context("deseq2 helpers")
source("helper.R")
test_that("we can extract different names from a deseq result", {
deseq.result <- readRDS(filesPath("test.deseq.result.RDS"))
expect_equal("log2 fold change (MAP): group group2 vs wt", getComparisonFoldChange(deseq.result))
expect_equal("group group2 vs wt", getComparisonTitle(deseq.result))
expect_equal("group2_vs_wt", getComparisonString(deseq.result))
expect_equal("group2 vs wt", getComparison(deseq.result))
})
test_that("we can the independent filtering threshold from the deseq.result", {
deseq.result <- readRDS(filesPath("test.deseq.result.RDS"))
expect_equivalent(0.0354, getFilterThreshold(deseq.result), tol = 1e-3 )
})
test_that("we get the normalised counts as a tibble", {
co <- getCounts(readRDS(filesPath("test.dds.r.RDS")))
expect_is(co, "tbl_df")
expect_equal(98, length(co$geneid))
expect_equal(16, ncol(co))
})
test_that("we get a deseq.result, but with the contrasts stored in metadata(comparison)", {
dds.r <- readRDS(filesPath("test.dds.r.RDS"))
dr <- deseqResult(dds.r, "group2", "group3")
expect_is(dr, 'DESeqResults')
expect_equal( c("group", "group2", "group3"), S4Vectors::metadata(dr)$comparison)
})
test_that("we get the normalised counts as a tibble but only from 2 groups", {
dds.r <- readRDS(filesPath("test.dds.r.RDS"))
grouping <- readGrouping(filesPath("test.grouping.tab"))
co <- getCounts(dds.r, groups=c("group1","group2"), grouping=grouping)
expect_is(co, "tbl_df")
expect_equal(98, length(co$geneid))
expect_equal(7, ncol(co))
expect_equal(colnames(co), c(as.character(83656:83661),"geneid"))
})
test_that("we get the normalised counts as a tibble for all groups", {
dds.r <- readRDS(filesPath("test.dds.r.RDS"))
co <- getCounts(dds.r)
expect_is(co, "tbl_df")
expect_equal(98, length(co$geneid))
expect_equal(16, ncol(co))
expect_equal(colnames(co)[ncol(co)], "geneid")
})
test_that("we create a sorted tibble for saving and for plotting of the data", {
ensembl <- readEnsembl(filesPath("test.ensembl.GRCh38.genes.tab"))
deseq.result <- readRDS(filesPath("test.deseq.result.RDS"))
comp <- toSortedTibble(deseq.result, ensembl, 0.01, ensembl_url)
expect_equal(nrow(comp), nrow(deseq.result) )
expect_equal(colnames(comp)[1],"geneid")
})
test_that("we create a sorted tibble for saving and for plotting of the data including normalised expression counts", {
ensembl <- readEnsembl(filesPath("test.ensembl.GRCh38.genes.tab"))
deseq.result <- readRDS(filesPath("test.deseq.m.result.RDS"))
grouping <- readGrouping(filesPath("test.grouping.tab"))
groups <- S4Vectors::metadata(deseq.result)$comparison[2:3]
countsdata <- getCounts(readRDS(filesPath("test.dds.r.RDS")),groups)
comp <- toSortedTibble(deseq.result, ensembl, 0.01, ensembl_url, countsdata)
expect_equal(nrow(comp), nrow(deseq.result))
#TODO: test width of comp
})
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