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CHECK report for SeqVarTools on tokay2

This page was generated on 2019-10-16 12:28:21 -0400 (Wed, 16 Oct 2019).

Package 1502/1741HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
SeqVarTools 1.22.0
Stephanie M. Gogarten
Snapshot Date: 2019-10-15 17:01:26 -0400 (Tue, 15 Oct 2019)
URL: https://git.bioconductor.org/packages/SeqVarTools
Branch: RELEASE_3_9
Last Commit: e2e9bcd
Last Changed Date: 2019-05-09 18:37:15 -0400 (Thu, 09 May 2019)
malbec2 Linux (Ubuntu 18.04.2 LTS) / x86_64  OK  OK  OK UNNEEDED, same version exists in internal repository
tokay2 Windows Server 2012 R2 Standard / x64  OK  OK [ OK ] OK UNNEEDED, same version exists in internal repository
celaya2 OS X 10.11.6 El Capitan / x86_64  OK  OK  OK  OK UNNEEDED, same version exists in internal repository

Summary

Package: SeqVarTools
Version: 1.22.0
Command: C:\Users\biocbuild\bbs-3.9-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:SeqVarTools.install-out.txt --library=C:\Users\biocbuild\bbs-3.9-bioc\R\library --no-vignettes --timings SeqVarTools_1.22.0.tar.gz
StartedAt: 2019-10-16 07:03:32 -0400 (Wed, 16 Oct 2019)
EndedAt: 2019-10-16 07:08:02 -0400 (Wed, 16 Oct 2019)
EllapsedTime: 269.9 seconds
RetCode: 0
Status:  OK  
CheckDir: SeqVarTools.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   C:\Users\biocbuild\bbs-3.9-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:SeqVarTools.install-out.txt --library=C:\Users\biocbuild\bbs-3.9-bioc\R\library --no-vignettes --timings SeqVarTools_1.22.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory 'C:/Users/biocbuild/bbs-3.9-bioc/meat/SeqVarTools.Rcheck'
* using R version 3.6.1 (2019-07-05)
* using platform: x86_64-w64-mingw32 (64-bit)
* using session charset: ISO8859-1
* using option '--no-vignettes'
* checking for file 'SeqVarTools/DESCRIPTION' ... OK
* checking extension type ... Package
* this is package 'SeqVarTools' version '1.22.0'
* checking package namespace information ... OK
* checking package dependencies ... OK
* checking if this is a source package ... OK
* checking if there is a namespace ... OK
* checking for hidden files and directories ... OK
* checking for portable file names ... OK
* checking whether package 'SeqVarTools' can be installed ... OK
* checking installed package size ... OK
* checking package directory ... OK
* checking 'build' directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... OK
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ... OK
* checking R files for non-ASCII characters ... OK
* checking R files for syntax errors ... OK
* loading checks for arch 'i386'
** checking whether the package can be loaded ... OK
** checking whether the package can be loaded with stated dependencies ... OK
** checking whether the package can be unloaded cleanly ... OK
** checking whether the namespace can be loaded with stated dependencies ... OK
** checking whether the namespace can be unloaded cleanly ... OK
* loading checks for arch 'x64'
** checking whether the package can be loaded ... OK
** checking whether the package can be loaded with stated dependencies ... OK
** checking whether the package can be unloaded cleanly ... OK
** checking whether the namespace can be loaded with stated dependencies ... OK
** checking whether the namespace can be unloaded cleanly ... OK
* checking dependencies in R code ... OK
* checking S3 generic/method consistency ... OK
* checking replacement functions ... OK
* checking foreign function calls ... OK
* checking R code for possible problems ... OK
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of 'data' directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking files in 'vignettes' ... OK
* checking examples ...
** running examples for arch 'i386' ... OK
** running examples for arch 'x64' ... OK
* checking for unstated dependencies in 'tests' ... OK
* checking tests ...
** running tests for arch 'i386' ...
  Running 'test.R'
 OK
** running tests for arch 'x64' ...
  Running 'test.R'
 OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes in 'inst/doc' ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE

Status: OK

Installation output

SeqVarTools.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   C:\cygwin\bin\curl.exe -O https://malbec2.bioconductor.org/BBS/3.9/bioc/src/contrib/SeqVarTools_1.22.0.tar.gz && rm -rf SeqVarTools.buildbin-libdir && mkdir SeqVarTools.buildbin-libdir && C:\Users\biocbuild\bbs-3.9-bioc\R\bin\R.exe CMD INSTALL --merge-multiarch --build --library=SeqVarTools.buildbin-libdir SeqVarTools_1.22.0.tar.gz && C:\Users\biocbuild\bbs-3.9-bioc\R\bin\R.exe CMD INSTALL SeqVarTools_1.22.0.zip && rm SeqVarTools_1.22.0.tar.gz SeqVarTools_1.22.0.zip
###
##############################################################################
##############################################################################


  % Total    % Received % Xferd  Average Speed   Time    Time     Time  Current
                                 Dload  Upload   Total   Spent    Left  Speed

  0     0    0     0    0     0      0      0 --:--:-- --:--:-- --:--:--     0
 69  527k   69  368k    0     0   725k      0 --:--:-- --:--:-- --:--:--  734k
100  527k  100  527k    0     0   791k      0 --:--:-- --:--:-- --:--:--  798k

install for i386

* installing *source* package 'SeqVarTools' ...
** using staged installation
** R
** data
*** moving datasets to lazyload DB
** inst
** byte-compile and prepare package for lazy loading
** help
*** installing help indices
  converting help for package 'SeqVarTools'
    finding HTML links ... done
    Iterator-class                          html  
    finding level-2 HTML links ... done

    SeqVarData-class                        html  
    SeqVarTools-package                     html  
    allele-methods                          html  
    alleleFrequency                         html  
    alternateAlleleDetection                html  
    applyMethod                             html  
    chromWithPAR                            html  
    countSingletons                         html  
    duplicateDiscordance                    html  
    getGenotype                             html  
    getVariableLengthData                   html  
    heterozygosity                          html  
    hwe                                     html  
    imputedDosage                           html  
    inbreedCoeff                            html  
    isSNV                                   html  
    isVariant                               html  
    meanBySample                            html  
    mendelErr                               html  
    missingGenotypeRate                     html  
    pca                                     html  
    pedigree                                html  
    refFrac                                 html  
    regression                              html  
    setVariantID                            html  
    titv                                    html  
    variantInfo                             html  
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path

install for x64

* installing *source* package 'SeqVarTools' ...
** testing if installed package can be loaded
* MD5 sums
packaged installation of 'SeqVarTools' as SeqVarTools_1.22.0.zip
* DONE (SeqVarTools)
* installing to library 'C:/Users/biocbuild/bbs-3.9-bioc/R/library'
package 'SeqVarTools' successfully unpacked and MD5 sums checked

Tests output

SeqVarTools.Rcheck/tests_i386/test.Rout


R version 3.6.1 (2019-07-05) -- "Action of the Toes"
Copyright (C) 2019 The R Foundation for Statistical Computing
Platform: i386-w64-mingw32/i386 (32-bit)

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> library(GenomicRanges)
Loading required package: stats4
Loading required package: BiocGenerics
Loading required package: parallel

Attaching package: 'BiocGenerics'

The following objects are masked from 'package:parallel':

    clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
    clusterExport, clusterMap, parApply, parCapply, parLapply,
    parLapplyLB, parRapply, parSapply, parSapplyLB

The following objects are masked from 'package:stats':

    IQR, mad, sd, var, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, append,
    as.data.frame, basename, cbind, colnames, dirname, do.call,
    duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
    lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
    pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table,
    tapply, union, unique, unsplit, which, which.max, which.min

Loading required package: S4Vectors

Attaching package: 'S4Vectors'

The following object is masked from 'package:base':

    expand.grid

Loading required package: IRanges

Attaching package: 'IRanges'

The following object is masked from 'package:grDevices':

    windows

Loading required package: GenomeInfoDb
> BiocGenerics:::testPackage("SeqVarTools")
Loading required package: Biobase
Welcome to Bioconductor

    Vignettes contain introductory material; view with
    'browseVignettes()'. To cite Bioconductor, see
    'citation("Biobase")', and for packages 'citation("pkgname")'.

# of selected samples: 5
# of selected variants: 5
# of selected samples: 85
# of selected variants: 9
# of selected samples: 5
# of selected variants: 5
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 3
# of selected samples: 3
matching samples... 2 pairs identified!
matching variants... 1346 non-overlapping variant matches identified!
# of selected samples: 2
# of selected variants: 1,346
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 2
# of selected variants: 50
# of selected samples: 2
# of selected variants: 51
matching samples... 2 pairs identified!
matching variants... 26 non-overlapping variant matches identified!
# of selected variants: 26
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
File: C:\Users\biocbuild\bbs-3.9-bioc\R\library\SeqArray\extdata\CEU_Exon.gds (299.1K)
+    [  ] *
|--+ description   [  ] *
|--+ sample.id   { Str8 90 LZMA_ra(35.8%), 258B } *
|--+ variant.id   { Int32 1348 LZMA_ra(16.8%), 906B } *
|--+ position   { Int32 1348 LZMA_ra(64.6%), 3.4K } *
|--+ chromosome   { Str8 1348 LZMA_ra(4.63%), 158B } *
|--+ allele   { Str8 1348 LZMA_ra(16.7%), 902B } *
|--+ genotype   [  ] *
|  |--+ data   { Bit2 2x90x1348 LZMA_ra(26.3%), 15.6K } *
|  |--+ ~data   { Bit2 2x1348x90 LZMA_ra(29.3%), 17.3K }
|  |--+ extra.index   { Int32 3x0 LZMA_ra, 19B } *
|  \--+ extra   { Int16 0 LZMA_ra, 19B }
|--+ phase   [  ]
|  |--+ data   { Bit1 90x1348 LZMA_ra(0.91%), 138B } *
|  |--+ ~data   { Bit1 1348x90 LZMA_ra(0.91%), 138B }
|  |--+ extra.index   { Int32 3x0 LZMA_ra, 19B } *
|  \--+ extra   { Bit1 0 LZMA_ra, 19B }
|--+ annotation   [  ]
|  |--+ id   { Str8 1348 LZMA_ra(38.4%), 5.5K } *
|  |--+ qual   { Float32 1348 LZMA_ra(2.26%), 122B } *
|  |--+ filter   { Int32,factor 1348 LZMA_ra(2.26%), 122B } *
|  |--+ info   [  ]
|  |  |--+ AA   { Str8 1348 LZMA_ra(25.6%), 690B } *
|  |  |--+ AC   { Int32 1348 LZMA_ra(24.2%), 1.3K } *
|  |  |--+ AN   { Int32 1348 LZMA_ra(19.8%), 1.0K } *
|  |  |--+ DP   { Int32 1348 LZMA_ra(47.9%), 2.5K } *
|  |  |--+ HM2   { Bit1 1348 LZMA_ra(150.3%), 254B } *
|  |  |--+ HM3   { Bit1 1348 LZMA_ra(150.3%), 254B } *
|  |  |--+ OR   { Str8 1348 LZMA_ra(20.1%), 342B } *
|  |  |--+ GP   { Str8 1348 LZMA_ra(24.4%), 3.8K } *
|  |  \--+ BN   { Int32 1348 LZMA_ra(20.9%), 1.1K } *
|  \--+ format   [  ]
|     \--+ DP   [  ] *
|        |--+ data   { Int32 90x1348 LZMA_ra(25.1%), 118.8K } *
|        \--+ ~data   { Int32 1348x90 LZMA_ra(24.1%), 114.2K }
\--+ sample.annotation   [  ]
   \--+ family   { Str8 90 LZMA_ra(57.1%), 222B }
# of selected variants: 142
# of selected samples: 90
# of selected variants: 1,348
# of selected variants: 5
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 5
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 3
# of selected samples: 3
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 2
# of selected variants: 50
# of selected samples: 2
# of selected variants: 51
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
# of selected variants: 26
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 3
# of selected samples: 3
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 2
# of selected variants: 50
# of selected samples: 2
# of selected variants: 51
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
# of selected variants: 26
Warning in SeqVarTools:::.samplePairs1(samples) :
  More than two samples for subject 4
Selecting first two samples: samp7, samp8
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected variants: 1,346
# of selected variants: 1,330
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 3
# of selected variants: 10
# of selected samples: 3
# of selected samples: 90
# of selected variants: 1,348
# of selected variants: 10
# of selected samples: 3
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected variants: 903
# of selected samples: 59
# of selected samples: 58
# of selected samples: 32
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 10
# of selected samples: 10
# of selected variants: 10
# of selected samples: 10


RUNIT TEST PROTOCOL -- Wed Oct 16 07:07:22 2019 
*********************************************** 
Number of test functions: 149 
Number of errors: 0 
Number of failures: 0 

 
1 Test Suite : 
SeqVarTools RUnit Tests - 149 test functions, 0 errors, 0 failures
Number of test functions: 149 
Number of errors: 0 
Number of failures: 0 
> 
> proc.time()
   user  system elapsed 
  24.60    1.43   26.48

SeqVarTools.Rcheck/tests_x64/test.Rout


R version 3.6.1 (2019-07-05) -- "Action of the Toes"
Copyright (C) 2019 The R Foundation for Statistical Computing
Platform: x86_64-w64-mingw32/x64 (64-bit)

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> library(GenomicRanges)
Loading required package: stats4
Loading required package: BiocGenerics
Loading required package: parallel

Attaching package: 'BiocGenerics'

The following objects are masked from 'package:parallel':

    clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
    clusterExport, clusterMap, parApply, parCapply, parLapply,
    parLapplyLB, parRapply, parSapply, parSapplyLB

The following objects are masked from 'package:stats':

    IQR, mad, sd, var, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, append,
    as.data.frame, basename, cbind, colnames, dirname, do.call,
    duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
    lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
    pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table,
    tapply, union, unique, unsplit, which, which.max, which.min

Loading required package: S4Vectors

Attaching package: 'S4Vectors'

The following object is masked from 'package:base':

    expand.grid

Loading required package: IRanges

Attaching package: 'IRanges'

The following object is masked from 'package:grDevices':

    windows

Loading required package: GenomeInfoDb
> BiocGenerics:::testPackage("SeqVarTools")
Loading required package: Biobase
Welcome to Bioconductor

    Vignettes contain introductory material; view with
    'browseVignettes()'. To cite Bioconductor, see
    'citation("Biobase")', and for packages 'citation("pkgname")'.

# of selected samples: 5
# of selected variants: 5
# of selected samples: 85
# of selected variants: 9
# of selected samples: 5
# of selected variants: 5
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 3
# of selected samples: 3
matching samples... 2 pairs identified!
matching variants... 1346 non-overlapping variant matches identified!
# of selected samples: 2
# of selected variants: 1,346
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 2
# of selected variants: 50
# of selected samples: 2
# of selected variants: 51
matching samples... 2 pairs identified!
matching variants... 26 non-overlapping variant matches identified!
# of selected variants: 26
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
File: C:\Users\biocbuild\bbs-3.9-bioc\R\library\SeqArray\extdata\CEU_Exon.gds (299.1K)
+    [  ] *
|--+ description   [  ] *
|--+ sample.id   { Str8 90 LZMA_ra(35.8%), 258B } *
|--+ variant.id   { Int32 1348 LZMA_ra(16.8%), 906B } *
|--+ position   { Int32 1348 LZMA_ra(64.6%), 3.4K } *
|--+ chromosome   { Str8 1348 LZMA_ra(4.63%), 158B } *
|--+ allele   { Str8 1348 LZMA_ra(16.7%), 902B } *
|--+ genotype   [  ] *
|  |--+ data   { Bit2 2x90x1348 LZMA_ra(26.3%), 15.6K } *
|  |--+ ~data   { Bit2 2x1348x90 LZMA_ra(29.3%), 17.3K }
|  |--+ extra.index   { Int32 3x0 LZMA_ra, 19B } *
|  \--+ extra   { Int16 0 LZMA_ra, 19B }
|--+ phase   [  ]
|  |--+ data   { Bit1 90x1348 LZMA_ra(0.91%), 138B } *
|  |--+ ~data   { Bit1 1348x90 LZMA_ra(0.91%), 138B }
|  |--+ extra.index   { Int32 3x0 LZMA_ra, 19B } *
|  \--+ extra   { Bit1 0 LZMA_ra, 19B }
|--+ annotation   [  ]
|  |--+ id   { Str8 1348 LZMA_ra(38.4%), 5.5K } *
|  |--+ qual   { Float32 1348 LZMA_ra(2.26%), 122B } *
|  |--+ filter   { Int32,factor 1348 LZMA_ra(2.26%), 122B } *
|  |--+ info   [  ]
|  |  |--+ AA   { Str8 1348 LZMA_ra(25.6%), 690B } *
|  |  |--+ AC   { Int32 1348 LZMA_ra(24.2%), 1.3K } *
|  |  |--+ AN   { Int32 1348 LZMA_ra(19.8%), 1.0K } *
|  |  |--+ DP   { Int32 1348 LZMA_ra(47.9%), 2.5K } *
|  |  |--+ HM2   { Bit1 1348 LZMA_ra(150.3%), 254B } *
|  |  |--+ HM3   { Bit1 1348 LZMA_ra(150.3%), 254B } *
|  |  |--+ OR   { Str8 1348 LZMA_ra(20.1%), 342B } *
|  |  |--+ GP   { Str8 1348 LZMA_ra(24.4%), 3.8K } *
|  |  \--+ BN   { Int32 1348 LZMA_ra(20.9%), 1.1K } *
|  \--+ format   [  ]
|     \--+ DP   [  ] *
|        |--+ data   { Int32 90x1348 LZMA_ra(25.1%), 118.8K } *
|        \--+ ~data   { Int32 1348x90 LZMA_ra(24.1%), 114.2K }
\--+ sample.annotation   [  ]
   \--+ family   { Str8 90 LZMA_ra(57.1%), 222B }
# of selected variants: 142
# of selected samples: 90
# of selected variants: 1,348
# of selected variants: 5
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 5
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 3
# of selected samples: 3
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 2
# of selected variants: 50
# of selected samples: 2
# of selected variants: 51
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
# of selected variants: 26
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 3
# of selected samples: 3
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 1346 variant matches identified!
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 2
# of selected variants: 50
# of selected samples: 2
# of selected variants: 51
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
matching samples... 2 pairs identified!
matching variants... 26 variant matches identified!
# of selected variants: 26
Warning in SeqVarTools:::.samplePairs1(samples) :
  More than two samples for subject 4
Selecting first two samples: samp7, samp8
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected variants: 1,346
# of selected variants: 1,330
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 3
# of selected variants: 10
# of selected samples: 3
# of selected samples: 90
# of selected variants: 1,348
# of selected variants: 10
# of selected samples: 3
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected variants: 903
# of selected samples: 59
# of selected samples: 58
# of selected samples: 32
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 5
# of selected variants: 10
# of selected samples: 90
# of selected variants: 1,348
# of selected samples: 5
# of selected variants: 10
# of selected samples: 10
# of selected samples: 10
# of selected variants: 10
# of selected samples: 10


RUNIT TEST PROTOCOL -- Wed Oct 16 07:07:56 2019 
*********************************************** 
Number of test functions: 149 
Number of errors: 0 
Number of failures: 0 

 
1 Test Suite : 
SeqVarTools RUnit Tests - 149 test functions, 0 errors, 0 failures
Number of test functions: 149 
Number of errors: 0 
Number of failures: 0 
> 
> proc.time()
   user  system elapsed 
  32.59    0.96   33.54

Example timings

SeqVarTools.Rcheck/examples_i386/SeqVarTools-Ex.timings

nameusersystemelapsed
Iterator-class1.500.061.56
SeqVarData-class0.130.010.14
allele-methods0.030.000.03
alleleFrequency0.040.000.03
alternateAlleleDetection000
applyMethod0.260.030.30
countSingletons0.080.040.11
duplicateDiscordance0.190.120.31
getGenotype0.040.020.06
getVariableLengthData0.050.000.05
heterozygosity0.190.140.33
hwe0.060.000.06
imputedDosage0.120.030.17
inbreedCoeff0.240.000.23
isSNV000
isVariant0.010.000.02
meanBySample0.060.000.06
mendelErr0.020.010.03
missingGenotypeRate0.010.000.02
pca0.990.131.11
pedigree0.010.000.01
refFrac0.100.010.19
regression0.150.000.16
setVariantID0.020.000.01
titv0.340.020.36
variantInfo0.050.050.10

SeqVarTools.Rcheck/examples_x64/SeqVarTools-Ex.timings

nameusersystemelapsed
Iterator-class1.050.001.05
SeqVarData-class0.070.010.08
allele-methods0.000.020.01
alleleFrequency0.020.000.02
alternateAlleleDetection000
applyMethod0.110.060.17
countSingletons0.040.020.06
duplicateDiscordance0.130.030.16
getGenotype0.050.000.04
getVariableLengthData0.010.020.04
heterozygosity0.160.000.15
hwe0.060.000.06
imputedDosage0.090.000.09
inbreedCoeff0.130.000.13
isSNV000
isVariant000
meanBySample0.030.000.04
mendelErr0.020.000.01
missingGenotypeRate0.010.000.02
pca0.950.010.97
pedigree000
refFrac0.070.020.07
regression0.080.010.10
setVariantID0.010.000.01
titv0.280.020.30
variantInfo0.080.000.08