Description

Genetic variant annotation and functional effect prediction toolbox

Input

Name (Type)
Description
Pattern

meta (map)

Groovy Map containing sample information
e.g. [ id:‘test’, single_end

]

vcf (file)

vcf to annotate

db (string)

which db to annotate with

cache (file)

path to snpEff cache (optional)

Output

Name (Type)
Description
Pattern

vcf (file)

annotated vcf

*.ann.vcf

report (file)

snpEff report csv file

*.csv

summary_html (file)

snpEff summary statistics in html file

*.html

genes_txt (file)

txt (tab separated) file having counts of the number of variants affecting each transcript and gene

*.genes.txt

versions (file)

File containing software versions

versions.yml

Tools

snpeff
MIT

SnpEff is a variant annotation and effect prediction tool. It annotates and predicts the effects of genetic variants on genes and proteins (such as amino acid changes).