Description

Derive off-target (“antitarget”) bins from target regions.

Input

name:type
description
pattern

meta

:map

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

targets

:file

File containing genomic regions

*.{bed}

Output

name:type
description
pattern

bed

meta

:map

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

*.bed

:file

File containing off-target regions

*.{bed}

versions_cnvkit

${task.process}

:string

The name of the process

cnvkit

:string

The name of the tool

cnvkit.py version | sed -e "s/cnvkit v//g"

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

The name of the process

cnvkit

:string

The name of the tool

cnvkit.py version | sed -e "s/cnvkit v//g"

:eval

The expression to obtain the version of the tool

Tools

cnvkit
Apache-2.0

CNVkit is a Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina and Ion Torrent.