExperiment_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RaggedExperiment_1.6.0.tgz vignettes: vignettes/RaggedExperiment/inst/doc/RaggedExperiment.html vignetteTitles: RaggedExperiment hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RaggedExperiment/inst/doc/RaggedExperiment.R dependsOnMe: TxRegInfra importsMe: omicsPrint, RTCGAToolbox, TCGAutils suggestsMe: MultiAssayExperiment, MultiDataSet Package: rain Version: 1.16.0 Depends: R (>= 2.10), gmp, multtest Suggests: lattice, BiocStyle License: GPL-2 MD5sum: f2ec7a42028c930beb3857c0e1292817 NeedsCompilation: no Title: Rhythmicity Analysis Incorporating Non-parametric Methods Description: This package uses non-parametric methods to detect rhythms in time series. It deals with outliers, missing values and is optimized for time series comprising 10-100 measurements. As it does not assume expect any distinct waveform it is optimal or detecting oscillating behavior (e.g. circadian or cell cycle) in e.g. genome- or proteome-wide biological measurements such as: micro arrays, proteome mass spectrometry, or metabolome measurements. biocViews: TimeCourse, Genetics, SystemsBiology, Proteomics, Microarray, MultipleComparison Author: Paul F. Thaben, Pål O. Westermark Maintainer: Paul F. Thaben git_url: https://git.bioconductor.org/packages/rain git_branch: RELEASE_3_8 git_last_commit: b0ffed8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rain_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rain_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rain_1.16.0.tgz vignettes: vignettes/rain/inst/doc/rain.pdf vignetteTitles: Rain Usage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rain/inst/doc/rain.R Package: rama Version: 1.56.0 Depends: R(>= 2.5.0) License: GPL (>= 2) MD5sum: 698c5d694e8e08c717ab7e0f7a6495d9 NeedsCompilation: yes Title: Robust Analysis of MicroArrays Description: Robust estimation of cDNA microarray intensities with replicates. The package uses a Bayesian hierarchical model for the robust estimation. Outliers are modeled explicitly using a t-distribution, and the model also addresses classical issues such as design effects, normalization, transformation, and nonconstant variance. biocViews: Microarray, TwoChannel, QualityControl, Preprocessing Author: Raphael Gottardo Maintainer: Raphael Gottardo git_url: https://git.bioconductor.org/packages/rama git_branch: RELEASE_3_8 git_last_commit: a611930 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rama_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rama_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rama_1.56.0.tgz vignettes: vignettes/rama/inst/doc/rama.pdf vignetteTitles: rama Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rama/inst/doc/rama.R dependsOnMe: bridge Package: ramwas Version: 1.6.0 Depends: R (>= 3.3.0), methods, filematrix Imports: graphics, stats, utils, digest, glmnet, KernSmooth, grDevices, GenomicAlignments, Rsamtools, parallel, biomaRt, Biostrings, BiocGenerics Suggests: knitr, rmarkdown, pander, BiocStyle, BSgenome.Ecoli.NCBI.20080805 License: LGPL-3 Archs: i386, x64 MD5sum: 63327d48803487a400eea7b0dcb09611 NeedsCompilation: yes Title: Fast Methylome-Wide Association Study Pipeline for Enrichment Platforms Description: A complete toolset for methylome-wide association studies (MWAS). It is specifically designed for data from enrichment based methylation assays, but can be applied to other data as well. The analysis pipeline includes seven steps: (1) scanning aligned reads from BAM files, (2) calculation of quality control measures, (3) creation of methylation score (coverage) matrix, (4) principal component analysis for capturing batch effects and detection of outliers, (5) association analysis with respect to phenotypes of interest while correcting for top PCs and known covariates, (6) annotation of significant findings, and (7) multi-marker analysis (methylation risk score) using elastic net. Additionally, RaMWAS include tools for joint analysis of methlyation and genotype data. This work is published in Bioinformatics, Shabalin et al. (2018) . biocViews: DNAMethylation, Sequencing, QualityControl, Coverage, Preprocessing, Normalization, BatchEffect, PrincipalComponent, DifferentialMethylation, Visualization Author: Andrey A Shabalin [aut, cre] (), Shaunna L Clark [aut], Mohammad W Hattab [aut], Karolina A Aberg [aut], Edwin J C G van den Oord [aut] Maintainer: Andrey A Shabalin URL: https://bioconductor.org/packages/ramwas/ VignetteBuilder: knitr BugReports: https://github.com/andreyshabalin/ramwas/issues git_url: https://git.bioconductor.org/packages/ramwas git_branch: RELEASE_3_8 git_last_commit: 2e1d8f6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ramwas_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ramwas_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ramwas_1.6.0.tgz vignettes: vignettes/ramwas/inst/doc/RW1_intro.html, vignettes/ramwas/inst/doc/RW2_CpG_sets.html, vignettes/ramwas/inst/doc/RW3_BAM_QCs.html, vignettes/ramwas/inst/doc/RW4_SNPs.html, vignettes/ramwas/inst/doc/RW5_matrix.html, vignettes/ramwas/inst/doc/RW6_param.html vignetteTitles: 1. Overview, 2. CpG sets, 3. BAM Quality Control Measures, 4. Joint Analysis of Methylation and Genotype Data, 5. Analyzing data from other sources, 6. RaMWAS parameters hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ramwas/inst/doc/RW1_intro.R, vignettes/ramwas/inst/doc/RW2_CpG_sets.R, vignettes/ramwas/inst/doc/RW3_BAM_QCs.R, vignettes/ramwas/inst/doc/RW4_SNPs.R, vignettes/ramwas/inst/doc/RW5_matrix.R, vignettes/ramwas/inst/doc/RW6_param.R Package: RandomWalkRestartMH Version: 1.2.0 Depends: R(>= 3.5.0) Imports: igraph, Matrix, dnet, methods Suggests: BiocStyle, testthat License: GPL (>= 2) Archs: i386, x64 MD5sum: 351404a67f4b115a3d24314cb60f9d20 NeedsCompilation: no Title: Random walk with restart on multiplex and heterogeneous Networks Description: This package performs Random Walk with Restart on multiplex and heterogeneous networks. It is described in the following article: "Random Walk With Restart On Multiplex And Heterogeneous Biological Networks". https://www.biorxiv.org/content/early/2017/08/30/134734 . biocViews: GenePrediction, NetworkInference, SomaticMutation, BiomedicalInformatics, MathematicalBiology, SystemsBiology, GraphAndNetwork, Pathways, BioCarta, KEGG, Reactome, Network Author: Alberto Valdeolivas Urbelz Maintainer: Alberto Valdeolivas Urbelz URL: https://www.biorxiv.org/content/early/2017/08/30/134734 git_url: https://git.bioconductor.org/packages/RandomWalkRestartMH git_branch: RELEASE_3_8 git_last_commit: f360f5c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RandomWalkRestartMH_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RandomWalkRestartMH_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RandomWalkRestartMH_1.2.0.tgz vignettes: vignettes/RandomWalkRestartMH/inst/doc/RandomWalkRestartMH1.pdf vignetteTitles: Random Walk with Restart on Multiplex and Heterogeneous Networks hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RandomWalkRestartMH/inst/doc/RandomWalkRestartMH1.R Package: randPack Version: 1.28.0 Depends: methods Imports: Biobase License: Artistic 2.0 MD5sum: 92c6a0d2bee12aa5cc9fae2882ac72f1 NeedsCompilation: no Title: Randomization routines for Clinical Trials Description: A suite of classes and functions for randomizing patients in clinical trials. biocViews: StatisticalMethod Author: Vincent Carey and Robert Gentleman Maintainer: Robert Gentleman git_url: https://git.bioconductor.org/packages/randPack git_branch: RELEASE_3_8 git_last_commit: 91e2504 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/randPack_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/randPack_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/randPack_1.28.0.tgz vignettes: vignettes/randPack/inst/doc/randPack.pdf vignetteTitles: Clinical trial randomization infrastructure hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/randPack/inst/doc/randPack.R Package: RankProd Version: 3.8.0 Depends: R (>= 3.2.1), stats, methods, Rmpfr, gmp Imports: graphics License: file LICENSE License_restricts_use: yes MD5sum: 86e2a46efa5edd1ad7ecaf7556b18208 NeedsCompilation: no Title: Rank Product method for identifying differentially expressed genes with application in meta-analysis Description: Non-parametric method for identifying differentially expressed (up- or down- regulated) genes based on the estimated percentage of false predictions (pfp). The method can combine data sets from different origins (meta-analysis) to increase the power of the identification. biocViews: DifferentialExpression, StatisticalMethod, Software, ResearchField, Metabolomics, Lipidomics, Proteomics, SystemsBiology, GeneExpression, Microarray, GeneSignaling Author: Francesco Del Carratore , Andris Jankevics Fangxin Hong , Ben Wittner , Rainer Breitling , and Florian Battke Maintainer: Francesco Del Carratore git_url: https://git.bioconductor.org/packages/RankProd git_branch: RELEASE_3_8 git_last_commit: 0215b84 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RankProd_3.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RankProd_3.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RankProd_3.8.0.tgz vignettes: vignettes/RankProd/inst/doc/RankProd.pdf vignetteTitles: RankProd Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RankProd/inst/doc/RankProd.R dependsOnMe: RNAither, tRanslatome importsMe: HTSanalyzeR, synlet Package: RareVariantVis Version: 2.10.0 Depends: BiocGenerics, VariantAnnotation, googleVis, GenomicFeatures Imports: S4Vectors, IRanges, GenomeInfoDb, GenomicRanges, gtools, BSgenome, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, phastCons100way.UCSC.hg19, SummarizedExperiment, GenomicScores Suggests: knitr License: Artistic-2.0 MD5sum: 193cfc429d07fdf039d3e2edea0893ae NeedsCompilation: no Title: A suite for analysis of rare genomic variants in whole genome sequencing data Description: Second version of RareVariantVis package aims to provide comprehensive information about rare variants for your genome data. It annotates, filters and presents genomic variants (especially rare ones) in a global, per chromosome way. For discovered rare variants CRISPR guide RNAs are designed, so the user can plan further functional studies. Large structural variants, including copy number variants are also supported. Package accepts variants directly from variant caller - for example GATK or Speedseq. Output of package are lists of variants together with adequate visualization. Visualization of variants is performed in two ways - standard that outputs png figures and interactive that uses JavaScript d3 package. Interactive visualization allows to analyze trio/family data, for example in search for causative variants in rare Mendelian diseases, in point-and-click interface. The package includes homozygous region caller and allows to analyse whole human genomes in less than 30 minutes on a desktop computer. RareVariantVis disclosed novel causes of several rare monogenic disorders, including one with non-coding causative variant - keratolythic winter erythema. biocViews: GenomicVariation, Sequencing, WholeGenome Author: Adam Gudys and Tomasz Stokowy Maintainer: Tomasz Stokowy VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RareVariantVis git_branch: RELEASE_3_8 git_last_commit: 8cf62cd git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/RareVariantVis_2.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RareVariantVis_2.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RareVariantVis_2.10.0.tgz vignettes: vignettes/RareVariantVis/inst/doc/RareVariantsVis.pdf vignetteTitles: RareVariantVis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RareVariantVis/inst/doc/RareVariantsVis.R Package: Rariant Version: 1.18.0 Depends: R (>= 3.0.2), GenomicRanges, VariantAnnotation Imports: methods, BiocGenerics, S4Vectors, IRanges, GenomeInfoDb, ggbio, ggplot2, exomeCopy, SomaticSignatures, Rsamtools, shiny, VGAM, dplyr, reshape2 Suggests: h5vcData, testthat, knitr, optparse, BSgenome.Hsapiens.UCSC.hg19 License: GPL-3 MD5sum: cc3ad6548566082286949d086014730c NeedsCompilation: no Title: Identification and Assessment of Single Nucleotide Variants through Shifts in Non-Consensus Base Call Frequencies Description: The 'Rariant' package identifies single nucleotide variants from sequencing data based on the difference of binomially distributed mismatch rates between matched samples. biocViews: Sequencing, StatisticalMethod, GenomicVariation, SomaticMutation, VariantDetection, Visualization Author: Julian Gehring, Simon Anders, Bernd Klaus Maintainer: Julian Gehring URL: https://github.com/juliangehring/Rariant VignetteBuilder: knitr BugReports: https://support.bioconductor.org git_url: https://git.bioconductor.org/packages/Rariant git_branch: RELEASE_3_8 git_last_commit: 76dec22 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rariant_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rariant_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rariant_1.18.0.tgz vignettes: vignettes/Rariant/inst/doc/Rariant-vignette.html vignetteTitles: Rariant hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rariant/inst/doc/Rariant-vignette.R Package: RbcBook1 Version: 1.50.0 Depends: R (>= 2.10), Biobase, graph, rpart License: Artistic-2.0 MD5sum: ab688a83dd3cb0dacea22caacd02c9cc NeedsCompilation: no Title: Support for Springer monograph on Bioconductor Description: tools for building book biocViews: Software Author: Vince Carey and Wolfgang Huber Maintainer: Vince Carey URL: http://www.biostat.harvard.edu/~carey git_url: https://git.bioconductor.org/packages/RbcBook1 git_branch: RELEASE_3_8 git_last_commit: 6e18a79 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RbcBook1_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RbcBook1_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RbcBook1_1.50.0.tgz vignettes: vignettes/RbcBook1/inst/doc/RbcBook1.pdf vignetteTitles: RbcBook1 Primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RbcBook1/inst/doc/RbcBook1.R Package: RBGL Version: 1.58.2 Depends: graph, methods Imports: methods Suggests: Rgraphviz, XML, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: cf5dd2e6dd3ebd8175d212bb86db0318 NeedsCompilation: yes Title: An interface to the BOOST graph library Description: A fairly extensive and comprehensive interface to the graph algorithms contained in the BOOST library. biocViews: GraphAndNetwork, Network Author: Vince Carey , Li Long , R. Gentleman Maintainer: Bioconductor Package Maintainer URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/RBGL git_branch: RELEASE_3_8 git_last_commit: 086ad0c git_last_commit_date: 2019-03-22 Date/Publication: 2019-03-22 source.ver: src/contrib/RBGL_1.58.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/RBGL_1.58.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RBGL_1.58.2.tgz vignettes: vignettes/RBGL/inst/doc/RBGL.pdf vignetteTitles: RBGL Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RBGL/inst/doc/RBGL.R dependsOnMe: apComplex, BioNet, CellNOptR, joda, pkgDepTools, RpsiXML importsMe: alpine, biocViews, CAMERA, Category, ChIPpeakAnno, CHRONOS, clipper, CytoML, DEGraph, DEsubs, EventPointer, flowWorkspace, GeneAnswers, GOSim, GOstats, MIGSA, NCIgraph, nem, OrganismDbi, pkgDepTools, predictionet, RDAVIDWebService, signet, Streamer, VariantFiltering suggestsMe: BiocCaseStudies, DEGraph, GeneNetworkBuilder, graph, gwascat, KEGGgraph, rBiopaxParser, VariantTools Package: RBioinf Version: 1.42.0 Depends: graph, methods Suggests: Rgraphviz License: Artistic-2.0 Archs: i386, x64 MD5sum: ccc0e1c81f86882eef47cef5b74b94d2 NeedsCompilation: yes Title: RBioinf Description: Functions and datasets and examples to accompany the monograph R For Bioinformatics. biocViews: GeneExpression, Microarray, Preprocessing, QualityControl, Classification, Clustering, MultipleComparison, Annotation Author: Robert Gentleman Maintainer: Robert Gentleman git_url: https://git.bioconductor.org/packages/RBioinf git_branch: RELEASE_3_8 git_last_commit: 677ac5e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RBioinf_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RBioinf_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RBioinf_1.42.0.tgz vignettes: vignettes/RBioinf/inst/doc/RBioinf.pdf vignetteTitles: RBioinf Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RBioinf/inst/doc/RBioinf.R Package: rBiopaxParser Version: 2.22.0 Depends: R (>= 3.0.0), data.table Imports: XML Suggests: Rgraphviz, RCurl, graph, RUnit, BiocGenerics, nem, RBGL, igraph License: GPL (>= 2) Archs: i386, x64 MD5sum: d83ba9fc20daeefc0ec70a01a4a99c07 NeedsCompilation: no Title: Parses BioPax files and represents them in R Description: Parses BioPAX files and represents them in R, at the moment BioPAX level 2 and level 3 are supported. biocViews: DataRepresentation Author: Frank Kramer Maintainer: Frank Kramer URL: https://github.com/frankkramer-lab/rBiopaxParser git_url: https://git.bioconductor.org/packages/rBiopaxParser git_branch: RELEASE_3_8 git_last_commit: 789779b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rBiopaxParser_2.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rBiopaxParser_2.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rBiopaxParser_2.22.0.tgz vignettes: vignettes/rBiopaxParser/inst/doc/rBiopaxParserVignette.pdf vignetteTitles: rBiopaxParser Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rBiopaxParser/inst/doc/rBiopaxParserVignette.R importsMe: AnnotationHubData, pwOmics suggestsMe: AnnotationHub, NetPathMiner Package: RBM Version: 1.14.0 Depends: R (>= 3.2.0), limma, marray License: GPL (>= 2) MD5sum: 3606f3c75a1198316189c26f7ea7ba85 NeedsCompilation: no Title: RBM: a R package for microarray and RNA-Seq data analysis Description: Use A Resampling-Based Empirical Bayes Approach to Assess Differential Expression in Two-Color Microarrays and RNA-Seq data sets. biocViews: Microarray, DifferentialExpression Author: Dongmei Li and Chin-Yuan Liang Maintainer: Dongmei Li git_url: https://git.bioconductor.org/packages/RBM git_branch: RELEASE_3_8 git_last_commit: bdb0f7b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RBM_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RBM_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RBM_1.14.0.tgz vignettes: vignettes/RBM/inst/doc/RBM.pdf vignetteTitles: RBM hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RBM/inst/doc/RBM.R Package: Rbowtie Version: 1.22.0 Suggests: parallel, BiocStyle, knitr, rmarkdown License: Artistic-1.0 | file LICENSE MD5sum: 4c1a3ec981370710eb6d526043a31965 NeedsCompilation: yes Title: R bowtie wrapper Description: This package provides an R wrapper around the popular bowtie short read aligner and around SpliceMap, a de novo splice junction discovery and alignment tool. The package is used by the QuasR bioconductor package. We recommend to use the QuasR package instead of using Rbowtie directly. biocViews: Sequencing, Alignment Author: Florian Hahne, Anita Lerch, Michael B Stadler Maintainer: Michael Stadler SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Rbowtie git_branch: RELEASE_3_8 git_last_commit: 5702a43 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rbowtie_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rbowtie_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rbowtie_1.22.0.tgz vignettes: vignettes/Rbowtie/inst/doc/Rbowtie-Overview.html vignetteTitles: An introduction to Rbowtie hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Rbowtie/inst/doc/Rbowtie-Overview.R dependsOnMe: QuasR importsMe: MACPET Package: Rbowtie2 Version: 1.4.0 Depends: R (>= 3.5) Suggests: knitr License: GPL (>= 3) Archs: x64 MD5sum: 8c6f2b4f4cf420132402458cc0431d96 NeedsCompilation: yes Title: An R Wrapper for Bowtie2 and AdapterRemoval Description: This package provides an R wrapper of the popular bowtie2 sequencing reads aligner and AdapterRemoval, a convenient tool for rapid adapter trimming, identification, and read merging. biocViews: Sequencing, Alignment, Preprocessing Author: Zheng Wei, Wei Zhang Maintainer: Zheng Wei SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Rbowtie2 git_branch: RELEASE_3_8 git_last_commit: e09f6d4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rbowtie2_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rbowtie2_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rbowtie2_1.4.0.tgz vignettes: vignettes/Rbowtie2/inst/doc/Rbowtie2-Introduction.html vignetteTitles: An Introduction to Rbowtie2 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rbowtie2/inst/doc/Rbowtie2-Introduction.R importsMe: esATAC Package: rbsurv Version: 2.40.0 Depends: R (>= 2.5.0), Biobase (>= 2.5.5), survival License: GPL (>= 2) Archs: x64 MD5sum: 1e470e032da134db83ae929adb8ff66a NeedsCompilation: no Title: Robust likelihood-based survival modeling with microarray data Description: This package selects genes associated with survival. biocViews: Microarray Author: HyungJun Cho , Sukwoo Kim , Soo-heang Eo , Jaewoo Kang Maintainer: Soo-heang Eo URL: http://www.korea.ac.kr/~stat2242/ git_url: https://git.bioconductor.org/packages/rbsurv git_branch: RELEASE_3_8 git_last_commit: 1d6cb54 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rbsurv_2.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rbsurv_2.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rbsurv_2.40.0.tgz vignettes: vignettes/rbsurv/inst/doc/rbsurv.pdf vignetteTitles: Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rbsurv/inst/doc/rbsurv.R Package: Rcade Version: 1.24.0 Depends: R (>= 2.14.0), methods, GenomicRanges, Rsamtools, baySeq Imports: utils, grDevices, stats, graphics, rgl, plotrix, S4Vectors, IRanges, GenomeInfoDb, GenomicAlignments Suggests: limma, biomaRt, RUnit, BiocGenerics, BiocStyle License: GPL-2 MD5sum: 33e6f9f825b0dabf32897a4044af6f7f NeedsCompilation: no Title: R-based analysis of ChIP-seq And Differential Expression - a tool for integrating a count-based ChIP-seq analysis with differential expression summary data Description: Rcade (which stands for "R-based analysis of ChIP-seq And Differential Expression") is a tool for integrating ChIP-seq data with differential expression summary data, through a Bayesian framework. A key application is in identifing the genes targeted by a transcription factor of interest - that is, we collect genes that are associated with a ChIP-seq peak, and differential expression under some perturbation related to that TF. biocViews: DifferentialExpression, GeneExpression, Transcription, ChIPSeq, Sequencing, Genetics Author: Jonathan Cairns Maintainer: Jonathan Cairns git_url: https://git.bioconductor.org/packages/Rcade git_branch: RELEASE_3_8 git_last_commit: c277672 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rcade_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rcade_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rcade_1.24.0.tgz vignettes: vignettes/Rcade/inst/doc/Rcade.pdf vignetteTitles: Rcade Vignette hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rcade/inst/doc/Rcade.R Package: RCAS Version: 1.8.0 Depends: R (>= 3.3.0), plotly (>= 4.5.2), DT (>= 0.2), data.table, topGO, motifRG Imports: biomaRt, AnnotationDbi, GenomicRanges, BSgenome.Hsapiens.UCSC.hg19, GenomeInfoDb (>= 1.12.0), Biostrings, rtracklayer, org.Hs.eg.db, GenomicFeatures, rmarkdown (>= 0.9.5), genomation (>= 1.5.5), knitr (>= 1.12.3), BiocGenerics, S4Vectors, stats, plotrix, pbapply, RSQLite, proxy, DBI, pheatmap, ggplot2, cowplot, ggseqlogo, methods, utils Suggests: BSgenome.Hsapiens.UCSC.hg38, BSgenome.Mmusculus.UCSC.mm10, BSgenome.Mmusculus.UCSC.mm9, BSgenome.Celegans.UCSC.ce10, BSgenome.Dmelanogaster.UCSC.dm3, org.Mm.eg.db, org.Ce.eg.db, org.Dm.eg.db, testthat, covr License: Artistic-2.0 MD5sum: 2146754031cbc929a628de63e7088388 NeedsCompilation: no Title: RNA Centric Annotation System Description: RCAS is an automated system that provides dynamic genome annotations for custom input files that contain transcriptomic regions. Such transcriptomic regions could be, for instance, peak regions detected by CLIP-Seq analysis that detect protein-RNA interactions, RNA modifications (alias the epitranscriptome), CAGE-tag locations, or any other collection of target regions at the level of the transcriptome. RCAS is designed as a reporting tool for the functional analysis of RNA-binding sites detected by high-throughput experiments. It takes as input a BED format file containing the genomic coordinates of the RNA binding sites and a GTF file that contains the genomic annotation features usually provided by publicly available databases such as Ensembl and UCSC. RCAS performs overlap operations between the genomic coordinates of the RNA binding sites and the genomic annotation features and produces in-depth annotation summaries such as the distribution of binding sites with respect to gene features (exons, introns, 5'/3' UTR regions, exon-intron boundaries, promoter regions, and whole transcripts). Moreover, by detecting the collection of targeted transcripts, RCAS can carry out functional annotation tables for enriched gene sets (annotated by the Molecular Signatures Database) and GO terms. As one of the most important questions that arise during protein-RNA interaction analysis; RCAS has a module for detecting sequence motifs enriched in the targeted regions of the transcriptome. A full interactive report in HTML format can be generated that contains interactive figures and tables that are ready for publication purposes. biocViews: Software, GeneTarget, MotifAnnotation, MotifDiscovery, GO, Transcriptomics, GenomeAnnotation, GeneSetEnrichment, Coverage Author: Bora Uyar [aut, cre], Dilmurat Yusuf [aut], Ricardo Wurmus [aut], Altuna Akalin [aut] Maintainer: Bora Uyar SystemRequirements: pandoc (>= 1.12.3) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RCAS git_branch: RELEASE_3_8 git_last_commit: a2f099e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RCAS_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RCAS_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RCAS_1.8.0.tgz vignettes: vignettes/RCAS/inst/doc/RCAS.metaAnalysis.vignette.html, vignettes/RCAS/inst/doc/RCAS.vignette.html vignetteTitles: How to do meta-analysis of multiple samples, Introduction - single sample analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RCAS/inst/doc/RCAS.metaAnalysis.vignette.R, vignettes/RCAS/inst/doc/RCAS.vignette.R Package: RCASPAR Version: 1.28.0 License: GPL (>=3) MD5sum: e479b18cfbc19c9ff633add554d85c2f NeedsCompilation: no Title: A package for survival time prediction based on a piecewise baseline hazard Cox regression model. Description: The package is the R-version of the C-based software \bold{CASPAR} (Kaderali,2006: \url{http://bioinformatics.oxfordjournals.org/content/22/12/1495}). It is meant to help predict survival times in the presence of high-dimensional explanatory covariates. The model is a piecewise baseline hazard Cox regression model with an Lq-norm based prior that selects for the most important regression coefficients, and in turn the most relevant covariates for survival analysis. It was primarily tried on gene expression and aCGH data, but can be used on any other type of high-dimensional data and in disciplines other than biology and medicine. biocViews: aCGH, GeneExpression, Genetics, Proteomics, Visualization Author: Douaa Mugahid, Lars Kaderali Maintainer: Douaa Mugahid , Lars Kaderali git_url: https://git.bioconductor.org/packages/RCASPAR git_branch: RELEASE_3_8 git_last_commit: be78240 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RCASPAR_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RCASPAR_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RCASPAR_1.28.0.tgz vignettes: vignettes/RCASPAR/inst/doc/RCASPAR.pdf vignetteTitles: RCASPAR: Software for high-dimentional-data driven survival time prediction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RCASPAR/inst/doc/RCASPAR.R Package: rcellminer Version: 2.4.0 Depends: R (>= 3.2), Biobase, rcdk, fingerprint, rcellminerData Imports: stringr, gplots, ggplot2, methods, stats, utils, shiny Suggests: knitr, RColorBrewer, sqldf, BiocGenerics, testthat, BiocStyle, jsonlite, d3heatmap, glmnet, foreach, doSNOW, parallel License: LGPL-3 + file LICENSE MD5sum: b4cc81cd0e95c5987a8bb9780abdf85c NeedsCompilation: no Title: rcellminer: Molecular Profiles and Drug Response for the NCI-60 Cell Lines Description: The NCI-60 cancer cell line panel has been used over the course of several decades as an anti-cancer drug screen. This panel was developed as part of the Developmental Therapeutics Program (DTP, http://dtp.nci.nih.gov/) of the U.S. National Cancer Institute (NCI). Thousands of compounds have been tested on the NCI-60, which have been extensively characterized by many platforms for gene and protein expression, copy number, mutation, and others (Reinhold, et al., 2012). The purpose of the CellMiner project (http://discover.nci.nih.gov/ cellminer) has been to integrate data from multiple platforms used to analyze the NCI-60 and to provide a powerful suite of tools for exploration of NCI-60 data. biocViews: aCGH, CellBasedAssays, CopyNumberVariation, GeneExpression, Pharmacogenomics, Pharmacogenetics, miRNA, Cheminformatics, Visualization, Software, SystemsBiology Author: Augustin Luna, Vinodh Rajapakse, Fabricio Sousa Maintainer: Augustin Luna , Vinodh Rajapakse , Fathi Elloumi URL: http://discover.nci.nih.gov/cellminer/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rcellminer git_branch: RELEASE_3_8 git_last_commit: e4c66ad git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rcellminer_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rcellminer_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rcellminer_2.4.0.tgz vignettes: vignettes/rcellminer/inst/doc/rcellminerUsage.html vignetteTitles: Using rcellminer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rcellminer/inst/doc/rcellminerUsage.R Package: rCGH Version: 1.12.0 Depends: R (>= 3.4),methods,stats,utils,graphics Imports: plyr,DNAcopy,lattice,ggplot2,grid,shiny (>= 0.11.1), limma,affy,mclust,TxDb.Hsapiens.UCSC.hg18.knownGene, TxDb.Hsapiens.UCSC.hg19.knownGene,TxDb.Hsapiens.UCSC.hg38.knownGene, org.Hs.eg.db,GenomicFeatures,GenomeInfoDb,GenomicRanges,AnnotationDbi, parallel,IRanges,grDevices,aCGH Suggests: BiocStyle, knitr, BiocGenerics, RUnit License: Artistic-2.0 MD5sum: eae2203e032108c2873331c9de08161e NeedsCompilation: no Title: Comprehensive Pipeline for Analyzing and Visualizing Array-Based CGH Data Description: A comprehensive pipeline for analyzing and interactively visualizing genomic profiles generated through commercial or custom aCGH arrays. As inputs, rCGH supports Agilent dual-color Feature Extraction files (.txt), from 44 to 400K, Affymetrix SNP6.0 and cytoScanHD probeset.txt, cychp.txt, and cnchp.txt files exported from ChAS or Affymetrix Power Tools. rCGH also supports custom arrays, provided data complies with the expected format. This package takes over all the steps required for individual genomic profiles analysis, from reading files to profiles segmentation and gene annotations. This package also provides several visualization functions (static or interactive) which facilitate individual profiles interpretation. Input files can be in compressed format, e.g. .bz2 or .gz. biocViews: aCGH,CopyNumberVariation,Preprocessing,FeatureExtraction Author: Frederic Commo [aut, cre] Maintainer: Frederic Commo URL: https://github.com/fredcommo/rCGH VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rCGH git_branch: RELEASE_3_8 git_last_commit: 9798df7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rCGH_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rCGH_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rCGH_1.12.0.tgz vignettes: vignettes/rCGH/inst/doc/rCGH.pdf vignetteTitles: using rCGH package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rCGH/inst/doc/rCGH.R Package: Rchemcpp Version: 2.20.1 Depends: R (>= 2.15.0) Imports: Rcpp (>= 0.11.1), methods, ChemmineR LinkingTo: Rcpp Suggests: apcluster, kernlab License: GPL (>= 2.1) MD5sum: 61d0cce0d63d013179eff08b850b684a NeedsCompilation: yes Title: Similarity measures for chemical compounds Description: The Rchemcpp package implements the marginalized graph kernel and extensions, Tanimoto kernels, graph kernels, pharmacophore and 3D kernels suggested for measuring the similarity of molecules. biocViews: ImmunoOncology, Bioinformatics, CellBasedAssays, Clustering, DataImport, Infrastructure, MicrotitrePlateAssay, Proteomics, Software, Visualization Author: Michael Mahr, Guenter Klambauer Maintainer: Guenter Klambauer URL: http://www.bioinf.jku.at/software/Rchemcpp SystemRequirements: GNU make git_url: https://git.bioconductor.org/packages/Rchemcpp git_branch: RELEASE_3_8 git_last_commit: 689ea65 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Rchemcpp_2.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rchemcpp_2.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rchemcpp_2.20.1.tgz vignettes: vignettes/Rchemcpp/inst/doc/Rchemcpp.pdf vignetteTitles: Rchemcpp hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rchemcpp/inst/doc/Rchemcpp.R Package: RchyOptimyx Version: 2.22.0 Depends: R (>= 2.10) Imports: Rgraphviz, sfsmisc, graphics, methods, graph, grDevices, flowType (>= 2.0.0) Suggests: flowCore License: Artistic-2.0 Archs: i386, x64 MD5sum: da60b35d34e9ca50d24128210ea043cd NeedsCompilation: yes Title: Optimyzed Cellular Hierarchies for Flow Cytometry Description: Constructs a hierarchy of cells using flow cytometry for maximization of an external variable (e.g., a clinical outcome or a cytokine response). biocViews: FlowCytometry Author: Adrin Jalali, Nima Aghaeepour Maintainer: Adrin Jalali , Nima Aghaeepour git_url: https://git.bioconductor.org/packages/RchyOptimyx git_branch: RELEASE_3_8 git_last_commit: 3759210 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RchyOptimyx_2.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RchyOptimyx_2.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RchyOptimyx_2.22.0.tgz vignettes: vignettes/RchyOptimyx/inst/doc/RchyOptimyx.pdf vignetteTitles: flowType package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RchyOptimyx/inst/doc/RchyOptimyx.R Package: RcisTarget Version: 1.2.1 Depends: R (>= 3.4) Imports: AUCell (>= 1.1.6), BiocGenerics, data.table, feather, graphics, GSEABase, methods, R.utils, stats, SummarizedExperiment, utils Suggests: Biobase, BiocStyle, BiocParallel, doParallel, DT, foreach, igraph, knitr, RcisTarget.hg19.motifDBs.cisbpOnly.500bp, rmarkdown, testthat, visNetwork Enhances: doMC, doRNG, zoo License: GPL-3 Archs: i386, x64 MD5sum: 436ba541859959c23c23c925d11f7342 NeedsCompilation: no Title: RcisTarget: Identify transcription factor binding motifs enriched on a gene list Description: RcisTarget identifies transcription factor binding motifs (TFBS) over-represented on a gene list. In a first step, RcisTarget selects DNA motifs that are significantly over-represented in the surroundings of the transcription start site (TSS) of the genes in the gene-set. This is achieved by using a database that contains genome-wide cross-species rankings for each motif. The motifs that are then annotated to TFs and those that have a high Normalized Enrichment Score (NES) are retained. Finally, for each motif and gene-set, RcisTarget predicts the candidate target genes (i.e. genes in the gene-set that are ranked above the leading edge). biocViews: GeneRegulation, MotifAnnotation, Transcriptomics, Transcription, GeneSetEnrichment, GeneTarget Author: Sara Aibar, Gert Hulselmans, Stein Aerts. Laboratory of Computational Biology. VIB-KU Leuven Center for Brain & Disease Research. Leuven, Belgium Maintainer: Sara Aibar URL: http://scenic.aertslab.org VignetteBuilder: knitr BugReports: https://github.com/aertslab/RcisTarget/issues git_url: https://git.bioconductor.org/packages/RcisTarget git_branch: RELEASE_3_8 git_last_commit: 35aa845 git_last_commit_date: 2019-01-31 Date/Publication: 2019-01-31 source.ver: src/contrib/RcisTarget_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RcisTarget_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RcisTarget_1.2.1.tgz vignettes: vignettes/RcisTarget/inst/doc/RcisTarget.html vignetteTitles: RcisTarget: Transcription factor binding motif enrichment hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RcisTarget/inst/doc/RcisTarget.R suggestsMe: universalmotif Package: Rcpi Version: 1.18.2 Depends: R (>= 3.0.2) Imports: stats, utils, methods, RCurl, rjson, foreach, doParallel, Biostrings, GOSemSim, ChemmineR, fmcsR, rcdk (>= 3.3.8) Suggests: knitr, rmarkdown, RUnit, BiocGenerics Enhances: ChemmineOB License: Artistic-2.0 | file LICENSE MD5sum: 0b023a6ef27b2606e4676d4a44ace932 NeedsCompilation: no Title: Molecular Informatics Toolkit for Compound-Protein Interaction in Drug Discovery Description: Rcpi offers a molecular informatics toolkit with a comprehensive integration of bioinformatics and chemoinformatics tools for drug discovery. biocViews: Software, DataImport, DataRepresentation, FeatureExtraction, Cheminformatics, BiomedicalInformatics, Proteomics, GO, SystemsBiology Author: Nan Xiao [aut, cre], Dong-Sheng Cao [aut], Qing-Song Xu [aut] Maintainer: Nan Xiao URL: https://nanx.me/Rcpi/, https://github.com/road2stat/Rcpi VignetteBuilder: knitr BugReports: https://github.com/road2stat/Rcpi/issues git_url: https://git.bioconductor.org/packages/Rcpi git_branch: RELEASE_3_8 git_last_commit: 7081799 git_last_commit_date: 2019-02-24 Date/Publication: 2019-02-27 source.ver: src/contrib/Rcpi_1.18.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rcpi_1.18.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rcpi_1.18.2.tgz vignettes: vignettes/Rcpi/inst/doc/Rcpi-quickref.html, vignettes/Rcpi/inst/doc/Rcpi.html vignetteTitles: Rcpi Quick Reference Card, Rcpi: R/Bioconductor Package as an Integrated Informatics Platform for Drug Discovery hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Rcpi/inst/doc/Rcpi.R Package: RCy3 Version: 2.2.9 Depends: R (>= 3.5) Imports: httr, methods, RJSONIO, XML, utils, BiocGenerics, igraph, stats, graph, R.utils Suggests: RUnit, RColorBrewer, BiocStyle, knitr, rmarkdown License: MIT + file LICENSE MD5sum: 8948fa8a1a771703485632e1d89b0929 NeedsCompilation: no Title: Functions to Access and Control Cytoscape Description: Vizualize, analyze and explore networks using Cytoscape via R. biocViews: Visualization, GraphAndNetwork, ThirdPartyClient, Network Author: Alexander Pico, Tanja Muetze, Ruth Isserlin, Shraddha Pai, Julia Gustavsen, Georgi Kolishovski, Paul Shannon Maintainer: Alexander Pico , Tanja Muetze , Paul Shannon URL: https://github.com/cytoscape/RCy3 SystemRequirements: Cytoscape (>= 3.7.0), CyREST (>= 3.8.0) VignetteBuilder: knitr BugReports: https://github.com/cytoscape/RCy3/issues git_url: https://git.bioconductor.org/packages/RCy3 git_branch: RELEASE_3_8 git_last_commit: 0578a69 git_last_commit_date: 2019-03-07 Date/Publication: 2019-03-08 source.ver: src/contrib/RCy3_2.2.9.tar.gz win.binary.ver: bin/windows/contrib/3.5/RCy3_2.2.9.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RCy3_2.2.9.tgz vignettes: vignettes/RCy3/inst/doc/Cancer-networks-and-data.html, vignettes/RCy3/inst/doc/Custom-Graphics.html, vignettes/RCy3/inst/doc/Cytoscape-and-graphNEL.html, vignettes/RCy3/inst/doc/Cytoscape-and-iGraph.html, vignettes/RCy3/inst/doc/Cytoscape-and-NDEx.html, vignettes/RCy3/inst/doc/Filtering-Networks.html, vignettes/RCy3/inst/doc/Group-nodes.html, vignettes/RCy3/inst/doc/Identifier-mapping.html, vignettes/RCy3/inst/doc/Importing-data.html, vignettes/RCy3/inst/doc/Network-functions-and-visualization.html, vignettes/RCy3/inst/doc/Overview-of-RCy3.html, vignettes/RCy3/inst/doc/Phylogenetic-trees.html, vignettes/RCy3/inst/doc/Upgrading-existing-scripts.html vignetteTitles: 06. Cancer networks and data ~40 min, 11. Custom Graphics and Labels ~10 min, 03. Cytoscape and graphNEL ~5 min, 02. Cytoscape and igraph ~5 min, 09. Cytoscape and NDEx ~20 min, 12. Filtering Networks ~10 min, 10. Group nodes ~15 min, 07. Identifier mapping ~20 min, 04. Importing data ~5 min, 05. Network functions and visualization ~15 min, 01. Overview of RCy3 ~25 min, 13. Phylogenetic Trees ~3 min, 08. Upgrading existing scripts ~15 min hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RCy3/inst/doc/Cancer-networks-and-data.R, vignettes/RCy3/inst/doc/Custom-Graphics.R, vignettes/RCy3/inst/doc/Cytoscape-and-graphNEL.R, vignettes/RCy3/inst/doc/Cytoscape-and-iGraph.R, vignettes/RCy3/inst/doc/Cytoscape-and-NDEx.R, vignettes/RCy3/inst/doc/Filtering-Networks.R, vignettes/RCy3/inst/doc/Group-nodes.R, vignettes/RCy3/inst/doc/Identifier-mapping.R, vignettes/RCy3/inst/doc/Importing-data.R, vignettes/RCy3/inst/doc/Network-functions-and-visualization.R, vignettes/RCy3/inst/doc/Overview-of-RCy3.R, vignettes/RCy3/inst/doc/Phylogenetic-trees.R, vignettes/RCy3/inst/doc/Upgrading-existing-scripts.R importsMe: categoryCompare, NCIgraph suggestsMe: graphite Package: RCyjs Version: 2.4.0 Depends: R (>= 3.5.0), BrowserViz (>= 2.0.0), graph (>= 1.56.0) Imports: methods, httpuv (>= 1.4.0), BiocGenerics, base64enc, utils Suggests: RUnit, BiocStyle, RefNet, knitr, rmarkdown License: MIT + file LICENSE MD5sum: 19c7f00c1017e0322bca3036a696fc66 NeedsCompilation: no Title: Display and manipulate graphs in cytoscape.js Description: Interactive viewing and exploration of graphs, connecting R to Cytoscape.js, using websockets. biocViews: Visualization, GraphAndNetwork, ThirdPartyClient Author: Paul Shannon Maintainer: Paul Shannon VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RCyjs git_branch: RELEASE_3_8 git_last_commit: 205545f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RCyjs_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RCyjs_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RCyjs_2.4.0.tgz vignettes: vignettes/RCyjs/inst/doc/RCyjs.pdf, vignettes/RCyjs/inst/doc/RCyjs.html vignetteTitles: "RCyjs: programmatic access to the web browser-based network viewer,, cytoscape.js", "RCyjs: programmatic access to the web browser-based network viewer,, cytoscape.js" hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RCyjs/inst/doc/RCyjs.R Package: RDAVIDWebService Version: 1.20.0 Depends: R (>= 2.14.1), methods, graph, GOstats, ggplot2 Imports: Category, GO.db, RBGL, rJava Suggests: Rgraphviz License: GPL (>=2) MD5sum: 21a1209b7e43d5753dcf84a4590d06e7 NeedsCompilation: no Title: An R Package for retrieving data from DAVID into R objects using Web Services API. Description: Tools for retrieving data from the Database for Annotation, Visualization and Integrated Discovery (DAVID) using Web Services into R objects. This package offers the main functionalities of DAVID website including: i) user friendly connectivity to upload gene/background list/s, change gene/background position, select current specie/s, select annotations, etc. ii) Reports of the submitted Gene List, Annotation Category Summary, Gene/Term Clusters, Functional Annotation Chart, Functional Annotation Table biocViews: Visualization, DifferentialExpression, GraphAndNetwork Author: Cristobal Fresno and Elmer A. Fernandez Maintainer: Cristobal Fresno URL: http://www.bdmg.com.ar, http://david.abcc.ncifcrf.gov/ git_url: https://git.bioconductor.org/packages/RDAVIDWebService git_branch: RELEASE_3_8 git_last_commit: 87bd43b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RDAVIDWebService_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RDAVIDWebService_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RDAVIDWebService_1.20.0.tgz vignettes: vignettes/RDAVIDWebService/inst/doc/RDavidWS-vignette.pdf vignetteTitles: RDAVIDWebService: a versatile R interface to DAVID hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RDAVIDWebService/inst/doc/RDavidWS-vignette.R dependsOnMe: CompGO suggestsMe: FGNet, IntramiRExploreR Package: rDGIdb Version: 1.8.0 Imports: jsonlite,httr,methods,graphics Suggests: BiocStyle,knitr,testthat License: MIT + file LICENSE MD5sum: b08e5cd64ac2af2f3fd05a7ec4472b1c NeedsCompilation: no Title: R Wrapper for DGIdb Description: The rDGIdb package provides a wrapper for the Drug Gene Interaction Database (DGIdb). For simplicity, the wrapper query function and output resembles the user interface and results format provided on the DGIdb website (http://www.dgidb.org/). biocViews: Software,ResearchField,Pharmacogenetics,Pharmacogenomics, FunctionalGenomics,WorkflowStep,Annotation Author: Thomas Thurnherr, Franziska Singer, Daniel J. Stekhoven, and Niko Beerenwinkel Maintainer: Thomas Thurnherr VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rDGIdb git_branch: RELEASE_3_8 git_last_commit: 864cc4b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rDGIdb_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rDGIdb_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rDGIdb_1.8.0.tgz vignettes: vignettes/rDGIdb/inst/doc/vignette.pdf vignetteTitles: Query DGIdb using R hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rDGIdb/inst/doc/vignette.R Package: Rdisop Version: 1.42.1 Depends: R (>= 2.0.0), RcppClassic LinkingTo: RcppClassic, Rcpp Suggests: RUnit License: GPL-2 MD5sum: 669585bc83dbc17643777baa37564444 NeedsCompilation: yes Title: Decomposition of Isotopic Patterns Description: Identification of metabolites using high precision mass spectrometry. MS Peaks are used to derive a ranked list of sum formulae, alternatively for a given sum formula the theoretical isotope distribution can be calculated to search in MS peak lists. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics Author: Anton Pervukhin , Steffen Neumann Maintainer: Steffen Neumann URL: https://github.com/sneumann/Rdisop SystemRequirements: None BugReports: https://github.com/sneumann/Rdisop/issues/new git_url: https://git.bioconductor.org/packages/Rdisop git_branch: RELEASE_3_8 git_last_commit: d0383fe git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Rdisop_1.42.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rdisop_1.42.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rdisop_1.42.1.tgz vignettes: vignettes/Rdisop/inst/doc/Rdisop.pdf vignetteTitles: Molecule Identification with Rdisop hasREADME: FALSE hasNEWS: FALSE hasINSTALL: TRUE hasLICENSE: FALSE suggestsMe: MSnbase Package: RDRToolbox Version: 1.32.0 Depends: R (>= 2.9.0) Imports: graphics, grDevices, methods, stats, MASS, rgl Suggests: golubEsets License: GPL (>= 2) Archs: i386, x64 MD5sum: 4878943bca03a276c3ad77772ae786cc NeedsCompilation: no Title: A package for nonlinear dimension reduction with Isomap and LLE. Description: A package for nonlinear dimension reduction using the Isomap and LLE algorithm. It also includes a routine for computing the Davis-Bouldin-Index for cluster validation, a plotting tool and a data generator for microarray gene expression data and for the Swiss Roll dataset. biocViews: DimensionReduction, FeatureExtraction, Visualization, Clustering, Microarray Author: Christoph Bartenhagen Maintainer: Christoph Bartenhagen git_url: https://git.bioconductor.org/packages/RDRToolbox git_branch: RELEASE_3_8 git_last_commit: 37af9c3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RDRToolbox_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RDRToolbox_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RDRToolbox_1.32.0.tgz vignettes: vignettes/RDRToolbox/inst/doc/vignette.pdf vignetteTitles: A package for nonlinear dimension reduction with Isomap and LLE. hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RDRToolbox/inst/doc/vignette.R Package: ReactomePA Version: 1.26.0 Depends: R (>= 3.4.0) Imports: AnnotationDbi, DOSE (>= 3.5.1), enrichplot, ggplot2, ggraph, reactome.db, igraph, graphite Suggests: BiocStyle, clusterProfiler, knitr, org.Hs.eg.db, prettydoc, testthat License: GPL-2 MD5sum: b240608152ce98d954046ecd1e14ba7b NeedsCompilation: no Title: Reactome Pathway Analysis Description: This package provides functions for pathway analysis based on REACTOME pathway database. It implements enrichment analysis, gene set enrichment analysis and several functions for visualization. biocViews: Pathways, Visualization, Annotation, MultipleComparison, GeneSetEnrichment, Reactome Author: Guangchuang Yu [aut, cre], Vladislav Petyuk [ctb] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/ReactomePA VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/ReactomePA/issues git_url: https://git.bioconductor.org/packages/ReactomePA git_branch: RELEASE_3_8 git_last_commit: cc07e54 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ReactomePA_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ReactomePA_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ReactomePA_1.26.0.tgz vignettes: vignettes/ReactomePA/inst/doc/ReactomePA.html vignetteTitles: An R package for Reactome Pathway Analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ReactomePA/inst/doc/ReactomePA.R importsMe: bioCancer, LINC, miRsponge suggestsMe: ChIPseeker, CINdex, clusterProfiler Package: readat Version: 1.8.0 Depends: R (>= 3.4.0) Imports: assertive.base (>= 0.0-7), assertive.files (>= 0.0-2), assertive.numbers (>= 0.0-2), assertive.properties (>= 0.0-4), assertive.sets (>= 0.0-3), assertive.types (>= 0.0-3), Biobase (>= 2.34.0), data.table (>= 1.10.4), dplyr (>= 0.5.0), magrittr (>= 1.5), openxlsx (>= 4.0.17), pathological (>= 0.1-2), reshape2 (>= 1.4.2), stats, stringi (>= 1.1.5), SummarizedExperiment (>= 1.4.0), testthat (>= 1.0.2), tidyr (>= 0.6.2), utils Suggests: knitr, MSnbase, rmarkdown, withr License: GPL-3 MD5sum: 5997fc86272923223432b715e16ba7be NeedsCompilation: no Title: Functionality to Read and Manipulate SomaLogic ADAT files Description: This package contains functionality to import, transform and annotate data from ADAT files generated by the SomaLogic SOMAscan platform. biocViews: GeneExpression, DataImport, Proteomics, OneChannel, ProprietaryPlatforms Author: Richard Cotton [cre, aut], Aditya Bhagwat [aut] Maintainer: Richard Cotton URL: https://bitbucket.org/graumannlabtools/readat VignetteBuilder: knitr BugReports: https://bitbucket.org/graumannlabtools/readat/issues git_url: https://git.bioconductor.org/packages/readat git_branch: RELEASE_3_8 git_last_commit: a5a144d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/readat_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/readat_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/readat_1.8.0.tgz vignettes: vignettes/readat/inst/doc/introduction.html vignetteTitles: Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/readat/inst/doc/introduction.R Package: ReadqPCR Version: 1.28.0 Depends: R(>= 2.14.0), Biobase, methods Suggests: qpcR License: LGPL-3 MD5sum: dff61efd77bb86fb720acd7c63b32976 NeedsCompilation: no Title: Read qPCR data Description: The package provides functions to read raw RT-qPCR data of different platforms. biocViews: DataImport, MicrotitrePlateAssay, GeneExpression, qPCR Author: James Perkins, Matthias Kohl, Nor Izayu Abdul Rahman Maintainer: James Perkins URL: http://www.bioconductor.org/packages/release/bioc/html/ReadqPCR.html git_url: https://git.bioconductor.org/packages/ReadqPCR git_branch: RELEASE_3_8 git_last_commit: 5d54273 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ReadqPCR_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ReadqPCR_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ReadqPCR_1.28.0.tgz vignettes: vignettes/ReadqPCR/inst/doc/ReadqPCR.pdf vignetteTitles: Functions to load RT-qPCR data into R hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ReadqPCR/inst/doc/ReadqPCR.R dependsOnMe: NormqPCR Package: reb Version: 1.60.0 Depends: R (>= 2.0), Biobase, idiogram (>= 1.5.3) License: GPL-2 MD5sum: b4e0632e5c9173414286e0dba2af409a NeedsCompilation: yes Title: Regional Expression Biases Description: A set of functions to dentify regional expression biases biocViews: Microarray, CopyNumberVariation, Visualization Author: Kyle A. Furge and Karl Dykema Maintainer: Karl J. Dykema git_url: https://git.bioconductor.org/packages/reb git_branch: RELEASE_3_8 git_last_commit: 20e853c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/reb_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/reb_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/reb_1.60.0.tgz vignettes: vignettes/reb/inst/doc/reb.pdf vignetteTitles: Smoothing of Microarray Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/reb/inst/doc/reb.R Package: REBET Version: 1.0.0 Depends: ASSET Imports: stats, utils Suggests: RUnit, BiocGenerics License: GPL-2 Archs: i386, x64 MD5sum: f48ce39437f7c86e3685d0426ba8083c NeedsCompilation: yes Title: The subREgion-based BurdEn Test (REBET) Description: There is an increasing focus to investigate the association between rare variants and diseases. The REBET package implements the subREgion-based BurdEn Test which is a powerful burden test that simultaneously identifies susceptibility loci and sub-regions. biocViews: Software, VariantAnnotation, SNP Author: Bill Wheeler [cre], Bin Zhu [aut], Lisa Mirabello [ctb], Nilanjan Chatterjee [ctb] Maintainer: Bill Wheeler git_url: https://git.bioconductor.org/packages/REBET git_branch: RELEASE_3_8 git_last_commit: 321c825 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/REBET_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/REBET_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/REBET_1.0.0.tgz vignettes: vignettes/REBET/inst/doc/vignette.pdf vignetteTitles: REBET Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/REBET/inst/doc/vignette.R Package: recount Version: 1.8.2 Depends: R (>= 3.3.0), SummarizedExperiment Imports: BiocParallel, derfinder, downloader, GEOquery, GenomeInfoDb, GenomicRanges, IRanges, methods, RCurl, rentrez, rtracklayer (>= 1.35.3), S4Vectors, stats, utils Suggests: AnnotationDbi, BiocManager, BiocStyle (>= 2.5.19), DESeq2, sessioninfo, EnsDb.Hsapiens.v79, GenomicFeatures, knitcitations, knitr (>= 1.6), org.Hs.eg.db, RefManageR, regionReport (>= 1.9.4), rmarkdown (>= 0.9.5), testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: f8414919e8dd691a9b89a8b6c0e48413 NeedsCompilation: no Title: Explore and download data from the recount project Description: Explore and download data from the recount project available at https://jhubiostatistics.shinyapps.io/recount/. Using the recount package you can download RangedSummarizedExperiment objects at the gene, exon or exon-exon junctions level, the raw counts, the phenotype metadata used, the urls to the sample coverage bigWig files or the mean coverage bigWig file for a particular study. The RangedSummarizedExperiment objects can be used by different packages for performing differential expression analysis. Using http://bioconductor.org/packages/derfinder you can perform annotation-agnostic differential expression analyses with the data from the recount project as described at http://www.nature.com/nbt/journal/v35/n4/full/nbt.3838.html. biocViews: Coverage, DifferentialExpression, GeneExpression, RNASeq, Sequencing, Software, DataImport, ImmunoOncology Author: Leonardo Collado-Torres [aut, cre], Abhinav Nellore [ctb], Andrew E. Jaffe [ctb], Margaret A. Taub [ctb], Kai Kammers [ctb], Shannon E. Ellis [ctb], Kasper Daniel Hansen [ctb], Ben Langmead [ctb], Jeffrey T. Leek [aut, ths] Maintainer: Leonardo Collado-Torres URL: https://github.com/leekgroup/recount VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/recount/ git_url: https://git.bioconductor.org/packages/recount git_branch: RELEASE_3_8 git_last_commit: ecd06f4 git_last_commit_date: 2019-02-14 Date/Publication: 2019-02-16 source.ver: src/contrib/recount_1.8.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/recount_1.8.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/recount_1.8.2.tgz vignettes: vignettes/recount/inst/doc/recount-quickstart.html, vignettes/recount/inst/doc/SRP009615-results.html vignetteTitles: recount quick start guide, Basic DESeq2 results exploration hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/recount/inst/doc/recount-quickstart.R, vignettes/recount/inst/doc/SRP009615-results.R importsMe: psichomics Package: recoup Version: 1.10.1 Depends: R (>= 2.13.0), GenomicRanges, GenomicAlignments, ggplot2, ComplexHeatmap Imports: BiocGenerics, biomaRt, circlize, graphics, grDevices, methods, rtracklayer, plyr, stats, utils Suggests: grid, GenomeInfoDb, Rsamtools, BiocStyle, knitr, rmarkdown, zoo, RUnit, BiocManager, BSgenome, RSQLite, RMySQL Enhances: parallel License: GPL (>= 3) MD5sum: 75f92e920049e9c4cbd689e55199cd81 NeedsCompilation: no Title: An R package for the creation of complex genomic profile plots Description: recoup calculates and plots signal profiles created from short sequence reads derived from Next Generation Sequencing technologies. The profiles provided are either sumarized curve profiles or heatmap profiles. Currently, recoup supports genomic profile plots for reads derived from ChIP-Seq and RNA-Seq experiments. The package uses ggplot2 and ComplexHeatmap graphics facilities for curve and heatmap coverage profiles respectively. biocViews: ImmunoOncology, Software, GeneExpression, Preprocessing, QualityControl, RNASeq, ChIPSeq, Sequencing, Coverage Author: Panagiotis Moulos Maintainer: Panagiotis Moulos URL: https://github.com/pmoulos/recoup VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/recoup git_branch: RELEASE_3_8 git_last_commit: 94b6d6d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/recoup_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/recoup_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/recoup_1.10.1.tgz vignettes: vignettes/recoup/inst/doc/recoup_intro.html vignetteTitles: Introduction to the recoup package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/recoup/inst/doc/recoup_intro.R Package: RedeR Version: 1.30.0 Depends: R (>= 3.3.3), methods Imports: igraph Suggests: pvclust, BiocStyle, knitr, rmarkdown License: GPL (>= 2) MD5sum: feec78beaad4c43950605f9fb6af3f9d NeedsCompilation: no Title: Interactive visualization and manipulation of nested networks Description: RedeR is an R-based package combined with a stand-alone Java application for interactive visualization and manipulation of modular structures, nested networks and multiple levels of hierarchical associations. biocViews: Infrastructure, GraphAndNetwork, Software, Network, Visualization, DataRepresentation Author: Mauro Castro, Xin Wang, Florian Markowetz Maintainer: Mauro Castro URL: http://genomebiology.com/2012/13/4/R29 SystemRequirements: Java Runtime Environment (>= 6) VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RedeR git_branch: RELEASE_3_8 git_last_commit: 47bcee9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RedeR_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RedeR_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RedeR_1.30.0.tgz vignettes: vignettes/RedeR/inst/doc/RedeR.html vignetteTitles: "RedeR: hierarchical network representation" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RedeR/inst/doc/RedeR.R importsMe: PANR, RTN, transcriptogramer Package: REDseq Version: 1.28.0 Depends: R (>= 2.15.0), BiocGenerics (>= 0.1.0), BSgenome.Celegans.UCSC.ce2, multtest, Biostrings, BSgenome, ChIPpeakAnno Imports: BiocGenerics, AnnotationDbi, Biostrings, ChIPpeakAnno, graphics, IRanges (>= 1.13.5), multtest, stats, utils License: GPL (>=2) MD5sum: 77974694af5810b7e9cbec3c126cc814 NeedsCompilation: no Title: Analysis of high-throughput sequencing data processed by restriction enzyme digestion Description: The package includes functions to build restriction enzyme cut site (RECS) map, distribute mapped sequences on the map with five different approaches, find enriched/depleted RECSs for a sample, and identify differentially enriched/depleted RECSs between samples. biocViews: Sequencing, SequenceMatching, Preprocessing Author: Lihua Julie Zhu and Thomas Fazzio Maintainer: Lihua Julie Zhu git_url: https://git.bioconductor.org/packages/REDseq git_branch: RELEASE_3_8 git_last_commit: 6278804 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/REDseq_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/REDseq_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/REDseq_1.28.0.tgz vignettes: vignettes/REDseq/inst/doc/REDseq.pdf vignetteTitles: REDseq Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/REDseq/inst/doc/REDseq.R Package: RefNet Version: 1.18.0 Depends: R (>= 2.15.0), methods, IRanges, PSICQUIC, AnnotationHub, RCurl, shiny Imports: BiocGenerics Suggests: RUnit, BiocStyle, org.Hs.eg.db License: Artistic-2.0 MD5sum: 5f543dd88c9275d0decf135bffa552dd NeedsCompilation: no Title: A queryable collection of molecular interactions, from many sources Description: Molecular interactions with metadata, some archived, some dynamically obtained biocViews: GraphAndNetwork Author: Paul Shannon Maintainer: Paul Shannon git_url: https://git.bioconductor.org/packages/RefNet git_branch: RELEASE_3_8 git_last_commit: 957a26e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RefNet_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RefNet_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RefNet_1.18.0.tgz vignettes: vignettes/RefNet/inst/doc/RefNet.pdf vignetteTitles: RefNet hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RefNet/inst/doc/RefNet.R suggestsMe: RCyjs Package: RefPlus Version: 1.52.0 Depends: R (>= 2.8.0), Biobase (>= 2.1.0), affy (>= 1.20.0), affyPLM (>= 1.18.0), preprocessCore (>= 1.4.0) Suggests: affydata License: GPL (>= 2) MD5sum: 1f3f27dfeccc81b91cef120849de5d1d NeedsCompilation: no Title: A function set for the Extrapolation Strategy (RMA+) and Extrapolation Averaging (RMA++) methods. Description: The package contains functions for pre-processing Affymetrix data using the RMA+ and the RMA++ methods. biocViews: Microarray, OneChannel, Preprocessing Author: Kai-Ming Chang , Chris Harbron , Marie C South Maintainer: Kai-Ming Chang git_url: https://git.bioconductor.org/packages/RefPlus git_branch: RELEASE_3_8 git_last_commit: ecabd0b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RefPlus_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RefPlus_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RefPlus_1.52.0.tgz vignettes: vignettes/RefPlus/inst/doc/RefPlus.pdf vignetteTitles: RefPlus Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RefPlus/inst/doc/RefPlus.R Package: regioneR Version: 1.14.0 Depends: GenomicRanges Imports: memoise, GenomicRanges, IRanges, BSgenome, Biostrings, rtracklayer, parallel, graphics, stats, utils, methods, GenomeInfoDb, S4Vectors Suggests: BiocStyle, knitr, BSgenome.Hsapiens.UCSC.hg19.masked, testthat License: Artistic-2.0 MD5sum: 526f133b01e3b43e3e1e72a1c34b4076 NeedsCompilation: no Title: Association analysis of genomic regions based on permutation tests Description: regioneR offers a statistical framework based on customizable permutation tests to assess the association between genomic region sets and other genomic features. biocViews: Genetics, ChIPSeq, DNASeq, MethylSeq, CopyNumberVariation Author: Anna Diez-Villanueva , Roberto Malinverni and Bernat Gel Maintainer: Bernat Gel VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/regioneR git_branch: RELEASE_3_8 git_last_commit: 1b54982 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/regioneR_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/regioneR_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/regioneR_1.14.0.tgz vignettes: vignettes/regioneR/inst/doc/regioneR.html vignetteTitles: regioneR vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/regioneR/inst/doc/regioneR.R dependsOnMe: karyoploteR importsMe: annotatr, ChIPpeakAnno, karyoploteR Package: regionReport Version: 1.16.1 Depends: R(>= 3.2) Imports: BiocStyle (>= 2.5.19), derfinder (>= 1.1.0), DEFormats, DESeq2, GenomeInfoDb, GenomicRanges, knitcitations (>= 1.0.1), knitr (>= 1.6), knitrBootstrap (>= 0.9.0), methods, RefManageR, rmarkdown (>= 0.9.5), S4Vectors, SummarizedExperiment Suggests: BiocManager, biovizBase, bumphunter (>= 1.7.6), derfinderPlot (>= 1.3.2), sessioninfo, DT, DESeq, edgeR, ggbio (>= 1.13.13), ggplot2, grid, gridExtra, IRanges, mgcv, pasilla, pheatmap, RColorBrewer, TxDb.Hsapiens.UCSC.hg19.knownGene, whisker License: Artistic-2.0 MD5sum: 52d87e72b67f0cbe611fbf647ccbff39 NeedsCompilation: no Title: Generate HTML or PDF reports for a set of genomic regions or DESeq2/edgeR results Description: Generate HTML or PDF reports to explore a set of regions such as the results from annotation-agnostic expression analysis of RNA-seq data at base-pair resolution performed by derfinder. You can also create reports for DESeq2 or edgeR results. biocViews: DifferentialExpression, Sequencing, RNASeq, Software, Visualization, Transcription, Coverage, ReportWriting, DifferentialMethylation, DifferentialPeakCalling, ImmunoOncology Author: Leonardo Collado-Torres [aut, cre], Andrew E. Jaffe [aut], Jeffrey T. Leek [aut, ths] Maintainer: Leonardo Collado-Torres URL: https://github.com/leekgroup/regionReport VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/regionReport/ git_url: https://git.bioconductor.org/packages/regionReport git_branch: RELEASE_3_8 git_last_commit: dacb49e git_last_commit_date: 2018-12-03 Date/Publication: 2018-12-03 source.ver: src/contrib/regionReport_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/regionReport_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/regionReport_1.16.1.tgz vignettes: vignettes/regionReport/inst/doc/bumphunterExample.html, vignettes/regionReport/inst/doc/bumphunterExampleOutput.html, vignettes/regionReport/inst/doc/regionReport.html vignetteTitles: Example report using bumphunter results, Basic genomic regions exploration, Introduction to regionReport hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/regionReport/inst/doc/bumphunterExample.R, vignettes/regionReport/inst/doc/bumphunterExampleOutput.R, vignettes/regionReport/inst/doc/regionReport.R suggestsMe: recount Package: regsplice Version: 1.8.1 Imports: glmnet, SummarizedExperiment, S4Vectors, limma, edgeR, stats, pbapply, utils, methods Suggests: testthat, BiocStyle, knitr, rmarkdown License: MIT + file LICENSE MD5sum: e9e8b4154fff0d4f9257a5778b5bf07f NeedsCompilation: no Title: L1-regularization based methods for detection of differential splicing Description: Statistical methods for detection of differential splicing (differential exon usage) in RNA-seq and exon microarray data, using L1-regularization (lasso) to improve power. biocViews: ImmunoOncology, AlternativeSplicing, DifferentialExpression, DifferentialSplicing, Sequencing, RNASeq, Microarray, ExonArray, ExperimentalDesign, Software Author: Lukas M. Weber [aut, cre] Maintainer: Lukas M. Weber URL: https://github.com/lmweber/regsplice VignetteBuilder: knitr BugReports: https://github.com/lmweber/regsplice/issues git_url: https://git.bioconductor.org/packages/regsplice git_branch: RELEASE_3_8 git_last_commit: 5569b4b git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/regsplice_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/regsplice_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/regsplice_1.8.1.tgz vignettes: vignettes/regsplice/inst/doc/regsplice-workflow.pdf vignetteTitles: Example workflow for regsplice package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/regsplice/inst/doc/regsplice-workflow.R Package: REMP Version: 1.6.1 Depends: R (>= 3.4), SummarizedExperiment(>= 1.1.6), minfi (>= 1.22.0), IlluminaHumanMethylation450kanno.ilmn12.hg19, IlluminaHumanMethylationEPICanno.ilm10b2.hg19 Imports: graphics, stats, utils, methods, settings, BiocGenerics, S4Vectors, Biostrings, GenomicRanges, IRanges, BiocParallel, doParallel, parallel, foreach, caret, kernlab, ranger, BSgenome, AnnotationHub, BSgenome.Hsapiens.UCSC.hg19, org.Hs.eg.db, impute, iterators Suggests: knitr, rmarkdown, minfiDataEPIC License: GPL-3 MD5sum: 0905f19c4e54251951492aa785130231 NeedsCompilation: no Title: Repetitive Element Methylation Prediction Description: Machine learning-based tools to predict DNA methylation of locus-specific repetitive elements (RE) by learning surrounding genetic and epigenetic information. These tools provide genomewide and single-base resolution of DNA methylation prediction on RE that are difficult to measure using array-based or sequencing-based platforms, which enables epigenome-wide association study (EWAS) and differentially methylated region (DMR) analysis on RE. biocViews: ImmunoOncology, DNAMethylation, Microarray, MethylationArray, GenePrediction, Sequencing, Alignment, Epigenetics, Normalization, Preprocessing, MultiChannel, TwoChannel, DifferentialMethylation, QualityControl, DataImport Author: Yinan Zheng [aut, cre], Lei Liu [aut], Wei Zhang [aut], Warren Kibbe [aut], Lifang Hou [aut, cph] Maintainer: Yinan Zheng URL: https://github.com/YinanZheng/REMP BugReports: https://github.com/YinanZheng/REMP/issues git_url: https://git.bioconductor.org/packages/REMP git_branch: RELEASE_3_8 git_last_commit: 4e47738 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-05 source.ver: src/contrib/REMP_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/REMP_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/REMP_1.6.1.tgz vignettes: vignettes/REMP/inst/doc/REMP.pdf vignetteTitles: An Introduction to the REMP Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/REMP/inst/doc/REMP.R Package: Repitools Version: 1.28.0 Depends: R (>= 3.0.0), methods, BiocGenerics (>= 0.8.0) Imports: parallel, S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), GenomeInfoDb, GenomicRanges, Biostrings, Rsamtools, GenomicAlignments, rtracklayer, BSgenome (>= 1.47.3), gplots, grid, MASS, gsmoothr, edgeR (>= 3.4.0), DNAcopy, Ringo, aroma.affymetrix, Rsolnp, cluster Suggests: ShortRead, BSgenome.Hsapiens.UCSC.hg18 License: LGPL (>= 2) MD5sum: 59c4e8b79e061909762b5e6d25f55510 NeedsCompilation: yes Title: Epigenomic tools Description: Tools for the analysis of enrichment-based epigenomic data. Features include summarization and visualization of epigenomic data across promoters according to gene expression context, finding regions of differential methylation/binding, BayMeth for quantifying methylation etc. biocViews: DNAMethylation, GeneExpression, MethylSeq Author: Mark Robinson , Dario Strbenac , Aaron Statham , Andrea Riebler Maintainer: Mark Robinson git_url: https://git.bioconductor.org/packages/Repitools git_branch: RELEASE_3_8 git_last_commit: 7aac8b7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Repitools_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Repitools_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Repitools_1.28.0.tgz vignettes: vignettes/Repitools/inst/doc/Repitools_vignette.pdf vignetteTitles: Using Repitools for Epigenomic Sequencing Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Repitools/inst/doc/Repitools_vignette.R Package: ReportingTools Version: 2.22.1 Depends: methods, knitr, utils Imports: Biobase,hwriter,Category,GOstats,limma(>= 3.17.5),lattice,AnnotationDbi,edgeR, annotate,PFAM.db, GSEABase, BiocGenerics(>= 0.1.6), grid, XML, R.utils, DESeq2(>= 1.3.41), ggplot2, ggbio, IRanges Suggests: RUnit, ALL, hgu95av2.db, org.Mm.eg.db, shiny, pasilla, org.Sc.sgd.db License: Artistic-2.0 Archs: i386, x64 MD5sum: 9f1b8a6037be14b4dc273334c6b57a58 NeedsCompilation: no Title: Tools for making reports in various formats Description: The ReportingTools software package enables users to easily display reports of analysis results generated from sources such as microarray and sequencing data. The package allows users to create HTML pages that may be viewed on a web browser such as Safari, or in other formats readable by programs such as Excel. Users can generate tables with sortable and filterable columns, make and display plots, and link table entries to other data sources such as NCBI or larger plots within the HTML page. Using the package, users can also produce a table of contents page to link various reports together for a particular project that can be viewed in a web browser. For more examples, please visit our site: http:// research-pub.gene.com/ReportingTools. biocViews: ImmunoOncology, Software, Visualization, Microarray, RNASeq, GO, DataRepresentation, GeneSetEnrichment Author: Jason A. Hackney, Melanie Huntley, Jessica L. Larson, Christina Chaivorapol, Gabriel Becker, and Josh Kaminker Maintainer: Jason A. Hackney , Gabriel Becker , Jessica L. Larson VignetteBuilder: utils, knitr git_url: https://git.bioconductor.org/packages/ReportingTools git_branch: RELEASE_3_8 git_last_commit: dce6af6 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ReportingTools_2.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ReportingTools_2.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ReportingTools_2.22.1.tgz vignettes: vignettes/ReportingTools/inst/doc/basicReportingTools.pdf, vignettes/ReportingTools/inst/doc/microarrayAnalysis.pdf, vignettes/ReportingTools/inst/doc/rnaseqAnalysis.pdf, vignettes/ReportingTools/inst/doc/shiny.pdf, vignettes/ReportingTools/inst/doc/knitr.html vignetteTitles: ReportingTools basics, Reporting on microarray differential expression, Reporting on RNA-seq differential expression, ReportingTools shiny, Knitr and ReportingTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ReportingTools/inst/doc/basicReportingTools.R, vignettes/ReportingTools/inst/doc/knitr.R, vignettes/ReportingTools/inst/doc/microarrayAnalysis.R, vignettes/ReportingTools/inst/doc/rnaseqAnalysis.R, vignettes/ReportingTools/inst/doc/shiny.R importsMe: affycoretools, EnrichmentBrowser suggestsMe: cpvSNP, GSEABase, npGSEA Package: ReQON Version: 1.28.0 Depends: R (>= 3.0.2), Rsamtools, seqbias Imports: rJava, graphics, stats, utils, grDevices Suggests: BiocStyle License: GPL-2 MD5sum: 4e9e1fd5a4b1c189e039a97dff587ccb NeedsCompilation: no Title: Recalibrating Quality Of Nucleotides Description: Algorithm for recalibrating the base quality scores for aligned sequencing data in BAM format. biocViews: Sequencing, HighThroughputSequencing, Preprocessing, QualityControl Author: Christopher Cabanski, Keary Cavin, Chris Bizon Maintainer: Christopher Cabanski SystemRequirements: Java version >= 1.6 git_url: https://git.bioconductor.org/packages/ReQON git_branch: RELEASE_3_8 git_last_commit: 1a68a91 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ReQON_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ReQON_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ReQON_1.28.0.tgz vignettes: vignettes/ReQON/inst/doc/ReQON.pdf vignetteTitles: ReQON Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ReQON/inst/doc/ReQON.R Package: restfulSE Version: 1.4.1 Depends: R (>= 3.5), SummarizedExperiment,DelayedArray Imports: utils, stats, methods, S4Vectors, Biobase,reshape2, AnnotationDbi, DBI, GO.db, rhdf5client, dplyr (>= 0.7.1), magrittr, bigrquery, ExperimentHub, AnnotationHub, rlang Suggests: knitr, testthat, Rtsne, org.Mm.eg.db, org.Hs.eg.db, BiocStyle License: Artistic-2.0 MD5sum: b5906075e8c499789ae0ac4a7678428a NeedsCompilation: no Title: Access matrix-like HDF5 server content or BigQuery content through a SummarizedExperiment interface Description: This package provides functions and classes to interface with remote data stores by operating on SummarizedExperiment-like objects. biocViews: ImmunoOncology, Infrastructure, SingleCell, Transcriptomics, Sequencing, Coverage Author: Vincent Carey [aut], Shweta Gopaulakrishnan [cre, aut] Maintainer: Shweta Gopaulakrishnan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/restfulSE git_branch: RELEASE_3_8 git_last_commit: f3f9d66 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/restfulSE_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/restfulSE_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/restfulSE_1.4.1.tgz vignettes: vignettes/restfulSE/inst/doc/restfulSE.pdf vignetteTitles: restfulSE -- experiments with SE interface to remote HDF5 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/restfulSE/inst/doc/restfulSE.R dependsOnMe: tenXplore suggestsMe: BiocOncoTK, BiocSklearn Package: rexposome Version: 1.4.0 Depends: R (>= 3.5), Biobase Imports: methods, utils, stats, lsr, FactoMineR, stringr, circlize, corrplot, ggplot2, reshape2, pryr, S4Vectors, imputeLCMD, scatterplot3d, glmnet, gridExtra, grid, Hmisc, gplots, gtools, scales, lme4, grDevices, graphics, ggrepel, mice Suggests: mclust, flexmix, testthat, BiocStyle, knitr, rmarkdown License: MIT + file LICENSE MD5sum: 3ba602e53b72ac2e89c0206164a9f6df NeedsCompilation: no Title: Exposome exploration and outcome data analysis Description: Package that allows to explore the exposome and to perform association analyses between exposures and health outcomes. biocViews: Software, BiologicalQuestion, Infrastructure, DataImport, DataRepresentation, BiomedicalInformatics, ExperimentalDesign, MultipleComparison, Classification, Clustering Author: Carles Hernandez-Ferrer [aut, cre], Juan R. Gonzalez [aut] Maintainer: Carles Hernandez-Ferrer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rexposome git_branch: RELEASE_3_8 git_last_commit: 5a5f209 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rexposome_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rexposome_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rexposome_1.4.0.tgz vignettes: vignettes/rexposome/inst/doc/exposome_data_analysis.html, vignettes/rexposome/inst/doc/mutiple_imputation_data_analysis.html vignetteTitles: Exposome Data Analysis, Dealing with Multiple Imputations hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rexposome/inst/doc/exposome_data_analysis.R, vignettes/rexposome/inst/doc/mutiple_imputation_data_analysis.R importsMe: omicRexposome Package: rfPred Version: 1.20.0 Depends: Rsamtools, GenomicRanges, IRanges, data.table, methods, parallel Suggests: BiocStyle License: GPL (>=2 ) MD5sum: 9d76d084ffbc2c95925accca4d39888b NeedsCompilation: yes Title: Assign rfPred functional prediction scores to a missense variants list Description: Based on external numerous data files where rfPred scores are pre-calculated on all genomic positions of the human exome, the package gives rfPred scores to missense variants identified by the chromosome, the position (hg19 version), the referent and alternative nucleotids and the uniprot identifier of the protein. Note that for using the package, the user has to be connected on the Internet or to download the TabixFile and index (approximately 3.3 Go). biocViews: Software, Annotation, Classification Author: Fabienne Jabot-Hanin, Hugo Varet and Jean-Philippe Jais Maintainer: Hugo Varet URL: http://www.sbim.fr/rfPred git_url: https://git.bioconductor.org/packages/rfPred git_branch: RELEASE_3_8 git_last_commit: 73789cf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rfPred_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rfPred_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rfPred_1.20.0.tgz vignettes: vignettes/rfPred/inst/doc/vignette.pdf vignetteTitles: CalculatingrfPredscoreswithpackagerfPred hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rfPred/inst/doc/vignette.R Package: rGADEM Version: 2.30.0 Depends: R (>= 2.11.0), Biostrings, IRanges, BSgenome, methods, seqLogo Imports: Biostrings, IRanges, methods, graphics, seqLogo Suggests: BSgenome.Hsapiens.UCSC.hg19 License: Artistic-2.0 Archs: i386, x64 MD5sum: 6c91a120a1451994f8a92d7a61b55662 NeedsCompilation: yes Title: de novo motif discovery Description: rGADEM is an efficient de novo motif discovery tool for large-scale genomic sequence data. It is an open-source R package, which is based on the GADEM software. biocViews: Microarray, ChIPchip, Sequencing, ChIPSeq, MotifDiscovery Author: Arnaud Droit, Raphael Gottardo, Gordon Robertson and Leiping Li Maintainer: Arnaud Droit git_url: https://git.bioconductor.org/packages/rGADEM git_branch: RELEASE_3_8 git_last_commit: f882304 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rGADEM_2.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rGADEM_2.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rGADEM_2.30.0.tgz vignettes: vignettes/rGADEM/inst/doc/rGADEM.pdf vignetteTitles: The rGADEM users guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rGADEM/inst/doc/rGADEM.R importsMe: MotIV suggestsMe: universalmotif Package: RGalaxy Version: 1.26.0 Depends: XML, methods, tools, optparse Imports: BiocGenerics, Biobase, roxygen2 Suggests: RUnit, hgu95av2.db, AnnotationDbi, knitr, formatR, Rserve Enhances: RSclient License: Artistic-2.0 Archs: i386, x64 MD5sum: b88c6f6f410d2f852096e69ebbe040d1 NeedsCompilation: no Title: Make an R function available in the Galaxy web platform Description: Given an R function and its manual page, make the documented function available in Galaxy. biocViews: Infrastructure Author: Dan Tenenbaum Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RGalaxy git_branch: RELEASE_3_8 git_last_commit: e3651a5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RGalaxy_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RGalaxy_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RGalaxy_1.26.0.tgz vignettes: vignettes/RGalaxy/inst/doc/RGalaxy-vignette.html vignetteTitles: Introduction to RGalaxy hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RGalaxy/inst/doc/RGalaxy-vignette.R Package: Rgin Version: 1.2.0 Depends: R (>= 3.5) LinkingTo: RcppEigen (>= 0.3.3.3.0) Suggests: knitr, rmarkdown License: MIT + file LICENSE MD5sum: 2d535bbeb2ba5810a0112f6c211a27a7 NeedsCompilation: yes Title: gin in R Description: C++ implementation of SConES. biocViews: Software, GenomeWideAssociation, SNP, GeneticVariability, Genetics, FeatureExtraction, GraphAndNetwork, Network Author: Hector Climente-Gonzalez [aut, cre], Dominik Gerhard Grimm [aut], Chloe-Agathe Azencott [aut] Maintainer: Hector Climente VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Rgin git_branch: RELEASE_3_8 git_last_commit: 91b6885 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rgin_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rgin_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rgin_1.2.0.tgz vignettes: vignettes/Rgin/inst/doc/Rgin-UsingCppLibraries.html vignetteTitles: Using Rgin C++ libraries hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE linksToMe: martini Package: RGMQL Version: 1.2.0 Depends: R(>= 3.4.2), RGMQLlib Imports: httr, rJava, GenomicRanges, rtracklayer, data.table, utils, plyr, xml2, methods, S4Vectors, dplyr, stats, glue, BiocGenerics Suggests: BiocStyle, knitr, rmarkdown License: Artistic-2.0 Archs: i386, x64 MD5sum: ecee8f65b339090d4a4d9a0db3311424 NeedsCompilation: no Title: GenoMetric Query Language for R/Bioconductor Description: This package brings the GenoMetric Query Language (GMQL) functionalities into the R environment. GMQL is a high-level, declarative language to manage heterogeneous genomic datasets for biomedical purposes, using simple queries to process genomic regions and their metadata and properties. GMQL adopts algorithms efficiently designed for big data using cloud-computing technologies (like Apache Hadoop and Spark) allowing GMQL to run on modern infrastructures, in order to achieve scalability and high performance. It allows to create, manipulate and extract genomic data from different data sources both locally and remotely. Our RGMQL functions allow complex queries and processing leveraging on the R idiomatic paradigm. The RGMQL package also provides a rich set of ancillary classes that allow sophisticated input/output management and sorting, such as: ASC, DESC, BAG, MIN, MAX, SUM, AVG, MEDIAN, STD, Q1, Q2, Q3 (and many others). Note that many RGMQL functions are not directly executed in R environment, but are deferred until real execution is issued. biocViews: Software, Infrastructure, DataImport, Network, SingleCell Author: Simone Pallotta, Marco Masseroli Maintainer: Simone Pallotta URL: http://www.bioinformatics.deib.polimi.it/genomic_computing/GMQL/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RGMQL git_branch: RELEASE_3_8 git_last_commit: 59df469 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RGMQL_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RGMQL_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RGMQL_1.2.0.tgz vignettes: vignettes/RGMQL/inst/doc/RGMQL-vignette.pdf vignetteTitles: RGMQL: GenoMetric Query Language for R/Bioconductor hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RGMQL/inst/doc/RGMQL-vignette.R Package: RGraph2js Version: 1.10.0 Imports: utils, whisker, rjson, digest, graph Suggests: RUnit, BiocStyle, BiocGenerics, xtable, sna License: GPL-2 MD5sum: e407635c0ffbdb22152a1313025a8b4a NeedsCompilation: no Title: Convert a Graph into a D3js Script Description: Generator of web pages which display interactive network/graph visualizations with D3js, jQuery and Raphael. biocViews: Visualization, Network, GraphAndNetwork, ThirdPartyClient Author: Stephane Cano [aut, cre], Sylvain Gubian [aut], Florian Martin [aut] Maintainer: Stephane Cano SystemRequirements: jQuery, jQueryUI, qTip2, D3js and Raphael are required Javascript libraries made available via the online CDNJS service (http://cdnjs.cloudflare.com). git_url: https://git.bioconductor.org/packages/RGraph2js git_branch: RELEASE_3_8 git_last_commit: a22fafc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RGraph2js_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RGraph2js_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RGraph2js_1.10.0.tgz vignettes: vignettes/RGraph2js/inst/doc/RGraph2js.pdf vignetteTitles: RGraph2js hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RGraph2js/inst/doc/RGraph2js.R Package: Rgraphviz Version: 2.26.0 Depends: R (>= 2.6.0), methods, utils, graph, grid Imports: stats4, graphics, grDevices Suggests: RUnit, BiocGenerics, XML License: EPL MD5sum: 148a37430c6f20d15b1564cb91796f00 NeedsCompilation: yes Title: Provides plotting capabilities for R graph objects Description: Interfaces R with the AT and T graphviz library for plotting R graph objects from the graph package. biocViews: GraphAndNetwork, Visualization Author: Kasper Daniel Hansen [cre, aut], Jeff Gentry [aut], Li Long [aut], Robert Gentleman [aut], Seth Falcon [aut], Florian Hahne [aut], Deepayan Sarkar [aut] Maintainer: Kasper Daniel Hansen SystemRequirements: optionally Graphviz (>= 2.16) git_url: https://git.bioconductor.org/packages/Rgraphviz git_branch: RELEASE_3_8 git_last_commit: e9b08c7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rgraphviz_2.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rgraphviz_2.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rgraphviz_2.26.0.tgz vignettes: vignettes/Rgraphviz/inst/doc/newRgraphvizInterface.pdf, vignettes/Rgraphviz/inst/doc/Rgraphviz.pdf vignetteTitles: A New Interface to Plot Graphs Using Rgraphviz, How To Plot A Graph Using Rgraphviz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rgraphviz/inst/doc/newRgraphvizInterface.R, vignettes/Rgraphviz/inst/doc/Rgraphviz.R dependsOnMe: biocGraph, BioMVCClass, CellNOptR, flowCL, GOFunction, MineICA, netresponse, paircompviz, pathRender, ROntoTools, SplicingGraphs, TDARACNE importsMe: apComplex, biocGraph, chimeraviz, CompGO, CytoML, DEGraph, EnrichmentBrowser, flowWorkspace, GeneNetworkBuilder, GOFunction, GOstats, hyperdraw, MIGSA, mirIntegrator, nem, OncoSimulR, paircompviz, pathview, Pigengene, qpgraph, RchyOptimyx, SplicingGraphs, trackViewer, TRONCO suggestsMe: altcdfenvs, annotate, BiocCaseStudies, Category, CNORfeeder, CNORfuzzy, DEGraph, flowCore, geneplotter, GlobalAncova, globaltest, GSEABase, KEGGgraph, MLP, NCIgraph, pcaGoPromoter, pkgDepTools, RBGL, RBioinf, rBiopaxParser, RDAVIDWebService, Rtreemix, safe, SPIA, SRAdb, Streamer, topGO, vtpnet Package: rGREAT Version: 1.14.0 Depends: R (>= 3.1.2), GenomicRanges, IRanges, methods Imports: rjson, GetoptLong (>= 0.0.9), RCurl, utils, stats Suggests: testthat (>= 0.3), knitr, circlize License: MIT + file LICENSE Archs: i386, x64 MD5sum: c7e906676ad1d4ce133a2d285e10b053 NeedsCompilation: no Title: Client for GREAT Analysis Description: This package makes GREAT (Genomic Regions Enrichment of Annotations Tool) analysis automatic by constructing a HTTP POST request according to user's input and automatically retrieving results from GREAT web server. biocViews: GeneSetEnrichment, GO, Pathways, Software, Sequencing, WholeGenome, GenomeAnnotation, Coverage Author: Zuguang Gu Maintainer: Zuguang Gu URL: https://github.com/jokergoo/rGREAT, http://great.stanford.edu/public/html/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rGREAT git_branch: RELEASE_3_8 git_last_commit: 0f4a457 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-03 source.ver: src/contrib/rGREAT_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rGREAT_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rGREAT_1.14.0.tgz vignettes: vignettes/rGREAT/inst/doc/rGREAT.html vignetteTitles: Analyze with GREAT hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rGREAT/inst/doc/rGREAT.R Package: RGSEA Version: 1.16.0 Depends: R(>= 2.10.0) Imports: BiocGenerics Suggests: BiocStyle, GEOquery, knitr, RUnit License: GPL(>=3) MD5sum: 7e45c90d4e1335e8fcc983f9a86e0ac0 NeedsCompilation: no Title: Random Gene Set Enrichment Analysis Description: Combining bootstrap aggregating and Gene set enrichment analysis (GSEA), RGSEA is a classfication algorithm with high robustness and no over-fitting problem. It performs well especially for the data generated from different exprements. biocViews: GeneSetEnrichment, StatisticalMethod, Classification Author: Chengcheng Ma Maintainer: Chengcheng Ma VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RGSEA git_branch: RELEASE_3_8 git_last_commit: 626324d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RGSEA_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RGSEA_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RGSEA_1.16.0.tgz vignettes: vignettes/RGSEA/inst/doc/RGSEA.pdf vignetteTitles: Introduction to RGSEA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RGSEA/inst/doc/RGSEA.R Package: rgsepd Version: 1.14.1 Depends: R (>= 3.5.0), DESeq2, goseq (>= 1.28) Imports: gplots, biomaRt, org.Hs.eg.db, GO.db, SummarizedExperiment, hash, AnnotationDbi Suggests: boot, tools, BiocGenerics, knitr, xtable License: GPL-3 MD5sum: 97ea9fa22cbd67ccc45ab0ae4e98f667 NeedsCompilation: no Title: Gene Set Enrichment / Projection Displays Description: R/GSEPD is a bioinformatics package for R to help disambiguate transcriptome samples (a matrix of RNA-Seq counts at RefSeq IDs) by automating differential expression (with DESeq2), then gene set enrichment (with GOSeq), and finally a N-dimensional projection to quantify in which ways each sample is like either treatment group. biocViews: ImmunoOncology, Software, DifferentialExpression, GeneSetEnrichment, RNASeq Author: Karl Stamm Maintainer: Karl Stamm VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rgsepd git_branch: RELEASE_3_8 git_last_commit: a8011b7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/rgsepd_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rgsepd_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rgsepd_1.14.1.tgz vignettes: vignettes/rgsepd/inst/doc/rgsepd.pdf vignetteTitles: An Introduction to the rgsepd package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rgsepd/inst/doc/rgsepd.R Package: rhdf5 Version: 2.26.2 Depends: R (>= 3.5.0), methods Imports: Rhdf5lib (>= 1.3.2) LinkingTo: Rhdf5lib Suggests: bit64, BiocStyle, knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: 519cea2559f9738d60ffc0041a8e61ce NeedsCompilation: yes Title: HDF5 interface to R Description: This package provides an interface between HDF5 and R. HDF5's main features are the ability to store and access very large and/or complex datasets and a wide variety of metadata on mass storage (disk) through a completely portable file format. The rhdf5 package is thus suited for the exchange of large and/or complex datasets between R and other software package, and for letting R applications work on datasets that are larger than the available RAM. biocViews: Infrastructure, DataImport Author: Bernd Fischer [aut], Gregoire Pau [aut], Mike Smith [aut, cre], Martin Morgan [ctb], Daniel van Twisk [ctb] Maintainer: Mike Smith URL: https://github.com/grimbough/rhdf5 VignetteBuilder: knitr BugReports: https://github.com/grimbough/rhdf5/issues git_url: https://git.bioconductor.org/packages/rhdf5 git_branch: RELEASE_3_8 git_last_commit: 81e1125 git_last_commit_date: 2019-01-02 Date/Publication: 2019-01-02 source.ver: src/contrib/rhdf5_2.26.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/rhdf5_2.26.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rhdf5_2.26.2.tgz vignettes: vignettes/rhdf5/inst/doc/rhdf5.html vignetteTitles: rhdf5 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rhdf5/inst/doc/rhdf5.R dependsOnMe: GenoGAM, GSCA, HDF5Array, HiCBricks, LoomExperiment importsMe: beachmat, biomformat, bsseq, CoGAPS, cTRAP, diffHic, DOQTL, DropletUtils, EventPointer, gep2pep, h5vc, IONiseR, phantasus, PureCN, scone, slinky suggestsMe: edgeR, slalom, SummarizedExperiment, tximport Package: rhdf5client Version: 1.4.1 Depends: R (>= 3.5), methods, DelayedArray Imports: S4Vectors, httr, R6, rjson, utils Suggests: knitr, testthat, BiocStyle, DT, reticulate License: Artistic-2.0 Archs: i386, x64 MD5sum: e0cbfdf98cc9d02133c133d80c169bf4 NeedsCompilation: yes Title: Access HDF5 content from h5serv Description: Provides functionality for reading data from h5serv server from within R. biocViews: DataImport, Software Author: Samuela Pollack [cre, aut], Shweta Gopaulakrishnan [aut], Vincent Carey [aut] Maintainer: Samuela Pollack VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rhdf5client git_branch: RELEASE_3_8 git_last_commit: 939791a git_last_commit_date: 2018-12-14 Date/Publication: 2018-12-14 source.ver: src/contrib/rhdf5client_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rhdf5client_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rhdf5client_1.4.1.tgz vignettes: vignettes/rhdf5client/inst/doc/delayed-array.html, vignettes/rhdf5client/inst/doc/h5sarray.html, vignettes/rhdf5client/inst/doc/main.html, vignettes/rhdf5client/inst/doc/multidim.html vignetteTitles: HSDSArray DelayedArray backend, h5client -- notes on Bioconductor and remote HDF5, Objects and methods in rhdf5client, Multidimensional verification hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rhdf5client/inst/doc/delayed-array.R, vignettes/rhdf5client/inst/doc/h5sarray.R, vignettes/rhdf5client/inst/doc/main.R, vignettes/rhdf5client/inst/doc/multidim.R importsMe: restfulSE Package: Rhdf5lib Version: 1.4.3 Suggests: BiocStyle, knitr, rmarkdown License: Artistic-2.0 Archs: i386, x64 MD5sum: 79b9c0902ae67edbc6faa63143fc2a9d NeedsCompilation: yes Title: hdf5 library as an R package Description: Provides C and C++ hdf5 libraries. biocViews: Infrastructure Author: Mike Smith Maintainer: Mike Smith SystemRequirements: GNU make VignetteBuilder: knitr BugReports: https://github.com/grimbough/Rhdf5lib git_url: https://git.bioconductor.org/packages/Rhdf5lib git_branch: RELEASE_3_8 git_last_commit: f6be8c2 git_last_commit_date: 2019-03-25 Date/Publication: 2019-03-25 source.ver: src/contrib/Rhdf5lib_1.4.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rhdf5lib_1.4.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rhdf5lib_1.4.3.tgz vignettes: vignettes/Rhdf5lib/inst/doc/Rhdf5lib.html vignetteTitles: Linking to Rhdf5lib hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rhdf5lib/inst/doc/Rhdf5lib.R importsMe: beachmat, rhdf5 linksToMe: beachmat, bsseq, DropletUtils, mzR, ncdfFlow, rhdf5, scater, scran Package: Rhtslib Version: 1.14.1 Imports: zlibbioc LinkingTo: zlibbioc Suggests: BiocStyle, knitr License: LGPL (>= 2) Archs: i386, x64 MD5sum: 6064e1d61f7f897adc0edac4b55fd3aa NeedsCompilation: yes Title: HTSlib high-throughput sequencing library as an R package Description: This package provides version 1.7 of the 'HTSlib' C library for high-throughput sequence analysis. The package is primarily useful to developers of other R packages who wish to make use of HTSlib. Motivation and instructions for use of this package are in the vignette, vignette(package="Rhtslib", "Rhtslib"). biocViews: DataImport, Sequencing Author: Nathaniel Hayden [led, aut], Martin Morgan [aut], Bioconductor Package Maintainer [cre] Maintainer: Bioconductor Package Maintainer URL: https://github.com/Bioconductor/Rhtslib, http://www.htslib.org/ VignetteBuilder: knitr BugReports: https://github.com/Bioconductor/Rhtslib git_url: https://git.bioconductor.org/packages/Rhtslib git_branch: RELEASE_3_8 git_last_commit: 4be2607 git_last_commit_date: 2019-02-12 Date/Publication: 2019-02-12 source.ver: src/contrib/Rhtslib_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rhtslib_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rhtslib_1.14.1.tgz vignettes: vignettes/Rhtslib/inst/doc/Rhtslib.html vignetteTitles: Motivation and use of Rhtslib hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rhtslib/inst/doc/Rhtslib.R dependsOnMe: deepSNV importsMe: deepSNV, diffHic, scPipe linksToMe: bamsignals, csaw, deepSNV, diffHic, methylKit, scPipe Package: rHVDM Version: 1.48.0 Depends: R (>= 2.10), R2HTML (>= 1.5), affy (>= 1.23.4), minpack.lm (>= 1.0-5), Biobase (>= 2.5.5) License: GPL-2 Archs: i386, x64 MD5sum: 03b3afcc36d32af3e5f32f14cbbdf79a NeedsCompilation: no Title: Hidden Variable Dynamic Modeling Description: A R implementation of HVDM (Genome Biol 2006, V7(3) R25) biocViews: Microarray, GraphAndNetwork, Transcription, Classification, NetworkInference Author: Martino Barenco Maintainer: Martino Barenco git_url: https://git.bioconductor.org/packages/rHVDM git_branch: RELEASE_3_8 git_last_commit: 99653d9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rHVDM_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rHVDM_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rHVDM_1.48.0.tgz vignettes: vignettes/rHVDM/inst/doc/rHVDM.pdf vignetteTitles: rHVDM primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rHVDM/inst/doc/rHVDM.R Package: RiboProfiling Version: 1.12.0 Depends: R (>= 3.2.2), Biostrings Imports: BiocGenerics, GenomeInfoDb, GenomicRanges, IRanges, reshape2, GenomicFeatures, grid, plyr, S4Vectors, GenomicAlignments, ggplot2, ggbio, Rsamtools, rtracklayer, data.table, sqldf Suggests: knitr, BiocStyle, TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome.Hsapiens.UCSC.hg19, testthat, SummarizedExperiment License: GPL-3 MD5sum: bde2fcd441936a57773f4c14fe283ffe NeedsCompilation: no Title: Ribosome Profiling Data Analysis: from BAM to Data Representation and Interpretation Description: Starting with a BAM file, this package provides the necessary functions for quality assessment, read start position recalibration, the counting of reads on CDS, 3'UTR, and 5'UTR, plotting of count data: pairs, log fold-change, codon frequency and coverage assessment, principal component analysis on codon coverage. biocViews: RiboSeq, Sequencing, Coverage, Alignment, QualityControl, Software, PrincipalComponent Author: Alexandra Popa Maintainer: A. Popa VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RiboProfiling git_branch: RELEASE_3_8 git_last_commit: edf20ed git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RiboProfiling_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RiboProfiling_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RiboProfiling_1.12.0.tgz vignettes: vignettes/RiboProfiling/inst/doc/RiboProfiling.pdf vignetteTitles: Analysing Ribo-Seq data with the "RiboProfiling" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RiboProfiling/inst/doc/RiboProfiling.R Package: riboSeqR Version: 1.16.0 Depends: R (>= 3.0.2), methods, GenomicRanges, abind Imports: Rsamtools, IRanges, baySeq, GenomeInfoDb, seqLogo Suggests: BiocStyle, RUnit, BiocGenerics License: GPL-3 MD5sum: 48f5aad232a33ca5f3ab9766c1b246f2 NeedsCompilation: no Title: Analysis of sequencing data from ribosome profiling experiments Description: Plotting functions, frameshift detection and parsing of sequencing data from ribosome profiling experiments. biocViews: Sequencing,Genetics,Visualization,RiboSeq Author: Thomas J. Hardcastle Maintainer: Thomas J. Hardcastle git_url: https://git.bioconductor.org/packages/riboSeqR git_branch: RELEASE_3_8 git_last_commit: 231a1bf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/riboSeqR_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/riboSeqR_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/riboSeqR_1.16.0.tgz vignettes: vignettes/riboSeqR/inst/doc/riboSeqR.pdf vignetteTitles: riboSeqR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/riboSeqR/inst/doc/riboSeqR.R Package: RImmPort Version: 1.10.0 Imports: plyr, dplyr, DBI, data.table, reshape2, methods, sqldf, tools, utils, RSQLite Suggests: knitr License: GPL-3 MD5sum: 6912d86ace8499a7be8bbcd2f2496ec5 NeedsCompilation: no Title: RImmPort: Enabling Ready-for-analysis Immunology Research Data Description: The RImmPort package simplifies access to ImmPort data for analysis in the R environment. It provides a standards-based interface to the ImmPort study data that is in a proprietary format. biocViews: BiomedicalInformatics, DataImport, DataRepresentation Author: Ravi Shankar Maintainer: Zicheng Hu , Ravi Shankar URL: http://bioconductor.org/packages/RImmPort/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RImmPort git_branch: RELEASE_3_8 git_last_commit: abbe516 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RImmPort_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RImmPort_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RImmPort_1.10.0.tgz vignettes: vignettes/RImmPort/inst/doc/RImmPort_Article.pdf, vignettes/RImmPort/inst/doc/RImmPort_QuickStart.pdf vignetteTitles: RImmPort: Enabling ready-for-analysis immunology research data, RImmPort: Quick Start Guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RImmPort/inst/doc/RImmPort_Article.R, vignettes/RImmPort/inst/doc/RImmPort_QuickStart.R Package: Ringo Version: 1.46.0 Depends: methods, Biobase (>= 1.14.1), RColorBrewer, limma, Matrix, grid, lattice Imports: BiocGenerics (>= 0.1.11), genefilter, limma, vsn, stats4 Suggests: rtracklayer (>= 1.3.1), mclust, topGO (>= 1.15.0) License: Artistic-2.0 MD5sum: 3436818ae4313f8dfab65d0db0e0b86f NeedsCompilation: yes Title: R Investigation of ChIP-chip Oligoarrays Description: The package Ringo facilitates the primary analysis of ChIP-chip data. The main functionalities of the package are data read-in, quality assessment, data visualisation and identification of genomic regions showing enrichment in ChIP-chip. The package has functions to deal with two-color oligonucleotide microarrays from NimbleGen used in ChIP-chip projects, but also contains more general functions for ChIP-chip data analysis, given that the data is supplied as RGList (raw) or ExpressionSet (pre- processed). The package employs functions from various other packages of the Bioconductor project and provides additional ChIP-chip-specific and NimbleGen-specific functionalities. biocViews: Microarray,TwoChannel,DataImport,QualityControl,Preprocessing Author: Joern Toedling, Oleg Sklyar, Tammo Krueger, Matt Ritchie, Wolfgang Huber Maintainer: J. Toedling git_url: https://git.bioconductor.org/packages/Ringo git_branch: RELEASE_3_8 git_last_commit: d9333cb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Ringo_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Ringo_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Ringo_1.46.0.tgz vignettes: vignettes/Ringo/inst/doc/Ringo.pdf vignetteTitles: R Investigation of NimbleGen Oligoarrays hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Ringo/inst/doc/Ringo.R dependsOnMe: SimBindProfiles, Starr importsMe: Repitools Package: RIPSeeker Version: 1.22.0 Depends: R (>= 2.15), methods, S4Vectors (>= 0.9.25), IRanges, GenomicRanges, SummarizedExperiment, Rsamtools, GenomicAlignments, rtracklayer Suggests: biomaRt, ChIPpeakAnno, parallel, GenomicFeatures License: GPL-2 Archs: i386, x64 MD5sum: ca82b8eb26b72bc28c55f133afcc7c2a NeedsCompilation: no Title: RIPSeeker: a statistical package for identifying protein-associated transcripts from RIP-seq experiments Description: Infer and discriminate RIP peaks from RIP-seq alignments using two-state HMM with negative binomial emission probability. While RIPSeeker is specifically tailored for RIP-seq data analysis, it also provides a suite of bioinformatics tools integrated within this self-contained software package comprehensively addressing issues ranging from post-alignments processing to visualization and annotation. biocViews: Sequencing, RIPSeq Author: Yue Li Maintainer: Yue Li URL: http://www.cs.utoronto.ca/~yueli/software.html git_url: https://git.bioconductor.org/packages/RIPSeeker git_branch: RELEASE_3_8 git_last_commit: 3b3bdfa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RIPSeeker_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RIPSeeker_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RIPSeeker_1.22.0.tgz vignettes: vignettes/RIPSeeker/inst/doc/RIPSeeker.pdf vignetteTitles: RIPSeeker: a statistical package for identifying protein-associated transcripts from RIP-seq experiments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RIPSeeker/inst/doc/RIPSeeker.R Package: Risa Version: 1.24.0 Depends: R (>= 2.0.9), Biobase (>= 2.4.0), methods, Rcpp (>= 0.9.13), biocViews, affy Imports: xcms Suggests: faahKO (>= 1.2.11) License: LGPL MD5sum: 7e0030432ea9e984265b3326e1cc08f9 NeedsCompilation: no Title: Converting experimental metadata from ISA-tab into Bioconductor data structures Description: The Investigation / Study / Assay (ISA) tab-delimited format is a general purpose framework with which to collect and communicate complex metadata (i.e. sample characteristics, technologies used, type of measurements made) from experiments employing a combination of technologies, spanning from traditional approaches to high-throughput techniques. Risa allows to access metadata/data in ISA-Tab format and build Bioconductor data structures. Currently, data generated from microarray, flow cytometry and metabolomics-based (i.e. mass spectrometry) assays are supported. The package is extendable and efforts are undergoing to support metadata associated to proteomics assays. biocViews: Annotation, DataImport, MassSpectrometry Author: Alejandra Gonzalez-Beltran, Audrey Kauffmann, Steffen Neumann, Gabriella Rustici, ISA Team Maintainer: Alejandra Gonzalez-Beltran URL: http://www.isa-tools.org/ BugReports: https://github.com/ISA-tools/Risa/issues git_url: https://git.bioconductor.org/packages/Risa git_branch: RELEASE_3_8 git_last_commit: 4b43070 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Risa_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Risa_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Risa_1.24.0.tgz vignettes: vignettes/Risa/inst/doc/Risa.pdf vignetteTitles: Risa: converts experimental metadata from ISA-tab into Bioconductor data structures hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Risa/inst/doc/Risa.R Package: RITAN Version: 1.6.0 Depends: R (>= 3.4), Imports: graphics, stats, utils, grid, gridExtra, reshape2, gplots, ggplot2, plotrix, RColorBrewer, STRINGdb, MCL, linkcomm, dynamicTreeCut, sqldf, gsubfn, hash, png, sqldf, igraph, BgeeDB, knitr, RITANdata Suggests: rmarkdown License: file LICENSE MD5sum: 922a970ba929bac0ecbc38e9f4496975 NeedsCompilation: no Title: Rapid Integration of Term Annotation and Network resources Description: Tools for comprehensive gene set enrichment and extraction of multi-resource high confidence subnetworks. RITAN facilitates bioinformatic tasks for enabling network biology research. biocViews: QualityControl, Network, NetworkEnrichment, NetworkInference, GeneSetEnrichment, FunctionalGenomics Author: Michael Zimmermann Maintainer: Michael Zimmermann VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RITAN git_branch: RELEASE_3_8 git_last_commit: 581a092 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RITAN_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RITAN_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RITAN_1.6.0.tgz vignettes: vignettes/RITAN/inst/doc/choosing_resources.html, vignettes/RITAN/inst/doc/enrichment.html, vignettes/RITAN/inst/doc/multi_tissue_analysis.html, vignettes/RITAN/inst/doc/resource_relationships.html, vignettes/RITAN/inst/doc/subnetworks.html vignetteTitles: Choosing Resources, Enrichment Vignette, Multi-Tissue Analysis, Relationships Among Resources, Network Biology Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RITAN/inst/doc/choosing_resources.R, vignettes/RITAN/inst/doc/enrichment.R, vignettes/RITAN/inst/doc/multi_tissue_analysis.R, vignettes/RITAN/inst/doc/resource_relationships.R, vignettes/RITAN/inst/doc/subnetworks.R Package: RIVER Version: 1.6.0 Depends: R (>= 3.3.2) Imports: glmnet, pROC, ggplot2, graphics, stats, Biobase, methods, utils Suggests: BiocStyle, knitr, rmarkdown, testthat, devtools License: GPL (>= 2) MD5sum: 1c71522aa5110c5e162019c2be4531ae NeedsCompilation: no Title: R package for RIVER (RNA-Informed Variant Effect on Regulation) Description: An implementation of a probabilistic modeling framework that jointly analyzes personal genome and transcriptome data to estimate the probability that a variant has regulatory impact in that individual. It is based on a generative model that assumes that genomic annotations, such as the location of a variant with respect to regulatory elements, determine the prior probability that variant is a functional regulatory variant, which is an unobserved variable. The functional regulatory variant status then influences whether nearby genes are likely to display outlier levels of gene expression in that person. See the RIVER website for more information, documentation and examples. biocViews: GeneExpression, GeneticVariability, SNP, Transcription, FunctionalPrediction, GeneRegulation, GenomicVariation, BiomedicalInformatics, FunctionalGenomics, Genetics, SystemsBiology, Transcriptomics, Bayesian, Clustering, TranscriptomeVariant, Regression Author: Yungil Kim [aut, cre], Alexis Battle [aut] Maintainer: Yungil Kim URL: https://github.com/ipw012/RIVER VignetteBuilder: knitr BugReports: https://github.com/ipw012/RIVER/issues git_url: https://git.bioconductor.org/packages/RIVER git_branch: RELEASE_3_8 git_last_commit: 9284298 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RIVER_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RIVER_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RIVER_1.6.0.tgz vignettes: vignettes/RIVER/inst/doc/RIVER.html vignetteTitles: RIVER hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RIVER/inst/doc/RIVER.R Package: RJMCMCNucleosomes Version: 1.6.0 Depends: R (>= 3.4), IRanges, GenomicRanges Imports: Rcpp (>= 0.12.5), consensusSeekeR, BiocGenerics, GenomeInfoDb, S4Vectors, BiocParallel, stats, graphics, methods, grDevices LinkingTo: Rcpp Suggests: BiocStyle, knitr, rmarkdown, nucleoSim, RUnit License: Artistic-2.0 MD5sum: 969be4b78d5429790fe5921118ba8b7e NeedsCompilation: yes Title: Bayesian hierarchical model for genome-wide nucleosome positioning with high-throughput short-read data (MNase-Seq) Description: This package does nucleosome positioning using informative Multinomial-Dirichlet prior in a t-mixture with reversible jump estimation of nucleosome positions for genome-wide profiling. biocViews: BiologicalQuestion, ChIPSeq, NucleosomePositioning, Software, StatisticalMethod, Bayesian, Sequencing, Coverage Author: Pascal Belleau [aut], Rawane Samb [aut], Astrid Deschênes [cre, aut], Khader Khadraoui [aut], Lajmi Lakhal-Chaieb [aut], Arnaud Droit [aut] Maintainer: Astrid Deschênes URL: https://github.com/ArnaudDroitLab/RJMCMCNucleosomes SystemRequirements: Rcpp VignetteBuilder: knitr BugReports: https://github.com/ArnaudDroitLab/RJMCMCNucleosomes/issues git_url: https://git.bioconductor.org/packages/RJMCMCNucleosomes git_branch: RELEASE_3_8 git_last_commit: e1c86d2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RJMCMCNucleosomes_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RJMCMCNucleosomes_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RJMCMCNucleosomes_1.6.0.tgz vignettes: vignettes/RJMCMCNucleosomes/inst/doc/RJMCMCNucleosomes.html vignetteTitles: Nucleosome Positioning hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RJMCMCNucleosomes/inst/doc/RJMCMCNucleosomes.R Package: RLMM Version: 1.44.0 Depends: R (>= 2.1.0) Imports: graphics, grDevices, MASS, stats, utils License: LGPL (>= 2) Archs: i386, x64 MD5sum: 8421a9bb66653cde951b58562ce7aaaf NeedsCompilation: no Title: A Genotype Calling Algorithm for Affymetrix SNP Arrays Description: A classification algorithm, based on a multi-chip, multi-SNP approach for Affymetrix SNP arrays. Using a large training sample where the genotype labels are known, this aglorithm will obtain more accurate classification results on new data. RLMM is based on a robust, linear model and uses the Mahalanobis distance for classification. The chip-to-chip non-biological variation is removed through normalization. This model-based algorithm captures the similarities across genotype groups and probes, as well as thousands other SNPs for accurate classification. NOTE: 100K-Xba only at for now. biocViews: Microarray, OneChannel, SNP, GeneticVariability Author: Nusrat Rabbee , Gary Wong Maintainer: Nusrat Rabbee URL: http://www.stat.berkeley.edu/users/nrabbee/RLMM SystemRequirements: Internal files Xba.CQV, Xba.regions (or other regions file) git_url: https://git.bioconductor.org/packages/RLMM git_branch: RELEASE_3_8 git_last_commit: f39e8cd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RLMM_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RLMM_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RLMM_1.44.0.tgz vignettes: vignettes/RLMM/inst/doc/RLMM.pdf vignetteTitles: RLMM Doc hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RLMM/inst/doc/RLMM.R Package: Rmagpie Version: 1.38.0 Depends: R (>= 2.6.1), Biobase (>= 2.5.5) Imports: Biobase (>= 2.5.5), e1071, graphics, grDevices, kernlab, methods, pamr, stats, utils Suggests: xtable License: GPL (>= 3) MD5sum: dcc38ce1cc7a63089db512988d0e5611 NeedsCompilation: no Title: MicroArray Gene-expression-based Program In Error rate estimation Description: Microarray Classification is designed for both biologists and statisticians. It offers the ability to train a classifier on a labelled microarray dataset and to then use that classifier to predict the class of new observations. A range of modern classifiers are available, including support vector machines (SVMs), nearest shrunken centroids (NSCs)... Advanced methods are provided to estimate the predictive error rate and to report the subset of genes which appear essential in discriminating between classes. biocViews: Microarray, Classification Author: Camille Maumet , with contributions from C. Ambroise J. Zhu Maintainer: Camille Maumet URL: http://www.bioconductor.org/ git_url: https://git.bioconductor.org/packages/Rmagpie git_branch: RELEASE_3_8 git_last_commit: 6e83386 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rmagpie_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rmagpie_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rmagpie_1.38.0.tgz vignettes: vignettes/Rmagpie/inst/doc/Magpie_examples.pdf vignetteTitles: Rmagpie Examples hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rmagpie/inst/doc/Magpie_examples.R Package: RMassBank Version: 2.10.1 Depends: Rcpp Imports: XML,RCurl,rjson,S4Vectors,digest, rcdk,yaml,mzR,methods,Biobase,MSnbase,httr Suggests: gplots,RMassBankData, xcms (>= 1.37.1), CAMERA, RUnit, enviPat License: Artistic-2.0 MD5sum: 47a3192d7b020db8dc92f01e42ecf0fa NeedsCompilation: no Title: Workflow to process tandem MS files and build MassBank records Description: Workflow to process tandem MS files and build MassBank records. Functions include automated extraction of tandem MS spectra, formula assignment to tandem MS fragments, recalibration of tandem MS spectra with assigned fragments, spectrum cleanup, automated retrieval of compound information from Internet databases, and export to MassBank records. biocViews: ImmunoOncology, Bioinformatics, MassSpectrometry, Metabolomics, Software Author: Michael Stravs, Emma Schymanski, Steffen Neumann, Erik Mueller, with contributions from Tobias Schulze Maintainer: RMassBank at Eawag SystemRequirements: OpenBabel git_url: https://git.bioconductor.org/packages/RMassBank git_branch: RELEASE_3_8 git_last_commit: b0ac42f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RMassBank_2.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RMassBank_2.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RMassBank_2.10.1.tgz vignettes: vignettes/RMassBank/inst/doc/RMassBank.pdf, vignettes/RMassBank/inst/doc/RMassBankNonstandard.pdf, vignettes/RMassBank/inst/doc/RMassBankXCMS.pdf vignetteTitles: RMassBank walkthrough, RMassBank non-standard usage, RMassBank using XCMS walkthrough hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RMassBank/inst/doc/RMassBank.R, vignettes/RMassBank/inst/doc/RMassBankNonstandard.R, vignettes/RMassBank/inst/doc/RMassBankXCMS.R Package: rMAT Version: 3.32.0 Depends: R(>= 2.9.0), BiocGenerics (>= 0.1.3), IRanges (>= 1.13.10), Biobase (>= 2.15.1), affxparser Imports: stats, methods, BiocGenerics, IRanges, Biobase, affxparser, stats4 Suggests: GenomeGraphs, rtracklayer License: Artistic-2.0 MD5sum: c37de71a14cb83a43f58db7c6ce5cbf2 NeedsCompilation: yes Title: R implementation from MAT program to normalize and analyze tiling arrays and ChIP-chip data. Description: This package is an R version of the package MAT and contains functions to parse and merge Affymetrix BPMAP and CEL tiling array files (using C++ based Fusion SDK and Bioconductor package affxparser), normalize tiling arrays using sequence specific models, detect enriched regions from ChIP-chip experiments. Note: users should have GSL and GenomeGraphs installed. Windows users: 'consult the README file available in the inst directory of the source distribution for necessary configuration instructions'. Snow Leopard users can take advantage of increase speed with Grand Central Dispatch! biocViews: Microarray, Preprocessing Author: Charles Cheung and Arnaud Droit and Raphael Gottardo Maintainer: Arnaud Droit and Raphael Gottardo URL: http://www.rglab.org SystemRequirements: GSL (GNU Scientific Library) git_url: https://git.bioconductor.org/packages/rMAT git_branch: RELEASE_3_8 git_last_commit: 34f2c25 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rMAT_3.32.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rMAT_3.32.0.tgz vignettes: vignettes/rMAT/inst/doc/rMAT.pdf vignetteTitles: The rMAT users guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rMAT/inst/doc/rMAT.R Package: RmiR Version: 1.38.0 Depends: R (>= 2.7.0), RmiR.Hs.miRNA, RSVGTipsDevice Imports: DBI, methods, stats Suggests: hgug4112a.db,org.Hs.eg.db License: Artistic-2.0 MD5sum: f4320c1b98aa85b078b9b4c2c55ded07 NeedsCompilation: no Title: Package to work with miRNAs and miRNA targets with R Description: Useful functions to merge microRNA and respective targets using differents databases biocViews: Software,GeneExpression,Microarray,TimeCourse,Visualization Author: Francesco Favero Maintainer: Francesco Favero git_url: https://git.bioconductor.org/packages/RmiR git_branch: RELEASE_3_8 git_last_commit: b725971 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RmiR_1.38.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RmiR_1.38.0.tgz vignettes: vignettes/RmiR/inst/doc/RmiR.pdf vignetteTitles: RmiR Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RmiR/inst/doc/RmiR.R Package: Rmmquant Version: 1.0.4 Depends: R (>= 3.5) Imports: Rcpp (>= 0.12.8), methods, S4Vectors, GenomicRanges, SummarizedExperiment, devtools, TBX20BamSubset, TxDb.Mmusculus.UCSC.mm9.knownGene, org.Mm.eg.db, DESeq2, BiocStyle LinkingTo: Rcpp Suggests: knitr, rmarkdown, testthat License: GPL-3 MD5sum: 2a6e079d5b19463538f7e41a4397e0ed NeedsCompilation: yes Title: RNA-Seq multi-mapping Reads Quantification Tool Description: RNA-Seq is currently used routinely, and it provides accurate information on gene transcription. However, the method cannot accurately estimate duplicated genes expression. Several strategies have been previously used, but all of them provide biased results. With Rmmquant, if a read maps at different positions, the tool detects that the corresponding genes are duplicated; it merges the genes and creates a merged gene. The counts of ambiguous reads is then based on the input genes and the merged genes. Rmmquant is a drop-in replacement of the widely used tools findOverlaps and featureCounts that handles multi-mapping reads in an unabiased way. biocViews: GeneExpression, Transcription Author: Zytnicki Matthias [aut, cre] Maintainer: Zytnicki Matthias SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Rmmquant git_branch: RELEASE_3_8 git_last_commit: d184ef0 git_last_commit_date: 2019-02-27 Date/Publication: 2019-02-27 source.ver: src/contrib/Rmmquant_1.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rmmquant_1.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rmmquant_1.0.4.tgz vignettes: vignettes/Rmmquant/inst/doc/Rmmquant.html vignetteTitles: The Rmmquant package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rmmquant/inst/doc/Rmmquant.R Package: RNAdecay Version: 1.2.1 Depends: R (>= 3.5) Imports: stats, grDevices, grid, ggplot2, gplots, utils, TMB, nloptr Suggests: parallel, knitr, reshape2, rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 46409994305fd5f78320b67590641bb5 NeedsCompilation: yes Title: Maximum Likelihood Decay Modeling of RNA Degradation Data Description: RNA degradation is monitored through measurement of RNA abundance after inhibiting RNA synthesis. This package has functions and example scripts to facilitate (1) data normalization, (2) data modeling using constant decay rate or time-dependent decay rate models, (3) the evaluation of treatment or genotype effects, and (4) plotting of the data and models. Data Normalization: functions and scripts make easy the normalization to the initial (T0) RNA abundance, as well as a method to correct for artificial inflation of Reads per Million (RPM) abundance in global assessments as the total size of the RNA pool decreases. Modeling: Normalized data is then modeled using maximum likelihood to fit parameters. For making treatment or genotype comparisons (up to four), the modeling step models all possible treatment effects on each gene by repeating the modeling with constraints on the model parameters (i.e., the decay rate of treatments A and B are modeled once with them being equal and again allowing them to both vary independently). Model Selection: The AICc value is calculated for each model, and the model with the lowest AICc is chosen. Modeling results of selected models are then compiled into a single data frame. Graphical Plotting: a function is provided to easily visualize the data and the selected model using ggplot2 package functions. biocViews: ImmunoOncology, Software, GeneExpression, GeneRegulation, DifferentialExpression, Transcription, Transcriptomics, TimeCourse, Regression, RNASeq, Normalization, WorkflowStep Author: Reed Sorenson [aut, cre], Katrina Johnson [aut], Frederick Adler [aut], Leslie Sieburth [aut] Maintainer: Reed Sorenson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RNAdecay git_branch: RELEASE_3_8 git_last_commit: 575aadd git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RNAdecay_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RNAdecay_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RNAdecay_1.2.1.tgz vignettes: vignettes/RNAdecay/inst/doc/RNAdecay_workflow.html vignetteTitles: RNAdecay hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RNAdecay/inst/doc/RNAdecay_workflow.R Package: RNAinteract Version: 1.30.1 Depends: R (>= 2.12.0), abind, locfit, Biobase Imports: RColorBrewer, ICS, ICSNP, cellHTS2, geneplotter, gplots, grid, hwriter, lattice, latticeExtra, limma, methods, splots (>= 1.13.12) License: Artistic-2.0 Archs: i386, x64 MD5sum: e225176e32d71d3bdef76657db673714 NeedsCompilation: no Title: Estimate Pairwise Interactions from multidimensional features Description: RNAinteract estimates genetic interactions from multi-dimensional read-outs like features extracted from images. The screen is assumed to be performed in multi-well plates or similar designs. Starting from a list of features (e.g. cell number, area, fluorescence intensity) per well, genetic interactions are estimated. The packages provides functions for reporting interacting gene pairs, plotting heatmaps and double RNAi plots. An HTML report can be written for quality control and analysis. biocViews: ImmunoOncology, CellBasedAssays, QualityControl, Preprocessing, Visualization Author: Bernd Fischer Maintainer: Bernd Fischer git_url: https://git.bioconductor.org/packages/RNAinteract git_branch: RELEASE_3_8 git_last_commit: 9f6d3b2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RNAinteract_1.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RNAinteract_1.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RNAinteract_1.30.1.tgz vignettes: vignettes/RNAinteract/inst/doc/RNAinteract.pdf vignetteTitles: RNAinteract hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RNAinteract/inst/doc/RNAinteract.R Package: RNAither Version: 2.30.1 Depends: R (>= 2.10), topGO, RankProd, prada Imports: geneplotter, limma, biomaRt, car, splots, methods License: Artistic-2.0 MD5sum: 887f8b55b34bf7cdbda598b701602576 NeedsCompilation: no Title: Statistical analysis of high-throughput RNAi screens Description: RNAither analyzes cell-based RNAi screens, and includes quality assessment, customizable normalization and statistical tests, leading to lists of significant genes and biological processes. biocViews: ImmunoOncology, CellBasedAssays, QualityControl, Preprocessing, Visualization, Annotation, GO Author: Nora Rieber and Lars Kaderali, University of Heidelberg, Viroquant Research Group Modeling, Im Neuenheimer Feld 267, 69120 Heidelberg, Germany Maintainer: Lars Kaderali git_url: https://git.bioconductor.org/packages/RNAither git_branch: RELEASE_3_8 git_last_commit: e1c1049 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RNAither_2.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RNAither_2.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RNAither_2.30.1.tgz vignettes: vignettes/RNAither/inst/doc/vignetteRNAither.pdf vignetteTitles: RNAither,, an automated pipeline for the statistical analysis of high-throughput RNAi screens hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RNAither/inst/doc/vignetteRNAither.R Package: RNAprobR Version: 1.14.0 Depends: R (>= 3.1.1), GenomicFeatures(>= 1.16.3), plyr(>= 1.8.1), BiocGenerics(>= 0.10.0) Imports: Biostrings(>= 2.32.1), GenomicRanges(>= 1.16.4), IRanges(>= 2.10.5), Rsamtools(>= 1.16.1), rtracklayer(>= 1.24.2), GenomicAlignments(>= 1.5.12), S4Vectors(>= 0.14.7), graphics, stats, utils Suggests: BiocStyle License: GPL (>=2) MD5sum: 7c4c5ed21a3b2594fe094e7b75f053bc NeedsCompilation: no Title: An R package for analysis of massive parallel sequencing based RNA structure probing data Description: This package facilitates analysis of Next Generation Sequencing data for which positional information with a single nucleotide resolution is a key. It allows for applying different types of relevant normalizations, data visualization and export in a table or UCSC compatible bedgraph file. biocViews: Coverage, Normalization, Sequencing, GenomeAnnotation Author: Lukasz Jan Kielpinski [aut], Nikos Sidiropoulos [cre, aut], Jeppe Vinther [aut] Maintainer: Nikos Sidiropoulos git_url: https://git.bioconductor.org/packages/RNAprobR git_branch: RELEASE_3_8 git_last_commit: d424ca9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RNAprobR_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RNAprobR_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RNAprobR_1.14.0.tgz vignettes: vignettes/RNAprobR/inst/doc/RNAprobR.pdf vignetteTitles: RNAprobR: An R package for analysis of the massive parallel sequencing based methods of RNA structure probing hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RNAprobR/inst/doc/RNAprobR.R Package: rnaseqcomp Version: 1.12.0 Depends: R (>= 3.2.0) Imports: RColorBrewer, methods Suggests: BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: 42917eebae09b1408fd29f6e929793bc NeedsCompilation: no Title: Benchmarks for RNA-seq Quantification Pipelines Description: Several quantitative and visualized benchmarks for RNA-seq quantification pipelines. Two-condition quantifications for genes, transcripts, junctions or exons by each pipeline with necessary meta information should be organized into numeric matrices in order to proceed the evaluation. biocViews: RNASeq, Visualization, QualityControl Author: Mingxiang Teng and Rafael A. Irizarry Maintainer: Mingxiang Teng URL: https://github.com/tengmx/rnaseqcomp VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/rnaseqcomp git_branch: RELEASE_3_8 git_last_commit: 7d7b2ce git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rnaseqcomp_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rnaseqcomp_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rnaseqcomp_1.12.0.tgz vignettes: vignettes/rnaseqcomp/inst/doc/rnaseqcomp.pdf vignetteTitles: The rnaseqcomp user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rnaseqcomp/inst/doc/rnaseqcomp.R suggestsMe: SummarizedBenchmark Package: rnaSeqMap Version: 2.40.1 Depends: R (>= 2.11.0), methods, Biobase, Rsamtools, GenomicAlignments Imports: GenomicRanges , IRanges, edgeR, DESeq, DBI License: GPL-2 MD5sum: 629d69ebfc6d6241ae954a5f61289966 NeedsCompilation: yes Title: rnaSeq secondary analyses Description: The rnaSeqMap library provides classes and functions to analyze the RNA-sequencing data using the coverage profiles in multiple samples at a time biocViews: ImmunoOncology, Annotation, ReportWriting, Transcription, GeneExpression, DifferentialExpression, Sequencing, RNASeq, SAGE, Visualization Author: Anna Lesniewska ; Michal Okoniewski Maintainer: Michal Okoniewski git_url: https://git.bioconductor.org/packages/rnaSeqMap git_branch: RELEASE_3_8 git_last_commit: c122d64 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/rnaSeqMap_2.40.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rnaSeqMap_2.40.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rnaSeqMap_2.40.1.tgz vignettes: vignettes/rnaSeqMap/inst/doc/rnaSeqMap.pdf vignetteTitles: rnaSeqMap primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rnaSeqMap/inst/doc/rnaSeqMap.R dependsOnMe: ampliQueso Package: RNASeqPower Version: 1.22.1 License: LGPL (>=2) Archs: i386, x64 MD5sum: 30691ae43fbcd92a8446ef972d6aad81 NeedsCompilation: no Title: Sample size for RNAseq studies Description: RNA-seq, sample size biocViews: ImmunoOncology, RNASeq Author: Terry M Therneau [aut, cre], Hart Stephen [ctb] Maintainer: Terry M Therneau git_url: https://git.bioconductor.org/packages/RNASeqPower git_branch: RELEASE_3_8 git_last_commit: 0ddd41e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RNASeqPower_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RNASeqPower_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RNASeqPower_1.22.1.tgz vignettes: vignettes/RNASeqPower/inst/doc/samplesize.pdf vignetteTitles: RNAseq samplesize hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RNASeqPower/inst/doc/samplesize.R Package: RNASeqR Version: 1.0.3 Depends: R(>= 3.5.0), ggplot2, pathview, edgeR, methods Imports: Rsamtools, tools, reticulate, ballgown, gridExtra, rafalib, FactoMineR, factoextra, corrplot, PerformanceAnalytics, reshape2, DESeq2, systemPipeR, systemPipeRdata, clusterProfiler, org.Hs.eg.db, org.Sc.sgd.db, stringr, pheatmap, grDevices, graphics, stats, utils, DOSE, Biostrings, parallel Suggests: knitr, png, grid, RNASeqRData License: Artistic-2.0 MD5sum: 41ef8cfd67effa33cca28f4a353edbd8 NeedsCompilation: no Title: RNASeqR: RNA-Seq workflow for case-control study Description: This R package is designed for case-control RNA-Seq analysis (two-group). There are six steps: "RNASeqRParam S4 Object Creation", "Environment Setup", "Quality Assessment", "Reads Alignment & Quantification", "Gene-level Differential Analyses" and "Functional Analyses". Each step corresponds to a function in this package. After running functions in order, a basic RNASeq analysis would be done easily. biocViews: Genetics, Infrastructure, DataImport, Sequencing, RNASeq, GeneExpression, GeneSetEnrichment, Alignment, QualityControl, DifferentialExpression, FunctionalPrediction, ExperimentalDesign, GO, KEGG, Visualization, Normalization, Pathways, Clustering, ImmunoOncology Author: Kuan-Hao Chao Maintainer: Kuan-Hao Chao URL: https://github.com/HowardChao/RNASeqR SystemRequirements: RNASeqR only support Linux and macOS. Window is not supported. Python2 is highly recommended. If your machine is Python3, make sure '2to3' command is available. VignetteBuilder: knitr BugReports: https://github.com/HowardChao/RNASeqR/issues git_url: https://git.bioconductor.org/packages/RNASeqR git_branch: RELEASE_3_8 git_last_commit: ba9f675 git_last_commit_date: 2018-12-04 Date/Publication: 2018-12-04 source.ver: src/contrib/RNASeqR_1.0.3.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RNASeqR_1.0.3.tgz vignettes: vignettes/RNASeqR/inst/doc/RNASeqR.html vignetteTitles: RNA-Seq analysis based on one independent variable hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RNASeqR/inst/doc/RNASeqR.R Package: RnaSeqSampleSize Version: 1.14.1 Depends: R (>= 2.10), RnaSeqSampleSizeData Imports: biomaRt,edgeR,heatmap3,matlab,KEGGREST,Rcpp (>= 0.11.2) LinkingTo: Rcpp Suggests: BiocStyle, knitr License: GPL (>= 2) MD5sum: 575a92cf0cb2ff0c085be098b8d1d019 NeedsCompilation: yes Title: RnaSeqSampleSize Description: RnaSeqSampleSize package provides a sample size calculation method based on negative binomial model and the exact test for assessing differential expression analysis of RNA-seq data biocViews: ImmunoOncology, ExperimentalDesign, Sequencing, RNASeq, GeneExpression, DifferentialExpression Author: Shilin Zhao, Chung-I Li, Yan Guo, Quanhu Sheng, Yu Shyr Maintainer: Shilin Zhao VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RnaSeqSampleSize git_branch: RELEASE_3_8 git_last_commit: 9d55430 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RnaSeqSampleSize_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RnaSeqSampleSize_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RnaSeqSampleSize_1.14.1.tgz vignettes: vignettes/RnaSeqSampleSize/inst/doc/RnaSeqSampleSize.pdf vignetteTitles: RnaSeqSampleSize: Sample size estimation by real data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RnaSeqSampleSize/inst/doc/RnaSeqSampleSize.R Package: RnBeads Version: 2.0.1 Depends: R (>= 3.0.0), BiocGenerics, S4Vectors (>= 0.9.25), GenomicRanges, MASS, cluster, ff, fields, ggplot2 (>= 0.9.2), gplots, gridExtra, limma, matrixStats, methods, illuminaio, methylumi, plyr Imports: IRanges Suggests: Category, GOstats, Gviz, IlluminaHumanMethylation450kmanifest, RPMM, RefFreeEWAS, RnBeads.hg19, XML, annotate, biomaRt, foreach, doParallel, ggbio, isva, mclust, mgcv, minfi, nlme, org.Hs.eg.db, org.Mm.eg.db, org.Rn.eg.db, quadprog, rtracklayer, qvalue, sva, wateRmelon, wordcloud, qvalue, argparse, glmnet, GLAD, IlluminaHumanMethylation450kanno.ilmn12.hg19, scales, missMethyl, impute, shiny, shinyjs, plotrix, hexbin, RUnit License: GPL-3 Archs: i386, x64 MD5sum: 815f0ce6e40b731a88d64658cbac28d1 NeedsCompilation: no Title: RnBeads Description: RnBeads facilitates comprehensive analysis of various types of DNA methylation data at the genome scale. biocViews: ImmunoOncology, DNAMethylation, MethylationArray, MethylSeq, Epigenetics, QualityControl, Preprocessing, BatchEffect, DifferentialMethylation, Sequencing, CpGIsland, TwoChannel, DataImport Author: Yassen Assenov [aut], Pavlo Lutsik [aut], Michael Scherer [aut], Fabian Mueller [aut, cre] Maintainer: Fabian Mueller git_url: https://git.bioconductor.org/packages/RnBeads git_branch: RELEASE_3_8 git_last_commit: 1e73169 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RnBeads_2.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RnBeads_2.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RnBeads_2.0.1.tgz vignettes: vignettes/RnBeads/inst/doc/RnBeads_Annotations.pdf, vignettes/RnBeads/inst/doc/RnBeads.pdf vignetteTitles: RnBeads Annotation, Comprehensive DNA Methylation Analysis with RnBeads hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RnBeads/inst/doc/RnBeads_Annotations.R, vignettes/RnBeads/inst/doc/RnBeads.R Package: Rnits Version: 1.16.0 Depends: R (>= 3.1.0), Biobase, ggplot2, limma, methods Imports: affy, boot, impute, splines, graphics, qvalue, reshape2 Suggests: BiocStyle, knitr, GEOquery, stringr License: GPL-3 MD5sum: 47d6ced6ce9154da7718e97178123f13 NeedsCompilation: no Title: R Normalization and Inference of Time Series data Description: R/Bioconductor package for normalization, curve registration and inference in time course gene expression data biocViews: GeneExpression, Microarray, TimeCourse, DifferentialExpression, Normalization Author: Dipen P. Sangurdekar Maintainer: Dipen P. Sangurdekar VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Rnits git_branch: RELEASE_3_8 git_last_commit: f03347f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rnits_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rnits_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rnits_1.16.0.tgz vignettes: vignettes/Rnits/inst/doc/Rnits-vignette.pdf vignetteTitles: R/Bioconductor package for normalization and differential expression inference in time series gene expression microarray data. hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rnits/inst/doc/Rnits-vignette.R Package: roar Version: 1.18.0 Depends: R (>= 3.0.1) Imports: methods, BiocGenerics, S4Vectors, IRanges, GenomicRanges, SummarizedExperiment, GenomicAlignments (>= 0.99.4), rtracklayer, GenomeInfoDb Suggests: RNAseqData.HNRNPC.bam.chr14, testthat License: GPL-3 MD5sum: af18fe575adeb3d3cddeea46774d9a07 NeedsCompilation: no Title: Identify differential APA usage from RNA-seq alignments Description: Identify preferential usage of APA sites, comparing two biological conditions, starting from known alternative sites and alignments obtained from standard RNA-seq experiments. biocViews: Sequencing, HighThroughputSequencing, RNAseq, Transcription Author: Elena Grassi Maintainer: Elena Grassi URL: https://github.com/vodkatad/roar/ git_url: https://git.bioconductor.org/packages/roar git_branch: RELEASE_3_8 git_last_commit: 119adf7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/roar_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/roar_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/roar_1.18.0.tgz vignettes: vignettes/roar/inst/doc/roar.pdf vignetteTitles: Identify differential APA usage from RNA-seq alignments hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/roar/inst/doc/roar.R importsMe: XBSeq Package: ROC Version: 1.58.0 Depends: R (>= 1.9.0), utils, methods Suggests: Biobase License: Artistic-2.0 MD5sum: d7a7d3f092af4fbba537c070c6f0efc0 NeedsCompilation: yes Title: utilities for ROC, with uarray focus Description: utilities for ROC, with uarray focus biocViews: DifferentialExpression Author: Vince Carey , Henning Redestig for C++ language enhancements Maintainer: Vince Carey URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/ROC git_branch: RELEASE_3_8 git_last_commit: da15bc4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ROC_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ROC_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ROC_1.58.0.tgz vignettes: vignettes/ROC/inst/doc/ROCnotes.pdf vignetteTitles: ROC notes hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ROC/inst/doc/ROCnotes.R dependsOnMe: TCC, wateRmelon importsMe: clst suggestsMe: genefilter, MCRestimate Package: Roleswitch Version: 1.20.0 Depends: R (>= 2.10), pracma, reshape, plotrix, microRNA, biomaRt, Biostrings, Biobase, DBI Suggests: ggplot2 License: GPL-2 Archs: i386, x64 MD5sum: e714b785159b4e22b1886d246a89adfc NeedsCompilation: no Title: Infer miRNA-mRNA interactions using paired expression data from a single sample Description: Infer Probabilities of MiRNA-mRNA Interaction Signature (ProMISe) using paired expression data from a single sample. Roleswitch operates in two phases by inferring the probability of mRNA (miRNA) being the targets ("targets") of miRNA (mRNA), taking into account the expression of all of the mRNAs (miRNAs) due to their potential competition for the same miRNA (mRNA). Due to dynamic miRNA repression in the cell, Roleswitch assumes that the total transcribed mRNA levels are higher than the observed (equilibrium) mRNA levels and iteratively updates the total transcription of each mRNA targets based on the above inference. NB: in the paper, we used ProMISe as both the model name and inferred score name. biocViews: miRNA Author: Yue Li Maintainer: Yue Li URL: http://www.cs.utoronto.ca/~yueli/roleswitch.html git_url: https://git.bioconductor.org/packages/Roleswitch git_branch: RELEASE_3_8 git_last_commit: 674fa20 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Roleswitch_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Roleswitch_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Roleswitch_1.20.0.tgz vignettes: vignettes/Roleswitch/inst/doc/Roleswitch.pdf vignetteTitles: Roleswitch hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Roleswitch/inst/doc/Roleswitch.R importsMe: miRLAB Package: rols Version: 2.10.1 Depends: methods Imports: httr, progress, jsonlite, utils, Biobase, BiocGenerics (>= 0.23.1) Suggests: GO.db, knitr (>= 1.1.0), BiocStyle (>= 2.5.19), testthat, lubridate, DT, rmarkdown, License: GPL-2 MD5sum: 8589367e96669e0c27f69d5c53954eba NeedsCompilation: no Title: An R interface to the Ontology Lookup Service Description: The rols package is an interface to the Ontology Lookup Service (OLS) to access and query hundred of ontolgies directly from R. biocViews: ImmunoOncology, Software, Annotation, MassSpectrometry, GO Author: Laurent Gatto , with contributions from Tiago Chedraoui Silva. Maintainer: Laurent Gatto URL: http://lgatto.github.com/rols/ VignetteBuilder: knitr BugReports: https://github.com/lgatto/rols/issues git_url: https://git.bioconductor.org/packages/rols git_branch: RELEASE_3_8 git_last_commit: 6648d28 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/rols_2.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rols_2.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rols_2.10.1.tgz vignettes: vignettes/rols/inst/doc/rols.html vignetteTitles: An R interface to the Ontology Lookup Service hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rols/inst/doc/rols.R suggestsMe: MSnbase Package: ROntoTools Version: 2.10.0 Depends: methods, graph, boot, KEGGREST, KEGGgraph, Rgraphviz Suggests: RUnit, BiocGenerics License: CC BY-NC-ND 4.0 + file LICENSE MD5sum: 75691c4b8aa9bf7bd9a948c2bd0d36e3 NeedsCompilation: no Title: R Onto-Tools suite Description: Suite of tools for functional analysis. biocViews: NetworkAnalysis, Microarray, GraphsAndNetworks Author: Calin Voichita and Sahar Ansari and Sorin Draghici Maintainer: Calin Voichita git_url: https://git.bioconductor.org/packages/ROntoTools git_branch: RELEASE_3_8 git_last_commit: c5535cd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ROntoTools_2.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ROntoTools_2.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ROntoTools_2.10.0.tgz vignettes: vignettes/ROntoTools/inst/doc/rontotools.pdf vignetteTitles: ROntoTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/ROntoTools/inst/doc/rontotools.R dependsOnMe: BLMA Package: ropls Version: 1.14.1 Imports: Biobase, methods Suggests: BiocGenerics, BiocStyle, knitr, multtest, rmarkdown, RUnit License: CeCILL MD5sum: ce9599d283318492c5873a1c11f816c1 NeedsCompilation: no Title: PCA, PLS(-DA) and OPLS(-DA) for multivariate analysis and feature selection of omics data Description: Latent variable modeling with Principal Component Analysis(PCA) and Partial Least Squares (PLS) are powerful methods for visualization, regression, classification, and feature selection of omics data where the number of variables exceeds the number of samples and with multicollinearity among variables. Orthogonal Partial Least Squares (OPLS) enables to separately model the variation correlated (predictive) to the factor of interest and the uncorrelated (orthogonal) variation. While performing similarly to PLS, OPLS facilitates interpretation. Successful applications of these chemometrics techniques include spectroscopic data such as Raman spectroscopy, nuclear magnetic resonance (NMR), mass spectrometry (MS) in metabolomics and proteomics, but also transcriptomics data. In addition to scores, loadings and weights plots, the package provides metrics and graphics to determine the optimal number of components (e.g. with the R2 and Q2 coefficients), check the validity of the model by permutation testing, detect outliers, and perform feature selection (e.g. with Variable Importance in Projection or regression coefficients). The package can be accessed via a user interface on the Workflow4Metabolomics.org online resource for computational metabolomics (built upon the Galaxy environment). biocViews: ImmunoOncology, Regression, Classification, PrincipalComponent, Transcriptomics, Proteomics, Metabolomics, Lipidomics, MassSpectrometry Author: Etienne A. Thevenot Maintainer: Etienne A. Thevenot URL: http://dx.doi.org/10.1021/acs.jproteome.5b00354 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ropls git_branch: RELEASE_3_8 git_last_commit: 8adbd25 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ropls_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ropls_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ropls_1.14.1.tgz vignettes: vignettes/ropls/inst/doc/ropls-vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ropls/inst/doc/ropls-vignette.R importsMe: ASICS, biosigner, proFIA Package: ROTS Version: 1.10.1 Depends: R (>= 3.3) Imports: Rcpp, stats, Biobase, methods LinkingTo: Rcpp Suggests: testthat License: GPL (>= 2) MD5sum: 430600d3a456ceeaddf9387721d2463d NeedsCompilation: yes Title: Reproducibility-Optimized Test Statistic Description: Calculates the Reproducibility-Optimized Test Statistic (ROTS) for differential testing in omics data. biocViews: ImmunoOncology, Software, GeneExpression, DifferentialExpression, Microarray, RNASeq, Proteomics Author: Fatemeh Seyednasrollah, Tomi Suomi, Laura L. Elo Maintainer: Fatemeh Seyednasrollah git_url: https://git.bioconductor.org/packages/ROTS git_branch: RELEASE_3_8 git_last_commit: 1733d3f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ROTS_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ROTS_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ROTS_1.10.1.tgz vignettes: vignettes/ROTS/inst/doc/ROTS.pdf vignetteTitles: ROTS: Reproducibility Optimized Test Statistic hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ROTS/inst/doc/ROTS.R importsMe: PECA, PowerExplorer Package: RPA Version: 1.38.0 Depends: R (>= 3.1.1), affy, BiocGenerics, methods Imports: phyloseq Suggests: affydata, knitr, parallel License: BSD_2_clause + file LICENSE Archs: i386, x64 MD5sum: 7b2d727e06ee9202a906a384a1514c01 NeedsCompilation: no Title: RPA: Robust Probabilistic Averaging for probe-level analysis Description: Probabilistic analysis of probe reliability and differential gene expression on short oligonucleotide arrays. biocViews: GeneExpression, Microarray, Preprocessing, QualityControl Author: Leo Lahti [aut, cre] Maintainer: Leo Lahti URL: https://github.com/antagomir/RPA VignetteBuilder: knitr BugReports: https://github.com/antagomir/RPA git_url: https://git.bioconductor.org/packages/RPA git_branch: RELEASE_3_8 git_last_commit: 7ce4005 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RPA_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RPA_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RPA_1.38.0.tgz vignettes: vignettes/RPA/inst/doc/RPA.html vignetteTitles: RPA R package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE dependsOnMe: prebs Package: RProtoBufLib Version: 1.4.0 License: BSD_3_clause MD5sum: 0aec534ff083127809f3313676f7b48e NeedsCompilation: yes Title: C++ headers and static libraries of Protocol buffers Description: This package provides the headers and static library of Protocol buffers 2.6.0 for other R packages to compile and link against. biocViews: Infrastructure Author: Mike Jiang Maintainer: Mike Jiang SystemRequirements: GNU make git_url: https://git.bioconductor.org/packages/RProtoBufLib git_branch: RELEASE_3_8 git_last_commit: 3b4d6a1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RProtoBufLib_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RProtoBufLib_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RProtoBufLib_1.4.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: FALSE linksToMe: cytolib, flowWorkspace Package: RpsiXML Version: 2.24.0 Depends: methods, annotate (>= 1.21.0), graph (>= 1.21.0), Biobase, RBGL (>= 1.17.0), XML (>= 2.4.0), hypergraph (>= 1.15.2), AnnotationDbi Suggests: org.Hs.eg.db, org.Mm.eg.db, org.Dm.eg.db, org.Rn.eg.db, org.Sc.sgd.db,hom.Hs.inp.db, hom.Mm.inp.db, hom.Dm.inp.db, hom.Rn.inp.db, hom.Sc.inp.db,Rgraphviz, ppiStats, ScISI License: LGPL-3 Archs: i386, x64 MD5sum: 7be74bec83e9b9afd74726a08f9e435b NeedsCompilation: no Title: R interface to PSI-MI 2.5 files Description: Queries, data structure and interface to visualization of interaction datasets. This package inplements the PSI-MI 2.5 standard and supports up to now 8 databases. Further databases supporting PSI-MI 2.5 standard will be added continuously. biocViews: Infrastructure, Proteomics Author: Jitao David Zhang, Stefan Wiemann, Marc Carlson, with contributions from Tony Chiang Maintainer: Jitao David Zhang URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/RpsiXML git_branch: RELEASE_3_8 git_last_commit: 89202e7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RpsiXML_2.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RpsiXML_2.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RpsiXML_2.24.0.tgz vignettes: vignettes/RpsiXML/inst/doc/RpsiXML.pdf, vignettes/RpsiXML/inst/doc/RpsiXMLApp.pdf vignetteTitles: Reading PSI-25 XML files, Application Examples of RpsiXML package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RpsiXML/inst/doc/RpsiXML.R, vignettes/RpsiXML/inst/doc/RpsiXMLApp.R dependsOnMe: ScISI importsMe: ScISI Package: rpx Version: 1.18.1 Depends: methods Imports: xml2, RCurl, utils Suggests: MSnbase, Biostrings, BiocStyle, testthat, knitr License: GPL-2 MD5sum: 9fafde1374e923e431d10c12c94ce787 NeedsCompilation: no Title: R Interface to the ProteomeXchange Repository Description: The rpx package implements an interface to proteomics data submitted to the ProteomeXchange consortium. biocViews: ImmunoOncology, Proteomics, MassSpectrometry, DataImport, ThirdPartyClient Author: Laurent Gatto Maintainer: Laurent Gatto URL: https://github.com/lgatto/rpx VignetteBuilder: knitr BugReports: https://github.com/lgatto/rpx/issues git_url: https://git.bioconductor.org/packages/rpx git_branch: RELEASE_3_8 git_last_commit: 15fac02 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/rpx_1.18.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rpx_1.18.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rpx_1.18.1.tgz vignettes: vignettes/rpx/inst/doc/rpx.html vignetteTitles: An R interface to the ProteomeXchange repository hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rpx/inst/doc/rpx.R importsMe: proteoQC suggestsMe: MSnbase Package: Rqc Version: 1.16.2 Depends: BiocParallel, ShortRead, ggplot2 Imports: BiocGenerics (>= 0.25.1), Biostrings, IRanges, methods, S4Vectors, knitr (>= 1.7), BiocStyle, plyr, markdown, grid, reshape2, digest, Rcpp (>= 0.11.6), biovizBase, shiny, Rsamtools, GenomicAlignments, GenomicFiles LinkingTo: Rcpp Suggests: testthat License: GPL (>= 2) MD5sum: 58558b854ed79b3950d6f83db6cbf554 NeedsCompilation: yes Title: Quality Control Tool for High-Throughput Sequencing Data Description: Rqc is an optimised tool designed for quality control and assessment of high-throughput sequencing data. It performs parallel processing of entire files and produces a report which contains a set of high-resolution graphics. biocViews: Sequencing, QualityControl, DataImport Author: Welliton Souza, Benilton Carvalho Maintainer: Welliton Souza URL: https://github.com/labbcb/Rqc VignetteBuilder: knitr BugReports: https://github.com/labbcb/Rqc/issues git_url: https://git.bioconductor.org/packages/Rqc git_branch: RELEASE_3_8 git_last_commit: eb418ff git_last_commit_date: 2018-11-02 Date/Publication: 2018-11-03 source.ver: src/contrib/Rqc_1.16.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rqc_1.16.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rqc_1.16.2.tgz vignettes: vignettes/Rqc/inst/doc/Rqc.html vignetteTitles: Using Rqc hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rqc/inst/doc/Rqc.R Package: rqt Version: 1.8.0 Depends: R (>= 3.4), SummarizedExperiment Imports: stats,Matrix,ropls,methods,car,RUnit,metap,CompQuadForm,glmnet,utils,pls Suggests: BiocStyle, knitr, rmarkdown License: GPL Archs: i386, x64 MD5sum: 7ce8c07744e2c70c68fb04ce7f7edab2 NeedsCompilation: no Title: rqt: utilities for gene-level meta-analysis Description: Despite the recent advances of modern GWAS methods, it still remains an important problem of addressing calculation an effect size and corresponding p-value for the whole gene rather than for single variant. The R- package rqt offers gene-level GWAS meta-analysis. For more information, see: "Gene-set association tests for next-generation sequencing data" by Lee et al (2016), Bioinformatics, 32(17), i611-i619, . biocViews: GenomeWideAssociation, Regression, Survival, PrincipalComponent, StatisticalMethod, Sequencing Author: I. Y. Zhbannikov, K. G. Arbeev, A. I. Yashin. Maintainer: Ilya Y. Zhbannikov URL: https://github.com/izhbannikov/rqt VignetteBuilder: knitr BugReports: https://github.com/izhbannikov/rqt/issues git_url: https://git.bioconductor.org/packages/rqt git_branch: RELEASE_3_8 git_last_commit: c66b6e5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rqt_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rqt_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rqt_1.8.0.tgz vignettes: vignettes/rqt/inst/doc/rqt-vignette.html vignetteTitles: Tutorial for rqt package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rqt/inst/doc/rqt-vignette.R Package: rqubic Version: 1.28.0 Imports: methods, Biobase, BiocGenerics, biclust Suggests: RColorBrewer License: GPL-2 MD5sum: 9a57a107dffeee5d00f42aaaeab6400c NeedsCompilation: yes Title: Qualitative biclustering algorithm for expression data analysis in R Description: This package implements the QUBIC algorithm introduced by Li et al. for the qualitative biclustering with gene expression data. biocViews: Microarray, Clustering Author: Jitao David Zhang, with inputs from Laura Badi and Martin Ebeling Maintainer: Jitao David Zhang git_url: https://git.bioconductor.org/packages/rqubic git_branch: RELEASE_3_8 git_last_commit: 3f1d19e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rqubic_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rqubic_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rqubic_1.28.0.tgz vignettes: vignettes/rqubic/inst/doc/rqubic.pdf vignetteTitles: Qualitative Biclustering with Bioconductor Package rqubic hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rqubic/inst/doc/rqubic.R importsMe: miRSM Package: rRDP Version: 1.16.1 Depends: Biostrings (>= 2.26.2) Suggests: rRDPData License: GPL-2 | file LICENSE Archs: i386, x64 MD5sum: 18f898327dcda77590dfe9352855ac2c NeedsCompilation: no Title: Interface to the RDP Classifier Description: Seamlessly interfaces RDP classifier (version 2.9). biocViews: ImmunoOncology, Genetics, Sequencing, Infrastructure, Classification, Microbiome Author: Michael Hahsler, Anurag Nagar Maintainer: Michael Hahsler SystemRequirements: Java git_url: https://git.bioconductor.org/packages/rRDP git_branch: RELEASE_3_8 git_last_commit: 993ae5e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/rRDP_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rRDP_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rRDP_1.16.1.tgz vignettes: vignettes/rRDP/inst/doc/rRDP.pdf vignetteTitles: rRDP: Interface to the RDP Classifier hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rRDP/inst/doc/rRDP.R Package: RRHO Version: 1.22.0 Depends: R (>= 2.10), grid Imports: VennDiagram Suggests: lattice License: GPL-2 MD5sum: 04b3d6a5bda498c229c22855b329bbb8 NeedsCompilation: no Title: Inference on agreement between ordered lists Description: The package is aimed at inference on the amount of agreement in two sorted lists using the Rank-Rank Hypergeometric Overlap test. biocViews: Genetics, SequenceMatching, Microarray, Transcription Author: Jonathan Rosenblatt and Jason Stein Maintainer: Jonathan Rosenblatt git_url: https://git.bioconductor.org/packages/RRHO git_branch: RELEASE_3_8 git_last_commit: 4ea5d2e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RRHO_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RRHO_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RRHO_1.22.0.tgz vignettes: vignettes/RRHO/inst/doc/RRHO.pdf vignetteTitles: RRHO hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RRHO/inst/doc/RRHO.R Package: Rsamtools Version: 1.34.1 Depends: methods, GenomeInfoDb (>= 1.1.3), GenomicRanges (>= 1.31.8), Biostrings (>= 2.47.6) Imports: utils, BiocGenerics (>= 0.25.1), S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), XVector (>= 0.19.7), zlibbioc, bitops, BiocParallel LinkingTo: S4Vectors, IRanges, XVector, Biostrings Suggests: GenomicAlignments, ShortRead (>= 1.19.10), GenomicFeatures, TxDb.Dmelanogaster.UCSC.dm3.ensGene, KEGG.db, TxDb.Hsapiens.UCSC.hg18.knownGene, RNAseqData.HNRNPC.bam.chr14, BSgenome.Hsapiens.UCSC.hg19, RUnit, BiocStyle License: Artistic-2.0 | file LICENSE MD5sum: e2060c9c832550ed3e72cd55506dc3c5 NeedsCompilation: yes Title: Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import Description: This package provides an interface to the 'samtools', 'bcftools', and 'tabix' utilities (see 'LICENCE') for manipulating SAM (Sequence Alignment / Map), FASTA, binary variant call (BCF) and compressed indexed tab-delimited (tabix) files. biocViews: DataImport, Sequencing, Coverage, Alignment, QualityControl Author: Martin Morgan, Herv\'e Pag\`es, Valerie Obenchain, Nathaniel Hayden Maintainer: Bioconductor Package Maintainer URL: http://bioconductor.org/packages/release/bioc/html/Rsamtools.html Video: https://www.youtube.com/watch?v=Rfon-DQYbWA&list=UUqaMSQd_h-2EDGsU6WDiX0Q git_url: https://git.bioconductor.org/packages/Rsamtools git_branch: RELEASE_3_8 git_last_commit: 0ec1d45 git_last_commit_date: 2019-01-30 Date/Publication: 2019-01-31 source.ver: src/contrib/Rsamtools_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rsamtools_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rsamtools_1.34.1.tgz vignettes: vignettes/Rsamtools/inst/doc/Rsamtools-Overview.pdf, vignettes/Rsamtools/inst/doc/Rsamtools-UsingCLibraries.pdf vignetteTitles: An introduction to Rsamtools, Using samtools C libraries hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Rsamtools/inst/doc/Rsamtools-Overview.R, vignettes/Rsamtools/inst/doc/Rsamtools-UsingCLibraries.R dependsOnMe: ArrayExpressHTS, BitSeq, chimera, CODEX, contiBAIT, CoverageView, esATAC, exomeCopy, exomePeak, GenomicAlignments, GenomicFiles, girafe, gmapR, Guitar, HelloRanges, IntEREst, MEDIPS, methylPipe, MMDiff2, podkat, qrqc, r3Cseq, Rcade, ReQON, rfPred, RIPSeeker, rnaSeqMap, SGSeq, ShortRead, SICtools, SNPhood, systemPipeR, TarSeqQC, TEQC, VariantAnnotation, wavClusteR importsMe: AllelicImbalance, alpine, AneuFinder, annmap, AnnotationHubData, appreci8R, ArrayExpressHTS, ASpli, ATACseqQC, BadRegionFinder, BBCAnalyzer, biovizBase, breakpointR, BSgenome, CAGEr, casper, cellbaseR, CexoR, chimeraviz, ChIPexoQual, ChIPpeakAnno, ChIPQC, ChIPSeqSpike, chromstaR, chromVAR, cn.mops, CNVPanelizer, CNVrd2, compEpiTools, consensusDE, CopywriteR, CrispRVariants, csaw, customProDB, derfinder, DEXSeq, DiffBind, diffHic, DOQTL, easyRNASeq, EDASeq, ensembldb, epigenomix, eudysbiome, FourCSeq, FunChIP, FunciSNP, gcapc, GeneGeneInteR, GenoGAM, genomation, GenomicAlignments, GenomicInteractions, GenVisR, ggbio, GGtools, GoogleGenomics, GOTHiC, GreyListChIP, GUIDEseq, Gviz, gwascat, h5vc, HTSeqGenie, icetea, IMAS, INSPEcT, karyoploteR, ldblock, MACPET, MADSEQ, MDTS, metagene, methylKit, mosaics, motifmatchr, msgbsR, MTseeker, NADfinder, nucleR, ORFik, panelcn.mops, PGA, PICS, plyranges, PureCN, QDNAseq, qsea, QuasR, R453Plus1Toolbox, ramwas, Rariant, Repitools, RiboProfiling, riboSeqR, RNAprobR, RNASeqR, Rqc, rtracklayer, scruff, segmentSeq, seqplots, seqsetvis, soGGi, SplicingGraphs, srnadiff, strandCheckR, TCseq, TitanCNA, tracktables, trackViewer, transcriptR, TransView, TSRchitect, TVTB, VariantFiltering, VariantTools suggestsMe: AnnotationHub, bamsignals, BaseSpaceR, BiocGenerics, BiocParallel, biomvRCNS, Chicago, epivizrChart, gage, GenomeInfoDb, GenomicDataCommons, GenomicFeatures, GenomicRanges, gQTLstats, IRanges, metaseqR, omicsPrint, recoup, SeqArray, seqbias, SigFuge, similaRpeak, Streamer, TFutils linksToMe: ArrayExpressHTS, BitSeq, DiffBind, h5vc, podkat, qrqc, QuasR, seqbias, TransView, VariantAnnotation Package: rsbml Version: 2.40.0 Depends: R (>= 2.6.0), BiocGenerics (>= 0.3.2), methods, utils Imports: BiocGenerics, graph, utils License: Artistic-2.0 Archs: i386, x64 MD5sum: c273ebb42e08542258b93904b3e132e4 NeedsCompilation: yes Title: R support for SBML, using libsbml Description: Links R to libsbml for SBML parsing, validating output, provides an S4 SBML DOM, converts SBML to R graph objects. Optionally links to the SBML ODE Solver Library (SOSLib) for simulating models. biocViews: GraphAndNetwork, Pathways, Network Author: Michael Lawrence Maintainer: Michael Lawrence URL: http://www.sbml.org SystemRequirements: libsbml (==5.10.2) git_url: https://git.bioconductor.org/packages/rsbml git_branch: RELEASE_3_8 git_last_commit: ea485fb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rsbml_2.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rsbml_2.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rsbml_2.40.0.tgz vignettes: vignettes/rsbml/inst/doc/quick-start.pdf vignetteTitles: Quick start for rsbml hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: FALSE Rfiles: vignettes/rsbml/inst/doc/quick-start.R dependsOnMe: BiGGR suggestsMe: piano, SBMLR Package: RSeqAn Version: 1.2.0 Suggests: knitr, rmarkdown License: BSD_3_clause + file LICENSE Archs: i386, x64 MD5sum: 3ccf58bab71c87b4df1c300b4766d750 NeedsCompilation: no Title: R SeqAn Description: Headers from the SeqAn C++ library for easy of usage in R. biocViews: Infrastructure, Software Author: August Guang [aut, cre] Maintainer: August Guang VignetteBuilder: knitr BugReports: https://github.com/compbiocore/RSeqAn/issues git_url: https://git.bioconductor.org/packages/RSeqAn git_branch: RELEASE_3_8 git_last_commit: ef55f8e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RSeqAn_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RSeqAn_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RSeqAn_1.2.0.tgz vignettes: vignettes/RSeqAn/inst/doc/first_example.html vignetteTitles: Introduction to Using RSeqAn hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RSeqAn/inst/doc/first_example.R Package: rSFFreader Version: 0.30.0 Depends: ShortRead (>= 1.23.17) Imports: methods, Biostrings, IRanges LinkingTo: S4Vectors (>= 0.13.8), IRanges, XVector, Biostrings Suggests: xtable License: Artistic-2.0 MD5sum: b3d8f6fb10462ef51867185257accc61 NeedsCompilation: yes Title: rSFFreader reads in sff files generated by Roche 454 and Life Sciences Ion Torrent sequencers Description: rSFFreader reads sequence, qualities and clip point values from sff files generated by Roche 454 and Life Sciences Ion Torrent sequencers into similar classes as are present for fastq files. biocViews: DataImport, Sequencing Author: Matt Settles , Sam Hunter, Brice Sarver, Ilia Zhbannikov, Kyu-Chul Cho Maintainer: Matt Settles git_url: https://git.bioconductor.org/packages/rSFFreader git_branch: RELEASE_3_8 git_last_commit: fdcb055 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rSFFreader_0.30.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rSFFreader_0.30.0.tgz vignettes: vignettes/rSFFreader/inst/doc/rSFFreader.pdf vignetteTitles: An introduction to rSFFreader hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rSFFreader/inst/doc/rSFFreader.R importsMe: hiReadsProcessor Package: Rsubread Version: 1.32.4 License: GPL-3 MD5sum: cb9e4136d89e2ddee5995672d436cc19 NeedsCompilation: yes Title: Subread sequence alignment and counting for R Description: Rsubread is a toolbox developed for the analyses of second and third generation sequencing data. It can be used for read mapping, read counting, SNP calling, structural variant detection and gene fusion discovery. It can be applied to all major sequencing techologies and is suitable for the analysis of both short and long reads. biocViews: Sequencing, Alignment, SequenceMatching, RNASeq, ChIPSeq, GeneExpression, GeneRegulation, Genetics, ImmunoOncology, SNP, GeneticVariability, Preprocessing, QualityControl, GenomeAnnotation, Software Author: Wei Shi, Yang Liao and Gordon K Smyth with contributions from Jenny Dai and Timothy Triche, Jr. Maintainer: Wei Shi , Yang Liao and Gordon K Smyth URL: http://bioconductor.org/packages/release/bioc/html/Rsubread.html git_url: https://git.bioconductor.org/packages/Rsubread git_branch: RELEASE_3_8 git_last_commit: c1d1d2b git_last_commit_date: 2019-03-05 Date/Publication: 2019-03-06 source.ver: src/contrib/Rsubread_1.32.4.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rsubread_1.32.4.tgz vignettes: vignettes/Rsubread/inst/doc/Rsubread.pdf, vignettes/Rsubread/inst/doc/SubreadUsersGuide.pdf vignetteTitles: Rsubread Vignette, SubreadUsersGuide.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rsubread/inst/doc/Rsubread.R dependsOnMe: ExCluster importsMe: dupRadar suggestsMe: icetea, scPipe, scruff, singleCellTK Package: RSVSim Version: 1.22.0 Depends: R (>= 3.0.0), Biostrings, GenomicRanges Imports: methods, IRanges, ShortRead Suggests: BSgenome.Hsapiens.UCSC.hg19, BSgenome.Hsapiens.UCSC.hg19.masked, MASS, rtracklayer License: LGPL-3 MD5sum: 161be094cdccdb551c4e702d1c687b4b NeedsCompilation: no Title: RSVSim: an R/Bioconductor package for the simulation of structural variations Description: RSVSim is a package for the simulation of deletions, insertions, inversion, tandem-duplications and translocations of various sizes in any genome available as FASTA-file or BSgenome data package. SV breakpoints can be placed uniformly accross the whole genome, with a bias towards repeat regions and regions of high homology (for hg19) or at user-supplied coordinates. biocViews: Sequencing Author: Christoph Bartenhagen Maintainer: Christoph Bartenhagen git_url: https://git.bioconductor.org/packages/RSVSim git_branch: RELEASE_3_8 git_last_commit: 4fee1e9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RSVSim_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RSVSim_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RSVSim_1.22.0.tgz vignettes: vignettes/RSVSim/inst/doc/vignette.pdf vignetteTitles: RSVSim: an R/Bioconductor package for the simulation of structural variations hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RSVSim/inst/doc/vignette.R Package: rTANDEM Version: 1.22.1 Depends: XML, Rcpp, data.table (>= 1.8.8) Imports: methods LinkingTo: Rcpp Suggests: biomaRt License: Artistic-1.0 | file LICENSE MD5sum: 3fd2dc74043c26e804771a32100d06e7 NeedsCompilation: yes Title: Interfaces the tandem protein identification algorithm in R Description: This package interfaces the tandem protein identification algorithm in R. Identification can be launched in the X!Tandem style, by using as sole parameter the path to a parameter file. But rTANDEM aslo provides extended syntax and functions to streamline launching analyses, as well as function to convert results, parameters and taxonomy to/from R. A related package, shinyTANDEM, provides visualization interface for result objects. biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Frederic Fournier , Charles Joly Beauparlant , Rene Paradis , Arnaud Droit Maintainer: Frederic Fournier SystemRequirements: rTANDEM uses expat and pthread libraries. See the README file for details. git_url: https://git.bioconductor.org/packages/rTANDEM git_branch: RELEASE_3_8 git_last_commit: 6149a8c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/rTANDEM_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rTANDEM_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rTANDEM_1.22.1.tgz vignettes: vignettes/rTANDEM/inst/doc/rTANDEM.pdf vignetteTitles: The rTANDEM users guide hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rTANDEM/inst/doc/rTANDEM.R dependsOnMe: PGA, shinyTANDEM importsMe: proteoQC Package: RTCA Version: 1.34.1 Depends: methods,stats,graphics,Biobase,RColorBrewer, gtools Suggests: xtable License: LGPL-3 Archs: i386, x64 MD5sum: 520f5e1e9f1d09b1f27e0fe95fd933da NeedsCompilation: no Title: Open-source toolkit to analyse data from xCELLigence System (RTCA) Description: Import, analyze and visualize data from Roche(R) xCELLigence RTCA systems. The package imports real-time cell electrical impedance data into R. As an alternative to commercial software shipped along the system, the Bioconductor package RTCA provides several unique transformation (normalization) strategies and various visualization tools. biocViews: ImmunoOncology, CellBasedAssays, Infrastructure, Visualization, TimeCourse Author: Jitao David Zhang Maintainer: Jitao David Zhang URL: http://code.google.com/p/xcelligence/,http://www.xcelligence.roche.com/,http://www.nextbiomotif.com/Home/scientific-programming git_url: https://git.bioconductor.org/packages/RTCA git_branch: RELEASE_3_8 git_last_commit: 791baeb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RTCA_1.34.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTCA_1.34.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTCA_1.34.1.tgz vignettes: vignettes/RTCA/inst/doc/aboutRTCA.pdf, vignettes/RTCA/inst/doc/RTCAtransformation.pdf vignetteTitles: Introduction to Data Analysis of the Roche xCELLigence System with RTCA Package, RTCAtransformation: Discussion of transformation methods of RTCA data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RTCA/inst/doc/aboutRTCA.R, vignettes/RTCA/inst/doc/RTCAtransformation.R Package: RTCGA Version: 1.12.1 Depends: R (>= 3.3.0) Imports: XML, assertthat, stringi, rvest, data.table, xml2, dplyr, purrr, survival, survminer, ggplot2, ggthemes, viridis, knitr, scales Suggests: devtools, testthat, pander, Biobase, GenomicRanges, IRanges, S4Vectors, RTCGA.rnaseq, RTCGA.clinical, RTCGA.mutations, RTCGA.RPPA, RTCGA.mRNA, RTCGA.miRNASeq, RTCGA.methylation, RTCGA.CNV, RTCGA.PANCAN12, magrittr, tidyr License: GPL-2 MD5sum: 1f7114fe41af1f41baed69a17c0610f7 NeedsCompilation: no Title: The Cancer Genome Atlas Data Integration Description: The Cancer Genome Atlas (TCGA) Data Portal provides a platform for researchers to search, download, and analyze data sets generated by TCGA. It contains clinical information, genomic characterization data, and high level sequence analysis of the tumor genomes. The key is to understand genomics to improve cancer care. RTCGA package offers download and integration of the variety and volume of TCGA data using patient barcode key, what enables easier data possession. This may have an benefcial infuence on impact on development of science and improvement of patients' treatment. Furthermore, RTCGA package transforms TCGA data to tidy form which is convenient to use. biocViews: ImmunoOncology, Software, DataImport, DataRepresentation, Preprocessing, RNASeq Author: Marcin Kosinski , Przemyslaw Biecek Maintainer: Marcin Kosinski URL: https://rtcga.github.io/RTCGA VignetteBuilder: knitr BugReports: https://github.com/RTCGA/RTCGA/issues git_url: https://git.bioconductor.org/packages/RTCGA git_branch: RELEASE_3_8 git_last_commit: 06aa512 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RTCGA_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTCGA_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTCGA_1.12.1.tgz vignettes: vignettes/RTCGA/inst/doc/RTCGA_Workflow.html vignetteTitles: Integrating TCGA Data - RTCGA Workflow hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: RTCGAToolbox Version: 2.12.1 Depends: R (>= 3.5.0) Imports: BiocGenerics, data.table, DelayedArray, GenomicRanges, GenomeInfoDb, IRanges, limma, methods, RaggedExperiment, RCircos, RCurl, RJSONIO, S4Vectors, stringr, SummarizedExperiment, survival, TCGAutils, XML Suggests: BiocStyle, Homo.sapiens, knitr, readr, rmarkdown License: file LICENSE MD5sum: 9644f99d8dea390f69387baf45f5fb9a NeedsCompilation: no Title: A new tool for exporting TCGA Firehose data Description: Managing data from large scale projects such as The Cancer Genome Atlas (TCGA) for further analysis is an important and time consuming step for research projects. Several efforts, such as Firehose project, make TCGA pre-processed data publicly available via web services and data portals but it requires managing, downloading and preparing the data for following steps. We developed an open source and extensible R based data client for Firehose pre-processed data and demonstrated its use with sample case studies. Results showed that RTCGAToolbox could improve data management for researchers who are interested with TCGA data. In addition, it can be integrated with other analysis pipelines for following data analysis. biocViews: DifferentialExpression, GeneExpression, Sequencing Author: Mehmet Samur [aut], Marcel Ramos [aut, cre], Ludwig Geistlinger [ctb] Maintainer: Marcel Ramos URL: http://mksamur.github.io/RTCGAToolbox/ VignetteBuilder: knitr BugReports: https://github.com/mksamur/RTCGAToolbox/issues git_url: https://git.bioconductor.org/packages/RTCGAToolbox git_branch: RELEASE_3_8 git_last_commit: 46aedee git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RTCGAToolbox_2.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTCGAToolbox_2.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTCGAToolbox_2.12.1.tgz vignettes: vignettes/RTCGAToolbox/inst/doc/RTCGAToolbox-vignette.html vignetteTitles: RTCGAToolbox Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RTCGAToolbox/inst/doc/RTCGAToolbox-vignette.R suggestsMe: CVE, TCGAutils Package: RTN Version: 2.6.3 Depends: R (>= 3.3.3), methods Imports: RedeR, minet, viper, mixtools, snow, limma, data.table, IRanges, igraph, S4Vectors, SummarizedExperiment Suggests: RUnit, BiocGenerics, BiocStyle, knitr, rmarkdown License: Artistic-2.0 MD5sum: 122e795cdf652c3ddcdd1b2aea554ec6 NeedsCompilation: no Title: Reconstruction of transcriptional networks and analysis of master regulators Description: This package provides classes and methods for transcriptional network inference and analysis. Modulators of transcription factor activity are assessed by conditional mutual information, and master regulators are mapped to phenotypes using different strategies, e.g., gene set enrichment, shadow and synergy analyses. Additionally, master regulators can be linked to genetic markers using eQTL/VSE analysis, taking advantage of the haplotype block structure mapped to the human genome in order to explore risk-associated SNPs identified in GWAS studies. biocViews: NetworkInference, NetworkEnrichment, GeneRegulation, GeneExpression, GraphAndNetwork, GeneSetEnrichment, GeneticVariability, SNP Author: Mauro Castro, Xin Wang, Michael Fletcher, Florian Markowetz and Kerstin Meyer Maintainer: Mauro Castro URL: http://dx.doi.org/10.1038/ncomms3464 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RTN git_branch: RELEASE_3_8 git_last_commit: ccc7d72 git_last_commit_date: 2019-03-25 Date/Publication: 2019-03-26 source.ver: src/contrib/RTN_2.6.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTN_2.6.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTN_2.6.3.tgz vignettes: vignettes/RTN/inst/doc/RTN.html vignetteTitles: "RTN: reconstruction of transcriptional networks and analysis of master regulators."" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RTN/inst/doc/RTN.R dependsOnMe: RTNduals, RTNsurvival suggestsMe: geneplast Package: RTNduals Version: 1.6.2 Depends: R(>= 3.5), RTN(>= 2.6.3), methods Imports: graphics, grDevices, stats, utils Suggests: knitr, rmarkdown, BiocStyle, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: c0fda5c20f0aa12cca0f17b52525e441 NeedsCompilation: no Title: Analysis of co-regulation and inference of 'dual regulons' Description: RTNduals is a tool that searches for possible co-regulatory loops between regulon pairs generated by the RTN package. It compares the shared targets in order to infer 'dual regulons', a new concept that tests whether regulators can co-operate or compete in influencing targets. biocViews: GeneRegulation, GeneExpression, NetworkEnrichment, NetworkInference, GraphAndNetwork Author: Vinicius S. Chagas, Clarice S. Groeneveld, Gordon Robertson, Kerstin B. Meyer, Mauro A. A. Castro Maintainer: Mauro Castro , Clarice Groeneveld VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RTNduals git_branch: RELEASE_3_8 git_last_commit: 64af553 git_last_commit_date: 2019-03-25 Date/Publication: 2019-03-26 source.ver: src/contrib/RTNduals_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTNduals_1.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTNduals_1.6.2.tgz vignettes: vignettes/RTNduals/inst/doc/RTNduals.html vignetteTitles: "RTNduals: analysis of co-regulation and inference of dual regulons." hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RTNduals/inst/doc/RTNduals.R dependsOnMe: RTNsurvival Package: RTNsurvival Version: 1.6.2 Depends: R(>= 3.5), RTN(>= 2.6.3), RTNduals(>= 1.6.1), methods Imports: survival, RColorBrewer, grDevices, graphics, stats, utils, viper, scales Suggests: Fletcher2013b, pheatmap, knitr, rmarkdown, BiocStyle, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: 6cc32e49aba3759fc786a3013e728f2c NeedsCompilation: no Title: Survival analysis using transcriptional networks inferred by the RTN package Description: RTNsurvival is a tool for integrating regulons generated by the RTN package with survival information. For a given regulon, the 2-tailed GSEA approach computes a differential Enrichment Score (dES) for each individual sample, and the dES distribution of all samples is then used to assess the survival statistics for the cohort. There are two main survival analysis workflows: a Cox Proportional Hazards approach used to model regulons as predictors of survival time, and a Kaplan-Meier analysis assessing the stratification of a cohort based on the regulon activity. All plots can be fine-tuned to the user's specifications. biocViews: NetworkEnrichment, Survival, GeneRegulation, GeneSetEnrichment, NetworkInference, GraphAndNetwork Author: Clarice S. Groeneveld, Vinicius S. Chagas, Mauro A. A. Castro Maintainer: Clarice Groeneveld , Mauro A. A. Castro VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RTNsurvival git_branch: RELEASE_3_8 git_last_commit: cf13753 git_last_commit_date: 2019-03-25 Date/Publication: 2019-03-26 source.ver: src/contrib/RTNsurvival_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTNsurvival_1.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTNsurvival_1.6.2.tgz vignettes: vignettes/RTNsurvival/inst/doc/RTNsurvival.html vignetteTitles: "RTNsurvival: multivariate survival analysis using transcriptional networks and regulons." hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RTNsurvival/inst/doc/RTNsurvival.R Package: RTopper Version: 1.28.0 Depends: R (>= 2.11.0), Biobase Imports: limma, multtest Suggests: limma, org.Hs.eg.db, KEGG.db, GO.db License: GPL (>= 3) MD5sum: 1248ca53c00dd4a687d62632bc75a1c5 NeedsCompilation: no Title: This package is designed to perform Gene Set Analysis across multiple genomic platforms Description: the RTopper package is designed to perform and integrate gene set enrichment results across multiple genomic platforms. biocViews: Microarray Author: Luigi Marchionni , Svitlana Tyekucheva Maintainer: Luigi Marchionni git_url: https://git.bioconductor.org/packages/RTopper git_branch: RELEASE_3_8 git_last_commit: 483ee0e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RTopper_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RTopper_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RTopper_1.28.0.tgz vignettes: vignettes/RTopper/inst/doc/RTopper.pdf vignetteTitles: RTopper user's manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/RTopper/inst/doc/RTopper.R Package: rtracklayer Version: 1.42.2 Depends: R (>= 3.3), methods, GenomicRanges (>= 1.31.8) Imports: XML (>= 1.98-0), BiocGenerics (>= 0.25.1), S4Vectors (>= 0.19.22), IRanges (>= 2.13.13), XVector (>= 0.19.7), GenomeInfoDb (>= 1.15.2), Biostrings (>= 2.47.6), zlibbioc, RCurl (>= 1.4-2), Rsamtools (>= 1.31.2), GenomicAlignments (>= 1.15.6), tools LinkingTo: S4Vectors, IRanges, XVector Suggests: BSgenome (>= 1.33.4), humanStemCell, microRNA (>= 1.1.1), genefilter, limma, org.Hs.eg.db, hgu133plus2.db, GenomicFeatures, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, RUnit License: Artistic-2.0 + file LICENSE MD5sum: b2748aa591c80c01d6b8fb940fc0a44f NeedsCompilation: yes Title: R interface to genome annotation files and the UCSC genome browser Description: Extensible framework for interacting with multiple genome browsers (currently UCSC built-in) and manipulating annotation tracks in various formats (currently GFF, BED, bedGraph, BED15, WIG, BigWig and 2bit built-in). The user may export/import tracks to/from the supported browsers, as well as query and modify the browser state, such as the current viewport. biocViews: Annotation,Visualization,DataImport Author: Michael Lawrence, Vince Carey, Robert Gentleman Maintainer: Michael Lawrence git_url: https://git.bioconductor.org/packages/rtracklayer git_branch: RELEASE_3_8 git_last_commit: 76702f6 git_last_commit_date: 2019-03-01 Date/Publication: 2019-03-01 source.ver: src/contrib/rtracklayer_1.42.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/rtracklayer_1.42.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rtracklayer_1.42.2.tgz vignettes: vignettes/rtracklayer/inst/doc/rtracklayer.pdf vignetteTitles: rtracklayer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: TRUE Rfiles: vignettes/rtracklayer/inst/doc/rtracklayer.R dependsOnMe: BSgenome, CAGEfightR, ChIPSeqSpike, CoverageView, cummeRbund, ExCluster, exomePeak, geneXtendeR, GenomicFiles, groHMM, Guitar, HelloRanges, igvR, LoomExperiment, MethylSeekR, r3Cseq, RIPSeeker importsMe: AnnotationHubData, annotatr, ATACseqQC, ballgown, BiSeq, branchpointer, BSgenome, CAGEr, casper, CexoR, chipenrich, ChIPseeker, ChromHeatMap, chromswitch, CNEr, coMET, CompGO, consensusSeekeR, contiBAIT, conumee, customProDB, DeepBlueR, derfinder, DEScan2, diffHic, diffloop, DMCHMM, dmrseq, ELMER, ensembldb, erma, esATAC, FourCSeq, FunciSNP, genbankr, geneAttribution, genomation, GenomicFeatures, GenomicInteractions, genotypeeval, ggbio, GGtools, gmapR, GOTHiC, gQTLBase, GreyListChIP, Gviz, gwascat, hiAnnotator, HiTC, HTSeqGenie, icetea, IsoformSwitchAnalyzeR, karyoploteR, MACPET, MADSEQ, maser, MEDIPS, metagene, methyAnalysis, methylKit, motifbreakR, MotifDb, MTseeker, NADfinder, normr, OMICsPCA, ORFik, Pbase, PGA, plyranges, primirTSS, proBAMr, PureCN, qsea, QuasR, RCAS, recount, recoup, regioneR, Repitools, RGMQL, RiboProfiling, RNAprobR, roar, scPipe, scruff, seqplots, seqsetvis, sevenC, SGSeq, soGGi, srnadiff, TFBSTools, trackViewer, transcriptR, tRNAscanImport, TSRchitect, VariantAnnotation, VariantTools, wavClusteR, wiggleplotr suggestsMe: alpine, AnnotationHub, BiocFileCache, biovizBase, bsseq, ChIPpeakAnno, cicero, CINdex, compEpiTools, CrispRVariants, epivizrChart, epivizrData, geneXtendeR, GenomicAlignments, GenomicRanges, goseq, InPAS, interactiveDisplay, metaseqR, methylumi, miRBaseConverter, MotIV, MutationalPatterns, NarrowPeaks, OrganismDbi, PICS, PING, pqsfinder, R453Plus1Toolbox, Ringo, rMAT, RnBeads, RSVSim, signeR, similaRpeak, triplex, tRNAdbImport, TSSi, TVTB Package: Rtreemix Version: 1.44.0 Depends: R (>= 2.5.0) Imports: methods, graph, Biobase, Hmisc Suggests: Rgraphviz License: LGPL Archs: i386, x64 MD5sum: 54dad4f9295a159b1358b3e09ab86f12 NeedsCompilation: yes Title: Rtreemix: Mutagenetic trees mixture models. Description: Rtreemix is a package that offers an environment for estimating the mutagenetic trees mixture models from cross-sectional data and using them for various predictions. It includes functions for fitting the trees mixture models, likelihood computations, model comparisons, waiting time estimations, stability analysis, etc. biocViews: StatisticalMethod Author: Jasmina Bogojeska Maintainer: Jasmina Bogojeska git_url: https://git.bioconductor.org/packages/Rtreemix git_branch: RELEASE_3_8 git_last_commit: 5519727 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Rtreemix_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Rtreemix_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Rtreemix_1.44.0.tgz vignettes: vignettes/Rtreemix/inst/doc/Rtreemix.pdf vignetteTitles: Rtreemix hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Rtreemix/inst/doc/Rtreemix.R Package: rTRM Version: 1.20.0 Depends: R (>= 2.10), igraph (>= 1.0) Imports: AnnotationDbi, DBI, RSQLite Suggests: RUnit, BiocGenerics, MotifDb, graph, PWMEnrich, biomaRt, knitr, Biostrings, BSgenome.Mmusculus.UCSC.mm8.masked, org.Hs.eg.db, org.Mm.eg.db, ggplot2 License: GPL-3 Archs: i386, x64 MD5sum: 2f3ca2f454102df0fb6790d11beb14e4 NeedsCompilation: no Title: Identification of transcriptional regulatory modules from PPI networks Description: rTRM identifies transcriptional regulatory modules (TRMs) from protein-protein interaction networks. biocViews: Transcription, Network, GeneRegulation, GraphAndNetwork Author: Diego Diez Maintainer: Diego Diez URL: https://github.com/ddiez/rTRM VignetteBuilder: knitr BugReports: https://github.com/ddiez/rTRM/issues git_url: https://git.bioconductor.org/packages/rTRM git_branch: RELEASE_3_8 git_last_commit: 2ee5bac git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rTRM_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rTRM_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rTRM_1.20.0.tgz vignettes: vignettes/rTRM/inst/doc/rTRM_Introduction.pdf vignetteTitles: Introduction to rTRM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rTRM/inst/doc/rTRM_Introduction.R importsMe: rTRMui Package: rTRMui Version: 1.20.0 Imports: shiny (>= 0.9), rTRM, MotifDb, org.Hs.eg.db, org.Mm.eg.db License: GPL-3 MD5sum: 1e0da9b0bbe347b9d4557d8dca91360f NeedsCompilation: no Title: A shiny user interface for rTRM Description: This package provides a web interface to compute transcriptional regulatory modules with rTRM. biocViews: Transcription, Network, GeneRegulation, GraphAndNetwork, GUI Author: Diego Diez Maintainer: Diego Diez URL: https://github.com/ddiez/rTRMui BugReports: https://github.com/ddiez/rTRMui/issues git_url: https://git.bioconductor.org/packages/rTRMui git_branch: RELEASE_3_8 git_last_commit: 42f8ece git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/rTRMui_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/rTRMui_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rTRMui_1.20.0.tgz vignettes: vignettes/rTRMui/inst/doc/rTRMui.pdf vignetteTitles: Introduction to rTRMui hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/rTRMui/inst/doc/rTRMui.R Package: runibic Version: 1.4.0 Depends: R (>= 3.4.0), biclust, SummarizedExperiment Imports: Rcpp (>= 0.12.12), testthat, methods LinkingTo: Rcpp Suggests: knitr, rmarkdown, GEOquery, affy, airway, QUBIC License: MIT + file LICENSE MD5sum: d0cedd151b4819370ba67bbde690ddf3 NeedsCompilation: yes Title: runibic: row-based biclustering algorithm for analysis of gene expression data in R Description: This package implements UbiBic algorithm in R. This biclustering algorithm for analysis of gene expression data was introduced by Zhenjia Wang et al. in 2016. It is currently considered the most promising biclustering method for identification of meaningful structures in complex and noisy data. biocViews: Microarray, Clustering, GeneExpression, Sequencing, Coverage Author: Patryk Orzechowski, Artur Pańszczyk Maintainer: Patryk Orzechowski URL: http://github.com/athril/runibic SystemRequirements: C++11, GNU make VignetteBuilder: knitr BugReports: http://github.com/athril/runibic/issues git_url: https://git.bioconductor.org/packages/runibic git_branch: RELEASE_3_8 git_last_commit: fa38dc2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/runibic_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/runibic_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/runibic_1.4.0.tgz vignettes: vignettes/runibic/inst/doc/runibic.html vignetteTitles: runibic: UniBic in R Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE importsMe: miRSM Package: RUVcorr Version: 1.14.0 Imports: corrplot, MASS, stats, lattice, grDevices, gridExtra, snowfall, psych, BiocParallel, grid, bladderbatch, reshape2 Suggests: knitr, BiocStyle, hgu133a2.db License: GPL-2 Archs: i386, x64 MD5sum: 158715467d2a0cb8bc83af04bd6ea3b4 NeedsCompilation: no Title: Removal of unwanted variation for gene-gene correlations and related analysis Description: RUVcorr allows to apply global removal of unwanted variation (ridged version of RUV) to real and simulated gene expression data. biocViews: GeneExpression, Normalization Author: Saskia Freytag Maintainer: Saskia Freytag VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RUVcorr git_branch: RELEASE_3_8 git_last_commit: a7abd8a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RUVcorr_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RUVcorr_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RUVcorr_1.14.0.tgz vignettes: vignettes/RUVcorr/inst/doc/RUVcorrVignetteNew.pdf vignetteTitles: RUVcorr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RUVcorr/inst/doc/RUVcorrVignetteNew.R Package: RUVnormalize Version: 1.16.0 Depends: R (>= 2.10.0) Imports: RUVnormalizeData, Biobase Enhances: spams License: GPL-3 MD5sum: 167b64fcfec25e40893b0170df327ed1 NeedsCompilation: no Title: RUV for normalization of expression array data Description: RUVnormalize is meant to remove unwanted variation from gene expression data when the factor of interest is not defined, e.g., to clean up a dataset for general use or to do any kind of unsupervised analysis. biocViews: StatisticalMethod, Normalization Author: Laurent Jacob Maintainer: Laurent Jacob git_url: https://git.bioconductor.org/packages/RUVnormalize git_branch: RELEASE_3_8 git_last_commit: 95ac490 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/RUVnormalize_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/RUVnormalize_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RUVnormalize_1.16.0.tgz vignettes: vignettes/RUVnormalize/inst/doc/RUVnormalize.pdf vignetteTitles: RUVnormalize hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RUVnormalize/inst/doc/RUVnormalize.R Package: RUVSeq Version: 1.16.1 Depends: Biobase, EDASeq (>= 1.99.1), edgeR Imports: methods, MASS Suggests: BiocStyle, knitr, RColorBrewer, zebrafishRNASeq, DESeq2 License: Artistic-2.0 MD5sum: 7ecef6b10da05f7d4ef04e9089928089 NeedsCompilation: no Title: Remove Unwanted Variation from RNA-Seq Data Description: This package implements the remove unwanted variation (RUV) methods of Risso et al. (2014) for the normalization of RNA-Seq read counts between samples. biocViews: ImmunoOncology, DifferentialExpression, Preprocessing, RNASeq, Software Author: Davide Risso [aut, cre, cph], Sandrine Dudoit [aut], Lorena Pantano [ctb], Kamil Slowikowski [ctb] Maintainer: Davide Risso URL: https://github.com/drisso/RUVSeq VignetteBuilder: knitr BugReports: https://github.com/drisso/RUVSeq/issues git_url: https://git.bioconductor.org/packages/RUVSeq git_branch: RELEASE_3_8 git_last_commit: 2edc83a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/RUVSeq_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/RUVSeq_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RUVSeq_1.16.1.tgz vignettes: vignettes/RUVSeq/inst/doc/RUVSeq.pdf vignetteTitles: RUVSeq: Remove Unwanted Variation from RNA-Seq Data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RUVSeq/inst/doc/RUVSeq.R importsMe: consensusDE, scone suggestsMe: DEScan2 Package: RVS Version: 1.4.4 Depends: R (>= 3.5.0) Imports: GENLIB, gRain, snpStats, kinship2, methods, stats, utils Suggests: knitr, testthat, rmarkdown, BiocStyle, VariantAnnotation License: GPL-2 MD5sum: 0ae328afcbe42af6893279fa285fd70a NeedsCompilation: no Title: Computes estimates of the probability of related individuals sharing a rare variant Description: Rare Variant Sharing (RVS) implements tests of association and linkage between rare genetic variant genotypes and a dichotomous phenotype, e.g. a disease status, in family samples. The tests are based on probabilities of rare variant sharing by relatives under the null hypothesis of absence of linkage and association between the rare variants and the phenotype and apply to single variants or multiple variants in a region (e.g. gene-based test). biocViews: ImmunoOncology, Genetics, GenomeWideAssociation, VariantDetection, ExomeSeq, WholeGenome Author: Alexandre Bureau, Ingo Ruczinski, Samuel Younkin, Thomas Sherman Maintainer: Thomas Sherman VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/RVS git_branch: RELEASE_3_8 git_last_commit: f9acc89 git_last_commit_date: 2019-04-02 Date/Publication: 2019-04-03 source.ver: src/contrib/RVS_1.4.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/RVS_1.4.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/RVS_1.4.4.tgz vignettes: vignettes/RVS/inst/doc/RVS.html vignetteTitles: The RVS Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/RVS/inst/doc/RVS.R Package: rWikiPathways Version: 1.2.1 Depends: R (>= 3.5) Imports: caTools, httr, RJSONIO, utils, XML Suggests: testthat, BiocStyle, knitr, rmarkdown License: MIT + file LICENSE MD5sum: e81638b838ab16d87f611e12ea189a3a NeedsCompilation: no Title: rWikiPathways - R client library for the WikiPathways API Description: Use this package to interface with the WikiPathways API. biocViews: Visualization, GraphAndNetwork, ThirdPartyClient, Network, Metabolomics Author: Egon Willighagen [aut, cre] (), Alex Pico [aut] () Maintainer: Egon Willighagen , Alexander Pico URL: https://github.com/wikipathways/rwikipathways VignetteBuilder: knitr BugReports: https://github.com/wikipathways/rwikipathways/issues git_url: https://git.bioconductor.org/packages/rWikiPathways git_branch: RELEASE_3_8 git_last_commit: 01cdd36 git_last_commit_date: 2019-02-06 Date/Publication: 2019-02-07 source.ver: src/contrib/rWikiPathways_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/rWikiPathways_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/rWikiPathways_1.2.1.tgz vignettes: vignettes/rWikiPathways/inst/doc/Overview.html, vignettes/rWikiPathways/inst/doc/Pathway-Analysis.html, vignettes/rWikiPathways/inst/doc/rWikiPathways-and-BridgeDbR.html, vignettes/rWikiPathways/inst/doc/rWikiPathways-and-RCy3.html vignetteTitles: 1. Overview, 4. Pathway Analysis, 2. rWikiPathways and BridgeDbR, 3. rWikiPathways and RCy3 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/rWikiPathways/inst/doc/Overview.R, vignettes/rWikiPathways/inst/doc/Pathway-Analysis.R, vignettes/rWikiPathways/inst/doc/rWikiPathways-and-BridgeDbR.R, vignettes/rWikiPathways/inst/doc/rWikiPathways-and-RCy3.R suggestsMe: TRONCO Package: S4Vectors Version: 0.20.1 Depends: R (>= 3.3.0), methods, utils, stats, stats4, BiocGenerics (>= 0.23.3) Suggests: IRanges, GenomicRanges, SummarizedExperiment, Matrix, DelayedArray, ShortRead, graph, data.table, RUnit, BiocStyle License: Artistic-2.0 MD5sum: 688d781fb673cfb94e9f1c164be1e24e NeedsCompilation: yes Title: S4 implementation of vector-like and list-like objects Description: The S4Vectors package defines the Vector and List virtual classes and a set of generic functions that extend the semantic of ordinary vectors and lists in R. Package developers can easily implement vector-like or list-like objects as concrete subclasses of Vector or List. In addition, a few low-level concrete subclasses of general interest (e.g. DataFrame, Rle, and Hits) are implemented in the S4Vectors package itself (many more are implemented in the IRanges package and in other Bioconductor infrastructure packages). biocViews: Infrastructure, DataRepresentation Author: H. Pagès, M. Lawrence and P. Aboyoun Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/S4Vectors git_branch: RELEASE_3_8 git_last_commit: 1878b29 git_last_commit_date: 2018-11-08 Date/Publication: 2018-11-09 source.ver: src/contrib/S4Vectors_0.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/S4Vectors_0.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/S4Vectors_0.20.1.tgz vignettes: vignettes/S4Vectors/inst/doc/RleTricks.pdf, vignettes/S4Vectors/inst/doc/S4QuickOverview.pdf, vignettes/S4Vectors/inst/doc/S4VectorsOverview.pdf vignetteTitles: Rle Tips and Tricks, A quick overview of the S4 class system, An Overview of the S4Vectors package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/S4Vectors/inst/doc/RleTricks.R, vignettes/S4Vectors/inst/doc/S4QuickOverview.R, vignettes/S4Vectors/inst/doc/S4VectorsOverview.R dependsOnMe: altcdfenvs, AnnotationHubData, ATACseqQC, Biostrings, BiSeq, BSgenome, bumphunter, Cardinal, CellMapper, CexoR, chimeraviz, ChIPpeakAnno, chipseq, ChIPseqR, ClassifyR, CODEX, coseq, CSAR, DelayedArray, DESeq2, DEXSeq, DirichletMultinomial, DMCHMM, DMRcaller, epigenomix, ExperimentHubData, ExpressionAtlas, fCCAC, GA4GHclient, GenoGAM, GenomeInfoDb, GenomicAlignments, GenomicFeatures, GenomicRanges, GenomicScores, GenomicTuples, girafe, groHMM, Gviz, HelloRanges, htSeqTools, InPAS, InTAD, IntEREst, IRanges, LoomExperiment, MotifDb, MSnbase, MTseeker, NADfinder, OTUbase, plethy, RIPSeeker, RnBeads, segmentSeq, SummarizedBenchmark, TimeSeriesExperiment, topdownr, triplex, VariantTools, vulcan, XVector importsMe: affycoretools, ALDEx2, AllelicImbalance, alpine, amplican, anamiR, AneuFinder, AnnotationDbi, AnnotationForge, AnnotationHub, annotatr, appreci8R, ArrayTV, ASpli, BadRegionFinder, ballgown, BASiCS, BiocNeighbors, BiocOncoTK, biotmle, biovizBase, BiSeq, BitSeq, bnbc, BPRMeth, branchpointer, breakpointR, BSgenome, bsseq, CAGEfightR, CAGEr, casper, CATALYST, ccfindR, celaref, ChIC, chipenrich, ChIPexoQual, ChIPQC, ChIPseeker, ChIPSeqSpike, chromstaR, chromswitch, chromVAR, cicero, cleaver, clusterExperiment, cn.mops, CNEr, CNPBayes, CNVPanelizer, COCOA, CoGAPS, coMET, compEpiTools, consensusDE, consensusSeekeR, contiBAIT, copynumber, CopywriteR, CoverageView, CRISPRseek, CrispRVariants, csaw, CTDquerier, cummeRbund, customProDB, cydar, DChIPRep, debrowser, DECIPHER, DEFormats, DEGreport, DelayedMatrixStats, derfinder, derfinderHelper, derfinderPlot, DEScan2, DiffBind, diffcyt, diffHic, diffloop, DMRcate, dmrseq, DOSE, DRIMSeq, DropletUtils, easyRNASeq, eegc, ELMER, EnrichmentBrowser, ensembldb, ensemblVEP, epivizr, epivizrData, epivizrStandalone, erma, esATAC, EventPointer, ExperimentHub, FastqCleaner, fastseg, FindMyFriends, FunciSNP, GA4GHshiny, gcapc, GDSArray, genbankr, genefilter, GeneRegionScan, GENESIS, genomation, genomeIntervals, GenomicAlignments, GenomicDataCommons, GenomicFiles, GenomicInteractions, genoset, GGBase, ggbio, GGtools, Glimma, gmapR, GoogleGenomics, GOpro, GOTHiC, gQTLBase, gQTLstats, GRmetrics, GSEABenchmarkeR, GUIDEseq, gwascat, h5vc, HDF5Array, HiCBricks, HiCcompare, hipathia, hmdbQuery, HTSeqGenie, icetea, ideal, IMAS, ImpulseDE2, INSPEcT, InteractionSet, InterMineR, iSEE, isomiRs, IVAS, ivygapSE, JunctionSeq, karyoploteR, kebabs, loci2path, LOLA, M3D, MACPET, MADSEQ, martini, MAST, mCSEA, MEAL, meshr, metagenomeFeatures, methInheritSim, methylInheritance, methylKit, methylPipe, methylumi, methyvim, mimager, minfi, MinimumDistance, MIRA, MiRaGE, missRows, MMDiff2, mosaics, motifbreakR, motifmatchr, MotIV, mpra, msa, msgbsR, MultiAssayExperiment, MultiDataSet, MutationalPatterns, mygene, myvariant, NarrowPeaks, nucleoSim, nucleR, oligoClasses, ontoProc, openPrimeR, ORFik, Organism.dplyr, OrganismDbi, OUTRIDER, panelcn.mops, PathwaySplice, Pbase, pcaExplorer, pdInfoBuilder, PGA, PICS, PING, plyranges, pogos, polyester, PowerExplorer, pqsfinder, prebs, primirTSS, procoil, PureCN, qcmetrics, qpgraph, QuasR, R3CPET, R453Plus1Toolbox, RaggedExperiment, RareVariantVis, Rariant, Rcade, RCAS, recount, regioneR, regionReport, regsplice, REMP, Repitools, restfulSE, rexposome, RGMQL, rhdf5client, RiboProfiling, RJMCMCNucleosomes, Rmmquant, RNAprobR, roar, Rqc, Rsamtools, RTCGAToolbox, RTN, rtracklayer, SC3, scater, scDD, scmap, SCnorm, scPipe, scran, scruff, SeqArray, seqCAT, seqplots, seqsetvis, SeqSQC, SeqVarTools, sesame, sevenbridges, sevenC, SGSeq, ShortRead, SingleCellExperiment, singleCellTK, skewr, SMITE, SNPchip, SNPhood, soGGi, SomaticSignatures, SplicingGraphs, SPLINTER, srnadiff, STAN, strandCheckR, SummarizedExperiment, TarSeqQC, TCGAbiolinks, TCGAutils, TFBSTools, TFHAZ, TnT, trackViewer, transcriptR, TransView, Trendy, tRNA, tRNAdbImport, tRNAscanImport, TSRchitect, TSSi, TVTB, twoddpcr, tximeta, TxRegInfra, VanillaICE, VariantAnnotation, VariantFiltering, wavClusteR, wiggleplotr, xcms, XVector, yamss suggestsMe: BiocGenerics, epivizrChart, globalSeq, GWASTools, RTCGA, splatter, TFEA.ChIP, TFutils linksToMe: Biostrings, CNEr, DECIPHER, DelayedArray, GenomicAlignments, GenomicRanges, IRanges, kebabs, MatrixRider, Rsamtools, rSFFreader, rtracklayer, ShortRead, triplex, VariantAnnotation, VariantFiltering, XVector Package: safe Version: 3.22.0 Depends: R (>= 2.4.0), AnnotationDbi, Biobase, methods, SparseM Suggests: GO.db, PFAM.db, reactome.db, hgu133a.db, breastCancerUPP, survival, foreach, doRNG, Rgraphviz, GOstats License: GPL (>= 2) Archs: i386, x64 MD5sum: 130b1a1220cb3703b2fc990ae2059378 NeedsCompilation: no Title: Significance Analysis of Function and Expression Description: SAFE is a resampling-based method for testing functional categories in gene expression experiments. SAFE can be applied to 2-sample and multi-class comparisons, or simple linear regressions. Other experimental designs can also be accommodated through user-defined functions. biocViews: DifferentialExpression, Pathways, GeneSetEnrichment, StatisticalMethod, Software Author: William T. Barry Maintainer: William T. Barry git_url: https://git.bioconductor.org/packages/safe git_branch: RELEASE_3_8 git_last_commit: 4031197 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/safe_3.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/safe_3.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/safe_3.22.0.tgz vignettes: vignettes/safe/inst/doc/SAFEmanual3.pdf vignetteTitles: SAFE manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/safe/inst/doc/SAFEmanual3.R importsMe: EGSEA, EnrichmentBrowser Package: sagenhaft Version: 1.52.0 Depends: R (>= 2.10), SparseM (>= 0.73), methods Imports: graphics, methods, SparseM, stats, utils License: GPL (>= 2) MD5sum: 582c5897ff5d4d7395a42f4655e33962 NeedsCompilation: no Title: Collection of functions for reading and comparing SAGE libraries Description: This package implements several functions useful for analysis of gene expression data by sequencing tags as done in SAGE (Serial Analysis of Gene Expressen) data, i.e. extraction of a SAGE library from sequence files, sequence error correction, library comparison. Sequencing error correction is implementing using an Expectation Maximization Algorithm based on a Mixture Model of tag counts. biocViews: SAGE Author: Tim Beissbarth , with contributions from Gordon Smyth and Lavinia Hyde . Maintainer: Tim Beissbarth URL: http://tagcalling.mbgproject.org git_url: https://git.bioconductor.org/packages/sagenhaft git_branch: RELEASE_3_8 git_last_commit: 0fd7107 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sagenhaft_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sagenhaft_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sagenhaft_1.52.0.tgz vignettes: vignettes/sagenhaft/inst/doc/SAGEnhaft.pdf vignetteTitles: SAGEnhaft hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sagenhaft/inst/doc/SAGEnhaft.R Package: SAGx Version: 1.56.0 Depends: R (>= 2.5.0), stats, multtest, methods Imports: Biobase, stats4 Suggests: KEGG.db, hu6800.db, MASS License: GPL-3 MD5sum: 3b4d03837b6be876bd3969c8f0d2a04f NeedsCompilation: yes Title: Statistical Analysis of the GeneChip Description: A package for retrieval, preparation and analysis of data from the Affymetrix GeneChip. In particular the issue of identifying differentially expressed genes is addressed. biocViews: Microarray, OneChannel, Preprocessing, DataImport, DifferentialExpression, Clustering, MultipleComparison, GeneExpression, GeneSetEnrichment, Pathways, Regression, KEGG Author: Per Broberg Maintainer: Per Broberg, URL: http://home.swipnet.se/pibroberg/expression_hemsida1.html git_url: https://git.bioconductor.org/packages/SAGx git_branch: RELEASE_3_8 git_last_commit: fd6e2d8 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SAGx_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SAGx_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SAGx_1.56.0.tgz vignettes: vignettes/SAGx/inst/doc/samroc-ex.pdf vignetteTitles: samroc - example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SAGx/inst/doc/samroc-ex.R Package: samExploreR Version: 1.6.1 Depends: ggplot2,Rsubread,RNAseqData.HNRNPC.bam.chr14,edgeR,R (>= 3.4.0) Imports: grDevices, stats, graphics Suggests: BiocStyle,RUnit,BiocGenerics,Matrix License: GPL-3 MD5sum: 9e9ec9ecbba16c9ea33e5a859e88cd1e NeedsCompilation: no Title: samExploreR package: high-performance read summarisation to count vectors with avaliability of sequencing depth reduction simulation Description: This R package is designed for subsampling procedure to simulate sequencing experiments with reduced sequencing depth. This package can be used to anlayze data generated from all major sequencing platforms such as Illumina GA, HiSeq, MiSeq, Roche GS-FLX, ABI SOLiD and LifeTech Ion PGM Proton sequencers. It supports multiple operating systems incluidng Linux, Mac OS X, FreeBSD and Solaris. Was developed with usage of Rsubread. biocViews: ImmunoOncology, Sequencing, SequenceMatching, RNASeq, ChIPSeq, DNASeq, WholeGenome, GeneTarget, Alignment, GeneExpression, GeneticVariability, GeneRegulation, Preprocessing, GenomeAnnotation, Software Author: Alexey Stupnikov, Shailesh Tripathi and Frank Emmert-Streib Maintainer: shailesh tripathi git_url: https://git.bioconductor.org/packages/samExploreR git_branch: RELEASE_3_8 git_last_commit: 7b821bb git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/samExploreR_1.6.1.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/samExploreR_1.6.1.tgz vignettes: vignettes/samExploreR/inst/doc/Manual.pdf vignetteTitles: samExploreR Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/samExploreR/inst/doc/Manual.R Package: sampleClassifier Version: 1.6.1 Depends: R (>= 3.4), MGFM, MGFR, annotate Imports: e1071, ggplot2, stats, utils Suggests: sampleClassifierData, BiocStyle, hgu133a.db, hgu133plus2.db License: Artistic-2.0 Archs: i386, x64 MD5sum: 22d21dd2507db7937d7774246d54cb1c NeedsCompilation: no Title: Sample Classifier Description: The package is designed to classify gene expression profiles. biocViews: ImmunoOncology, Classification, Microarray, RNASeq, GeneExpression Author: Khadija El-Amrani Maintainer: Khadija El Amrani git_url: https://git.bioconductor.org/packages/sampleClassifier git_branch: RELEASE_3_8 git_last_commit: 282b044 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sampleClassifier_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sampleClassifier_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sampleClassifier_1.6.1.tgz vignettes: vignettes/sampleClassifier/inst/doc/sampleClassifier.pdf vignetteTitles: sampleClassifier Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sampleClassifier/inst/doc/sampleClassifier.R Package: SamSPECTRAL Version: 1.36.1 Depends: R (>= 3.3.3) Imports: methods License: GPL (>= 2) MD5sum: e1aa6f4c3e8f4dc05539f92719c19e24 NeedsCompilation: yes Title: Identifies cell population in flow cytometry data. Description: Samples large data such that spectral clustering is possible while preserving density information in edge weights. More specifically, given a matrix of coordinates as input, SamSPECTRAL first builds the communities to sample the data points. Then, it builds a graph and after weighting the edges by conductance computation, the graph is passed to a classic spectral clustering algorithm to find the spectral clusters. The last stage of SamSPECTRAL is to combine the spectral clusters. The resulting "connected components" estimate biological cell populations in the data. See the vignette for more details on how to use this package, some illustrations, and simple examples. biocViews: ImmunoOncology, FlowCytometry, CellBiology, Clustering, Cancer, FlowCytometry, StemCells, HIV Author: Habil Zare and Parisa Shooshtari Maintainer: Habil git_url: https://git.bioconductor.org/packages/SamSPECTRAL git_branch: RELEASE_3_8 git_last_commit: 65d4c9d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SamSPECTRAL_1.36.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SamSPECTRAL_1.36.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SamSPECTRAL_1.36.1.tgz vignettes: vignettes/SamSPECTRAL/inst/doc/Clustering_by_SamSPECTRAL.pdf vignetteTitles: A modified spectral clustering method for clustering Flow Cytometry Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SamSPECTRAL/inst/doc/Clustering_by_SamSPECTRAL.R importsMe: ddPCRclust Package: sangerseqR Version: 1.18.0 Depends: R (>= 3.0.2), Biostrings Imports: methods, shiny Suggests: BiocStyle, knitr, RUnit, BiocGenerics License: GPL-2 Archs: i386, x64 MD5sum: a9087a41aa05c312e686f3b5578f82ab NeedsCompilation: no Title: Tools for Sanger Sequencing Data in R Description: This package contains several tools for analyzing Sanger Sequencing data files in R, including reading .scf and .ab1 files, making basecalls and plotting chromatograms. biocViews: Sequencing, SNP, Visualization Author: Jonathon T. Hill, Bradley Demarest Maintainer: Jonathon Hill VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/sangerseqR git_branch: RELEASE_3_8 git_last_commit: b42e866 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sangerseqR_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sangerseqR_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sangerseqR_1.18.0.tgz vignettes: vignettes/sangerseqR/inst/doc/sangerseq_walkthrough.pdf vignetteTitles: sangerseqR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sangerseqR/inst/doc/sangerseq_walkthrough.R suggestsMe: CrispRVariants Package: SANTA Version: 2.20.0 Depends: R (>= 2.14), igraph Imports: Matrix, snow Suggests: RUnit, BiocGenerics, knitr, knitcitations, formatR, org.Sc.sgd.db, BioNet, DLBCL, msm License: GPL (>= 2) MD5sum: 2d2c95468044819a5b1b41c4a563e636 NeedsCompilation: yes Title: Spatial Analysis of Network Associations Description: This package provides methods for measuring the strength of association between a network and a phenotype. It does this by measuring clustering of the phenotype across the network (Knet). Vertices can also be individually ranked by their strength of association with high-weight vertices (Knode). biocViews: Network, NetworkEnrichment, Clustering Author: Alex J. Cornish and Florian Markowetz Maintainer: Alex J. Cornish VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SANTA git_branch: RELEASE_3_8 git_last_commit: c90410f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SANTA_2.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SANTA_2.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SANTA_2.20.0.tgz vignettes: vignettes/SANTA/inst/doc/SANTA-vignette.html vignetteTitles: Introduction to SANTA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SANTA/inst/doc/SANTA-vignette.R Package: sapFinder Version: 1.20.1 Depends: R (>= 3.0.0),rTANDEM (>= 1.3.5) Imports: pheatmap,Rcpp (>= 0.10.6),graphics,grDevices,stats, utils LinkingTo: Rcpp Suggests: RUnit, BiocGenerics, BiocStyle License: GPL-2 Archs: i386, x64 MD5sum: 1d4171bf15a1a4b7eb67ef1154f37abe NeedsCompilation: yes Title: A package for variant peptides detection and visualization in shotgun proteomics. Description: sapFinder is developed to automate (1) variation-associated database construction, (2) database searching, (3) post-processing, (4) HTML-based report generation in shotgun proteomics. biocViews: ImmunoOncology, MassSpectrometry, Proteomics, SNP, RNASeq, Visualization, ReportWriting Author: Shaohang Xu, Bo Wen Maintainer: Shaohang Xu , Bo Wen git_url: https://git.bioconductor.org/packages/sapFinder git_branch: RELEASE_3_8 git_last_commit: 8e0868c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sapFinder_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sapFinder_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sapFinder_1.20.1.tgz vignettes: vignettes/sapFinder/inst/doc/sapFinder.pdf vignetteTitles: sapFinder Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sapFinder/inst/doc/sapFinder.R Package: savR Version: 1.20.0 Depends: ggplot2 Imports: methods, reshape2, scales, gridExtra, XML Suggests: Cairo, testthat License: AGPL-3 Archs: i386, x64 MD5sum: 765521fb53c6b8ab25bbd2ff26efe67b NeedsCompilation: no Title: Parse and analyze Illumina SAV files Description: Parse Illumina Sequence Analysis Viewer (SAV) files, access data, and generate QC plots. biocViews: Sequencing Author: R. Brent Calder Maintainer: R. Brent Calder URL: https://github.com/bcalder/savR BugReports: https://github.com/bcalder/savR/issues git_url: https://git.bioconductor.org/packages/savR git_branch: RELEASE_3_8 git_last_commit: a209204 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/savR_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/savR_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/savR_1.20.0.tgz vignettes: vignettes/savR/inst/doc/savR.pdf vignetteTitles: Using savR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/savR/inst/doc/savR.R Package: SBMLR Version: 1.78.0 Depends: XML, deSolve Suggests: rsbml License: GPL-2 MD5sum: 8263d9957245263681e6349e13058a2c NeedsCompilation: no Title: SBML-R Interface and Analysis Tools Description: This package contains a systems biology markup language (SBML) interface to R. biocViews: GraphAndNetwork, Pathways, Network Author: Tomas Radivoyevitch, Vishak Venkateswaran Maintainer: Tomas Radivoyevitch URL: http://epbi-radivot.cwru.edu/SBMLR/SBMLR.html git_url: https://git.bioconductor.org/packages/SBMLR git_branch: RELEASE_3_8 git_last_commit: 1985c63 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SBMLR_1.78.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SBMLR_1.78.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SBMLR_1.78.0.tgz vignettes: vignettes/SBMLR/inst/doc/quick-start.pdf vignetteTitles: Quick intro to SBMLR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SBMLR/inst/doc/quick-start.R Package: SC3 Version: 1.10.1 Depends: R(>= 3.3) Imports: graphics, stats, utils, methods, e1071, parallel, foreach, doParallel, doRNG, shiny, ggplot2, pheatmap (>= 1.0.8), ROCR, robustbase, rrcov, cluster, WriteXLS, Rcpp (>= 0.11.1), SummarizedExperiment, SingleCellExperiment, BiocGenerics, S4Vectors LinkingTo: Rcpp, RcppArmadillo Suggests: knitr, rmarkdown, mclust, scater License: GPL-3 MD5sum: 6063f7314acc80fc7a9a0c3d00813dc3 NeedsCompilation: yes Title: Single-Cell Consensus Clustering Description: A tool for unsupervised clustering and analysis of single cell RNA-Seq data. biocViews: ImmunoOncology, SingleCell, Software, Classification, Clustering, DimensionReduction, SupportVectorMachine, RNASeq, Visualization, Transcriptomics, DataRepresentation, GUI, DifferentialExpression, Transcription Author: Vladimir Kiselev Maintainer: Vladimir Kiselev URL: https://github.com/hemberg-lab/SC3 VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/sc3/ git_url: https://git.bioconductor.org/packages/SC3 git_branch: RELEASE_3_8 git_last_commit: b2e9122 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SC3_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SC3_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SC3_1.10.1.tgz vignettes: vignettes/SC3/inst/doc/SC3.html vignetteTitles: SC3 package manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SC3/inst/doc/SC3.R Package: Scale4C Version: 1.4.0 Depends: R (>= 3.4), smoothie, GenomicRanges, IRanges, SummarizedExperiment Imports: methods, grDevices, graphics, utils License: LGPL-3 Archs: i386, x64 MD5sum: 42129ff892946f7832161ae468afd8cf NeedsCompilation: no Title: Scale4C: an R/Bioconductor package for scale-space transformation of 4C-seq data Description: Scale4C is an R/Bioconductor package for scale-space transformation and visualization of 4C-seq data. The scale-space transformation is a multi-scale visualization technique to transform a 2D signal (e.g. 4C-seq reads on a genomic interval of choice) into a tesselation in the scale space (2D, genomic position x scale factor) by applying different smoothing kernels (Gauss, with increasing sigma). This transformation allows for explorative analysis and comparisons of the data's structure with other samples. biocViews: Visualization, QualityControl, DataImport, Sequencing, Coverage Author: Carolin Walter Maintainer: Carolin Walter git_url: https://git.bioconductor.org/packages/Scale4C git_branch: RELEASE_3_8 git_last_commit: a3fa0c3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Scale4C_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Scale4C_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Scale4C_1.4.0.tgz vignettes: vignettes/Scale4C/inst/doc/vignette.pdf vignetteTitles: Scale4C: an R/Bioconductor package for scale-space transformation of 4C-seq data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Scale4C/inst/doc/vignette.R Package: SCAN.UPC Version: 2.24.1 Depends: R (>= 2.14.0), Biobase (>= 2.6.0), oligo, Biostrings, GEOquery, affy, affyio, foreach, sva Imports: utils, methods, MASS, tools, IRanges Suggests: pd.hg.u95a License: MIT MD5sum: 41c135cf7832a54404fbe1d060aa6eb3 NeedsCompilation: no Title: Single-channel array normalization (SCAN) and Universal exPression Codes (UPC) Description: SCAN is a microarray normalization method to facilitate personalized-medicine workflows. Rather than processing microarray samples as groups, which can introduce biases and present logistical challenges, SCAN normalizes each sample individually by modeling and removing probe- and array-specific background noise using only data from within each array. SCAN can be applied to one-channel (e.g., Affymetrix) or two-channel (e.g., Agilent) microarrays. The Universal exPression Codes (UPC) method is an extension of SCAN that estimates whether a given gene/transcript is active above background levels in a given sample. The UPC method can be applied to one-channel or two-channel microarrays as well as to RNA-Seq read counts. Because UPC values are represented on the same scale and have an identical interpretation for each platform, they can be used for cross-platform data integration. biocViews: ImmunoOncology, Software, Microarray, Preprocessing, RNASeq, TwoChannel, OneChannel Author: Stephen R. Piccolo and Andrea H. Bild and W. Evan Johnson Maintainer: Stephen R. Piccolo URL: http://bioconductor.org, http://jlab.bu.edu/software/scan-upc git_url: https://git.bioconductor.org/packages/SCAN.UPC git_branch: RELEASE_3_8 git_last_commit: 427d523 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SCAN.UPC_2.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SCAN.UPC_2.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SCAN.UPC_2.24.1.tgz vignettes: vignettes/SCAN.UPC/inst/doc/SCAN.vignette.pdf vignetteTitles: Primer hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SCAN.UPC/inst/doc/SCAN.vignette.R Package: scater Version: 1.10.1 Depends: R (>= 3.5), SingleCellExperiment, ggplot2, BiocParallel Imports: BiocGenerics, SummarizedExperiment, Matrix, dplyr, ggbeeswarm, grid, DelayedMatrixStats, methods, plyr, reshape2, S4Vectors, stats, utils, viridis, Rcpp (>= 0.12.14), DelayedArray LinkingTo: Rhdf5lib, Rcpp, beachmat Suggests: BiocStyle, biomaRt, beachmat, cowplot, cluster, destiny, knitr, monocle, mvoutlier, rmarkdown, Rtsne, umap, testthat, magrittr, pheatmap, irlba, tximport, tximportData, tximeta, Biobase, limma License: GPL-3 MD5sum: faa6a6ab933d20c4ded77a10040b50ca NeedsCompilation: yes Title: Single-Cell Analysis Toolkit for Gene Expression Data in R Description: A collection of tools for doing various analyses of single-cell RNA-seq gene expression data, with a focus on quality control and visualization. biocViews: ImmunoOncology, SingleCell, RNASeq, QualityControl, Preprocessing, Normalization, Visualization, DimensionReduction, Transcriptomics, GeneExpression, Sequencing, Software, DataImport, DataRepresentation, Infrastructure, Coverage Author: Davis McCarthy [aut, cre], Kieran Campbell [aut], Aaron Lun [aut, ctb], Quin Wills [aut], Vladimir Kiselev [ctb] Maintainer: Davis McCarthy URL: http://bioconductor.org/packages/scater/ SystemRequirements: C++11 VignetteBuilder: knitr BugReports: https://support.bioconductor.org/ git_url: https://git.bioconductor.org/packages/scater git_branch: RELEASE_3_8 git_last_commit: 2e6694a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scater_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scater_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scater_1.10.1.tgz vignettes: vignettes/scater/inst/doc/vignette-dataviz.html, vignettes/scater/inst/doc/vignette-intro.html, vignettes/scater/inst/doc/vignette-qc.html vignetteTitles: Data visualisation methods in scater, An introduction to the scater package, Quality control with scater hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scater/inst/doc/vignette-dataviz.R, vignettes/scater/inst/doc/vignette-intro.R, vignettes/scater/inst/doc/vignette-qc.R dependsOnMe: netSmooth importsMe: CATALYST, scran, splatter suggestsMe: CellTrails, iSEE, MAST, monocle, SC3, slalom, SummarizedBenchmark Package: SCBN Version: 1.0.0 Depends: R (>= 3.5.0) Imports: stats Suggests: knitr,rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 36f0eef432e32fd3a5aa9c63b0bf2dda NeedsCompilation: no Title: A novel normalization method and differential expression analysis of RNA-seq d between different species Description: This package provides a scale based normalization (SCBN) method to identify genes with differential expression between different species. It takes into account the available knowledge of conserved orthologous genes and the hypothesis testing framework to detect differentially expressed orthologous genes. The method on this package are described in the article 'A statistical normalization method and differential expression analysis for RNA-seq data between different species' by Yan Zhou, Jiadi Zhu, Tiejun Tong, Junhui Wang, Bingqing Lin, Jun Zhang (2018, pending publication). biocViews: DifferentialExpression, GeneExpression, Normalization Author: Yan Zhou Maintainer: Yan Zhou <2160090406@email.szu.edu.cn> VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SCBN git_branch: RELEASE_3_8 git_last_commit: 3e0b5c0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SCBN_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SCBN_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SCBN_1.0.0.tgz vignettes: vignettes/SCBN/inst/doc/SCBN.html vignetteTitles: SCBN Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SCBN/inst/doc/SCBN.R Package: scDD Version: 1.6.1 Depends: R (>= 3.4) Imports: fields, mclust, BiocParallel, outliers, ggplot2, EBSeq, arm, SingleCellExperiment, SummarizedExperiment, grDevices, graphics, stats, S4Vectors, scran Suggests: BiocStyle, knitr, gridExtra License: GPL-2 MD5sum: b72aa48c7bbe0cf488c4bc444132e514 NeedsCompilation: yes Title: Mixture modeling of single-cell RNA-seq data to identify genes with differential distributions Description: This package implements a method to analyze single-cell RNA- seq Data utilizing flexible Dirichlet Process mixture models. Genes with differential distributions of expression are classified into several interesting patterns of differences between two conditions. The package also includes functions for simulating data with these patterns from negative binomial distributions. biocViews: ImmunoOncology, Bayesian, Clustering, RNASeq, SingleCell, MultipleComparison, Visualization, DifferentialExpression Author: Keegan Korthauer Maintainer: Keegan Korthauer URL: https://github.com/kdkorthauer/scDD VignetteBuilder: knitr BugReports: https://github.com/kdkorthauer/scDD/issues git_url: https://git.bioconductor.org/packages/scDD git_branch: RELEASE_3_8 git_last_commit: 38f09d1 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scDD_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scDD_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scDD_1.6.1.tgz vignettes: vignettes/scDD/inst/doc/scDD.pdf vignetteTitles: scDD Quickstart hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scDD/inst/doc/scDD.R suggestsMe: splatter Package: scde Version: 2.10.1 Depends: R (>= 3.0.0), flexmix Imports: Rcpp (>= 0.10.4), RcppArmadillo (>= 0.5.400.2.0), mgcv, Rook, rjson, MASS, Cairo, RColorBrewer, edgeR, quantreg, methods, nnet, RMTstat, extRemes, pcaMethods, BiocParallel, parallel LinkingTo: Rcpp, RcppArmadillo Suggests: knitr, cba, fastcluster, WGCNA, GO.db, org.Hs.eg.db, rmarkdown License: GPL-2 MD5sum: 911bc20284db73f8f3db95d65101c9d1 NeedsCompilation: yes Title: Single Cell Differential Expression Description: The scde package implements a set of statistical methods for analyzing single-cell RNA-seq data. scde fits individual error models for single-cell RNA-seq measurements. These models can then be used for assessment of differential expression between groups of cells, as well as other types of analysis. The scde package also contains the pagoda framework which applies pathway and gene set overdispersion analysis to identify and characterize putative cell subpopulations based on transcriptional signatures. The overall approach to the differential expression analysis is detailed in the following publication: "Bayesian approach to single-cell differential expression analysis" (Kharchenko PV, Silberstein L, Scadden DT, Nature Methods, doi: 10.1038/nmeth.2967). The overall approach to subpopulation identification and characterization is detailed in the following pre-print: "Characterizing transcriptional heterogeneity through pathway and gene set overdispersion analysis" (Fan J, Salathia N, Liu R, Kaeser G, Yung Y, Herman J, Kaper F, Fan JB, Zhang K, Chun J, and Kharchenko PV, Nature Methods, doi:10.1038/nmeth.3734). biocViews: ImmunoOncology, RNASeq, StatisticalMethod, DifferentialExpression, Bayesian, Transcription, Software Author: Peter Kharchenko [aut, cre], Jean Fan [aut] Maintainer: Jean Fan URL: http://pklab.med.harvard.edu/scde VignetteBuilder: knitr BugReports: https://github.com/hms-dbmi/scde/issues git_url: https://git.bioconductor.org/packages/scde git_branch: RELEASE_3_8 git_last_commit: f186785 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scde_2.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scde_2.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scde_2.10.1.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: scFeatureFilter Version: 1.2.1 Depends: R (>= 3.5) Imports: dplyr (>= 0.7.3), ggplot2 (>= 2.1.0), magrittr (>= 1.5), rlang (>= 0.1.2), tibble (>= 1.3.4), stats, methods Suggests: testthat, knitr, rmarkdown, SingleCellExperiment, SummarizedExperiment, scRNAseq, cowplot License: MIT + file LICENSE Archs: i386, x64 MD5sum: 8c1bfa91efbaa3bd6f6734bdc98cebdf NeedsCompilation: no Title: A correlation-based method for quality filtering of single-cell RNAseq data Description: An R implementation of the correlation-based method developed in the Joshi laboratory to analyse and filter processed single-cell RNAseq data. It returns a filtered version of the data containing only genes expression values unaffected by systematic noise. biocViews: ImmunoOncology, SingleCell, RNASeq, Preprocessing, GeneExpression Author: Angeles Arzalluz-Luque [aut], Guillaume Devailly [aut, cre], Anagha Joshi [aut] Maintainer: Guillaume Devailly VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/scFeatureFilter git_branch: RELEASE_3_8 git_last_commit: 2f8b2b1 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scFeatureFilter_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scFeatureFilter_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scFeatureFilter_1.2.1.tgz vignettes: vignettes/scFeatureFilter/inst/doc/Introduction.html vignetteTitles: Introduction to scFeatureFilter hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/scFeatureFilter/inst/doc/Introduction.R Package: scfind Version: 1.4.1 Depends: R(>= 3.4) Imports: SingleCellExperiment, SummarizedExperiment, methods, stats, bit, dplyr, hash, reshape2, Rcpp(>= 0.12.12) LinkingTo: Rcpp Suggests: knitr, rmarkdown, testthat License: GPL-3 MD5sum: 7734053eefd07f06fa726e8e643b971d NeedsCompilation: yes Title: A search tool for single cell RNA-seq data by gene lists Description: Recently a very large collection of single-cell RNA-seq (scRNA-seq) datasets has been generated and publicly released. For the collection to be useful, the information must be organized in a way that supports queries that are relevant to researchers. `scfind` builds an index from scRNA-seq datasets which organizes the information in a suitable and compact manner so that the datasets can be very efficiently searched for either cells or cell types in which a given list of genes is expressed. biocViews: ImmunoOncology, SingleCell, Software, RNASeq, Transcriptomics, DataRepresentation, Transcription, Sequencing, GeneExpression Author: Vladimir Kiselev Maintainer: Vladimir Kiselev URL: https://github.com/hemberg-lab/scfind VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/scfind/ git_url: https://git.bioconductor.org/packages/scfind git_branch: RELEASE_3_8 git_last_commit: 69ba6c2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scfind_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scfind_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scfind_1.4.1.tgz vignettes: vignettes/scfind/inst/doc/scfind.html vignetteTitles: `scfind` package vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scfind/inst/doc/scfind.R Package: ScISI Version: 1.54.0 Depends: R (>= 2.10), GO.db, RpsiXML, annotate, apComplex Imports: AnnotationDbi, GO.db, RpsiXML, annotate, methods, org.Sc.sgd.db, utils Suggests: ppiData, xtable License: LGPL Archs: i386, x64 MD5sum: 88cc06d0227f9111004afc9da312fed3 NeedsCompilation: no Title: In Silico Interactome Description: Package to create In Silico Interactomes biocViews: GraphAndNetwork, Proteomics, NetworkInference, DecisionTree Author: Tony Chiang Maintainer: Tony Chiang git_url: https://git.bioconductor.org/packages/ScISI git_branch: RELEASE_3_8 git_last_commit: c9a6a97 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ScISI_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ScISI_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ScISI_1.54.0.tgz vignettes: vignettes/ScISI/inst/doc/vignette.pdf vignetteTitles: ScISI Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ScISI/inst/doc/vignette.R dependsOnMe: PCpheno, ppiStats, SLGI importsMe: PCpheno, SLGI suggestsMe: RpsiXML Package: scmap Version: 1.4.1 Depends: R(>= 3.4) Imports: Biobase, SingleCellExperiment, SummarizedExperiment, BiocGenerics, S4Vectors, dplyr, reshape2, matrixStats, proxy, utils, googleVis, ggplot2, methods, stats, e1071, randomForest, Rcpp (>= 0.12.12) LinkingTo: Rcpp, RcppArmadillo Suggests: knitr, rmarkdown License: GPL-3 MD5sum: 67ddac6e3aca54496073d2eea4fc667f NeedsCompilation: yes Title: A tool for unsupervised projection of single cell RNA-seq data Description: Single-cell RNA-seq (scRNA-seq) is widely used to investigate the composition of complex tissues since the technology allows researchers to define cell-types using unsupervised clustering of the transcriptome. However, due to differences in experimental methods and computational analyses, it is often challenging to directly compare the cells identified in two different experiments. scmap is a method for projecting cells from a scRNA-seq experiment on to the cell-types or individual cells identified in a different experiment. biocViews: ImmunoOncology, SingleCell, Software, Classification, SupportVectorMachine, RNASeq, Visualization, Transcriptomics, DataRepresentation, Transcription, Sequencing, Preprocessing, GeneExpression, DataImport Author: Vladimir Kiselev Maintainer: Vladimir Kiselev URL: https://github.com/hemberg-lab/scmap VignetteBuilder: knitr BugReports: https://support.bioconductor.org/t/scmap/ git_url: https://git.bioconductor.org/packages/scmap git_branch: RELEASE_3_8 git_last_commit: 1e83b1a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scmap_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scmap_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scmap_1.4.1.tgz vignettes: vignettes/scmap/inst/doc/scmap.html vignetteTitles: `scmap` package vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scmap/inst/doc/scmap.R Package: scmeth Version: 1.2.2 Depends: R (>= 3.5.0) Imports: knitr, rmarkdown, bsseq, AnnotationHub, GenomicRanges, reshape2, stats, utils, BSgenome, DelayedArray (>= 0.5.15), annotatr, SummarizedExperiment (>= 1.5.6), GenomeInfoDb, Biostrings, DT, HDF5Array (>= 1.7.5) Suggests: BSgenome.Mmusculus.UCSC.mm10, BSgenome.Hsapiens.NCBI.GRCh38, TxDb.Hsapiens.UCSC.hg38.knownGene, org.Hs.eg.db, Biobase, BiocGenerics, ggplot2, ggthemes License: GPL-2 Archs: i386, x64 MD5sum: 15b825f27990acd25f180511c8bfc9ff NeedsCompilation: no Title: Functions to conduct quality control analysis in methylation data Description: Functions to analyze methylation data can be found here. Some functions are relevant for single cell methylation data but most other functions can be used for any methylation data. Highlight of this workflow is the comprehensive quality control report. biocViews: ImmunoOncology, DNAMethylation, QualityControl, Preprocessing, SingleCell Author: Divy Kangeyan Maintainer: Divy Kangeyan VignetteBuilder: knitr BugReports: https://github.com/aryeelab/scmeth/issues git_url: https://git.bioconductor.org/packages/scmeth git_branch: RELEASE_3_8 git_last_commit: 091a232 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scmeth_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/scmeth_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scmeth_1.2.2.tgz vignettes: vignettes/scmeth/inst/doc/my-vignette.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scmeth/inst/doc/my-vignette.R Package: SCnorm Version: 1.4.7 Depends: R (>= 3.4.0), Imports: stats, methods, graphics, grDevices, parallel, quantreg, cluster, moments, data.table, BiocParallel, SingleCellExperiment, SummarizedExperiment, S4Vectors, ggplot2, forcats Suggests: BiocStyle, knitr, rmarkdown, devtools License: GPL (>= 2) MD5sum: 2e3c409def6758790c99c79e2f3f74b4 NeedsCompilation: no Title: Normalization of single cell RNA-seq data Description: This package implements SCnorm — a method to normalize single-cell RNA-seq data. biocViews: Normalization, RNASeq, SingleCell, ImmunoOncology Author: Rhonda Bacher Maintainer: Rhonda Bacher URL: https://github.com/rhondabacher/SCnorm VignetteBuilder: knitr BugReports: https://github.com/rhondabacher/SCnorm/issues git_url: https://git.bioconductor.org/packages/SCnorm git_branch: RELEASE_3_8 git_last_commit: 77b094f git_last_commit_date: 2019-02-18 Date/Publication: 2019-02-18 source.ver: src/contrib/SCnorm_1.4.7.tar.gz win.binary.ver: bin/windows/contrib/3.5/SCnorm_1.4.7.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SCnorm_1.4.7.tgz vignettes: vignettes/SCnorm/inst/doc/SCnorm.pdf vignetteTitles: SCnorm Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SCnorm/inst/doc/SCnorm.R Package: scone Version: 1.6.1 Depends: R (>= 3.4), methods, SummarizedExperiment Imports: graphics, stats, utils, aroma.light, BiocParallel, class, cluster, compositions, diptest, edgeR, fpc, gplots, grDevices, hexbin, limma, matrixStats, mixtools, RColorBrewer, boot, rhdf5, RUVSeq, rARPACK Suggests: BiocStyle, DT, ggplot2, knitr, miniUI, NMF, plotly, reshape2, rmarkdown, scran, scRNAseq, shiny, testthat, visNetwork License: Artistic-2.0 MD5sum: 555e5a118ab8bcd2f13d125499094226 NeedsCompilation: no Title: Single Cell Overview of Normalized Expression data Description: SCONE is an R package for comparing and ranking the performance of different normalization schemes for single-cell RNA-seq and other high-throughput analyses. biocViews: ImmunoOncology, Normalization, Preprocessing, QualityControl, GeneExpression, RNASeq, Software, Transcriptomics, Sequencing, SingleCell, Coverage Author: Michael Cole [aut, cre, cph], Davide Risso [aut, cph] Maintainer: Michael Cole VignetteBuilder: knitr BugReports: https://github.com/YosefLab/scone/issues git_url: https://git.bioconductor.org/packages/scone git_branch: RELEASE_3_8 git_last_commit: ad564e5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scone_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scone_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scone_1.6.1.tgz vignettes: vignettes/scone/inst/doc/sconeTutorial.html vignetteTitles: scone Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scone/inst/doc/sconeTutorial.R Package: Sconify Version: 1.2.1 Depends: R (>= 3.5) Imports: tibble, dplyr, FNN, flowCore, Rtsne, ggplot2, magrittr, utils, stats, readr Suggests: knitr, rmarkdown, testthat License: Artistic-2.0 MD5sum: 5f184dbb6823b5d6ad3e03644cbb3b24 NeedsCompilation: no Title: A toolkit for performing KNN-based statistics for flow and mass cytometry data Description: This package does k-nearest neighbor based statistics and visualizations with flow and mass cytometery data. This gives tSNE maps"fold change" functionality and provides a data quality metric by assessing manifold overlap between fcs files expected to be the same. Other applications using this package include imputation, marker redundancy, and testing the relative information loss of lower dimension embeddings compared to the original manifold. biocViews: ImmunoOncology, SingleCell, FlowCytometry, Software, MultipleComparison, Visualization Author: Tyler J Burns Maintainer: Tyler J Burns VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Sconify git_branch: RELEASE_3_8 git_last_commit: 940b0c7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Sconify_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Sconify_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Sconify_1.2.1.tgz vignettes: vignettes/Sconify/inst/doc/DataQuality.html, vignettes/Sconify/inst/doc/FindingIdealK.html, vignettes/Sconify/inst/doc/Step1.PreProcessing.html, vignettes/Sconify/inst/doc/Step2.TheSconeWorkflow.html, vignettes/Sconify/inst/doc/Step3.PostProcessing.html vignetteTitles: Data Quality, Finding Ideal K, How to process FCS files for downstream use in R, General Scone Analysis, Final Post-Processing Steps for Scone hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Sconify/inst/doc/DataQuality.R, vignettes/Sconify/inst/doc/FindingIdealK.R, vignettes/Sconify/inst/doc/Step1.PreProcessing.R, vignettes/Sconify/inst/doc/Step2.TheSconeWorkflow.R, vignettes/Sconify/inst/doc/Step3.PostProcessing.R Package: scoreInvHap Version: 1.4.0 Depends: R (>= 3.4.0) Imports: Biostrings, methods, snpStats, VariantAnnotation, GenomicRanges, BiocParallel, graphics, SummarizedExperiment Suggests: testthat, knitr, BiocStyle, rmarkdown License: file LICENSE MD5sum: 2ad194689a37b11ae8e50c00056c2e86 NeedsCompilation: no Title: Get inversion status in predefined regions Description: scoreInvHap can get the samples' inversion status of known inversions. scoreInvHap uses SNP data as input and requires the following information about the inversion: genotype frequencies in the different haplotypes, R2 between the region SNPs and inversion status and heterozygote genotypes in the reference. The package include this data for two well known inversions (8p23 and 17q21.31) and for two additional regions. biocViews: SNP, Genetics, GenomicVariation Author: Carlos Ruiz [aut, cre], Juan R. Gonzalez [aut] Maintainer: Carlos Ruiz VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/scoreInvHap git_branch: RELEASE_3_8 git_last_commit: f460bf0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/scoreInvHap_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/scoreInvHap_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scoreInvHap_1.4.0.tgz vignettes: vignettes/scoreInvHap/inst/doc/scoreInvHap.html vignetteTitles: Call haplotype inversions with scoreInvHap hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/scoreInvHap/inst/doc/scoreInvHap.R Package: scPipe Version: 1.4.1 Depends: R (>= 3.4), ggplot2, methods, SingleCellExperiment Imports: Rhtslib, biomaRt, GGally, MASS, mclust, Rcpp (>= 0.11.3), reshape, BiocGenerics, robustbase, scales, utils, stats, S4Vectors, SummarizedExperiment, AnnotationDbi, org.Hs.eg.db, org.Mm.eg.db, stringr, rtracklayer, hashmap, dplyr, GenomicRanges, magrittr, glue LinkingTo: Rcpp, Rhtslib (>= 1.13.1), zlibbioc, testthat Suggests: Rsubread, knitr, rmarkdown, testthat License: GPL (>= 2) MD5sum: 6a4ef0adf5fcfc0e94db6b8caf6486ca NeedsCompilation: yes Title: pipeline for single cell RNA-seq data analysis Description: A preprocessing pipeline for single cell RNA-seq data that starts from the fastq files and produces a gene count matrix with associated quality control information. It can process fastq data generated by CEL-seq, MARS-seq, Drop-seq, Chromium 10x and SMART-seq protocols. biocViews: ImmunoOncology, Software, Sequencing, RNASeq, GeneExpression, SingleCell, Visualization, SequenceMatching, Preprocessing, QualityControl, GenomeAnnotation Author: Luyi Tian Maintainer: Luyi Tian URL: https://github.com/LuyiTian/scPipe VignetteBuilder: knitr BugReports: https://github.com/LuyiTian/scPipe git_url: https://git.bioconductor.org/packages/scPipe git_branch: RELEASE_3_8 git_last_commit: 90a617d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scPipe_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/scPipe_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scPipe_1.4.1.tgz vignettes: vignettes/scPipe/inst/doc/scPipe_tutorial.html vignetteTitles: scPipe: flexible data preprocessing pipeline for 3' end scRNA-seq data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scPipe/inst/doc/scPipe_tutorial.R Package: scran Version: 1.10.2 Depends: R (>= 3.5), BiocParallel, SingleCellExperiment Imports: SummarizedExperiment, S4Vectors, BiocGenerics, Rcpp (>= 0.12.14), stats, methods, utils, Matrix, scater, edgeR, limma, dynamicTreeCut, BiocNeighbors, igraph, statmod, DelayedArray, DelayedMatrixStats LinkingTo: beachmat, Rcpp, Rhdf5lib Suggests: testthat, BiocStyle, knitr, beachmat, HDF5Array, irlba, org.Mm.eg.db, DESeq2, monocle, pracma, Biobase, aroma.light License: GPL-3 Archs: i386, x64 MD5sum: 7e7cc6ff1b30df7f92b682cd0ca61aac NeedsCompilation: yes Title: Methods for Single-Cell RNA-Seq Data Analysis Description: Implements functions for low-level analyses of single-cell RNA-seq data. Methods are provided for normalization of cell-specific biases, assignment of cell cycle phase, detection of highly variable and significantly correlated genes, correction of batch effects, identification of marker genes, and other common tasks in single-cell analysis workflows. biocViews: ImmunoOncology, Normalization, Sequencing, RNASeq, Software, GeneExpression, Transcriptomics, SingleCell, Visualization, BatchEffect, Clustering Author: Aaron Lun [aut, cre], Karsten Bach [aut], Jong Kyoung Kim [ctb], Antonio Scialdone [ctb], Laleh Haghverdi [ctb] Maintainer: Aaron Lun SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/scran git_branch: RELEASE_3_8 git_last_commit: b4191ec git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/scran_1.10.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/scran_1.10.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scran_1.10.2.tgz vignettes: vignettes/scran/inst/doc/scran.html vignetteTitles: Using scran to analyze scRNA-seq data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scran/inst/doc/scran.R importsMe: BASiCS, scDD suggestsMe: CellTrails, clusterExperiment, scone, splatter Package: scruff Version: 1.0.3 Depends: R (>= 3.5.0) Imports: data.table, GenomicAlignments, GenomicFeatures, GenomicRanges, Rsamtools, ShortRead, parallel, plyr, BiocGenerics, BiocParallel, S4Vectors, AnnotationDbi, Biostrings, methods, ggplot2, ggthemes, scales, GenomeInfoDb, stringdist, ggbio, rtracklayer, SingleCellExperiment, SummarizedExperiment Suggests: BiocStyle, knitr, rmarkdown, Rsubread, testthat License: MIT + file LICENSE MD5sum: c39f6292f1f1064e7d457ea3963dfdf0 NeedsCompilation: no Title: Single Cell RNA-Seq UMI Filtering Facilitator (scruff) Description: A pipeline which processes single cell RNA-seq (scRNA-seq) reads from CEL-seq and CEL-seq2 protocols. Demultiplex scRNA-seq FASTQ files, align reads to reference genome using Rsubread, and generate UMI filtered count matrix. Also provide visualizations of read alignments and pre- and post-alignment QC metrics. biocViews: Software, Technology, Sequencing, Alignment, RNASeq, SingleCell, WorkflowStep, Preprocessing, QualityControl, Visualization, ImmunoOncology Author: Zhe Wang [aut, cre], Junming Hu [aut], Joshua Campbell [aut] Maintainer: Zhe Wang VignetteBuilder: knitr BugReports: https://github.com/campbio/scruff/issues git_url: https://git.bioconductor.org/packages/scruff git_branch: RELEASE_3_8 git_last_commit: 6edc6bf git_last_commit_date: 2019-03-28 Date/Publication: 2019-03-28 source.ver: src/contrib/scruff_1.0.3.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scruff_1.0.3.tgz vignettes: vignettes/scruff/inst/doc/scruff.pdf vignetteTitles: Process Single Cell RNA-Seq reads using _scruff_ hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/scruff/inst/doc/scruff.R Package: scsR Version: 1.18.0 Depends: R (>= 2.14.0), STRINGdb, methods, BiocGenerics, Biostrings, IRanges, plyr, tcltk Imports: sqldf, hash, ggplot2, graphics,grDevices, RColorBrewer Suggests: RUnit License: GPL-2 Archs: i386, x64 MD5sum: 0f4b6a6a4da4a834cf90834a9d93f83b NeedsCompilation: no Title: SiRNA correction for seed mediated off-target effect Description: Corrects genome-wide siRNA screens for seed mediated off-target effect. Suitable functions to identify the effective seeds/miRNAs and to visualize their effect are also provided in the package. biocViews: Preprocessing Author: Andrea Franceschini Maintainer: Andrea Franceschini , Roger Meier , Christian von Mering git_url: https://git.bioconductor.org/packages/scsR git_branch: RELEASE_3_8 git_last_commit: 1a01bfa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/scsR_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/scsR_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/scsR_1.18.0.tgz vignettes: vignettes/scsR/inst/doc/scsR.pdf vignetteTitles: scsR Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/scsR/inst/doc/scsR.R Package: SDAMS Version: 1.2.1 Depends: R(>= 3.5), SummarizedExperiment Imports: trust, qvalue, methods, stats, utils Suggests: testthat License: GPL MD5sum: c835846ec1bbc21a26d041a7c14e5401 NeedsCompilation: no Title: Differential Abundant Analysis for Metabolomics and Proteomics Data Description: This Package utilizes a Semi-parametric Differential Abundance analysis (SDA) method for metabolomics and proteomics data from mass spectrometry. SDA is able to robustly handle non-normally distributed data and provides a clear quantification of the effect size. biocViews: ImmunoOncology, DifferentialExpression, Metabolomics, Proteomics, MassSpectrometry Author: Yuntong Li , Chi Wang , Li Chen Maintainer: Yuntong Li git_url: https://git.bioconductor.org/packages/SDAMS git_branch: RELEASE_3_8 git_last_commit: ec66e1e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SDAMS_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SDAMS_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SDAMS_1.2.1.tgz vignettes: vignettes/SDAMS/inst/doc/SDAMS.pdf vignetteTitles: SDAMS Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SDAMS/inst/doc/SDAMS.R Package: segmentSeq Version: 2.16.0 Depends: R (>= 3.0.0), methods, baySeq (>= 2.9.0), S4Vectors, parallel, GenomicRanges, ShortRead, stats Imports: Rsamtools, IRanges, GenomeInfoDb, graphics, grDevices, utils, abind Suggests: BiocStyle, BiocGenerics License: GPL-3 MD5sum: d824a0fa29add988a1ce56eb6fe3dcdb NeedsCompilation: no Title: Methods for identifying small RNA loci from high-throughput sequencing data Description: High-throughput sequencing technologies allow the production of large volumes of short sequences, which can be aligned to the genome to create a set of matches to the genome. By looking for regions of the genome which to which there are high densities of matches, we can infer a segmentation of the genome into regions of biological significance. The methods in this package allow the simultaneous segmentation of data from multiple samples, taking into account replicate data, in order to create a consensus segmentation. This has obvious applications in a number of classes of sequencing experiments, particularly in the discovery of small RNA loci and novel mRNA transcriptome discovery. biocViews: MultipleComparison, Sequencing, Alignment, DifferentialExpression, QualityControl, DataImport Author: Thomas J. Hardcastle Maintainer: Thomas J. Hardcastle git_url: https://git.bioconductor.org/packages/segmentSeq git_branch: RELEASE_3_8 git_last_commit: 41e5cbb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/segmentSeq_2.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/segmentSeq_2.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/segmentSeq_2.16.0.tgz vignettes: vignettes/segmentSeq/inst/doc/methylationAnalysis.pdf, vignettes/segmentSeq/inst/doc/segmentSeq.pdf vignetteTitles: segmentsSeq: Methylation locus identification, segmentSeq: small RNA locus detection hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/segmentSeq/inst/doc/methylationAnalysis.R, vignettes/segmentSeq/inst/doc/segmentSeq.R Package: SELEX Version: 1.14.0 Depends: R (>= 2.7.0), rJava (>= 0.5-0), Biostrings (>= 2.26.0) License: GPL (>=2) MD5sum: 50fc8dc5e8723d5c1d93f7e1b9140ca8 NeedsCompilation: no Title: Functions for analyzing SELEX-seq data Description: Tools for quantifying DNA binding specificities based on SELEX-seq data biocViews: Software, MotifDiscovery, MotifAnnotation, GeneRegulation, Transcription Author: Chaitanya Rastogi, Dahong Liu, and Harmen Bussemaker Maintainer: Harmen Bussemaker URL: http://bussemakerlab.org/software/SELEX/ SystemRequirements: Java (>= 1.5) git_url: https://git.bioconductor.org/packages/SELEX git_branch: RELEASE_3_8 git_last_commit: 00b9541 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SELEX_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SELEX_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SELEX_1.14.0.tgz vignettes: vignettes/SELEX/inst/doc/SELEX.pdf vignetteTitles: Motif Discovery with SELEX-seq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SELEX/inst/doc/SELEX.R Package: SemDist Version: 1.16.0 Depends: R (>= 3.1), AnnotationDbi, GO.db, annotate Suggests: GOSemSim License: GPL (>= 2) MD5sum: eab03908affcfa4650727b2d59de3a1e NeedsCompilation: no Title: Information Accretion-based Function Predictor Evaluation Description: This package implements methods to calculate information accretion for a given version of the gene ontology and uses this data to calculate remaining uncertainty, misinformation, and semantic similarity for given sets of predicted annotations and true annotations from a protein function predictor. biocViews: Classification, Annotation, GO, Software Author: Ian Gonzalez and Wyatt Clark Maintainer: Ian Gonzalez URL: http://github.com/iangonzalez/SemDist git_url: https://git.bioconductor.org/packages/SemDist git_branch: RELEASE_3_8 git_last_commit: fc74e13 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SemDist_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SemDist_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SemDist_1.16.0.tgz vignettes: vignettes/SemDist/inst/doc/introduction.pdf vignetteTitles: introduction.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SemDist/inst/doc/introduction.R Package: semisup Version: 1.6.0 Depends: R (>= 3.0.0) Imports: SummarizedExperiment, VGAM Suggests: knitr, testthat License: GPL-3 MD5sum: 7de301d6f0da4d2fb6c7b720c33d0801 NeedsCompilation: no Title: Semi-Supervised Mixture Model Description: Useful for detecting SNPs with interactive effects on a quantitative trait. This R packages moves away from testing interaction terms, and moves towards testing whether an individual SNP is involved in any interaction. This reduces the multiple testing burden to one test per SNP, and allows for interactions with unobserved factors. Analysing one SNP at a time, it splits the individuals into two groups, based on the number of minor alleles. If the quantitative trait differs in mean between the two groups, the SNP has a main effect. If the quantitative trait differs in distribution between some individuals in one group and all other individuals, it possibly has an interactive effect. Implicitly, the membership probabilities may suggest potential interacting variables. biocViews: SNP, GenomicVariation, SomaticMutation, Genetics, Classification, Clustering, DNASeq, Microarray, MultipleComparison Author: Armin Rauschenberger [aut, cre] Maintainer: Armin Rauschenberger URL: https://github.com/rauschenberger/semisup VignetteBuilder: knitr BugReports: https://github.com/rauschenberger/semisup/issues git_url: https://git.bioconductor.org/packages/semisup git_branch: RELEASE_3_8 git_last_commit: ae6f2b4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/semisup_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/semisup_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/semisup_1.6.0.tgz vignettes: vignettes/semisup/inst/doc/semisup.pdf, vignettes/semisup/inst/doc/article.html, vignettes/semisup/inst/doc/vignette.html vignetteTitles: semisup, pkgdown, pkgdown hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/semisup/inst/doc/semisup.R Package: SEPA Version: 1.12.0 Depends: R(>= 2.10.0) Imports: ggplot2, shiny, topGO, segmented, reshape2, org.Hs.eg.db, org.Mm.eg.db Suggests: knitr License: GPL(>=2) MD5sum: 8e24d376c6932b319c7220271d2ac3d9 NeedsCompilation: no Title: SEPA Description: Given single-cell RNA-seq data and true experiment time of cells or pseudo-time cell ordering, SEPA provides convenient functions for users to assign genes into different gene expression patterns such as constant, monotone increasing and increasing then decreasing. SEPA then performs GO enrichment analysis to analysis the functional roles of genes with same or similar patterns. biocViews: GeneExpression, Visualization, GUI, GO Author: Zhicheng Ji, Hongkai Ji Maintainer: Zhicheng Ji VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SEPA git_branch: RELEASE_3_8 git_last_commit: 0b21a28 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SEPA_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SEPA_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SEPA_1.12.0.tgz vignettes: vignettes/SEPA/inst/doc/SEPA.pdf vignetteTitles: SEPA: Single-Cell Gene Expression Pattern Analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SEPA/inst/doc/SEPA.R Package: SEPIRA Version: 1.2.0 Depends: R (>= 3.5.0) Imports: limma (>= 3.32.5), corpcor (>= 1.6.9), parallel (>= 3.3.1), stats Suggests: knitr, rmarkdown, testthat, igraph License: GPL-3 MD5sum: 9c692e31570fd41c696bb62f2f48b45e NeedsCompilation: no Title: Systems EPigenomics Inference of Regulatory Activity Description: SEPIRA (Systems EPigenomics Inference of Regulatory Activity) is an algorithm that infers sample-specific transcription factor activity from the genome-wide expression or DNA methylation profile of the sample. biocViews: GeneExpression, Transcription, GeneRegulation, GeneTarget, NetworkInference, Network, Software Author: Yuting Chen [aut, cre], Andrew Teschendorff [aut] Maintainer: Yuting Chen VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SEPIRA git_branch: RELEASE_3_8 git_last_commit: 89e49a9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SEPIRA_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SEPIRA_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SEPIRA_1.2.0.tgz vignettes: vignettes/SEPIRA/inst/doc/SEPIRA.html vignetteTitles: Introduction to `SEPIRA` hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SEPIRA/inst/doc/SEPIRA.R Package: seq2pathway Version: 1.14.0 Depends: R (>= 2.10.0) Imports: nnet, WGCNA, GSA, biomaRt, GenomicRanges, seq2pathway.data License: GPL-2 MD5sum: 3902ddfb016b893e874cd6eadc13c1d2 NeedsCompilation: no Title: a novel tool for functional gene-set (or termed as pathway) analysis of next-generation sequencing data Description: Seq2pathway is a novel tool for functional gene-set (or termed as pathway) analysis of next-generation sequencing data, consisting of "seq2gene" and "gene2path" components. The seq2gene links sequence-level measurements of genomic regions (including SNPs or point mutation coordinates) to gene-level scores, and the gene2pathway summarizes gene scores to pathway-scores for each sample. The seq2gene has the feasibility to assign both coding and non-exon regions to a broader range of neighboring genes than only the nearest one, thus facilitating the study of functional non-coding regions. The gene2pathway takes into account the quantity of significance for gene members within a pathway compared those outside a pathway. The output of seq2pathway is a general structure of quantitative pathway-level scores, thus allowing one to functional interpret such datasets as RNA-seq, ChIP-seq, GWAS, and derived from other next generational sequencing experiments. biocViews: Software Author: Xinan Yang ; Bin Wang Maintainer: Xinan Yang with contribution from Lorenzo Pesce and Ana Marija Sokovic git_url: https://git.bioconductor.org/packages/seq2pathway git_branch: RELEASE_3_8 git_last_commit: 11464ae git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/seq2pathway_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/seq2pathway_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seq2pathway_1.14.0.tgz vignettes: vignettes/seq2pathway/inst/doc/seq2pathwaypackage.pdf vignetteTitles: An R package for sequence hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seq2pathway/inst/doc/seq2pathwaypackage.R Package: SeqArray Version: 1.22.6 Depends: R (>= 3.5.0), gdsfmt (>= 1.18.0) Imports: methods, parallel, IRanges, GenomicRanges, GenomeInfoDb, Biostrings, S4Vectors LinkingTo: gdsfmt Suggests: Biobase, BiocGenerics, BiocParallel, RUnit, Rcpp, SNPRelate, digest, crayon, knitr, Rsamtools, VariantAnnotation License: GPL-3 MD5sum: d84251ce933fd3e82b00f141739de0d0 NeedsCompilation: yes Title: Data Management of Large-scale Whole-genome Sequence Variant Calls Description: Data management of large-scale whole-genome sequencing variant calls with thousands of individuals: genotypic data (e.g., SNVs, indels and structural variation calls) and annotations in SeqArray files are stored in an array-oriented and compressed manner, with efficient data access using the R programming language. biocViews: Infrastructure, DataRepresentation, Sequencing, Genetics Author: Xiuwen Zheng [aut, cre], Stephanie Gogarten [aut], David Levine [ctb], Cathy Laurie [ctb] Maintainer: Xiuwen Zheng URL: http://github.com/zhengxwen/SeqArray VignetteBuilder: knitr BugReports: http://github.com/zhengxwen/SeqArray/issues git_url: https://git.bioconductor.org/packages/SeqArray git_branch: RELEASE_3_8 git_last_commit: 585cb72 git_last_commit_date: 2019-03-10 Date/Publication: 2019-03-10 source.ver: src/contrib/SeqArray_1.22.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/SeqArray_1.22.6.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SeqArray_1.22.6.tgz vignettes: vignettes/SeqArray/inst/doc/OverviewSlides.html, vignettes/SeqArray/inst/doc/R_Integration.html, vignettes/SeqArray/inst/doc/SeqArrayTutorial.html vignetteTitles: SeqArray Overview, R Integration, SeqArray Data Format and Access hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SeqArray/inst/doc/R_Integration.R, vignettes/SeqArray/inst/doc/SeqArrayTutorial.R dependsOnMe: SeqVarTools importsMe: GDSArray, GENESIS Package: seqbias Version: 1.30.0 Depends: R (>= 2.13.0), GenomicRanges (>= 0.1.0), Biostrings (>= 2.15.0), methods Imports: zlibbioc LinkingTo: Rsamtools (>= 1.19.38) Suggests: Rsamtools, ggplot2 License: LGPL-3 Archs: i386, x64 MD5sum: a7246cbe2d95208f29cf3651e25b9688 NeedsCompilation: yes Title: Estimation of per-position bias in high-throughput sequencing data Description: This package implements a model of per-position sequencing bias in high-throughput sequencing data using a simple Bayesian network, the structure and parameters of which are trained on a set of aligned reads and a reference genome sequence. biocViews: Sequencing Author: Daniel Jones Maintainer: Daniel Jones git_url: https://git.bioconductor.org/packages/seqbias git_branch: RELEASE_3_8 git_last_commit: 498bb37 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/seqbias_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqbias_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqbias_1.30.0.tgz vignettes: vignettes/seqbias/inst/doc/overview.pdf vignetteTitles: Assessing and Adjusting for Technical Bias in High Throughput Sequencing Data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqbias/inst/doc/overview.R dependsOnMe: ReQON Package: seqCAT Version: 1.4.1 Depends: R (>= 3.5), GenomicRanges (>= 1.26.4), VariantAnnotation(>= 1.20.3) Imports: dplyr (>= 0.5.0), GenomeInfoDb (>= 1.13.4), ggplot2 (>= 2.2.1), grid (>= 3.5.0), IRanges (>= 2.8.2), lazyeval (>= 0.2.0), methods, scales (>= 0.4.1), S4Vectors (>= 0.12.2), stats, SummarizedExperiment (>= 1.4.0), tidyr (>= 0.6.1), utils Suggests: knitr, BiocStyle, rmarkdown, testthat, BiocManager License: MIT + file LICENCE Archs: i386, x64 MD5sum: e2742e15dd741cb9369fbafc2da0b3e4 NeedsCompilation: no Title: High Throughput Sequencing Cell Authentication Toolkit Description: The seqCAT package uses variant calling data (in the form of VCF files) from high throughput sequencing technologies to authenticate and validate the source, function and characteristics of biological samples used in scientific endeavours. biocViews: Coverage, GenomicVariation, Sequencing, VariantAnnotation Author: Erik Fasterius [aut, cre] Maintainer: Erik Fasterius VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/seqCAT git_branch: RELEASE_3_8 git_last_commit: 5cb2793 git_last_commit_date: 2019-01-14 Date/Publication: 2019-01-14 source.ver: src/contrib/seqCAT_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqCAT_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqCAT_1.4.1.tgz vignettes: vignettes/seqCAT/inst/doc/seqCAT.html vignetteTitles: seqCAT: The High Throughput Sequencing Cell Authentication Toolkit hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqCAT/inst/doc/seqCAT.R Package: seqCNA Version: 1.28.0 Depends: R (>= 3.0), GLAD (>= 2.14), doSNOW (>= 1.0.5), adehabitatLT (>= 0.3.4), seqCNA.annot (>= 0.99), methods License: GPL-3 MD5sum: 0942b2ccaa95004fcf5b5155bede0e76 NeedsCompilation: yes Title: Copy number analysis of high-throughput sequencing cancer data Description: Copy number analysis of high-throughput sequencing cancer data with fast summarization, extensive filtering and improved normalization biocViews: CopyNumberVariation, Genetics, Sequencing Author: David Mosen-Ansorena Maintainer: David Mosen-Ansorena SystemRequirements: samtools git_url: https://git.bioconductor.org/packages/seqCNA git_branch: RELEASE_3_8 git_last_commit: c0ef4aa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/seqCNA_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqCNA_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqCNA_1.28.0.tgz vignettes: vignettes/seqCNA/inst/doc/seqCNA.pdf hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqCNA/inst/doc/seqCNA.R Package: seqcombo Version: 1.4.1 Depends: R (>= 3.4.0) Imports: Biostrings, cowplot, dplyr, ggplot2, grid, igraph, magrittr, methods, rvcheck, utils Suggests: emojifont, knitr, prettydoc, tibble License: Artistic-2.0 Archs: i386, x64 MD5sum: 20e6e4f63d060aff6e88d0004df5e92e NeedsCompilation: no Title: Visualization Tool for Sequence Recombination and Reassortment Description: Provides useful functions for visualizing sequence recombination and virus reassortment events. biocViews: Alignment, Software, Visualization Author: Guangchuang Yu [aut, cre] Maintainer: Guangchuang Yu VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/seqcombo/issues git_url: https://git.bioconductor.org/packages/seqcombo git_branch: RELEASE_3_8 git_last_commit: d3b8579 git_last_commit_date: 2019-01-01 Date/Publication: 2019-01-02 source.ver: src/contrib/seqcombo_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqcombo_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqcombo_1.4.1.tgz vignettes: vignettes/seqcombo/inst/doc/reassortment.html, vignettes/seqcombo/inst/doc/seqcombo.html vignetteTitles: Reassortment, seqcombo introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqcombo/inst/doc/reassortment.R, vignettes/seqcombo/inst/doc/seqcombo.R Package: SeqGSEA Version: 1.22.1 Depends: Biobase, doParallel, DESeq Imports: methods, biomaRt Suggests: easyRNASeq, GenomicRanges License: GPL (>= 3) MD5sum: d7d5fe974beaea34e30ac28a1cd767e5 NeedsCompilation: no Title: Gene Set Enrichment Analysis (GSEA) of RNA-Seq Data: integrating differential expression and splicing Description: The package generally provides methods for gene set enrichment analysis of high-throughput RNA-Seq data by integrating differential expression and splicing. It uses negative binomial distribution to model read count data, which accounts for sequencing biases and biological variation. Based on permutation tests, statistical significance can also be achieved regarding each gene's differential expression and splicing, respectively. biocViews: ImmunoOncology, Sequencing, RNASeq, GeneSetEnrichment, GeneExpression, DifferentialExpression Author: Xi Wang Maintainer: Xi Wang git_url: https://git.bioconductor.org/packages/SeqGSEA git_branch: RELEASE_3_8 git_last_commit: 9ef68f0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SeqGSEA_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SeqGSEA_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SeqGSEA_1.22.1.tgz vignettes: vignettes/SeqGSEA/inst/doc/SeqGSEA.pdf vignetteTitles: Gene set enrichment analysis of RNA-Seq data with the SeqGSEA package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SeqGSEA/inst/doc/SeqGSEA.R Package: seqLogo Version: 1.48.0 Depends: methods, grid Imports: stats4 License: LGPL (>= 2) MD5sum: 435a5d989d6fcb86466ab7bbd546bf70 NeedsCompilation: no Title: Sequence logos for DNA sequence alignments Description: seqLogo takes the position weight matrix of a DNA sequence motif and plots the corresponding sequence logo as introduced by Schneider and Stephens (1990). biocViews: SequenceMatching Author: Oliver Bembom Maintainer: Oliver Bembom git_url: https://git.bioconductor.org/packages/seqLogo git_branch: RELEASE_3_8 git_last_commit: dde8558 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/seqLogo_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqLogo_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqLogo_1.48.0.tgz vignettes: vignettes/seqLogo/inst/doc/seqLogo.pdf vignetteTitles: Sequence logos for DNA sequence alignments hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqLogo/inst/doc/seqLogo.R dependsOnMe: motifRG, rGADEM importsMe: IntEREst, PWMEnrich, rGADEM, riboSeqR, SPLINTER, TFBSTools suggestsMe: BCRANK, DiffLogo, Logolas, motifcounter, universalmotif Package: seqPattern Version: 1.14.0 Depends: methods, R (>= 2.15.0) Imports: Biostrings, GenomicRanges, IRanges, KernSmooth, plotrix Suggests: BSgenome.Drerio.UCSC.danRer7, CAGEr, RUnit, BiocGenerics, BiocStyle Enhances: parallel License: GPL-3 MD5sum: eaa324090a3e3aea517439104aff6721 NeedsCompilation: no Title: Visualising oligonucleotide patterns and motif occurrences across a set of sorted sequences Description: Visualising oligonucleotide patterns and sequence motifs occurrences across a large set of sequences centred at a common reference point and sorted by a user defined feature. biocViews: Visualization, SequenceMatching Author: Vanja Haberle Maintainer: Vanja Haberle git_url: https://git.bioconductor.org/packages/seqPattern git_branch: RELEASE_3_8 git_last_commit: 0bf8fd0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/seqPattern_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqPattern_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqPattern_1.14.0.tgz vignettes: vignettes/seqPattern/inst/doc/seqPattern.pdf vignetteTitles: seqPattern hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqPattern/inst/doc/seqPattern.R importsMe: genomation Package: seqplots Version: 1.20.1 Depends: R (>= 3.2.0) Imports: methods, IRanges, BSgenome, digest, rtracklayer, GenomicRanges, Biostrings, shiny (>= 0.13.0), DBI, RSQLite, plotrix, fields, grid, kohonen, parallel, GenomeInfoDb, class, S4Vectors, ggplot2, reshape2, gridExtra, jsonlite, DT (>= 0.1.0), RColorBrewer, Rsamtools, GenomicAlignments, BiocManager Suggests: testthat, BiocStyle, knitr, rmarkdown, covr License: GPL-3 MD5sum: 4030865144e8d321585adc6804da6d37 NeedsCompilation: no Title: An interactive tool for visualizing NGS signals and sequence motif densities along genomic features using average plots and heatmaps Description: SeqPlots is a tool for plotting next generation sequencing (NGS) based experiments' signal tracks, e.g. reads coverage from ChIP-seq, RNA-seq and DNA accessibility assays like DNase-seq and MNase-seq, over user specified genomic features, e.g. promoters, gene bodies, etc. It can also calculate sequence motif density profiles from reference genome. The data are visualized as average signal profile plot, with error estimates (standard error and 95% confidence interval) shown as fields, or as series of heatmaps that can be sorted and clustered using hierarchical clustering, k-means algorithm and self organising maps. Plots can be prepared using R programming language or web browser based graphical user interface (GUI) implemented using Shiny framework. The dual-purpose implementation allows running the software locally on desktop or deploying it on server. SeqPlots is useful for both for exploratory data analyses and preparing replicable, publication quality plots. Other features of the software include collaboration and data sharing capabilities, as well as ability to store pre-calculated result matrixes, that combine many sequencing experiments and in-silico generated tracks with multiple different features. These binaries can be further used to generate new combination plots on fly, run automated batch operations or share with colleagues, who can adjust their plotting parameters without loading actual tracks and recalculating numeric values. SeqPlots relays on Bioconductor packages, mainly on rtracklayer for data input and BSgenome packages for reference genome sequence and annotations. biocViews: ImmunoOncology, ChIPSeq, RNASeq, Sequencing, Software, Visualization Author: Przemyslaw Stempor [aut, cph, cre] Maintainer: Przemyslaw Stempor URL: http://github.com/przemol/seqplots VignetteBuilder: knitr BugReports: http://github.com/przemol/seqplots/issues git_url: https://git.bioconductor.org/packages/seqplots git_branch: RELEASE_3_8 git_last_commit: 85f7caa git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/seqplots_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqplots_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqplots_1.20.1.tgz vignettes: vignettes/seqplots/inst/doc/QuickStart.html, vignettes/seqplots/inst/doc/SeqPlotsGUI.html vignetteTitles: Vignette Title, Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqplots/inst/doc/QuickStart.R, vignettes/seqplots/inst/doc/SeqPlotsGUI.R importsMe: ChIPSeqSpike Package: seqsetvis Version: 1.2.1 Depends: R (>= 3.5), ggplot2 Imports: data.table, eulerr, GenomeInfoDb, GenomicAlignments, GenomicRanges, grDevices, grid, IRanges, limma, methods, png, RColorBrewer, Rsamtools, rtracklayer, S4Vectors, stats Suggests: BiocFileCache, BiocManager, BiocStyle, ChIPpeakAnno, covr, cowplot, knitr, rmarkdown, testthat License: MIT + file LICENSE MD5sum: d552623ed8752b0c16305fd5a8b8345b NeedsCompilation: no Title: Set Based Visualizations for Next-Gen Sequencing Data Description: seqsetvis enables the visualization and analysis of multiple genomic datasets. Although seqsetvis was designed for the comparison of mulitple ChIP-seq datasets, this package is domain-agnostic and allows the processing of multiple genomic coordinate files (bed-like files) and signal files (bigwig files or bam pileups). biocViews: Software, ChIPSeq, Sequencing, Visualization Author: Joseph R Boyd [aut, cre] Maintainer: Joseph R Boyd VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/seqsetvis git_branch: RELEASE_3_8 git_last_commit: 10f20ae git_last_commit_date: 2019-02-15 Date/Publication: 2019-02-19 source.ver: src/contrib/seqsetvis_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqsetvis_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqsetvis_1.2.1.tgz vignettes: vignettes/seqsetvis/inst/doc/seqsetvis_overview.html vignetteTitles: Overview and Use Cases hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/seqsetvis/inst/doc/seqsetvis_overview.R Package: SeqSQC Version: 1.4.0 Depends: R (>= 3.4), ExperimentHub (>= 1.3.7), SNPRelate (>= 1.10.2) Imports: e1071, GenomicRanges, gdsfmt, ggplot2, GGally, IRanges, methods, rbokeh, RColorBrewer, reshape2, rmarkdown, S4Vectors, stats, utils Suggests: BiocStyle, knitr, testthat License: GPL-3 MD5sum: 567ec0880b33d8207b237e337e17fb98 NeedsCompilation: no Title: A bioconductor package for sample quality check with next generation sequencing data Description: The SeqSQC is designed to identify problematic samples in NGS data, including samples with gender mismatch, contamination, cryptic relatedness, and population outlier. biocViews: Experiment Data, Homo_sapiens_Data, Sequencing Data, Project1000genomes, Genome Author: Qian Liu [aut, cre] Maintainer: Qian Liu URL: https://github.com/Liubuntu/SeqSQC VignetteBuilder: knitr BugReports: https://github.com/Liubuntu/SeqSQC/issues git_url: https://git.bioconductor.org/packages/SeqSQC git_branch: RELEASE_3_8 git_last_commit: 6a30e5e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SeqSQC_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SeqSQC_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SeqSQC_1.4.0.tgz vignettes: vignettes/SeqSQC/inst/doc/vignette.html vignetteTitles: Sample Quality Check for Next-Generation Sequencing Data with SeqSQC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SeqSQC/inst/doc/vignette.R Package: seqTools Version: 1.16.0 Depends: methods,utils,zlibbioc LinkingTo: zlibbioc Suggests: RUnit, BiocGenerics License: Artistic-2.0 MD5sum: fb3f61a5e3916be5eb4ab19e44b857d5 NeedsCompilation: yes Title: Analysis of nucleotide, sequence and quality content on fastq files Description: Analyze read length, phred scores and alphabet frequency and DNA k-mers on uncompressed and compressed fastq files. biocViews: QualityControl,Sequencing Author: Wolfgang Kaisers Maintainer: Wolfgang Kaisers git_url: https://git.bioconductor.org/packages/seqTools git_branch: RELEASE_3_8 git_last_commit: 420c3f6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/seqTools_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/seqTools_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/seqTools_1.16.0.tgz vignettes: vignettes/seqTools/inst/doc/seqTools_qual_report.pdf, vignettes/seqTools/inst/doc/seqTools.pdf vignetteTitles: seqTools_qual_report, Introduction hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/seqTools/inst/doc/seqTools_qual_report.R, vignettes/seqTools/inst/doc/seqTools.R Package: SeqVarTools Version: 1.20.2 Depends: SeqArray Imports: grDevices, graphics, stats, methods, Biobase, gdsfmt, GenomicRanges, IRanges, S4Vectors, GWASExactHW, logistf, Matrix, dplyr, rlang, tidyr Suggests: BiocGenerics, BiocStyle, RUnit, stringr License: GPL-3 Archs: i386, x64 MD5sum: d3a7c78c788be05f37e3a9ff572b6039 NeedsCompilation: no Title: Tools for variant data Description: An interface to the fast-access storage format for VCF data provided in SeqArray, with tools for common operations and analysis. biocViews: SNP, GeneticVariability, Sequencing, Genetics Author: Stephanie M. Gogarten, Xiuwen Zheng, Adrienne Stilp Maintainer: Stephanie M. Gogarten URL: https://github.com/smgogarten/SeqVarTools git_url: https://git.bioconductor.org/packages/SeqVarTools git_branch: RELEASE_3_8 git_last_commit: 92fe035 git_last_commit_date: 2019-02-26 Date/Publication: 2019-02-27 source.ver: src/contrib/SeqVarTools_1.20.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/SeqVarTools_1.20.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SeqVarTools_1.20.2.tgz vignettes: vignettes/SeqVarTools/inst/doc/SeqVarTools.pdf vignetteTitles: Introduction to SeqVarTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SeqVarTools/inst/doc/SeqVarTools.R importsMe: GENESIS Package: sesame Version: 1.0.0 Depends: R (>= 3.5), sesameData, methods Imports: R6, grDevices, utils, illuminaio, MASS, GenomicRanges, IRanges, grid, preprocessCore, stats, S4Vectors, randomForest, wheatmap, ggplot2, parallel, DNAcopy Suggests: scales, knitr, rmarkdown, testthat, minfi, SummarizedExperiment, FlowSorted.CordBloodNorway.450k License: Artistic-2.0 MD5sum: 39b48bfe5a5aca7b74685fd0a922aed4 NeedsCompilation: no Title: Tools For Analyzing Illumina Infinium DNA Methylation Arrays Description: Tools For analyzing Illumina Infinium DNA methylation arrays. biocViews: DNAMethylation, MethylationArray, Preprocessing, QualityControl Author: Wanding Zhou [aut, cre], Hui Shen [aut], Timothy Triche [ctb] Maintainer: Wanding Zhou URL: https://github.com/zwdzwd/sesame VignetteBuilder: knitr BugReports: https://github.com/zwdzwd/sesame/issues git_url: https://git.bioconductor.org/packages/sesame git_branch: RELEASE_3_8 git_last_commit: 8a9c43d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sesame_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sesame_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sesame_1.0.0.tgz vignettes: vignettes/sesame/inst/doc/sesame.html vignetteTitles: SeSAMe User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sesame/inst/doc/sesame.R importsMe: TCGAbiolinks, TCGAbiolinksGUI Package: sevenbridges Version: 1.12.5 Depends: methods, utils, stats Imports: httr, jsonlite, yaml, objectProperties, stringr, S4Vectors, docopt, curl, uuid, dplyr Suggests: knitr, rmarkdown, testthat, readr License: Apache License 2.0 | file LICENSE MD5sum: d2552e8cc90601590215e4b124a69d37 NeedsCompilation: no Title: Seven Bridges Platform API Client and Common Workflow Language Tool Builder in R Description: R client and utilities for Seven Bridges platform API, from Cancer Genomics Cloud to other Seven Bridges supported platforms. biocViews: Software, DataImport, ThirdPartyClient Author: Nan Xiao [aut, cre], Tengfei Yin [aut], Emile Young [ctb], Dusan Randjelovic [ctb], Seven Bridges Genomics [cph, fnd] Maintainer: Nan Xiao URL: https://www.sevenbridges.com, https://sbg.github.io/sevenbridges-r/, https://github.com/sbg/sevenbridges-r VignetteBuilder: knitr BugReports: https://github.com/sbg/sevenbridges-r/issues git_url: https://git.bioconductor.org/packages/sevenbridges git_branch: RELEASE_3_8 git_last_commit: 9b8e0ef git_last_commit_date: 2019-03-21 Date/Publication: 2019-03-21 source.ver: src/contrib/sevenbridges_1.12.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/sevenbridges_1.12.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sevenbridges_1.12.5.tgz vignettes: vignettes/sevenbridges/inst/doc/api.html, vignettes/sevenbridges/inst/doc/apps.html, vignettes/sevenbridges/inst/doc/bioc-workflow.html, vignettes/sevenbridges/inst/doc/cgc-datasets.html, vignettes/sevenbridges/inst/doc/docker.html, vignettes/sevenbridges/inst/doc/rstudio.html vignetteTitles: Complete Guide for Seven Bridges API R Client, Describe and Execute CWL Tools/Workflows in R, Master Tutorial: Use R for Cancer Genomics Cloud, Find Data on CGC via Data Browser and Datasets API, Creating Your Docker Container and Command Line Interface (with docopt), IDE Container: RStudio Server,, Shiny Server,, and More hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/sevenbridges/inst/doc/api.R, vignettes/sevenbridges/inst/doc/apps.R, vignettes/sevenbridges/inst/doc/bioc-workflow.R, vignettes/sevenbridges/inst/doc/cgc-datasets.R, vignettes/sevenbridges/inst/doc/docker.R, vignettes/sevenbridges/inst/doc/rstudio.R Package: sevenC Version: 1.2.0 Depends: R (>= 3.5), InteractionSet (>= 1.2.0) Imports: rtracklayer (>= 1.34.1), BiocGenerics (>= 0.22.0), GenomeInfoDb (>= 1.12.2), GenomicRanges (>= 1.28.5), IRanges (>= 2.10.3), S4Vectors (>= 0.14.4), readr (>= 1.1.0), purrr (>= 0.2.2), data.table (>= 1.10.4), boot (>= 1.3-20), methods (>= 3.4.1) Suggests: testthat, BiocStyle, knitr, rmarkdown, GenomicInteractions, covr License: GPL-3 MD5sum: 276812bfe5e2ed5a8d6e7cd28c4effb9 NeedsCompilation: no Title: Computational Chromosome Conformation Capture by Correlation of ChIP-seq at CTCF motifs Description: Chromatin looping is an essential feature of eukaryotic genomes and can bring regulatory sequences, such as enhancers or transcription factor binding sites, in the close physical proximity of regulated target genes. Here, we provide sevenC, an R package that uses protein binding signals from ChIP-seq and sequence motif information to predict chromatin looping events. Cross-linking of proteins that bind close to loop anchors result in ChIP-seq signals at both anchor loci. These signals are used at CTCF motif pairs together with their distance and orientation to each other to predict whether they interact or not. The resulting chromatin loops might be used to associate enhancers or transcription factor binding sites (e.g., ChIP-seq peaks) to regulated target genes. biocViews: DNA3DStructure, ChIPchip, Coverage, DataImport, Epigenetics, FunctionalGenomics, Classification, Regression, ChIPSeq, HiC, Annotation Author: Jonas Ibn-Salem [aut, cre] Maintainer: Jonas Ibn-Salem URL: https://github.com/ibn-salem/sevenC VignetteBuilder: knitr BugReports: https://github.com/ibn-salem/sevenC/issues git_url: https://git.bioconductor.org/packages/sevenC git_branch: RELEASE_3_8 git_last_commit: 73bde3f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sevenC_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sevenC_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sevenC_1.2.0.tgz vignettes: vignettes/sevenC/inst/doc/sevenC.html vignetteTitles: Introduction to sevenC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sevenC/inst/doc/sevenC.R Package: SGSeq Version: 1.16.2 Depends: IRanges (>= 2.13.15), GenomicRanges (>= 1.31.10), Rsamtools (>= 1.31.2), SummarizedExperiment, methods Imports: AnnotationDbi, BiocGenerics, Biostrings (>= 2.47.6), GenomicAlignments (>= 1.15.7), GenomicFeatures (>= 1.31.5), GenomeInfoDb, RUnit, S4Vectors (>= 0.17.28), grDevices, graphics, igraph, parallel, rtracklayer (>= 1.39.7), stats Suggests: BiocStyle, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, knitr, rmarkdown License: Artistic-2.0 MD5sum: 031623023d4aae8f1ea43b159ffe13ab NeedsCompilation: no Title: Splice event prediction and quantification from RNA-seq data Description: SGSeq is a software package for analyzing splice events from RNA-seq data. Input data are RNA-seq reads mapped to a reference genome in BAM format. Genes are represented as a splice graph, which can be obtained from existing annotation or predicted from the mapped sequence reads. Splice events are identified from the graph and are quantified locally using structurally compatible reads at the start or end of each splice variant. The software includes functions for splice event prediction, quantification, visualization and interpretation. biocViews: AlternativeSplicing, ImmunoOncology, RNASeq, Transcription Author: Leonard Goldstein Maintainer: Leonard Goldstein VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SGSeq git_branch: RELEASE_3_8 git_last_commit: ac7e0ff git_last_commit_date: 2018-12-18 Date/Publication: 2018-12-19 source.ver: src/contrib/SGSeq_1.16.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/SGSeq_1.16.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SGSeq_1.16.2.tgz vignettes: vignettes/SGSeq/inst/doc/SGSeq.html vignetteTitles: SGSeq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SGSeq/inst/doc/SGSeq.R dependsOnMe: EventPointer Package: shinyMethyl Version: 1.18.0 Depends: methods, BiocGenerics (>= 0.3.2), shiny (>= 0.13.2), minfi (>= 1.18.2), IlluminaHumanMethylation450kmanifest, matrixStats, R (>= 3.0.0) Imports: RColorBrewer Suggests: shinyMethylData, minfiData, BiocStyle, RUnit, digest, knitr License: Artistic-2.0 MD5sum: fb818769476e39badee29c91a49736dc NeedsCompilation: no Title: Interactive visualization for Illumina methylation arrays Description: Interactive tool for visualizing Illumina methylation array data. Both the 450k and EPIC array are supported. biocViews: DNAMethylation, Microarray, TwoChannel, Preprocessing, QualityControl Author: Jean-Philippe Fortin [cre, aut], Kasper Daniel Hansen [aut] Maintainer: Jean-Philippe Fortin VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/shinyMethyl git_branch: RELEASE_3_8 git_last_commit: 0a65e01 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/shinyMethyl_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/shinyMethyl_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/shinyMethyl_1.18.0.tgz vignettes: vignettes/shinyMethyl/inst/doc/shinyMethyl.pdf vignetteTitles: shinyMethyl: interactive visualization of Illumina 450K methylation arrays hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/shinyMethyl/inst/doc/shinyMethyl.R Package: shinyTANDEM Version: 1.20.1 Depends: rTANDEM (>= 1.3.5), shiny, mixtools, methods, xtable License: GPL-3 MD5sum: 214390e95f00e0aa251e71caae2f37c9 NeedsCompilation: no Title: Provides a GUI for rTANDEM Description: This package provides a GUI interface for rTANDEM. The GUI is primarily designed to visualize rTANDEM result object or result xml files. But it will also provides an interface for creating parameter objects, launching searches or performing conversions between R objects and xml files. biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Frederic Fournier , Arnaud Droit Maintainer: Frederic Fournier git_url: https://git.bioconductor.org/packages/shinyTANDEM git_branch: RELEASE_3_8 git_last_commit: e6558f0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/shinyTANDEM_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/shinyTANDEM_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/shinyTANDEM_1.20.1.tgz vignettes: vignettes/shinyTANDEM/inst/doc/shinyTANDEM.pdf vignetteTitles: shinyTANDEM user guide hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: ShortRead Version: 1.40.0 Depends: BiocGenerics (>= 0.23.3), BiocParallel, Biostrings (>= 2.47.6), Rsamtools (>= 1.31.2), GenomicAlignments (>= 1.15.6) Imports: Biobase, S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), GenomeInfoDb (>= 1.15.2), GenomicRanges (>= 1.31.8), hwriter, methods, zlibbioc, lattice, latticeExtra, LinkingTo: S4Vectors, IRanges, XVector, Biostrings Suggests: BiocStyle, RUnit, biomaRt, GenomicFeatures, yeastNagalakshmi License: Artistic-2.0 MD5sum: 455d4397ae013d40ad8f5eb6e215d6b7 NeedsCompilation: yes Title: FASTQ input and manipulation Description: This package implements sampling, iteration, and input of FASTQ files. The package includes functions for filtering and trimming reads, and for generating a quality assessment report. Data are represented as DNAStringSet-derived objects, and easily manipulated for a diversity of purposes. The package also contains legacy support for early single-end, ungapped alignment formats. biocViews: DataImport, Sequencing, QualityControl Author: Martin Morgan, Michael Lawrence, Simon Anders Maintainer: Bioconductor Package Maintainer git_url: https://git.bioconductor.org/packages/ShortRead git_branch: RELEASE_3_8 git_last_commit: 0cbe4b6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ShortRead_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ShortRead_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ShortRead_1.40.0.tgz vignettes: vignettes/ShortRead/inst/doc/Overview.pdf vignetteTitles: An introduction to ShortRead hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ShortRead/inst/doc/Overview.R dependsOnMe: chipseq, EDASeq, esATAC, girafe, HTSeqGenie, OTUbase, Rqc, rSFFreader, segmentSeq, systemPipeR importsMe: amplican, ArrayExpressHTS, basecallQC, BEAT, chipseq, ChIPseqR, ChIPsim, dada2, easyRNASeq, FastqCleaner, GOTHiC, icetea, IONiseR, MACPET, nucleR, QuasR, R453Plus1Toolbox, RSVSim, scruff suggestsMe: BiocParallel, CSAR, DBChIP, GenomicAlignments, Genominator, PICS, PING, Repitools, Rsamtools, S4Vectors Package: SIAMCAT Version: 1.2.1 Depends: R (>= 3.5.0), mlr, phyloseq Imports: beanplot, glmnet, graphics, grDevices, grid, gridBase, gridExtra, LiblineaR, matrixStats, methods, ParamHelpers, pROC, PRROC, RColorBrewer, scales, stats, stringr, utils, infotheo, corrplot Suggests: BiocStyle, optparse, testthat, knitr, rmarkdown License: GPL-3 Archs: i386, x64 MD5sum: 727a0a4ace5609d95fd51dc44bdf5284 NeedsCompilation: no Title: Statistical Inference of Associations between Microbial Communities And host phenoTypes Description: Pipeline for Statistical Inference of Associations between Microbial Communities And host phenoTypes (SIAMCAT). A primary goal of analyzing microbiome data is to determine changes in community composition that are associated with environmental factors. In particular, linking human microbiome composition to host phenotypes such as diseases has become an area of intense research. For this, robust statistical modeling and biomarker extraction toolkits are crucially needed. SIAMCAT provides a full pipeline supporting data preprocessing, statistical association testing, statistical modeling (LASSO logistic regression) including tools for evaluation and interpretation of these models (such as cross validation, parameter selection, ROC analysis and diagnostic model plots). biocViews: ImmunoOncology, Metagenomics, Classification, Microbiome, Sequencing, Preprocessing, Clustering, FeatureExtraction, GeneticVariability, MultipleComparison, Regression Author: Konrad Zych [aut, cre] (), Jakob Wirbel [aut] (), Georg Zeller [aut] (), Morgan Essex [ctb], Nicolai Karcher [ctb], Kersten Breuer [ctb] Maintainer: Konrad Zych VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SIAMCAT git_branch: RELEASE_3_8 git_last_commit: 4f0a7ca git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SIAMCAT_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SIAMCAT_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SIAMCAT_1.2.1.tgz vignettes: vignettes/SIAMCAT/inst/doc/SIAMCAT_holdout.html, vignettes/SIAMCAT/inst/doc/SIAMCAT_read-in.html, vignettes/SIAMCAT/inst/doc/SIAMCAT_vignette.html vignetteTitles: SIAMCAT holdout testing vignette, SIAMCAT.input, SIAMCAT basic vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SIAMCAT/inst/doc/SIAMCAT_holdout.R, vignettes/SIAMCAT/inst/doc/SIAMCAT_read-in.R, vignettes/SIAMCAT/inst/doc/SIAMCAT_vignette.R Package: SICtools Version: 1.12.0 Depends: R (>= 3.0.0), methods, Rsamtools (>= 1.18.1), doParallel (>= 1.0.8), Biostrings (>= 2.32.1), stringr (>= 0.6.2), matrixStats (>= 0.10.0), plyr (>= 1.8.3), GenomicRanges (>= 1.22.4), IRanges (>= 2.4.8) Suggests: knitr, RUnit, BiocGenerics License: GPL (>=2) MD5sum: 4e9730f2194cfb50c7808bfe43f0c3af NeedsCompilation: yes Title: Find SNV/Indel differences between two bam files with near relationship Description: This package is to find SNV/Indel differences between two bam files with near relationship in a way of pairwise comparison thourgh each base position across the genome region of interest. The difference is inferred by fisher test and euclidean distance, the input of which is the base count (A,T,G,C) in a given position and read counts for indels that span no less than 2bp on both sides of indel region. biocViews: Alignment, Sequencing, Coverage, SequenceMatching, QualityControl, DataImport, Software, SNP, VariantDetection Author: Xiaobin Xing, Wu Wei Maintainer: Xiaobin Xing VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SICtools git_branch: RELEASE_3_8 git_last_commit: 5e62f40 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SICtools_1.12.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SICtools_1.12.0.tgz vignettes: vignettes/SICtools/inst/doc/SICtools.pdf vignetteTitles: Using SICtools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SICtools/inst/doc/SICtools.R Package: sigaR Version: 1.30.0 Depends: Biobase, CGHbase, methods, mvtnorm, Imports: corpcor (>= 1.6.2), graphics, igraph, limma, marray, MASS, penalized, quadprog, snowfall, stats Suggests: CGHcall License: GPL (>= 2) MD5sum: f27d79fb98bc4327fbc638f140a3f0d7 NeedsCompilation: no Title: Statistics for Integrative Genomics Analyses in R Description: Facilitates the joint analysis of high-throughput data from multiple molecular levels. Contains functions for manipulation of objects, various analysis types, and some visualization. biocViews: Microarray, DifferentialExpression, aCGH, GeneExpression, Pathways Author: Wessel N. van Wieringen Maintainer: Wessel N. van Wieringen URL: http://www.few.vu.nl/~wvanwie git_url: https://git.bioconductor.org/packages/sigaR git_branch: RELEASE_3_8 git_last_commit: c2a13ff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sigaR_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sigaR_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sigaR_1.30.0.tgz vignettes: vignettes/sigaR/inst/doc/sigaR.pdf vignetteTitles: sigaR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sigaR/inst/doc/sigaR.R Package: SigCheck Version: 2.14.0 Depends: R (>= 3.2.0), MLInterfaces, Biobase, e1071, BiocParallel, survival Imports: graphics, stats, utils, methods Suggests: BiocStyle, breastCancerNKI, qusage License: Artistic-2.0 MD5sum: f63b63b11545697c94145639594dd0bb NeedsCompilation: no Title: Check a gene signature's prognostic performance against random signatures, known signatures, and permuted data/metadata Description: While gene signatures are frequently used to predict phenotypes (e.g. predict prognosis of cancer patients), it it not always clear how optimal or meaningful they are (cf David Venet, Jacques E. Dumont, and Vincent Detours' paper "Most Random Gene Expression Signatures Are Significantly Associated with Breast Cancer Outcome"). Based on suggestions in that paper, SigCheck accepts a data set (as an ExpressionSet) and a gene signature, and compares its performance on survival and/or classification tasks against a) random gene signatures of the same length; b) known, related and unrelated gene signatures; and c) permuted data and/or metadata. biocViews: GeneExpression, Classification, GeneSetEnrichment Author: Rory Stark and Justin Norden Maintainer: Rory Stark git_url: https://git.bioconductor.org/packages/SigCheck git_branch: RELEASE_3_8 git_last_commit: ce2b1bb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SigCheck_2.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SigCheck_2.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SigCheck_2.14.0.tgz vignettes: vignettes/SigCheck/inst/doc/SigCheck.pdf vignetteTitles: Checking gene expression signatures against random and known signatures with SigCheck hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SigCheck/inst/doc/SigCheck.R Package: sigFeature Version: 1.0.0 Depends: R (>= 3.5.0) Imports: biocViews, nlme, e1071, openxlsx, pheatmap, RColorBrewer, Matrix, SparseM, graphics, stats, utils, SummarizedExperiment, BiocParallel, methods Suggests: RUnit, BiocGenerics, knitr License: GPL MD5sum: 5e75e6f3818225a0b8135d9cd4acaaa6 NeedsCompilation: no Title: sigFeature: Significant feature selection using SVM-RFE & t-statistic Description: This package provides a novel feature selection algorithm for binary classification using support vector machine recursive feature elimination SVM-RFE and t-statistic. In this feature selection process, the selected features are differentially significant between the two classes and also they are good classifier with higher degree of classification accuracy. biocViews: FeatureExtraction, GeneExpression, Microarray, Transcription, mRNAMicroarray, GenePrediction, Normalization, Classification, SupportVectorMachine Author: Pijush Das Developer [aut, cre], Dr. Susanta Roychudhury User [ctb], Dr. Sucheta Tripathy User [ctb] Maintainer: Pijush Das Developer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/sigFeature git_branch: RELEASE_3_8 git_last_commit: 40d2a91 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sigFeature_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sigFeature_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sigFeature_1.0.0.tgz vignettes: vignettes/sigFeature/inst/doc/vignettes.pdf vignetteTitles: sigFeature hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/sigFeature/inst/doc/vignettes.R Package: SigFuge Version: 1.20.0 Depends: R (>= 3.1.1), GenomicRanges Imports: ggplot2, matlab, reshape, sigclust Suggests: org.Hs.eg.db, prebsdata, Rsamtools (>= 1.17.0), TxDb.Hsapiens.UCSC.hg19.knownGene, BiocStyle License: GPL-3 MD5sum: 617321ada3ea3a85d48d9643d6d64ecc NeedsCompilation: no Title: SigFuge Description: Algorithm for testing significance of clustering in RNA-seq data. biocViews: Clustering, Visualization, RNASeq Author: Patrick Kimes, Christopher Cabanski Maintainer: Patrick Kimes git_url: https://git.bioconductor.org/packages/SigFuge git_branch: RELEASE_3_8 git_last_commit: c97e0e1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SigFuge_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SigFuge_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SigFuge_1.20.0.tgz vignettes: vignettes/SigFuge/inst/doc/SigFuge.pdf vignetteTitles: SigFuge Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SigFuge/inst/doc/SigFuge.R Package: siggenes Version: 1.56.0 Depends: methods, Biobase, multtest, splines, graphics Imports: stats4 Suggests: affy, annotate, genefilter, KernSmooth, scrime (>= 1.2.5) License: LGPL (>= 2) MD5sum: 28a8f05b99d9576b8ace9ea342efe70c NeedsCompilation: no Title: Multiple testing using SAM and Efron's empirical Bayes approaches Description: Identification of differentially expressed genes and estimation of the False Discovery Rate (FDR) using both the Significance Analysis of Microarrays (SAM) and the Empirical Bayes Analyses of Microarrays (EBAM). biocViews: MultipleComparison, Microarray, GeneExpression, SNP, ExonArray, DifferentialExpression Author: Holger Schwender Maintainer: Holger Schwender git_url: https://git.bioconductor.org/packages/siggenes git_branch: RELEASE_3_8 git_last_commit: 3e929fe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/siggenes_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/siggenes_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/siggenes_1.56.0.tgz vignettes: vignettes/siggenes/inst/doc/siggenes.pdf vignetteTitles: siggenes Manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/siggenes/inst/doc/siggenes.R dependsOnMe: KCsmart importsMe: charm, coexnet, DAPAR, GeneSelector, minfi, XDE suggestsMe: GeneSelector, logicFS, trio Package: sights Version: 1.8.1 Depends: R(>= 3.3) Imports: MASS(>= 7.3), qvalue(>= 2.2), ggplot2(>= 2.0), reshape2(>= 1.4), lattice(>= 0.2), stats(>= 3.3) Suggests: testthat, knitr, rmarkdown, ggthemes, gridExtra, xlsx License: GPL-3 | file LICENSE MD5sum: dcde5fa8f307cd2169f574b72abb32ec NeedsCompilation: no Title: Statistics and dIagnostic Graphs for HTS Description: SIGHTS is a suite of normalization methods, statistical tests, and diagnostic graphical tools for high throughput screening (HTS) assays. HTS assays use microtitre plates to screen large libraries of compounds for their biological, chemical, or biochemical activity. biocViews: ImmunoOncology, CellBasedAssays, MicrotitrePlateAssay, Normalization, MultipleComparison, Preprocessing, QualityControl, BatchEffect, Visualization Author: Elika Garg [aut, cre], Carl Murie [aut], Heydar Ensha [ctb], Robert Nadon [aut] Maintainer: Elika Garg URL: https://eg-r.github.io/sights/ VignetteBuilder: knitr BugReports: https://github.com/eg-r/sights/issues git_url: https://git.bioconductor.org/packages/sights git_branch: RELEASE_3_8 git_last_commit: 94a5d74 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sights_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sights_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sights_1.8.1.tgz vignettes: vignettes/sights/inst/doc/sights.html vignetteTitles: Using **SIGHTS** R-package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/sights/inst/doc/sights.R Package: signeR Version: 1.8.0 Depends: VariantAnnotation, NMF Imports: BiocGenerics, Biostrings, class, graphics, grDevices, GenomicRanges, nloptr, methods, stats, utils, PMCMR LinkingTo: Rcpp, RcppArmadillo (>= 0.7.100) Suggests: knitr, rtracklayer, BSgenome.Hsapiens.UCSC.hg19 License: GPL-3 MD5sum: 79074171d5f1f9af6f93abcfcc96cbe1 NeedsCompilation: yes Title: Empirical Bayesian approach to mutational signature discovery Description: The signeR package provides an empirical Bayesian approach to mutational signature discovery. It is designed to analyze single nucleotide variaton (SNV) counts in cancer genomes, but can also be applied to other features as well. Functionalities to characterize signatures or genome samples according to exposure patterns are also provided. biocViews: GenomicVariation, SomaticMutation, StatisticalMethod, Visualization Author: Rafael Rosales, Rodrigo Drummond, Renan Valieris, Israel Tojal da Silva Maintainer: Renan Valieris URL: https://github.com/rvalieris/signeR SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/signeR git_branch: RELEASE_3_8 git_last_commit: a99d4d7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/signeR_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/signeR_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/signeR_1.8.0.tgz vignettes: vignettes/signeR/inst/doc/signeR-vignette.html vignetteTitles: signeR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/signeR/inst/doc/signeR-vignette.R Package: signet Version: 1.2.3 Depends: R (>= 3.4.0) Imports: graph, igraph, RBGL, graphics, utils, stats, methods Suggests: graphite, BiocStyle, knitr, rmarkdown License: GPL-2 Archs: i386, x64 MD5sum: 2fc1635f464735f6255c820c777d568a NeedsCompilation: no Title: signet: Selection Inference in Gene NETworks Description: An R package to detect selection in biological pathways. Using gene selection scores and biological pathways data, one can search for high-scoring subnetworks of genes within pathways and test their significance. biocViews: Software, Pathways, DifferentialExpression, GeneExpression, NetworkEnrichment, GraphAndNetwork, KEGG Author: Alexandre Gouy [aut, cre] Maintainer: Alexandre Gouy VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/signet git_branch: RELEASE_3_8 git_last_commit: d9e212e git_last_commit_date: 2019-04-11 Date/Publication: 2019-04-14 source.ver: src/contrib/signet_1.2.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/signet_1.2.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/signet_1.2.3.tgz vignettes: vignettes/signet/inst/doc/signet.html vignetteTitles: signet tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/signet/inst/doc/signet.R Package: sigPathway Version: 1.50.0 Depends: R (>= 2.10) Suggests: hgu133a.db (>= 1.10.0), XML (>= 1.6-3), AnnotationDbi (>= 1.3.12) License: GPL-2 MD5sum: b825fbbd08a65e76c61fef39eab3492b NeedsCompilation: yes Title: Pathway Analysis Description: Conducts pathway analysis by calculating the NT_k and NE_k statistics as described in Tian et al. (2005) biocViews: DifferentialExpression, MultipleComparison Author: Weil Lai (optimized R and C code), Lu Tian and Peter Park (algorithm development and initial R code) Maintainer: Weil Lai URL: http://www.pnas.org/cgi/doi/10.1073/pnas.0506577102, http://www.chip.org/~ppark/Supplements/PNAS05.html git_url: https://git.bioconductor.org/packages/sigPathway git_branch: RELEASE_3_8 git_last_commit: 2050a1e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sigPathway_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sigPathway_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sigPathway_1.50.0.tgz vignettes: vignettes/sigPathway/inst/doc/sigPathway-vignette.pdf vignetteTitles: sigPathway hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sigPathway/inst/doc/sigPathway-vignette.R dependsOnMe: tRanslatome Package: sigsquared Version: 1.14.0 Depends: R (>= 3.2.0), methods Imports: Biobase, survival Suggests: RUnit, BiocGenerics License: GPL version 3 Archs: i386, x64 MD5sum: 3cc54becc997d3072a3c626a4267462b NeedsCompilation: no Title: Gene signature generation for functionally validated signaling pathways Description: By leveraging statistical properties (log-rank test for survival) of patient cohorts defined by binary thresholds, poor-prognosis patients are identified by the sigsquared package via optimization over a cost function reducing type I and II error. Author: UnJin Lee Maintainer: UnJin Lee git_url: https://git.bioconductor.org/packages/sigsquared git_branch: RELEASE_3_8 git_last_commit: 689d036 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sigsquared_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sigsquared_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sigsquared_1.14.0.tgz vignettes: vignettes/sigsquared/inst/doc/sigsquared.pdf vignetteTitles: SigSquared hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sigsquared/inst/doc/sigsquared.R Package: SIM Version: 1.52.0 Depends: R (>= 2.4), quantreg Imports: graphics, stats, globaltest, quantsmooth Suggests: biomaRt, RColorBrewer License: GPL (>= 2) MD5sum: 1c7164bbcfbc8d3dfb2495875c3aa478 NeedsCompilation: yes Title: Integrated Analysis on two human genomic datasets Description: Finds associations between two human genomic datasets. biocViews: Microarray, Visualization Author: Renee X. de Menezes and Judith M. Boer Maintainer: Renee X. de Menezes git_url: https://git.bioconductor.org/packages/SIM git_branch: RELEASE_3_8 git_last_commit: 0d16b7e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SIM_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SIM_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SIM_1.52.0.tgz vignettes: vignettes/SIM/inst/doc/SIM.pdf vignetteTitles: SIM vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SIM/inst/doc/SIM.R Package: SIMAT Version: 1.14.1 Depends: R (>= 3.5.0), Rcpp (>= 0.11.3) Imports: mzR, ggplot2, grid, reshape2, grDevices, stats, utils Suggests: RUnit, BiocGenerics License: GPL-2 Archs: i386, x64 MD5sum: e8179ed6f60f1fa1f071a58b60ef5e52 NeedsCompilation: no Title: GC-SIM-MS data processing and alaysis tool Description: This package provides a pipeline for analysis of GC-MS data acquired in selected ion monitoring (SIM) mode. The tool also provides a guidance in choosing appropriate fragments for the targets of interest by using an optimization algorithm. This is done by considering overlapping peaks from a provided library by the user. biocViews: ImmunoOncology, Software, Metabolomics, MassSpectrometry Author: M. R. Nezami Ranjbar Maintainer: M. R. Nezami Ranjbar URL: http://omics.georgetown.edu/SIMAT.html git_url: https://git.bioconductor.org/packages/SIMAT git_branch: RELEASE_3_8 git_last_commit: 8a168c6 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SIMAT_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SIMAT_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SIMAT_1.14.1.tgz vignettes: vignettes/SIMAT/inst/doc/SIMAT-vignette.pdf vignetteTitles: SIMAT Usage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SIMAT/inst/doc/SIMAT-vignette.R Package: SimBindProfiles Version: 1.20.0 Depends: R (>= 2.10), methods, Ringo Imports: limma, mclust, Biobase License: GPL-3 MD5sum: 1bebc53f15f0afdd77b7512beaf06c28 NeedsCompilation: no Title: Similar Binding Profiles Description: SimBindProfiles identifies common and unique binding regions in genome tiling array data. This package does not rely on peak calling, but directly compares binding profiles processed on the same array platform. It implements a simple threshold approach, thus allowing retrieval of commonly and differentially bound regions between datasets as well as events of compensation and increased binding. biocViews: Microarray, Software Author: Bettina Fischer, Enrico Ferrero, Robert Stojnic, Steve Russell Maintainer: Bettina Fischer git_url: https://git.bioconductor.org/packages/SimBindProfiles git_branch: RELEASE_3_8 git_last_commit: 2fad013 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SimBindProfiles_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SimBindProfiles_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SimBindProfiles_1.20.0.tgz vignettes: vignettes/SimBindProfiles/inst/doc/SimBindProfiles.pdf vignetteTitles: SimBindProfiles: Similar Binding Profiles,, identifies common and unique regions in array genome tiling array data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SimBindProfiles/inst/doc/SimBindProfiles.R Package: SIMD Version: 1.0.0 Depends: R (>= 3.5.0) Imports: edgeR, statmod, methylMnM, stats, utils Suggests: BiocStyle, knitr,rmarkdown License: GPL-3 MD5sum: 385e8cbf0131d3ef3707b6ba582948e8 NeedsCompilation: yes Title: Statistical Inferences with MeDIP-seq Data (SIMD) to infer the methylation level for each CpG site Description: This package provides a inferential analysis method for detecting differentially expressed CpG sites in MeDIP-seq data. It uses statistical framework and EM algorithm, to identify differentially expressed CpG sites. The methods on this package are described in the article 'Methylation-level Inferences and Detection of Differential Methylation with Medip-seq Data' by Yan Zhou, Jiadi Zhu, Mingtao Zhao, Baoxue Zhang, Chunfu Jiang and Xiyan Yang (2018, pending publication). biocViews: DifferentialMethylation,SingleCell, DifferentialExpression Author: Yan Zhou Maintainer: Jiadi Zhu <2160090406@email.szu.edu.cn> VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SIMD git_branch: RELEASE_3_8 git_last_commit: d18a51d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SIMD_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SIMD_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SIMD_1.0.0.tgz vignettes: vignettes/SIMD/inst/doc/SIMD.html vignetteTitles: SIMD Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SIMD/inst/doc/SIMD.R Package: similaRpeak Version: 1.14.0 Depends: R6 (>= 2.0) Imports: stats Suggests: RUnit, BiocGenerics, knitr, Rsamtools, GenomicAlignments, rtracklayer, rmarkdown, BiocStyle License: Artistic-2.0 Archs: i386, x64 MD5sum: 5131bceb89b919a1df752c9047a55671 NeedsCompilation: no Title: Metrics to estimate a level of similarity between two ChIP-Seq profiles Description: This package calculates metrics which assign a level of similarity between ChIP-Seq profiles. biocViews: BiologicalQuestion, ChIPSeq, Genetics, MultipleComparison, DifferentialExpression Author: Astrid Deschenes [cre, aut], Elsa Bernatchez [aut], Charles Joly Beauparlant [aut], Fabien Claude Lamaze [aut], Rawane Samb [aut], Pascal Belleau [aut], Arnaud Droit [aut] Maintainer: Astrid Deschenes URL: https://github.com/adeschen/similaRpeak VignetteBuilder: knitr BugReports: https://github.com/adeschen/similaRpeak/issues git_url: https://git.bioconductor.org/packages/similaRpeak git_branch: RELEASE_3_8 git_last_commit: 2c725a6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/similaRpeak_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/similaRpeak_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/similaRpeak_1.14.0.tgz vignettes: vignettes/similaRpeak/inst/doc/similaRpeak.html vignetteTitles: Similarity between two ChIP-Seq profiles hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/similaRpeak/inst/doc/similaRpeak.R suggestsMe: metagene Package: SIMLR Version: 1.8.1 Depends: R (>= 3.5), Imports: parallel, Matrix, stats, methods, Rcpp, pracma, RcppAnnoy, RSpectra LinkingTo: Rcpp Suggests: BiocGenerics, BiocStyle, testthat, knitr, igraph License: file LICENSE MD5sum: e3b90e0d215caef03ff0522962420118 NeedsCompilation: yes Title: Single-cell Interpretation via Multi-kernel LeaRning (SIMLR) Description: Single-cell RNA-seq technologies enable high throughput gene expression measurement of individual cells, and allow the discovery of heterogeneity within cell populations. Measurement of cell-to-cell gene expression similarity is critical for the identification, visualization and analysis of cell populations. However, single-cell data introduce challenges to conventional measures of gene expression similarity because of the high level of noise, outliers and dropouts. We develop a novel similarity-learning framework, SIMLR (Single-cell Interpretation via Multi-kernel LeaRning), which learns an appropriate distance metric from the data for dimension reduction, clustering and visualization. biocViews: ImmunoOncology, Clustering, GeneExpression, Sequencing, SingleCell Author: Daniele Ramazzotti [aut, cre], Bo Wang [aut], Luca De Sano [aut], Serafim Batzoglou [ctb] Maintainer: Luca De Sano URL: https://github.com/BatzoglouLabSU/SIMLR VignetteBuilder: knitr BugReports: https://github.com/BatzoglouLabSU/SIMLR git_url: https://git.bioconductor.org/packages/SIMLR git_branch: RELEASE_3_8 git_last_commit: b0105de git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SIMLR_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SIMLR_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SIMLR_1.8.1.tgz vignettes: vignettes/SIMLR/inst/doc/vignette.pdf vignetteTitles: Single-cell Interpretation via Multi-kernel LeaRning (\Biocpkg{SIMLR}) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/SIMLR/inst/doc/vignette.R Package: simpleaffy Version: 2.58.0 Depends: R (>= 2.0.0), methods, utils, grDevices, graphics, stats, BiocGenerics (>= 0.1.12), Biobase, affy (>= 1.33.6), genefilter, gcrma Imports: methods, utils, grDevices, graphics, stats, BiocGenerics, Biobase, affy, genefilter, gcrma License: GPL (>= 2) Archs: i386, x64 MD5sum: f6d7cbd0c17d30f74cf54782be74fbba NeedsCompilation: yes Title: Very simple high level analysis of Affymetrix data Description: Provides high level functions for reading Affy .CEL files, phenotypic data, and then computing simple things with it, such as t-tests, fold changes and the like. Makes heavy use of the affy library. Also has some basic scatter plot functions and mechanisms for generating high resolution journal figures... biocViews: Microarray, OneChannel, QualityControl, Preprocessing, Transcription, DataImport, DifferentialExpression, Annotation, ReportWriting, Visualization Author: Crispin J Miller Maintainer: Crispin Miller URL: http://www.bioconductor.org, http://bioinformatics.picr.man.ac.uk/simpleaffy/ git_url: https://git.bioconductor.org/packages/simpleaffy git_branch: RELEASE_3_8 git_last_commit: 70cf119 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/simpleaffy_2.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/simpleaffy_2.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/simpleaffy_2.58.0.tgz vignettes: vignettes/simpleaffy/inst/doc/simpleAffy.pdf vignetteTitles: simpleaffy primer hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/simpleaffy/inst/doc/simpleAffy.R dependsOnMe: yaqcaffy importsMe: affyQCReport, arrayMvout suggestsMe: AffyExpress, ArrayTools, ELBOW Package: simulatorZ Version: 1.16.0 Depends: R (>= 3.5), Biobase, SummarizedExperiment, survival, CoxBoost, BiocGenerics Imports: graphics, stats, gbm, Hmisc, GenomicRanges, methods Suggests: RUnit, BiocStyle, curatedOvarianData, parathyroidSE, superpc License: Artistic-2.0 Archs: i386, x64 MD5sum: 23b14912a86f22445fa0b20ccb9a8769 NeedsCompilation: yes Title: Simulator for Collections of Independent Genomic Data Sets Description: simulatorZ is a package intended primarily to simulate collections of independent genomic data sets, as well as performing training and validation with predicting algorithms. It supports ExpressionSet and RangedSummarizedExperiment objects. biocViews: Survival Author: Yuqing Zhang, Christoph Bernau, Levi Waldron Maintainer: Yuqing Zhang URL: https://github.com/zhangyuqing/simulatorZ BugReports: https://github.com/zhangyuqing/simulatorZ git_url: https://git.bioconductor.org/packages/simulatorZ git_branch: RELEASE_3_8 git_last_commit: 8aa14af git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/simulatorZ_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/simulatorZ_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/simulatorZ_1.16.0.tgz vignettes: vignettes/simulatorZ/inst/doc/simulatorZ-vignette.pdf vignetteTitles: SimulatorZ hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/simulatorZ/inst/doc/simulatorZ-vignette.R suggestsMe: doppelgangR Package: sincell Version: 1.14.1 Depends: R (>= 3.0.2), igraph Imports: Rcpp (>= 0.11.2), entropy, scatterplot3d, MASS, TSP, ggplot2, reshape2, fields, proxy, parallel, Rtsne, fastICA, cluster, statmod LinkingTo: Rcpp Suggests: BiocStyle, knitr, biomaRt, stringr, monocle License: GPL (>= 2) Archs: i386, x64 MD5sum: 8a94aea3ba1a97114386f0d05daaab01 NeedsCompilation: yes Title: R package for the statistical assessment of cell state hierarchies from single-cell RNA-seq data Description: Cell differentiation processes are achieved through a continuum of hierarchical intermediate cell-states that might be captured by single-cell RNA seq. Existing computational approaches for the assessment of cell-state hierarchies from single-cell data might be formalized under a general workflow composed of i) a metric to assess cell-to-cell similarities (combined or not with a dimensionality reduction step), and ii) a graph-building algorithm (optionally making use of a cells-clustering step). Sincell R package implements a methodological toolbox allowing flexible workflows under such framework. Furthermore, Sincell contributes new algorithms to provide cell-state hierarchies with statistical support while accounting for stochastic factors in single-cell RNA seq. Graphical representations and functional association tests are provided to interpret hierarchies. biocViews: ImmunoOncology, Sequencing, RNASeq, Clustering, GraphAndNetwork, Visualization, GeneExpression, GeneSetEnrichment, BiomedicalInformatics, CellBiology, FunctionalGenomics, SystemsBiology Author: Miguel Julia , Amalio Telenti , Antonio Rausell Maintainer: Miguel Julia , Antonio Rausell URL: http://bioconductor.org/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/sincell git_branch: RELEASE_3_8 git_last_commit: 80edf44 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sincell_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sincell_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sincell_1.14.1.tgz vignettes: vignettes/sincell/inst/doc/sincell-vignette.pdf vignetteTitles: Sincell: Analysis of cell state hierarchies from single-cell RNA-seq hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sincell/inst/doc/sincell-vignette.R Package: SingleCellExperiment Version: 1.4.1 Depends: R (>= 3.5), SummarizedExperiment Imports: S4Vectors, methods, BiocGenerics, utils, stats Suggests: testthat, BiocStyle, knitr, rmarkdown, scRNAseq, magrittr, Rtsne License: GPL-3 Archs: i386, x64 MD5sum: 65b08e06d67ef97a6cafaad5696ebb6a NeedsCompilation: no Title: S4 Classes for Single Cell Data Description: Defines a S4 class for storing data from single-cell experiments. This includes specialized methods to store and retrieve spike-in information, dimensionality reduction coordinates and size factors for each cell, along with the usual metadata for genes and libraries. biocViews: ImmunoOncology, DataRepresentation, DataImport, Infrastructure, SingleCell Author: Aaron Lun [aut, cph], Davide Risso [aut, cre, cph], Keegan Korthauer [ctb] Maintainer: Davide Risso VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SingleCellExperiment git_branch: RELEASE_3_8 git_last_commit: b1efcb3 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SingleCellExperiment_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SingleCellExperiment_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SingleCellExperiment_1.4.1.tgz vignettes: vignettes/SingleCellExperiment/inst/doc/devel.html, vignettes/SingleCellExperiment/inst/doc/intro.html vignetteTitles: 2. Developing around the SingleCellExperiment class, 1. An introduction to the SingleCellExperiment class hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SingleCellExperiment/inst/doc/devel.R, vignettes/SingleCellExperiment/inst/doc/intro.R dependsOnMe: BASiCS, CellTrails, clusterExperiment, cydar, DropletUtils, iSEE, LoomExperiment, MAST, scater, scPipe, scran, singleCellTK, splatter, switchde, zinbwave importsMe: bayNorm, BEARscc, CATALYST, ccfindR, CoGAPS, LineagePulse, netSmooth, SC3, scDD, scfind, scmap, SCnorm, scruff, slalom, slingshot suggestsMe: DEsingle, destiny, FCBF, phenopath, scFeatureFilter Package: singleCellTK Version: 1.2.3 Depends: R (>= 3.5), SummarizedExperiment, SingleCellExperiment, DelayedArray, Biobase Imports: ape, colourpicker, cluster, ComplexHeatmap, data.table, DESeq2, DT, ggplot2, ggtree, gridExtra, GSVA (>= 1.26.0), GSVAdata, limma, MAST, matrixStats, methods, multtest, plotly, RColorBrewer, Rtsne, S4Vectors, shiny, shinyjs, sva, reshape2, AnnotationDbi, shinyalert, circlize, enrichR, shinycssloaders Suggests: testthat, Rsubread, BiocStyle, knitr, bladderbatch, rmarkdown, org.Mm.eg.db, org.Hs.eg.db, scRNAseq, xtable, spelling License: MIT + file LICENSE MD5sum: 52c4647995b617eba6f157ee2678c058 NeedsCompilation: no Title: Interactive Analysis of Single Cell RNA-Seq Data Description: Run common single cell analysis directly through your browser including differential expression, downsampling analysis, and clustering. biocViews: SingleCell, GeneExpression, DifferentialExpression, Alignment, Clustering, ImmunoOncology Author: David Jenkins Maintainer: David Jenkins URL: https://compbiomed.github.io/sctk_docs/ VignetteBuilder: knitr BugReports: https://github.com/compbiomed/singleCellTK/issues git_url: https://git.bioconductor.org/packages/singleCellTK git_branch: RELEASE_3_8 git_last_commit: 445cc42 git_last_commit_date: 2018-11-29 Date/Publication: 2018-12-01 source.ver: src/contrib/singleCellTK_1.2.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/singleCellTK_1.2.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/singleCellTK_1.2.3.tgz vignettes: vignettes/singleCellTK/inst/doc/v01-Introduction_to_singleCellTK.html, vignettes/singleCellTK/inst/doc/v02-Processing_and_Visualizing_Data_in_the_SingleCellTK.html vignetteTitles: 1. Introduction to singleCellTK, 2. Processing and Visualizing Data in the Single Cell Toolkit hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/singleCellTK/inst/doc/v01-Introduction_to_singleCellTK.R, vignettes/singleCellTK/inst/doc/v02-Processing_and_Visualizing_Data_in_the_SingleCellTK.R Package: singscore Version: 1.2.2 Depends: R (>= 3.5),GSEABase Imports: methods, stats, graphics, ggplot2, ggsci, grDevices, ggrepel, plotly, tidyr, plyr, magrittr, reshape, edgeR, RColorBrewer, Biobase, BiocParallel, SummarizedExperiment, matrixStats Suggests: knitr, rmarkdown, testthat License: GPL-3 MD5sum: 8e278c32b376aafa623be1dd5e33d78b NeedsCompilation: no Title: Rank-based single-sample gene set scoring method Description: A simple single-sample gene signature scoring method that uses rank-based statistics to analyze the sample's gene expression profile. It scores the expression activities of gene sets at a single-sample level. biocViews: Software, GeneExpression, GeneSetEnrichment,GO,KEGG,GraphAndNetwork Author: Momeneh Foroutan [aut, ctb], Dharmesh Bhuva [aut, ctb], Ruqian Lyu [aut, cre] Maintainer: Ruqian Lyu URL: https://github.com/DavisLaboratory/singscore VignetteBuilder: knitr BugReports: https://github.com/DavisLaboratory/singscore/issues git_url: https://git.bioconductor.org/packages/singscore git_branch: RELEASE_3_8 git_last_commit: ecfb21e git_last_commit_date: 2018-11-11 Date/Publication: 2018-11-11 source.ver: src/contrib/singscore_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/singscore_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/singscore_1.2.2.tgz vignettes: vignettes/singscore/inst/doc/singscore.html vignetteTitles: singscore hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/singscore/inst/doc/singscore.R Package: SISPA Version: 1.12.0 Depends: R (>= 3.2),genefilter,GSVA,changepoint Imports: data.table, plyr, ggplot2 Suggests: knitr License: GPL-2 MD5sum: 31a2981180fb569f9bceaedf950c2ac0 NeedsCompilation: no Title: SISPA: Method for Sample Integrated Set Profile Analysis Description: Sample Integrated Set Profile Analysis (SISPA) is a method designed to define sample groups with similar gene set enrichment profiles. biocViews: GeneSetEnrichment,GenomeWideAssociation Author: Bhakti Dwivedi and Jeanne Kowalski Maintainer: Bhakti Dwivedi VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SISPA git_branch: RELEASE_3_8 git_last_commit: 0e95271 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SISPA_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SISPA_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SISPA_1.12.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: sizepower Version: 1.52.0 Depends: stats License: LGPL MD5sum: bdccb70dcc32782ba50646a7f9e521fe NeedsCompilation: no Title: Sample Size and Power Calculation in Micorarray Studies Description: This package has been prepared to assist users in computing either a sample size or power value for a microarray experimental study. The user is referred to the cited references for technical background on the methodology underpinning these calculations. This package provides support for five types of sample size and power calculations. These five types can be adapted in various ways to encompass many of the standard designs encountered in practice. biocViews: Microarray Author: Weiliang Qiu and Mei-Ling Ting Lee and George Alex Whitmore Maintainer: Weiliang Qiu git_url: https://git.bioconductor.org/packages/sizepower git_branch: RELEASE_3_8 git_last_commit: 4c1ba97 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sizepower_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sizepower_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sizepower_1.52.0.tgz vignettes: vignettes/sizepower/inst/doc/sizepower.pdf vignetteTitles: Sample Size and Power Calculation in Microarray Studies Using the \Rpackage{sizepower} package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sizepower/inst/doc/sizepower.R Package: skewr Version: 1.14.0 Depends: R (>= 3.1.1), methylumi, wateRmelon, mixsmsn, IlluminaHumanMethylation450kmanifest Imports: minfi, S4Vectors (>= 0.19.1), RColorBrewer Suggests: GEOquery, knitr, minfiData License: GPL-2 MD5sum: 96a073b45b0870dedd69129cc678075a NeedsCompilation: no Title: Visualize Intensities Produced by Illumina's Human Methylation 450k BeadChip Description: The skewr package is a tool for visualizing the output of the Illumina Human Methylation 450k BeadChip to aid in quality control. It creates a panel of nine plots. Six of the plots represent the density of either the methylated intensity or the unmethylated intensity given by one of three subsets of the 485,577 total probes. These subsets include Type I-red, Type I-green, and Type II.The remaining three distributions give the density of the Beta-values for these same three subsets. Each of the nine plots optionally displays the distributions of the "rs" SNP probes and the probes associated with imprinted genes as series of 'tick' marks located above the x-axis. biocViews: DNAMethylation, TwoChannel, Preprocessing, QualityControl Author: Ryan Putney [cre, aut], Steven Eschrich [aut], Anders Berglund [aut] Maintainer: Ryan Putney VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/skewr git_branch: RELEASE_3_8 git_last_commit: f354f7a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/skewr_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/skewr_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/skewr_1.14.0.tgz vignettes: vignettes/skewr/inst/doc/skewr.pdf vignetteTitles: An Introduction to the skewr Package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/skewr/inst/doc/skewr.R Package: slalom Version: 1.4.1 Depends: R (>= 3.4) Imports: Rcpp (>= 0.12.8), RcppArmadillo, BH, ggplot2, grid, GSEABase, methods, rsvd, SingleCellExperiment, SummarizedExperiment, stats LinkingTo: Rcpp, RcppArmadillo, BH Suggests: knitr, rhdf5, scater, testthat License: GPL-2 MD5sum: 920a089b8e6c917ad80a825bfaec1775 NeedsCompilation: yes Title: Factorial Latent Variable Modeling of Single-Cell RNA-Seq Data Description: slalom is a scalable modelling framework for single-cell RNA-seq data that uses gene set annotations to dissect single-cell transcriptome heterogeneity, thereby allowing to identify biological drivers of cell-to-cell variability and model confounding factors. biocViews: ImmunoOncology, SingleCell, RNASeq, Normalization, Visualization, DimensionReduction, Transcriptomics, GeneExpression, Sequencing, Software, Reactome Author: Florian Buettner [aut], Naruemon Pratanwanich [aut], Davis McCarthy [aut, cre], John Marioni [aut], Oliver Stegle [aut] Maintainer: Davis McCarthy VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/slalom git_branch: RELEASE_3_8 git_last_commit: 80469d2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/slalom_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/slalom_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/slalom_1.4.1.tgz vignettes: vignettes/slalom/inst/doc/vignette.html vignetteTitles: Introduction to slalom hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/slalom/inst/doc/vignette.R Package: SLGI Version: 1.42.0 Depends: R (>= 2.10), ScISI, lattice Imports: AnnotationDbi, Biobase, GO.db, ScISI, graphics, lattice, methods, stats, BiocGenerics Suggests: GO.db, org.Sc.sgd.db License: Artistic-2.0 Archs: i386, x64 MD5sum: ea0839feb33db33273540c5495db717a NeedsCompilation: no Title: Synthetic Lethal Genetic Interaction Description: A variety of data files and functions for the analysis of genetic interactions biocViews: GraphAndNetwork, Proteomics, Genetics, Network Author: Nolwenn LeMeur, Zhen Jiang, Ting-Yuan Liu, Jess Mar and Robert Gentleman Maintainer: Nolwenn Le Meur git_url: https://git.bioconductor.org/packages/SLGI git_branch: RELEASE_3_8 git_last_commit: 78f38a7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SLGI_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SLGI_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SLGI_1.42.0.tgz vignettes: vignettes/SLGI/inst/doc/SLGI.pdf vignetteTitles: SLGI Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SLGI/inst/doc/SLGI.R dependsOnMe: PCpheno Package: slingshot Version: 1.0.0 Depends: R (>= 3.5), princurve (>= 2.0.4), stats Imports: ape, clusterExperiment, graphics, grDevices, igraph, matrixStats, methods, rgl, SingleCellExperiment, SummarizedExperiment Suggests: BiocGenerics, destiny, gam, knitr, mclust, RColorBrewer, rmarkdown, splatter, testthat, covr License: Artistic-2.0 MD5sum: 429308c9bbe073d329feedfe57ae773e NeedsCompilation: no Title: Tools for ordering single-cell sequencing Description: Provides functions for inferring continuous, branching lineage structures in low-dimensional data. Slingshot was designed to model developmental trajectories in single-cell RNA sequencing data and serve as a component in an analysis pipeline after dimensionality reduction and clustering. It is flexible enough to handle arbitrarily many branching events and allows for the incorporation of prior knowledge through supervised graph construction. biocViews: Clustering, DifferentialExpression, GeneExpression, RNASeq, Sequencing, Software, Sequencing, SingleCell, Transcriptomics, Visualization Author: Kelly Street [aut, cre, cph], Davide Risso [aut], Diya Das [aut], Sandrine Dudoit [ths], Koen Van den Berge [ctb], Robrecht Cannoodt [ctb] Maintainer: Kelly Street VignetteBuilder: knitr BugReports: https://github.com/kstreet13/slingshot/issues git_url: https://git.bioconductor.org/packages/slingshot git_branch: RELEASE_3_8 git_last_commit: d111b64 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/slingshot_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/slingshot_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/slingshot_1.0.0.tgz vignettes: vignettes/slingshot/inst/doc/slingshot.html vignetteTitles: slingshot Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/slingshot/inst/doc/slingshot.R Package: slinky Version: 1.0.2 Depends: R (>= 3.5.0) Imports: SummarizedExperiment, curl, dplyr, foreach, httr, stats, utils, methods, readr, rhdf5, jsonlite, tidyr Suggests: GeoDE, doParallel, testthat, knitr, rmarkdown, ggplot2, Rtsne, Biobase, BiocStyle License: MIT + file LICENSE MD5sum: 9a8618cc6e2788fcf4da36f4e598e0ec NeedsCompilation: no Title: Putting the fun in LINCS L1000 data analysis Description: Wrappers to query the L1000 metadata available via the clue.io REST API as well as helpers for dealing with LINCS gctx files, extracting data sets of interest, converting to SummarizedExperiment objects, and some facilities for performing streamlined differential expression analysis of these data sets. biocViews: DataImport, ThirdPartyClient, GeneExpression, DifferentialExpression, GeneSetEnrichment, PatternLogic Author: Eric J. Kort Maintainer: Eric J. Kort VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/slinky git_branch: RELEASE_3_8 git_last_commit: 02e88c4 git_last_commit_date: 2019-02-28 Date/Publication: 2019-02-28 source.ver: src/contrib/slinky_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/slinky_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/slinky_1.0.2.tgz vignettes: vignettes/slinky/inst/doc/LINCS-analysis.html vignetteTitles: "LINCS analysis with slinky" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/slinky/inst/doc/LINCS-analysis.R Package: SLqPCR Version: 1.48.0 Depends: R(>= 2.4.0) Imports: stats Suggests: RColorBrewer License: GPL (>= 2) MD5sum: e1902128c0521f0f1c815fa130cccf05 NeedsCompilation: no Title: Functions for analysis of real-time quantitative PCR data at SIRS-Lab GmbH Description: Functions for analysis of real-time quantitative PCR data at SIRS-Lab GmbH biocViews: MicrotitrePlateAssay, qPCR Author: Matthias Kohl Maintainer: Matthias Kohl git_url: https://git.bioconductor.org/packages/SLqPCR git_branch: RELEASE_3_8 git_last_commit: 8c8d554 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SLqPCR_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SLqPCR_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SLqPCR_1.48.0.tgz vignettes: vignettes/SLqPCR/inst/doc/SLqPCR.pdf vignetteTitles: SLqPCR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SLqPCR/inst/doc/SLqPCR.R suggestsMe: EasyqpcR Package: SMAP Version: 1.46.0 Depends: R (>= 2.10), methods License: GPL-2 MD5sum: abf9f359b95a13d9b914fb977ad1b6b7 NeedsCompilation: yes Title: A Segmental Maximum A Posteriori Approach to Array-CGH Copy Number Profiling Description: Functions and classes for DNA copy number profiling of array-CGH data biocViews: Microarray, TwoChannel, CopyNumberVariation Author: Robin Andersson Maintainer: Robin Andersson git_url: https://git.bioconductor.org/packages/SMAP git_branch: RELEASE_3_8 git_last_commit: 1980da1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SMAP_1.46.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SMAP_1.46.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SMAP_1.46.0.tgz vignettes: vignettes/SMAP/inst/doc/SMAP.pdf vignetteTitles: SMAP hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SMAP/inst/doc/SMAP.R Package: SMITE Version: 1.10.1 Depends: R (>= 3.3), GenomicRanges Imports: scales, plyr, Hmisc, AnnotationDbi, org.Hs.eg.db, ggplot2, reactome.db, KEGG.db, BioNet, goseq, methods, IRanges, igraph, Biobase,tools, S4Vectors, geneLenDataBase, grDevices, graphics, stats, utils Suggests: knitr License: GPL (>=2) Archs: i386, x64 MD5sum: 1d200829e8965757023b445b3ebe1f4e NeedsCompilation: no Title: Significance-based Modules Integrating the Transcriptome and Epigenome Description: This package builds on the Epimods framework which facilitates finding weighted subnetworks ("modules") on Illumina Infinium 27k arrays using the SpinGlass algorithm, as implemented in the iGraph package. We have created a class of gene centric annotations associated with p-values and effect sizes and scores from any researchers prior statistical results to find functional modules. biocViews: ImmunoOncology, DifferentialMethylation, DifferentialExpression, SystemsBiology, NetworkEnrichment,GenomeAnnotation,Network, Sequencing, RNASeq, Coverage Author: Neil Ari Wijetunga, Andrew Damon Johnston, John Murray Greally Maintainer: Neil Ari Wijetunga , Andrew Damon Johnston URL: https://github.com/GreallyLab/SMITE VignetteBuilder: knitr BugReports: https://github.com/GreallyLab/SMITE/issues git_url: https://git.bioconductor.org/packages/SMITE git_branch: RELEASE_3_8 git_last_commit: fbe69e0 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SMITE_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SMITE_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SMITE_1.10.1.tgz vignettes: vignettes/SMITE/inst/doc/SMITE.pdf vignetteTitles: SMITE Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SMITE/inst/doc/SMITE.R Package: SNAGEE Version: 1.22.0 Depends: R (>= 2.6.0), SNAGEEdata Suggests: ALL, hgu95av2.db Enhances: parallel License: Artistic-2.0 MD5sum: d1587c20f9e38e9a8d85219ff149ce1d NeedsCompilation: no Title: Signal-to-Noise applied to Gene Expression Experiments Description: Signal-to-Noise applied to Gene Expression Experiments. Signal-to-noise ratios can be used as a proxy for quality of gene expression studies and samples. The SNRs can be calculated on any gene expression data set as long as gene IDs are available, no access to the raw data files is necessary. This allows to flag problematic studies and samples in any public data set. biocViews: Microarray, OneChannel, TwoChannel, QualityControl Author: David Venet Maintainer: David Venet URL: http://bioconductor.org/ git_url: https://git.bioconductor.org/packages/SNAGEE git_branch: RELEASE_3_8 git_last_commit: d4636e0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SNAGEE_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SNAGEE_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SNAGEE_1.22.0.tgz vignettes: vignettes/SNAGEE/inst/doc/SNAGEE.pdf vignetteTitles: SNAGEE Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SNAGEE/inst/doc/SNAGEE.R Package: snapCGH Version: 1.52.0 Depends: limma, DNAcopy, methods Imports: aCGH, cluster, DNAcopy, GLAD, graphics, grDevices, limma, methods, stats, tilingArray, utils License: GPL MD5sum: 6aefaf2fe3f35acb952a03488c44ffb9 NeedsCompilation: yes Title: Segmentation, normalisation and processing of aCGH data. Description: Methods for segmenting, normalising and processing aCGH data; including plotting functions for visualising raw and segmented data for individual and multiple arrays. biocViews: Microarray, CopyNumberVariation, TwoChannel, Preprocessing Author: Mike L. Smith, John C. Marioni, Steven McKinney, Thomas Hardcastle, Natalie P. Thorne Maintainer: John Marioni git_url: https://git.bioconductor.org/packages/snapCGH git_branch: RELEASE_3_8 git_last_commit: 7f9020f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/snapCGH_1.52.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/snapCGH_1.52.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/snapCGH_1.52.0.tgz vignettes: vignettes/snapCGH/inst/doc/snapCGHguide.pdf vignetteTitles: Segmentation Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/snapCGH/inst/doc/snapCGHguide.R importsMe: ADaCGH2 suggestsMe: beadarraySNP Package: snm Version: 1.30.0 Depends: R (>= 2.12.0) Imports: corpcor, lme4 (>= 1.0), splines License: LGPL Archs: i386, x64 MD5sum: c3d4d6770565f32fb9b1b3e1bbaf30ee NeedsCompilation: no Title: Supervised Normalization of Microarrays Description: SNM is a modeling strategy especially designed for normalizing high-throughput genomic data. The underlying premise of our approach is that your data is a function of what we refer to as study-specific variables. These variables are either biological variables that represent the target of the statistical analysis, or adjustment variables that represent factors arising from the experimental or biological setting the data is drawn from. The SNM approach aims to simultaneously model all study-specific variables in order to more accurately characterize the biological or clinical variables of interest. biocViews: Microarray, OneChannel, TwoChannel, MultiChannel, DifferentialExpression, ExonArray, GeneExpression, Transcription, MultipleComparison, Preprocessing, QualityControl Author: Brig Mecham and John D. Storey Maintainer: John D. Storey git_url: https://git.bioconductor.org/packages/snm git_branch: RELEASE_3_8 git_last_commit: d8ae381 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/snm_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/snm_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/snm_1.30.0.tgz vignettes: vignettes/snm/inst/doc/snm.pdf vignetteTitles: snm Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/snm/inst/doc/snm.R importsMe: edge Package: SNPchip Version: 2.28.0 Depends: R (>= 2.14.0) Imports: methods, graphics, lattice, grid, foreach, utils, Biobase, S4Vectors (>= 0.9.25), IRanges, GenomeInfoDb, GenomicRanges, SummarizedExperiment, oligoClasses (>= 1.31.1) Suggests: crlmm (>= 1.17.14), RUnit Enhances: doSNOW, VanillaICE (>= 1.21.24), RColorBrewer License: LGPL (>= 2) MD5sum: 6aa3050529ceb3c1500f56d0eb663982 NeedsCompilation: no Title: Visualizations for copy number alterations Description: Functions for plotting SNP array data; maintained for historical reasons biocViews: CopyNumberVariation, SNP, GeneticVariability, Visualization Author: Robert Scharpf and Ingo Ruczinski Maintainer: Robert Scharpf URL: http://www.biostat.jhsph.edu/~iruczins/software/snpchip.html git_url: https://git.bioconductor.org/packages/SNPchip git_branch: RELEASE_3_8 git_last_commit: b59939b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SNPchip_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SNPchip_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SNPchip_2.28.0.tgz vignettes: vignettes/SNPchip/inst/doc/PlottingIdiograms.pdf vignetteTitles: Plotting Idiograms hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SNPchip/inst/doc/PlottingIdiograms.R dependsOnMe: mBPCR importsMe: crlmm, phenoTest suggestsMe: Category, MinimumDistance, oligoClasses, VanillaICE Package: SNPediaR Version: 1.8.0 Depends: R (>= 3.0.0) Imports: RCurl, jsonlite Suggests: BiocStyle, knitr, rmarkdown, testthat License: GPL-2 MD5sum: a1ee826e42e3caa1231e1616d5a0944f NeedsCompilation: no Title: Query data from SNPedia Description: SNPediaR provides some tools for downloading and parsing data from the SNPedia web site . The implemented functions allow users to import the wiki text available in SNPedia pages and to extract the most relevant information out of them. If some information in the downloaded pages is not automatically processed by the library functions, users can easily implement their own parsers to access it in an efficient way. biocViews: SNP, VariantAnnotation Author: David Montaner [aut, cre] Maintainer: David Montaner URL: https://github.com/genometra/SNPediaR VignetteBuilder: knitr BugReports: https://github.com/genometra/SNPediaR/issues git_url: https://git.bioconductor.org/packages/SNPediaR git_branch: RELEASE_3_8 git_last_commit: d9ee8b3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SNPediaR_1.8.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SNPediaR_1.8.0.tgz vignettes: vignettes/SNPediaR/inst/doc/SNPediaR.html vignetteTitles: SNPediaR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SNPediaR/inst/doc/SNPediaR.R Package: SNPhood Version: 1.12.0 Depends: R (>= 3.1), GenomicRanges, Rsamtools, data.table, checkmate Imports: DESeq2, cluster, ggplot2, lattice, GenomeInfoDb, BiocParallel, VariantAnnotation, BiocGenerics, IRanges, methods, SummarizedExperiment, RColorBrewer, Biostrings, grDevices, gridExtra, stats, grid, utils, reshape2, scales, S4Vectors Suggests: BiocStyle, knitr, pryr, rmarkdown, SNPhoodData, corrplot License: LGPL (>= 3) MD5sum: 7f665ce6a2a88a8df7aee41bd46d4930 NeedsCompilation: no Title: SNPhood: Investigate, quantify and visualise the epigenomic neighbourhood of SNPs using NGS data Description: To date, thousands of single nucleotide polymorphisms (SNPs) have been found to be associated with complex traits and diseases. However, the vast majority of these disease-associated SNPs lie in the non-coding part of the genome, and are likely to affect regulatory elements, such as enhancers and promoters, rather than function of a protein. Thus, to understand the molecular mechanisms underlying genetic traits and diseases, it becomes increasingly important to study the effect of a SNP on nearby molecular traits such as chromatin environment or transcription factor (TF) binding. Towards this aim, we developed SNPhood, a user-friendly *Bioconductor* R package to investigate and visualize the local neighborhood of a set of SNPs of interest for NGS data such as chromatin marks or transcription factor binding sites from ChIP-Seq or RNA- Seq experiments. SNPhood comprises a set of easy-to-use functions to extract, normalize and summarize reads for a genomic region, perform various data quality checks, normalize read counts using additional input files, and to cluster and visualize the regions according to the binding pattern. The regions around each SNP can be binned in a user-defined fashion to allow for analysis of very broad patterns as well as a detailed investigation of specific binding shapes. Furthermore, SNPhood supports the integration with genotype information to investigate and visualize genotype-specific binding patterns. Finally, SNPhood can be employed for determining, investigating, and visualizing allele-specific binding patterns around the SNPs of interest. biocViews: Software Author: Christian Arnold [aut, cre], Pooja Bhat [aut], Judith Zaugg [aut] Maintainer: Christian Arnold URL: https://bioconductor.org/packages/SNPhood VignetteBuilder: knitr BugReports: christian.arnold@embl.de git_url: https://git.bioconductor.org/packages/SNPhood git_branch: RELEASE_3_8 git_last_commit: f6e5f8e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SNPhood_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SNPhood_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SNPhood_1.12.0.tgz vignettes: vignettes/SNPhood/inst/doc/IntroductionToSNPhood.html, vignettes/SNPhood/inst/doc/workflow.html vignetteTitles: Introduction and Methodological Details, Workflow example hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SNPhood/inst/doc/IntroductionToSNPhood.R, vignettes/SNPhood/inst/doc/workflow.R Package: SNPRelate Version: 1.16.0 Depends: R (>= 2.15), gdsfmt (>= 1.8.3) Imports: methods LinkingTo: gdsfmt Suggests: parallel, Matrix, RUnit, knitr, MASS, BiocGenerics Enhances: SeqArray (>= 1.12.0) License: GPL-3 MD5sum: 9c7ebe9e6249405c2982d1cb812bec74 NeedsCompilation: yes Title: Parallel Computing Toolset for Relatedness and Principal Component Analysis of SNP Data Description: Genome-wide association studies (GWAS) are widely used to investigate the genetic basis of diseases and traits, but they pose many computational challenges. We developed an R package SNPRelate to provide a binary format for single-nucleotide polymorphism (SNP) data in GWAS utilizing CoreArray Genomic Data Structure (GDS) data files. The GDS format offers the efficient operations specifically designed for integers with two bits, since a SNP could occupy only two bits. SNPRelate is also designed to accelerate two key computations on SNP data using parallel computing for multi-core symmetric multiprocessing computer architectures: Principal Component Analysis (PCA) and relatedness analysis using Identity-By-Descent measures. The SNP GDS format is also used by the GWASTools package with the support of S4 classes and generic functions. The extended GDS format is implemented in the SeqArray package to support the storage of single nucleotide variations (SNVs), insertion/deletion polymorphism (indel) and structural variation calls. biocViews: Infrastructure, Genetics, StatisticalMethod, PrincipalComponent Author: Xiuwen Zheng [aut, cre, cph], Stephanie Gogarten [ctb], Cathy Laurie [ctb], Bruce Weir [ctb, ths] Maintainer: Xiuwen Zheng URL: http://github.com/zhengxwen/SNPRelate, http://corearray.sourceforge.net/tutorials/SNPRelate/ VignetteBuilder: knitr BugReports: http://github.com/zhengxwen/SNPRelate/issues git_url: https://git.bioconductor.org/packages/SNPRelate git_branch: RELEASE_3_8 git_last_commit: 0e38e8d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SNPRelate_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SNPRelate_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SNPRelate_1.16.0.tgz vignettes: vignettes/SNPRelate/inst/doc/SNPRelateTutorial.html vignetteTitles: SNPRelate Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SNPRelate/inst/doc/SNPRelateTutorial.R dependsOnMe: SeqSQC importsMe: GDSArray, GENESIS, gwasurvivr suggestsMe: GWASTools, HIBAG, SeqArray Package: snpStats Version: 1.32.0 Depends: R(>= 2.10.0), survival, Matrix, methods Imports: graphics, grDevices, stats, utils, BiocGenerics, zlibbioc Suggests: hexbin License: GPL-3 Archs: i386, x64 MD5sum: 1c1a4fecfb47e7fd1e567eed1dbf2e26 NeedsCompilation: yes Title: SnpMatrix and XSnpMatrix classes and methods Description: Classes and statistical methods for large SNP association studies. This extends the earlier snpMatrix package, allowing for uncertainty in genotypes. biocViews: Microarray, SNP, GeneticVariability Author: David Clayton Maintainer: David Clayton git_url: https://git.bioconductor.org/packages/snpStats git_branch: RELEASE_3_8 git_last_commit: 7c31158 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/snpStats_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/snpStats_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/snpStats_1.32.0.tgz vignettes: vignettes/snpStats/inst/doc/data-input-vignette.pdf, vignettes/snpStats/inst/doc/differences.pdf, vignettes/snpStats/inst/doc/Fst-vignette.pdf, vignettes/snpStats/inst/doc/imputation-vignette.pdf, vignettes/snpStats/inst/doc/ld-vignette.pdf, vignettes/snpStats/inst/doc/pca-vignette.pdf, vignettes/snpStats/inst/doc/snpStats-vignette.pdf, vignettes/snpStats/inst/doc/tdt-vignette.pdf vignetteTitles: Data input, snpMatrix-differences, Fst, Imputation and meta-analysis, LD statistics, Principal components analysis, snpStats introduction, TDT tests hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/snpStats/inst/doc/data-input-vignette.R, vignettes/snpStats/inst/doc/Fst-vignette.R, vignettes/snpStats/inst/doc/imputation-vignette.R, vignettes/snpStats/inst/doc/ld-vignette.R, vignettes/snpStats/inst/doc/pca-vignette.R, vignettes/snpStats/inst/doc/snpStats-vignette.R, vignettes/snpStats/inst/doc/tdt-vignette.R dependsOnMe: GGBase importsMe: FunciSNP, GeneGeneInteR, GGtools, gQTLstats, gwascat, ldblock, martini, RVS, scoreInvHap suggestsMe: crlmm, GWASTools, omicRexposome, omicsPrint, VariantAnnotation Package: soGGi Version: 1.14.0 Depends: R (>= 3.2.0), BiocGenerics, SummarizedExperiment Imports: methods, reshape2, ggplot2, S4Vectors, IRanges, GenomeInfoDb, GenomicRanges, Biostrings, Rsamtools, GenomicAlignments, rtracklayer, preprocessCore, chipseq, BiocParallel Suggests: testthat, BiocStyle, knitr License: GPL (>= 3) Archs: i386, x64 MD5sum: e5d0416ddfb35676209c266b0899cbf2 NeedsCompilation: no Title: Visualise ChIP-seq, MNase-seq and motif occurrence as aggregate plots Summarised Over Grouped Genomic Intervals Description: The soGGi package provides a toolset to create genomic interval aggregate/summary plots of signal or motif occurence from BAM and bigWig files as well as PWM, rlelist, GRanges and GAlignments Bioconductor objects. soGGi allows for normalisation, transformation and arithmetic operation on and between summary plot objects as well as grouping and subsetting of plots by GRanges objects and user supplied metadata. Plots are created using the GGplot2 libary to allow user defined manipulation of the returned plot object. Coupled together, soGGi features a broad set of methods to visualise genomics data in the context of groups of genomic intervals such as genes, superenhancers and transcription factor binding events. biocViews: Sequencing, ChIPSeq, Coverage Author: Gopuraja Dharmalingam, Tom Carroll Maintainer: Tom Carroll VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/soGGi git_branch: RELEASE_3_8 git_last_commit: 90cc6b6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/soGGi_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/soGGi_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/soGGi_1.14.0.tgz vignettes: vignettes/soGGi/inst/doc/soggi.pdf vignetteTitles: soggi hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/soGGi/inst/doc/soggi.R importsMe: DChIPRep Package: SomaticSignatures Version: 2.18.0 Depends: R (>= 3.1.0), VariantAnnotation, GenomicRanges, NMF Imports: S4Vectors, IRanges, GenomeInfoDb, Biostrings, ggplot2, ggbio, reshape2, NMF, pcaMethods, Biobase, methods, proxy Suggests: testthat, knitr, parallel, BSgenome.Hsapiens.1000genomes.hs37d5, SomaticCancerAlterations, ggdendro, fastICA, sva License: MIT + file LICENSE MD5sum: aecea0dbbe1b16434e7e47466cfea941 NeedsCompilation: no Title: Somatic Signatures Description: The SomaticSignatures package identifies mutational signatures of single nucleotide variants (SNVs). It provides a infrastructure related to the methodology described in Nik-Zainal (2012, Cell), with flexibility in the matrix decomposition algorithms. biocViews: Sequencing, SomaticMutation, Visualization, Clustering, GenomicVariation, StatisticalMethod Author: Julian Gehring Maintainer: Julian Gehring URL: https://github.com/juliangehring/SomaticSignatures VignetteBuilder: knitr BugReports: https://support.bioconductor.org git_url: https://git.bioconductor.org/packages/SomaticSignatures git_branch: RELEASE_3_8 git_last_commit: facccd6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SomaticSignatures_2.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SomaticSignatures_2.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SomaticSignatures_2.18.0.tgz vignettes: vignettes/SomaticSignatures/inst/doc/SomaticSignatures-vignette.html vignetteTitles: SomaticSignatures hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/SomaticSignatures/inst/doc/SomaticSignatures-vignette.R importsMe: Rariant, YAPSA Package: SpacePAC Version: 1.20.0 Depends: R(>= 2.15),iPAC Suggests: RUnit, BiocGenerics, rgl License: GPL-2 MD5sum: f5a76a8b5ee150030fcaec81b61c6119 NeedsCompilation: no Title: Identification of Mutational Clusters in 3D Protein Space via Simulation. Description: Identifies clustering of somatic mutations in proteins via a simulation approach while considering the protein's tertiary structure. biocViews: Clustering, Proteomics Author: Gregory Ryslik, Hongyu Zhao Maintainer: Gregory Ryslik git_url: https://git.bioconductor.org/packages/SpacePAC git_branch: RELEASE_3_8 git_last_commit: 20b6f47 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SpacePAC_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SpacePAC_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SpacePAC_1.20.0.tgz vignettes: vignettes/SpacePAC/inst/doc/SpacePAC.pdf vignetteTitles: SpacePAC: Identifying mutational clusters in 3D protein space using simulation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SpacePAC/inst/doc/SpacePAC.R dependsOnMe: QuartPAC Package: sparseDOSSA Version: 1.6.1 Imports: stats, utils, optparse, MASS, tmvtnorm (>= 1.4.10), MCMCpack Suggests: knitr, BiocStyle, BiocGenerics, rmarkdown License: MIT + file LICENSE MD5sum: 9e7046fa4bc0bd007589073a9784f89b NeedsCompilation: no Title: Sparse Data Observations for Simulating Synthetic Abundance Description: The package is to provide a model based Bayesian method to characterize and simulate microbiome data. sparseDOSSA's model captures the marginal distribution of each microbial feature as a truncated, zero-inflated log-normal distribution, with parameters distributed as a parent log-normal distribution. The model can be effectively fit to reference microbial datasets in order to parameterize their microbes and communities, or to simulate synthetic datasets of similar population structure. Most importantly, it allows users to include both known feature-feature and feature-metadata correlation structures and thus provides a gold standard to enable benchmarking of statistical methods for metagenomic data analysis. biocViews: ImmunoOncology, Bayesian, Microbiome, Metagenomics, Software Author: Boyu Ren, Emma Schwager, Timothy Tickle, Curtis Huttenhower Maintainer: Boyu Ren, Emma Schwager , George Weingart VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/sparseDOSSA git_branch: RELEASE_3_8 git_last_commit: 441b30c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sparseDOSSA_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sparseDOSSA_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sparseDOSSA_1.6.1.tgz vignettes: vignettes/sparseDOSSA/inst/doc/sparsedossa-vignette.html vignetteTitles: Sparse Data Observations for the Simulation of Synthetic Abundances (sparseDOSSA) hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/sparseDOSSA/inst/doc/sparsedossa-vignette.R Package: sparsenetgls Version: 1.0.1 Depends: R (>= 3.5.0), Matrix, MASS Imports: methods, glmnet, parcor, huge, stats, graphics, utils Suggests: testthat, lme4, BiocStyle, knitr, rmarkdown, roxygen2 (>= 5.0.0) License: GPL-3 MD5sum: 7ef7d3b5a974cbdcaca5c4db001fab0a NeedsCompilation: no Title: Using Gaussian graphical structue learning estimation in generalized least squared regression for multivariate normal regression Description: The package provides methods of combining the graph structure learning and generalized least squares regression to improve the regression estimation. The main function sparsenetgls() provides solutions for multivariate regression with Gaussian distributed dependant variables and explanatory variables utlizing multiple well-known graph structure learning approaches to estimating the precision matrix, and uses a penalized variance covariance matrix with a distance tuning parameter of the graph structure in deriving the sandwich estimators in generalized least squares (gls) regression. This package also provides functions for assessing a Gaussian graphical model which uses the penalized approach. It uses Receiver Operative Characteristics curve as a visualization tool in the assessment. biocViews: ImmunoOncology, GraphAndNetwork,Regression,Metabolomics,CopyNumberVariation,MassSpectrometry,Proteomics,Software,Visualization Author: Irene Zeng [aut, cre], Thomas Lumley [ctb] Maintainer: Irene Zeng SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/sparsenetgls git_branch: RELEASE_3_8 git_last_commit: 1eec6fe git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sparsenetgls_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sparsenetgls_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sparsenetgls_1.0.1.tgz vignettes: vignettes/sparsenetgls/inst/doc/vignettes_sparsenetgls.html vignetteTitles: Introduction to sparsenetgls hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sparsenetgls/inst/doc/vignettes_sparsenetgls.R Package: SparseSignatures Version: 1.2.0 Depends: R (>= 3.5), NMF Imports: nnlasso, nnls, parallel, data.table, Biostrings, GenomicRanges, IRanges, BSgenome, BSgenome.Hsapiens.1000genomes.hs37d5, GenomeInfoDb, ggplot2, gridExtra Suggests: BiocGenerics, BiocStyle, testthat, knitr, License: file LICENSE MD5sum: dcbc3c8a105ae46137b771ba2ec0735f NeedsCompilation: no Title: SparseSignatures Description: Point mutations occurring in a genome can be divided into 96 categories based on the base being mutated, the base it is mutated into and its two flanking bases. Therefore, for any patient, it is possible to represent all the point mutations occurring in that patient’s tumor as a vector of length 96, where each element represents the count of mutations for a given category in the patient. A mutational signature represents the pattern of mutations produced by a mutagen or mutagenic process inside the cell. Each signature can also be represented by a vector of length 96, where each element represents the probability that this particular mutagenic process generates a mutation of the 96 above mentioned categories. In this R package, we provide a set of functions to extract and visualize the mutational signatures that best explain the mutation counts of a large number of patients. biocViews: BiomedicalInformatics, SomaticMutation Author: Daniele Ramazzotti [cre, aut], Avantika Lal [aut], Keli Liu [ctb], Luca De Sano [ctb], Robert Tibshirani [ctb], Arend Sidow [aut] Maintainer: Luca De Sano URL: https://github.com/danro9685/SparseSignatures VignetteBuilder: knitr BugReports: https://github.com/danro9685/SparseSignatures git_url: https://git.bioconductor.org/packages/SparseSignatures git_branch: RELEASE_3_8 git_last_commit: 555f164 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SparseSignatures_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SparseSignatures_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SparseSignatures_1.2.0.tgz vignettes: vignettes/SparseSignatures/inst/doc/vignette.pdf vignetteTitles: SparseSignatures hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/SparseSignatures/inst/doc/vignette.R Package: specL Version: 1.16.1 Depends: R (>= 3.3.2), DBI (>= 0.5.1), methods (>= 3.3.2), protViz (>= 0.2.45), RSQLite (>= 1.1.2), seqinr (>= 3.3.3) Suggests: BiocGenerics, BiocStyle (>= 2.2.1), knitr (>= 1.15.1), msqc1 (>= 1.0.0), plotrix (>= 3.6.4), prozor (>= 0.2.2), RUnit (>= 0.4.31) License: GPL-3 MD5sum: 774f0ddb159c33a064c365095404f807 NeedsCompilation: no Title: specL - Prepare Peptide Spectrum Matches for Use in Targeted Proteomics Description: provides a function for generating spectra libraries which can be used for MRM SRM MS workflows in proteomics. The package provides a BiblioSpec reader, a function which can add the protein information using a FASTA formatted amino acid file, and an export method for using the created library in the Spectronaut software. biocViews: ImmunoOncology, MassSpectrometry, Proteomics Author: Christian Trachsel [aut], Christian Panse [aut, cre] (0000-0003-1975-3064), Jonas Grossmann [aut] (0000-0002-6899-9020), Witold E. Wolski [ctb] Maintainer: Christian Panse , Witold E. Wolski URL: https://github.com/fgcz/specL VignetteBuilder: knitr BugReports: https://github.com/fgcz/specL/issues git_url: https://git.bioconductor.org/packages/specL git_branch: RELEASE_3_8 git_last_commit: f49026a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/specL_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/specL_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/specL_1.16.1.tgz vignettes: vignettes/specL/inst/doc/specL.pdf, vignettes/specL/inst/doc/cdsw.html, vignettes/specL/inst/doc/report.html, vignettes/specL/inst/doc/ssrc.html vignetteTitles: Introduction to specL, Computing Dynamic SWATH Windows, Automatic Workflow, Retention Time Prediction using the ssrc Method hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/specL/inst/doc/cdsw.R, vignettes/specL/inst/doc/report.R, vignettes/specL/inst/doc/specL.R, vignettes/specL/inst/doc/ssrc.R Package: SpeCond Version: 1.36.0 Depends: R (>= 2.10.0), mclust (>= 3.3.1), Biobase (>= 1.15.13), fields, hwriter (>= 1.1), RColorBrewer, methods License: LGPL (>=2) MD5sum: 917e0149bfc0891249d1008f26e5ffb4 NeedsCompilation: no Title: Condition specific detection from expression data Description: This package performs a gene expression data analysis to detect condition-specific genes. Such genes are significantly up- or down-regulated in a small number of conditions. It does so by fitting a mixture of normal distributions to the expression values. Conditions can be environmental conditions, different tissues, organs or any other sources that you wish to compare in terms of gene expression. biocViews: Microarray, DifferentialExpression, MultipleComparison, Clustering, ReportWriting Author: Florence Cavalli Maintainer: Florence Cavalli git_url: https://git.bioconductor.org/packages/SpeCond git_branch: RELEASE_3_8 git_last_commit: a425ae7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SpeCond_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SpeCond_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SpeCond_1.36.0.tgz vignettes: vignettes/SpeCond/inst/doc/SpeCond.pdf vignetteTitles: SpeCond hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SpeCond/inst/doc/SpeCond.R Package: SPEM Version: 1.22.0 Depends: R (>= 2.15.1), Rsolnp, Biobase, methods License: GPL-2 MD5sum: ef4d7302fe48373c81e008ad7e21a1f6 NeedsCompilation: no Title: S-system parameter estimation method Description: This package can optimize the parameter in S-system models given time series data biocViews: Network, NetworkInference, Software Author: Xinyi YANG Developer, Jennifer E. DENT Developer and Christine NARDINI Supervisor Maintainer: Xinyi YANG git_url: https://git.bioconductor.org/packages/SPEM git_branch: RELEASE_3_8 git_last_commit: fddb7cd git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SPEM_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SPEM_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SPEM_1.22.0.tgz vignettes: vignettes/SPEM/inst/doc/SPEM-package.pdf vignetteTitles: Vignette for SPEM hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SPEM/inst/doc/SPEM-package.R importsMe: TMixClust Package: SPIA Version: 2.34.0 Depends: R (>= 2.14.0), graphics, KEGGgraph Imports: graphics Suggests: graph, Rgraphviz, hgu133plus2.db License: file LICENSE License_restricts_use: yes MD5sum: b78883062aeacd45a6739f7f23e551b9 NeedsCompilation: no Title: Signaling Pathway Impact Analysis (SPIA) using combined evidence of pathway over-representation and unusual signaling perturbations Description: This package implements the Signaling Pathway Impact Analysis (SPIA) which uses the information form a list of differentially expressed genes and their log fold changes together with signaling pathways topology, in order to identify the pathways most relevant to the condition under the study. biocViews: Microarray, GraphAndNetwork Author: Adi Laurentiu Tarca , Purvesh Kathri and Sorin Draghici Maintainer: Adi Laurentiu Tarca URL: http://bioinformatics.oxfordjournals.org/cgi/reprint/btn577v1 git_url: https://git.bioconductor.org/packages/SPIA git_branch: RELEASE_3_8 git_last_commit: febbfe2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SPIA_2.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SPIA_2.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SPIA_2.34.0.tgz vignettes: vignettes/SPIA/inst/doc/SPIA.pdf vignetteTitles: SPIA hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/SPIA/inst/doc/SPIA.R importsMe: EnrichmentBrowser suggestsMe: graphite, KEGGgraph Package: SpidermiR Version: 1.12.1 Depends: R (>= 3.0.0) Imports: networkD3, httr, igraph, utils, stats, miRNAtap, miRNAtap.db, AnnotationDbi, org.Hs.eg.db, ggplot2, gridExtra, gplots, grDevices, lattice, latticeExtra, visNetwork, TCGAbiolinks, gdata Suggests: BiocStyle, knitr, rmarkdown, testthat, devtools, roxygen2 License: GPL (>= 3) MD5sum: 24a7367b2db2b1785afa2ef026556197 NeedsCompilation: no Title: SpidermiR: An R/Bioconductor package for integrative network analysis with miRNA data Description: The aims of SpidermiR are : i) facilitate the network open-access data retrieval from GeneMania data, ii) prepare the data using the appropriate gene nomenclature, iii) integration of miRNA data in a specific network, iv) provide different standard analyses and v) allow the user to visualize the results. In more detail, the package provides multiple methods for query, prepare and download network data (GeneMania), and the integration with validated and predicted miRNA data (mirWalk, miRTarBase, miRandola,Pharmaco-miR,DIANA, Miranda, PicTar and TargetScan) and the use of standard analysis (igraph) and visualization methods (networkD3). biocViews: GeneRegulation, miRNA, Network Author: Claudia Cava, Antonio Colaprico, Alex Graudenzi, Gloria Bertoli, Tiago C. Silva, Catharina Olsen, Houtan Noushmehr, Gianluca Bontempi, Giancarlo Mauri, Isabella Castiglioni Maintainer: Claudia Cava URL: https://github.com/claudiacava/SpidermiR VignetteBuilder: knitr BugReports: https://github.com/claudiacava/SpidermiR/issues git_url: https://git.bioconductor.org/packages/SpidermiR git_branch: RELEASE_3_8 git_last_commit: c728d83 git_last_commit_date: 2019-02-04 Date/Publication: 2019-02-04 source.ver: src/contrib/SpidermiR_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SpidermiR_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SpidermiR_1.12.1.tgz vignettes: vignettes/SpidermiR/inst/doc/SpidermiR.html vignetteTitles: Working with SpidermiR package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SpidermiR/inst/doc/SpidermiR.R importsMe: StarBioTrek Package: spikeLI Version: 2.42.0 Imports: graphics, grDevices, stats, utils License: GPL-2 MD5sum: fede6083947ebb7ce4bacafce63b56c6 NeedsCompilation: no Title: Affymetrix Spike-in Langmuir Isotherm Data Analysis Tool Description: SpikeLI is a package that performs the analysis of the Affymetrix spike-in data using the Langmuir Isotherm. The aim of this package is to show the advantages of a physical-chemistry based analysis of the Affymetrix microarray data compared to the traditional methods. The spike-in (or Latin square) data for the HGU95 and HGU133 chipsets have been downloaded from the Affymetrix web site. The model used in the spikeLI package is described in details in E. Carlon and T. Heim, Physica A 362, 433 (2006). biocViews: Microarray, QualityControl Author: Delphine Baillon, Paul Leclercq , Sarah Ternisien, Thomas Heim, Enrico Carlon Maintainer: Enrico Carlon git_url: https://git.bioconductor.org/packages/spikeLI git_branch: RELEASE_3_8 git_last_commit: d5ef71c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/spikeLI_2.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/spikeLI_2.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/spikeLI_2.42.0.tgz vignettes: vignettes/spikeLI/inst/doc/spikeLI.pdf vignetteTitles: spikeLI hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: spkTools Version: 1.38.0 Depends: R (>= 2.7.0), Biobase (>= 2.5.5) Imports: Biobase (>= 2.5.5), graphics, grDevices, gtools, methods, RColorBrewer, stats, utils Suggests: xtable License: GPL (>= 2) MD5sum: 5a5c7b1b12e15ddcead01e006f4d8294 NeedsCompilation: no Title: Methods for Spike-in Arrays Description: The package contains functions that can be used to compare expression measures on different array platforms. biocViews: Software, Technology, Microarray Author: Matthew N McCall , Rafael A Irizarry Maintainer: Matthew N McCall URL: http://bioconductor.org git_url: https://git.bioconductor.org/packages/spkTools git_branch: RELEASE_3_8 git_last_commit: e60c5d0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/spkTools_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/spkTools_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/spkTools_1.38.0.tgz vignettes: vignettes/spkTools/inst/doc/spkDoc.pdf vignetteTitles: spkTools: Spike-in Data Analysis and Visualization hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/spkTools/inst/doc/spkDoc.R Package: splatter Version: 1.6.1 Depends: R (>= 3.4), SingleCellExperiment Imports: akima, BiocGenerics, BiocParallel, checkmate, edgeR, fitdistrplus, ggplot2, locfit, matrixStats, methods, scales, scater (>= 1.7.4), stats, SummarizedExperiment, utils, crayon Suggests: BiocStyle, covr, cowplot, knitr, limSolve, lme4, progress, pscl, testthat, rmarkdown, S4Vectors, scDD, scran, mfa, phenopath, BASiCS, zinbwave, SparseDC, BiocManager License: GPL-3 + file LICENSE MD5sum: d191f036bf700775249fceb024f61dc1 NeedsCompilation: no Title: Simple Simulation of Single-cell RNA Sequencing Data Description: Splatter is a package for the simulation of single-cell RNA sequencing count data. It provides a simple interface for creating complex simulations that are reproducible and well-documented. Parameters can be estimated from real data and functions are provided for comparing real and simulated datasets. biocViews: SingleCell, RNASeq, Transcriptomics, GeneExpression, Sequencing, Software, ImmunoOncology Author: Luke Zappia Maintainer: Luke Zappia URL: https://github.com/Oshlack/splatter VignetteBuilder: knitr BugReports: https://github.com/Oshlack/splatter/issues git_url: https://git.bioconductor.org/packages/splatter git_branch: RELEASE_3_8 git_last_commit: b809a81 git_last_commit_date: 2018-12-05 Date/Publication: 2018-12-06 source.ver: src/contrib/splatter_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/splatter_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/splatter_1.6.1.tgz vignettes: vignettes/splatter/inst/doc/splatter.html vignetteTitles: An introduction to the Splatter package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/splatter/inst/doc/splatter.R suggestsMe: slingshot, SummarizedBenchmark Package: splicegear Version: 1.54.0 Depends: R (>= 2.6.0), methods, Biobase(>= 2.5.5) Imports: annotate, Biobase, graphics, grDevices, grid, methods, utils, XML License: LGPL MD5sum: 16c969a97b03236c8d94b1edf5ba43fd NeedsCompilation: no Title: splicegear Description: A set of tools to work with alternative splicing biocViews: Infrastructure, Transcription Author: Laurent Gautier Maintainer: Laurent Gautier git_url: https://git.bioconductor.org/packages/splicegear git_branch: RELEASE_3_8 git_last_commit: 6b897ff git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/splicegear_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/splicegear_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/splicegear_1.54.0.tgz vignettes: vignettes/splicegear/inst/doc/splicegear.pdf vignetteTitles: splicegear Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/splicegear/inst/doc/splicegear.R Package: spliceSites Version: 1.30.0 Depends: methods,rbamtools (>= 2.14.3),refGenome (>= 1.6.0),Biobase,Biostrings (>= 2.28.0) Imports: BiocGenerics,doBy,seqLogo,IRanges License: GPL-2 MD5sum: cfcde22a0fadd95d33faf18e95e1182f NeedsCompilation: yes Title: A bioconductor package for exploration of alignment gap positions from RNA-seq data Description: Performs splice centered analysis on RNA-seq data. biocViews: RNAseq,GeneExpression,DifferentialExpression,Proteomics Author: Wolfgang Kaisers Maintainer: Wolfgang Kaisers git_url: https://git.bioconductor.org/packages/spliceSites git_branch: RELEASE_3_8 git_last_commit: faa0748 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/spliceSites_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/spliceSites_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/spliceSites_1.30.0.tgz vignettes: vignettes/spliceSites/inst/doc/spliceSites.pdf vignetteTitles: spliceSites hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/spliceSites/inst/doc/spliceSites.R Package: SplicingGraphs Version: 1.22.2 Depends: GenomicFeatures (>= 1.17.13), GenomicAlignments (>= 1.1.22), Rgraphviz (>= 2.3.7) Imports: methods, utils, graphics, igraph, BiocGenerics, S4Vectors (>= 0.17.5), BiocParallel, IRanges (>= 2.3.21), GenomeInfoDb, GenomicRanges (>= 1.23.21), GenomicFeatures, Rsamtools, GenomicAlignments, graph, Rgraphviz Suggests: igraph, Gviz, TxDb.Hsapiens.UCSC.hg19.knownGene, RNAseqData.HNRNPC.bam.chr14, RUnit License: Artistic-2.0 Archs: i386, x64 MD5sum: 522bfe2bfe0b2f62f6814e5ddcf2989d NeedsCompilation: no Title: Create, manipulate, visualize splicing graphs, and assign RNA-seq reads to them Description: This package allows the user to create, manipulate, and visualize splicing graphs and their bubbles based on a gene model for a given organism. Additionally it allows the user to assign RNA-seq reads to the edges of a set of splicing graphs, and to summarize them in different ways. biocViews: Genetics, Annotation, DataRepresentation, Visualization, Sequencing, RNASeq, GeneExpression, AlternativeSplicing, Transcription, ImmunoOncology Author: D. Bindreither, M. Carlson, M. Morgan, H. Pagès Maintainer: H. Pagès git_url: https://git.bioconductor.org/packages/SplicingGraphs git_branch: RELEASE_3_8 git_last_commit: df10695 git_last_commit_date: 2019-01-28 Date/Publication: 2019-01-31 source.ver: src/contrib/SplicingGraphs_1.22.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/SplicingGraphs_1.22.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SplicingGraphs_1.22.2.tgz vignettes: vignettes/SplicingGraphs/inst/doc/SplicingGraphs.pdf vignetteTitles: Splicing graphs and RNA-seq data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SplicingGraphs/inst/doc/SplicingGraphs.R Package: splineTimeR Version: 1.10.0 Depends: R (>= 3.3), Biobase, igraph, limma, GSEABase, gtools, splines, GeneNet (>= 1.2.13), longitudinal (>= 1.1.12), FIs Suggests: knitr License: GPL-3 MD5sum: 62d088b9c08349611d18aee11eb7612e NeedsCompilation: no Title: Time-course differential gene expression data analysis using spline regression models followed by gene association network reconstruction Description: This package provides functions for differential gene expression analysis of gene expression time-course data. Natural cubic spline regression models are used. Identified genes may further be used for pathway enrichment analysis and/or the reconstruction of time dependent gene regulatory association networks. biocViews: GeneExpression, DifferentialExpression, TimeCourse, Regression, GeneSetEnrichment, NetworkEnrichment, NetworkInference, GraphAndNetwork Author: Agata Michna Maintainer: Herbert Braselmann VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/splineTimeR git_branch: RELEASE_3_8 git_last_commit: f1c2020 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/splineTimeR_1.10.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/splineTimeR_1.10.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/splineTimeR_1.10.0.tgz vignettes: vignettes/splineTimeR/inst/doc/splineTimeR.pdf vignetteTitles: splineTimeR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/splineTimeR/inst/doc/splineTimeR.R Package: SPLINTER Version: 1.8.1 Depends: R (>= 3.4.0), grDevices, stats Imports: graphics, ggplot2, seqLogo, Biostrings, biomaRt, GenomicAlignments, GenomicRanges, GenomicFeatures, Gviz, IRanges, S4Vectors, GenomeInfoDb, utils, plyr,stringr, methods, BSgenome.Mmusculus.UCSC.mm9, googleVis Suggests: BiocStyle, knitr, rmarkdown License: GPL-2 MD5sum: b4c6645041c811cf9806e69e6d0fb934 NeedsCompilation: no Title: Splice Interpreter Of Transcripts Description: SPLINTER provides tools to analyze alternative splicing sites, interpret outcomes based on sequence information, select and design primers for site validiation and give visual representation of the event to guide downstream experiments. biocViews: ImmunoOncology, GeneExpression, RNASeq, Visualization, AlternativeSplicing Author: Diana Low Maintainer: Diana Low VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SPLINTER git_branch: RELEASE_3_8 git_last_commit: c0320af git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SPLINTER_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SPLINTER_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SPLINTER_1.8.1.tgz vignettes: vignettes/SPLINTER/inst/doc/vignette.pdf vignetteTitles: SPLINTER hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SPLINTER/inst/doc/vignette.R Package: splots Version: 1.48.0 Imports: grid, RColorBrewer License: LGPL MD5sum: 58d6a7e42306390dffe15484f0540ffb NeedsCompilation: no Title: Visualization of high-throughput assays in microtitre plate or slide format Description: The splots package provides the plotScreen function for visualising data in microtitre plate or slide format. biocViews: Visualization, Sequencing, MicrotitrePlateAssay Author: Wolfgang Huber, Oleg Sklyar Maintainer: Wolfgang Huber git_url: https://git.bioconductor.org/packages/splots git_branch: RELEASE_3_8 git_last_commit: 5d95a03 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/splots_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/splots_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/splots_1.48.0.tgz vignettes: vignettes/splots/inst/doc/splotsHOWTO.pdf vignetteTitles: Visualization of data from assays in microtitre plate or slide format hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/splots/inst/doc/splotsHOWTO.R dependsOnMe: cellHTS2 importsMe: RNAinteract, RNAither Package: SPONGE Version: 1.4.0 Depends: R (>= 3.4) Imports: Biobase, stats, ppcor, logging, foreach, doRNG, data.table, MASS, expm, gRbase, glmnet, igraph, iterators, Suggests: testthat, knitr, rmarkdown, visNetwork, ggplot2, ggrepel, gridExtra, digest, doParallel, bigmemory License: GPL (>=3) MD5sum: 6761d96ab04189f01b7bd9260428e22c NeedsCompilation: no Title: Sparse Partial Correlations On Gene Expression Description: This package provides methods to efficiently detect competitive endogeneous RNA interactions between two genes. Such interactions are mediated by one or several miRNAs such that both gene and miRNA expression data for a larger number of samples is needed as input. biocViews: GeneExpression, Transcription, GeneRegulation, NetworkInference, Transcriptomics, SystemsBiology, Regression Author: Markus List, Azim Dehghani Amirabad, Dennis Kostka, Marcel H. Schulz Maintainer: Markus List VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SPONGE git_branch: RELEASE_3_8 git_last_commit: 4123d4f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SPONGE_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SPONGE_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SPONGE_1.4.0.tgz vignettes: vignettes/SPONGE/inst/doc/SPONGE.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SPONGE/inst/doc/SPONGE.R Package: spotSegmentation Version: 1.56.0 Depends: R (>= 2.10), mclust License: GPL (>= 2) MD5sum: 1ea2481528bffefd86889ec081f29124 NeedsCompilation: no Title: Microarray Spot Segmentation and Gridding for Blocks of Microarray Spots Description: Spot segmentation via model-based clustering and gridding for blocks within microarray slides, as described in Li et al, Robust Model-Based Segmentation of Microarray Images, Technical Report no. 473, Department of Statistics, University of Washington. biocViews: Microarray, TwoChannel, QualityControl, Preprocessing Author: Qunhua Li, Chris Fraley, Adrian Raftery Department of Statistics, University of Washington Maintainer: Chris Fraley URL: http://www.stat.washington.edu/fraley git_url: https://git.bioconductor.org/packages/spotSegmentation git_branch: RELEASE_3_8 git_last_commit: 20273de git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/spotSegmentation_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/spotSegmentation_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/spotSegmentation_1.56.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: SQUADD Version: 1.32.0 Depends: R (>= 2.11.0) Imports: graphics, grDevices, methods, RColorBrewer, stats, utils License: GPL (>=2) MD5sum: 6ec1ec80c00a53aa607426cfa2c15f8b NeedsCompilation: no Title: Add-on of the SQUAD Software Description: This package SQUADD is a SQUAD add-on. It permits to generate SQUAD simulation matrix, prediction Heat-Map and Correlation Circle from PCA analysis. biocViews: GraphAndNetwork, Network, Visualization Author: Martial Sankar, supervised by Christian Hardtke and Ioannis Xenarios Maintainer: Martial Sankar URL: http://www.unil.ch/dbmv/page21142_en.html git_url: https://git.bioconductor.org/packages/SQUADD git_branch: RELEASE_3_8 git_last_commit: 0609efc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SQUADD_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SQUADD_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SQUADD_1.32.0.tgz vignettes: vignettes/SQUADD/inst/doc/SQUADD_ERK.pdf, vignettes/SQUADD/inst/doc/SQUADD.pdf vignetteTitles: SQUADD package, SQUADD package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SQUADD/inst/doc/SQUADD_ERK.R, vignettes/SQUADD/inst/doc/SQUADD.R Package: SRAdb Version: 1.44.0 Depends: RSQLite, graph, RCurl Imports: GEOquery Suggests: Rgraphviz License: Artistic-2.0 MD5sum: a37d04633f80e87dd7e9a5398712445f NeedsCompilation: no Title: A compilation of metadata from NCBI SRA and tools Description: The Sequence Read Archive (SRA) is the largest public repository of sequencing data from the next generation of sequencing platforms including Roche 454 GS System, Illumina Genome Analyzer, Applied Biosystems SOLiD System, Helicos Heliscope, and others. However, finding data of interest can be challenging using current tools. SRAdb is an attempt to make access to the metadata associated with submission, study, sample, experiment and run much more feasible. This is accomplished by parsing all the NCBI SRA metadata into a SQLite database that can be stored and queried locally. Fulltext search in the package make querying metadata very flexible and powerful. fastq and sra files can be downloaded for doing alignment locally. Beside ftp protocol, the SRAdb has funcitons supporting fastp protocol (ascp from Aspera Connect) for faster downloading large data files over long distance. The SQLite database is updated regularly as new data is added to SRA and can be downloaded at will for the most up-to-date metadata. biocViews: Infrastructure, Sequencing, DataImport Author: Jack Zhu and Sean Davis Maintainer: Jack Zhu URL: http://gbnci.abcc.ncifcrf.gov/sra/ BugReports: https://github.com/seandavi/SRAdb/issues/new git_url: https://git.bioconductor.org/packages/SRAdb git_branch: RELEASE_3_8 git_last_commit: 090ce6e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SRAdb_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SRAdb_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SRAdb_1.44.0.tgz vignettes: vignettes/SRAdb/inst/doc/SRAdb.pdf vignetteTitles: Using SRAdb to Query the Sequence Read Archive hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SRAdb/inst/doc/SRAdb.R Package: sRAP Version: 1.22.0 Depends: WriteXLS Imports: gplots, pls, ROCR, qvalue License: GPL-3 MD5sum: 5ae1daf3d036da49f0c51a31658604a3 NeedsCompilation: no Title: Simplified RNA-Seq Analysis Pipeline Description: This package provides a pipeline for gene expression analysis (primarily for RNA-Seq data). The normalization function is specific for RNA-Seq analysis, but all other functions (Quality Control Figures, Differential Expression and Visualization, and Functional Enrichment via BD-Func) will work with any type of gene expression data. biocViews: GeneExpression, RNAseq, Microarray, Preprocessing, QualityControl, Statistics, DifferentialExpression, Visualization, GeneSetEnrichment, GO Author: Charles Warden Maintainer: Charles Warden git_url: https://git.bioconductor.org/packages/sRAP git_branch: RELEASE_3_8 git_last_commit: ca77558 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sRAP_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sRAP_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sRAP_1.22.0.tgz vignettes: vignettes/sRAP/inst/doc/sRAP.pdf vignetteTitles: sRAP Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sRAP/inst/doc/sRAP.R Package: SRGnet Version: 1.8.0 Depends: R (>= 3.3.1), EBcoexpress, MASS, igraph, pvclust (>= 2.0-0), gbm (>= 2.1.1), limma, DMwR (>= 0.4.1), matrixStats, Hmisc Suggests: knitr, rmarkdown License: GPL-2 MD5sum: ee9c754e6be1b8a5fb9653285327c1fc NeedsCompilation: no Title: SRGnet: An R package for studying synergistic response to gene mutations from transcriptomics data from transcriptomics data Description: We developed SRGnet to analyze synergistic regulatory mechanisms in transcriptome profiles that act to enhance the overall cell response to combination of mutations, drugs or environmental exposure. This package can be used to identify regulatory modules downstream of synergistic response genes, prioritize synergistic regulatory genes that may be potential intervention targets, and contextualize gene perturbation experiments. biocViews: Software, StatisticalMethod, Regression Author: Isar Nassiri [aut, cre], Matthew McCall [aut, cre] Maintainer: Isar Nassiri VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SRGnet git_branch: RELEASE_3_8 git_last_commit: 34aae51 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SRGnet_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SRGnet_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SRGnet_1.8.0.tgz vignettes: vignettes/SRGnet/inst/doc/vignette.html vignetteTitles: SRGnet An R package for studying synergistic response to gene mutations from transcriptomics data \ hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: srnadiff Version: 1.2.1 Depends: R (>= 3.5) Imports: Rcpp (>= 0.12.8), methods, utils, devtools, BiocStyle, S4Vectors, GenomeInfoDb, rtracklayer, SummarizedExperiment, IRanges, GenomicRanges, DESeq2, Rsamtools, GenomicFeatures, GenomicAlignments, ggplot2, BiocParallel LinkingTo: Rcpp Suggests: knitr, rmarkdown, testthat License: GPL-3 MD5sum: be35c8421a289b89e5a3e753cc44cd08 NeedsCompilation: yes Title: Differential Expression of Small RNA-Seq Description: Differential expression of small RNA-seq when reference annotation is not given. biocViews: ImmunoOncology, GeneExpression, Coverage, SmallRNA, Epigenetics, StatisticalMethod, Preprocessing, DifferentialExpression Author: Zytnicki Matthias [aut, cre] Maintainer: Matthias Zytnicki SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/srnadiff git_branch: RELEASE_3_8 git_last_commit: 1c2d7d9 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/srnadiff_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/srnadiff_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/srnadiff_1.2.1.tgz vignettes: vignettes/srnadiff/inst/doc/srnadiff.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/srnadiff/inst/doc/srnadiff.R Package: sscore Version: 1.54.0 Depends: R (>= 1.8.0), affy, affyio Suggests: affydata License: GPL (>= 2) Archs: i386, x64 MD5sum: 8d7cc52c819e22d0264a1ca6fff19327 NeedsCompilation: no Title: S-Score Algorithm for Affymetrix Oligonucleotide Microarrays Description: This package contains an implementation of the S-Score algorithm as described by Zhang et al (2002). biocViews: DifferentialExpression Author: Richard Kennedy , based on C++ code from Li Zhang and Borland Delphi code from Robnet Kerns . Maintainer: Richard Kennedy URL: http://home.att.net/~richard-kennedy/professional.html git_url: https://git.bioconductor.org/packages/sscore git_branch: RELEASE_3_8 git_last_commit: 3ef1a75 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sscore_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sscore_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sscore_1.54.0.tgz vignettes: vignettes/sscore/inst/doc/sscore.pdf vignetteTitles: SScore primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sscore/inst/doc/sscore.R Package: sscu Version: 2.12.0 Depends: R (>= 3.3) Imports: Biostrings (>= 2.36.4), seqinr (>= 3.1-3), BiocGenerics (>= 0.16.1) Suggests: knitr, rmarkdown License: GPL (>= 2) MD5sum: ddbb17a9eb6ef4599fd888772c389faa NeedsCompilation: no Title: Strength of Selected Codon Usage Description: The package calculates the indexes for selective stength in codon usage in bacteria species. (1) The package can calculate the strength of selected codon usage bias (sscu, also named as s_index) based on Paul Sharp's method. The method take into account of background mutation rate, and focus only on four pairs of codons with universal translational advantages in all bacterial species. Thus the sscu index is comparable among different species. (2) The package can detect the strength of translational accuracy selection by Akashi's test. The test tabulating all codons into four categories with the feature as conserved/variable amino acids and optimal/non-optimal codons. (3) Optimal codon lists (selected codons) can be calculated by either op_highly function (by using the highly expressed genes compared with all genes to identify optimal codons), or op_corre_CodonW/op_corre_NCprime function (by correlative method developed by Hershberg & Petrov). Users will have a list of optimal codons for further analysis, such as input to the Akashi's test. (4) The detailed codon usage information, such as RSCU value, number of optimal codons in the highly/all gene set, as well as the genomic gc3 value, can be calculate by the optimal_codon_statistics and genomic_gc3 function. (5) Furthermore, we added one test function low_frequency_op in the package. The function try to find the low frequency optimal codons, among all the optimal codons identified by the op_highly function. biocViews: Genetics, GeneExpression, WholeGenome Author: Yu Sun Maintainer: Yu Sun VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/sscu git_branch: RELEASE_3_8 git_last_commit: 50b310f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/sscu_2.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/sscu_2.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sscu_2.12.0.tgz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: sSeq Version: 1.20.1 Depends: R (>= 3.0), caTools, RColorBrewer License: GPL (>= 3) MD5sum: 114ded3d58a185fce7c6623e2b548faf NeedsCompilation: no Title: Shrinkage estimation of dispersion in Negative Binomial models for RNA-seq experiments with small sample size Description: The purpose of this package is to discover the genes that are differentially expressed between two conditions in RNA-seq experiments. Gene expression is measured in counts of transcripts and modeled with the Negative Binomial (NB) distribution using a shrinkage approach for dispersion estimation. The method of moment (MM) estimates for dispersion are shrunk towards an estimated target, which minimizes the average squared difference between the shrinkage estimates and the initial estimates. The exact per-gene probability under the NB model is calculated, and used to test the hypothesis that the expected expression of a gene in two conditions identically follow a NB distribution. biocViews: ImmunoOncology, RNASeq Author: Danni Yu , Wolfgang Huber and Olga Vitek Maintainer: Danni Yu git_url: https://git.bioconductor.org/packages/sSeq git_branch: RELEASE_3_8 git_last_commit: 91f3144 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sSeq_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sSeq_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sSeq_1.20.1.tgz vignettes: vignettes/sSeq/inst/doc/sSeq.pdf vignetteTitles: sSeq hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sSeq/inst/doc/sSeq.R importsMe: MLSeq Package: ssize Version: 1.56.0 Depends: gdata, xtable License: LGPL MD5sum: 0f17e8554718d39959b9edaa732f3c5e NeedsCompilation: no Title: Estimate Microarray Sample Size Description: Functions for computing and displaying sample size information for gene expression arrays. biocViews: Microarray, DifferentialExpression Author: Gregory R. Warnes, Peng Liu, and Fasheng Li Maintainer: Gregory R. Warnes git_url: https://git.bioconductor.org/packages/ssize git_branch: RELEASE_3_8 git_last_commit: a20017b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ssize_1.56.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ssize_1.56.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ssize_1.56.0.tgz vignettes: vignettes/ssize/inst/doc/ssize.pdf vignetteTitles: Sample Size Estimation for Microarray Experiments Using the \code{ssize} package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ssize/inst/doc/ssize.R Package: SSPA Version: 2.22.1 Depends: R (>= 2.12), methods, qvalue, lattice, limma Imports: graphics, stats Suggests: BiocStyle, genefilter, edgeR, DESeq License: GPL (>= 2) MD5sum: 76570fc7a92c3d5619cd407574f1b597 NeedsCompilation: yes Title: General Sample Size and Power Analysis for Microarray and Next-Generation Sequencing Data Description: General Sample size and power analysis for microarray and next-generation sequencing data. biocViews: ImmunoOncology, GeneExpression, RNASeq, Microarray, StatisticalMethod Author: Maarten van Iterson Maintainer: Maarten van Iterson URL: http://www.humgen.nl/MicroarrayAnalysisGroup.html git_url: https://git.bioconductor.org/packages/SSPA git_branch: RELEASE_3_8 git_last_commit: 2ece27d git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SSPA_2.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SSPA_2.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SSPA_2.22.1.tgz vignettes: vignettes/SSPA/inst/doc/SSPA.pdf vignetteTitles: SSPA Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SSPA/inst/doc/SSPA.R Package: ssviz Version: 1.16.1 Depends: R (>= 2.15.1),methods,Rsamtools,Biostrings,reshape,ggplot2,RColorBrewer,stats Suggests: knitr License: GPL-2 Archs: i386, x64 MD5sum: ca33d8dab66899d614d5b6588f33419b NeedsCompilation: no Title: A small RNA-seq visualizer and analysis toolkit Description: Small RNA sequencing viewer biocViews: ImmunoOncology, Sequencing,RNASeq,Visualization,MultipleComparison,Genetics Author: Diana Low Maintainer: Diana Low VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ssviz git_branch: RELEASE_3_8 git_last_commit: c105418 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ssviz_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ssviz_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ssviz_1.16.1.tgz vignettes: vignettes/ssviz/inst/doc/ssviz.pdf vignetteTitles: ssviz hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ssviz/inst/doc/ssviz.R Package: stageR Version: 1.4.0 Depends: R (>= 3.4), SummarizedExperiment Imports: methods, stats Suggests: knitr, rmarkdown, BiocStyle, methods, Biobase, edgeR, limma, DEXSeq, testthat License: GNU General Public License version 3 MD5sum: 3940cc6f065042cc8dd0c135109ec057 NeedsCompilation: no Title: stageR: stage-wise analysis of high throughput gene expression data in R Description: The stageR package allows automated stage-wise analysis of high-throughput gene expression data. The method is published in Genome Biology at https://genomebiology.biomedcentral.com/articles/10.1186/s13059-017-1277-0 biocViews: Software, StatisticalMethod Author: Koen Van den Berge and Lieven Clement Maintainer: Koen Van den Berge VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/stageR git_branch: RELEASE_3_8 git_last_commit: bf61ea3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/stageR_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/stageR_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/stageR_1.4.0.tgz vignettes: vignettes/stageR/inst/doc/stageRVignette.html vignetteTitles: stageR: stage-wise analysis of high-throughput gene expression data in R hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/stageR/inst/doc/stageRVignette.R Package: STAN Version: 2.10.1 Depends: methods, poilog, parallel Imports: GenomicRanges, IRanges, S4Vectors, BiocGenerics, GenomeInfoDb, Gviz, Rsolnp Suggests: BiocStyle, gplots, knitr License: GPL (>= 2) MD5sum: 4db6654de1c2de94e1ad1e6be1c50123 NeedsCompilation: yes Title: The Genomic STate ANnotation Package Description: Genome segmentation with hidden Markov models has become a useful tool to annotate genomic elements, such as promoters and enhancers. STAN (genomic STate ANnotation) implements (bidirectional) hidden Markov models (HMMs) using a variety of different probability distributions, which can model a wide range of current genomic data (e.g. continuous, discrete, binary). STAN de novo learns and annotates the genome into a given number of 'genomic states'. The 'genomic states' may for instance reflect distinct genome-associated protein complexes (e.g. 'transcription states') or describe recurring patterns of chromatin features (referred to as 'chromatin states'). Unlike other tools, STAN also allows for the integration of strand-specific (e.g. RNA) and non-strand-specific data (e.g. ChIP). biocViews: ImmunoOncology, HiddenMarkovModel, GenomeAnnotation, Microarray, Sequencing, ChIPSeq, RNASeq, ChipOnChip, Transcription Author: Benedikt Zacher, Julia Ertl, Julien Gagneur, Achim Tresch Maintainer: Rafael Campos-Martin VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/STAN git_branch: RELEASE_3_8 git_last_commit: b0dc295 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/STAN_2.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/STAN_2.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/STAN_2.10.1.tgz vignettes: vignettes/STAN/inst/doc/STAN-knitr.pdf vignetteTitles: The genomic STate ANnotation package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/STAN/inst/doc/STAN-knitr.R Package: staRank Version: 1.24.1 Depends: methods, cellHTS2, R (>= 2.10) License: GPL Archs: i386, x64 MD5sum: f120f8fea27077644d6f929a995fef73 NeedsCompilation: no Title: Stability Ranking Description: Detecting all relevant variables from a data set is challenging, especially when only few samples are available and data is noisy. Stability ranking provides improved variable rankings of increased robustness using resampling or subsampling. biocViews: ImmunoOncology, MultipleComparison, CellBiology, CellBasedAssays, MicrotitrePlateAssay Author: Juliane Siebourg, Niko Beerenwinkel Maintainer: Juliane Siebourg git_url: https://git.bioconductor.org/packages/staRank git_branch: RELEASE_3_8 git_last_commit: ba921ee git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/staRank_1.24.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/staRank_1.24.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/staRank_1.24.1.tgz vignettes: vignettes/staRank/inst/doc/staRank.pdf vignetteTitles: Using staRank hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/staRank/inst/doc/staRank.R Package: StarBioTrek Version: 1.8.5 Depends: R (>= 3.3) Imports: SpidermiR, graphite, AnnotationDbi, e1071, ROCR, MLmetrics, grDevices, igraph, reshape2, ggplot2 Suggests: BiocStyle, knitr, rmarkdown, testthat, devtools, roxygen2, qgraph, png, grid License: GPL (>= 3) MD5sum: 6ed931472cc1d76b6e0278342cb6b85c NeedsCompilation: no Title: StarBioTrek Description: This tool StarBioTrek presents some methodologies to measure pathway activity and cross-talk among pathways integrating also the information of network data. biocViews: GeneRegulation, Network, Pathways, KEGG Author: Claudia Cava, Isabella Castiglioni Maintainer: Claudia Cava URL: https://github.com/claudiacava/StarBioTrek VignetteBuilder: knitr BugReports: https://github.com/claudiacava/StarBioTrek/issues git_url: https://git.bioconductor.org/packages/StarBioTrek git_branch: RELEASE_3_8 git_last_commit: c5cb148 git_last_commit_date: 2019-04-15 Date/Publication: 2019-04-15 source.ver: src/contrib/StarBioTrek_1.8.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/StarBioTrek_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/StarBioTrek_1.8.5.tgz vignettes: vignettes/StarBioTrek/inst/doc/StarBioTrek.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/StarBioTrek/inst/doc/StarBioTrek.R Package: Starr Version: 1.38.0 Depends: Ringo, affy, affxparser Imports: pspline, MASS, zlibbioc License: Artistic-2.0 MD5sum: eec8e43bb3dc5d143b06de2f7cda0982 NeedsCompilation: yes Title: Simple tiling array analysis of Affymetrix ChIP-chip data Description: Starr facilitates the analysis of ChIP-chip data, in particular that of Affymetrix tiling arrays. The package provides functions for data import, quality assessment, data visualization and exploration. Furthermore, it includes high-level analysis features like association of ChIP signals with annotated features, correlation analysis of ChIP signals and other genomic data (e.g. gene expression), peak-finding with the CMARRT algorithm and comparative display of multiple clusters of ChIP-profiles. It uses the basic Bioconductor classes ExpressionSet and probeAnno for maximum compatibility with other software on Bioconductor. All functions from Starr can be used to investigate preprocessed data from the Ringo package, and vice versa. An important novel tool is the the automated generation of correct, up-to-date microarray probe annotation (bpmap) files, which relies on an efficient mapping of short sequences (e.g. the probe sequences on a microarray) to an arbitrary genome. biocViews: Microarray,OneChannel,DataImport,QualityControl,Preprocessing,ChIPchip Author: Benedikt Zacher, Johannes Soeding, Pei Fen Kuan, Matthias Siebert, Achim Tresch Maintainer: Benedikt Zacher git_url: https://git.bioconductor.org/packages/Starr git_branch: RELEASE_3_8 git_last_commit: a8d2dc2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Starr_1.38.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Starr_1.38.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Starr_1.38.0.tgz vignettes: vignettes/Starr/inst/doc/Starr.pdf vignetteTitles: Simple tiling array analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Starr/inst/doc/Starr.R suggestsMe: nucleR Package: STATegRa Version: 1.18.0 Depends: R (>= 2.10) Imports: Biobase, gridExtra, ggplot2, methods, stats, grid, MASS, calibrate, gplots, edgeR, limma, foreach, affy Suggests: RUnit, BiocGenerics, knitr (>= 1.6), rmarkdown, BiocStyle (>= 1.3), roxygen2, doSNOW License: GPL-2 Archs: i386, x64 MD5sum: 12ca7c3e81a4757ca68d7eb69a95e65a NeedsCompilation: no Title: Classes and methods for multi-omics data integration Description: Classes and tools for multi-omics data integration. biocViews: Software, StatisticalMethod, Clustering, DimensionReduction, PrincipalComponent Author: STATegra Consortia Maintainer: David Gomez-Cabrero , Núria Planell VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/STATegRa git_branch: RELEASE_3_8 git_last_commit: b7a1407 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/STATegRa_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/STATegRa_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/STATegRa_1.18.0.tgz vignettes: vignettes/STATegRa/inst/doc/STATegRa.html vignetteTitles: STATegRa User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/STATegRa/inst/doc/STATegRa.R Package: statTarget Version: 1.12.1 Depends: R (>= 3.3.0) Imports: randomForest,plyr,pdist,ROC,utils,grDevices,graphics,rrcov,stats, pls,impute Suggests: testthat, BiocStyle, knitr, rmarkdown, gWidgets2,gWidgets2RGtk2,RGtk2 License: LGPL (>= 3) MD5sum: 033a2af56846419c8771654a167fc41e NeedsCompilation: no Title: Statistical Analysis of Molecular Profiles Description: A streamlined tool provides a graphical user interface for quality control based signal drift correction (QC-RFSC), integration of data from multi-batch MS-based experiments, and the comprehensive statistical analysis in metabolomics and proteomics. biocViews: ImmunoOncology, Metabolomics, Proteomics, Machine Learning, MassSpectrometry, QualityControl, Normalization, DifferentialExpression, BatchEffect, Visualization, MultipleComparison,Preprocessing, GUI, Software Author: Hemi Luan Maintainer: Hemi Luan URL: https://stattarget.github.io VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/statTarget git_branch: RELEASE_3_8 git_last_commit: b3e9c8a git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/statTarget_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/statTarget_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/statTarget_1.12.1.tgz vignettes: vignettes/statTarget/inst/doc/statTarget.html vignetteTitles: statTarget2 On using the Graphical User Interface hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/statTarget/inst/doc/statTarget.R Package: stepNorm Version: 1.54.0 Depends: R (>= 1.8.0), marray, methods Imports: marray, MASS, methods, stats License: LGPL MD5sum: 76233358af8236df8f33b593e9699f05 NeedsCompilation: no Title: Stepwise normalization functions for cDNA microarrays Description: Stepwise normalization functions for cDNA microarray data. biocViews: Microarray, TwoChannel, Preprocessing Author: Yuanyuan Xiao , Yee Hwa (Jean) Yang Maintainer: Yuanyuan Xiao URL: http://www.biostat.ucsf.edu/jean/ git_url: https://git.bioconductor.org/packages/stepNorm git_branch: RELEASE_3_8 git_last_commit: 422b547 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/stepNorm_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/stepNorm_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/stepNorm_1.54.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: strandCheckR Version: 1.0.0 Imports: dplyr, magrittr, GenomeInfoDb, GenomicAlignments, GenomicRanges, IRanges, Rsamtools, S4Vectors, grid, BiocGenerics, ggplot2, reshape2, stats, gridExtra, TxDb.Hsapiens.UCSC.hg38.knownGene, methods, stringr Suggests: BiocStyle, knitr, testthat License: GPL (>= 2) MD5sum: 3db4172a54f75b10ab4bde8805a76d43 NeedsCompilation: no Title: Calculate strandness information of a bam file Description: This package aims to quantify and remove putative double strand DNA from a strand-specific RNA sample. There are also options and methods to plot the positive/negative proportions of all sliding windows, which allow users to have an idea of how much the sample was contaminated and the appropriate threshold to be used for filtering. biocViews: RNASeq, Alignment, QualityControl, Coverage Author: Thu-Hien To [aut, cre], Steve Pederson [aut] Maintainer: Thu-Hien To VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/strandCheckR git_branch: RELEASE_3_8 git_last_commit: a1e7d02 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/strandCheckR_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/strandCheckR_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/strandCheckR_1.0.0.tgz vignettes: vignettes/strandCheckR/inst/doc/strandCheckR.html vignetteTitles: An Introduction To strandCheckR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/strandCheckR/inst/doc/strandCheckR.R Package: Streamer Version: 1.28.1 Imports: methods, graph, RBGL, parallel, BiocGenerics Suggests: RUnit, Rsamtools (>= 1.5.53), GenomicAlignments, Rgraphviz License: Artistic-2.0 MD5sum: 9fb476a6e9d7f2c10314c740c873eb35 NeedsCompilation: yes Title: Enabling stream processing of large files Description: Large data files can be difficult to work with in R, where data generally resides in memory. This package encourages a style of programming where data is 'streamed' from disk into R via a `producer' and through a series of `consumers' that, typically reduce the original data to a manageable size. The package provides useful Producer and Consumer stream components for operations such as data input, sampling, indexing, and transformation; see package?Streamer for details. biocViews: Infrastructure, DataImport Author: Martin Morgan, Nishant Gopalakrishnan Maintainer: Martin Morgan git_url: https://git.bioconductor.org/packages/Streamer git_branch: RELEASE_3_8 git_last_commit: 62f37cb git_last_commit_date: 2019-03-06 Date/Publication: 2019-03-06 source.ver: src/contrib/Streamer_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Streamer_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Streamer_1.28.1.tgz vignettes: vignettes/Streamer/inst/doc/Streamer.pdf vignetteTitles: Streamer: A simple example hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Streamer/inst/doc/Streamer.R importsMe: plethy Package: STRINGdb Version: 1.22.0 Depends: R (>= 2.14.0) Imports: png, sqldf, plyr, igraph, RCurl, methods, RColorBrewer, gplots, hash, plotrix Suggests: RUnit, BiocGenerics License: GPL-2 Archs: i386, x64 MD5sum: bf498d4d580ffc25bca94edcc21934b5 NeedsCompilation: no Title: STRINGdb (Search Tool for the Retrieval of Interacting proteins database) Description: The STRINGdb package provides a R interface to the STRING protein-protein interactions database (http://www.string-db.org). biocViews: Network Author: Andrea Franceschini Maintainer: Damian Szklarczyk git_url: https://git.bioconductor.org/packages/STRINGdb git_branch: RELEASE_3_8 git_last_commit: d0d3549 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/STRINGdb_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/STRINGdb_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/STRINGdb_1.22.0.tgz vignettes: vignettes/STRINGdb/inst/doc/STRINGdb.pdf vignetteTitles: STRINGdb Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/STRINGdb/inst/doc/STRINGdb.R dependsOnMe: PPInfer, scsR importsMe: coexnet, glmSparseNet, IMMAN, pwOmics, RITAN, XINA suggestsMe: epiNEM, GeneNetworkBuilder, netSmooth, PCAN Package: STROMA4 Version: 1.6.1 Depends: R (>= 3.4), Biobase, BiocParallel, cluster, matrixStats, stats, graphics, utils Suggests: breastCancerMAINZ License: GPL-3 MD5sum: a6893280968165456534c330999336ee NeedsCompilation: no Title: Assign Properties to TNBC Patients Description: This package estimates four stromal properties identified in TNBC patients in each patient of a gene expression datasets. These stromal property assignments can be combined to subtype patients. These four stromal properties were identified in Triple negative breast cancer (TNBC) patients and represent the presence of different cells in the stroma: T-cells (T), B-cells (B), stromal infiltrating epithelial cells (E), and desmoplasia (D). Additionally this package can also be used to estimate generative properties for the Lehmann subtypes, an alternative TNBC subtyping scheme (PMID: 21633166). biocViews: ImmunoOncology, GeneExpression, BiomedicalInformatics, Classification, Microarray, RNASeq, Software Author: Sadiq Saleh [aut, cre], Michael Hallett [aut] Maintainer: Sadiq Saleh git_url: https://git.bioconductor.org/packages/STROMA4 git_branch: RELEASE_3_8 git_last_commit: e50340f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/STROMA4_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/STROMA4_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/STROMA4_1.6.1.tgz vignettes: vignettes/STROMA4/inst/doc/STROMA4-vignette.pdf vignetteTitles: Using the STROMA4 package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/STROMA4/inst/doc/STROMA4-vignette.R Package: subSeq Version: 1.12.1 Depends: R (>= 3.2) Imports: data.table, dplyr, tidyr, ggplot2, magrittr, qvalue (>= 1.99), digest, Biobase Suggests: limma, edgeR, DESeq2, DEXSeq (>= 1.9.7), testthat, knitr License: MIT + file LICENSE MD5sum: 1923737c7ce61c7f1b9ecdfa1590beb6 NeedsCompilation: no Title: Subsampling of high-throughput sequencing count data Description: Subsampling of high throughput sequencing count data for use in experiment design and analysis. biocViews: ImmunoOncology, Sequencing, Transcription, RNASeq, GeneExpression, DifferentialExpression Author: David Robinson, John D. Storey, with contributions from Andrew J. Bass Maintainer: Andrew J. Bass , John D. Storey URL: http://github.com/StoreyLab/subSeq VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/subSeq git_branch: RELEASE_3_8 git_last_commit: fa7cd77 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/subSeq_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/subSeq_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/subSeq_1.12.1.tgz vignettes: vignettes/subSeq/inst/doc/subSeq.pdf vignetteTitles: subSeq Example hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/subSeq/inst/doc/subSeq.R Package: SummarizedBenchmark Version: 2.0.1 Depends: R (>= 3.5), tidyr, SummarizedExperiment, S4Vectors, BiocGenerics, methods, UpSetR, rlang, stringr, utils, BiocParallel, ggplot2, mclust, dplyr, digest, sessioninfo, crayon, tibble Suggests: iCOBRA, BiocStyle, knitr, magrittr, IHW, qvalue, testthat, DESeq2, edgeR, limma, tximport, readr, scRNAseq, splatter, scater, rnaseqcomp, biomaRt License: GPL (>= 3) MD5sum: 49e6155796cc9333be354ccf157a76b7 NeedsCompilation: no Title: Classes and methods for performing benchmark comparisons Description: This package defines the BenchDesign and SummarizedBenchmark classes for building, executing, and evaluating benchmark experiments of computational methods. The SummarizedBenchmark class extends the RangedSummarizedExperiment object, and is designed to provide infrastructure to store and compare the results of applying different methods to a shared data set. This class provides an integrated interface to store metadata such as method parameters and software versions as well as ground truths (when these are available) and evaluation metrics. biocViews: Software, Infrastructure Author: Alejandro Reyes , Patrick Kimes Maintainer: Alejandro Reyes , Patrick Kimes VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SummarizedBenchmark git_branch: RELEASE_3_8 git_last_commit: 7eee513 git_last_commit_date: 2019-01-20 Date/Publication: 2019-01-20 source.ver: src/contrib/SummarizedBenchmark_2.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SummarizedBenchmark_2.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SummarizedBenchmark_2.0.1.tgz vignettes: vignettes/SummarizedBenchmark/inst/doc/Appendix.html, vignettes/SummarizedBenchmark/inst/doc/QuantificationBenchmark.html, vignettes/SummarizedBenchmark/inst/doc/SingleCellBenchmark.html, vignettes/SummarizedBenchmark/inst/doc/SummarizedBenchmark.html vignetteTitles: Data objects and non-standard use., Case Study: Benchmarking Methods Not Written in R, Case Study: Single-Cell RNA-Seq Simulation, Benchmarking with SummarizedBenchmark hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SummarizedBenchmark/inst/doc/Appendix.R, vignettes/SummarizedBenchmark/inst/doc/QuantificationBenchmark.R, vignettes/SummarizedBenchmark/inst/doc/SingleCellBenchmark.R, vignettes/SummarizedBenchmark/inst/doc/SummarizedBenchmark.R Package: SummarizedExperiment Version: 1.12.0 Depends: R (>= 3.2), methods, GenomicRanges (>= 1.33.6), Biobase, DelayedArray (>= 0.3.20) Imports: utils, stats, tools, Matrix, BiocGenerics (>= 0.15.3), S4Vectors (>= 0.17.25), IRanges (>= 2.13.16), GenomeInfoDb (>= 1.13.1) Suggests: annotate, AnnotationDbi, hgu95av2.db, GenomicFeatures, TxDb.Hsapiens.UCSC.hg19.knownGene, BiocStyle, knitr, rmarkdown, digest, jsonlite, rhdf5, HDF5Array (>= 1.7.5), airway, RUnit, testthat License: Artistic-2.0 MD5sum: 5738caa020eb8f8c7f399d9e799500ad NeedsCompilation: no Title: SummarizedExperiment container Description: The SummarizedExperiment container contains one or more assays, each represented by a matrix-like object of numeric or other mode. The rows typically represent genomic ranges of interest and the columns represent samples. biocViews: Genetics, Infrastructure, Sequencing, Annotation, Coverage, GenomeAnnotation Author: Martin Morgan, Valerie Obenchain, Jim Hester, Hervé Pagès Maintainer: Bioconductor Package Maintainer VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SummarizedExperiment git_branch: RELEASE_3_8 git_last_commit: 5f84168 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SummarizedExperiment_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SummarizedExperiment_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SummarizedExperiment_1.12.0.tgz vignettes: vignettes/SummarizedExperiment/inst/doc/Extensions.html, vignettes/SummarizedExperiment/inst/doc/SummarizedExperiment.html vignetteTitles: 2. Extending the SummarizedExperiment class, 1. SummarizedExperiment for Coordinating Experimental Assays,, Samples,, and Regions of Interest hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SummarizedExperiment/inst/doc/Extensions.R, vignettes/SummarizedExperiment/inst/doc/SummarizedExperiment.R dependsOnMe: AffiXcan, AllelicImbalance, BDMMAcorrect, BiocSklearn, BiSeq, bnbc, bsseq, CAGEfightR, celaref, clusterExperiment, coseq, csaw, DaMiRseq, deepSNV, DESeq2, DEXSeq, DiffBind, diffcoexp, diffHic, DMCHMM, ENmix, EnrichmentBrowser, epigenomix, EventPointer, ExpressionAtlas, GenoGAM, GenomicAlignments, GenomicFiles, genoset, GRmetrics, GSEABenchmarkeR, HelloRanges, hipathia, InteractionSet, IntEREst, iSEE, isomiRs, ivygapSE, JunctionSeq, LoomExperiment, MBASED, methylPipe, minfi, miRmine, mpra, MultiAssayExperiment, NADfinder, OUTRIDER, PowerExplorer, recount, REMP, RIPSeeker, rqt, runibic, Scale4C, scone, SDAMS, SGSeq, simulatorZ, SingleCellExperiment, singleCellTK, soGGi, stageR, SummarizedBenchmark, TimeSeriesExperiment, TissueEnrich, VanillaICE, VariantAnnotation, yamss, zinbwave importsMe: adaptest, ALDEx2, alpine, anamiR, anota2seq, apeglm, appreci8R, ASICS, AUCell, BASiCS, bayNorm, BBCAnalyzer, BiocOncoTK, biotmle, biovizBase, BiSeq, BUMHMM, BUScorrect, CAGEr, CAMTHC, CATALYST, ccfindR, CellTrails, CHARGE, ChIPpeakAnno, chromVAR, CNPBayes, coexnet, CoGAPS, compartmap, consensusDE, countsimQC, cydar, DChIPRep, debrowser, DEComplexDisease, DEFormats, DEGreport, DEP, DEScan2, destiny, diffcyt, DominoEffect, doppelgangR, easyRNASeq, ELMER, ensemblVEP, epivizrData, erma, FCBF, FourCSeq, GARS, GenomicDataCommons, GGBase, ggbio, glmSparseNet, gQTLBase, gQTLstats, GreyListChIP, gwascat, gwasurvivr, HTSeqGenie, iasva, icetea, ideal, ImpulseDE2, INSPEcT, InterMineR, iteremoval, LineagePulse, M3D, MADSEQ, MAST, mCSEA, MEAL, MetaNeighbor, methyAnalysis, MethylAid, methylumi, methyvim, MinimumDistance, miRSM, MLSeq, MoonlightR, motifmatchr, MPRAnalyze, msgbsR, MTseeker, MultiDataSet, multiOmicsViz, MutationalPatterns, MWASTools, netSmooth, NormalyzerDE, oligoClasses, omicRexposome, omicsPrint, oncomix, pcaExplorer, phenopath, psichomics, PureCN, R453Plus1Toolbox, RaggedExperiment, RareVariantVis, RcisTarget, readat, regionReport, regsplice, rgsepd, Rmmquant, roar, RTCGAToolbox, RTN, SC3, scater, scDD, scfind, scmap, scmeth, SCnorm, scoreInvHap, scPipe, scran, scruff, semisup, seqCAT, sigFeature, singscore, slalom, slingshot, slinky, SNPchip, SNPhood, splatter, srnadiff, SVAPLSseq, switchde, systemPipeR, TCGAbiolinks, TCGAbiolinksGUI, TCGAutils, TCseq, tenXplore, Trendy, TSRchitect, TTMap, TVTB, tximeta, TxRegInfra, VariantFiltering, vidger, zFPKM suggestsMe: AnnotationHub, biobroom, DelayedArray, epivizr, epivizrChart, esetVis, GENIE3, GenomicRanges, Glimma, globalSeq, gsean, HDF5Array, interactiveDisplay, MSnbase, pathprint, podkat, RiboProfiling, S4Vectors, scFeatureFilter, sesame, TFutils Package: supraHex Version: 1.20.0 Depends: R (>= 3.3), hexbin Imports: ape, MASS, grDevices, graphics, stats, utils License: GPL-2 MD5sum: 6a9ce3e5a00dca2709dfbb1569546767 NeedsCompilation: no Title: supraHex: a supra-hexagonal map for analysing tabular omics data Description: A supra-hexagonal map is a giant hexagon on a 2-dimensional grid seamlessly consisting of smaller hexagons. It is supposed to train, analyse and visualise a high-dimensional omics input data. The supraHex is able to carry out gene clustering/meta-clustering and sample correlation, plus intuitive visualisations to facilitate exploratory analysis. More importantly, it allows for overlaying additional data onto the trained map to explore relations between input and additional data. So with supraHex, it is also possible to carry out multilayer omics data comparisons. Newly added utilities are advanced heatmap visualisation and tree-based analysis of sample relationships. Uniquely to this package, users can ultrafastly understand any tabular omics data, both scientifically and artistically, especially in a sample-specific fashion but without loss of information on large genes. biocViews: Software, Clustering, Visualization, GeneExpression Author: Hai Fang and Julian Gough Maintainer: Hai Fang URL: http://suprahex.r-forge.r-project.org git_url: https://git.bioconductor.org/packages/supraHex git_branch: RELEASE_3_8 git_last_commit: 3a7fe24 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/supraHex_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/supraHex_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/supraHex_1.20.0.tgz vignettes: vignettes/supraHex/inst/doc/supraHex_vignettes.pdf vignetteTitles: supraHex User Manual hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/supraHex/inst/doc/supraHex_vignettes.R importsMe: Pi suggestsMe: TCGAbiolinks Package: survcomp Version: 1.32.0 Depends: survival, prodlim, R (>= 3.4) Imports: ipred, SuppDists, KernSmooth, survivalROC, bootstrap, grid, rmeta, stats, graphics Suggests: Hmisc, CPE, clinfun, xtable, Biobase, BiocManager License: Artistic-2.0 MD5sum: 9deb430d0aa94bc4738bbed9828cbf08 NeedsCompilation: yes Title: Performance Assessment and Comparison for Survival Analysis Description: Assessment and Comparison for Performance of Risk Prediction (Survival) Models. biocViews: GeneExpression, DifferentialExpression, Visualization Author: Benjamin Haibe-Kains, Markus Schroeder, Catharina Olsen, Christos Sotiriou, Gianluca Bontempi, John Quackenbush, Samuel Branders, Zhaleh Safikhani Maintainer: Benjamin Haibe-Kains , Markus Schroeder , Catharina Olsen URL: http://www.pmgenomics.ca/bhklab/ git_url: https://git.bioconductor.org/packages/survcomp git_branch: RELEASE_3_8 git_last_commit: d23b602 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/survcomp_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/survcomp_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/survcomp_1.32.0.tgz vignettes: vignettes/survcomp/inst/doc/survcomp.pdf vignetteTitles: SurvComp: a package for performance assessment and comparison for survival analysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/survcomp/inst/doc/survcomp.R dependsOnMe: genefu importsMe: GenRank suggestsMe: glmSparseNet, metaseqR Package: Sushi Version: 1.20.0 Depends: R (>= 2.10), zoo,biomaRt Imports: graphics, grDevices License: GPL (>= 2) Archs: i386, x64 MD5sum: 1dd42cecf0f9fcc2ce3e5da994e42c4a NeedsCompilation: no Title: Tools for visualizing genomics data Description: Flexible, quantitative, and integrative genomic visualizations for publication-quality multi-panel figures biocViews: DataRepresentation, Visualization, Genetics, Sequencing, Infrastructure, HiC Author: Douglas H Phanstiel Maintainer: Douglas H Phanstiel git_url: https://git.bioconductor.org/packages/Sushi git_branch: RELEASE_3_8 git_last_commit: fea3c6c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Sushi_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Sushi_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Sushi_1.20.0.tgz vignettes: vignettes/Sushi/inst/doc/Sushi.pdf vignetteTitles: Sushi hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Sushi/inst/doc/Sushi.R importsMe: diffloop, Ularcirc Package: sva Version: 3.30.1 Depends: R (>= 3.2), mgcv, genefilter, BiocParallel Imports: matrixStats, stats, graphics, utils, limma, Suggests: pamr, bladderbatch, BiocStyle, zebrafishRNASeq, testthat License: Artistic-2.0 MD5sum: 3041abd22f3a7769982bb290b8b628ea NeedsCompilation: yes Title: Surrogate Variable Analysis Description: The sva package contains functions for removing batch effects and other unwanted variation in high-throughput experiment. Specifically, the sva package contains functions for the identifying and building surrogate variables for high-dimensional data sets. Surrogate variables are covariates constructed directly from high-dimensional data (like gene expression/RNA sequencing/methylation/brain imaging data) that can be used in subsequent analyses to adjust for unknown, unmodeled, or latent sources of noise. The sva package can be used to remove artifacts in three ways: (1) identifying and estimating surrogate variables for unknown sources of variation in high-throughput experiments (Leek and Storey 2007 PLoS Genetics,2008 PNAS), (2) directly removing known batch effects using ComBat (Johnson et al. 2007 Biostatistics) and (3) removing batch effects with known control probes (Leek 2014 biorXiv). Removing batch effects and using surrogate variables in differential expression analysis have been shown to reduce dependence, stabilize error rate estimates, and improve reproducibility, see (Leek and Storey 2007 PLoS Genetics, 2008 PNAS or Leek et al. 2011 Nat. Reviews Genetics). biocViews: ImmunoOncology, Microarray, StatisticalMethod, Preprocessing, MultipleComparison, Sequencing, RNASeq, BatchEffect, Normalization Author: Jeffrey T. Leek , W. Evan Johnson , Hilary S. Parker , Elana J. Fertig , Andrew E. Jaffe , John D. Storey , Yuqing Zhang , Leonardo Collado Torres Maintainer: Jeffrey T. Leek , John D. Storey , W. Evan Johnson git_url: https://git.bioconductor.org/packages/sva git_branch: RELEASE_3_8 git_last_commit: fdb98bc git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/sva_3.30.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/sva_3.30.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/sva_3.30.1.tgz vignettes: vignettes/sva/inst/doc/sva.pdf vignetteTitles: sva tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/sva/inst/doc/sva.R dependsOnMe: SCAN.UPC importsMe: ASSIGN, ballgown, BatchQC, bnbc, charm, crossmeta, DaMiRseq, debrowser, doppelgangR, edge, LINC, MAGeCKFlute, omicRexposome, PAA, PROPS, singleCellTK, TCGAbiolinks, trigger suggestsMe: Harman, iasva, RnBeads, SomaticSignatures Package: SVAPLSseq Version: 1.8.1 Depends: R (>= 3.4) Imports: methods, stats, SummarizedExperiment, edgeR, ggplot2, limma, lmtest, parallel, pls Suggests: BiocStyle License: GPL-3 Archs: i386, x64 MD5sum: f5c96fa7eb7d472cd2ddedaee359fdce NeedsCompilation: no Title: SVAPLSseq-An R package to estimate the hidden factors of unwanted variability and adjust for them to enable a more powerful and accurate differential expression analysis based on RNAseq data Description: The package contains functions that are intended for extracting the signatures of latent variation in RNAseq data and using them to perform an improved differential expression analysis for a set of features (genes, transcripts) between two specified biological groups. biocViews: ImmunoOncology, GeneExpression, RNASeq, Normalization, BatchEffect Author: Sutirtha Chakraborty Maintainer: Sutirtha Chakraborty git_url: https://git.bioconductor.org/packages/SVAPLSseq git_branch: RELEASE_3_8 git_last_commit: afebc26 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/SVAPLSseq_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SVAPLSseq_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SVAPLSseq_1.8.1.tgz vignettes: vignettes/SVAPLSseq/inst/doc/SVAPLSseq.pdf vignetteTitles: SVAPLSseq tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SVAPLSseq/inst/doc/SVAPLSseq.R Package: SVM2CRM Version: 1.14.0 Depends: R (>= 3.2.0), LiblineaR, SVM2CRMdata Imports: AnnotationDbi, mclust, GenomicRanges, IRanges, zoo, squash, pls,rtracklayer,ROCR,verification License: GPL-3 MD5sum: 406904f28e8238f547ecc79b2d562ffd NeedsCompilation: no Title: SVM2CRM: support vector machine for cis-regulatory elements detections Description: Detection of cis-regulatory elements using svm implemented in LiblineaR. biocViews: ChIPSeq, SupportVectorMachine, Software, Preprocessing, ChipOnChip Author: Guidantonio Malagoli Tagliazucchi Maintainer: Guidantonio Malagoli Tagliazucchi git_url: https://git.bioconductor.org/packages/SVM2CRM git_branch: RELEASE_3_8 git_last_commit: e1e185a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SVM2CRM_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SVM2CRM_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SVM2CRM_1.14.0.tgz vignettes: vignettes/SVM2CRM/inst/doc/SVM2CRM.pdf vignetteTitles: The \Rpackage{SVM2CRM} Package hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SVM2CRM/inst/doc/SVM2CRM.R Package: SWATH2stats Version: 1.12.1 Depends: R(>= 2.10.0) Imports: data.table, reshape2, grid, ggplot2, stats, grDevices, graphics, utils, biomaRt Suggests: testthat, aLFQ, knitr, PECA Enhances: imsbInfer, MSstats License: GPL-3 MD5sum: b9a0757b467c76b415777e94fd0e2da9 NeedsCompilation: no Title: Transform and Filter SWATH Data for Statistical Packages Description: This package is intended to transform SWATH data from the OpenSWATH software into a format readable by other statistics packages while performing filtering, annotation and FDR estimation. biocViews: Proteomics, Annotation, ExperimentalDesign, Preprocessing, MassSpectrometry, ImmunoOncology Author: Peter Blattmann, Moritz Heusel and Ruedi Aebersold Maintainer: Peter Blattmann VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/SWATH2stats git_branch: RELEASE_3_8 git_last_commit: af27a5f git_last_commit_date: 2018-11-30 Date/Publication: 2018-12-01 source.ver: src/contrib/SWATH2stats_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/SWATH2stats_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SWATH2stats_1.12.1.tgz vignettes: vignettes/SWATH2stats/inst/doc/SWATH2stats_example_script.pdf, vignettes/SWATH2stats/inst/doc/SWATH2stats_vignette.pdf vignetteTitles: SWATH2stats example script, SWATH2stats package Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SWATH2stats/inst/doc/SWATH2stats_example_script.R, vignettes/SWATH2stats/inst/doc/SWATH2stats_vignette.R Package: SwathXtend Version: 2.4.0 Depends: e1071, openxlsx, VennDiagram, lattice License: GPL-2 MD5sum: 4be2d18fb48add8b1212d8c1e906ecec NeedsCompilation: no Title: SWATH extended library generation and statistical data analysis Description: Contains utility functions for integrating spectral libraries for SWATH and statistical data analysis for SWATH generated data. biocViews: Software Author: J WU and D Pascovici Maintainer: Jemma Wu git_url: https://git.bioconductor.org/packages/SwathXtend git_branch: RELEASE_3_8 git_last_commit: 054a7db git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SwathXtend_2.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SwathXtend_2.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SwathXtend_2.4.0.tgz vignettes: vignettes/SwathXtend/inst/doc/SwathXtend_vignette.pdf vignetteTitles: SwathXtend hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SwathXtend/inst/doc/SwathXtend_vignette.R Package: swfdr Version: 1.8.0 Depends: R (>= 3.4) Imports: stats4, ggplot2, reshape2, stats, dplyr Suggests: BiocStyle, knitr, rmarkdown License: GPL (>= 3) MD5sum: edaa6e7aa6de877fd3b61d4c03daa5fe NeedsCompilation: no Title: Science-wise false discovery rate and proportion of true null hypotheses estimation Description: This package allows users to estimate the science-wise false discovery rate from Jager and Leek, "Empirical estimates suggest most published medical research is true," 2013, Biostatistics, using an EM approach due to the presence of rounding and censoring. It also allows users to estimate the proportion of true null hypotheses in the presence of covariates, using a regression framework, as per Boca and Leek, "A regression framework for the proportion of true null hypotheses," 2015, bioRxiv preprint. biocViews: MultipleComparison, StatisticalMethod, Software Author: Jeffrey T. Leek, Leah Jager, Simina M. Boca Maintainer: Simina M. Boca , Jeffrey T. Leek VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/swfdr git_branch: RELEASE_3_8 git_last_commit: c275ab1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/swfdr_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/swfdr_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/swfdr_1.8.0.tgz vignettes: vignettes/swfdr/inst/doc/swfdrTutorial.pdf vignetteTitles: Tutorial for swfdr package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/swfdr/inst/doc/swfdrTutorial.R Package: SwimR Version: 1.20.0 Depends: R (>= 3.0.0), methods, gplots (>= 2.10.1), heatmap.plus (>= 1.3), signal (>= 0.7), R2HTML (>= 2.2.1) Imports: methods License: LGPL-2 MD5sum: 98716966952df5504255e41de4e57055 NeedsCompilation: no Title: SwimR: A Suite of Analytical Tools for Quantification of C. elegans Swimming Behavior Description: SwimR is an R-based suite that calculates, analyses, and plots the frequency of C. elegans swimming behavior over time. It places a particular emphasis on identifying paralysis and quantifying the kinetic elements of paralysis during swimming. Data is input to SwipR from a custom built program that fits a 5 point morphometric spine to videos of single worms swimming in a buffer called Worm Tracker. biocViews: Visualization Author: Jing Wang , Andrew Hardaway and Bing Zhang Maintainer: Randy Blakely git_url: https://git.bioconductor.org/packages/SwimR git_branch: RELEASE_3_8 git_last_commit: 99d8fe2 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/SwimR_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/SwimR_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/SwimR_1.20.0.tgz vignettes: vignettes/SwimR/inst/doc/SwimR.pdf vignetteTitles: SwimR hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/SwimR/inst/doc/SwimR.R Package: switchBox Version: 1.18.0 Depends: R (>= 2.13.1), pROC, gplots License: GPL-2 MD5sum: 383194e52f750c3c3ef7764ca66bcdb3 NeedsCompilation: yes Title: Utilities to train and validate classifiers based on pair switching using the K-Top-Scoring-Pair (KTSP) algorithm Description: The package offer different classifiers based on comparisons of pair of features (TSP), using various decision rules (e.g., majority wins principle). biocViews: Software, StatisticalMethod, Classification Author: Bahman Afsari , Luigi Marchionni , Wikum Dinalankara Maintainer: Bahman Afsari , Luigi Marchionni , Wikum Dinalankara git_url: https://git.bioconductor.org/packages/switchBox git_branch: RELEASE_3_8 git_last_commit: 93b5398 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/switchBox_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/switchBox_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/switchBox_1.18.0.tgz vignettes: vignettes/switchBox/inst/doc/switchBox.pdf vignetteTitles: Working with the switchBox package hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/switchBox/inst/doc/switchBox.R Package: switchde Version: 1.8.1 Depends: R (>= 3.4), SingleCellExperiment Imports: SummarizedExperiment, dplyr, ggplot2, methods, stats Suggests: knitr, rmarkdown, BiocStyle, testthat, numDeriv, tidyr License: GPL (>= 2) Archs: i386, x64 MD5sum: 3ae58b96d83d20e299dfa4550014d062 NeedsCompilation: no Title: Switch-like differential expression across single-cell trajectories Description: Inference and detection of switch-like differential expression across single-cell RNA-seq trajectories. biocViews: ImmunoOncology, Software, Transcriptomics, GeneExpression, RNASeq, Regression, DifferentialExpression, SingleCell Author: Kieran Campbell [aut, cre] Maintainer: Kieran Campbell URL: https://github.com/kieranrcampbell/switchde VignetteBuilder: knitr BugReports: https://github.com/kieranrcampbell/switchde git_url: https://git.bioconductor.org/packages/switchde git_branch: RELEASE_3_8 git_last_commit: d1b6157 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/switchde_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/switchde_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/switchde_1.8.1.tgz vignettes: vignettes/switchde/inst/doc/switchde_vignette.html vignetteTitles: An overview of the switchde package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/switchde/inst/doc/switchde_vignette.R Package: synapter Version: 2.6.1 Depends: R (>= 3.1.0), methods, MSnbase (>= 2.1.2) Imports: RColorBrewer, lattice, qvalue, multtest, utils, tools, Biobase, knitr, Biostrings, cleaver (>= 1.3.3), readr (>= 0.2), rmarkdown (>= 1.0) Suggests: synapterdata (>= 1.13.2), xtable, testthat (>= 0.8), BRAIN, BiocStyle License: GPL-2 MD5sum: 9a66a45988875d007038bae143ce4ea7 NeedsCompilation: no Title: Label-free data analysis pipeline for optimal identification and quantitation Description: The synapter package provides functionality to reanalyse label-free proteomics data acquired on a Synapt G2 mass spectrometer. One or several runs, possibly processed with additional ion mobility separation to increase identification accuracy can be combined to other quantitation files to maximise identification and quantitation accuracy. biocViews: ImmunoOncology, MassSpectrometry, Proteomics, QualityControl Author: Laurent Gatto, Nick J. Bond, Pavel V. Shliaha and Sebastian Gibb. Maintainer: Laurent Gatto and Sebastian Gibb URL: https://lgatto.github.io/synapter/ VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/synapter git_branch: RELEASE_3_8 git_last_commit: 0dcf262 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/synapter_2.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/synapter_2.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/synapter_2.6.1.tgz vignettes: vignettes/synapter/inst/doc/fragmentmatching.html, vignettes/synapter/inst/doc/synapter.html, vignettes/synapter/inst/doc/synapter2.html vignetteTitles: Fragment matching using 'synapter', Combining HDMSe/MSe data using 'synapter' to optimise identification and quantitation, Synapter2 and synergise2 hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/synapter/inst/doc/fragmentmatching.R, vignettes/synapter/inst/doc/synapter.R, vignettes/synapter/inst/doc/synapter2.R suggestsMe: pRoloc Package: synergyfinder Version: 1.8.0 Imports: drc (>= 2.5-12), reshape2 (>= 1.4.1), SpatialExtremes (>= 2.0-2), ggplot2 (>= 2.1.0), gridBase (>= 0.4-7), grid (>= 3.2.4), lattice (>= 0.20-33), gplots (>= 3.0.0), nleqslv(>= 3.0), stats (>= 3.3.0), graphics (>= 3.3.0), grDevices (>= 3.3.0) Suggests: knitr, rmarkdown License: Mozilla Public License 2.0 + file LICENSE MD5sum: e3f9aa7ba027416ec0644f9bf85f5376 NeedsCompilation: no Title: Calculate and Visualize Synergy Scores for Drug Combinations Description: Efficient implementations for all the popular synergy scoring models for drug combinations, including HSA, Loewe, Bliss and ZIP and visualization of the synergy scores as either a two-dimensional or a three-dimensional interaction surface over the dose matrix. biocViews: Software, Statistical Method Author: Liye He , Jing Tang Maintainer: Liye He VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/synergyfinder git_branch: RELEASE_3_8 git_last_commit: 488b89f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/synergyfinder_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/synergyfinder_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/synergyfinder_1.8.0.tgz vignettes: vignettes/synergyfinder/inst/doc/synergyfinder.pdf vignetteTitles: synergyfinder hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/synergyfinder/inst/doc/synergyfinder.R Package: synlet Version: 1.12.1 Depends: R (>= 3.2.0), ggplot2 Imports: doBy, dplyr, grid, magrittr, RColorBrewer, RankProd, reshape2 Suggests: knitr, testthat License: GPL-3 MD5sum: 3c47339f0b3fb2606e620029e2001b10 NeedsCompilation: no Title: Hits Selection for Synthetic Lethal RNAi Screen Data Description: Select hits from synthetic lethal RNAi screen data. For example, there are two identical celllines except one gene is knocked-down in one cellline. The interest is to find genes that lead to stronger lethal effect when they are knocked-down further by siRNA. Quality control and various visualisation tools are implemented. Four different algorithms could be used to pick up the interesting hits. This package is designed based on 384 wells plates, but may apply to other platforms with proper configuration. biocViews: ImmunoOncology, CellBasedAssays, QualityControl, Preprocessing, Visualization, FeatureExtraction Author: Chunxuan Shao Maintainer: Chunxuan Shao VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/synlet git_branch: RELEASE_3_8 git_last_commit: ea52064 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/synlet_1.12.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/synlet_1.12.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/synlet_1.12.1.tgz vignettes: vignettes/synlet/inst/doc/synlet-vignette.html vignetteTitles: A working Demo for synlet hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/synlet/inst/doc/synlet-vignette.R Package: systemPipeR Version: 1.16.1 Depends: Rsamtools (>= 1.31.2), Biostrings, ShortRead (>= 1.37.1), methods Imports: BiocGenerics, GenomicRanges, GenomicFeatures (>= 1.31.3), SummarizedExperiment, VariantAnnotation (>= 1.25.11), rjson, ggplot2, grid, limma, edgeR, DESeq2, GOstats, GO.db, annotate, pheatmap, BatchJobs Suggests: ape, RUnit, BiocStyle, knitr, rmarkdown, biomaRt, BiocParallel, BiocManager License: Artistic-2.0 MD5sum: 0498828a65dbfdaa91825082ec8fe382 NeedsCompilation: no Title: systemPipeR: NGS workflow and report generation environment Description: R package for building and running automated end-to-end analysis workflows for a wide range of next generation sequence (NGS) applications such as RNA-Seq, ChIP-Seq, VAR-Seq and Ribo-Seq. Important features include a uniform workflow interface across different NGS applications, automated report generation, and support for running both R and command-line software, such as NGS aligners or peak/variant callers, on local computers or compute clusters. Efficient handling of complex sample sets and experimental designs is facilitated by a consistently implemented sample annotation infrastructure. Instructions for using systemPipeR are given in the Overview Vignette (HTML). The remaining Vignettes, linked below, are workflow templates for common NGS use cases. biocViews: ImmunoOncology, Genetics, Infrastructure, DataImport, Sequencing, RNASeq, RiboSeq, ChIPSeq, MethylSeq, SNP, GeneExpression, Coverage, GeneSetEnrichment, Alignment, QualityControl Author: Thomas Girke Maintainer: Thomas Girke URL: http://tgirke.github.io/systemPipeR SystemRequirements: systemPipeR can be used to run external command-line software (e.g. short read aligners), but the corresponding tool needs to be installed on a system. VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/systemPipeR git_branch: RELEASE_3_8 git_last_commit: 6f1a478 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/systemPipeR_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/systemPipeR_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/systemPipeR_1.16.1.tgz vignettes: vignettes/systemPipeR/inst/doc/systemPipeChIPseq.pdf, vignettes/systemPipeR/inst/doc/systemPipeRIBOseq.pdf, vignettes/systemPipeR/inst/doc/systemPipeRNAseq.pdf, vignettes/systemPipeR/inst/doc/systemPipeVARseq.pdf, vignettes/systemPipeR/inst/doc/systemPipeR.html vignetteTitles: ChIP-Seq Workflow Template, Ribo-Seq Workflow Template, RNA-Seq Workflow Template, VAR-Seq Workflow Template, Overview Vignette hasREADME: TRUE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/systemPipeR/inst/doc/systemPipeChIPseq.R, vignettes/systemPipeR/inst/doc/systemPipeR.R, vignettes/systemPipeR/inst/doc/systemPipeRIBOseq.R, vignettes/systemPipeR/inst/doc/systemPipeRNAseq.R, vignettes/systemPipeR/inst/doc/systemPipeVARseq.R importsMe: DiffBind, RNASeqR Package: TargetScore Version: 1.20.0 Depends: pracma, Matrix Suggests: TargetScoreData, gplots, Biobase, GEOquery License: GPL-2 MD5sum: 4334b96fdaf7f911bc922ba9d7d1c1a4 NeedsCompilation: no Title: TargetScore: Infer microRNA targets using microRNA-overexpression data and sequence information Description: Infer the posterior distributions of microRNA targets by probabilistically modelling the likelihood microRNA-overexpression fold-changes and sequence-based scores. Variaitonal Bayesian Gaussian mixture model (VB-GMM) is applied to log fold-changes and sequence scores to obtain the posteriors of latent variable being the miRNA targets. The final targetScore is computed as the sigmoid-transformed fold-change weighted by the averaged posteriors of target components over all of the features. biocViews: miRNA Author: Yue Li Maintainer: Yue Li URL: http://www.cs.utoronto.ca/~yueli/software.html git_url: https://git.bioconductor.org/packages/TargetScore git_branch: RELEASE_3_8 git_last_commit: 3f9a5fe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TargetScore_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TargetScore_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TargetScore_1.20.0.tgz vignettes: vignettes/TargetScore/inst/doc/TargetScore.pdf vignetteTitles: TargetScore: Infer microRNA targets using microRNA-overexpression data and sequence information hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TargetScore/inst/doc/TargetScore.R Package: TargetSearch Version: 1.38.2 Depends: ncdf4 Imports: graphics, grDevices, methods, stats, tcltk, utils Suggests: TargetSearchData, BiocStyle, knitr License: GPL (>= 2) MD5sum: 4bbfc850bba21f660f42127c3ca87407 NeedsCompilation: yes Title: A package for the analysis of GC-MS metabolite profiling data Description: This packages provides a targeted pre-processing method for GC-MS data. biocViews: MassSpectrometry, Preprocessing, DecisionTree, ImmunoOncology Author: Alvaro Cuadros-Inostroza , Jan Lisec, Henning Redestig, Matt Hannah Maintainer: Alvaro Cuadros-Inostroza URL: https://github.com/acinostroza/TargetSearch VignetteBuilder: knitr BugReports: https://github.com/acinostroza/TargetSearch/issues git_url: https://git.bioconductor.org/packages/TargetSearch git_branch: RELEASE_3_8 git_last_commit: 5711849 git_last_commit_date: 2019-02-25 Date/Publication: 2019-02-27 source.ver: src/contrib/TargetSearch_1.38.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/TargetSearch_1.38.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TargetSearch_1.38.2.tgz vignettes: vignettes/TargetSearch/inst/doc/RICorrection.pdf, vignettes/TargetSearch/inst/doc/TargetSearch.pdf vignetteTitles: RI correction extra, The TargetSearch Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TargetSearch/inst/doc/RetentionIndexCorrection.R, vignettes/TargetSearch/inst/doc/RICorrection.R, vignettes/TargetSearch/inst/doc/TargetSearch.R Package: TarSeqQC Version: 1.12.0 Depends: R (>= 3.4.1), methods, GenomicRanges, Rsamtools (>= 1.20.4), ggplot2, plyr, openxlsx Imports: grDevices, stats, utils, S4Vectors, IRanges, BiocGenerics, reshape2, GenomeInfoDb, BiocParallel, Biostrings, cowplot, graphics, GenomicAlignments, Hmisc Suggests: BiocManager, RUnit License: GPL (>=2) Archs: i386, x64 MD5sum: d63b65c61556d88e875ac624b4142756 NeedsCompilation: no Title: TARgeted SEQuencing Experiment Quality Control Description: The package allows the representation of targeted experiment in R. This is based on current packages and incorporates functions to do a quality control over this kind of experiments and a fast exploration of the sequenced regions. An xlsx file is generated as output. biocViews: Software, Sequencing, TargetedResequencing, QualityControl, Visualization, Coverage, Alignment, DataImport Author: Gabriela A. Merino, Cristobal Fresno, Yanina Murua, Andrea S. Llera and Elmer A. Fernandez Maintainer: Gabriela Merino URL: http://www.bdmg.com.ar git_url: https://git.bioconductor.org/packages/TarSeqQC git_branch: RELEASE_3_8 git_last_commit: 5a68300 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TarSeqQC_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TarSeqQC_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TarSeqQC_1.12.0.tgz vignettes: vignettes/TarSeqQC/inst/doc/TarSeqQC-vignette.pdf vignetteTitles: TarSeqQC: Targeted Sequencing Experiment Quality Control hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TarSeqQC/inst/doc/TarSeqQC-vignette.R Package: TCC Version: 1.22.1 Depends: R (>= 3.0), methods, DESeq, DESeq2, edgeR, baySeq, ROC Suggests: RUnit, BiocGenerics Enhances: snow License: GPL-2 MD5sum: 1f552da47b59798539ea0191be509ebd NeedsCompilation: no Title: TCC: Differential expression analysis for tag count data with robust normalization strategies Description: This package provides a series of functions for performing differential expression analysis from RNA-seq count data using robust normalization strategy (called DEGES). The basic idea of DEGES is that potential differentially expressed genes or transcripts (DEGs) among compared samples should be removed before data normalization to obtain a well-ranked gene list where true DEGs are top-ranked and non-DEGs are bottom ranked. This can be done by performing a multi-step normalization strategy (called DEGES for DEG elimination strategy). A major characteristic of TCC is to provide the robust normalization methods for several kinds of count data (two-group with or without replicates, multi-group/multi-factor, and so on) by virtue of the use of combinations of functions in depended packages. biocViews: ImmunoOncology, Sequencing, DifferentialExpression, RNASeq Author: Jianqiang Sun, Tomoaki Nishiyama, Kentaro Shimizu, and Koji Kadota Maintainer: Jianqiang Sun , Tomoaki Nishiyama git_url: https://git.bioconductor.org/packages/TCC git_branch: RELEASE_3_8 git_last_commit: bb586e8 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/TCC_1.22.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TCC_1.22.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TCC_1.22.1.tgz vignettes: vignettes/TCC/inst/doc/TCC.pdf vignetteTitles: TCC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TCC/inst/doc/TCC.R suggestsMe: compcodeR Package: TCGAbiolinks Version: 2.10.5 Depends: R (>= 3.2) Imports: downloader (>= 0.4), survminer, grDevices, dplyr, gridExtra, graphics, tibble, grid, GenomicRanges, XML (>= 3.98.0), data.table, EDASeq (>= 2.0.0), edgeR (>= 3.0.0), jsonlite (>= 1.0.0), plyr, knitr, methods, biomaRt, ggplot2, ggthemes, survival, stringr (>= 1.0.0), IRanges, scales, rvest (>= 0.3.0), stats, utils, selectr, S4Vectors, ComplexHeatmap (>= 1.10.2), R.utils, SummarizedExperiment (>= 1.4.0), genefilter, ConsensusClusterPlus, readr, RColorBrewer, doParallel, GenomeInfoDb, GenomicFeatures, parallel, tools, sesame, tidyr, sva, limma, xml2, httr (>= 1.2.1), matlab, circlize, ggrepel (>= 0.6.3) Suggests: png, BiocStyle, rmarkdown, devtools, maftools, parmigene, c3net, minet, dnet, Biobase, affy, testthat, pathview, clusterProfiler, igraph, supraHex License: GPL (>= 3) MD5sum: 4c635e11b988b2226d2eb6662798cf95 NeedsCompilation: no Title: TCGAbiolinks: An R/Bioconductor package for integrative analysis with GDC data Description: The aim of TCGAbiolinks is : i) facilitate the GDC open-access data retrieval, ii) prepare the data using the appropriate pre-processing strategies, iii) provide the means to carry out different standard analyses and iv) to easily reproduce earlier research results. In more detail, the package provides multiple methods for analysis (e.g., differential expression analysis, identifying differentially methylated regions) and methods for visualization (e.g., survival plots, volcano plots, starburst plots) in order to easily develop complete analysis pipelines. biocViews: DNAMethylation, DifferentialMethylation, GeneRegulation, GeneExpression, MethylationArray, DifferentialExpression, Pathways, Network, Sequencing, Survival Author: Antonio Colaprico, Tiago Chedraoui Silva, Catharina Olsen, Luciano Garofano, Davide Garolini, Claudia Cava, Thais Sabedot, Tathiane Malta, Stefano M. Pagnotta, Isabella Castiglioni, Michele Ceccarelli, Gianluca Bontempi, Houtan Noushmehr Maintainer: Antonio Colaprico , Tiago Chedraoui Silva URL: https://github.com/BioinformaticsFMRP/TCGAbiolinks VignetteBuilder: knitr BugReports: https://github.com/BioinformaticsFMRP/TCGAbiolinks/issues git_url: https://git.bioconductor.org/packages/TCGAbiolinks git_branch: RELEASE_3_8 git_last_commit: c51253f git_last_commit_date: 2019-03-20 Date/Publication: 2019-03-20 source.ver: src/contrib/TCGAbiolinks_2.10.5.tar.gz win.binary.ver: bin/windows/contrib/3.5/TCGAbiolinks_2.10.5.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TCGAbiolinks_2.10.5.tgz vignettes: vignettes/TCGAbiolinks/inst/doc/analysis.html, vignettes/TCGAbiolinks/inst/doc/casestudy.html, vignettes/TCGAbiolinks/inst/doc/clinical.html, vignettes/TCGAbiolinks/inst/doc/download_prepare.html, vignettes/TCGAbiolinks/inst/doc/extension.html, vignettes/TCGAbiolinks/inst/doc/gui.html, vignettes/TCGAbiolinks/inst/doc/index.html, vignettes/TCGAbiolinks/inst/doc/mutation.html, vignettes/TCGAbiolinks/inst/doc/query.html, vignettes/TCGAbiolinks/inst/doc/subtypes.html vignetteTitles: 7. Analyzing and visualizing TCGA data, 8. Case Studies, "4. Clinical data", "3. Downloading and preparing files for analysis", "10. TCGAbiolinks_Extension", "9. Graphical User Interface (GUI)", "1. Introduction", "5. Mutation data", "2. Searching GDC database", 6. Compilation of TCGA molecular subtypes hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TCGAbiolinks/inst/doc/analysis.R, vignettes/TCGAbiolinks/inst/doc/casestudy.R, vignettes/TCGAbiolinks/inst/doc/clinical.R, vignettes/TCGAbiolinks/inst/doc/download_prepare.R, vignettes/TCGAbiolinks/inst/doc/extension.R, vignettes/TCGAbiolinks/inst/doc/gui.R, vignettes/TCGAbiolinks/inst/doc/index.R, vignettes/TCGAbiolinks/inst/doc/mutation.R, vignettes/TCGAbiolinks/inst/doc/query.R, vignettes/TCGAbiolinks/inst/doc/subtypes.R importsMe: ELMER, MoonlightR, SpidermiR, TCGAbiolinksGUI Package: TCGAbiolinksGUI Version: 1.8.1 Depends: R (>= 3.3.1), shinydashboard (>= 0.5.3), TCGAbiolinksGUI.data Imports: shiny (>= 0.14.1), downloader (>= 0.4), grid, DT, plotly, readr, maftools, stringr (>= 1.1.0), SummarizedExperiment, ggrepel, data.table, caret, shinyFiles (>= 0.6.2), ggplot2 (>= 2.1.0), pathview, ELMER (>= 2.0.0), clusterProfiler, parallel, TCGAbiolinks (>= 2.5.5), shinyjs (>= 0.7), colourpicker, sesame, sesameData, shinyBS (>= 0.61) Suggests: testthat, dplyr, knitr, roxygen2, devtools, rvest, xml2, BiocStyle, animation, pander License: GPL (>= 3) MD5sum: 6b6661d875a92fbf472cb6e1df48285b NeedsCompilation: no Title: "TCGAbiolinksGUI: A Graphical User Interface to analyze cancer molecular and clinical data" Description: "TCGAbiolinksGUI: A Graphical User Interface to analyze cancer molecular and clinical data. A demo version of GUI is found in https://tcgabiolinksgui.shinyapps.io/tcgabiolinks/" biocViews: Genetics, GUI, DNAMethylation, StatisticalMethod, DifferentialMethylation, GeneRegulation, GeneExpression, MethylationArray, DifferentialExpression, Sequencing, Pathways, Network, DNASeq Author: Tiago Chedraoui Silva , Antonio Colaprico , Catharina Olsen , Michele Ceccarelli, Gianluca Bontempi , Benjamin P. Berman , Houtan Noushmehr Maintainer: Tiago C. Silva VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TCGAbiolinksGUI git_branch: RELEASE_3_8 git_last_commit: 8bb61bd git_last_commit_date: 2019-02-15 Date/Publication: 2019-02-15 source.ver: src/contrib/TCGAbiolinksGUI_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TCGAbiolinksGUI_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TCGAbiolinksGUI_1.8.1.tgz vignettes: vignettes/TCGAbiolinksGUI/inst/doc/analysis.html, vignettes/TCGAbiolinksGUI/inst/doc/Cases.html, vignettes/TCGAbiolinksGUI/inst/doc/data.html, vignettes/TCGAbiolinksGUI/inst/doc/index.html, vignettes/TCGAbiolinksGUI/inst/doc/integrative.html vignetteTitles: "3. Analysis menu", "5. Cases study", "2. Data menu", "1. Introduction", "4. Integrative analysis menu" hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TCGAbiolinksGUI/inst/doc/data.R, vignettes/TCGAbiolinksGUI/inst/doc/index.R Package: TCGAutils Version: 1.2.2 Depends: R (>= 3.5.0) Imports: AnnotationDbi, BiocGenerics, GenomeInfoDb, GenomicFeatures, GenomicRanges, GenomicDataCommons, IRanges, methods, MultiAssayExperiment, RaggedExperiment (>= 1.5.7), rvest, S4Vectors, stats, stringr, SummarizedExperiment, utils, xml2 Suggests: BiocStyle, curatedTCGAData, devtools, impute, knitr, magrittr, mirbase.db, org.Hs.eg.db, readr, RTCGAToolbox (>= 2.7.5), testthat, TxDb.Hsapiens.UCSC.hg19.knownGene, License: Artistic-2.0 MD5sum: d47efffef898763c70e5e5241af113bd NeedsCompilation: no Title: TCGA utility functions for data management Description: A suite of helper functions for checking and manipulating TCGA data including data obtained from the curatedTCGAData experiment package. These functions aim to simplify and make working with TCGA data more manageable. biocViews: Software, WorkflowStep, Preprocessing Author: Marcel Ramos [aut, cre], Lucas Schiffer [aut], Sean Davis [ctb], Levi Waldron [aut] Maintainer: Marcel Ramos VignetteBuilder: knitr BugReports: https://github.com/waldronlab/TCGAutils/issues git_url: https://git.bioconductor.org/packages/TCGAutils git_branch: RELEASE_3_8 git_last_commit: b8b085b git_last_commit_date: 2019-02-13 Date/Publication: 2019-02-13 source.ver: src/contrib/TCGAutils_1.2.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/TCGAutils_1.2.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TCGAutils_1.2.2.tgz vignettes: vignettes/TCGAutils/inst/doc/TCGAutils.html vignetteTitles: TCGAutils Essentials hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TCGAutils/inst/doc/TCGAutils.R importsMe: RTCGAToolbox suggestsMe: glmSparseNet Package: TCseq Version: 1.6.1 Depends: R (>= 3.4) Imports: edgeR, BiocGenerics, reshape2, GenomicRanges, IRanges, SummarizedExperiment, GenomicAlignments, Rsamtools, e1071, cluster, ggplot2, grid, grDevices, stats, utils, methods, locfit Suggests: testthat License: GPL (>= 2) MD5sum: a5256db53d8413d4d479c4328b66a360 NeedsCompilation: no Title: Time course sequencing data analysis Description: Quantitative and differential analysis of epigenomic and transcriptomic time course sequencing data, clustering analysis and visualization of temporal patterns of time course data. biocViews: ImmunoOncology, Epigenetics, TimeCourse, Sequencing, ChIPSeq, RNASeq, DifferentialExpression, Clustering, Visualization Author: Mengjun Wu , Lei Gu Maintainer: Mengjun Wu git_url: https://git.bioconductor.org/packages/TCseq git_branch: RELEASE_3_8 git_last_commit: bd2c43e git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/TCseq_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TCseq_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TCseq_1.6.1.tgz vignettes: vignettes/TCseq/inst/doc/TCseq.pdf vignetteTitles: TCseq Vignette hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TCseq/inst/doc/TCseq.R Package: TDARACNE Version: 1.32.0 Depends: GenKern, Rgraphviz, Biobase License: GPL-2 MD5sum: 5d2edadc66ee9cc1e3984fb1845314fb NeedsCompilation: no Title: Network reverse engineering from time course data. Description: To infer gene networks from time-series measurements is a current challenge into bioinformatics research area. In order to detect dependencies between genes at different time delays, we propose an approach to infer gene regulatory networks from time-series measurements starting from a well known algorithm based on information theory. The proposed algorithm is expected to be useful in reconstruction of small biological directed networks from time course data. biocViews: Microarray, TimeCourse Author: Zoppoli P.,Morganella S., Ceccarelli M. Maintainer: Zoppoli Pietro git_url: https://git.bioconductor.org/packages/TDARACNE git_branch: RELEASE_3_8 git_last_commit: e091645 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TDARACNE_1.32.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TDARACNE_1.32.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TDARACNE_1.32.0.tgz vignettes: vignettes/TDARACNE/inst/doc/TDARACNE.pdf vignetteTitles: TDARACNE hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TDARACNE/inst/doc/TDARACNE.R Package: tenXplore Version: 1.4.1 Depends: R (>= 3.4), shiny, restfulSE (>= 0.99.12) Imports: methods, ontoProc (>= 0.99.7), SummarizedExperiment, AnnotationDbi, matrixStats, org.Mm.eg.db, stats, utils Suggests: org.Hs.eg.db, testthat, knitr License: Artistic-2.0 MD5sum: 8095bfd5b39517eb131405153f410b2f NeedsCompilation: no Title: ontological exploration of scRNA-seq of 1.3 million mouse neurons from 10x genomics Description: Perform ontological exploration of scRNA-seq of 1.3 million mouse neurons from 10x genomics. biocViews: ImmunoOncology, DimensionReduction, PrincipalComponent, Transcriptomics, SingleCell Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tenXplore git_branch: RELEASE_3_8 git_last_commit: b65bcf4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/tenXplore_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/tenXplore_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tenXplore_1.4.1.tgz vignettes: vignettes/tenXplore/inst/doc/tenXplore.pdf vignetteTitles: tenXplore: ontology for scRNA-seq,, applied to 10x 1.3 million neurons hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tenXplore/inst/doc/tenXplore.R Package: TEQC Version: 4.4.0 Depends: methods, BiocGenerics (>= 0.1.0), IRanges (>= 1.13.5), Rsamtools, hwriter Imports: Biobase (>= 2.15.1) License: GPL (>= 2) MD5sum: 85ceae4d51ead9716d90df8bc38e60a8 NeedsCompilation: no Title: Quality control for target capture experiments Description: Target capture experiments combine hybridization-based (in solution or on microarrays) capture and enrichment of genomic regions of interest (e.g. the exome) with high throughput sequencing of the captured DNA fragments. This package provides functionalities for assessing and visualizing the quality of the target enrichment process, like specificity and sensitivity of the capture, per-target read coverage and so on. biocViews: QualityControl, Microarray, Sequencing, Genetics Author: M. Hummel, S. Bonnin, E. Lowy, G. Roma Maintainer: Manuela Hummel git_url: https://git.bioconductor.org/packages/TEQC git_branch: RELEASE_3_8 git_last_commit: b4a9d5a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TEQC_4.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TEQC_4.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TEQC_4.4.0.tgz vignettes: vignettes/TEQC/inst/doc/TEQC.pdf vignetteTitles: TEQC hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TEQC/inst/doc/TEQC.R Package: ternarynet Version: 1.26.0 Depends: R (>= 2.10.0), methods Imports: utils, igraph License: GPL (>= 2) MD5sum: fcc0042c1e0dbfc502572cd0f4b0a3cf NeedsCompilation: yes Title: Ternary Network Estimation Description: A computational Bayesian approach to ternary gene regulatory network estimation from gene perturbation experiments. biocViews: Software, CellBiology, GraphAndNetwork Author: Matthew N. McCall , Anthony Almudevar , David Burton , Harry Stern Maintainer: Matthew N. McCall git_url: https://git.bioconductor.org/packages/ternarynet git_branch: RELEASE_3_8 git_last_commit: 846cf9e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/ternarynet_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/ternarynet_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ternarynet_1.26.0.tgz vignettes: vignettes/ternarynet/inst/doc/ternarynet.pdf vignetteTitles: ternarynet: A Computational Bayesian Approach to Ternary Network Estimation hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ternarynet/inst/doc/ternarynet.R Package: TFARM Version: 1.4.0 Depends: R (>= 3.4) Imports: arules, fields, GenomicRanges, graphics, grDevices, stringr, methods, stats Suggests: BiocStyle, knitr, plyr License: Artistic-2.0 Archs: i386, x64 MD5sum: de70bbb6c08b094687d9a0c8c1b80307 NeedsCompilation: no Title: Transcription Factors Association Rules Miner Description: It searches for relevant associations of transcription factors with a transcription factor target, in specific genomic regions. It also allows to evaluate the Importance Index distribution of transcription factors (and combinations of transcription factors) in association rules. biocViews: BiologicalQuestion, Infrastructure, StatisticalMethod, Transcription Author: Liuba Nausicaa Martino, Alice Parodi, Gaia Ceddia, Piercesare Secchi, Stefano Campaner, Marco Masseroli Maintainer: Liuba Nausicaa Martino VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TFARM git_branch: RELEASE_3_8 git_last_commit: ac05e23 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TFARM_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TFARM_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TFARM_1.4.0.tgz vignettes: vignettes/TFARM/inst/doc/TFARM.pdf vignetteTitles: Transcription Factor Association Rule Miner hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TFARM/inst/doc/TFARM.R Package: TFBSTools Version: 1.20.0 Depends: R (>= 3.2.2) Imports: Biobase(>= 2.28), Biostrings(>= 2.36.4), BiocGenerics(>= 0.14.0), BiocParallel(>= 1.2.21), BSgenome(>= 1.36.3), caTools(>= 1.17.1), CNEr(>= 1.4.0), DirichletMultinomial(>= 1.10.0), GenomeInfoDb(>= 1.6.1), GenomicRanges(>= 1.20.6), gtools(>= 3.5.0), grid, IRanges(>= 2.2.7), methods, DBI (>= 0.6), RSQLite(>= 1.0.0), rtracklayer(>= 1.28.10), seqLogo(>= 1.34.0), S4Vectors(>= 0.9.25), TFMPvalue(>= 0.0.5), XML(>= 3.98-1.3), XVector(>= 0.8.0), parallel Suggests: BiocStyle(>= 1.7.7), JASPAR2014(>= 1.4.0), knitr(>= 1.11), testthat, JASPAR2016(>= 1.0.0) License: GPL-2 MD5sum: e3c9e0fb66c9e32d883aaa5f22d86201 NeedsCompilation: yes Title: Software Package for Transcription Factor Binding Site (TFBS) Analysis Description: TFBSTools is a package for the analysis and manipulation of transcription factor binding sites. It includes matrices conversion between Position Frequency Matirx (PFM), Position Weight Matirx (PWM) and Information Content Matrix (ICM). It can also scan putative TFBS from sequence/alignment, query JASPAR database and provides a wrapper of de novo motif discovery software. biocViews: MotifAnnotation, GeneRegulation, MotifDiscovery, Transcription, Alignment Author: Ge Tan [aut, cre] Maintainer: Ge Tan URL: https://github.com/ge11232002/TFBSTools VignetteBuilder: knitr BugReports: https://github.com/ge11232002/TFBSTools/issues git_url: https://git.bioconductor.org/packages/TFBSTools git_branch: RELEASE_3_8 git_last_commit: 74035fc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TFBSTools_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TFBSTools_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TFBSTools_1.20.0.tgz vignettes: vignettes/TFBSTools/inst/doc/TFBSTools.html vignetteTitles: Transcription factor binding site (TFBS) analysis with the "TFBSTools" package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TFBSTools/inst/doc/TFBSTools.R importsMe: chromVAR, esATAC, MatrixRider, motifmatchr, primirTSS suggestsMe: universalmotif Package: TFEA.ChIP Version: 1.2.3 Depends: R (>= 3.3), dplyr, TxDb.Hsapiens.UCSC.hg19.knownGene, org.Hs.eg.db Imports: GenomicRanges, IRanges, biomaRt, GenomicFeatures, grDevices, stats, utils, R.utils Suggests: knitr, rmarkdown, S4Vectors, plotly, scales, tidyr, ggplot2, GSEABase, DESeq2, BiocGenerics License: Artistic-2.0 Archs: i386, x64 MD5sum: 98861c5d58b41f70c8d7a91114d4fd9a NeedsCompilation: no Title: Analyze Transcription Factor Enrichment Description: Package to analize transcription factor enrichment in a gene set using data from ChIP-Seq experiments. biocViews: ImmunoOncology, Transcription, GeneRegulation, GeneSetEnrichment, Transcriptomics, Sequencing, ChIPSeq, RNASeq Author: Laura Puente Santamaría, Luis del Peso Maintainer: Laura Puente Santamaría VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TFEA.ChIP git_branch: RELEASE_3_8 git_last_commit: 7c2991d git_last_commit_date: 2019-01-22 Date/Publication: 2019-01-22 source.ver: src/contrib/TFEA.ChIP_1.2.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/TFEA.ChIP_1.2.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TFEA.ChIP_1.2.3.tgz vignettes: vignettes/TFEA.ChIP/inst/doc/TFEA.ChIP.html vignetteTitles: Vignette Title hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TFEA.ChIP/inst/doc/TFEA.ChIP.R Package: TFHAZ Version: 1.4.0 Depends: R(>= 3.4) Imports: GenomicRanges, S4Vectors, grDevices, graphics, stats, utils, IRanges, methods Suggests: BiocStyle, knitr, rmarkdown License: Artistic-2.0 MD5sum: b2e9eef46b67621c17b58309ff630b22 NeedsCompilation: no Title: Transcription Factor High Accumulation Zones Description: It finds trascription factor (TF) high accumulation DNA zones, i.e., regions along the genome where there is a high presence of different transcription factors. Starting from a dataset containing the genomic positions of TF binding regions, for each base of the selected chromosome the accumulation of TFs is computed. Three different types of accumulation (TF, region and base accumulation) are available, together with the possibility of considering, in the single base accumulation computing, the TFs present not only in that single base, but also in its neighborhood, within a window of a given width. Two different methods for the search of TF high accumulation DNA zones, called "binding regions" and "overlaps", are available. In addition, some functions are provided in order to analyze, visualize and compare results obtained with different input parameters. biocViews: Software, BiologicalQuestion, Transcription, ChIPSeq, Coverage Author: Alberto Marchesi, Marco Masseroli Maintainer: Alberto Marchesi VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TFHAZ git_branch: RELEASE_3_8 git_last_commit: edb4d1e git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TFHAZ_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TFHAZ_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TFHAZ_1.4.0.tgz vignettes: vignettes/TFHAZ/inst/doc/TFHAZ.html vignetteTitles: TFHAZ hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TFHAZ/inst/doc/TFHAZ.R Package: TFutils Version: 1.2.0 Depends: R (>= 3.5.0) Imports: methods, dplyr, magrittr, miniUI, shiny Suggests: knitr, data.table, GSEABase, testthat, AnnotationDbi, AnnotationFilter, Biobase, GenomicFeatures, GenomicRanges, Gviz, IRanges, Rsamtools, S4Vectors, org.Hs.eg.db, EnsDb.Hsapiens.v75, BiocParallel, BiocStyle, GO.db, GenomicFiles, GenomeInfoDb, SummarizedExperiment, UpSetR, ggplot2, png, gwascat License: Artistic-2.0 MD5sum: f8cdec899590e3cd9198bd3e63c27d01 NeedsCompilation: no Title: TFutils Description: Package to work with TF data. biocViews: Transcriptomics Author: Vincent Carey [aut], Shweta Gopaulakrishnan [cre, aut] Maintainer: Shweta Gopaulakrishnan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TFutils git_branch: RELEASE_3_8 git_last_commit: f97d49d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TFutils_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TFutils_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TFutils_1.2.0.tgz vignettes: vignettes/TFutils/inst/doc/TFutils.html vignetteTitles: TFutils -- representing TFBS and TF target sets hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TFutils/inst/doc/TFutils.R Package: tigre Version: 1.36.0 Depends: R (>= 2.11.0), BiocGenerics, Biobase Imports: methods, AnnotationDbi, gplots, graphics, grDevices, stats, utils, annotate, DBI, RSQLite Suggests: drosgenome1.db, puma, lumi, BiocStyle, BiocManager License: AGPL-3 MD5sum: 96d6f5cdec071763b3695fab44ae87cb NeedsCompilation: yes Title: Transcription factor Inference through Gaussian process Reconstruction of Expression Description: The tigre package implements our methodology of Gaussian process differential equation models for analysis of gene expression time series from single input motif networks. The package can be used for inferring unobserved transcription factor (TF) protein concentrations from expression measurements of known target genes, or for ranking candidate targets of a TF. biocViews: Microarray, TimeCourse, GeneExpression, Transcription, GeneRegulation, NetworkInference, Bayesian Author: Antti Honkela, Pei Gao, Jonatan Ropponen, Miika-Petteri Matikainen, Magnus Rattray, Neil D. Lawrence Maintainer: Antti Honkela URL: https://github.com/ahonkela/tigre BugReports: https://github.com/ahonkela/tigre/issues git_url: https://git.bioconductor.org/packages/tigre git_branch: RELEASE_3_8 git_last_commit: 6ce82a1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tigre_1.36.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tigre_1.36.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tigre_1.36.0.tgz vignettes: vignettes/tigre/inst/doc/tigre_quick.pdf, vignettes/tigre/inst/doc/tigre.pdf vignetteTitles: tigre Quick Guide, tigre User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tigre/inst/doc/tigre_quick.R, vignettes/tigre/inst/doc/tigre.R Package: tilingArray Version: 1.60.0 Depends: R (>= 2.11.0), Biobase, methods, pixmap Imports: strucchange, affy, vsn, genefilter, RColorBrewer, grid, stats4 License: Artistic-2.0 Archs: i386, x64 MD5sum: eae54973c3f6bd1f99ddb4df77d0377a NeedsCompilation: yes Title: Transcript mapping with high-density oligonucleotide tiling arrays Description: The package provides functionality that can be useful for the analysis of high-density tiling microarray data (such as from Affymetrix genechips) for measuring transcript abundance and architecture. The main functionalities of the package are: 1. the class 'segmentation' for representing partitionings of a linear series of data; 2. the function 'segment' for fitting piecewise constant models using a dynamic programming algorithm that is both fast and exact; 3. the function 'confint' for calculating confidence intervals using the strucchange package; 4. the function 'plotAlongChrom' for generating pretty plots; 5. the function 'normalizeByReference' for probe-sequence dependent response adjustment from a (set of) reference hybridizations. biocViews: Microarray, OneChannel, Preprocessing, Visualization Author: Wolfgang Huber, Zhenyu Xu, Joern Toedling with contributions from Matt Ritchie Maintainer: Zhenyu Xu git_url: https://git.bioconductor.org/packages/tilingArray git_branch: RELEASE_3_8 git_last_commit: be5c18c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tilingArray_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tilingArray_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tilingArray_1.60.0.tgz vignettes: vignettes/tilingArray/inst/doc/assessNorm.pdf, vignettes/tilingArray/inst/doc/costMatrix.pdf, vignettes/tilingArray/inst/doc/findsegments.pdf, vignettes/tilingArray/inst/doc/plotAlongChrom.pdf, vignettes/tilingArray/inst/doc/segmentation.pdf vignetteTitles: Normalisation with the normalizeByReference function in the tilingArray package, Supplement. Calculation of the cost matrix, Introduction to using the segment function to fit a piecewise constant curve, Introduction to the plotAlongChrom function, Segmentation demo hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tilingArray/inst/doc/findsegments.R, vignettes/tilingArray/inst/doc/plotAlongChrom.R importsMe: ADaCGH2, snapCGH Package: timecourse Version: 1.54.0 Depends: R (>= 2.1.1), MASS, methods Imports: Biobase, graphics, limma (>= 1.8.6), MASS, marray, methods, stats License: LGPL Archs: i386, x64 MD5sum: f951b9aa3b8398f16a99b0534c58c94f NeedsCompilation: no Title: Statistical Analysis for Developmental Microarray Time Course Data Description: Functions for data analysis and graphical displays for developmental microarray time course data. biocViews: Microarray, TimeCourse, DifferentialExpression Author: Yu Chuan Tai Maintainer: Yu Chuan Tai URL: http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/timecourse git_branch: RELEASE_3_8 git_last_commit: 1a12deb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/timecourse_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/timecourse_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/timecourse_1.54.0.tgz vignettes: vignettes/timecourse/inst/doc/timecourse.pdf vignetteTitles: timecourse manual hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/timecourse/inst/doc/timecourse.R Package: timescape Version: 1.6.0 Depends: R (>= 3.3) Imports: htmlwidgets (>= 0.5), jsonlite (>= 0.9.19), stringr (>= 1.0.0), dplyr (>= 0.4.3), gtools (>= 3.5.0) Suggests: knitr, rmarkdown License: GPL-3 MD5sum: 4559bf51a0edf576108683f5b8e96652 NeedsCompilation: no Title: Patient Clonal Timescapes Description: TimeScape is an automated tool for navigating temporal clonal evolution data. The key attributes of this implementation involve the enumeration of clones, their evolutionary relationships and their shifting dynamics over time. TimeScape requires two inputs: (i) the clonal phylogeny and (ii) the clonal prevalences. Optionally, TimeScape accepts a data table of targeted mutations observed in each clone and their allele prevalences over time. The output is the TimeScape plot showing clonal prevalence vertically, time horizontally, and the plot height optionally encoding tumour volume during tumour-shrinking events. At each sampling time point (denoted by a faint white line), the height of each clone accurately reflects its proportionate prevalence. These prevalences form the anchors for bezier curves that visually represent the dynamic transitions between time points. biocViews: Visualization, BiomedicalInformatics Author: Maia Smith [aut, cre] Maintainer: Maia Smith VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/timescape git_branch: RELEASE_3_8 git_last_commit: 0742f27 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/timescape_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/timescape_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/timescape_1.6.0.tgz vignettes: vignettes/timescape/inst/doc/timescape_vignette.html vignetteTitles: TimeScape vignette hasREADME: TRUE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/timescape/inst/doc/timescape_vignette.R Package: TimeSeriesExperiment Version: 1.0.4 Depends: R (>= 3.5.0), S4Vectors (>= 0.19.23), SummarizedExperiment (>= 1.11.6) Imports: dynamicTreeCut, dplyr, edgeR, DESeq2, ggplot2 (>= 3.0.0), graphics, Hmisc, limma, methods, magrittr, proxy, stats, tibble, tidyr, vegan, viridis, utils Suggests: Biobase, BiocFileCache (>= 1.5.8), circlize, ComplexHeatmap, GO.db, grDevices, grid, knitr, org.Mm.eg.db, org.Hs.eg.db, MASS, RColorBrewer, rmarkdown, UpSetR, License: LGPL (>= 3) MD5sum: 505f3d1a4e1b9f17d0a1e799e28fcec0 NeedsCompilation: no Title: Analysis for short time-series data Description: Visualization and analysis toolbox for short time course data which includes dimensionality reduction, clustering, two-sample differential expression testing and gene ranking techniques. The package also provides methods for retrieving enriched pathways. biocViews: TimeCourse, Sequencing, RNASeq, Microbiome, GeneExpression, ImmunoOncology, Transcription, Normalization, DifferentialExpression, PrincipalComponent, Clustering, Visualization, Pathways Author: Lan Huong Nguyen Maintainer: Lan Huong Nguyen URL: https://github.com/nlhuong/TimeSeriesExperiment VignetteBuilder: knitr BugReports: https://github.com/nlhuong/TimeSeriesExperiment/issues git_url: https://git.bioconductor.org/packages/TimeSeriesExperiment git_branch: RELEASE_3_8 git_last_commit: 63f9597 git_last_commit_date: 2019-01-14 Date/Publication: 2019-01-15 source.ver: src/contrib/TimeSeriesExperiment_1.0.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/TimeSeriesExperiment_1.0.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TimeSeriesExperiment_1.0.4.tgz vignettes: vignettes/TimeSeriesExperiment/inst/doc/cop1_knockout_timecourse.html vignetteTitles: Gene expression time course data analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TimeSeriesExperiment/inst/doc/cop1_knockout_timecourse.R Package: TIN Version: 1.14.0 Depends: R (>= 2.12.0), data.table, impute, aroma.affymetrix Imports: WGCNA, squash, stringr Suggests: knitr, aroma.light, affxparser, RUnit, BiocGenerics License: Artistic-2.0 MD5sum: 924d7dc26022c2ca5d9923d05de34c83 NeedsCompilation: no Title: Transcriptome instability analysis Description: The TIN package implements a set of tools for transcriptome instability analysis based on exon expression profiles. Deviating exon usage is studied in the context of splicing factors to analyse to what degree transcriptome instability is correlated to splicing factor expression. In the transcriptome instability correlation analysis, the data is compared to both random permutations of alternative splicing scores and expression of random gene sets. biocViews: ExonArray, Microarray, GeneExpression, AlternativeSplicing, Genetics, DifferentialSplicing Author: Bjarne Johannessen, Anita Sveen and Rolf I. Skotheim Maintainer: Bjarne Johannessen VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TIN git_branch: RELEASE_3_8 git_last_commit: c2851cb git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TIN_1.14.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TIN_1.14.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TIN_1.14.0.tgz vignettes: vignettes/TIN/inst/doc/TIN.pdf vignetteTitles: Introduction to the TIN package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TIN/inst/doc/TIN.R Package: TissueEnrich Version: 1.2.1 Depends: R (>= 3.5), ensurer (>= 1.1.0), ggplot2 (>= 2.2.1), tidyr (>= 0.8.0), SummarizedExperiment (>= 1.6.5), GSEABase (>= 1.38.2) Imports: dplyr (>= 0.7.3), stats Suggests: knitr, rmarkdown, testthat License: MIT + file LICENSE MD5sum: e35456c0b1b802568e099654a8d933e6 NeedsCompilation: no Title: Tissue-specific gene enrichment analysis Description: The TissueEnrich package is used to calculate enrichment of tissue-specific genes in a set of input genes. For example, the user can input the most highly expressed genes from RNA-Seq data, or gene co-expression modules to determine which tissue-specific genes are enriched in those datasets. Tissue-specific genes were defined by processing RNA-Seq data from the Human Protein Atlas (HPA) (Uhlén et al. 2015), GTEx (Ardlie et al. 2015), and mouse ENCODE (Shen et al. 2012) using the algorithm from the HPA (Uhlén et al. 2015).The hypergeometric test is being used to determine if the tissue-specific genes are enriched among the input genes. Along with tissue-specific gene enrichment, the TissueEnrich package can also be used to define tissue-specific genes from expression datasets provided by the user, which can then be used to calculate tissue-specific gene enrichments. biocViews: GeneSetEnrichment, GeneExpression, Sequencing Author: Ashish Jain [aut, cre], Geetu Tuteja [aut] Maintainer: Ashish Jain VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TissueEnrich git_branch: RELEASE_3_8 git_last_commit: c3a1633 git_last_commit_date: 2018-12-12 Date/Publication: 2018-12-12 source.ver: src/contrib/TissueEnrich_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TissueEnrich_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TissueEnrich_1.2.1.tgz vignettes: vignettes/TissueEnrich/inst/doc/TissueEnrich.html vignetteTitles: TissueEnrich hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/TissueEnrich/inst/doc/TissueEnrich.R Package: TitanCNA Version: 1.20.1 Depends: R (>= 3.3.2) Imports: IRanges (>= 2.6.1), GenomicRanges (>= 1.24.3), VariantAnnotation (>= 1.18.7), foreach (>= 1.4.3), Rsamtools (>= 1.24.0), GenomeInfoDb (>= 1.8.7), data.table (>= 1.10.4), dplyr (>= 0.5.0), License: GPL-3 MD5sum: 024bfa5afdfeaf0b6bc40cad677cdb5c NeedsCompilation: yes Title: Subclonal copy number and LOH prediction from whole genome sequencing of tumours Description: Hidden Markov model to segment and predict regions of subclonal copy number alterations (CNA) and loss of heterozygosity (LOH), and estimate cellular prevalenece of clonal clusters in tumour whole genome sequencing data. biocViews: ImmunoOncology, Sequencing, WholeGenome, DNASeq, ExomeSeq, StatisticalMethod, CopyNumberVariation, HiddenMarkovModel, Genetics, GenomicVariation Author: Gavin Ha, Sohrab P Shah Maintainer: Gavin Ha , Sohrab P Shah URL: https://github.com/gavinha/TitanCNA git_url: https://git.bioconductor.org/packages/TitanCNA git_branch: RELEASE_3_8 git_last_commit: 3636b53 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/TitanCNA_1.20.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TitanCNA_1.20.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TitanCNA_1.20.1.tgz vignettes: vignettes/TitanCNA/inst/doc/TitanCNA.pdf hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TitanCNA/inst/doc/TitanCNA.R Package: tkWidgets Version: 1.60.0 Depends: R (>= 2.0.0), methods, widgetTools (>= 1.1.7), DynDoc (>= 1.3.0), tools Suggests: Biobase, hgu95av2 License: Artistic-2.0 Archs: i386, x64 MD5sum: 0e005bd310c9b2eceacac768781a3a61 NeedsCompilation: no Title: R based tk widgets Description: Widgets to provide user interfaces. tcltk should have been installed for the widgets to run. biocViews: Infrastructure Author: J. Zhang Maintainer: J. Zhang git_url: https://git.bioconductor.org/packages/tkWidgets git_branch: RELEASE_3_8 git_last_commit: 81906e7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tkWidgets_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tkWidgets_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tkWidgets_1.60.0.tgz vignettes: vignettes/tkWidgets/inst/doc/importWizard.pdf, vignettes/tkWidgets/inst/doc/tkWidgets.pdf vignetteTitles: tkWidgets importWizard, tkWidgets contents hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tkWidgets/inst/doc/importWizard.R, vignettes/tkWidgets/inst/doc/tkWidgets.R importsMe: Mfuzz, OLINgui suggestsMe: affy, affyQCReport, annotate, Biobase, genefilter, marray Package: TMixClust Version: 1.4.0 Depends: R (>= 3.4) Imports: gss, mvtnorm, stats, zoo, cluster, utils, BiocParallel, flexclust, grDevices, graphics, Biobase, SPEM Suggests: rmarkdown, knitr, BiocStyle, testthat License: GPL (>=2) MD5sum: 60760731b1fdae8cf110d2407173bdb5 NeedsCompilation: no Title: Time Series Clustering of Gene Expression with Gaussian Mixed-Effects Models and Smoothing Splines Description: Implementation of a clustering method for time series gene expression data based on mixed-effects models with Gaussian variables and non-parametric cubic splines estimation. The method can robustly account for the high levels of noise present in typical gene expression time series datasets. biocViews: Software, StatisticalMethod, Clustering, TimeCourse, GeneExpression Author: Monica Golumbeanu Maintainer: Monica Golumbeanu VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TMixClust git_branch: RELEASE_3_8 git_last_commit: a52fcae git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TMixClust_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TMixClust_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TMixClust_1.4.0.tgz vignettes: vignettes/TMixClust/inst/doc/TMixClust.pdf vignetteTitles: Clustering time series gene expression data with TMixClust hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TMixClust/inst/doc/TMixClust.R Package: TnT Version: 1.4.0 Depends: R (>= 3.4), GenomicRanges Imports: methods, stats, utils, grDevices, htmlwidgets, jsonlite, data.table, Biobase, GenomeInfoDb, IRanges, S4Vectors, knitr Suggests: GenomicFeatures, shiny, BiocManager, rmarkdown, testthat License: AGPL-3 MD5sum: fe8a6e7598825b862f8fcba6bddebc71 NeedsCompilation: no Title: Interactive Visualization for Genomic Features Description: A R interface to the TnT javascript library (https://github.com/ tntvis) to provide interactive and flexible visualization of track-based genomic data. biocViews: Infrastructure, Visualization Author: Jialin Ma [cre, aut], Miguel Pignatelli [aut], Toby Hocking [aut] Maintainer: Jialin Ma URL: https://github.com/Marlin-Na/TnT VignetteBuilder: knitr BugReports: https://github.com/Marlin-Na/TnT/issues git_url: https://git.bioconductor.org/packages/TnT git_branch: RELEASE_3_8 git_last_commit: d7d17ed git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TnT_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TnT_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TnT_1.4.0.tgz vignettes: vignettes/TnT/inst/doc/introduction.html vignetteTitles: Introduction to TnT hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TnT/inst/doc/introduction.R Package: tofsims Version: 1.10.1 Depends: R (>= 3.3.0), methods, utils, ProtGenerics Imports: Rcpp (>= 0.11.2), ALS, ChemometricsWithR, signal, KernSmooth, graphics, grDevices, stats LinkingTo: Rcpp, RcppArmadillo Suggests: EBImage, knitr, rmarkdown, testthat, tofsimsData, BiocParallel, RColorBrewer Enhances: parallel License: GPL-3 MD5sum: c2dd08ba481e1d82632d1f7a33eda2c3 NeedsCompilation: yes Title: Import, process and analysis of Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) imaging data Description: This packages offers a pipeline for import, processing and analysis of ToF-SIMS 2D image data. Import of Iontof and Ulvac-Phi raw or preprocessed data is supported. For rawdata, mass calibration, peak picking and peak integration exist. General funcionality includes data binning, scaling, image subsetting and visualization. A range of multivariate tools common in the ToF-SIMS community are implemented (PCA, MCR, MAF, MNF). An interface to the bioconductor image processing package EBImage offers image segmentation functionality. biocViews: ImmunoOncology, Infrastructure, DataImport, MassSpectrometry, ImagingMassSpectrometry, Proteomics, Metabolomics Author: Lorenz Gerber, Viet Mai Hoang Maintainer: Lorenz Gerber URL: https://github.com/lorenzgerber/tofsims VignetteBuilder: knitr BugReports: https://github.com/lorenzgerber/tofsims/issues git_url: https://git.bioconductor.org/packages/tofsims git_branch: RELEASE_3_8 git_last_commit: 59e42aa git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/tofsims_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/tofsims_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tofsims_1.10.1.tgz vignettes: vignettes/tofsims/inst/doc/workflow.html vignetteTitles: Workflow with the `tofsims` package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tofsims/inst/doc/workflow.R Package: ToPASeq Version: 1.16.1 Depends: R(>= 3.5.0), graphite Imports: Rcpp, graph, methods LinkingTo: Rcpp Suggests: BiocStyle, EnrichmentBrowser, airway, knitr, rmarkdown License: AGPL-3 Archs: i386, x64 MD5sum: edd0e4da44815a02ca4c6df5b59423ca NeedsCompilation: yes Title: Topology-based pathway analysis of RNA-seq data Description: Implementation of methods for topology-based pathway analysis of RNA-seq data. This includes Topological Analysis of Pathway Phenotype Association (TAPPA; Gao and Wang, 2007), PathWay Enrichment Analysis (PWEA; Hung et al., 2010), and the Pathway Regulation Score (PRS; Ibrahim et al., 2012). biocViews: ImmunoOncology, GeneExpression, RNASeq, DifferentialExpression, GraphAndNetwork, Pathways, NetworkEnrichment, Visualization Author: Ivana Ihnatova, Eva Budinska, Ludwig Geistlinger Maintainer: Ludwig Geistlinger VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/ToPASeq git_branch: RELEASE_3_8 git_last_commit: c4c0bb7 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/ToPASeq_1.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/ToPASeq_1.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/ToPASeq_1.16.1.tgz vignettes: vignettes/ToPASeq/inst/doc/ToPASeq.html vignetteTitles: Topology-based pathway analysis of RNA-seq data hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/ToPASeq/inst/doc/ToPASeq.R Package: topdownr Version: 1.4.1 Depends: R (>= 3.4), methods, BiocGenerics (>= 0.20.0), ProtGenerics (>= 1.10.0), Biostrings (>= 2.42.1), S4Vectors (>= 0.12.2) Imports: grDevices, stats, tools, utils, Biobase, Matrix (>= 1.2.10), MSnbase (>= 2.3.10), ggplot2 (>= 2.2.1), mzR (>= 2.11.4) Suggests: topdownrdata (>= 0.2), knitr, ranger, testthat, BiocStyle License: GPL (>= 3) Archs: i386, x64 MD5sum: adc072328cc05e4faf4523c59dd94ca7 NeedsCompilation: no Title: Investigation of Fragmentation Conditions in Top-Down Proteomics Description: The topdownr package allows automatic and systemic investigation of fragment conditions. It creates Thermo Orbitrap Fusion Lumos method files to test hundreds of fragmentation conditions. Additionally it provides functions to analyse and process the generated MS data and determine the best conditions to maximise overall fragment coverage. biocViews: ImmunoOncology, Infrastructure, Proteomics, MassSpectrometry, Coverage Author: Sebastian Gibb [aut, cre] (), Pavel Shliaha [aut] (), Ole Nørregaard Jensen [aut] () Maintainer: Sebastian Gibb URL: https://github.com/sgibb/topdownr/ VignetteBuilder: knitr BugReports: https://github.com/sgibb/topdownr/issues/ git_url: https://git.bioconductor.org/packages/topdownr git_branch: RELEASE_3_8 git_last_commit: 6e2f8b5 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/topdownr_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/topdownr_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/topdownr_1.4.1.tgz vignettes: vignettes/topdownr/inst/doc/analysis.html, vignettes/topdownr/inst/doc/data-generation.html vignetteTitles: Fragmentation Analysis with topdownr, Data Generation for topdownr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/topdownr/inst/doc/analysis.R, vignettes/topdownr/inst/doc/data-generation.R Package: topGO Version: 2.34.0 Depends: R (>= 2.10.0), methods, BiocGenerics (>= 0.13.6), graph (>= 1.14.0), Biobase (>= 2.0.0), GO.db (>= 2.3.0), AnnotationDbi (>= 1.7.19), SparseM (>= 0.73) Imports: lattice, matrixStats, DBI Suggests: ALL, hgu95av2.db, hgu133a.db, genefilter, xtable, multtest, Rgraphviz, globaltest License: LGPL MD5sum: c46fdfda730504443c46c4b4bed95f00 NeedsCompilation: no Title: Enrichment Analysis for Gene Ontology Description: topGO package provides tools for testing GO terms while accounting for the topology of the GO graph. Different test statistics and different methods for eliminating local similarities and dependencies between GO terms can be implemented and applied. biocViews: Microarray, Visualization Author: Adrian Alexa, Jorg Rahnenfuhrer Maintainer: Adrian Alexa git_url: https://git.bioconductor.org/packages/topGO git_branch: RELEASE_3_8 git_last_commit: 44cb5ea git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/topGO_2.34.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/topGO_2.34.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/topGO_2.34.0.tgz vignettes: vignettes/topGO/inst/doc/topGO.pdf vignetteTitles: topGO hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/topGO/inst/doc/topGO.R dependsOnMe: BgeeDB, cellTree, compEpiTools, EGSEA, ideal, RCAS, RNAither, tRanslatome importsMe: cellity, EnrichmentBrowser, FoldGO, GOSim, OmaDB, pcaExplorer, psygenet2r, SEPA, transcriptogramer suggestsMe: FGNet, IntramiRExploreR, miRNAtap, Ringo Package: TPP Version: 3.10.1 Depends: R (>= 3.4), Biobase, dplyr, magrittr, tidyr Imports: biobroom, broom, data.table, doParallel, foreach, futile.logger, ggplot2, grDevices, gridExtra, grid, knitr, limma, MASS, mefa, nls2, openxlsx (>= 2.4.0), parallel, plyr, purrr, RColorBrewer, RCurl, reshape2, rmarkdown, sme, splines, stats, stringr, utils, VennDiagram, VGAM Suggests: BiocStyle, testthat License: Artistic-2.0 MD5sum: aa7ba75a54c3bb9c9c34efdf1a6208a7 NeedsCompilation: no Title: Analyze thermal proteome profiling (TPP) experiments Description: Analyze thermal proteome profiling (TPP) experiments with varying temperatures (TR) or compound concentrations (CCR). biocViews: ImmunoOncology, Proteomics, MassSpectrometry Author: Dorothee Childs, Nils Kurzawa, Holger Franken, Carola Doce, Mikhail Savitski and Wolfgang Huber Maintainer: Dorothee Childs VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TPP git_branch: RELEASE_3_8 git_last_commit: 7543797 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/TPP_3.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TPP_3.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TPP_3.10.1.tgz vignettes: vignettes/TPP/inst/doc/NPARC_analysis_of_TPP_TR_data.pdf, vignettes/TPP/inst/doc/TPP_introduction_1D.pdf, vignettes/TPP/inst/doc/TPP_introduction_2D.pdf vignetteTitles: TPP_introduction_NPARC, TPP_introduction_1D, TPP_introduction_2D hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TPP/inst/doc/NPARC_analysis_of_TPP_TR_data.R, vignettes/TPP/inst/doc/TPP_introduction_1D.R, vignettes/TPP/inst/doc/TPP_introduction_2D.R Package: tracktables Version: 1.16.0 Depends: R (>= 3.0.0) Imports: IRanges, GenomicRanges, XVector, Rsamtools, XML, tractor.base, stringr, RColorBrewer, methods Suggests: knitr, BiocStyle License: GPL (>= 3) MD5sum: 838950811dd0ae1fc902181f7ecca4ab NeedsCompilation: no Title: Build IGV tracks and HTML reports Description: Methods to create complex IGV genome browser sessions and dynamic IGV reports in HTML pages. biocViews: Sequencing, ReportWriting Author: Tom Carroll, Sanjay Khadayate, Anne Pajon, Ziwei Liang Maintainer: Tom Carroll VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tracktables git_branch: RELEASE_3_8 git_last_commit: 7a1f02a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tracktables_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tracktables_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tracktables_1.16.0.tgz vignettes: vignettes/tracktables/inst/doc/tracktables.pdf vignetteTitles: Creating IGV HTML reports with tracktables hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tracktables/inst/doc/tracktables.R Package: trackViewer Version: 1.18.3 Depends: R (>= 3.1.0), grDevices, methods, GenomicRanges, grid Imports: GenomeInfoDb, GenomicAlignments, GenomicFeatures, Gviz, Rsamtools, S4Vectors, rtracklayer, BiocGenerics, scales, tools, IRanges, AnnotationDbi, grImport, htmlwidgets, plotrix, Rgraphviz, InteractionSet, graph Suggests: biomaRt, TxDb.Hsapiens.UCSC.hg19.knownGene, RUnit, org.Hs.eg.db, BiocStyle, knitr, VariantAnnotation License: GPL (>= 2) MD5sum: bbd6d7b32021cf66e055af85a9412f2d NeedsCompilation: no Title: A R/Bioconductor package for drawing elegant interactive tracks or lollipop plot to facilitate integrated analysis of multi-omics data Description: Visualize mapped reads along with annotation as track layers for NGS dataset such as ChIP-seq, RNA-seq, miRNA-seq, DNA-seq, SNPs and methylation data. biocViews: Visualization Author: Jianhong Ou, Yong-Xu Wang, Lihua Julie Zhu Maintainer: Jianhong Ou VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/trackViewer git_branch: RELEASE_3_8 git_last_commit: be07a8e git_last_commit_date: 2019-03-14 Date/Publication: 2019-03-14 source.ver: src/contrib/trackViewer_1.18.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/trackViewer_1.18.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/trackViewer_1.18.3.tgz vignettes: vignettes/trackViewer/inst/doc/trackViewer.html vignetteTitles: trackViewer Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/trackViewer/inst/doc/trackViewer.R importsMe: NADfinder suggestsMe: ATACseqQC, ChIPpeakAnno Package: transcriptogramer Version: 1.4.1 Depends: R (>= 3.4), methods Imports: biomaRt, data.table, doSNOW, foreach, ggplot2, graphics, grDevices, igraph, limma, parallel, progress, RedeR, snow, stats, tidyr, topGO Suggests: BiocStyle, knitr, rmarkdown, RUnit, BiocGenerics License: GPL (>= 2) MD5sum: f47441df0de365c755ad232153eb8082 NeedsCompilation: no Title: Transcriptional analysis based on transcriptograms Description: R package for transcriptional analysis based on transcriptograms, a method to analyze transcriptomes that projects expression values on a set of ordered proteins, arranged such that the probability that gene products participate in the same metabolic pathway exponentially decreases with the increase of the distance between two proteins of the ordering. Transcriptograms are, hence, genome wide gene expression profiles that provide a global view for the cellular metabolism, while indicating gene sets whose expression are altered. biocViews: Software, Network, Visualization, SystemsBiology, GeneExpression, GeneSetEnrichment, GraphAndNetwork, Clustering, DifferentialExpression, Microarray, RNASeq, Transcription, ImmunoOncology Author: Diego Morais [aut, cre], Rodrigo Dalmolin [aut] Maintainer: Diego Morais URL: https://github.com/arthurvinx/transcriptogramer SystemRequirements: Java Runtime Environment (>= 6) VignetteBuilder: knitr BugReports: https://github.com/arthurvinx/transcriptogramer/issues git_url: https://git.bioconductor.org/packages/transcriptogramer git_branch: RELEASE_3_8 git_last_commit: 3759ba7 git_last_commit_date: 2018-11-29 Date/Publication: 2018-11-29 source.ver: src/contrib/transcriptogramer_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/transcriptogramer_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/transcriptogramer_1.4.1.tgz vignettes: vignettes/transcriptogramer/inst/doc/transcriptogramer.html vignetteTitles: The transcriptogramer user's guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/transcriptogramer/inst/doc/transcriptogramer.R Package: transcriptR Version: 1.10.1 Depends: methods, R (>= 3.3) Imports: BiocGenerics, caret, chipseq, e1071, GenomicAlignments, GenomicRanges, GenomicFeatures, GenomeInfoDb, ggplot2, graphics, grDevices, IRanges (>= 2.11.15), pROC, reshape2, Rsamtools, rtracklayer, S4Vectors, stats, utils Suggests: BiocStyle, knitr, rmarkdown, TxDb.Hsapiens.UCSC.hg19.knownGene, testthat License: GPL-3 MD5sum: 684c388c37c55d7626d7aeea1c950ac3 NeedsCompilation: no Title: An Integrative Tool for ChIP- And RNA-Seq Based Primary Transcripts Detection and Quantification Description: The differences in the RNA types being sequenced have an impact on the resulting sequencing profiles. mRNA-seq data is enriched with reads derived from exons, while GRO-, nucRNA- and chrRNA-seq demonstrate a substantial broader coverage of both exonic and intronic regions. The presence of intronic reads in GRO-seq type of data makes it possible to use it to computationally identify and quantify all de novo continuous regions of transcription distributed across the genome. This type of data, however, is more challenging to interpret and less common practice compared to mRNA-seq. One of the challenges for primary transcript detection concerns the simultaneous transcription of closely spaced genes, which needs to be properly divided into individually transcribed units. The R package transcriptR combines RNA-seq data with ChIP-seq data of histone modifications that mark active Transcription Start Sites (TSSs), such as, H3K4me3 or H3K9/14Ac to overcome this challenge. The advantage of this approach over the use of, for example, gene annotations is that this approach is data driven and therefore able to deal also with novel and case specific events. Furthermore, the integration of ChIP- and RNA-seq data allows the identification all known and novel active transcription start sites within a given sample. biocViews: ImmunoOncology, Transcription, Software, Sequencing, RNASeq, Coverage Author: Armen R. Karapetyan Maintainer: Armen R. Karapetyan VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/transcriptR git_branch: RELEASE_3_8 git_last_commit: 777abcd git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/transcriptR_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/transcriptR_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/transcriptR_1.10.1.tgz vignettes: vignettes/transcriptR/inst/doc/transcriptR.pdf vignetteTitles: transcriptR: an integrative tool for ChIP- and RNA-seq based primary transcripts detection and quantification hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/transcriptR/inst/doc/transcriptR.R Package: transite Version: 1.0.2 Depends: R (>= 3.5) Imports: BiocGenerics (>= 0.26.0), Biostrings (>= 2.48.0), dplyr (>= 0.7.6), GenomicRanges (>= 1.32.6), ggplot2 (>= 3.0.0), ggseqlogo (>= 0.1), gridExtra (>= 2.3), methods, parallel, Rcpp (>= 0.12.18), scales (>= 1.0.0), stats, TFMPvalue (>= 0.0.8), utils LinkingTo: Rcpp (>= 0.12.18) Suggests: knitr (>= 1.20), rmarkdown (>= 1.10), roxygen2 (>= 6.1.0) License: MIT + file LICENSE MD5sum: 0c1afa12b4673222cbc42ae63cebc9bf NeedsCompilation: yes Title: RNA-binding protein motif analysis Description: transite is a computational method that allows comprehensive analysis of the regulatory role of RNA-binding proteins in various cellular processes by leveraging preexisting gene expression data and current knowledge of binding preferences of RNA-binding proteins. biocViews: GeneExpression, Transcription, DifferentialExpression, Microarray, mRNAMicroarray, Genetics, GeneSetEnrichment Author: Konstantin Krismer [aut, cre, cph] (), Anna Gattinger [aut] (), Michael Yaffe [ths, cph] (), Ian Cannell [ths] () Maintainer: Konstantin Krismer URL: https://transite.mit.edu SystemRequirements: C++11 VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/transite git_branch: RELEASE_3_8 git_last_commit: cd25324 git_last_commit_date: 2019-02-22 Date/Publication: 2019-02-22 source.ver: src/contrib/transite_1.0.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/transite_1.0.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/transite_1.0.2.tgz vignettes: vignettes/transite/inst/doc/spma.html vignetteTitles: Spectrum Motif Analysis (SPMA) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/transite/inst/doc/spma.R Package: tRanslatome Version: 1.20.0 Depends: R (>= 2.15.0), methods, limma, sigPathway, anota, DESeq, edgeR, RankProd, topGO, org.Hs.eg.db, GOSemSim, Heatplus, gplots, plotrix, Biobase License: GPL-3 Archs: i386, x64 MD5sum: b426345db745c8c6e163c2a6a15a533e NeedsCompilation: no Title: Comparison between multiple levels of gene expression Description: Detection of differentially expressed genes (DEGs) from the comparison of two biological conditions (treated vs. untreated, diseased vs. normal, mutant vs. wild-type) among different levels of gene expression (transcriptome ,translatome, proteome), using several statistical methods: Rank Product, Translational Efficiency, t-test, Limma, ANOTA, DESeq, edgeR. Possibility to plot the results with scatterplots, histograms, MA plots, standard deviation (SD) plots, coefficient of variation (CV) plots. Detection of significantly enriched post-transcriptional regulatory factors (RBPs, miRNAs, etc) and Gene Ontology terms in the lists of DEGs previously identified for the two expression levels. Comparison of GO terms enriched only in one of the levels or in both. Calculation of the semantic similarity score between the lists of enriched GO terms coming from the two expression levels. Visual examination and comparison of the enriched terms with heatmaps, radar plots and barplots. biocViews: CellBiology, GeneRegulation, Regulation, GeneExpression, DifferentialExpression, Microarray, HighThroughputSequencing, QualityControl, GO, MultipleComparisons, Bioinformatics Author: Toma Tebaldi, Erik Dassi, Galena Kostoska Maintainer: Toma Tebaldi , Erik Dassi git_url: https://git.bioconductor.org/packages/tRanslatome git_branch: RELEASE_3_8 git_last_commit: 8119726 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tRanslatome_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tRanslatome_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tRanslatome_1.20.0.tgz vignettes: vignettes/tRanslatome/inst/doc/tRanslatome_package.pdf vignetteTitles: tRanslatome hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tRanslatome/inst/doc/tRanslatome_package.R Package: TransView Version: 1.26.1 Depends: methods, GenomicRanges Imports: BiocGenerics, S4Vectors (>= 0.9.25), IRanges, Rsamtools (>= 1.19.38), zlibbioc, gplots LinkingTo: Rsamtools Suggests: RUnit, pasillaBamSubset, BiocManager License: GPL-3 MD5sum: 357f2e92589edff33b3e9d8d910b805f NeedsCompilation: yes Title: Read density map construction and accession. Visualization of ChIPSeq and RNASeq data sets Description: This package provides efficient tools to generate, access and display read densities of sequencing based data sets such as from RNA-Seq and ChIP-Seq. biocViews: ImmunoOncology, DNAMethylation, GeneExpression, Transcription, Microarray, Sequencing, Sequencing, ChIPSeq, RNASeq, MethylSeq, DataImport, Visualization, Clustering, MultipleComparison Author: Julius Muller Maintainer: Julius Muller URL: http://bioconductor.org/packages/release/bioc/html/TransView.html git_url: https://git.bioconductor.org/packages/TransView git_branch: RELEASE_3_8 git_last_commit: 4393040 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/TransView_1.26.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TransView_1.26.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TransView_1.26.1.tgz vignettes: vignettes/TransView/inst/doc/TransView.pdf vignetteTitles: An introduction to TransView hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TransView/inst/doc/TransView.R Package: traseR Version: 1.12.0 Depends: R (>= 3.2.0),GenomicRanges,IRanges,BSgenome.Hsapiens.UCSC.hg19 Suggests: BiocStyle,RUnit, BiocGenerics License: GPL Archs: i386, x64 MD5sum: bcd587ebb46cd8b95863d9e31fe95bbc NeedsCompilation: no Title: GWAS trait-associated SNP enrichment analyses in genomic intervals Description: traseR performs GWAS trait-associated SNP enrichment analyses in genomic intervals using different hypothesis testing approaches, also provides various functionalities to explore and visualize the results. biocViews: Genetics,Sequencing, Coverage, Alignment, QualityControl, DataImport Author: Li Chen, Zhaohui S.Qin Maintainer: li chen git_url: https://git.bioconductor.org/packages/traseR git_branch: RELEASE_3_8 git_last_commit: 2405ddf git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/traseR_1.12.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/traseR_1.12.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/traseR_1.12.0.tgz vignettes: vignettes/traseR/inst/doc/traseR.pdf vignetteTitles: Perform GWAS trait-associated SNP enrichment analyses in genomic intervals hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/traseR/inst/doc/traseR.R Package: treeio Version: 1.6.2 Depends: R (>= 3.4.0) Imports: ape, dplyr, jsonlite, magrittr, methods, rlang, rvcheck, tibble, tidytree (>= 0.1.7), utils Suggests: ggplot2, ggtree, knitr, prettydoc, testthat, tidyr License: Artistic-2.0 MD5sum: 716e1ecd082083202d3a5ea60c105aa5 NeedsCompilation: no Title: Base Classes and Functions for Phylogenetic Tree Input and Output Description: Base classes and functions for parsing and exporting phylogenetic trees. 'treeio' supports parsing analysis findings from commonly used software packages, allows linking external data to phylogeny and merging tree data obtained from different sources. It also supports exporting phylogenetic tree with heterogeneous associated data to a single tree file. biocViews: Software, Annotation, Clustering, DataImport, DataRepresentation, Alignment, MultipleSequenceAlignment Author: Guangchuang Yu [aut, cre] (), Tommy Tsan-Yuk Lam [ctb, ths], Casey Dunn [ctb], Bradley Jones [ctb], Tyler Bradley [ctb] Maintainer: Guangchuang Yu URL: https://guangchuangyu.github.io/software/treeio VignetteBuilder: knitr BugReports: https://github.com/GuangchuangYu/treeio/issues git_url: https://git.bioconductor.org/packages/treeio git_branch: RELEASE_3_8 git_last_commit: 4fb11e8 git_last_commit_date: 2019-01-25 Date/Publication: 2019-01-25 source.ver: src/contrib/treeio_1.6.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/treeio_1.6.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/treeio_1.6.2.tgz vignettes: vignettes/treeio/inst/doc/Exporter.html, vignettes/treeio/inst/doc/Importer.html vignetteTitles: 02 Exporting trees with data, 01 Importing trees with data hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/treeio/inst/doc/Exporter.R, vignettes/treeio/inst/doc/Importer.R importsMe: ggtree Package: trena Version: 1.4.2 Depends: R (>= 3.4.0), utils, glmnet (>= 2.0.3), MotifDb (>= 1.19.17) Imports: RSQLite, lassopv, randomForest, flare, vbsr, BiocParallel, RPostgreSQL, RMariaDB, methods, DBI, BSgenome, BSgenome.Hsapiens.UCSC.hg38, BSgenome.Hsapiens.UCSC.hg19, BSgenome.Mmusculus.UCSC.mm10, SNPlocs.Hsapiens.dbSNP150.GRCh38, org.Hs.eg.db, Biostrings, GenomicRanges, biomaRt, AnnotationDbi Suggests: RUnit, plyr, knitr, BiocGenerics, rmarkdown License: GPL-3 MD5sum: 2860c7d847193071a608d566bcccf9ba NeedsCompilation: no Title: Fit transcriptional regulatory networks using gene expression, priors, machine learning Description: Methods for reconstructing transcriptional regulatory networks, especially in species for which genome-wide TF binding site information is available. biocViews: Transcription, GeneRegulation, NetworkInference, FeatureExtraction, Regression, SystemsBiology, GeneExpression Author: Seth Ament , Paul Shannon , Matthew Richards Maintainer: Paul Shannon VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/trena git_branch: RELEASE_3_8 git_last_commit: 927f446 git_last_commit_date: 2018-11-18 Date/Publication: 2018-11-18 source.ver: src/contrib/trena_1.4.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/trena_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/trena_1.4.2.tgz vignettes: vignettes/trena/inst/doc/TReNA_Vignette.html vignetteTitles: A Brief Introduction to TReNA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/trena/inst/doc/TReNA_Vignette.R Package: Trendy Version: 1.4.6 Depends: R (>= 3.4) Imports: stats, utils, graphics, grDevices, segmented, gplots, parallel, magrittr, BiocParallel, DT, S4Vectors, SummarizedExperiment, methods, shiny, shinyFiles Suggests: BiocStyle, knitr, rmarkdown, devtools License: GPL-3 MD5sum: c3d34b81738efeaaf79aafb072624d3b NeedsCompilation: no Title: Breakpoint analysis of time-course expression data Description: Trendy implements segmented (or breakpoint) regression models to estimate breakpoints which represent changes in expression for each feature/gene in high throughput data with ordered conditions. biocViews: TimeCourse, RNASeq, Regression, ImmunoOncology Author: Rhonda Bacher and Ning Leng Maintainer: Rhonda Bacher URL: https://github.com/rhondabacher/Trendy VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Trendy git_branch: RELEASE_3_8 git_last_commit: 1f39572 git_last_commit_date: 2019-03-28 Date/Publication: 2019-03-29 source.ver: src/contrib/Trendy_1.4.6.tar.gz win.binary.ver: bin/windows/contrib/3.5/Trendy_1.4.6.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Trendy_1.4.6.tgz vignettes: vignettes/Trendy/inst/doc/Trendy_vignette.pdf vignetteTitles: Trendy Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Trendy/inst/doc/Trendy_vignette.R Package: triform Version: 1.24.0 Depends: R (>= 2.11.0), IRanges, yaml Imports: BiocGenerics, IRanges (>= 2.5.27), yaml Suggests: RUnit License: GPL-2 MD5sum: 5d97100c4ecccc587a7c339338499e6a NeedsCompilation: no Title: Triform finds enriched regions (peaks) in transcription factor ChIP-sequencing data Description: The Triform algorithm uses model-free statistics to identify peak-like distributions of TF ChIP sequencing reads, taking advantage of an improved peak definition in combination with known profile characteristics. biocViews: Sequencing, ChIPSeq Author: Karl Kornacker Developer [aut], Tony Handstad Developer [aut, cre] Maintainer: Thomas Carroll git_url: https://git.bioconductor.org/packages/triform git_branch: RELEASE_3_8 git_last_commit: 7d64cf7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/triform_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/triform_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/triform_1.24.0.tgz vignettes: vignettes/triform/inst/doc/triform.pdf vignetteTitles: Triform users guide hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/triform/inst/doc/triform.R Package: trigger Version: 1.28.0 Depends: R (>= 2.14.0), corpcor, qtl Imports: qvalue, methods, graphics, sva License: GPL-3 MD5sum: 26b0b707b709215845adcd78059c142f NeedsCompilation: yes Title: Transcriptional Regulatory Inference from Genetics of Gene ExpRession Description: This R package provides tools for the statistical analysis of integrative genomic data that involve some combination of: genotypes, high-dimensional intermediate traits (e.g., gene expression, protein abundance), and higher-order traits (phenotypes). The package includes functions to: (1) construct global linkage maps between genetic markers and gene expression; (2) analyze multiple-locus linkage (epistasis) for gene expression; (3) quantify the proportion of genome-wide variation explained by each locus and identify eQTL hotspots; (4) estimate pair-wise causal gene regulatory probabilities and construct gene regulatory networks; and (5) identify causal genes for a quantitative trait of interest. biocViews: GeneExpression, SNP, GeneticVariability, Microarray, Genetics Author: Lin S. Chen , Dipen P. Sangurdekar and John D. Storey Maintainer: John D. Storey git_url: https://git.bioconductor.org/packages/trigger git_branch: RELEASE_3_8 git_last_commit: 0c58b84 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/trigger_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/trigger_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/trigger_1.28.0.tgz vignettes: vignettes/trigger/inst/doc/trigger.pdf vignetteTitles: Trigger Tutorial hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/trigger/inst/doc/trigger.R Package: trio Version: 3.20.0 Depends: R (>= 3.0.1) Suggests: survival, haplo.stats, mcbiopi, siggenes, splines, LogicReg (>= 1.5.3), logicFS (>= 1.28.1), KernSmooth, VariantAnnotation License: LGPL-2 Archs: i386, x64 MD5sum: 742ef152b1d4cd230c557dba4bd308a8 NeedsCompilation: no Title: Testing of SNPs and SNP Interactions in Case-Parent Trio Studies Description: Testing SNPs and SNP interactions with a genotypic TDT. This package furthermore contains functions for computing pairwise values of LD measures and for identifying LD blocks, as well as functions for setting up matched case pseudo-control genotype data for case-parent trios in order to run trio logic regression, for imputing missing genotypes in trios, for simulating case-parent trios with disease risk dependent on SNP interaction, and for power and sample size calculation in trio data. biocViews: SNP, GeneticVariability, Microarray, Genetics Author: Holger Schwender, Qing Li, Philipp Berger, Christoph Neumann, Margaret Taub, Ingo Ruczinski Maintainer: Holger Schwender git_url: https://git.bioconductor.org/packages/trio git_branch: RELEASE_3_8 git_last_commit: 16aad35 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/trio_3.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/trio_3.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/trio_3.20.0.tgz vignettes: vignettes/trio/inst/doc/trio.pdf vignetteTitles: Trio Logic Regression and genotypic TDT hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/trio/inst/doc/trio.R Package: triplex Version: 1.22.0 Depends: R (>= 2.15.0), S4Vectors (>= 0.5.14), IRanges (>= 2.5.27), XVector (>= 0.11.6), Biostrings (>= 2.39.10) Imports: methods, grid, GenomicRanges LinkingTo: S4Vectors, IRanges, XVector, Biostrings Suggests: rgl (>= 0.93.932), BSgenome.Celegans.UCSC.ce10, rtracklayer, GenomeGraphs License: BSD_2_clause + file LICENSE MD5sum: a155c67050549f90fb2e1565b36e7f6f NeedsCompilation: yes Title: Search and visualize intramolecular triplex-forming sequences in DNA Description: This package provides functions for identification and visualization of potential intramolecular triplex patterns in DNA sequence. The main functionality is to detect the positions of subsequences capable of folding into an intramolecular triplex (H-DNA) in a much larger sequence. The potential H-DNA (triplexes) should be made of as many cannonical nucleotide triplets as possible. The package includes visualization showing the exact base-pairing in 1D, 2D or 3D. biocViews: SequenceMatching, GeneRegulation Author: Jiri Hon, Matej Lexa, Tomas Martinek and Kamil Rajdl with contributions from Daniel Kopecek Maintainer: Jiri Hon URL: http://www.fi.muni.cz/~lexa/triplex/ git_url: https://git.bioconductor.org/packages/triplex git_branch: RELEASE_3_8 git_last_commit: 8426061 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/triplex_1.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/triplex_1.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/triplex_1.22.0.tgz vignettes: vignettes/triplex/inst/doc/triplex.pdf vignetteTitles: Triplex User Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/triplex/inst/doc/triplex.R Package: tRNA Version: 1.0.0 Depends: R (>= 3.5), GenomicRanges Imports: stringr, S4Vectors, methods, assertive, BiocGenerics, IRanges, XVector, Biostrings, ggplot2, scales Suggests: knitr, rmarkdown, testthat, BiocStyle, tRNAscanImport License: GPL-3 + file LICENSE Archs: i386, x64 MD5sum: f53b7c910a0519debc047e4df784a63a NeedsCompilation: no Title: tRNA: Analyzing tRNA sequences and structures Description: The tRNA package allows tRNA sequences and structures to be accessed and used for subsetting. In addition, it provides visualization tools to compare feature parameters of multiple tRNA sets and correlate them to additional data. The tRNA package uses GRanges objects as inputs requiring only few additional column data sets. biocViews: Software, Visualization Author: Felix GM Ernst [aut, cre] Maintainer: Felix GM Ernst VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tRNA git_branch: RELEASE_3_8 git_last_commit: e6048b1 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tRNA_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tRNA_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tRNA_1.0.0.tgz vignettes: vignettes/tRNA/inst/doc/tRNA.html vignetteTitles: tRNA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/tRNA/inst/doc/tRNA.R dependsOnMe: tRNAdbImport, tRNAscanImport Package: tRNAdbImport Version: 1.0.0 Depends: R (>= 3.5), GenomicRanges, tRNA Imports: Biostrings, stringr, xml2, S4Vectors, assertive, methods, httr, IRanges, utils Suggests: knitr, rmarkdown, testthat, httptest, BiocStyle, rtracklayer License: GPL-3 + file LICENSE MD5sum: 97017b574dee15ec399bab8a5cf095c4 NeedsCompilation: no Title: Importing from tRNAdb and mitotRNAdb as GRanges objects Description: tRNAdbImport imports the entries of the tRNAdb and mtRNAdb (http://trna.bioinf.uni-leipzig.de) as GRanges object. biocViews: Software, Visualization, DataImport Author: Felix GM Ernst [aut, cre] Maintainer: Felix GM Ernst VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tRNAdbImport git_branch: RELEASE_3_8 git_last_commit: 5648b27 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tRNAdbImport_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tRNAdbImport_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tRNAdbImport_1.0.0.tgz vignettes: vignettes/tRNAdbImport/inst/doc/tRNAdbImport.html vignetteTitles: tRNAdbImport hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/tRNAdbImport/inst/doc/tRNAdbImport.R Package: tRNAscanImport Version: 1.2.0 Depends: R (>= 3.5), GenomicRanges, tRNA Imports: methods, assertive, stringr, BiocGenerics, Biostrings, S4Vectors, GenomeInfoDb, rtracklayer Suggests: BiocStyle, knitr, rmarkdown, testthat, ggplot2 License: GPL-3 + file LICENSE MD5sum: 00c52e3ddec9433db1e2422ee3da4b4f NeedsCompilation: no Title: Imports a tRNAscan-SE result file as GRanges object Description: The package imports the result of tRNAscan-SE as a GRanges object. biocViews: Software, DataImport, WorkflowStep, Preprocessing, Visualization Author: Felix GM Ernst [aut, cre] Maintainer: Felix GM Ernst VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tRNAscanImport git_branch: RELEASE_3_8 git_last_commit: a8e7293 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tRNAscanImport_1.2.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tRNAscanImport_1.2.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tRNAscanImport_1.2.0.tgz vignettes: vignettes/tRNAscanImport/inst/doc/tRNAscanImport.html vignetteTitles: tRNAscanImport hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/tRNAscanImport/inst/doc/tRNAscanImport.R suggestsMe: tRNA Package: TRONCO Version: 2.14.2 Depends: R (>= 3.5), Imports: bnlearn, Rgraphviz, gtools, parallel, foreach, doParallel, iterators, RColorBrewer, circlize, cgdsr, igraph, grid, gridExtra, xtable, gtable, scales, R.matlab, grDevices, graphics, stats, utils, methods Suggests: BiocGenerics, BiocStyle, testthat, knitr, rWikiPathways License: file LICENSE MD5sum: e93b2f90880b287243cee99769f1efc6 NeedsCompilation: no Title: TRONCO, an R package for TRanslational ONCOlogy Description: The TRONCO (TRanslational ONCOlogy) R package collects algorithms to infer progression models via the approach of Suppes-Bayes Causal Network, both from an ensemble of tumors (cross-sectional samples) and within an individual patient (multi-region or single-cell samples). The package provides parallel implementation of algorithms that process binary matrices where each row represents a tumor sample and each column a single-nucleotide or a structural variant driving the progression; a 0/1 value models the absence/presence of that alteration in the sample. The tool can import data from plain, MAF or GISTIC format files, and can fetch it from the cBioPortal for cancer genomics. Functions for data manipulation and visualization are provided, as well as functions to import/export such data to other bioinformatics tools for, e.g, clustering or detection of mutually exclusive alterations. Inferred models can be visualized and tested for their confidence via bootstrap and cross-validation. TRONCO is used for the implementation of the Pipeline for Cancer Inference (PICNIC). biocViews: BiomedicalInformatics, Bayesian, GraphAndNetwork, SomaticMutation, NetworkInference, Network, Clustering, DataImport, SingleCell, ImmunoOncology Author: Marco Antoniotti [ctb], Giulio Caravagna [aut, cre], Luca De Sano [aut], Alex Graudenzi [aut], Giancarlo Mauri [ctb], Bud Mishra [ctb], Daniele Ramazzotti [aut] Maintainer: Luca De Sano URL: https://sites.google.com/site/troncopackage/ VignetteBuilder: knitr BugReports: https://github.com/BIMIB-DISCo/TRONCO git_url: https://git.bioconductor.org/packages/TRONCO git_branch: RELEASE_3_8 git_last_commit: fe79b24 git_last_commit_date: 2018-12-10 Date/Publication: 2018-12-10 source.ver: src/contrib/TRONCO_2.14.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/TRONCO_2.14.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TRONCO_2.14.2.tgz vignettes: vignettes/TRONCO/inst/doc/vignette.pdf vignetteTitles: An R Package for TRanslational ONCOlogy hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/TRONCO/inst/doc/vignette.R Package: TSCAN Version: 1.20.0 Depends: R(>= 2.10.0) Imports: ggplot2, shiny, plyr, grid, fastICA, igraph, combinat, mgcv, mclust, gplots Suggests: knitr License: GPL(>=2) MD5sum: 88f8eead43b40eeacfd6546d0f7ad3e5 NeedsCompilation: no Title: TSCAN: Tools for Single-Cell ANalysis Description: TSCAN enables users to easily construct and tune pseudotemporal cell ordering as well as analyzing differentially expressed genes. TSCAN comes with a user-friendly GUI written in shiny. More features will come in the future. biocViews: GeneExpression, Visualization, GUI Author: Zhicheng Ji, Hongkai Ji Maintainer: Zhicheng Ji VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TSCAN git_branch: RELEASE_3_8 git_last_commit: 0acbe64 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TSCAN_1.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TSCAN_1.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TSCAN_1.20.0.tgz vignettes: vignettes/TSCAN/inst/doc/TSCAN.pdf vignetteTitles: TSCAN: Tools for Single-Cell ANalysis hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TSCAN/inst/doc/TSCAN.R Package: tspair Version: 1.40.0 Depends: R (>= 2.10), Biobase (>= 2.4.0) License: GPL-2 MD5sum: 8f240fd93f65564edf17897732940e17 NeedsCompilation: yes Title: Top Scoring Pairs for Microarray Classification Description: These functions calculate the pair of genes that show the maximum difference in ranking between two user specified groups. This "top scoring pair" maximizes the average of sensitivity and specificity over all rank based classifiers using a pair of genes in the data set. The advantage of classifying samples based on only the relative rank of a pair of genes is (a) the classifiers are much simpler and often more interpretable than more complicated classification schemes and (b) if arrays can be classified using only a pair of genes, PCR based tests could be used for classification of samples. See the references for the tspcalc() function for references regarding TSP classifiers. biocViews: Microarray Author: Jeffrey T. Leek Maintainer: Jeffrey T. Leek git_url: https://git.bioconductor.org/packages/tspair git_branch: RELEASE_3_8 git_last_commit: 88743ae git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/tspair_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/tspair_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tspair_1.40.0.tgz vignettes: vignettes/tspair/inst/doc/tsp.pdf vignetteTitles: tspTutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tspair/inst/doc/tsp.R Package: TSRchitect Version: 1.8.9 Depends: R (>= 3.5) Imports: AnnotationHub, BiocGenerics, BiocParallel, GenomicAlignments, GenomeInfoDb, GenomicRanges, gtools, IRanges, methods, Rsamtools (>= 1.14.3), rtracklayer, S4Vectors, SummarizedExperiment, utils Suggests: ENCODExplorer, ggplot2, knitr, rmarkdown License: GPL-3 Archs: i386, x64 MD5sum: ffb55c47e0e9ba14edd48bcd48bb0330 NeedsCompilation: no Title: Promoter identification from large-scale TSS profiling data Description: In recent years, large-scale transcriptional sequence data has yielded considerable insights into the nature of gene expression and regulation in eukaryotes. Techniques that identify the 5' end of mRNAs, most notably CAGE, have mapped the promoter landscape across a number of model organisms. Due to the variability of TSS distributions and the transcriptional noise present in datasets, precisely identifying the active promoter(s) for genes from these datasets is not straightforward. TSRchitect allows the user to efficiently identify the putative promoter (the transcription start region, or TSR) from a variety of TSS profiling data types, including both single-end (e.g. CAGE) as well as paired-end (RAMPAGE, PEAT, STRIPE-seq). In addition, (new with version 1.3.0) TSRchitect provides the ability to import aligned EST and cDNA data. Along with the coordiantes of identified TSRs, TSRchitect also calculates the width, abundance and two forms of the Shape Index, and handles biological replicates for expression profiling. Finally, TSRchitect imports annotation files, allowing the user to associate identified promoters with genes and other genomic features. Three detailed examples of TSRchitect's utility are provided in the User's Guide, included with this package. biocViews: Clustering, FunctionalGenomics, GeneExpression, GeneRegulation, GenomeAnnotation, Sequencing, Transcription Author: R. Taylor Raborn [aut, cre, cph] Volker P. Brendel [aut, cph] Krishnakumar Sridharan [ctb] Maintainer: R. Taylor Raborn URL: https://github.com/brendelgroup/tsrchitect VignetteBuilder: knitr BugReports: https://github.com/brendelgroup/tsrchitect/issues git_url: https://git.bioconductor.org/packages/TSRchitect git_branch: RELEASE_3_8 git_last_commit: eea6a50 git_last_commit_date: 2018-11-15 Date/Publication: 2018-11-17 source.ver: src/contrib/TSRchitect_1.8.9.tar.gz win.binary.ver: bin/windows/contrib/3.5/TSRchitect_1.8.9.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TSRchitect_1.8.9.tgz vignettes: vignettes/TSRchitect/inst/doc/TSRchitectUsersGuide.pdf, vignettes/TSRchitect/inst/doc/TSRchitect.html, vignettes/TSRchitect/inst/doc/TSRchitectUsersGuide.html vignetteTitles: TSRchitect User's Guide, TSRchitect vignette, TSRchitect User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TSRchitect/inst/doc/TSRchitect.R Package: TSSi Version: 1.28.0 Depends: R (>= 2.13.2) Imports: methods, BiocGenerics (>= 0.3.2), S4Vectors, Hmisc, minqa, stats, Biobase (>= 0.3.2), plyr, IRanges Suggests: rtracklayer Enhances: parallel License: GPL-3 MD5sum: 71fb81d19b05b106eaf0a34f8975d6b1 NeedsCompilation: yes Title: Transcription Start Site Identification Description: Identify and normalize transcription start sites in high-throughput sequencing data. biocViews: Sequencing, RNASeq, Genetics, Preprocessing Author: Julian Gehring, Clemens Kreutz Maintainer: Julian Gehring git_url: https://git.bioconductor.org/packages/TSSi git_branch: RELEASE_3_8 git_last_commit: 55b5404 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TSSi_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TSSi_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TSSi_1.28.0.tgz vignettes: vignettes/TSSi/inst/doc/TSSi.pdf vignetteTitles: Introduction to the TSSi package: Identification of Transcription Start Sites hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TSSi/inst/doc/TSSi.R Package: TTMap Version: 1.4.0 Depends: rgl, colorRamps Imports: grDevices,graphics,stats,utils, methods, SummarizedExperiment, Biobase Suggests: BiocStyle, airway License: GPL-2 Archs: i386, x64 MD5sum: b9749313b878fae1dd4ed81a16b7271d NeedsCompilation: no Title: Two-Tier Mapper: a clustering tool based on topological data analysis Description: TTMap is a clustering method that groups together samples with the same deviation in comparison to a control group. It is specially useful when the data is small. It is parameter free. biocViews: Software, Microarray, DifferentialExpression, MultipleComparison, Clustering, Classification Author: Rachel Jeitziner Maintainer: Rachel Jeitziner git_url: https://git.bioconductor.org/packages/TTMap git_branch: RELEASE_3_8 git_last_commit: 973fa80 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TTMap_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TTMap_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TTMap_1.4.0.tgz vignettes: vignettes/TTMap/inst/doc/TTMap.pdf vignetteTitles: Manual for the TTMap library hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TTMap/inst/doc/TTMap.R Package: TurboNorm Version: 1.30.0 Depends: R (>= 2.12.0), convert, limma (>= 1.7.0), marray Imports: stats, grDevices, affy, lattice Suggests: BiocStyle, affydata License: LGPL MD5sum: c258665eba34296ed6a5f6e4b7e8ddd5 NeedsCompilation: yes Title: A fast scatterplot smoother suitable for microarray normalization Description: A fast scatterplot smoother based on B-splines with second-order difference penalty. Functions for microarray normalization of single-colour data i.e. Affymetrix/Illumina and two-colour data supplied as marray MarrayRaw-objects or limma RGList-objects are available. biocViews: Microarray, OneChannel, TwoChannel, Preprocessing, DNAMethylation, CpGIsland, MethylationArray, Normalization Author: Maarten van Iterson and Chantal van Leeuwen Maintainer: Maarten van Iterson URL: http://www.humgen.nl/MicroarrayAnalysisGroup.html git_url: https://git.bioconductor.org/packages/TurboNorm git_branch: RELEASE_3_8 git_last_commit: 1be548c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TurboNorm_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TurboNorm_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TurboNorm_1.30.0.tgz vignettes: vignettes/TurboNorm/inst/doc/turbonorm.pdf vignetteTitles: TurboNorm Overview hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TurboNorm/inst/doc/turbonorm.R Package: TVTB Version: 1.8.0 Depends: R (>= 3.4), methods, utils, stats Imports: AnnotationFilter, BiocGenerics (>= 0.25.1), BiocParallel, Biostrings, ensembldb, ensemblVEP, GenomeInfoDb, GenomicRanges, GGally, ggplot2, Gviz, limma, IRanges (>= 2.7.1), reshape2, Rsamtools, S4Vectors (>= 0.11.11), SummarizedExperiment, VariantAnnotation (>= 1.19.9) Suggests: EnsDb.Hsapiens.v75 (>= 0.99.7), shiny (>= 0.13.2.9005), DT (>= 0.1.67), rtracklayer, BiocStyle (>= 2.5.19), knitr (>= 1.12), rmarkdown, testthat, covr, pander License: Artistic-2.0 MD5sum: cba10d6dc0358c99d2ab92e861786a9b NeedsCompilation: no Title: TVTB: The VCF Tool Box Description: The package provides S4 classes and methods to filter, summarise and visualise genetic variation data stored in VCF files. In particular, the package extends the FilterRules class (S4Vectors package) to define news classes of filter rules applicable to the various slots of VCF objects. Functionalities are integrated and demonstrated in a Shiny web-application, the Shiny Variant Explorer (tSVE). biocViews: Software, Genetics, GeneticVariability, GenomicVariation, DataRepresentation, GUI, Genetics, DNASeq, WholeGenome, Visualization, MultipleComparison, DataImport, VariantAnnotation, Sequencing, Coverage, Alignment, SequenceMatching Author: Kevin Rue-Albrecht [aut, cre] Maintainer: Kevin Rue-Albrecht URL: https://github.com/kevinrue/TVTB VignetteBuilder: knitr BugReports: https://github.com/kevinrue/TVTB/issues git_url: https://git.bioconductor.org/packages/TVTB git_branch: RELEASE_3_8 git_last_commit: 67e1b0c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TVTB_1.8.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TVTB_1.8.0.tgz vignettes: vignettes/TVTB/inst/doc/tSVE.pdf, vignettes/TVTB/inst/doc/Introduction.html, vignettes/TVTB/inst/doc/VcfFilterRules.html vignetteTitles: The Shiny Variant Explorer, Introduction to TVTB, VCF filter rules hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TVTB/inst/doc/Introduction.R, vignettes/TVTB/inst/doc/tSVE.R, vignettes/TVTB/inst/doc/VcfFilterRules.R Package: tweeDEseq Version: 1.28.1 Depends: R (>= 2.12.0) Imports: MASS, limma, edgeR, parallel, cqn Suggests: tweeDEseqCountData, xtable License: GPL (>= 2) Archs: i386, x64 MD5sum: 0b4fcd5b9cf52acb8bbf3292d4dd2aac NeedsCompilation: yes Title: RNA-seq data analysis using the Poisson-Tweedie family of distributions Description: Differential expression analysis of RNA-seq using the Poisson-Tweedie family of distributions. biocViews: ImmunoOncology, StatisticalMethod, DifferentialExpression, Sequencing, RNASeq Author: Juan R Gonzalez and Mikel Esnaola (with contributions from Robert Castelo ) Maintainer: Juan R Gonzalez URL: http://www.creal.cat/jrgonzalez/software.htm git_url: https://git.bioconductor.org/packages/tweeDEseq git_branch: RELEASE_3_8 git_last_commit: 95ffd20 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/tweeDEseq_1.28.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/tweeDEseq_1.28.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tweeDEseq_1.28.1.tgz vignettes: vignettes/tweeDEseq/inst/doc/tweeDEseq.pdf vignetteTitles: tweeDEseq: analysis of RNA-seq data using the Poisson-Tweedie family of distributions hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tweeDEseq/inst/doc/tweeDEseq.R Package: twilight Version: 1.58.0 Depends: R (>= 2.10), splines (>= 2.2.0), stats (>= 2.2.0), Biobase(>= 1.12.0) Imports: Biobase, graphics, grDevices, stats Suggests: golubEsets (>= 1.4.2), vsn (>= 1.7.2) License: GPL (>= 2) Archs: i386, x64 MD5sum: bdc31d1f7e094aa3d2e3eb436b9b6306 NeedsCompilation: yes Title: Estimation of local false discovery rate Description: In a typical microarray setting with gene expression data observed under two conditions, the local false discovery rate describes the probability that a gene is not differentially expressed between the two conditions given its corrresponding observed score or p-value level. The resulting curve of p-values versus local false discovery rate offers an insight into the twilight zone between clear differential and clear non-differential gene expression. Package 'twilight' contains two main functions: Function twilight.pval performs a two-condition test on differences in means for a given input matrix or expression set and computes permutation based p-values. Function twilight performs a stochastic downhill search to estimate local false discovery rates and effect size distributions. The package further provides means to filter for permutations that describe the null distribution correctly. Using filtered permutations, the influence of hidden confounders could be diminished. biocViews: Microarray, DifferentialExpression, MultipleComparison Author: Stefanie Scheid Maintainer: Stefanie Scheid URL: http://compdiag.molgen.mpg.de/software/twilight.shtml git_url: https://git.bioconductor.org/packages/twilight git_branch: RELEASE_3_8 git_last_commit: 3271710 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/twilight_1.58.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/twilight_1.58.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/twilight_1.58.0.tgz vignettes: vignettes/twilight/inst/doc/tr_2004_01.pdf vignetteTitles: Estimation of Local False Discovery Rates hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/twilight/inst/doc/tr_2004_01.R dependsOnMe: OrderedList importsMe: OrderedList Package: twoddpcr Version: 1.6.0 Depends: R (>= 3.4) Imports: class, ggplot2, hexbin, methods, scales, shiny, stats, utils, RColorBrewer, S4Vectors Suggests: devtools, knitr, reshape2, rmarkdown, testthat, BiocStyle License: GPL-3 Archs: i386, x64 MD5sum: 42ab6dd8305e75b8029b4c69abeb5b7d NeedsCompilation: no Title: Classify 2-d Droplet Digital PCR (ddPCR) data and quantify the number of starting molecules Description: The twoddpcr package takes Droplet Digital PCR (ddPCR) droplet amplitude data from Bio-Rad's QuantaSoft and can classify the droplets. A summary of the positive/negative droplet counts can be generated, which can then be used to estimate the number of molecules using the Poisson distribution. This is the first open source package that facilitates the automatic classification of general two channel ddPCR data. Previous work includes 'definetherain' (Jones et al., 2014) and 'ddpcRquant' (Trypsteen et al., 2015) which both handle one channel ddPCR experiments only. The 'ddpcr' package available on CRAN (Attali et al., 2016) supports automatic gating of a specific class of two channel ddPCR experiments only. biocViews: ddPCR, Software, Classification Author: Anthony Chiu [aut, cre] Maintainer: Anthony Chiu URL: http://github.com/CRUKMI-ComputationalBiology/twoddpcr/ VignetteBuilder: knitr BugReports: http://github.com/CRUKMI-ComputationalBiology/twoddpcr/issues/ git_url: https://git.bioconductor.org/packages/twoddpcr git_branch: RELEASE_3_8 git_last_commit: 81366aa git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/twoddpcr_1.6.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/twoddpcr_1.6.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/twoddpcr_1.6.0.tgz vignettes: vignettes/twoddpcr/inst/doc/twoddpcr.html vignetteTitles: twoddpcr: A package for Droplet Digital PCR analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/twoddpcr/inst/doc/twoddpcr.R Package: tximeta Version: 1.0.3 Imports: SummarizedExperiment, tximport, jsonlite, S4Vectors, AnnotationDbi, GenomicFeatures, ensembldb, BiocFileCache, tibble, GenomeInfoDb, rappdirs, utils, methods Suggests: knitr, rmarkdown, testthat, tximportData, org.Dm.eg.db, DESeq2, devtools License: GPL-2 MD5sum: ee9fda484e8a56ee554d4f6bf85773d0 NeedsCompilation: no Title: Transcript Quantification Import with Automatic Metadata Description: Transcript quantification import from Salmon with automatic population of metadata and transcript ranges. Filtered, combined, or de novo transcriptomes can be linked to the appropriate sources with linkedTxomes and shared for reproducible analyses. biocViews: ImmunoOncology, Annotation, DataImport, Preprocessing, RNASeq, Transcriptomics, Transcription, GeneExpression Author: Michael Love [aut, cre], Rob Patro [aut, ctb], Peter Hickey [aut, ctb], Charlotte Soneson [aut, ctb] Maintainer: Michael Love VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tximeta git_branch: RELEASE_3_8 git_last_commit: dd036ee git_last_commit_date: 2019-01-11 Date/Publication: 2019-01-11 source.ver: src/contrib/tximeta_1.0.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/tximeta_1.0.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tximeta_1.0.3.tgz vignettes: vignettes/tximeta/inst/doc/tximeta.html vignetteTitles: Transcript quantification import with automatic metadata hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tximeta/inst/doc/tximeta.R suggestsMe: scater Package: tximport Version: 1.10.1 Imports: utils, stats Suggests: knitr, rmarkdown, testthat, tximportData, TxDb.Hsapiens.UCSC.hg19.knownGene, readr (>= 0.2.2), limma, edgeR, DESeq2 (>= 1.11.6), rhdf5, jsonlite, matrixStats License: GPL (>=2) MD5sum: 3b7cbbd9da1defe0c23224a3035f361e NeedsCompilation: no Title: Import and summarize transcript-level estimates for transcript- and gene-level analysis Description: Imports transcript-level abundance, estimated counts and transcript lengths, and summarizes into matrices for use with downstream gene-level analysis packages. Average transcript length, weighted by sample-specific transcript abundance estimates, is provided as a matrix which can be used as an offset for different expression of gene-level counts. biocViews: ImmunoOncology, RNASeq, Transcription, GeneExpression, DataImport Author: Michael Love [cre,aut], Charlotte Soneson [aut], Mark Robinson [aut], Rob Patro [ctb], Andrew Parker Morgan [ctb], Ryan C. Thompson [ctb], Matt Shirley [ctb] Maintainer: Michael Love VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/tximport git_branch: RELEASE_3_8 git_last_commit: cd8f81c git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/tximport_1.10.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/tximport_1.10.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/tximport_1.10.1.tgz vignettes: vignettes/tximport/inst/doc/tximport.html vignetteTitles: Importing transcript abundance datasets with tximport hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/tximport/inst/doc/tximport.R importsMe: IsoformSwitchAnalyzeR, tximeta suggestsMe: DESeq2, scater, SummarizedBenchmark, variancePartition Package: TxRegInfra Version: 1.2.1 Depends: RaggedExperiment (>= 1.3.11), mongolite Imports: methods, rjson, GenomicRanges, IRanges, BiocParallel, GenomeInfoDb, S4Vectors, SummarizedExperiment, utils Suggests: knitr, GenomicFiles, EnsDb.Hsapiens.v75, testthat, biovizBase (>= 1.27.2), Gviz, AnnotationFilter, ensembldb License: Artistic-2.0 MD5sum: 4715d2324f8b49342a65820b6b303089 NeedsCompilation: no Title: Metadata management for multiomic specification of transcriptional regulatory networks Description: This package provides interfaces to genomic metadata employed in regulatory network creation, with a focus on noSQL solutions. Currently quantitative representations of eQTLs, DnaseI hypersensitivity sites and digital genomic footprints are assembled using an out-of-memory extension of the RaggedExperiment API. biocViews: Network Author: Vince Carey Maintainer: VJ Carey VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/TxRegInfra git_branch: RELEASE_3_8 git_last_commit: 2028a2f git_last_commit_date: 2019-03-08 Date/Publication: 2019-03-08 source.ver: src/contrib/TxRegInfra_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/TxRegInfra_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TxRegInfra_1.2.1.tgz vignettes: vignettes/TxRegInfra/inst/doc/TxRegInfra.html vignetteTitles: TxRegInfra -- classes and methods for TxRegQuery hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TxRegInfra/inst/doc/TxRegInfra.R Package: TypeInfo Version: 1.48.0 Depends: methods Suggests: Biobase License: BSD MD5sum: 1923e893a75108abebee8fc64984144e NeedsCompilation: no Title: Optional Type Specification Prototype Description: A prototype for a mechanism for specifying the types of parameters and the return value for an R function. This is meta-information that can be used to generate stubs for servers and various interfaces to these functions. Additionally, the arguments in a call to a typed function can be validated using the type specifications. We allow types to be specified as either i) by class name using either inheritance - is(x, className), or strict instance of - class(x) %in% className, or ii) a dynamic test given as an R expression which is evaluated at run-time. More precise information and interesting tests can be done via ii), but it is harder to use this information as meta-data as it requires more effort to interpret it and it is of course run-time information. It is typically more meaningful. biocViews: Infrastructure Author: Duncan Temple Lang Robert Gentleman () Maintainer: Duncan Temple Lang git_url: https://git.bioconductor.org/packages/TypeInfo git_branch: RELEASE_3_8 git_last_commit: bbed433 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/TypeInfo_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/TypeInfo_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/TypeInfo_1.48.0.tgz vignettes: vignettes/TypeInfo/inst/doc/TypeInfoNews.pdf vignetteTitles: TypeInfo R News hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/TypeInfo/inst/doc/TypeInfoNews.R Package: Ularcirc Version: 1.0.0 Depends: R (>= 3.5.0) Imports: data.table (>= 1.9.4), shiny, shinyFiles, gsubfn, Biostrings, GenomicFeatures, GenomeInfoDb, GenomeInfoDbData, Sushi, moments, DT, yaml, AnnotationHub, BSgenome, httpuv, mirbase.db Suggests: knitr, rmarkdown License: file LICENSE MD5sum: e8b3ed9cba2d1b3f52f2a1252107ec0f NeedsCompilation: no Title: Shiny app for canonical and back splicing analysis (i.e. circular and mRNA analysis) Description: Ularcirc reads in STAR aligned splice junction files and provides visualisation and analysis tools for splicing analysis. Users can assess backsplice junctions and forward canonical junctions. biocViews: DataRepresentation,Visualization, Genetics, Sequencing, Annotation, Coverage, AlternativeSplicing, DifferentialSplicing Author: David Humphreys [aut, cre] Maintainer: David Humphreys VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Ularcirc git_branch: RELEASE_3_8 git_last_commit: 95e51c5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Ularcirc_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Ularcirc_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Ularcirc_1.0.0.tgz vignettes: vignettes/Ularcirc/inst/doc/Ularcirc.html vignetteTitles: Ularcirc.html hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/Ularcirc/inst/doc/Ularcirc.R Package: UNDO Version: 1.24.0 Depends: R (>= 2.15.2), methods, BiocGenerics, Biobase Imports: MASS, boot, nnls, stats, utils License: GPL-2 MD5sum: f1e2a4e8cc746b0f2e99793229b09d79 NeedsCompilation: no Title: Unsupervised Deconvolution of Tumor-Stromal Mixed Expressions Description: UNDO is an R package for unsupervised deconvolution of tumor and stromal mixed expression data. It detects marker genes and deconvolutes the mixing expression data without any prior knowledge. biocViews: Software Author: Niya Wang Maintainer: Niya Wang git_url: https://git.bioconductor.org/packages/UNDO git_branch: RELEASE_3_8 git_last_commit: 721e930 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/UNDO_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/UNDO_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/UNDO_1.24.0.tgz vignettes: vignettes/UNDO/inst/doc/UNDO-vignette.pdf vignetteTitles: UNDO Usage hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/UNDO/inst/doc/UNDO-vignette.R Package: unifiedWMWqPCR Version: 1.18.0 Depends: methods Imports: BiocGenerics, stats, graphics, HTqPCR License: GPL (>=2) MD5sum: d0bc72990976a0e11766f9f46402a588 NeedsCompilation: no Title: Unified Wilcoxon-Mann Whitney Test for testing differential expression in qPCR data Description: This packages implements the unified Wilcoxon-Mann-Whitney Test for qPCR data. This modified test allows for testing differential expression in qPCR data. biocViews: DifferentialExpression, GeneExpression, MicrotitrePlateAssay, MultipleComparison, QualityControl, Software, Visualization, qPCR Author: Jan R. De Neve & Joris Meys Maintainer: Joris Meys git_url: https://git.bioconductor.org/packages/unifiedWMWqPCR git_branch: RELEASE_3_8 git_last_commit: 8abf2d5 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/unifiedWMWqPCR_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/unifiedWMWqPCR_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/unifiedWMWqPCR_1.18.0.tgz vignettes: vignettes/unifiedWMWqPCR/inst/doc/unifiedWMWqPCR.pdf vignetteTitles: Using unifiedWMWqPCR hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/unifiedWMWqPCR/inst/doc/unifiedWMWqPCR.R Package: UniProt.ws Version: 2.22.0 Depends: methods, utils, RSQLite, RCurl, BiocGenerics (>= 0.13.8) Imports: AnnotationDbi, BiocFileCache, rappdirs Suggests: RUnit License: Artistic License 2.0 MD5sum: 54f202f10a75478ae02ca20a309c231b NeedsCompilation: no Title: R Interface to UniProt Web Services Description: A collection of functions for retrieving, processing and repackaging the UniProt web services. biocViews: Annotation, Infrastructure, GO, KEGG, BioCarta Author: Marc Carlson [aut, cre], Csaba Ortutay [ctb] Maintainer: Marc Carlson git_url: https://git.bioconductor.org/packages/UniProt.ws git_branch: RELEASE_3_8 git_last_commit: dd22a96 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/UniProt.ws_2.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/UniProt.ws_2.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/UniProt.ws_2.22.0.tgz vignettes: vignettes/UniProt.ws/inst/doc/UniProt.ws.pdf vignetteTitles: UniProt.ws: A package for retrieving data from the UniProt web service hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/UniProt.ws/inst/doc/UniProt.ws.R suggestsMe: cleaver, dagLogo, qPLEXanalyzer Package: Uniquorn Version: 2.2.1 Depends: R (>= 3.5) Imports: stringr, R.utils, WriteXLS, stats, data.table, doParallel, foreach, GenomicRanges, IRanges, VariantAnnotation Suggests: testthat, knitr, rmarkdown, BiocGenerics, RUnit License: Artistic-2.0 MD5sum: e0522179a1f9939d1ec1c73677dfe936 NeedsCompilation: no Title: Identification of cancer cell lines based on their weighted mutational/ variational fingerprint Description: This packages enables users to identify cancer cell lines. Cancer cell line misidentification and cross-contamination reprents a significant challenge for cancer researchers. The identification is vital and in the frame of this package based on the locations/ loci of somatic and germline mutations/ variations. The input format is vcf/ vcf.gz and the files have to contain a single cancer cell line sample (i.e. a single member/genotype/gt column in the vcf file). The implemented method is optimized for the Next-generation whole exome and whole genome DNA-sequencing technology. RNA-seq data is very likely to work as well but hasn't been rigiously tested yet. Panel-seq will require manual adjustment of thresholds biocViews: ImmunoOncology, Software, StatisticalMethod, WholeGenome, ExomeSeq Author: Raik Otto Maintainer: 'Raik Otto' VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/Uniquorn git_branch: RELEASE_3_8 git_last_commit: 9a1b9e4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/Uniquorn_2.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/Uniquorn_2.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Uniquorn_2.2.1.tgz vignettes: vignettes/Uniquorn/inst/doc/Uniquorn.html vignetteTitles: Uniquorn vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Uniquorn/inst/doc/Uniquorn.R Package: universalmotif Version: 1.0.22 Depends: R (>= 3.5.0) Imports: methods, ggplot2, ape, ggtree, ggseqlogo, stats, utils, gtools, Rdpack (>= 0.7), Biostrings, BiocGenerics, Rcpp, processx LinkingTo: Rcpp Suggests: knitr, BiocStyle, TFBSTools, MotIV, PWMEnrich, motifStack, seqLogo, rmarkdown, MotifDb, testthat, rGADEM, motifRG, motifbreakR, RcisTarget, motifcounter, Logolas, BiocParallel, BCRANK License: GPL-3 MD5sum: e65ff5cccdb18f65487bca242726aead NeedsCompilation: yes Title: Import, Modify, and Export Motifs with R Description: Allows for importing most common motif types into R for use by functions provided by other Bioconductor motif-related packages. Motifs can be exported into most major motif formats from various classes as defined by other Bioconductor packages. A suite of motif and sequence manipulation and analysis functions are included, including enrichment, comparison, P-value calculation, shuffling, trimming, higher-order motifs, and others. biocViews: MotifAnnotation, MotifDiscovery, DataImport, GeneRegulation Author: Benjamin Jean-Marie Tremblay [aut, cre] Maintainer: Benjamin Jean-Marie Tremblay URL: https://github.com/bjmt/universalmotif VignetteBuilder: knitr BugReports: https://github.com/bjmt/universalmotif/issues git_url: https://git.bioconductor.org/packages/universalmotif git_branch: RELEASE_3_8 git_last_commit: 34a663f git_last_commit_date: 2019-03-06 Date/Publication: 2019-03-06 source.ver: src/contrib/universalmotif_1.0.22.tar.gz win.binary.ver: bin/windows/contrib/3.5/universalmotif_1.0.22.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/universalmotif_1.0.22.tgz vignettes: vignettes/universalmotif/inst/doc/AdvancedUsage.pdf, vignettes/universalmotif/inst/doc/Introduction.pdf, vignettes/universalmotif/inst/doc/IntroductionToSequenceMotifs.pdf, vignettes/universalmotif/inst/doc/MotifManipulation.pdf, vignettes/universalmotif/inst/doc/SequenceSearches.pdf vignetteTitles: Advanced usage: motif and sequence analysis, Introduction to "universalmotif", Introduction to sequence motifs, Motif import,, export,, and manipulation, Sequence manipulation and scanning hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/universalmotif/inst/doc/AdvancedUsage.R, vignettes/universalmotif/inst/doc/Introduction.R, vignettes/universalmotif/inst/doc/IntroductionToSequenceMotifs.R, vignettes/universalmotif/inst/doc/MotifManipulation.R, vignettes/universalmotif/inst/doc/SequenceSearches.R Package: uSORT Version: 1.8.1 Depends: R (>= 3.3.0), tcltk Imports: igraph, Matrix, RANN, RSpectra, VGAM, gplots, parallel, plyr, methods, cluster, Biobase, fpc, BiocGenerics, monocle, grDevices, graphics, stats, utils Suggests: knitr, RUnit, testthat, ggplot2 License: Artistic-2.0 Archs: i386, x64 MD5sum: 134a1fcc450f3d5ba2d8356cc2b260f8 NeedsCompilation: no Title: uSORT: A self-refining ordering pipeline for gene selection Description: This package is designed to uncover the intrinsic cell progression path from single-cell RNA-seq data. It incorporates data pre-processing, preliminary PCA gene selection, preliminary cell ordering, feature selection, refined cell ordering, and post-analysis interpretation and visualization. biocViews: ImmunoOncology, RNASeq, GUI, CellBiology, DNASeq Author: Mai Chan Lau, Hao Chen, Jinmiao Chen Maintainer: Hao Chen VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/uSORT git_branch: RELEASE_3_8 git_last_commit: 2b2c850 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/uSORT_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/uSORT_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/uSORT_1.8.1.tgz vignettes: vignettes/uSORT/inst/doc/uSORT_quick_start.html vignetteTitles: Quick Start hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/uSORT/inst/doc/uSORT_quick_start.R Package: VanillaICE Version: 1.44.0 Depends: R (>= 3.0.0), BiocGenerics (>= 0.13.6), GenomicRanges (>= 1.27.6), SummarizedExperiment (>= 1.5.3) Imports: Biobase, S4Vectors (>= 0.9.25), IRanges (>= 1.14.0), oligoClasses (>= 1.31.1), foreach, matrixStats, data.table, grid, lattice, methods, GenomeInfoDb (>= 1.11.4), crlmm, tools, stats, utils, BSgenome.Hsapiens.UCSC.hg18 Suggests: RUnit, SNPchip, human610quadv1bCrlmm, ArrayTV Enhances: doMC, doMPI, doSNOW, doParallel, doRedis License: LGPL-2 MD5sum: ea6bd436eab15fa26a9809990494a9a2 NeedsCompilation: yes Title: A Hidden Markov Model for high throughput genotyping arrays Description: Hidden Markov Models for characterizing chromosomal alterations in high throughput SNP arrays. biocViews: CopyNumberVariation Author: Robert Scharpf , Kevin Scharpf, and Ingo Ruczinski Maintainer: Robert Scharpf git_url: https://git.bioconductor.org/packages/VanillaICE git_branch: RELEASE_3_8 git_last_commit: c5d853d git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/VanillaICE_1.44.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/VanillaICE_1.44.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/VanillaICE_1.44.0.tgz vignettes: vignettes/VanillaICE/inst/doc/crlmmDownstream.pdf, vignettes/VanillaICE/inst/doc/VanillaICE.pdf vignetteTitles: crlmmDownstream, VanillaICE Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/VanillaICE/inst/doc/crlmmDownstream.R, vignettes/VanillaICE/inst/doc/VanillaICE.R dependsOnMe: MinimumDistance suggestsMe: CNPBayes, oligoClasses Package: variancePartition Version: 1.12.3 Depends: R (>= 3.0.0), ggplot2, limma, foreach, scales, Biobase, methods Imports: MASS, pbkrtest (>= 0.4-4), lmerTest, iterators, splines, colorRamps, gplots, progress, reshape2, lme4 (>= 1.1-10), doParallel, grDevices, graphics, utils, stats Suggests: BiocStyle, knitr, pander, rmarkdown, edgeR, dendextend, tximport, tximportData, ballgown, DESeq2, RUnit, BiocGenerics, r2glmm, readr License: GPL (>= 2) Archs: i386, x64 MD5sum: f6b97c4cfd9972eeb64e2c2b67622130 NeedsCompilation: no Title: Quantify and interpret divers of variation in multilevel gene expression experiments Description: Quantify and interpret multiple sources of biological and technical variation in gene expression experiments. Uses a linear mixed model to quantify variation in gene expression attributable to individual, tissue, time point, or technical variables. Includes dream differential expression analysis for repeated measures. biocViews: RNASeq, GeneExpression, GeneSetEnrichment, DifferentialExpression, BatchEffect, QualityControl, Regression, Epigenetics, FunctionalGenomics, Transcriptomics, Normalization, Preprocessing, Microarray, ImmunoOncology, Software Author: Gabriel E. Hoffman Maintainer: Gabriel E. Hoffman VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/variancePartition git_branch: RELEASE_3_8 git_last_commit: ffd2458 git_last_commit_date: 2019-03-21 Date/Publication: 2019-03-21 source.ver: src/contrib/variancePartition_1.12.3.tar.gz win.binary.ver: bin/windows/contrib/3.5/variancePartition_1.12.3.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/variancePartition_1.12.3.tgz vignettes: vignettes/variancePartition/inst/doc/additional_visualization.pdf, vignettes/variancePartition/inst/doc/theory_practice_random_effects.pdf, vignettes/variancePartition/inst/doc/variancePartition.pdf, vignettes/variancePartition/inst/doc/dream.html vignetteTitles: 2) Additional visualizations, 3) Theory and practice of random effects, 1) Tutorial on using variancePartition, 4) Differential expression testing with repeated measures designs hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/variancePartition/inst/doc/additional_visualization.R, vignettes/variancePartition/inst/doc/dream.R, vignettes/variancePartition/inst/doc/theory_practice_random_effects.R, vignettes/variancePartition/inst/doc/variancePartition.R Package: VariantAnnotation Version: 1.28.13 Depends: R (>= 2.8.0), methods, BiocGenerics (>= 0.15.3), GenomeInfoDb (>= 1.15.2), GenomicRanges (>= 1.31.8), SummarizedExperiment (>= 1.9.9), Rsamtools (>= 1.33.6) Imports: utils, DBI, zlibbioc, Biobase, S4Vectors (>= 0.17.24), IRanges (>= 2.13.13), XVector (>= 0.19.7), Biostrings (>= 2.47.6), AnnotationDbi (>= 1.27.9), rtracklayer (>= 1.39.7), BSgenome (>= 1.47.3), GenomicFeatures (>= 1.31.3) LinkingTo: S4Vectors, IRanges, XVector, Biostrings, Rsamtools Suggests: RUnit, AnnotationHub, BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, SNPlocs.Hsapiens.dbSNP.20101109, SIFT.Hsapiens.dbSNP132, SIFT.Hsapiens.dbSNP137, PolyPhen.Hsapiens.dbSNP131, snpStats, ggplot2, BiocStyle License: Artistic-2.0 MD5sum: 9b8a421a65890353ed2b16d483f88684 NeedsCompilation: yes Title: Annotation of Genetic Variants Description: Annotate variants, compute amino acid coding changes, predict coding outcomes. biocViews: DataImport, Sequencing, SNP, Annotation, Genetics, VariantAnnotation Author: Valerie Obenchain [aut, cre], Martin Morgan [aut], Michael Lawrence [aut], Stephanie Gogarten [ctb] Maintainer: Valerie Obenchain Video: https://www.youtube.com/watch?v=Ro0lHQ_J--I&list=UUqaMSQd_h-2EDGsU6WDiX0Q git_url: https://git.bioconductor.org/packages/VariantAnnotation git_branch: RELEASE_3_8 git_last_commit: 0393347 git_last_commit_date: 2019-03-19 Date/Publication: 2019-03-19 source.ver: src/contrib/VariantAnnotation_1.28.13.tar.gz win.binary.ver: bin/windows/contrib/3.5/VariantAnnotation_1.28.13.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/VariantAnnotation_1.28.13.tgz vignettes: vignettes/VariantAnnotation/inst/doc/filterVcf.pdf, vignettes/VariantAnnotation/inst/doc/VariantAnnotation.pdf vignetteTitles: 2. Using filterVcf to Select Variants from VCF Files, 1. Introduction to VariantAnnotation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/VariantAnnotation/inst/doc/filterVcf.R, vignettes/VariantAnnotation/inst/doc/VariantAnnotation.R dependsOnMe: CNVrd2, deepSNV, DOQTL, ensemblVEP, genotypeeval, GoogleGenomics, HelloRanges, HTSeqGenie, igvR, MTseeker, myvariant, PureCN, R453Plus1Toolbox, RareVariantVis, Rariant, seqCAT, signeR, SomaticSignatures, VariantFiltering, VariantTools importsMe: AllelicImbalance, appreci8R, BadRegionFinder, BBCAnalyzer, biovizBase, customProDB, DominoEffect, FunciSNP, GA4GHclient, genbankr, GenomicFiles, GenVisR, ggbio, GGtools, gmapR, gQTLstats, gwascat, gwasurvivr, icetea, ldblock, MADSEQ, methyAnalysis, motifbreakR, MutationalPatterns, PGA, scoreInvHap, SNPhood, systemPipeR, TitanCNA, TVTB, Uniquorn, YAPSA suggestsMe: AnnotationHub, BiocParallel, cellbaseR, CrispRVariants, GenomicRanges, GenomicScores, GWASTools, omicsPrint, podkat, RVS, SeqArray, trackViewer, trio, vtpnet Package: VariantFiltering Version: 1.18.0 Depends: R (>= 3.0.0), methods, BiocGenerics (>= 0.25.1), VariantAnnotation (>= 1.13.29) Imports: utils, stats, Biobase, S4Vectors (>= 0.9.25), IRanges (>= 2.3.23), RBGL, graph, AnnotationDbi, BiocParallel, Biostrings (>= 2.33.11), GenomeInfoDb (>= 1.3.6), GenomicRanges (>= 1.19.13), SummarizedExperiment, GenomicFeatures, Rsamtools (>= 1.17.8), BSgenome, GenomicScores (>= 1.0.0), Gviz, shiny, shinythemes, shinyjs, DT, shinyTree LinkingTo: S4Vectors, IRanges, XVector, Biostrings Suggests: RUnit, BiocStyle, org.Hs.eg.db, BSgenome.Hsapiens.1000genomes.hs37d5, TxDb.Hsapiens.UCSC.hg19.knownGene, SNPlocs.Hsapiens.dbSNP144.GRCh37, MafDb.1Kgenomes.phase1.hs37d5, phastCons100way.UCSC.hg19, PolyPhen.Hsapiens.dbSNP131, SIFT.Hsapiens.dbSNP137 License: Artistic-2.0 Archs: i386, x64 MD5sum: 1ce3cd46b70fd5e9ca215f125d36317f NeedsCompilation: yes Title: Filtering of coding and non-coding genetic variants Description: Filter genetic variants using different criteria such as inheritance model, amino acid change consequence, minor allele frequencies across human populations, splice site strength, conservation, etc. biocViews: Genetics, Homo_sapiens, Annotation, SNP, Sequencing, HighThroughputSequencing Author: Robert Castelo [aut, cre], Dei Martinez Elurbe [ctb], Pau Puigdevall [ctb], Joan Fernandez [ctb] Maintainer: Robert Castelo URL: https://github.com/rcastelo/VariantFiltering BugReports: https://github.com/rcastelo/VariantFiltering/issues git_url: https://git.bioconductor.org/packages/VariantFiltering git_branch: RELEASE_3_8 git_last_commit: e217023 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/VariantFiltering_1.18.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/VariantFiltering_1.18.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/VariantFiltering_1.18.0.tgz vignettes: vignettes/VariantFiltering/inst/doc/usingVariantFiltering.pdf vignetteTitles: VariantFiltering: filter coding and non-coding genetic variants hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/VariantFiltering/inst/doc/usingVariantFiltering.R Package: VariantTools Version: 1.24.0 Depends: S4Vectors (>= 0.17.33), IRanges (>= 2.13.12), GenomicRanges (>= 1.31.8), VariantAnnotation (>= 1.11.16), methods Imports: Rsamtools (>= 1.31.2), BiocGenerics, Biostrings, parallel, GenomicFeatures (>= 1.31.3), Matrix, rtracklayer (>= 1.39.7), BiocParallel, GenomeInfoDb, BSgenome, Biobase Suggests: RUnit, LungCancerLines (>= 0.0.6), RBGL, graph, gmapR (>= 1.21.3) License: Artistic-2.0 Archs: i386, x64 MD5sum: 58f5a5c644464fcac6ee6eb7ef3b1aa9 NeedsCompilation: no Title: Tools for Exploratory Analysis of Variant Calls Description: Explore, diagnose, and compare variant calls using filters. biocViews: Genetics, GeneticVariability, Sequencing Author: Michael Lawrence, Jeremiah Degenhardt, Robert Gentleman Maintainer: Michael Lawrence git_url: https://git.bioconductor.org/packages/VariantTools git_branch: RELEASE_3_8 git_last_commit: 8528ff3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-11-01 source.ver: src/contrib/VariantTools_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/VariantTools_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/VariantTools_1.24.0.tgz vignettes: vignettes/VariantTools/inst/doc/tutorial.pdf, vignettes/VariantTools/inst/doc/VariantTools.pdf vignetteTitles: tutorial.pdf, Introduction to VariantTools hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/VariantTools/inst/doc/VariantTools.R importsMe: HTSeqGenie, MTseeker Package: vbmp Version: 1.50.0 Depends: R (>= 2.10) Suggests: Biobase (>= 2.5.5), statmod License: GPL (>= 2) MD5sum: 775146794e65565df652e53d0330aff5 NeedsCompilation: no Title: Variational Bayesian Multinomial Probit Regression Description: Variational Bayesian Multinomial Probit Regression with Gaussian Process Priors. It estimates class membership posterior probability employing variational and sparse approximation to the full posterior. This software also incorporates feature weighting by means of Automatic Relevance Determination. biocViews: Classification Author: Nicola Lama , Mark Girolami Maintainer: Nicola Lama URL: http://bioinformatics.oxfordjournals.org/cgi/content/short/btm535v1 git_url: https://git.bioconductor.org/packages/vbmp git_branch: RELEASE_3_8 git_last_commit: ef6c49f git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/vbmp_1.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/vbmp_1.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/vbmp_1.50.0.tgz vignettes: vignettes/vbmp/inst/doc/vbmp.pdf vignetteTitles: vbmp Tutorial hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/vbmp/inst/doc/vbmp.R Package: Vega Version: 1.30.0 Depends: R (>= 2.10) License: GPL-2 MD5sum: 909008499be8b351162b36976db05a5b NeedsCompilation: yes Title: An R package for copy number data segmentation Description: Vega (Variational Estimator for Genomic Aberrations) is an algorithm that adapts a very popular variational model (Mumford and Shah) used in image segmentation so that chromosomal aberrant regions can be efficiently detected. biocViews: aCGH, CopyNumberVariation Author: Sandro Morganella Maintainer: Sandro Morganella git_url: https://git.bioconductor.org/packages/Vega git_branch: RELEASE_3_8 git_last_commit: 2c5365a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Vega_1.30.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Vega_1.30.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Vega_1.30.0.tgz vignettes: vignettes/Vega/inst/doc/Vega.pdf vignetteTitles: Vega hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Vega/inst/doc/Vega.R Package: VegaMC Version: 3.20.0 Depends: R (>= 2.10.0), biomaRt, Biobase Imports: methods, genoset License: GPL-2 Archs: i386, x64 MD5sum: c3e60f589acb272536f80e01eb14e83f NeedsCompilation: yes Title: VegaMC: A Package Implementing a Variational Piecewise Smooth Model for Identification of Driver Chromosomal Imbalances in Cancer Description: This package enables the detection of driver chromosomal imbalances including loss of heterozygosity (LOH) from array comparative genomic hybridization (aCGH) data. VegaMC performs a joint segmentation of a dataset and uses a statistical framework to distinguish between driver and passenger mutation. VegaMC has been implemented so that it can be immediately integrated with the output produced by PennCNV tool. In addition, VegaMC produces in output two web pages that allows a rapid navigation between both the detected regions and the altered genes. In the web page that summarizes the altered genes, the link to the respective Ensembl gene web page is reported. biocViews: aCGH, CopyNumberVariation Author: S. Morganella and M. Ceccarelli Maintainer: Sandro Morganella git_url: https://git.bioconductor.org/packages/VegaMC git_branch: RELEASE_3_8 git_last_commit: aa7cbb9 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/VegaMC_3.20.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/VegaMC_3.20.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/VegaMC_3.20.0.tgz vignettes: vignettes/VegaMC/inst/doc/VegaMC.pdf vignetteTitles: VegaMC hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/VegaMC/inst/doc/VegaMC.R Package: vidger Version: 1.2.1 Depends: R (>= 3.5) Imports: Biobase, DESeq2, edgeR, GGally, ggplot2, ggrepel, knitr, RColorBrewer, rmarkdown, scales, stats, SummarizedExperiment, tidyr, utils Suggests: BiocStyle, testthat License: GPL-3 | file LICENSE Archs: i386, x64 MD5sum: e188f6749e30227e0355a808fbd41824 NeedsCompilation: no Title: Create rapid visualizations of RNAseq data in R Description: The aim of vidger is to rapidly generate information-rich visualizations for the interpretation of differential gene expression results from three widely-used tools: Cuffdiff, DESeq2, and edgeR. biocViews: ImmunoOncology, Visualization, RNASeq, DifferentialExpression, GeneExpression Author: Brandon Monier [aut, cre], Adam McDermaid [aut], Jing Zhao [aut], Qin Ma [aut, fnd] Maintainer: Brandon Monier URL: https://github.com/btmonier/vidger, https://bioconductor.org/packages/release/bioc/html/vidger.html VignetteBuilder: knitr BugReports: https://github.com/btmonier/vidger/issues git_url: https://git.bioconductor.org/packages/vidger git_branch: RELEASE_3_8 git_last_commit: e997581 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/vidger_1.2.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/vidger_1.2.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/vidger_1.2.1.tgz vignettes: vignettes/vidger/inst/doc/vidger.html vignetteTitles: Visualizing RNA-seq data with ViDGER hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/vidger/inst/doc/vidger.R Package: viper Version: 1.16.0 Depends: R (>= 2.14.0), Biobase, methods Imports: mixtools, stats, parallel, e1071, KernSmooth Suggests: bcellViper License: file LICENSE MD5sum: 88466e58bd88dc075343d450c2688b68 NeedsCompilation: no Title: Virtual Inference of Protein-activity by Enriched Regulon analysis Description: Inference of protein activity from gene expression data, including the VIPER and msVIPER algorithms biocViews: SystemsBiology, NetworkEnrichment, GeneExpression, FunctionalPrediction, GeneRegulation Author: Mariano J Alvarez Maintainer: Mariano J Alvarez git_url: https://git.bioconductor.org/packages/viper git_branch: RELEASE_3_8 git_last_commit: c95d6fe git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/viper_1.16.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/viper_1.16.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/viper_1.16.0.tgz vignettes: vignettes/viper/inst/doc/viper.pdf vignetteTitles: Using VIPER hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/viper/inst/doc/viper.R dependsOnMe: vulcan importsMe: diggit, RTN, RTNsurvival Package: vsn Version: 3.50.0 Depends: R (>= 3.4.0), Biobase Imports: methods, affy, limma, lattice, ggplot2 Suggests: affydata, hgu95av2cdf, BiocStyle, knitr, dplyr, testthat License: Artistic-2.0 MD5sum: bf53a681b9b9bdfce2b27cb556e2b9d0 NeedsCompilation: yes Title: Variance stabilization and calibration for microarray data Description: The package implements a method for normalising microarray intensities, and works for single- and multiple-color arrays. It can also be used for data from other technologies, as long as they have similar format. The method uses a robust variant of the maximum-likelihood estimator for an additive-multiplicative error model and affine calibration. The model incorporates data calibration step (a.k.a. normalization), a model for the dependence of the variance on the mean intensity and a variance stabilizing data transformation. Differences between transformed intensities are analogous to "normalized log-ratios". However, in contrast to the latter, their variance is independent of the mean, and they are usually more sensitive and specific in detecting differential transcription. biocViews: Microarray, OneChannel, TwoChannel, Preprocessing Author: Wolfgang Huber, with contributions from Anja von Heydebreck. Many comments and suggestions by users are acknowledged, among them Dennis Kostka, David Kreil, Hans-Ulrich Klein, Robert Gentleman, Deepayan Sarkar and Gordon Smyth Maintainer: Wolfgang Huber URL: http://www.r-project.org, http://www.ebi.ac.uk/huber VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/vsn git_branch: RELEASE_3_8 git_last_commit: ad49fcc git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/vsn_3.50.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/vsn_3.50.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/vsn_3.50.0.tgz vignettes: vignettes/vsn/inst/doc/C-likelihoodcomputations.pdf, vignettes/vsn/inst/doc/D-convergence.pdf, vignettes/vsn/inst/doc/A-vsn.html vignetteTitles: Likelihood Calculations for vsn, Verifying and assessing the performance with simulated data, Introduction to vsn (HTML version) hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/vsn/inst/doc/A-vsn.R, vignettes/vsn/inst/doc/C-likelihoodcomputations.R dependsOnMe: affyPara, cellHTS2, MmPalateMiRNA, webbioc importsMe: arrayQualityMetrics, coexnet, DAPAR, DEP, Doscheda, imageHTS, LVSmiRNA, metaseqR, MSnbase, NormalyzerDE, PowerExplorer, pvca, Ringo, tilingArray suggestsMe: adSplit, beadarray, BiocCaseStudies, DESeq, DESeq2, ggbio, GlobalAncova, globaltest, limma, lumi, PAA, twilight Package: vtpnet Version: 0.22.0 Depends: R (>= 3.0.0), graph, GenomicRanges, gwascat, doParallel, foreach Suggests: MotifDb, VariantAnnotation, Rgraphviz License: Artistic-2.0 Archs: i386, x64 MD5sum: c72d10bf3d20932c1847fa2aad5f914e NeedsCompilation: no Title: variant-transcription factor-phenotype networks Description: variant-transcription factor-phenotype networks, inspired by Maurano et al., Science (2012), PMID 22955828 biocViews: Network Author: VJ Carey Maintainer: VJ Carey git_url: https://git.bioconductor.org/packages/vtpnet git_branch: RELEASE_3_8 git_last_commit: f45d71c git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/vtpnet_0.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/vtpnet_0.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/vtpnet_0.22.0.tgz vignettes: vignettes/vtpnet/inst/doc/vtpnet.pdf vignetteTitles: vtpnet: variant-transcription factor-network tools hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/vtpnet/inst/doc/vtpnet.R Package: vulcan Version: 1.4.0 Depends: R (>= 3.4), ChIPpeakAnno,TxDb.Hsapiens.UCSC.hg19.knownGene, zoo, GenomicRanges, S4Vectors, viper, DiffBind, locfit Imports: wordcloud, csaw, gplots, stats, utils, caTools, graphics, DESeq, Biobase Suggests: vulcandata License: LGPL-3 MD5sum: bdec6ffd2a60d2f83183dd2c76bcb637 NeedsCompilation: no Title: VirtUaL ChIP-Seq data Analysis using Networks Description: Vulcan (VirtUaL ChIP-Seq Analysis through Networks) is a package that interrogates gene regulatory networks to infer cofactors significantly enriched in a differential binding signature coming from ChIP-Seq data. In order to do so, our package combines strategies from different BioConductor packages: DESeq for data normalization, ChIPpeakAnno and DiffBind for annotation and definition of ChIP-Seq genomic peaks, csaw to define optimal peak width and viper for applying a regulatory network over a differential binding signature. biocViews: SystemsBiology, NetworkEnrichment, GeneExpression, ChIPSeq Author: Federico M. Giorgi, Andrew N. Holding, Florian Markowetz Maintainer: Federico M. Giorgi git_url: https://git.bioconductor.org/packages/vulcan git_branch: RELEASE_3_8 git_last_commit: 5848876 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/vulcan_1.4.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/vulcan_1.4.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/vulcan_1.4.0.tgz vignettes: vignettes/vulcan/inst/doc/vulcan.pdf vignetteTitles: Vulcan: VirtUaL ChIP-Seq Analysis through Networks hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/vulcan/inst/doc/vulcan.R Package: wateRmelon Version: 1.26.0 Depends: R (>= 2.10), Biobase, limma, methods, matrixStats, methylumi, lumi, ROC, IlluminaHumanMethylation450kanno.ilmn12.hg19, illuminaio Imports: Biobase Suggests: RPMM, IlluminaHumanMethylationEPICanno.ilm10b2.hg19, IlluminaHumanMethylationEPICmanifest, irlba Enhances: minfi License: GPL-3 MD5sum: 850367d09d233968ac5b418f29de23a4 NeedsCompilation: no Title: Illumina 450 methylation array normalization and metrics Description: 15 flavours of betas and three performance metrics, with methods for objects produced by methylumi and minfi packages. biocViews: DNAMethylation, Microarray, TwoChannel, Preprocessing, QualityControl Author: Leonard C Schalkwyk, Ruth Pidsley, Chloe CY Wong, with functions contributed by Nizar Touleimat, Matthieu Defrance, Andrew Teschendorff, Jovana Maksimovic, Tyler Gorrie-Stone, Louis El Khoury Maintainer: Leo git_url: https://git.bioconductor.org/packages/wateRmelon git_branch: RELEASE_3_8 git_last_commit: b9c14c3 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/wateRmelon_1.26.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/wateRmelon_1.26.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/wateRmelon_1.26.0.tgz vignettes: vignettes/wateRmelon/inst/doc/wateRmelon.pdf vignetteTitles: The \Rpackage{wateRmelon} Package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/wateRmelon/inst/doc/wateRmelon.R dependsOnMe: bigmelon, skewr importsMe: ChAMP suggestsMe: RnBeads Package: wavClusteR Version: 2.16.1 Depends: R (>= 3.2), GenomicRanges (>= 1.31.8), Rsamtools Imports: methods, BiocGenerics, S4Vectors (>= 0.17.25), IRanges (>= 2.13.12), Biostrings (>= 2.47.6), foreach, GenomicFeatures (>= 1.31.3), ggplot2, Hmisc, mclust, rtracklayer (>= 1.39.7), seqinr, stringr, wmtsa Suggests: BiocStyle, knitr, rmarkdown, BSgenome.Hsapiens.UCSC.hg19 Enhances: doMC License: GPL-2 MD5sum: 8d4730f9b60865bffadb4d7fde122b1c NeedsCompilation: no Title: Sensitive and highly resolved identification of RNA-protein interaction sites in PAR-CLIP data Description: The package provides an integrated pipeline for the analysis of PAR-CLIP data. PAR-CLIP-induced transitions are first discriminated from sequencing errors, SNPs and additional non-experimental sources by a non- parametric mixture model. The protein binding sites (clusters) are then resolved at high resolution and cluster statistics are estimated using a rigorous Bayesian framework. Post-processing of the results, data export for UCSC genome browser visualization and motif search analysis are provided. In addition, the package allows to integrate RNA-Seq data to estimate the False Discovery Rate of cluster detection. Key functions support parallel multicore computing. Note: while wavClusteR was designed for PAR-CLIP data analysis, it can be applied to the analysis of other NGS data obtained from experimental procedures that induce nucleotide substitutions (e.g. BisSeq). biocViews: ImmunoOncology, Sequencing, Technology, RIPSeq, RNASeq, Bayesian Author: Federico Comoglio and Cem Sievers Maintainer: Federico Comoglio VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/wavClusteR git_branch: RELEASE_3_8 git_last_commit: 454c3d4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/wavClusteR_2.16.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/wavClusteR_2.16.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/wavClusteR_2.16.1.tgz vignettes: vignettes/wavClusteR/inst/doc/wavCluster_vignette.html vignetteTitles: wavClusteR: a workflow for PAR-CLIP data analysis hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/wavClusteR/inst/doc/wavCluster_vignette.R Package: waveTiling Version: 1.24.0 Depends: oligo, oligoClasses, Biobase, Biostrings, GenomeGraphs Imports: methods, affy, preprocessCore, GenomicRanges, waveslim, IRanges Suggests: BSgenome, BSgenome.Athaliana.TAIR.TAIR9, waveTilingData, pd.atdschip.tiling, TxDb.Athaliana.BioMart.plantsmart22 License: GPL (>=2) MD5sum: 80d2a5104b88c2621ded2314d7a986ba NeedsCompilation: yes Title: Wavelet-Based Models for Tiling Array Transcriptome Analysis Description: This package is designed to conduct transcriptome analysis for tiling arrays based on fast wavelet-based functional models. biocViews: Microarray, DifferentialExpression, TimeCourse, GeneExpression Author: Kristof De Beuf , Peter Pipelers and Lieven Clement Maintainer: Kristof De Beuf URL: https://r-forge.r-project.org/projects/wavetiling/ git_url: https://git.bioconductor.org/packages/waveTiling git_branch: RELEASE_3_8 git_last_commit: 9e16d0a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/waveTiling_1.24.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/waveTiling_1.24.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/waveTiling_1.24.0.tgz vignettes: vignettes/waveTiling/inst/doc/waveTiling-vignette.pdf vignetteTitles: The waveTiling package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/waveTiling/inst/doc/waveTiling-vignette.R Package: weaver Version: 1.48.0 Depends: R (>= 2.5.0), digest, tools, utils, codetools Suggests: codetools License: GPL-2 Archs: i386, x64 MD5sum: 9b2abdd081e7f54dff55bfd0fe27512c NeedsCompilation: no Title: Tools and extensions for processing Sweave documents Description: This package provides enhancements on the Sweave() function in the base package. In particular a facility for caching code chunk results is included. biocViews: Infrastructure Author: Seth Falcon Maintainer: Seth Falcon git_url: https://git.bioconductor.org/packages/weaver git_branch: RELEASE_3_8 git_last_commit: 4ed114b git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/weaver_1.48.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/weaver_1.48.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/weaver_1.48.0.tgz vignettes: vignettes/weaver/inst/doc/weaver_howTo.pdf vignetteTitles: Using weaver to process Sweave documents hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/weaver/inst/doc/weaver_howTo.R suggestsMe: BiocCaseStudies Package: webbioc Version: 1.54.0 Depends: R (>= 1.8.0), Biobase, affy, multtest, annaffy, vsn, gcrma, qvalue Imports: multtest, qvalue, stats, utils, BiocManager License: GPL (>= 2) MD5sum: d08d8ccc53dc8c06d1472dc5e6e528d4 NeedsCompilation: no Title: Bioconductor Web Interface Description: An integrated web interface for doing microarray analysis using several of the Bioconductor packages. It is intended to be deployed as a centralized bioinformatics resource for use by many users. (Currently only Affymetrix oligonucleotide analysis is supported.) biocViews: Infrastructure, Microarray, OneChannel, DifferentialExpression Author: Colin A. Smith Maintainer: Colin A. Smith URL: http://www.bioconductor.org/ SystemRequirements: Unix, Perl (>= 5.6.0), Netpbm git_url: https://git.bioconductor.org/packages/webbioc git_branch: RELEASE_3_8 git_last_commit: bcbfed6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/webbioc_1.54.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/webbioc_1.54.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/webbioc_1.54.0.tgz vignettes: vignettes/webbioc/inst/doc/demoscript.pdf, vignettes/webbioc/inst/doc/webbioc.pdf vignetteTitles: webbioc Demo Script, webbioc Overview hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Package: widgetTools Version: 1.60.0 Depends: R (>= 2.4.0), methods, utils, tcltk Suggests: Biobase License: LGPL MD5sum: c317790521ce4176632769af78d89b4f NeedsCompilation: no Title: Creates an interactive tcltk widget Description: This packages contains tools to support the construction of tcltk widgets biocViews: Infrastructure Author: Jianhua Zhang Maintainer: Jianhua Zhang git_url: https://git.bioconductor.org/packages/widgetTools git_branch: RELEASE_3_8 git_last_commit: ed404f6 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/widgetTools_1.60.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/widgetTools_1.60.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/widgetTools_1.60.0.tgz vignettes: vignettes/widgetTools/inst/doc/widgetTools.pdf vignetteTitles: widgetTools Introduction hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/widgetTools/inst/doc/widgetTools.R dependsOnMe: tkWidgets importsMe: OLINgui suggestsMe: affy Package: wiggleplotr Version: 1.6.1 Depends: R (>= 3.4) Imports: dplyr, ggplot2 (>= 2.2.0), GenomicRanges, rtracklayer, cowplot, assertthat, purrr, S4Vectors, IRanges, GenomeInfoDb Suggests: knitr, rmarkdown, biomaRt, GenomicFeatures, testthat, ensembldb, EnsDb.Hsapiens.v86, org.Hs.eg.db, TxDb.Hsapiens.UCSC.hg38.knownGene, AnnotationDbi, AnnotationFilter License: Apache License 2.0 MD5sum: 4d8df675778183878622324b7727bd50 NeedsCompilation: no Title: Make read coverage plots from BigWig files Description: Tools to visualise read coverage from sequencing experiments together with genomic annotations (genes, transcripts, peaks). Introns of long transcripts can be rescaled to a fixed length for better visualisation of exonic read coverage. biocViews: ImmunoOncology, Coverage, RNASeq, ChIPSeq, Sequencing, Visualization, GeneExpression, Transcription, AlternativeSplicing Author: Kaur Alasoo [aut, cre] Maintainer: Kaur Alasoo VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/wiggleplotr git_branch: RELEASE_3_8 git_last_commit: 2fe7de2 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/wiggleplotr_1.6.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/wiggleplotr_1.6.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/wiggleplotr_1.6.1.tgz vignettes: vignettes/wiggleplotr/inst/doc/wiggleplotr.html vignetteTitles: Introduction to wiggleplotr hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/wiggleplotr/inst/doc/wiggleplotr.R Package: Wrench Version: 1.0.0 Depends: R (>= 3.5.0) Imports: limma, matrixStats, locfit, stats, graphics Suggests: knitr, rmarkdown, metagenomeSeq, DESeq2, edgeR License: Artistic-2.0 MD5sum: a13adf697da0006944f1f36b3c5748e5 NeedsCompilation: no Title: Wrench normalization for sparse count data Description: Wrench is a package for normalization sparse genomic count data, like that arising from 16s metagenomic surveys. biocViews: Normalization, Sequencing, Software Author: Senthil Kumar Muthiah [aut], Hector Corrada Bravo [aut, cre] Maintainer: Hector Corrada Bravo URL: https://github.com/HCBravoLab/Wrench VignetteBuilder: knitr BugReports: https://github.com/HCBravoLab/Wrench/issues git_url: https://git.bioconductor.org/packages/Wrench git_branch: RELEASE_3_8 git_last_commit: ea2cb42 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/Wrench_1.0.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/Wrench_1.0.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/Wrench_1.0.0.tgz vignettes: vignettes/Wrench/inst/doc/vignette.html vignetteTitles: Wrench hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/Wrench/inst/doc/vignette.R Package: XBSeq Version: 1.14.1 Depends: DESeq2, R (>= 3.3) Imports: pracma, matrixStats, locfit, ggplot2, methods, Biobase, dplyr, magrittr, roar Suggests: knitr, DESeq, rmarkdown, BiocStyle, testthat License: GPL (>=3) MD5sum: 27d568ac864612bbd7096f1b49a1db92 NeedsCompilation: no Title: Test for differential expression for RNA-seq data Description: We developed a novel algorithm, XBSeq, where a statistical model was established based on the assumption that observed signals are the convolution of true expression signals and sequencing noises. The mapped reads in non-exonic regions are considered as sequencing noises, which follows a Poisson distribution. Given measureable observed and noise signals from RNA-seq data, true expression signals, assuming governed by the negative binomial distribution, can be delineated and thus the accurate detection of differential expressed genes. biocViews: ImmunoOncology, RNASeq, DifferentialExpression, Sequencing, Software, ExperimentalDesign Author: Yuanhang Liu Maintainer: Yuanhang Liu URL: https://github.com/Liuy12/XBSeq VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/XBSeq git_branch: RELEASE_3_8 git_last_commit: 09c6bd4 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/XBSeq_1.14.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/XBSeq_1.14.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/XBSeq_1.14.1.tgz vignettes: vignettes/XBSeq/inst/doc/XBSeq.html vignetteTitles: Differential expression and apa usage analysis of count data using XBSeq package hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/XBSeq/inst/doc/XBSeq.R Package: xcms Version: 3.4.4 Depends: R (>= 2.14.0), methods, Biobase, BiocParallel (>= 1.8.0), MSnbase (>= 2.7.8) Imports: mzR (>= 2.13.1), BiocGenerics, ProtGenerics, lattice, RColorBrewer, plyr, RANN, multtest, MassSpecWavelet (>= 1.5.2), S4Vectors, robustbase Suggests: BiocStyle, caTools, knitr (>= 1.1.0), faahKO, msdata, ncdf4, rgl, microbenchmark, testthat, pander, magrittr, MALDIquant Enhances: Rgraphviz, Rmpi, XML License: GPL (>= 2) + file LICENSE MD5sum: 5bcf252ec53c7720a67f1785e4693005 NeedsCompilation: yes Title: LC/MS and GC/MS Data Analysis Description: Framework for processing and visualization of chromatographically separated and single-spectra mass spectral data. Imports from AIA/ANDI NetCDF, mzXML, mzData and mzML files. Preprocesses data for high-throughput, untargeted analyte profiling. biocViews: ImmunoOncology, MassSpectrometry, Metabolomics Author: Colin A. Smith , Ralf Tautenhahn , Steffen Neumann , Paul Benton , Christopher Conley , Johannes Rainer Maintainer: Steffen Neumann URL: http://metlin.scripps.edu/download/ and https://github.com/sneumann/xcms VignetteBuilder: knitr BugReports: https://github.com/sneumann/xcms/issues/new git_url: https://git.bioconductor.org/packages/xcms git_branch: RELEASE_3_8 git_last_commit: 6a9e67f git_last_commit_date: 2019-02-20 Date/Publication: 2019-02-20 source.ver: src/contrib/xcms_3.4.4.tar.gz win.binary.ver: bin/windows/contrib/3.5/xcms_3.4.4.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/xcms_3.4.4.tgz vignettes: vignettes/xcms/inst/doc/new_functionality.html, vignettes/xcms/inst/doc/xcms-direct-injection.html, vignettes/xcms/inst/doc/xcms.html, vignettes/xcms/inst/doc/xcmsMSn.html vignetteTitles: New and modified functionality in xcms, Grouping FTICR-MS data with xcms, LCMS data preprocessing and analysis with xcms, Processing Tandem-MS and MSn data with xcms hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/xcms/inst/doc/new_functionality.R, vignettes/xcms/inst/doc/xcms-direct-injection.R, vignettes/xcms/inst/doc/xcms.R, vignettes/xcms/inst/doc/xcmsMSn.R dependsOnMe: CAMERA, flagme, IPO, LOBSTAHS, Metab, metaMS, proFIA importsMe: CAMERA, cosmiq, Risa suggestsMe: MassSpecWavelet, msPurity, RMassBank Package: XDE Version: 2.28.0 Depends: R (>= 2.10.0), Biobase (>= 2.5.5) Imports: BiocGenerics, genefilter, graphics, grDevices, gtools, MergeMaid, methods, stats, utils, mvtnorm, RColorBrewer, GeneMeta, siggenes Suggests: MASS, RUnit Enhances: coda License: LGPL-2 Archs: i386, x64 MD5sum: be18c127b068e92c2811ceaf408326e0 NeedsCompilation: yes Title: XDE: a Bayesian hierarchical model for cross-study analysis of differential gene expression Description: Multi-level model for cross-study detection of differential gene expression. biocViews: Microarray, DifferentialExpression Author: R.B. Scharpf, G. Parmigiani, A.B. Nobel, and H. Tjelmeland Maintainer: Robert Scharpf git_url: https://git.bioconductor.org/packages/XDE git_branch: RELEASE_3_8 git_last_commit: b8cc7d0 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/XDE_2.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/XDE_2.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/XDE_2.28.0.tgz vignettes: vignettes/XDE/inst/doc/XDE.pdf, vignettes/XDE/inst/doc/XdeParameterClass.pdf vignetteTitles: XDE Vignette, XdeParameterClass Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/XDE/inst/doc/XDE.R, vignettes/XDE/inst/doc/XdeParameterClass.R Package: XINA Version: 1.0.1 Depends: R (>= 3.5), Biobase Imports: mclust, plyr, alluvial, ggplot2, igraph, gridExtra, tools, grDevices, graphics, utils, STRINGdb Suggests: knitr, rmarkdown License: GPL-3 Archs: i386, x64 MD5sum: 408813249f4f5dc4a4a140c97027fa40 NeedsCompilation: no Title: Multiplexes isobaric mass tagged-based kinetics data for network analysis Description: An intuitive R package simplifies network analyses output from multiplexed high-dimensional proteomics/trascriptomics kinetics data. biocViews: ImmunoOncology, SystemsBiology, Proteomics, RNASeq, Network Author: Lee, Lang Ho and Singh, Sasha A. Maintainer: Lang Ho Lee and Sasha A. Singh VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/XINA git_branch: RELEASE_3_8 git_last_commit: 5941b22 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/XINA_1.0.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/XINA_1.0.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/XINA_1.0.1.tgz vignettes: vignettes/XINA/inst/doc/xina_user_code.html vignetteTitles: xina_user_code hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/XINA/inst/doc/xina_user_code.R Package: xmapbridge Version: 1.40.0 Depends: R (>= 2.0), methods Suggests: RUnit, RColorBrewer License: LGPL-3 MD5sum: aad45dacbe7c31b2569b42e38cea5131 NeedsCompilation: no Title: Export plotting files to the xmapBridge for visualisation in X:Map Description: xmapBridge can plot graphs in the X:Map genome browser. This package exports plotting files in a suitable format. biocViews: Annotation, ReportWriting, Visualization Author: Tim Yates and Crispin J Miller Maintainer: Chris Wirth URL: http://xmap.picr.man.ac.uk, http://www.bioconductor.org git_url: https://git.bioconductor.org/packages/xmapbridge git_branch: RELEASE_3_8 git_last_commit: 00a2993 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/xmapbridge_1.40.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/xmapbridge_1.40.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/xmapbridge_1.40.0.tgz vignettes: vignettes/xmapbridge/inst/doc/xmapbridge.pdf vignetteTitles: xmapbridge primer hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/xmapbridge/inst/doc/xmapbridge.R Package: xps Version: 1.42.0 Depends: R (>= 2.6.0), methods, utils Suggests: tools License: GPL (>= 2.0) MD5sum: 7778907ce1572ac8dddb9cf753dd1b68 NeedsCompilation: yes Title: Processing and Analysis of Affymetrix Oligonucleotide Arrays including Exon Arrays, Whole Genome Arrays and Plate Arrays Description: The package handles pre-processing, normalization, filtering and analysis of Affymetrix GeneChip expression arrays, including exon arrays (Exon 1.0 ST: core, extended, full probesets), gene arrays (Gene 1.0 ST) and plate arrays on computers with 1 GB RAM only. It imports Affymetrix .CDF, .CLF, .PGF and .CEL as well as annotation files, and computes e.g. RMA, MAS5, FARMS, DFW, FIRMA, tRMA, MAS5-calls, DABG-calls, I/NI-calls. It is an R wrapper to XPS (eXpression Profiling System), which is based on ROOT, an object-oriented framework developed at CERN. Thus, the prior installation of ROOT is a prerequisite for the usage of this package, however, no knowledge of ROOT is required. ROOT is licensed under LGPL and can be downloaded from http://root.cern.ch. biocViews: ExonArray, GeneExpression, Microarray, OneChannel, DataImport, Preprocessing, Transcription, DifferentialExpression Author: Christian Stratowa, Vienna, Austria Maintainer: Christian Stratowa SystemRequirements: GNU make, root_v5.34.36 - See README file for installation instructions. git_url: https://git.bioconductor.org/packages/xps git_branch: RELEASE_3_8 git_last_commit: 34409b4 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/xps_1.42.0.tar.gz mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/xps_1.42.0.tgz vignettes: vignettes/xps/inst/doc/APTvsXPS.pdf, vignettes/xps/inst/doc/xps.pdf, vignettes/xps/inst/doc/xpsClasses.pdf, vignettes/xps/inst/doc/xpsPreprocess.pdf vignetteTitles: 3. XPS Vignette: Comparison APT vs XPS, 1. XPS Vignette: Overview, 2. XPS Vignette: Classes, 4. XPS Vignette: Function express() hasREADME: TRUE hasNEWS: TRUE hasINSTALL: TRUE hasLICENSE: FALSE Rfiles: vignettes/xps/inst/doc/APTvsXPS.R, vignettes/xps/inst/doc/xps.R, vignettes/xps/inst/doc/xpsClasses.R, vignettes/xps/inst/doc/xpsPreprocess.R Package: XVector Version: 0.22.0 Depends: R (>= 2.8.0), methods, BiocGenerics (>= 0.19.2), S4Vectors (>= 0.19.15), IRanges (>= 2.15.12) Imports: methods, utils, zlibbioc, BiocGenerics, S4Vectors, IRanges LinkingTo: S4Vectors, IRanges Suggests: Biostrings, drosophila2probe, RUnit License: Artistic-2.0 MD5sum: 464c4abd6b6134b894a885f7f42e2ff8 NeedsCompilation: yes Title: Representation and manipulation of external sequences Description: Memory efficient S4 classes for storing sequences "externally" (behind an R external pointer, or on disk). biocViews: Infrastructure, DataRepresentation Author: Hervé Pagès and Patrick Aboyoun Maintainer: Hervé Pagès git_url: https://git.bioconductor.org/packages/XVector git_branch: RELEASE_3_8 git_last_commit: b5e107a git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/XVector_0.22.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/XVector_0.22.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/XVector_0.22.0.tgz hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: FALSE dependsOnMe: Biostrings, motifRG, triplex importsMe: BSgenome, ChIPsim, CNEr, compEpiTools, dada2, DECIPHER, gcrma, GenomicFeatures, GenomicRanges, Gviz, IONiseR, kebabs, MatrixRider, R453Plus1Toolbox, Rsamtools, rtracklayer, TFBSTools, tracktables, tRNA, VariantAnnotation suggestsMe: IRanges linksToMe: Biostrings, CNEr, DECIPHER, kebabs, MatrixRider, Rsamtools, rSFFreader, rtracklayer, ShortRead, triplex, VariantAnnotation, VariantFiltering Package: yamss Version: 1.8.1 Depends: R (>= 3.3.0), methods, BiocGenerics (>= 0.15.3), SummarizedExperiment Imports: IRanges, stats, S4Vectors, EBImage, Matrix, mzR, data.table, grDevices, limma Suggests: BiocStyle, knitr, rmarkdown, digest, mtbls2, testthat License: Artistic-2.0 Archs: i386, x64 MD5sum: 2eae19bf5906a912a04d9fb0c2a31445 NeedsCompilation: no Title: Tools for high-throughput metabolomics Description: Tools to analyze and visualize high-throughput metabolomics data aquired using chromatography-mass spectrometry. These tools preprocess data in a way that enables reliable and powerful differential analysis. biocViews: MassSpectrometry, Metabolomics, ImmunoOncology, Software Author: Leslie Myint [cre, aut], Kasper Daniel Hansen [aut] Maintainer: Leslie Myint URL: https://github.com/hansenlab/yamss VignetteBuilder: knitr BugReports: https://github.com/hansenlab/yamss/issues git_url: https://git.bioconductor.org/packages/yamss git_branch: RELEASE_3_8 git_last_commit: 93b6947 git_last_commit_date: 2018-12-01 Date/Publication: 2018-12-01 source.ver: src/contrib/yamss_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/yamss_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/yamss_1.8.1.tgz vignettes: vignettes/yamss/inst/doc/yamss.html vignetteTitles: yamss User's Guide hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/yamss/inst/doc/yamss.R Package: YAPSA Version: 1.8.0 Depends: R (>= 3.3.0), GenomicRanges, ggplot2, grid Imports: lsei, SomaticSignatures, VariantAnnotation, GenomeInfoDb, reshape2, gridExtra, corrplot, dendextend, GetoptLong, circlize, gtrellis, PMCMR, ComplexHeatmap, KEGGREST, grDevices Suggests: BSgenome.Hsapiens.UCSC.hg19, testthat, BiocStyle, knitr, rmarkdown License: GPL-3 MD5sum: 09ee5f1de2127297df5914ec0082103b NeedsCompilation: no Title: Yet Another Package for Signature Analysis Description: This package provides functions and routines useful in the analysis of somatic signatures (cf. L. Alexandrov et al., Nature 2013). In particular, functions to perform a signature analysis with known signatures (LCD = linear combination decomposition) and a signature analysis on stratified mutational catalogue (SMC = stratify mutational catalogue) are provided. biocViews: Sequencing, DNASeq, SomaticMutation, Visualization, Clustering, GenomicVariation, StatisticalMethod, BiologicalQuestion Author: Daniel Huebschmann, Zuguang Gu, Matthias Schlesner Maintainer: Daniel Huebschmann VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/YAPSA git_branch: RELEASE_3_8 git_last_commit: 402f3f7 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/YAPSA_1.8.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/YAPSA_1.8.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/YAPSA_1.8.0.tgz vignettes: vignettes/YAPSA/inst/doc/YAPSA.html vignetteTitles: YAPSA hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/YAPSA/inst/doc/YAPSA.R Package: yaqcaffy Version: 1.42.0 Depends: simpleaffy (>= 2.19.3), methods Imports: stats4 Suggests: MAQCsubsetAFX, affydata, xtable, tcltk2, tcltk License: Artistic-2.0 MD5sum: 0ac961004e53ff216bcfa89616c92b56 NeedsCompilation: no Title: Affymetrix expression data quality control and reproducibility analysis Description: Quality control of Affymetrix GeneChip expression data and reproducibility analysis of human whole genome chips with the MAQC reference datasets. biocViews: Microarray,OneChannel,QualityControl,ReportWriting Author: Laurent Gatto Maintainer: Laurent Gatto git_url: https://git.bioconductor.org/packages/yaqcaffy git_branch: RELEASE_3_8 git_last_commit: a4af673 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/yaqcaffy_1.42.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/yaqcaffy_1.42.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/yaqcaffy_1.42.0.tgz vignettes: vignettes/yaqcaffy/inst/doc/yaqcaffy.pdf vignetteTitles: yaqcaffy: Affymetrix quality control and MAQC reproducibility hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/yaqcaffy/inst/doc/yaqcaffy.R suggestsMe: qcmetrics Package: yarn Version: 1.8.1 Depends: Biobase Imports: biomaRt, downloader, edgeR, gplots, graphics, limma, matrixStats, preprocessCore, readr, RColorBrewer, stats, quantro Suggests: knitr, rmarkdown, testthat (>= 0.8) License: Artistic-2.0 MD5sum: 6b167461ec52111beace3a17e36fadd8 NeedsCompilation: no Title: YARN: Robust Multi-Condition RNA-Seq Preprocessing and Normalization Description: Expedite large RNA-Seq analyses using a combination of previously developed tools. YARN is meant to make it easier for the user in performing basic mis-annotation quality control, filtering, and condition-aware normalization. YARN leverages many Bioconductor tools and statistical techniques to account for the large heterogeneity and sparsity found in very large RNA-seq experiments. biocViews: Software, QualityControl, GeneExpression, Sequencing, Preprocessing, Normalization, Annotation, Visualization, Clustering Author: Joseph N Paulson [aut, cre], Cho-Yi Chen [aut], Camila Lopes-Ramos [aut], Marieke Kuijjer [aut], John Platig [aut], Abhijeet Sonawane [aut], Maud Fagny [aut], Kimberly Glass [aut], John Quackenbush [aut] Maintainer: Joseph N Paulson VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/yarn git_branch: RELEASE_3_8 git_last_commit: ee0723d git_last_commit_date: 2019-03-14 Date/Publication: 2019-03-14 source.ver: src/contrib/yarn_1.8.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/yarn_1.8.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/yarn_1.8.1.tgz vignettes: vignettes/yarn/inst/doc/yarn.pdf vignetteTitles: YARN: Robust Multi-Tissue RNA-Seq Preprocessing and Normalization hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/yarn/inst/doc/yarn.R Package: zFPKM Version: 1.4.1 Depends: R (>= 3.4.0) Imports: checkmate, dplyr, ggplot2, tidyr, SummarizedExperiment Suggests: knitr, limma, edgeR, GEOquery, stringr, printr License: GPL-3 | file LICENSE MD5sum: d8966bc7e55ba3d432ede5cf18b2a4f9 NeedsCompilation: no Title: A suite of functions to facilitate zFPKM transformations Description: Perform the zFPKM transform on RNA-seq FPKM data. This algorithm is based on the publication by Hart et al., 2013 (Pubmed ID 24215113). Reference recommends using zFPKM > -3 to select expressed genes. Validated with encode open/closed chromosome data. Works well for gene level data using FPKM or TPM. Does not appear to calibrate well for transcript level data. biocViews: ImmunoOncology, RNASeq, FeatureExtraction, Software, GeneExpression Author: Ron Ammar [aut, cre], John Thompson [aut] Maintainer: Ron Ammar URL: https://github.com/ronammar/zFPKM/ VignetteBuilder: knitr BugReports: https://github.com/ronammar/zFPKM/issues git_url: https://git.bioconductor.org/packages/zFPKM git_branch: RELEASE_3_8 git_last_commit: e1c2a03 git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 source.ver: src/contrib/zFPKM_1.4.1.tar.gz win.binary.ver: bin/windows/contrib/3.5/zFPKM_1.4.1.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/zFPKM_1.4.1.tgz vignettes: vignettes/zFPKM/inst/doc/zFPKM.html vignetteTitles: Introduction to zFPKM Transformation hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: TRUE Rfiles: vignettes/zFPKM/inst/doc/zFPKM.R Package: zinbwave Version: 1.4.2 Depends: R (>= 3.4), methods, SummarizedExperiment, SingleCellExperiment Imports: copula, glmnet, BiocParallel, softImpute, stats, genefilter, edgeR, Matrix Suggests: knitr, rmarkdown, testthat, matrixStats, magrittr, scRNAseq, ggplot2, biomaRt, BiocStyle, Rtsne, DESeq2, Seurat License: Artistic-2.0 MD5sum: 3ca35d29cb395030acb1286bc7399cf7 NeedsCompilation: no Title: Zero-Inflated Negative Binomial Model for RNA-Seq Data Description: Implements a general and flexible zero-inflated negative binomial model that can be used to provide a low-dimensional representations of single-cell RNA-seq data. The model accounts for zero inflation (dropouts), over-dispersion, and the count nature of the data. The model also accounts for the difference in library sizes and optionally for batch effects and/or other covariates, avoiding the need for pre-normalize the data. biocViews: ImmunoOncology, DimensionReduction, GeneExpression, RNASeq, Software, Transcriptomics, Sequencing, SingleCell Author: Davide Risso [aut, cre, cph], Svetlana Gribkova [aut], Fanny Perraudeau [aut], Jean-Philippe Vert [aut] Maintainer: Davide Risso VignetteBuilder: knitr BugReports: https://github.com/drisso/zinbwave/issues git_url: https://git.bioconductor.org/packages/zinbwave git_branch: RELEASE_3_8 git_last_commit: fe932f7 git_last_commit_date: 2019-03-11 Date/Publication: 2019-03-11 source.ver: src/contrib/zinbwave_1.4.2.tar.gz win.binary.ver: bin/windows/contrib/3.5/zinbwave_1.4.2.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/zinbwave_1.4.2.tgz vignettes: vignettes/zinbwave/inst/doc/intro.html vignetteTitles: zinbwave Vignette hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Rfiles: vignettes/zinbwave/inst/doc/intro.R importsMe: clusterExperiment suggestsMe: splatter Package: zlibbioc Version: 1.28.0 License: Artistic-2.0 + file LICENSE MD5sum: a92d411b500d3f88434653351a8e9aea NeedsCompilation: yes Title: An R packaged zlib-1.2.5 Description: This package uses the source code of zlib-1.2.5 to create libraries for systems that do not have these available via other means (most Linux and Mac users should have system-level access to zlib, and no direct need for this package). See the vignette for instructions on use. biocViews: Infrastructure Author: Martin Morgan Maintainer: Bioconductor Package Maintainer URL: http://bioconductor.org/packages/release/bioc/html/Zlibbioc.html git_url: https://git.bioconductor.org/packages/zlibbioc git_branch: RELEASE_3_8 git_last_commit: b825b04 git_last_commit_date: 2018-10-30 Date/Publication: 2018-10-30 source.ver: src/contrib/zlibbioc_1.28.0.tar.gz win.binary.ver: bin/windows/contrib/3.5/zlibbioc_1.28.0.zip mac.binary.el-capitan.ver: bin/macosx/el-capitan/contrib/3.5/zlibbioc_1.28.0.tgz vignettes: vignettes/zlibbioc/inst/doc/UsingZlibbioc.pdf vignetteTitles: Using zlibbioc C libraries hasREADME: FALSE hasNEWS: FALSE hasINSTALL: FALSE hasLICENSE: TRUE dependsOnMe: BitSeq importsMe: affy, affyio, affyPLM, bamsignals, ChemmineOB, DiffBind, LVSmiRNA, MADSEQ, makecdfenv, oligo, polyester, QuasR, Rhtslib, Rsamtools, rtracklayer, seqbias, ShortRead, snpStats, Starr, TransView, VariantAnnotation, XVector linksToMe: bamsignals, BitSeq, csaw, diffHic, methylKit, mzR, Rhtslib, scPipe, seqTools Package: mlm4omics Version: 1.0.1 Depends: R (>= 3.5.0), Rcpp (>= 0.12.17), methods, stats Imports: rstan (>= 2.17.3),rstantools (>= 1.5.0),MASS,Matrix,stats4,ggplot2 LinkingTo: StanHeaders (>= 2.17.2), rstan (>= 2.17.3), BH (>= 1.66.0-1), Rcpp (>= 0.12.17), RcppEigen (>= 0.3.3.4.0) Suggests: testthat, BiocStyle, knitr, rmarkdown, roxygen2 (>= 5.0.0) License: GPL-3 Archs: i386, x64 NeedsCompilation: yes Title: Multilevel Model for Multivariate Responses with Missing Values Description: To conduct Bayesian inference regression for responses with multilevel explanatory variables and missing values; It uses function from 'Stan', a software to implement posterior sampling using Hamiltonian MC and its variation Non-U-Turn algorithms. It implements the posterior sampling of regression coefficients from the multilevel regression models. The package has two main functions to handle not-missing-at-random missing responses and left-censored with not-missing-at random responses. The purpose is to provide a similar format as the other R regression functions but using 'Stan' models. biocViews: ImmunoOncology, Bayesian,CopyNumberVariation,Classification,Regression,MassSpectrometry,Proteomics,Software Author: Irene Zeng [aut, cre], Thomas Lumley [ctb] Maintainer: Irene SL Zeng URL: https://doi.org/10.1101/153049 SystemRequirements: GNU make VignetteBuilder: knitr git_url: https://git.bioconductor.org/packages/mlm4omics git_branch: RELEASE_3_8 git_last_commit: 308441f git_last_commit_date: 2019-01-04 Date/Publication: 2019-01-04 win.binary.ver: bin/windows/contrib/3.5/mlm4omics_1.0.1.zip hasREADME: FALSE hasNEWS: TRUE hasINSTALL: FALSE hasLICENSE: FALSE Package: nudge Version: 1.48.0 Imports: stats License: GPL-2 Title: Normal Uniform Differential Gene Expression detection Description: Package for normalizing microarray data in single and multiple replicate experiments and fitting a normal-uniform mixture to detect differentially expressed genes in the cases where the two samples are being compared directly or indirectly (via a common reference sample) biocViews: Microarray, TwoChannel, DifferentialExpression Author: N. Dean and A. E. Raftery Maintainer: N. Dean PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/nudge git_branch: RELEASE_3_8 git_last_commit: 538a9ed git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: flowQ Version: 1.42.0 Depends: R (>= 2.10.0), methods, BiocGenerics, outliers, lattice, flowViz, mvoutlier, bioDist, parody, RColorBrewer, latticeExtra Imports: methods, BiocGenerics, geneplotter, flowCore, flowViz, IRanges Suggests: flowStats License: Artistic-2.0 Title: Quality control for flow cytometry Description: Provides quality control and quality assessment tools for flow cytometry data. biocViews: Infrastructure, FlowCytometry, CellBasedAssays Author: R. Gentleman, F. Hahne, J. Kettman, N. Le Meur, N. Gopalakrishnan Maintainer: Mike Jiang SystemRequirements: ImageMagick git_url: https://git.bioconductor.org/packages/flowQ git_branch: RELEASE_3_8 git_last_commit: 854ed71 git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: RamiGO Version: 1.30.0 Depends: gsubfn,methods Imports: igraph,RCurl,png,graph License: Artistic-2.0 Title: AmiGO visualize R interface Description: R interface sending requests to AmiGO visualize, retrieving DAG GO trees, parsing GraphViz DOT format files and exporting GML files for Cytoscape. Deprecated:Also uses RCytoscape to interactively display AmiGO trees in Cytoscape. biocViews: GO, Visualization, GraphAndNetwork, Classification, ThirdPartyClient Author: Markus Schroeder, Daniel Gusenleitner, John Quackenbush, Aedin Culhane, Benjamin Haibe-Kains Maintainer: Markus Schroeder PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/RamiGO git_branch: RELEASE_3_8 git_last_commit: 2f84aae git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: ProCoNA Version: 1.20.0 Depends: R (>= 2.10), methods, WGCNA, MSnbase, flashClust Imports: BiocGenerics, GOstats Suggests: RUnit License: GPL (>= 2) Title: Protein co-expression network analysis (ProCoNA). Description: Protein co-expression network construction using peptide level data, with statisical analysis. (Journal of Clinical Bioinformatics 2013, 3:11 doi:10.1186/2043-9113-3-11) biocViews: GraphAndNetwork, Software, Proteomics Author: David L Gibbs Maintainer: David L Gibbs git_url: https://git.bioconductor.org/packages/ProCoNA git_branch: RELEASE_3_8 git_last_commit: bd633f7 git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: gaucho Version: 1.18.0 Depends: R (>= 3.0.0), compiler, GA, graph, heatmap.plus, png, Rgraphviz Suggests: knitr License: GPL-3 Title: Genetic Algorithms for Understanding Clonal Heterogeneity and Ordering Description: Use genetic algorithms to determine the relationship between clones in heterogenous populations such as cancer sequencing samples biocViews: Software,Genetics,SNP,Sequencing,SomaticMutation Author: Alex Murison [aut, cre], Christopher Wardell [aut, cre] Maintainer: Alex Murison , Christopher Wardell VignetteBuilder: knitr PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/gaucho git_branch: RELEASE_3_8 git_last_commit: 8df20f1 git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: mQTL.NMR Version: 1.16.0 Depends: R (>= 2.15.0) Imports: qtl, GenABEL, MASS, outliers, graphics, stats, utils Suggests: BiocStyle License: Artistic-2.0 NeedsCompilation: yes Title: Metabolomic Quantitative Trait Locus Mapping for 1H NMR data Description: mQTL.NMR provides a complete mQTL analysis pipeline for 1H NMR data. Distinctive features include normalisation using most-used approaches, peak alignment using RSPA approach, dimensionality reduction using SRV and binning approaches, and mQTL analysis for animal and human cohorts. biocViews: Cheminformatics, Metabolomics, Genetics, SNP Author: Lyamine Hedjazi and Jean-Baptiste Cazier Maintainer: Lyamine Hedjazi URL: http://www.ican-institute.org/tools/ PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/mQTL.NMR git_branch: RELEASE_3_8 git_last_commit: 9d7b548 git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: facopy Version: 1.16.0 Depends: R (>= 3.0), methods, cgdsr (>= 1.1.30), coin (>= 1.0), ggplot2, gridExtra, facopy.annot, grid Imports: annotate, data.table, DOSE, FactoMineR, GO.db, GOstats, graphite, igraph, S4Vectors, IRanges, MASS, nnet, reshape2, Rgraphviz, scales License: CC BY-NC 4.0 Title: Feature-based association and gene-set enrichment for copy number alteration analysis in cancer Description: facopy is an R package for fine-tuned cancer CNA association modeling. Association is measured directly at the genomic features of interest and, in the case of genes, downstream gene-set enrichment analysis can be performed thanks to novel internal processing of the data. The software opens a way to systematically scrutinize the differences in CNA distribution across tumoral phenotypes, such as those that relate to tumor type, location and progression. Currently, the output format from 11 different methods that analyze data from whole-genome/exome sequencing and SNP microarrays, is supported. Multiple genomes, alteration types and variable types are also supported. biocViews: Software, CopyNumberVariation, GeneSetEnrichment, GenomicVariation, Genetics, Microarray, Sequencing, Visualization Author: David Mosen-Ansorena Maintainer: David Mosen-Ansorena PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/facopy git_branch: RELEASE_3_8 git_last_commit: 037d864 git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: cytofkit Version: 1.14.0 Depends: R (>= 3.4.0), ggplot2, plyr Imports: tcltk, grDevices, graphics, utils, stats, Rtsne, e1071, flowCore, gplots, colourpicker, VGAM, reshape2, ggrepel, shiny, shinyFiles, vegan, Biobase, doParallel, parallel, pdist, methods, destiny, FlowSOM(>= 1.4.0), igraph(>= 1.1.2), RANN(>= 2.5), Rcpp (>= 0.12.0) LinkingTo: Rcpp Suggests: knitr, RUnit, testthat, BiocGenerics License: Artistic-2.0 Title: cytofkit: an integrated mass cytometry data analysis pipeline Description: An integrated mass cytometry data analysis pipeline that enables simultaneous illustration of cellular diversity and progression. biocViews: FlowCytometry, GUI, CellBiology, Clustering, DimensionReduction, BiomedicalInformatics Author: Jinmiao Chen, Hao Chen, Matthew Myint Maintainer: Jinmiao Chen , Matthew Myint URL: https://github.com/JinmiaoChenLab/cytofkit VignetteBuilder: knitr BugReports: https://github.com/JinmiaoChenLab/cytofkit/issues PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/cytofkit git_branch: RELEASE_3_8 git_last_commit: 854ad07 git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15 Package: pbcmc Version: 1.10.1 Depends: R (>= 3.4), genefu Imports: Biobase, BiocGenerics, BiocParallel (>= 1.3.13), parallel, reshape2, grid, utils, cowplot, methods, limma, ggplot2, gridExtra, grDevices, stats Suggests: breastCancerUPP, breastCancerNKI, breastCancerVDX, breastCancerTRANSBIG, breastCancerMAINZ, breastCancerUNT License: GPL (>=2) NeedsCompilation: no Title: Permutation-Based Confidence for Molecular Classification Description: The pbcmc package characterizes uncertainty assessment on gene expression classifiers, a. k. a. molecular signatures, based on a permutation test. In order to achieve this goal, synthetic simulated subjects are obtained by permutations of gene labels. Then, each synthetic subject is tested against the corresponding subtype classifier to build the null distribution. Thus, classification confidence measurement can be provided for each subject, to assist physician therapy choice. At present, it is only available for PAM50 implementation in genefu package but it can easily be extend to other molecular signatures. biocViews: Classification, GeneExpression, Microarray, MultipleComparison, QualityControl, Normalization, Clustering, mRNAMicroarray, OneChannel, TwoChannel, RNASeq, KEGG, DifferentialExpression Author: Cristobal Fresno, German A. Gonzalez, Andrea S. Llera and Elmer A. Fernandez Maintainer: Cristobal Fresno URL: http://www.bdmg.com.ar/ PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/pbcmc git_branch: RELEASE_3_8 git_last_commit: bb53ec7 git_last_commit_date: 2018-11-30 Date/Publication: 2019-04-15 Package: IrisSpatialFeatures Version: 1.6.0 Depends: R (>= 3.4) Imports: Rcpp (>= 0.12.7), SpatialTools, gplots, spatstat, tiff, RColorBrewer, methods, grDevices, graphics, stats, utils, data.table, ggplot2, dplyr, magrittr, tibble LinkingTo: Rcpp Suggests: knitr, rmarkdown, testthat License: MIT + file LICENSE NeedsCompilation: yes Title: A package to extract spatial features based on multiplex IF images Description: IrisSpatialFeatures reads the output of the PerkinElmer inForm software and calculates a variety of spatial statistics. In addition to simple counts, it can derive average nearest neighbors for each cell-type and interaction summary profiles for each celltype. These statistics are derived across images, both overall and regions of interest as defined by user defined masks. biocViews: FeatureExtraction, SingleCell Author: Daniel Gusenleitner, Jason L. Weirather Maintainer: Daniel Gusenleitner VignetteBuilder: knitr PackageStatus: Deprecated git_url: https://git.bioconductor.org/packages/IrisSpatialFeatures git_branch: RELEASE_3_8 git_last_commit: 4b4e0bd git_last_commit_date: 2018-10-30 Date/Publication: 2019-04-15