Description

Copy number variant detection from high-throughput sequencing data

Input

name:type
description
pattern

meta

:map

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

cnr

:file

CNR file

*.cnr

cns

:file

CNS file [Optional]

*.cns

Output

name:type
description
pattern

tsv

meta

:map

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

*.tsv

:file

TSV file

*.tsv

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.