Description

Calculates the allele-specific read counts for allele-specific expression analysis of RNAseq data

Input

name:type
description
pattern

meta

:map

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

bam

:file

BAM file

*.{bam}

bai

:file

index file for BAM file

*.{bai}

vcf

:file

VCF file

*.{vcf.gz}

tbi

:file

index file for VCF file

*.{vcf.gz.tbi}

meta2

:map

Groovy Map containing reference information e.g. [ id:'reference' ]

fasta

:file

fasta file

*.{fasta,fa}

meta3

:map

Groovy Map containing reference information e.g. [ id:'reference' ]

fai

:file

fasta index file

*.{fai}

meta4

:map

Groovy Map containing reference information e.g. [ id:'reference' ]

dict

:file

dictionary file

*.{dict}

intervals

:file

interval file

Output

name:type
description
pattern

csv

meta

:map

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

versions_gatk4

${task.process}

:string

The name of the process

gatk4

:string

The name of the tool

gatk --version | sed -n '/GATK.*v/s/.*v//p'

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

The name of the process

gatk4

:string

The name of the tool

gatk --version | sed -n '/GATK.*v/s/.*v//p'

:eval

The expression to obtain the version of the tool

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.