Description

Exclude variant identifiers from plink bfiles

Input

name:type
description
pattern

meta:map

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

]

bed:file

PLINK binary biallelic genotype table

*.{bed}

bim:file

PLINK extended MAP file

*.{bim}

fam:file

PLINK sample information file

*.{fam}

variants:file

A text file containing variant identifiers to remove (one per line)

*.{txt}

Output

name:type
description
pattern

bed

meta:map

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

]

*.bed:file

PLINK binary biallelic genotype table file

*.{bed}

bim

meta:map

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

]

*.bim:file

PLINK extended MAP file

*.{bim}

fam

meta:map

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

]

*.fam:file

PLINK sample information file

*.{fam}

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.