enrichDGNv | R Documentation |
Enrichment analysis based on the DisGeNET (http://www.disgenet.org/)
enrichDGNv(
snp,
pvalueCutoff = 0.05,
pAdjustMethod = "BH",
universe,
minGSSize = 10,
maxGSSize = 500,
qvalueCutoff = 0.2,
readable = FALSE
)
snp |
a vector of SNP |
pvalueCutoff |
pvalue cutoff |
pAdjustMethod |
one of "holm", "hochberg", "hommel", "bonferroni", "BH", "BY", "fdr", "none" |
universe |
background genes |
minGSSize |
minimal size of genes annotated by NCG category for testing |
maxGSSize |
maximal size of each geneSet for analyzing |
qvalueCutoff |
qvalue cutoff |
readable |
whether mapping gene ID to gene Name |
given a vector of genes, this function will return the enrichment NCG categories with FDR control
A enrichResult
instance
Guangchuang Yu
Janet et al. (2015) DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes. Database bav028 http://database.oxfordjournals.org/content/2015/bav028.long
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