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).
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()# 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:
Now compute the pseudobulk using standard code:
sce$id <- paste0(sce$StimStatus, sce$ind)
# Create pseudobulk
pb <- aggregateToPseudoBulk(sce,
assay = "counts",
cluster_id = "cell",
sample_id = "id",
verbose = FALSE
)The means per variable, cell type, and sample are stored in the
pseudobulk SingleCellExperiment object:
## # A tibble: 128 × 5
## # Groups: cell [8]
## cell id cluster value1 value2
## <fct> <fct> <dbl> <dbl> <dbl>
## 1 B cells ctrl101 3.96 0.0189 -0.0274
## 2 B cells ctrl1015 4.00 -0.0584 0.0767
## 3 B cells ctrl1016 4 -0.0218 0.0614
## 4 B cells ctrl1039 4.04 0.0607 0.167
## 5 B cells ctrl107 4 -0.266 -0.180
## 6 B cells ctrl1244 4 0.0341 0.0893
## 7 B cells ctrl1256 4.01 -0.0424 0.0393
## 8 B cells ctrl1488 4.02 0.0465 -0.0960
## 9 B cells stim101 4.09 0.0529 0.0511
## 10 B cells stim1015 4.06 -0.0176 0.0799
## # ℹ 118 more rows
Including these variables in a regression formula uses the summarized
values from the corresponding cell type. This happens behind the scenes,
so the user doesn’t need to distinguish bewteen sample-level variables
stored in colData(pb) and cell-level variables stored in
metadata(pb)$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 value2
A variable in colData(sce) is handled according to if
the variable is
metadata(pb)$aggr_meanscolData(pb)## R version 4.5.1 (2025-06-13)
## Platform: x86_64-pc-linux-gnu
## Running under: Ubuntu 24.04.3 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
## LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/libopenblasp-r0.3.26.so; LAPACK version 3.12.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=C
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: Etc/UTC
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats4 stats graphics grDevices utils datasets methods
## [8] base
##
## other attached packages:
## [1] muscData_1.23.0 scater_1.37.0
## [3] scuttle_1.19.0 ExperimentHub_2.99.6
## [5] AnnotationHub_3.99.6 BiocFileCache_2.99.6
## [7] dbplyr_2.5.1 muscat_1.23.2
## [9] dreamlet_1.9.0 SingleCellExperiment_1.31.1
## [11] SummarizedExperiment_1.39.2 Biobase_2.69.1
## [13] GenomicRanges_1.61.8 Seqinfo_0.99.4
## [15] IRanges_2.43.8 S4Vectors_0.47.6
## [17] BiocGenerics_0.55.4 generics_0.1.4
## [19] MatrixGenerics_1.21.0 matrixStats_1.5.0
## [21] variancePartition_1.39.3 BiocParallel_1.43.4
## [23] limma_3.65.7 ggplot2_4.0.0
## [25] BiocStyle_2.37.1
##
## loaded via a namespace (and not attached):
## [1] bitops_1.0-9 httr_1.4.7
## [3] RColorBrewer_1.1-3 doParallel_1.0.17
## [5] Rgraphviz_2.53.0 numDeriv_2016.8-1.1
## [7] tools_4.5.1 sctransform_0.4.2
## [9] backports_1.5.0 utf8_1.2.6
## [11] R6_2.6.1 metafor_4.8-0
## [13] mgcv_1.9-3 GetoptLong_1.0.5
## [15] withr_3.0.2 prettyunits_1.2.0
## [17] gridExtra_2.3 fdrtool_1.2.18
## [19] cli_3.6.5 sandwich_3.1-1
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## [23] sass_0.4.10 KEGGgraph_1.69.0
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