Description

Transform bait intervals into targets more suitable for CNVkit.

Input

name:type
description
pattern

meta

:map

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

baits

:file

BED or interval file listing the targeted regions.

*.{bed}

meta2

:map

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

annotation

:file

Use gene models from this file to assign names to the target regions.

*.{txt,bed,gff3,pil}

Output

name:type
description
pattern

bed

meta

:map

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

*.bed

:file

File containing 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.