Nothing
test_that("idwas TCGA CNV branch uses filtered 01A drug predictions", {
drug_prediction <- data.frame(
drugA=c(-10, 10, 0),
row.names=c(
"TCGA-AA-ZZZZ-11A",
"TCGA-AA-0002-01A",
"TCGA-AA-0001-01A"
)
)
cnv_data <- data.frame(
`TCGA-AA-0001-01A`=c(0, 0),
`TCGA-AA-0002-01A`=c(2, 0),
row.names=c("geneA", "geneB"),
check.names=FALSE
)
output <- idwas(drug_prediction, cnv_data, n=0, cnv=TRUE, folder=FALSE)
expect_gt(output$betas["geneA.drugA"], 0)
})
test_that("idwas TCGA mutation branch handles one commonly mutated gene", {
samples <- paste0("TCGA-AA-000", 1:4, "-01A")
drug_prediction <- data.frame(
drugA=c(0, 1, 10, 11),
row.names=samples
)
mutation_data <- data.frame(
Tumor_Sample_Barcode=c(samples, samples[3], samples[1:2]),
Variant_Classification=c(
"Silent",
"Silent",
"Missense_Mutation",
"Missense_Mutation",
"Missense_Mutation",
"Missense_Mutation",
"Missense_Mutation"
),
Hugo_Symbol=c("noise1", "noise2", "geneA", "geneA", "geneB",
"Unknown", "Unknown")
)
output <- idwas(drug_prediction, mutation_data, n=2, cnv=FALSE, folder=FALSE)
expect_true("drugA.geneA" %in% rownames(output))
expect_gt(output["drugA.geneA", "betaVal"], 0)
expect_false(any(grepl("Unknown", rownames(output), fixed=TRUE)))
})
test_that("idwas non-TCGA mutation branch removes Unknown rows by name", {
samples <- paste0("sample", seq_len(4))
drug_prediction <- data.frame(
drugA=c(0, 1, 10, 11),
row.names=samples
)
mutation_data <- data.frame(
Tumor_Sample_Barcode=c(samples[3:4], samples[1:2]),
Variant_Classification=rep("Missense_Mutation", 4),
Hugo_Symbol=c("geneA", "geneA", "Unknown", "Unknown")
)
output <- idwas(drug_prediction, mutation_data, n=2, cnv=FALSE, folder=FALSE)
expect_true("geneA:drugA" %in% rownames(output))
expect_false(any(grepl("Unknown", rownames(output), fixed=TRUE)))
})
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