## ----setup, include=FALSE------------------------------------------------ knitr::opts_chunk$set(echo = TRUE) knitr::opts_knit$set(progress = FALSE) ## ----message=FALSE, warning=FALSE, include=FALSE------------------------- library(TCGAbiolinks) library(SummarizedExperiment) library(dplyr) library(DT) ## ----results = 'hide', echo=TRUE, message=FALSE, warning=FALSE----------- acc.maf <- GDCquery_Maf("ACC", pipelines = "muse") ## ----echo = TRUE, message = FALSE, warning = FALSE----------------------- # Only first 50 to make render faster datatable(acc.maf[1:50,], filter = 'top', options = list(scrollX = TRUE, keys = TRUE, pageLength = 5), rownames = FALSE) ## ----results = 'hide', echo=TRUE, message=FALSE, warning=FALSE----------- query.maf.hg19 <- GDCquery(project = "TCGA-CHOL", data.category = "Simple nucleotide variation", data.type = "Simple somatic mutation", access = "open", legacy = TRUE) ## ----echo = TRUE, message = FALSE, warning = FALSE----------------------- # Check maf availables datatable(select(getResults(query.maf.hg19),-contains("cases")), filter = 'top', options = list(scrollX = TRUE, keys = TRUE, pageLength = 10), rownames = FALSE) ## ----results = 'hide', echo=TRUE, message=FALSE, warning=FALSE----------- query.maf.hg19 <- GDCquery(project = "TCGA-CHOL", data.category = "Simple nucleotide variation", data.type = "Simple somatic mutation", access = "open", file.type = "bcgsc.ca_CHOL.IlluminaHiSeq_DNASeq.1.somatic.maf", legacy = TRUE) GDCdownload(query.maf.hg19) maf <- GDCprepare(query.maf.hg19) ## ----echo = TRUE, message = FALSE, warning = FALSE----------------------- # Only first 50 to make render faster datatable(maf[1:50,], filter = 'top', options = list(scrollX = TRUE, keys = TRUE, pageLength = 5), rownames = FALSE)