#' Performs gene set enrichment analysis using KEGG terms
#'
#' @param proteins numeric vector of proteins scores
#' @param pvalueCutoff p-value cutoff for annotations
#' @param pAdjustMethod one of "none", "BH" (Benjamini-Hochberg correction), "hochberg", "bonferroni", "holm", "hommel", "BY", "fdr"
#' @param qvalueCutoff q-value cutoff for annotations
#' @param minGSSize minimum number of annotated proteins to be included
#' @param maxGSSize maximum number of annotated proteins to be included
#' @param dataset dataset
#' @param view view results
#' @param return.all return enrichResult object; useful for further analysis of enrichment results
#' @param add.info add additional information to the results data frame
#'
#' @return
#' @export
#'
#'
do_GSEA_KEGG <- function(proteins, pvalueCutoff = 0.05, pAdjustMethod = "none", qvalueCutoff = 0.2, minGSSize = 10,
maxGSSize = 120, dataset = dataset, view = T, return.all = F, add.info = F) {
# Get dataset
dataset <- get_dataset(dataset)
# Kegg organism code
kegg_code <- get_dataset_attr(which = "kegg_code",
dataset = dataset)
# Prepare protein list
proteins.sorted <- sort(rank(proteins), decreasing = T)
# Perform enrichment
kegg.results <- clusterProfiler::gseKEGG(geneList = proteins.sorted,
organism = kegg_code,
minGSSize = minGSSize,
maxGSSize = maxGSSize,
pvalueCutoff = pvalueCutoff,
pAdjustMethod = pAdjustMethod,
verbose = FALSE,
keyType = "uniprot",
scoreType = "pos")
results <- tibble::as_tibble(kegg.results@result) %>%
dplyr::filter(p.adjust < pvalueCutoff) %>%
dplyr::rowwise() %>%
dplyr::mutate(Proteins = paste(strsplit(core_enrichment, split = "/")[[1]], collapse = ";"), .before = core_enrichment) %>%
dplyr::select(-c(core_enrichment, leading_edge, rank)) %>%
dplyr::mutate(Genes = paste(p2g(strsplit(Proteins, split = ";")[[1]]), collapse = ";"), .before = Proteins)
# View data frame immediately
if (view) View(results)
# Return
if (!return.all) return(results)
else return(list(results = results,
enrichResult = kegg.result))
}
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