enrichDGNv {DOSE} | R Documentation

## enrichDGN

### Description

Enrichment analysis based on the DisGeNET (http://www.disgenet.org/)

### Usage

    enrichDGNv(snp, pvalueCutoff = 0.05, pAdjustMethod = "BH", universe,
      minGSSize = 10, maxGSSize = 500, qvalueCutoff = 0.2,
      readable = FALSE)

### Arguments

`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

### Details

given a vector of genes, this function will return the enrichment NCG categories with FDR control

### Value

A `enrichResult` instance

### Author(s)

Guangchuang Yu

### References

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

[Package DOSE version 3.10.2 Index]