Description

Left align and trim variants using GATK4 LeftAlignAndTrimVariants.

Input

name:type
description
pattern

meta:map

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

]

vcf:file

The vcf file to be normalized e.g. ‘file1.vcf.gz’

tbi:file

Index of the vcf file to be normalized e.g. ‘file1.vcf.gz.tbi’

intervals:file

Bed file with the genomic regions included in the library (optional)

fasta:file

The reference fasta file

*.fasta

fai:file

Index of reference fasta file

*.fasta.fai

dict:file

GATK sequence dictionary

*.dict

Output

name:type
description
pattern

vcf

meta:map

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

]

*.vcf.gz:file

VCF normalized output file

*.{vcf.gz}

tbi

meta:map

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

]

*.tbi:file

Tbi index for VCF file

*.tbi

versions

versions.yml:file

File containing software versions

versions.yml

Tools

gatk4
Apache-2.0

Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size.

gatk.broadinstitute.org/hc/en-us gatk.broadinstitute.org/hc/en-us/categories/360002369672s 10.1158/1538-7445.AM2017-3590
included in
variantcatalogue
maintainer
Github user adamrtalbot
get in touch
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