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Merge pull request #172 from biomage-ltd/test-prepare-experiment
Test prepare_experiment
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pipeline-runner/tests/testthat/_snaps/gem2s-6-prepare_experiment.md
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# prepare_experiment generates qc_config that matches snapshot | ||
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Code | ||
str(task_out$qc_config) | ||
Output | ||
List of 7 | ||
$ cellSizeDistribution:List of 4 | ||
..$ enabled : logi FALSE | ||
..$ auto : logi TRUE | ||
..$ filterSettings:List of 2 | ||
.. ..$ minCellSize: num 1080 | ||
.. ..$ binStep : num 200 | ||
..$ sample_a :List of 4 | ||
.. ..$ enabled : logi FALSE | ||
.. ..$ auto : logi TRUE | ||
.. ..$ filterSettings :List of 2 | ||
.. .. ..$ minCellSize: num 10 | ||
.. .. ..$ binStep : num 200 | ||
.. ..$ defaultFilterSettings:List of 2 | ||
.. .. ..$ minCellSize: num 10 | ||
.. .. ..$ binStep : num 200 | ||
$ mitochondrialContent:List of 4 | ||
..$ enabled : logi TRUE | ||
..$ auto : logi TRUE | ||
..$ filterSettings:List of 2 | ||
.. ..$ method : chr "absolute_threshold" | ||
.. ..$ methodSettings:List of 1 | ||
.. .. ..$ absolute_threshold:List of 2 | ||
.. .. .. ..$ maxFraction: num 0.1 | ||
.. .. .. ..$ binStep : num 0.05 | ||
..$ sample_a :List of 3 | ||
.. ..$ auto : logi TRUE | ||
.. ..$ filterSettings :List of 2 | ||
.. .. ..$ method : chr "absolute_threshold" | ||
.. .. ..$ methodSettings:List of 1 | ||
.. .. .. ..$ absolute_threshold:List of 2 | ||
.. .. .. .. ..$ maxFraction: num 0.1 | ||
.. .. .. .. ..$ binStep : num 0.05 | ||
.. ..$ defaultFilterSettings:List of 2 | ||
.. .. ..$ method : chr "absolute_threshold" | ||
.. .. ..$ methodSettings:List of 1 | ||
.. .. .. ..$ absolute_threshold:List of 2 | ||
.. .. .. .. ..$ maxFraction: num 0.1 | ||
.. .. .. .. ..$ binStep : num 0.05 | ||
$ classifier :List of 4 | ||
..$ enabled : logi TRUE | ||
..$ auto : logi TRUE | ||
..$ filterSettings:List of 1 | ||
.. ..$ FDR: num 0.01 | ||
..$ sample_a :List of 4 | ||
.. ..$ enabled : logi TRUE | ||
.. ..$ auto : logi TRUE | ||
.. ..$ filterSettings :List of 1 | ||
.. .. ..$ FDR: num 0.01 | ||
.. ..$ defaultFilterSettings:List of 1 | ||
.. .. ..$ FDR: num 0.01 | ||
$ numGenesVsNumUmis :List of 4 | ||
..$ enabled : logi TRUE | ||
..$ auto : logi TRUE | ||
..$ filterSettings:List of 2 | ||
.. ..$ regressionType : chr "gam" | ||
.. ..$ regressionTypeSettings:List of 1 | ||
.. .. ..$ gam:List of 1 | ||
.. .. .. ..$ p.level: num 0.001 | ||
..$ sample_a :List of 4 | ||
.. ..$ enabled : logi TRUE | ||
.. ..$ auto : logi TRUE | ||
.. ..$ filterSettings :List of 2 | ||
.. .. ..$ regressionType : chr "gam" | ||
.. .. ..$ regressionTypeSettings:List of 1 | ||
.. .. .. ..$ gam:List of 1 | ||
.. .. .. .. ..$ p.level: num 0.00013 | ||
.. ..$ defaultFilterSettings:List of 2 | ||
.. .. ..$ regressionType : chr "gam" | ||
.. .. ..$ regressionTypeSettings:List of 1 | ||
.. .. .. ..$ gam:List of 1 | ||
.. .. .. .. ..$ p.level: num 0.00013 | ||
$ doubletScores :List of 4 | ||
..$ enabled : logi TRUE | ||
..$ auto : logi TRUE | ||
..$ filterSettings:List of 2 | ||
.. ..$ probabilityThreshold: num 0.5 | ||
.. ..$ binStep : num 0.05 | ||
..$ sample_a :List of 4 | ||
.. ..$ enabled : logi TRUE | ||
.. ..$ auto : logi TRUE | ||
.. ..$ filterSettings :List of 2 | ||
.. .. ..$ probabilityThreshold: num 0.8 | ||
.. .. ..$ binStep : num 0.05 | ||
.. ..$ defaultFilterSettings:List of 2 | ||
.. .. ..$ probabilityThreshold: num 0.8 | ||
.. .. ..$ binStep : num 0.05 | ||
$ dataIntegration :List of 2 | ||
..$ dataIntegration :List of 2 | ||
.. ..$ method : chr "harmony" | ||
.. ..$ methodSettings:List of 4 | ||
.. .. ..$ seuratv4 :List of 2 | ||
.. .. .. ..$ numGenes : num 2000 | ||
.. .. .. ..$ normalisation: chr "logNormalize" | ||
.. .. ..$ unisample:List of 2 | ||
.. .. .. ..$ numGenes : num 2000 | ||
.. .. .. ..$ normalisation: chr "logNormalize" | ||
.. .. ..$ harmony :List of 2 | ||
.. .. .. ..$ numGenes : num 2000 | ||
.. .. .. ..$ normalisation: chr "logNormalize" | ||
.. .. ..$ fastmnn :List of 2 | ||
.. .. .. ..$ numGenes : num 2000 | ||
.. .. .. ..$ normalisation: chr "logNormalize" | ||
..$ dimensionalityReduction:List of 3 | ||
.. ..$ method : chr "rpca" | ||
.. ..$ numPCs : num 30 | ||
.. ..$ excludeGeneCategories: list() | ||
$ configureEmbedding :List of 2 | ||
..$ embeddingSettings :List of 2 | ||
.. ..$ method : chr "umap" | ||
.. ..$ methodSettings:List of 2 | ||
.. .. ..$ umap:List of 2 | ||
.. .. .. ..$ minimumDistance: num 0.3 | ||
.. .. .. ..$ distanceMetric : chr "cosine" | ||
.. .. ..$ tsne:List of 2 | ||
.. .. .. ..$ perplexity : num 30 | ||
.. .. .. ..$ learningRate: num 640 | ||
..$ clusteringSettings:List of 2 | ||
.. ..$ method : chr "louvain" | ||
.. ..$ methodSettings:List of 1 | ||
.. .. ..$ louvain:List of 1 | ||
.. .. .. ..$ resolution: num 0.8 | ||
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pipeline-runner/tests/testthat/test-gem2s-6-prepare_experiment.R
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mock_counts <- function() { | ||
read.table( | ||
file = system.file("extdata", "pbmc_raw.txt", package = "Seurat"), | ||
as.is = TRUE | ||
) | ||
} | ||
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mock_doublet_scores <- function(counts) { | ||
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doublet_scores <- runif(ncol(counts)) | ||
doublet_class <- ifelse(doublet_scores < 0.8, 'singlet', 'doublet') | ||
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data.frame( | ||
row.names = colnames(counts), | ||
barcodes = colnames(counts), | ||
doublet_class = doublet_class, | ||
doublet_scores = doublet_scores | ||
) | ||
} | ||
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mock_prev_out <- function(samples = 'sample_a', counts = NULL) { | ||
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if (is.null(counts)) { | ||
counts <- DropletUtils:::simCounts() | ||
colnames(counts) <- paste0('cell', seq_len(ncol(counts))) | ||
} | ||
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eout <- DropletUtils::emptyDrops(counts) | ||
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counts_list <- list() | ||
edrops <- list() | ||
doublet_scores <- list() | ||
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for (sample in samples) { | ||
counts_list[[sample]] <- counts | ||
edrops[[sample]] <- eout | ||
doublet_scores[[sample]] <- mock_doublet_scores(counts) | ||
} | ||
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# as passed to create_seurat | ||
prev_out <- list( | ||
counts_list = counts_list, | ||
edrops = edrops, | ||
doublet_scores = doublet_scores, | ||
annot = data.frame(name = row.names(counts), input = row.names(counts)), | ||
config = list(name = 'project name') | ||
) | ||
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# call create_seurat to get prev_out to pass to prepare_experiment | ||
create_seurat(NULL, NULL, prev_out)$output | ||
} | ||
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test_that("prepare_experiment merges multiple SeuratObjects", { | ||
prev_out <- mock_prev_out(samples = c('a', 'b', 'c')) | ||
scdata_list <- prev_out$scdata_list | ||
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task_out <- expect_warning(prepare_experiment(NULL, NULL, prev_out)$output) | ||
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scdata <- task_out$scdata | ||
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expect_equal(ncol(scdata), sum(sapply(scdata_list, ncol))) | ||
}) | ||
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test_that("prepare_experiment ensures gene_annotations are indexed the same as scdata", { | ||
prev_out <- mock_prev_out() | ||
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# shuffle gene order of annot | ||
annot <- prev_out$annot | ||
prev_out$annot <- annot[sample(nrow(annot)), ] | ||
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scdata <- prepare_experiment(NULL, NULL, prev_out)$output$scdata | ||
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expect_equal(row.names(scdata), scdata@misc$gene_annotations$input) | ||
}) | ||
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test_that("prepare_experiment adds 0 indexed cell_ids and other metadata to scdata", { | ||
prev_out <- mock_prev_out() | ||
input <- list(experimentId = '1234') | ||
scdata <- prepare_experiment(input, NULL, prev_out)$output$scdata | ||
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added_to_misc <- c('gene_annotations', 'color_pool', 'experimentId', 'ingestionDate') | ||
expect_true(all(added_to_misc %in% names(scdata@misc))) | ||
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added_ids <- unname(scdata$cells_id) | ||
expected_ids <- seq(0, ncol(scdata)-1) | ||
expect_equal(added_ids, expected_ids) | ||
}) | ||
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test_that("prepare_experiment generates qc_config that matches snapshot", { | ||
prev_out <- mock_prev_out() | ||
input <- list(experimentId = '1234') | ||
task_out <- prepare_experiment(input, NULL, prev_out)$output | ||
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expect_snapshot(str(task_out$qc_config)) | ||
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}) |