Description

Calculate the sequence-accessible coordinates in chromosomes from the given reference genome, output as a BED file.

Input

name:type
description
pattern

meta

:map

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

fasta

:file

Genome FASTA.

*.fasta

meta2

:map

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

exclude_bed

:file

Additional regions to exclude, in BED format. Can be used multiple times.

Output

name:type
description
pattern

bed

meta

:map

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

*.bed

:file

File containing accessible regions.

*.{bed}

versions_cnvkit

${task.process}

:string

The process the versions were collected from

cnvkit

:string

The tool name

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 process the versions were collected from

cnvkit

:string

The tool name

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.