has_RcppPlanc <- requireNamespace("RcppPlanc", quietly = TRUE) data("pbmc", package = "rliger") withNewH5Copy <- function(fun) { ctrlpath.orig <- system.file("extdata/ctrl.h5", package = "rliger") stimpath.orig <- system.file("extdata/stim.h5", package = "rliger") if (!file.exists(ctrlpath.orig)) stop("Cannot find original h5 file at: ", ctrlpath.orig) if (file.exists("ctrltest.h5")) file.remove("ctrltest.h5") if (file.exists("stimtest.h5")) file.remove("stimtest.h5") pwd <- getwd() # Temp setting for GitHub Actions fsep <- ifelse(Sys.info()["sysname"] == "Windows", "\\", "/") if (Sys.info()["sysname"] == "Windows") { pwd <- file.path("C:\\Users", Sys.info()["user"], "Documents", fsep = fsep) } ctrlpath <- file.path(pwd, "ctrltest.h5", fsep = fsep) stimpath <- file.path(pwd, "stimtest.h5", fsep = fsep) cat("Working ctrl H5 file path: ", ctrlpath, "\n") cat("Working stim H5 file path: ", stimpath, "\n") file.copy(ctrlpath.orig, ctrlpath, copy.mode = TRUE) file.copy(stimpath.orig, stimpath, copy.mode = TRUE) if (!file.exists(ctrlpath)) stop("Cannot find copied h5 file at: ", ctrlpath) fun(list(ctrl = ctrlpath, stim = stimpath)) if (file.exists(ctrlpath)) unlink(ctrlpath) if (file.exists(stimpath)) unlink(stimpath) } closeH5Liger <- function(object) { for (d in names(object)) { if (isH5Liger(object, d)) { h5file <- getH5File(object, d) h5file$close() } } } process <- function(object, f = TRUE, q = TRUE) { object <- normalize(object) object <- selectGenes(object) object <- scaleNotCenter(object) if (f) object <- runOnlineINMF(object, k = 20, minibatchSize = 100) if (q) object <- quantileNorm(object) return(object) } is_online <- function() { tryCatch({ readLines("https://cran.r-project.org/", n = 1) TRUE }, warning = function(w) invokeRestart("muffleWarning"), error = function(e) FALSE) } #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% # Clustering #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% context("Clustering") test_that("clustering", { skip_if_not(has_RcppPlanc) pbmc <- process(pbmc, f = FALSE, q = FALSE) expect_error(runCluster(pbmc), "No cell factor loading available") pbmc <- runOnlineINMF(pbmc, k = 20, minibatchSize = 100) expect_message(runCluster(pbmc, nRandomStarts = 1), "leiden clustering on unnormalized") expect_message(runCluster(pbmc, nRandomStarts = 1, method = "louvain"), "louvain clustering on unnormalized") pbmc <- quantileNorm(pbmc) expect_message(runCluster(pbmc, nRandomStarts = 1), "leiden clustering on quantile normalized") expect_message(runCluster(pbmc, nRandomStarts = 1, method = "louvain"), "louvain clustering on quantile normalized") # Tests for singleton grouping. Need to find the case where there are singletons # expect_message(runCluster(pbmc, nRandomStarts = 1, # partitionType = "CPMVertexPartition"), # "63 singletons identified. 112 final clusters") # pbmc <- runCluster(pbmc, nRandomStarts = 1, # partitionType = "CPMVertexPartition", # groupSingletons = FALSE) # expect_equal(nlevels(pbmc$leiden_cluster), 113) # expect_true("singleton" %in% pbmc$leiden_cluster) # Test downsampling with the info already here pbmc.small1 <- downsample(pbmc, maxCells = 100) expect_true(all.equal(sapply(pbmc.small1@datasets, ncol), c(ctrl = 44, stim = 56))) idx <- downsample(pbmc, balance = c("dataset"), maxCells = 100, returnIndex = TRUE) expect_is(idx, "integer") expect_equal(length(idx), 200) pbmc <- mapCellMeta(pbmc, from = "dataset", newTo = "pseudo", `ctrl` = "CTRL") expect_identical(pbmc$pseudo, setNames(factor(c(rep("CTRL", 300), rep("stim", 300))), colnames(pbmc))) }) #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% # Dimensionality reduction #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% context("dimensionality reduction") test_that("dimensionality reduction", { skip_if_not(has_RcppPlanc) pbmc <- process(pbmc) expect_message(runUMAP(pbmc, useRaw = TRUE), "Generating UMAP on unnormalized") expect_message(pbmc <- runUMAP(pbmc, useRaw = FALSE), "Generating UMAP on quantile normalized") expect_equal(dim(dimRed(pbmc, "UMAP")), c(ncol(pbmc), 2)) expect_message(runTSNE(pbmc, useRaw = TRUE), "Generating TSNE \\(Rtsne\\) on unnormalized") expect_message(pbmc <- runTSNE(pbmc, useRaw = FALSE), "Generating TSNE \\(Rtsne\\) on quantile normalized") expect_equal(dim(dimRed(pbmc, "TSNE")), c(ncol(pbmc), 2)) expect_error(runTSNE(pbmc, method = "fft"), "Please pass in path to FIt-SNE directory as fitsne.path.") }) #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% # Differential Expression #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% context("Differential Expression") test_that("wilcoxon", { skip_if_not(has_RcppPlanc) expect_error(runMarkerDEG(pbmc), "No `conditionBy` given or default cluster not set") pbmc <- process(pbmc) pbmc <- runCluster(pbmc, nRandomStarts = 1) res0 <- runMarkerDEG(pbmc, conditionBy = "dataset", useDatasets = 1) expect_true(all(is.nan(res0$pval))) res1 <- runMarkerDEG(pbmc) expect_equal(dim(res1), c(249 * nlevels(pbmc$leiden_cluster), 10)) res2 <- runMarkerDEG(pbmc, conditionBy = "dataset", splitBy = "leiden_cluster") expect_is(res2, "list") hm1 <- plotMarkerHeatmap(pbmc, res1, dedupBy = "l") hm2 <- plotMarkerHeatmap(pbmc, res1, dedupBy = "p") expect_is(hm1, "HeatmapList") expect_is(hm2, "HeatmapList") expect_is(plotVolcano(res1, 0), "ggplot") expect_is(plotEnhancedVolcano(res1, 0), "ggplot") expect_error(getFactorMarkers(pbmc, "ctrl", "stim", factorShareThresh = 0), "No factor passed the dataset specificity threshold") expect_message( res3 <- getFactorMarkers(pbmc, "ctrl", "stim", printGenes = TRUE) ) expect_is(res3, "list") expect_identical(names(res3), c("ctrl", "shared", "stim", "num_factors_V1", "num_factors_V2")) expect_error(runGOEnrich(res1, group = "a"), "Selected groups not available") expect_error(runGOEnrich(res1, group = 0, orderBy = c("logFC", "pval")), "Only one `orderBy`") expect_error(runGOEnrich(res1, orderBy = "score"), "`orderBy` should be one of") if (is_online()) { go1 <- runGOEnrich(res1, group = 0, orderBy = "logFC", significant = FALSE) expect_is(go1, "list") expect_is(go1$`0`$result, "data.frame") go2 <- runGOEnrich(res1, group = 0, orderBy = "pval", significant = FALSE) expect_is(go2, "list") expect_is(go2$`0`$result, "data.frame") } }) test_that("pseudo bulk", { skip_if_not(has_RcppPlanc) pbmc <- process(pbmc) pbmc <- runCluster(pbmc, nRandomStarts = 1) res1 <- runPairwiseDEG(pbmc, groupTest = pbmc$leiden_cluster == 1, groupCtrl = pbmc$leiden_cluster == 2, method = "pseudo") expect_is(res1, "data.frame") expect_true(all.equal(dim(res1), c(238, 5))) res2 <- runPairwiseDEG(pbmc, groupTest = 1, groupCtrl = 2, variable1 = "leiden_cluster", method = "pseudo", useReplicate = "dataset") expect_is(res2, "data.frame") expect_true(all.equal(dim(res2), c(238, 5))) res3 <- runPairwiseDEG(pbmc, groupTest = 1, groupCtrl = 2, variable1 = "leiden_cluster", method = "pseudo") expect_true(identical(res1[,-2], res3[,-2])) # Different in "group" column pbmc$leiden2 <- pbmc$leiden_cluster res4 <- runPairwiseDEG(pbmc, groupTest = 1, groupCtrl = 2, variable1 = "leiden_cluster", variable2 = "leiden2", method = "pseudo", useReplicate = "dataset") expect_true(all.equal(res2[,-2], res4[,-2])) # Different in "group" column expect_error(runPairwiseDEG(pbmc, variable2 = "yo"), "Please see") expect_error( runPairwiseDEG( pbmc, groupTest = pbmc$dataset == "ctrl" & pbmc$leiden_cluster == 0, groupCtrl = pbmc$dataset == "stim" & pbmc$leiden_cluster == 0, method = "pseudo", useReplicate = "dataset" ), "Too few replicates for condition" ) pbmc@datasets$ctrl@rawData <- NULL expect_error( runPairwiseDEG( pbmc, groupTest = 1, groupCtrl = 2, variable1 = "leiden_cluster",　method = "pseudo", useReplicate = "dataset" ), "not all available for involved datasets" ) }) #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% # GSEA #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% context("GSEA") custom <- list( `Immune System` = c("9636", "2633", "6282", "6280", "6279", "2207", "2214", "6402", "91543", "6233", "10578", "3553", "5473", "3627", "51316", "929", "972") ) if (is_online()) { test_that("gsea", { expect_warning({ expect_is(runGSEA(pbmcPlot, genesets = "Immune System"), "list") expect_is(runGSEA(pbmcPlot, customGenesets = custom), "list") }) }) } #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% # ATAC #%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% context("ATAC") data("bmmc") test_that("ATAC", { skip_if_not(has_RcppPlanc) bmmc <- normalize(bmmc) bmmc <- selectGenes(bmmc) bmmc <- scaleNotCenter(bmmc) bmmc <- runOnlineINMF(bmmc, minibatchSize = 80) bmmc <- quantileNorm(bmmc) bmmc <- normalizePeak(bmmc) bmmc <- imputeKNN(bmmc, reference = "atac", queries = "rna") expect_is(dataset(bmmc, "rna"), "ligerATACDataset") corr <- linkGenesAndPeaks( bmmc, useDataset = "rna", pathToCoords = system.file("extdata/hg19_genes.bed", package = "rliger") ) expect_is(corr, "dgCMatrix") })