Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

extension for gs descriptions #23

Open
wants to merge 4 commits into
base: main
Choose a base branch
from
Open
Changes from 1 commit
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
Next Next commit
update msigdbr_collections()
add the major groups and their individual descriptions
ozturan authored Dec 7, 2022
commit 8c60233652fd2751cf5f1deca726b364c506ab37
37 changes: 34 additions & 3 deletions R/msigdbr-collections.R
Original file line number Diff line number Diff line change
@@ -8,8 +8,39 @@
#' @examples
#' msigdbr_collections()
msigdbr_collections <- function() {
msigdbr_geneset_desc <- c("POSITIONAL GENE SETS",
"CHEMICAL AND GENETIC PERTURBATIONS",
"CANONICAL PATHWAYS",
"CANONICAL PATHWAYS - BIOCARTA",
"CANONICAL PATHWAYS - KEGG",
"CANONICAL PATHWAYS - PID",
"CANONICAL PATHWAYS - REACTOME",
"CANONICAL PATHWAYS - WIKIPATHWAYS",
"CURATED GENES SETS",
"MICRORNA TARGETS - LEGACY",
"MICRORNA TARGETS - MIR",
"TRANSCRIPTION FACTOR TARGETS - GTRD",
"TRANSCRIPTION FACTOR TARGETS - LEGACY",
"REGULATORY TARGET GENES",
"CANCER GENE NEIGHBOURHOODS",
"CANCER MODULES",
"COMPUTATIONAL GENE SETS",
"GENE ONTOLOGY - BIOLOGICAL PROCESS",
"GENE ONTOLOGY - CELLULAR COMPONENT",
"GENE ONTOLOGY - MOLECULAR FUNCTION",
"HUMAN PHENOTYPE ONTOLOGY",
"ONTOLOGY GENE SETS",
"ONCOGENIC SIGNATURE GENE SETS",
"IMMUNESIGDB",
"VACCINE RESPONSE GENE SETS",
"IMMUNOLOGIC SIGNATURE GENE SETS",
"CELL TYPE SIGNATURE GENE SETS",
"HALLMARK GENE SETS")
msigdbr_genesets %>%
distinct(.data$gs_cat, .data$gs_subcat, .data$gs_id) %>%
count(.data$gs_cat, .data$gs_subcat, name = "num_genesets") %>%
arrange(.data$gs_cat, .data$gs_subcat)
distinct(.data$gs_cat, .data$gs_subcat, .data$gs_id) %>%
count(.data$gs_cat, .data$gs_subcat, name = "num_genesets") %>%
arrange(.data$gs_cat, .data$gs_subcat) %>%
group_by(gs_cat) %>%
bind_rows(summarise_all(., ~if(is.numeric(.)) sum(.) else "")) %>%
unique() %>% arrange(gs_cat, desc=T) %>% cbind(msigdbr_geneset_desc)
}