knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "man/figures/README-", out.width = "100%" )
The goal of enrichr.db is to provide the data from Enrichr in a format that makes it easy to access the gene sets programmatically from R.
The current Enrichr release included is from 2019-01-23.
You can install the released version of enrichr.db from Github with:
if (!requireNamespace("remotes", quietly = TRUE)) install.packages("remotes") remotes::install_url("https://github.com/labsyspharm/enrichr.db/releases/download/v0.1/enrichr.db_0.1.tar.gz")
This is a basic example which shows how to query the gene set database and use the gene sets for enrichment analysis using fgsea.
library(tidyverse) library(enrichr.db) # Finding all libraries that have something to do with drug treatments drug_gene_sets <- enrichr_terms %>% filter(grepl("drug", library, ignore.case = TRUE))
This gives a data frame of gene set libraries. The gene sets are in the data
column of the data frame and are implemented as lists. Each list element is
a gene set and contains a vector of HGCN gene symbols.
knitr::kable(drug_gene_sets %>% mutate(data = paste0("<", map_int(data, length), " gene sets>")))
We can have a look a the first five gene sets in the
Drug_Perturbations_from_GEO_2014 library. We can print the first 10 genes of
each gene set.
print( # Drug_Perturbations_from_GEO_2014 is the first library drug_gene_sets$data[[1]] %>% head(n = 5) %>% map(head, n = 10) )
We can use the gene sets in the data column directly for gene set enrichment
analysis using fgsea. Again, we're using the first library that we found
(Drug_Perturbations_from_GEO_2014).
library(fgsea) # Making random fake expression results genes <- Reduce(union, drug_gene_sets$data[[1]]) expression_res <- setNames( rnorm(length(genes), 0, 0.5), genes ) enrichment_res <- fgseaMultilevel( pathways = drug_gene_sets$data[[1]], stats = expression_res, sampleSize = 101, minSize = 15 )
knitr::kable( enrichment_res %>% arrange(padj) %>% select(-leadingEdge) %>% head() )
We gratefully acknowledge support by NIH Grant 1U54CA225088-01: Systems Pharmacology of Therapeutic and Adverse Responses to Immune Checkpoint and Small Molecule Drugs.
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