# Skip these tests on CRAN skip_on_cran() context("test-basic-workflow") data("XenaData", package = "UCSCXenaTools") head(XenaData) test_that("Load XenaData works", { expect_is(XenaData, "data.frame") }) xe <- XenaGenerate(subset = XenaHostNames == "tcgaHub") test_that("XenaGenerate works", { expect_is(xe, "XenaHub") }) test_that("Xena Scan works", { XenaScan() XenaScan(pattern = "zzzzzzzzzzz") x1 <- XenaScan(pattern = "Blood") x2 <- XenaScan(pattern = "LUNG", ignore.case = FALSE) x1 %>% XenaGenerate() x2 %>% XenaGenerate() }) xe2 <- XenaFilter(xe, filterDatasets = "clinical") xe2 <- XenaFilter(xe2, filterDatasets = "LUAD|LUSC") test_that("XenaFilter works", { expect_is(xe2, "XenaHub") }) xe2_query <- XenaQuery(xe2) test_that("XenaQuery works", { expect_is(xe2_query, "data.frame") }) xe2_download <- XenaDownload(xe2_query, trans_slash = FALSE, download_probeMap = TRUE) xe2_download <- XenaDownload(xe2_query, trans_slash = TRUE, destdir = file.path(tempdir(), "test_ucscxenatools") ) # 4 ways to prepare data dt1 <- XenaPrepare(file.path(tempdir(), "test_ucscxenatools")) dt1 <- XenaPrepare(file.path(tempdir(), "test_ucscxenatools"), use_chunk = TRUE) dt2 <- XenaPrepare(xe2_download$destfiles[1]) dt2 <- XenaPrepare(xe2_download$destfiles[1], use_chunk = TRUE) dt3 <- XenaPrepare(xe2_download$url[1]) dt3 <- XenaPrepare(xe2_download$url[1], use_chunk = TRUE) dt3 <- XenaPrepare(xe2_download$url, use_chunk = TRUE) dt4 <- XenaPrepare(xe2_download) dt4 <- XenaPrepare(xe2_download, use_chunk = TRUE) ### Simplified functions expect_error(getTCGAdata("xxx")) expect_error(getTCGAdata(c("UVM", "LUAD"), mRNASeq = TRUE, mRNASeqType = "xxx")) expect_error(getTCGAdata(c("UVM", "LUAD"), Methylation = TRUE, MethylationType = "xxx", RPPAArray = TRUE, ReplicateBaseNormalization = FALSE )) getTCGAdata(c("UVM", "LUAD"), GisticCopyNumber = TRUE, Gistic2Threshold = FALSE, CopyNumberSegment = TRUE, RemoveGermlineCNV = FALSE ) getTCGAdata("LUNG", download = TRUE) getTCGAdata("LUAD", clinical = FALSE, mRNASeq = TRUE, mRNAArray = TRUE, miRNASeq = TRUE, exonRNASeq = TRUE, RPPAArray = TRUE, ReplicateBaseNormalization = TRUE, Methylation = TRUE, GeneMutation = TRUE, SomaticMutation = TRUE, GisticCopyNumber = TRUE, Gistic2Threshold = TRUE, CopyNumberSegment = TRUE, RemoveGermlineCNV = TRUE ) downloadTCGA( project = "UVM", data_type = "Phenotype", file_type = "Clinical Information" ) downloadTCGA("xxx", data_type = "Phenotype", file_type = "Clinical Information" ) availTCGA() availTCGA(which = "ProjectID") availTCGA(which = "DataType") availTCGA(which = "FileType") showTCGA() showTCGA("LUAD") # clean all rm(list = ls())