Description

Generate Hardy-Weinberg statistics for provided input

Input

name:type
description
pattern

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ] meta is associated to PLINK native files input

bed:file

PLINK binary biallelic genotype table file

*.{bed}

bim:file

PLINK extended MAP file

*.{bim}

fam:file

PLINK sample information file

*.{fam}

meta2:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ] meta2 is associated to VCF files input

vcf:file

VCF format input file

*.{vcf} | *{vcf.gz}

meta3:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ] meta is associated to BCF files input

bcf:file

BCF format input file

*.{bcf}

Output

name:type
description
pattern

hwe

meta:map

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

*.hwe:file

Summary file containing observed vs expected heterozygous frequencies and the p-value of the hardy-weinberg statistics

versions

versions.yml:file

File containing software versions

versions.yml

Tools

plink
GPL

Whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner.