Description

Calculates the fraction of reads from cross-sample contamination based on summary tables from getpileupsummaries. Output to be used with filtermutectcalls.

Input

name:type
description
pattern

meta

:map

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

pileup

:file

File containing the pileups summary table of a tumor sample to be used to calculate contamination.

*.pileups.table

matched

:file

File containing the pileups summary table of a normal sample that matches with the tumor sample specified in pileup argument. This is an optional input.

*.pileups.table

Output

name:type
description
pattern

contamination

meta

:file

File containing the contamination table.

*.contamination.table

*.contamination.table

:file

File containing the contamination table.

*.contamination.table

segmentation

meta

:file

File containing the contamination table.

*.contamination.table

*.segmentation.table

:file

output table containing segmentation of tumor minor allele fractions (optional)

*.segmentation.table

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.