Parallelize 'DESeq2' functions
Henrik Bengtsson
Source:vignettes/futurize-81-DESeq2.md
futurize-81-DESeq2.Rmd
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The futurize package allows you to easily turn
sequential code into parallel code by piping the sequential code to the
futurize() function. Easy!
Introduction
This vignette demonstrates how to use this approach to parallelize
the DESeq2
DESeq() function.
The DESeq2
Bioconductor package provides methods to test for differential
expression in RNA-seq data. The main function DESeq() runs
a pipeline of gene-wise dispersion estimation, fitting, and statistical
testing, which can be parallelized across genes.
Example: Running DESeq() in parallel
The DESeq() function performs the full differential
expression analysis:
library(DESeq2)
# Simulate data
n_genes <- 100L
n_samples <- 8L
counts <- matrix(
as.integer(runif(n_genes * n_samples, min = 0, max = 1000)),
nrow = n_genes,
ncol = n_samples,
dimnames = list(
paste0("gene", seq_len(n_genes)),
paste0("sample", seq_len(n_samples))
)
)
col_data <- data.frame(
condition = factor(rep(c("control", "treated"), each = n_samples / 2L)),
row.names = colnames(counts)
)
dds <- DESeqDataSetFromMatrix(
countData = counts,
colData = col_data,
design = ~ condition
)
dds <- DESeq(dds)
res <- results(dds)Here DESeq() runs sequentially, but we can easily make
it run in parallel by piping to futurize():
This will distribute the work across the available parallel workers, given that we have set up parallel workers, e.g.
plan(multisession)The built-in multisession backend parallelizes on your
local computer and works on all operating systems. There are other parallel
backends to choose from, including alternatives to parallelize
locally as well as distributed across remote machines, e.g.
plan(future.mirai::mirai_multisession)and
plan(future.batchtools::batchtools_slurm)Supported Functions
The following DESeq2 functions are supported by
futurize():