pseudobulk_deseq2: Pseudobulk differential expression with DESeq2

In presto: Fast Functions for Differential Expression Using Wilcoxon and AUC

Pseudobulk differential expression with DESeq2

Description

Runs DESeq2::DESeq() on a feature-by-pseudobulk count matrix to identify genes whose expression differs between groups of pseudobulks. Three test designs are supported, selected by mode:

• "one_vs_all" (default) - test each level of the contrast variable against the union of all others. Useful for marker discovery. Dispatched to pseudobulk_one_vs_all().

• "pairwise" - test every ordered pair of levels separately. Useful for high-confidence markers; combine with summarize_dge_pairs() to keep the most conservative pair. Dispatched to pseudobulk_pairwise().

• "within" - split on the first term of dge_formula and test the second term within each split level. Useful for condition / case-vs-control comparisons restricted to one cluster at a time. Dispatched to pseudobulk_within().

Pseudobulk inputs are typically produced by collapse_counts(). Genes with low counts across pseudobulks are filtered out before fitting (controlled by min_counts_per_sample and present_in_min_samples). See the pseudobulk vignette for an end-to-end walkthrough on a real single-cell dataset.

Usage

pseudobulk_deseq2(
  dge_formula,
  meta_data,
  counts_df,
  verbose = TRUE,
  min_counts_per_sample = 10,
  present_in_min_samples = 5,
  collapse_background = TRUE,
  vals_test = NULL,
  mode = c("one_vs_all", "pairwise", "within")[1]
)

Arguments

dge_formula	One-sided formula such as ~cluster + donor. The first term is treated as the contrast variable in "one_vs_all" and "pairwise" modes, or as the split variable in "within" mode (in which case the second term becomes the contrast variable). Additional terms are kept as covariates in the DESeq2 design.
meta_data	data.frame of pseudobulk metadata. One row per pseudobulk; should contain only the variables used in dge_formula.
counts_df	Feature-by-pseudobulk integer count matrix. Rows are features; columns must align with rows of meta_data.
verbose	Logical. Print progress messages. Default TRUE.
min_counts_per_sample	Minimum count per pseudobulk for a gene to be considered expressed in that pseudobulk. Default 10.
present_in_min_samples	Minimum number of pseudobulks in which a gene must reach min_counts_per_sample to be retained. Default 5.
collapse_background	Used only when mode = "one_vs_all". If TRUE, background pseudobulks are collapsed across the contrast variable before each DESeq2 fit, which helps when donor representation is unbalanced across clusters. Default TRUE.
vals_test	Character vector of contrast levels to test. If NULL (default), every level of the contrast variable is tested.
mode	One of "one_vs_all" (default), "pairwise", or "within". See description.

Value

A long-form data.frame of DESeq2 results. Columns include the group identifier(s) (group, or group1 / group2 in pairwise mode), feature, and the DESeq2 columns baseMean, log2FoldChange, lfcSE, stat, pvalue, padj.

See Also

collapse_counts(), top_markers_dds(), summarize_dge_pairs()

Examples

if (requireNamespace("DESeq2", quietly = TRUE)) {
    ## 40 genes x 300 cells from 2 clusters across 6 donors
    m <- matrix(sample.int(8, 40 * 300, replace = TRUE), nrow = 40)
    rownames(m) <- paste0("G", 1:40)
    colnames(m) <- paste0("C", 1:300)
    meta <- data.frame(
        cluster = sample(c("a", "b"), 300, replace = TRUE),
        donor = sample(paste0("d", 1:6), 300, replace = TRUE)
    )

    ## collapse cells into per-(cluster, donor) pseudobulks
    dc <- collapse_counts(m, meta, c("cluster", "donor"))

    ## test each cluster against the rest
    res <- pseudobulk_deseq2(
        ~cluster,
        dc$meta_data["cluster"],
        dc$counts_mat,
        verbose = FALSE,
        present_in_min_samples = 1,
        collapse_background = FALSE,
        mode = "one_vs_all"
    )
    head(res)
}

presto documentation built on Sept. 30, 2026, 5:13 p.m.