View source: R/enrichment_depletion_test.R
enrichment_depletion_test | R Documentation |
This function aggregates mutations per group (optional) and performs an enrichment depletion test.
enrichment_depletion_test(x, by = NA, p_cutoffs = 0.05, fdr_cutoffs = 0.1)
x |
data.frame result from genomic_distribution() |
by |
Optional grouping variable, e.g. tissue type |
p_cutoffs |
Significance cutoff for the p value. Default: 0.05 |
fdr_cutoffs |
Significance cutoff for the fdr. Default: 0.1 |
data.frame with the observed and expected number of mutations per genomic region per group (by) or sample
genomic_distribution
,
plot_enrichment_depletion
## See the 'genomic_distribution()' example for how we obtained the ## following data: distr <- readRDS(system.file("states/distr_data.rds", package = "MutationalPatterns" )) tissue <- c(rep("colon", 3), rep("intestine", 3), rep("liver", 3)) ## Perform the enrichment/depletion test by tissue type. distr_test <- enrichment_depletion_test(distr, by = tissue) ## Or without specifying the 'by' parameter, to pool all samples. distr_single_sample <- enrichment_depletion_test(distr) ## Use different significance cutoffs for the pvalue and fdr distr_strict <- enrichment_depletion_test(distr, by = tissue, p_cutoffs = 0.01, fdr_cutoffs = 0.05 ) ## Use multiple (max 3) significance cutoffs. ## This will vary the number of significance stars. distr_multistars <- enrichment_depletion_test(distr, by = tissue, p_cutoffs = c(0.05, 0.01, 0.005), fdr_cutoffs = c(0.1, 0.05, 0.01) )
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