Gene Set Enrichment Analysis (GSEA) is a computational method that determines whether an a priori defined set of genes shows statistically significant, concordant differences between two biological states. The original algorithm is detailed in Subramanian, Tamayo, et al. with Java implementations available through the Broad Institute.
The liger
package provides a lightweight R implementation of this enrichment test on a list of values. Given a list of values, such as p-values or log-fold changes derived from differential expression analysis or other analyses comparing biological states, this package enables you to test a priori defined set of genes for enrichment to enable interpretability of highly significant or high fold-change genes.
Consider an example, simulated dataset.
library(liger)
# load gene set
data("org.Hs.GO2Symbol.list")
# get universe
universe <- unique(unlist(org.Hs.GO2Symbol.list))
# get a gene set
gs <- org.Hs.GO2Symbol.list[[1]]
# fake dummy example where everything in gene set is perfectly enriched
vals <- rnorm(length(universe), 0, 10)
names(vals) <- universe
vals[gs] <- rnorm(length(gs), 100, 10)
head(vals) # look at vals
## AKT3 C10orf2 DNA2 LIG3 MEF2A MGME1
## 92.04368 91.18714 102.78193 81.08097 94.94418 87.07168
Here, vals
can be seen as representing a list of log-fold changes derived from differential expression analysis on samples in two biological states. We want to interpret the set of differentially expressed genes with high positive fold changes using gene set enrichment analysis.
To test for enrichment of a particular gene set:
names(org.Hs.GO2Symbol.list)[[1]]
## [1] "GO:0000002"
gs # look at gs
## [1] "AKT3" "C10orf2" "DNA2" "LIG3" "MEF2A" "MGME1"
## [7] "MPV17" "OPA1" "PID1" "PRIMPOL" "SLC25A33" "SLC25A36"
## [13] "SLC25A4" "STOML2" "TYMP"
gsea(values=vals, geneset=gs, mc.cores=1, plot=TRUE, n.rand=500)
## [1] 0.002
In this simulation, we created vals
such that gs
was obviously enriched. And indeed, we see that this gene set exhibits significant enrichment.
Now to test for enrichment of another gene set:
gs.new <- org.Hs.GO2Symbol.list[[2]]
names(org.Hs.GO2Symbol.list)[[2]]
## [1] "GO:0000003"
head(gs.new) # look at gs.new
## [1] "ACE" "ACR" "ADAM2" "ADAM20" "ADAM21" "ADAM28"
gsea(values=vals, geneset=gs.new, mc.cores=1, n.rand=500)
## [1] 0.604
In this simulation, we created vals
such that gs.new
was obviously not enriched. And indeed, we see that this gene set does not exhibit significant enrichment.
If we simulate a more ambiguous case:
# add some noise
vals[sample(1:length(universe), 1000)] <- rnorm(1000, 100, 10)
# test previously perfectly enriched gene set again
gs <- org.Hs.GO2Symbol.list[[1]]
gsea(values=vals, geneset=gs, mc.cores=1, n.rand=500)
## [1] 0.044
The enrichment plots and p-values are affected as expected.
We can also test a number of gene sets:
bulk.gsea(values=vals, set.list=org.Hs.GO2Symbol.list[1:5], mc.cores=1, n.rand=500)
## p.val q.val sscore edge
## GO:0000002 0.001996008 0.0000000 1.9279433 81.08097
## GO:0000003 0.189620758 0.2626667 -0.8531194 105.20476
## GO:0000012 0.017964072 0.0260000 -1.3714705 12.45331
## GO:0000014 0.013972056 0.0260000 -1.3772795 10.36180
To save on computation time, we can also iterative assess significance:
iterative.bulk.gsea(values=vals, set.list=org.Hs.GO2Symbol.list[1:5], mc.cores=1, n.rand=500)
## initial: [5e+02 - 3] done
## p.val q.val sscore edge
## GO:0000002 0.001996008 0.007984032 1.9279433 81.08097
## GO:0000003 0.189620758 0.189620758 -0.8531194 105.20476
## GO:0000012 0.017964072 0.023952096 -1.3714705 12.45331
## GO:0000014 0.013972056 0.023952096 -1.3772795 10.36180
sessionInfo()
## R version 3.6.0 (2019-04-26)
## Platform: x86_64-apple-darwin15.6.0 (64-bit)
## Running under: macOS Mojave 10.14.6
##
## Matrix products: default
## BLAS: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRblas.0.dylib
## LAPACK: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRlapack.dylib
##
## locale:
## [1] C/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
##
## attached base packages:
## [1] stats graphics grDevices utils datasets methods base
##
## other attached packages:
## [1] liger_1.1.2
##
## loaded via a namespace (and not attached):
## [1] compiler_3.6.0 magrittr_1.5 parallel_3.6.0 tools_3.6.0
## [5] Rcpp_1.0.4.6 stringi_1.4.6 highr_0.8 knitr_1.28
## [9] stringr_1.4.0 xfun_0.14 matrixStats_0.56.0 evaluate_0.14