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test_polyenrich_slow = function(geneset, gpw, n_cores) {
# Restrict our genes/weights/peaks to only those genes in the genesets.
# Here, geneset is not all combined, but GOBP, GOCC, etc.
gpw = subset(gpw, gpw$gene_id %in% geneset@all.genes)
# Construct model formula.
model = "num_peaks ~ goterm + s(log10_length,bs='cr')"
# Run tests. NOTE: If os == 'Windows', n_cores is reset to 1 for this to work
results_list = parallel::mclapply(as.list(ls(geneset@set.gene)), function(go_id) {
single_polyenrich_slow(go_id, geneset, gpw, 'polyenrich_slow', model)
}, mc.cores = n_cores)
# Collapse results into one table
results = Reduce(rbind,results_list)
# Correct for multiple testing
results$FDR = p.adjust(results$P.value, method="BH")
# Create enriched/depleted status column
results$Status = ifelse(results$Effect > 0, 'enriched', 'depleted')
results = results[order(results$P.value),]
return(results)
}
single_polyenrich_slow = function(go_id, geneset, gpw, method, model) {
final_model = as.formula(model)
# Genes in the geneset
go_genes = geneset@set.gene[[go_id]]
# Background genes and the background presence of a peak
b_genes = gpw$gene_id %in% go_genes
sg_go = gpw$peak[b_genes]
# Information about the geneset
r_go_id = go_id
r_go_genes_num = length(go_genes)
r_go_genes_avg_length = mean(gpw$length[b_genes])
# Information about peak genes
go_genes_peak = gpw$gene_id[b_genes][sg_go==1]
r_go_genes_peak = paste(go_genes_peak,collapse=", ")
r_go_genes_peak_num = length(go_genes_peak)
fit = mgcv::gam(final_model,data=cbind(gpw,goterm=as.numeric(b_genes)),family='nb')
# Results from the logistic regression
r_effect = coef(fit)[2]
r_pval = summary(fit)$p.table[2,4]
out = data.frame(
"P.value"=r_pval,
"Geneset ID"=r_go_id,
"N Geneset Genes"=r_go_genes_num,
"Geneset Peak Genes"=r_go_genes_peak,
"N Geneset Peak Genes"=r_go_genes_peak_num,
"Effect"=r_effect,
"Odds.Ratio"=exp(r_effect),
"Geneset Avg Gene Length"=r_go_genes_avg_length,
stringsAsFactors = FALSE)
return(out)
}
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