View source: R/enriched_pathways.R
enriched_pathways | R Documentation |
returns pathways from enrichR
enriched_pathways( genes, drop_terms = c("User", "Enrichr"), keep_terms = c(), dbs = NULL, cutoff = 0.05, min_N = 2, remove_old = TRUE, libraries = c("Transcription", "Pathways"), plot_cap = 20, plot_pcutoff = 0.01, plot_colour = "Combined.Score", plot_x = "P.value", plot_vline = NA, check_for_updates = TRUE )
genes |
List of gene names |
drop_terms |
terms in databases not to search. If NULL only keep_terms used |
keep_terms |
terms in databases to search. If NULL only all except drop_terms used |
dbs |
database of enrichR pathways. If NULL all are selected minus those removed by drop_terms. See listEnrichrDbs(). |
cutoff |
pvalue cutoff |
min_N |
minimum number of genes to consider |
remove_old |
Whether to remove legacy libraries () |
libraries |
Which type of libraries to check for enrichment. Options include c('Transcription', 'Pathways', 'Ontologies', 'Diseases_Drugs', 'Cell_Types', 'Misc')) |
plot_cap |
Maximum number of terms to plot |
plot_pcutoff |
Pvalue cutoff for plotting |
plot_colour |
Parameter for the colour scaling |
plot_x |
Parameter to plot on the x-axis |
plot_vline |
Position for vertical line |
check_for_updates |
Whether to check for updates in the enrichR database |
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