Modeling continuous cell-level covariates
Collapse using mean value for pseudobulk data
Run on 2026-04-14 17:25:11
1 Introduction
Since read counts are summed across cells in a pseudobulk approach, modeling continuous cell-level covariates also requires a collapsing step. Here we summarize the values of a variable from a set of cells using the mean, and store the value for each cell type. Including these variables in a regression formula uses the summarized values from the corresponding cell type.
We demonstrate this feature on a lightly modified analysis of PBMCs from 8 individuals stimulated with interferon-β (Kang, et al, 2018, Nature Biotech).
2 Standard processing
Here is the code from the main vignette:
library(dreamlet)
library(muscat)
library(ExperimentHub)
library(scater)
# Download data, specifying EH2259 for the Kang, et al study
eh <- ExperimentHub()
sce <- eh[["EH2259"]]
# only keep singlet cells with sufficient reads
sce <- sce[rowSums(counts(sce) > 0) > 0, ]
sce <- sce[, colData(sce)$multiplets == "singlet"]
# compute QC metrics
qc <- perCellQCMetrics(sce)
# remove cells with few or many detected genes
ol <- isOutlier(metric = qc$detected, nmads = 2, log = TRUE)
sce <- sce[, !ol]
# set variable indicating stimulated (stim) or control (ctrl)
sce$StimStatus <- sce$stimIn many datasets, continuous cell-level variables could be mapped reads, gene count, mitochondrial rate, etc. There are no continuous cell-level variables in this dataset, so we can simulate two from a normal distribution:
sce$value1 <- rnorm(ncol(sce))
sce$value2 <- rnorm(ncol(sce))3 Pseudobulk
Now compute the pseudobulk using standard code:
sce$id <- paste0(sce$StimStatus, sce$ind)
# Create pseudobulk
pb <- aggregateToPseudoBulk(sce,
assay = "counts",
cluster_id = "cell",
sample_id = "id",
verbose = FALSE
)The means per variable, cell type, and sample are stored in the pseudobulk SingleCellExperiment object:
metadata(pb)$aggr_means## # A tibble: 128 × 5
## # Groups: cell [8]
## cell id cluster value1 value2
## <fct> <fct> <dbl> <dbl> <dbl>
## 1 B cells ctrl101 3.96 -0.0393 -0.159
## 2 B cells ctrl1015 4.00 0.0249 0.00488
## 3 B cells ctrl1016 4 -0.0588 0.138
## 4 B cells ctrl1039 4.04 -0.0784 0.262
## 5 B cells ctrl107 4 0.198 0.0241
## 6 B cells ctrl1244 4 0.161 -0.180
## 7 B cells ctrl1256 4.01 -0.106 0.0500
## 8 B cells ctrl1488 4.02 -0.128 -0.138
## 9 B cells stim101 4.09 0.0735 -0.0556
## 10 B cells stim1015 4.06 0.0891 -0.117
## # ℹ 118 more rows4 Analysis
Including these variables in a regression formula uses the summarized values from the corresponding cell type. This happens behind the scenes, so the user doesn’t need to distinguish bewteen sample-level variables stored in colData(pb) and cell-level variables stored in metadata(pb)$aggr_means.
Variance partition and hypothesis testing proceeds as ususal:
form <- ~ StimStatus + value1 + value2
# Normalize and apply voom/voomWithDreamWeights
res.proc <- processAssays(pb, form, min.count = 5)
# run variance partitioning analysis
vp.lst <- fitVarPart(res.proc, form)
# Summarize variance fractions genome-wide for each cell type
plotVarPart(vp.lst, label.angle = 60)
# Differential expression analysis within each assay
res.dl <- dreamlet(res.proc, form)
# dreamlet results include coefficients for value1 and value2
res.dl## class: dreamletResult
## assays(8): B cells CD14+ Monocytes ... Megakaryocytes NK cells
## Genes:
## min: 164
## max: 5262
## details(7): assay n_retain ... n_errors error_initial
## coefNames(4): (Intercept) StimStatusstim value1 value25 Details
A variable in colData(sce) is handled according to if the variable is
- continuous: the mean per donor/cell type is stored in
metadata(pb)$aggr_means - discrete
- [constant within each donor/cell type] it is stored in
colData(pb) - [varies within each donor/cell type] there is no good way to summarize it. The variable is dropped.
- [constant within each donor/cell type] it is stored in
6 Session Info
## R version 4.6.0 alpha (2026-04-05 r89794)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.4 LTS
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## Matrix products: default
## BLAS: /home/biocbuild/bbs-3.23-bioc/R/lib/libRblas.so
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0 LAPACK version 3.12.0
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## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
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## time zone: America/New_York
## tzcode source: system (glibc)
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## attached base packages:
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## other attached packages:
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