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nf-core/cnvkit/genemetrics @ 0.0.0-0c7146d

Copy number variant detection from high-throughput sequencing data

Latest version: 0.0.0-0c7146d
Total downloads: 1
Source: nf-core/modules

Summary

Copy number variant detection from high-throughput sequencing data

Get started

Add the following snippet to your workflow script to include this module.

include { CNVKIT_GENEMETRICS } from 'nf-core/cnvkit/genemetrics'

License

MIT License

Process
Name CNVKIT_GENEMETRICS
Input 1 channel
#1 tuple
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 2 channels
#1 tsv tuple
meta map

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

*.tsv file

TSV file

*.tsv
#2 versions_cnvkit tuple
${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

Tool Description Homepage
cnvkit 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. https://cnvkit.readthedocs.io/en/stable/index.html
Version 0.0.0-0c7146d
Commit ID 135d883a43b1a2324b4112cd270cf22e20835533
Release Date 08 Apr 2026 18:31:49 (UTC)
Download URL https://registry-stage.nextflow.io/api/v1/modules/nf-core%2Fcnvkit%2Fgenemetrics/0.0.0-0c7146d/download
OCI Store URL https://public.cr.stage-seqera.io/v2/nextflow/plugin-stage/modules/nf-core/cnvkit/genemetrics/blobs/sha256:5addad045ffa5465e82297f626cf29071576d53c886726bb2a22b1d3ecde6e98
Size 2.4 KB
Checksum sha256:5addad045ffa5465e82297f626cf29071576d53c886726bb2a22b1d3ecde6e98
Downloads 1
Version Date Status Downloads Size Diff
0.0.0-0c7146d 08 Apr 2026 18:31:49 (UTC) 1 2.4 KB -