785 lines
30 KiB
R
785 lines
30 KiB
R
de_analysis_arg_parser <- function() {
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parser <- argparser::arg_parser("Run DESeq2 and DEXSeq on bambu output.")
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parser <- argparser::add_argument(parser, "--transcript_rds", help = "bambu transcript RDS.")
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parser <- argparser::add_argument(parser, "--gene_rds", help = "bambu gene RDS.")
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parser <- argparser::add_argument(parser, "--sample_sheet", help = "Sample sheet CSV.")
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parser <- argparser::add_argument(
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parser,
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"--condition_column",
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help = "Primary condition column.",
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default = "condition"
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)
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parser <- argparser::add_argument(parser, "--covariates", help = "Comma-separated nuisance covariates.")
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parser <- argparser::add_argument(parser, "--reference_level", help = "Reference level for the condition column.")
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argparser::add_argument(parser, "--out_dir", help = "Output directory.", default = "de_analysis")
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}
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de_parse_covariates <- function(value) {
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workflow_glue_r_parse_csv_list(value)
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}
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de_validate_inputs <- function(tx_se, gene_se, sample_df, argv) {
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workflow_glue_r_require_args(argv, c("transcript_rds", "gene_rds", "sample_sheet"))
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covariates <- de_parse_covariates(argv$covariates)
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workflow_glue_r_validate_r_formula_names(
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c(argv$condition_column, covariates),
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label = "Design column"
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)
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if (!"alias" %in% names(sample_df)) {
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stop("Sample sheet must contain an 'alias' column.", call. = FALSE)
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}
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duplicate_sample_aliases <- unique(sample_df$alias[duplicated(sample_df$alias)])
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if (length(duplicate_sample_aliases) > 0) {
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stop(
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sprintf(
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"Sample sheet aliases must be unique; duplicated aliases: %s",
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paste(duplicate_sample_aliases, collapse = ", ")
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),
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call. = FALSE
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)
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}
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if (!(argv$condition_column %in% names(sample_df))) {
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stop(
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sprintf("Sample sheet must contain the '%s' column.", argv$condition_column),
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call. = FALSE
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)
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}
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missing_covariates <- setdiff(covariates, names(sample_df))
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if (length(missing_covariates) > 0) {
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stop(
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sprintf(
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"Missing covariate columns: %s",
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paste(missing_covariates, collapse = ", ")
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),
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call. = FALSE
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)
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}
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if (any(duplicated(colnames(tx_se)))) {
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stop("Transcript RDS sample names must be unique.", call. = FALSE)
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}
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if (any(duplicated(colnames(gene_se)))) {
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stop("Gene RDS sample names must be unique.", call. = FALSE)
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}
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if (!setequal(colnames(tx_se), colnames(gene_se))) {
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stop("Transcript and gene RDS sample names must match.", call. = FALSE)
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}
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tx_counts <- SummarizedExperiment::assays(tx_se)$counts
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gene_counts <- SummarizedExperiment::assays(gene_se)$counts
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if (is.null(tx_counts)) {
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stop("Transcript RDS must contain a 'counts' assay.", call. = FALSE)
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}
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if (is.null(gene_counts)) {
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stop("Gene RDS must contain a 'counts' assay.", call. = FALSE)
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}
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if (!is.numeric(tx_counts) || !is.numeric(gene_counts)) {
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stop("Count matrices must be numeric.", call. = FALSE)
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}
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if (anyNA(tx_counts) || anyNA(gene_counts)) {
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stop("Count matrices must not contain NA values.", call. = FALSE)
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}
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zero_count_samples <- unique(c(
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colnames(tx_counts)[colSums(tx_counts) == 0],
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colnames(gene_counts)[colSums(gene_counts) == 0]
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))
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if (length(zero_count_samples) > 0) {
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stop(
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sprintf(
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"Count matrices contain samples with zero total counts: %s",
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paste(zero_count_samples, collapse = ", ")
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),
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call. = FALSE
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)
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}
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sample_df <- sample_df[match(colnames(tx_se), sample_df$alias), , drop = FALSE]
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if (any(is.na(sample_df$alias))) {
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stop("Sample sheet aliases do not match the bambu output sample names.", call. = FALSE)
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}
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condition_values <- unique(sample_df[[argv$condition_column]])
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if (length(condition_values) < 2) {
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stop("Differential analysis requires at least two condition levels.", call. = FALSE)
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}
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reference_level <- argv$reference_level
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if (workflow_glue_r_arg_missing(reference_level)) {
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if ("control" %in% condition_values) {
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reference_level <- "control"
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} else {
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stop(
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"Provide --reference_level when the condition column does not contain 'control'.",
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call. = FALSE
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)
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}
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}
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if (!(reference_level %in% condition_values)) {
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stop("The requested reference level is not present in the condition column.", call. = FALSE)
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}
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sample_df[[argv$condition_column]] <- factor(sample_df[[argv$condition_column]])
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for (covariate in covariates) {
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sample_df[[covariate]] <- factor(sample_df[[covariate]])
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}
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list(
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tx_se = tx_se,
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gene_se = gene_se,
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sample_df = sample_df,
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covariates = covariates,
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condition_values = condition_values,
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reference_level = reference_level
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)
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}
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de_build_contrast_name <- function(condition_column, target_level, reference_level) {
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sprintf("%s_%s_vs_%s", condition_column, target_level, reference_level)
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}
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de_set_dispersions <- function(object, value) {
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setter <- get("dispersions<-", envir = asNamespace("DESeq2"))
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setter(object, value = value)
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}
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de_run_deseq_with_fallback <- function(dds, contrast_name, out_dir) {
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tryCatch(
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DESeq2::DESeq(dds, quiet = TRUE),
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error = function(err) {
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if (!grepl(
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"all gene-wise dispersion estimates are within 2 orders of magnitude",
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conditionMessage(err),
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fixed = TRUE
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)) {
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stop(err)
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}
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warning(
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"STATISTICAL POWER REDUCED: DESeq2 dispersion estimation failed for ",
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contrast_name,
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".\n",
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"This usually indicates:\n",
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" 1. Too few replicates (recommend n>=3 per group)\n",
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" 2. High biological variability\n",
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" 3. Poor data quality\n",
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"Falling back to gene-wise dispersion (no information sharing).\n",
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"Results will have reduced power and wider confidence intervals."
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)
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dds <- DESeq2::estimateSizeFactors(dds)
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dds <- DESeq2::estimateDispersionsGeneEst(dds)
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dds <- de_set_dispersions(dds, S4Vectors::mcols(dds)$dispGeneEst)
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diag_content <- c(
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"DESeq2 Dispersion Estimation Fallback Applied",
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"==============================================",
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"",
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sprintf("Timestamp: %s", format(Sys.time(), "%Y-%m-%d %H:%M:%S")),
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sprintf("Contrast: %s", contrast_name),
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sprintf("Samples: %d", ncol(dds)),
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sprintf("Genes tested: %d", nrow(dds)),
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sprintf(
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"Dispersion range: %.3f to %.3f",
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min(DESeq2::dispersions(dds)),
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max(DESeq2::dispersions(dds))
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),
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"",
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"WHAT HAPPENED:",
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" Curve fitting failed. Using gene-wise dispersion estimates.",
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"",
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"IMPLICATIONS:",
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" - No information sharing across genes",
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" - Reduced statistical power",
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" - Wider confidence intervals",
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" - More conservative results (fewer discoveries)",
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"",
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"LIKELY CAUSES:",
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" 1. Too few replicates (recommend n>=3 per group)",
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" 2. High biological variability",
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" 3. Poor data quality or outlier samples",
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"",
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"RECOMMENDATIONS:",
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" - Add more biological replicates if possible",
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" - Check sample quality metrics",
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" - Consider filtering low-count genes more stringently"
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)
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diag_file <- file.path(
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out_dir,
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sprintf(
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"DESeq2_dispersion_fallback_%s.txt",
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gsub("[^A-Za-z0-9_-]", "_", contrast_name)
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)
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)
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writeLines(diag_content, diag_file)
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DESeq2::nbinomWaldTest(dds)
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}
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)
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}
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de_estimate_dispersions_with_fallback <- function(object, context_label, allow_gene_est = TRUE) {
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tryCatch(
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DESeq2::estimateDispersions(object),
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error = function(err) {
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if (!grepl(
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"all gene-wise dispersion estimates are within 2 orders of magnitude",
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conditionMessage(err),
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fixed = TRUE
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)) {
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stop(err)
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}
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message(context_label, " dispersion fitting failed; retrying with fitType='local'.")
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tryCatch(
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DESeq2::estimateDispersions(object, fitType = "local"),
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error = function(local_err) {
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if (!grepl(
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"all gene-wise dispersion estimates are within 2 orders of magnitude",
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conditionMessage(local_err),
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fixed = TRUE
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)) {
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stop(local_err)
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}
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message(context_label, " local-fit dispersion retry failed; retrying with fitType='mean'.")
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tryCatch(
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DESeq2::estimateDispersions(object, fitType = "mean"),
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error = function(mean_err) {
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if (!grepl(
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"all gene-wise dispersion estimates are within 2 orders of magnitude",
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conditionMessage(mean_err),
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fixed = TRUE
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)) {
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stop(mean_err)
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}
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if (!allow_gene_est) {
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stop(mean_err)
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}
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message(
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context_label,
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" mean-fit dispersion retry failed; falling back to gene-wise dispersion estimates."
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)
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object <- DESeq2::estimateDispersionsGeneEst(object)
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object <- de_set_dispersions(object, S4Vectors::mcols(object)$dispGeneEst)
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object
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}
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)
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}
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)
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}
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)
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}
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de_is_recoverable_dexseq_error <- function(message_text) {
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grepl(
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"all gene-wise dispersion estimates are within 2 orders of magnitude",
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message_text,
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fixed = TRUE
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) || grepl(
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"model matrix is not full rank",
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message_text,
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fixed = TRUE
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) || grepl(
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"replacement has 1 row, data has 0",
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message_text,
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fixed = TRUE
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)
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}
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de_write_placeholder_pdf <- function(path, label) {
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grDevices::pdf(path)
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graphics::plot.new()
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graphics::text(0.5, 0.5, label, cex = 0.9)
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grDevices::dev.off()
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}
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de_run_deseq2_result <- function(
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count_mat,
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coldata,
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target_level,
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reference_level,
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condition_column,
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covariates,
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out_dir,
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contrast_name
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) {
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design_terms <- c(covariates, condition_column)
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design_formula <- stats::as.formula(paste("~", paste(design_terms, collapse = " + ")))
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dds <- DESeq2::DESeqDataSetFromMatrix(
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countData = round(count_mat),
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colData = coldata,
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design = design_formula
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)
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dds <- de_run_deseq_with_fallback(dds, contrast_name, out_dir)
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result <- DESeq2::results(
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dds,
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contrast = c(condition_column, target_level, reference_level),
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independentFiltering = TRUE
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)
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list(dds = dds, result = result)
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}
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de_run_dexseq_result <- function(
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tx_counts,
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tx_meta,
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coldata,
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condition_column,
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covariates
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) {
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coldata$sample <- factor(coldata$alias)
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coldata[[condition_column]] <- factor(coldata[[condition_column]])
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for (covariate in covariates) {
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coldata[[covariate]] <- factor(coldata[[covariate]])
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}
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run_inner <- function(active_covariates) {
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covariate_exon_terms <- if (length(active_covariates) > 0) {
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paste0(active_covariates, ":exon")
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} else {
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character(0)
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}
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design_terms <- c("sample", "exon", covariate_exon_terms, paste0(condition_column, ":exon"))
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reduced_terms <- c("sample", "exon", covariate_exon_terms)
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full_formula <- stats::as.formula(paste("~", paste(design_terms, collapse = " + ")))
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reduced_formula <- stats::as.formula(paste("~", paste(reduced_terms, collapse = " + ")))
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tryCatch({
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dxd <- DEXSeq::DEXSeqDataSet(
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countData = round(tx_counts),
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sampleData = as.data.frame(coldata),
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design = full_formula,
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featureID = tx_meta$TXNAME,
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groupID = tx_meta$GENEID
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)
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dxd <- DESeq2::estimateSizeFactors(dxd)
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dxd <- de_estimate_dispersions_with_fallback(dxd, "DEXSeq", allow_gene_est = TRUE)
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dxd <- DEXSeq::testForDEU(dxd, reducedModel = reduced_formula)
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dxd <- DEXSeq::estimateExonFoldChanges(dxd, fitExpToVar = condition_column)
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dxr <- DEXSeq::DEXSeqResults(dxd, independentFiltering = FALSE)
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list(dxd = dxd, dxr = dxr)
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}, error = function(err) {
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if (length(active_covariates) == 0 || !grepl(
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"model matrix is not full rank",
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conditionMessage(err),
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fixed = TRUE
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)) {
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stop(err)
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}
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dropped_covariate <- tail(active_covariates, 1)
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kept_covariates <- head(active_covariates, -1)
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message(
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"DEXSeq design was not full rank with covariate '",
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dropped_covariate,
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"'; retrying without it."
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)
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run_inner(kept_covariates)
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})
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}
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run_inner(covariates)
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}
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main_run_de_analysis <- function(
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argv,
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deseq_runner = de_run_deseq2_result,
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dexseq_runner = de_run_dexseq_result,
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pdf_fn = grDevices::pdf,
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dev_off_fn = grDevices::dev.off,
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plot_ma_fn = DESeq2::plotMA,
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plot_disp_fn = DESeq2::plotDispEsts,
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per_gene_q_fn = DEXSeq::perGeneQValue,
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placeholder_pdf_fn = de_write_placeholder_pdf
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) {
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set.seed(42)
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dir.create(argv$out_dir, showWarnings = FALSE, recursive = TRUE)
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tx_se <- readRDS(argv$transcript_rds)
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gene_se <- readRDS(argv$gene_rds)
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sample_df <- workflow_glue_r_read_csv(argv$sample_sheet)
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validated <- de_validate_inputs(tx_se, gene_se, sample_df, argv)
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sample_df <- validated$sample_df
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covariates <- validated$covariates
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condition_values <- validated$condition_values
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reference_level <- validated$reference_level
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tx_meta <- as.data.frame(SummarizedExperiment::rowData(tx_se))
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if (!"TXNAME" %in% names(tx_meta)) {
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tx_meta$TXNAME <- rownames(tx_se)
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}
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if (!"GENEID" %in% names(tx_meta)) {
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stop("Transcript rowData must contain GENEID for DEXSeq.", call. = FALSE)
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}
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gene_meta <- as.data.frame(SummarizedExperiment::rowData(gene_se))
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if (!"GENEID" %in% names(gene_meta)) {
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gene_meta$GENEID <- rownames(gene_se)
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}
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targets <- setdiff(as.character(condition_values), reference_level)
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de_qc_stats <- list(
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timestamp = format(Sys.time(), "%Y-%m-%d %H:%M:%S"),
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total_samples = nrow(sample_df),
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condition_column = argv$condition_column,
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reference_level = reference_level,
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covariates = if (length(covariates) > 0) covariates else "none",
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num_contrasts = length(targets),
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contrasts = list()
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)
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n_per_group <- table(sample_df[[argv$condition_column]])
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de_qc_stats$samples_per_group <- as.list(n_per_group)
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sample_size_warnings <- character(0)
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if (any(n_per_group < 3)) {
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warning(
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"WARNING: Some condition groups have fewer than 3 replicates.\n",
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"Recommended minimum for DGE: n=3 per group\n",
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"Current sample sizes: ",
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paste(names(n_per_group), "=", n_per_group, collapse = ", "),
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"\nResults may have reduced statistical power."
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)
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sample_size_warnings <- c(sample_size_warnings, "Some groups have n<3 (recommended minimum)")
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}
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if (any(n_per_group < 2)) {
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stop(
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"ERROR: Some condition groups have fewer than 2 replicates. Cannot perform statistical testing.",
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call. = FALSE
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)
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}
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de_qc_stats$sample_size_warnings <- if (length(sample_size_warnings) > 0) {
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sample_size_warnings
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} else {
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"none"
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}
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if (length(targets) > 1) {
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fwer <- (1 - (1 - 0.05)^length(targets)) * 100
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mt_warning <- sprintf(
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"Multiple contrasts tested (%d). Per-contrast FDR < 0.05 yields family-wise error rate of ~%.1f%%",
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length(targets),
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fwer
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)
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message("WARNING: ", mt_warning)
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de_qc_stats$multiple_testing_note <- mt_warning
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mt_content <- c(
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"Multiple Testing Across Contrasts",
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"==================================",
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"",
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sprintf("Timestamp: %s", format(Sys.time(), "%Y-%m-%d %H:%M:%S")),
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sprintf("Number of contrasts tested: %d", length(targets)),
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sprintf("Contrasts: %s", paste(sprintf("%s vs %s", targets, reference_level), collapse = ", ")),
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"",
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"PER-CONTRAST FDR THRESHOLD: 0.05",
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sprintf("FAMILY-WISE ERROR RATE: ~%.1f%%", fwer),
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"",
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"WHAT THIS MEANS:",
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" Each contrast uses FDR < 0.05 independently.",
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" When testing multiple contrasts, the overall false positive rate increases.",
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sprintf(" Expected: %.1f%% chance of at least one false positive across all contrasts", fwer),
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"",
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"RECOMMENDATIONS:",
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|
sprintf(" 1. Bonferroni correction: 0.05 / %d = %.4f", length(targets), 0.05 / length(targets)),
|
|
" 2. Focus on pre-specified contrasts of interest",
|
|
" 3. Treat results as exploratory and validate key findings",
|
|
" 4. Consider using hierarchical testing procedures",
|
|
""
|
|
)
|
|
writeLines(mt_content, file.path(argv$out_dir, "MULTIPLE_TESTING_WARNING.txt"))
|
|
}
|
|
|
|
for (target_level in targets) {
|
|
contrast_name <- de_build_contrast_name(argv$condition_column, target_level, reference_level)
|
|
contrast_dir <- file.path(argv$out_dir, contrast_name)
|
|
dir.create(contrast_dir, showWarnings = FALSE, recursive = TRUE)
|
|
|
|
keep_samples <- sample_df[[argv$condition_column]] %in% c(reference_level, target_level)
|
|
contrast_samples <- droplevels(sample_df[keep_samples, , drop = FALSE])
|
|
contrast_samples[[argv$condition_column]] <- stats::relevel(
|
|
factor(contrast_samples[[argv$condition_column]]),
|
|
ref = reference_level
|
|
)
|
|
|
|
contrast_qc <- list(
|
|
name = contrast_name,
|
|
target_level = target_level,
|
|
reference_level = reference_level,
|
|
n_samples = nrow(contrast_samples),
|
|
n_target = sum(contrast_samples[[argv$condition_column]] == target_level),
|
|
n_reference = sum(contrast_samples[[argv$condition_column]] == reference_level)
|
|
)
|
|
|
|
if (nrow(contrast_samples) < 6) {
|
|
contrast_qc$dtu_power_warning <- sprintf(
|
|
"DTU analysis may be underpowered (n=%d, recommend n>=6 with >=3 per group)",
|
|
nrow(contrast_samples)
|
|
)
|
|
warning(contrast_qc$dtu_power_warning)
|
|
}
|
|
|
|
gene_counts <- SummarizedExperiment::assays(gene_se)$counts[, contrast_samples$alias, drop = FALSE]
|
|
tx_counts <- SummarizedExperiment::assays(tx_se)$counts[, contrast_samples$alias, drop = FALSE]
|
|
contrast_qc$genes_tested <- nrow(gene_counts)
|
|
contrast_qc$transcripts_tested <- nrow(tx_counts)
|
|
|
|
dge_run <- deseq_runner(
|
|
gene_counts,
|
|
contrast_samples,
|
|
target_level,
|
|
reference_level,
|
|
argv$condition_column,
|
|
covariates,
|
|
argv$out_dir,
|
|
contrast_name
|
|
)
|
|
dge_res <- as.data.frame(dge_run$result)
|
|
dge_res$GENEID <- rownames(dge_res)
|
|
dge_res <- merge(gene_meta, dge_res, by = "GENEID", all.y = TRUE, sort = FALSE)
|
|
dge_res <- workflow_glue_r_normalise_tsv_df(dge_res)
|
|
|
|
contrast_qc$dge_total_genes <- nrow(dge_res)
|
|
contrast_qc$dge_significant_fdr05 <- sum(dge_res$padj < 0.05, na.rm = TRUE)
|
|
contrast_qc$dge_significant_fdr01 <- sum(dge_res$padj < 0.01, na.rm = TRUE)
|
|
contrast_qc$dge_upregulated <- sum(
|
|
dge_res$padj < 0.05 & dge_res$log2FoldChange > 0,
|
|
na.rm = TRUE
|
|
)
|
|
contrast_qc$dge_downregulated <- sum(
|
|
dge_res$padj < 0.05 & dge_res$log2FoldChange < 0,
|
|
na.rm = TRUE
|
|
)
|
|
|
|
utils::write.table(
|
|
dge_res[order(dge_res$padj), ],
|
|
file = file.path(contrast_dir, "results_dge.tsv"),
|
|
sep = "\t",
|
|
quote = FALSE,
|
|
row.names = FALSE
|
|
)
|
|
|
|
pdf_fn(file.path(contrast_dir, "results_dge.pdf"))
|
|
plot_ma_fn(dge_run$result)
|
|
dev_off_fn()
|
|
|
|
dex_res <- tryCatch(
|
|
dexseq_runner(
|
|
tx_counts,
|
|
tx_meta,
|
|
contrast_samples,
|
|
argv$condition_column,
|
|
covariates
|
|
),
|
|
error = function(err) {
|
|
message_text <- conditionMessage(err)
|
|
if (!de_is_recoverable_dexseq_error(message_text)) {
|
|
stop(err)
|
|
}
|
|
|
|
warning(
|
|
"DEXSeq failed for contrast ",
|
|
target_level,
|
|
" vs ",
|
|
reference_level,
|
|
"\nError: ",
|
|
message_text
|
|
)
|
|
|
|
failure_content <- c(
|
|
"DTU Analysis Failed",
|
|
"===================",
|
|
"",
|
|
sprintf("Timestamp: %s", format(Sys.time(), "%Y-%m-%d %H:%M:%S")),
|
|
sprintf("Contrast: %s vs %s", target_level, reference_level),
|
|
sprintf(
|
|
"Samples: %d (%d %s, %d %s)",
|
|
nrow(contrast_samples),
|
|
sum(contrast_samples[[argv$condition_column]] == target_level),
|
|
target_level,
|
|
sum(contrast_samples[[argv$condition_column]] == reference_level),
|
|
reference_level
|
|
),
|
|
sprintf("Transcripts: %d", nrow(tx_counts)),
|
|
"",
|
|
"ERROR MESSAGE:",
|
|
sprintf(" %s", message_text),
|
|
"",
|
|
"DTU RESULTS CANNOT BE INTERPRETED",
|
|
""
|
|
)
|
|
writeLines(failure_content, file.path(contrast_dir, "DTU_ANALYSIS_FAILED.txt"))
|
|
NULL
|
|
}
|
|
)
|
|
|
|
if (is.null(dex_res)) {
|
|
dex_df <- workflow_glue_r_empty_tsv(c(
|
|
"featureID",
|
|
"groupID",
|
|
"log2fold",
|
|
"pvalue",
|
|
"padj",
|
|
"exonBaseMean"
|
|
))
|
|
tx_dtu <- dex_df
|
|
gene_dtu <- workflow_glue_r_empty_tsv(c("GENEID", "qval"))
|
|
placeholder_pdf_fn(
|
|
file.path(contrast_dir, "results_dtu.pdf"),
|
|
"DEXSeq did not converge for this contrast.\nSee DTU_ANALYSIS_FAILED.txt for details."
|
|
)
|
|
contrast_qc$dtu_status <- "FAILED"
|
|
contrast_qc$dtu_significant_transcripts <- 0
|
|
contrast_qc$dtu_significant_genes <- 0
|
|
} else {
|
|
dex_df <- as.data.frame(dex_res$dxr)
|
|
dex_df <- workflow_glue_r_normalise_tsv_df(dex_df)
|
|
tx_dtu <- dex_df[, intersect(
|
|
c("featureID", "groupID", "log2fold", "pvalue", "padj", "exonBaseMean"),
|
|
names(dex_df)
|
|
), drop = FALSE]
|
|
tx_dtu <- workflow_glue_r_normalise_tsv_df(tx_dtu)
|
|
|
|
gene_q <- per_gene_q_fn(dex_res$dxr)
|
|
gene_dtu <- data.frame(
|
|
GENEID = names(gene_q),
|
|
qval = unname(gene_q),
|
|
row.names = NULL
|
|
)
|
|
|
|
contrast_qc$dtu_status <- "SUCCESS"
|
|
contrast_qc$dtu_significant_transcripts <- sum(tx_dtu$padj < 0.05, na.rm = TRUE)
|
|
contrast_qc$dtu_significant_genes <- sum(gene_dtu$qval < 0.05, na.rm = TRUE)
|
|
|
|
pdf_fn(file.path(contrast_dir, "results_dtu.pdf"))
|
|
plot_ma_fn(dex_res$dxr, cex = 0.8, alpha = 0.05)
|
|
plot_disp_fn(dex_res$dxd)
|
|
dev_off_fn()
|
|
}
|
|
|
|
utils::write.table(
|
|
dex_df,
|
|
file = file.path(contrast_dir, "results_dexseq.tsv"),
|
|
sep = "\t",
|
|
quote = FALSE,
|
|
row.names = FALSE
|
|
)
|
|
utils::write.table(
|
|
tx_dtu[order(tx_dtu$padj), ],
|
|
file = file.path(contrast_dir, "results_dtu_transcript.tsv"),
|
|
sep = "\t",
|
|
quote = FALSE,
|
|
row.names = FALSE
|
|
)
|
|
utils::write.table(
|
|
gene_dtu[order(gene_dtu$qval), ],
|
|
file = file.path(contrast_dir, "results_dtu_gene.tsv"),
|
|
sep = "\t",
|
|
quote = FALSE,
|
|
row.names = FALSE
|
|
)
|
|
utils::write.table(
|
|
contrast_samples,
|
|
file = file.path(contrast_dir, "samples_used.tsv"),
|
|
sep = "\t",
|
|
quote = FALSE,
|
|
row.names = FALSE
|
|
)
|
|
|
|
contrast_qc_summary <- c(
|
|
sprintf("Contrast QC Summary: %s", contrast_name),
|
|
paste(rep("=", 50), collapse = ""),
|
|
"",
|
|
"Sample Information:",
|
|
sprintf(" Target level (%s): %d samples", target_level, contrast_qc$n_target),
|
|
sprintf(" Reference level (%s): %d samples", reference_level, contrast_qc$n_reference),
|
|
sprintf(" Total samples: %d", contrast_qc$n_samples),
|
|
"",
|
|
"DGE Results:",
|
|
sprintf(" Genes tested: %d", contrast_qc$genes_tested),
|
|
sprintf(" Significant (FDR < 0.05): %d", contrast_qc$dge_significant_fdr05),
|
|
sprintf(" Significant (FDR < 0.01): %d", contrast_qc$dge_significant_fdr01),
|
|
sprintf(" Upregulated: %d", contrast_qc$dge_upregulated),
|
|
sprintf(" Downregulated: %d", contrast_qc$dge_downregulated),
|
|
"",
|
|
"DTU Results:",
|
|
sprintf(" Status: %s", contrast_qc$dtu_status),
|
|
sprintf(" Transcripts tested: %d", contrast_qc$transcripts_tested),
|
|
if (contrast_qc$dtu_status == "SUCCESS") {
|
|
c(
|
|
sprintf(
|
|
" Significant transcripts (FDR < 0.05): %d",
|
|
contrast_qc$dtu_significant_transcripts
|
|
),
|
|
sprintf(" Genes with DTU (q < 0.05): %d", contrast_qc$dtu_significant_genes)
|
|
)
|
|
} else {
|
|
" See DTU_ANALYSIS_FAILED.txt for details"
|
|
},
|
|
if (!is.null(contrast_qc$dtu_power_warning)) paste0(" WARNING: ", contrast_qc$dtu_power_warning) else NULL,
|
|
""
|
|
)
|
|
writeLines(contrast_qc_summary, file.path(contrast_dir, "contrast_qc_summary.txt"))
|
|
de_qc_stats$contrasts[[contrast_name]] <- contrast_qc
|
|
}
|
|
|
|
jsonlite::write_json(
|
|
de_qc_stats,
|
|
file.path(argv$out_dir, "de_qc_stats.json"),
|
|
pretty = TRUE,
|
|
auto_unbox = TRUE
|
|
)
|
|
|
|
overall_summary <- c(
|
|
"Differential Expression/Usage Analysis Summary",
|
|
paste(rep("=", 50), collapse = ""),
|
|
"",
|
|
sprintf("Timestamp: %s", de_qc_stats$timestamp),
|
|
sprintf("Total samples: %d", de_qc_stats$total_samples),
|
|
sprintf("Condition column: %s", de_qc_stats$condition_column),
|
|
sprintf("Reference level: %s", de_qc_stats$reference_level),
|
|
sprintf("Covariates: %s", paste(de_qc_stats$covariates, collapse = ", ")),
|
|
"",
|
|
"Sample Sizes:",
|
|
sapply(names(de_qc_stats$samples_per_group), function(grp) {
|
|
sprintf(" %s: %d samples", grp, de_qc_stats$samples_per_group[[grp]])
|
|
}),
|
|
if (de_qc_stats$sample_size_warnings != "none") paste0(" WARNING: ", de_qc_stats$sample_size_warnings) else NULL,
|
|
"",
|
|
sprintf("Number of contrasts tested: %d", de_qc_stats$num_contrasts),
|
|
if (!is.null(de_qc_stats$multiple_testing_note)) paste0(" NOTE: ", de_qc_stats$multiple_testing_note) else NULL,
|
|
"",
|
|
"Per-Contrast Results:",
|
|
sapply(names(de_qc_stats$contrasts), function(cname) {
|
|
cqc <- de_qc_stats$contrasts[[cname]]
|
|
c(
|
|
"",
|
|
sprintf(" %s:", cname),
|
|
sprintf(" Samples: %d (%d vs %d)", cqc$n_samples, cqc$n_target, cqc$n_reference),
|
|
sprintf(" DGE significant: %d genes (FDR<0.05)", cqc$dge_significant_fdr05),
|
|
sprintf(" DTU status: %s", cqc$dtu_status),
|
|
if (cqc$dtu_status == "SUCCESS") sprintf(" DTU significant: %d genes", cqc$dtu_significant_genes) else NULL
|
|
)
|
|
}),
|
|
"",
|
|
"For detailed per-contrast statistics, see:",
|
|
" - <contrast>/contrast_qc_summary.txt",
|
|
" - <contrast>/results_dge.tsv",
|
|
" - <contrast>/results_dtu_gene.tsv",
|
|
""
|
|
)
|
|
writeLines(unlist(overall_summary), file.path(argv$out_dir, "de_overall_summary.txt"))
|
|
writeLines(capture.output(sessionInfo()), file.path(argv$out_dir, "session_info.txt"))
|
|
|
|
invisible(list(qc = de_qc_stats))
|
|
}
|
|
|
|
run_de_analysis_cli <- function(argv = commandArgs(trailingOnly = TRUE)) {
|
|
parsed <- argparser::parse_args(de_analysis_arg_parser(), argv = argv)
|
|
main_run_de_analysis(parsed)
|
|
}
|