SnpEff: SnpEff

View source: R/SnpEff.R

SnpEffR Documentation

SnpEff

Description

Function to make the SnpEff-based vcf readable by extracting the functional annotation and splitting each gene transcript into single rows.

Usage

SnpEff(vcf,modifier=F,amino=F,rm_dup=T)

Arguments

vcf

SnpEff-based annotated vcf file

modifier

if TRUE variants with no impact on gene will be removed

amino

if TRUE variants that do not change the amino acid sequence will be removed

rm_dup

if TRUE duplicated transcripts for each variant will be removed

Examples

SnpEff(vcf,modifier=F,amino=F,rm_dup=T)

mdelcorvo/rgumbo documentation built on Jan. 3, 2025, 2:12 p.m.