mirror of
https://github.com/MillironX/nf-core_modules.git
synced 2024-12-23 03:28:17 +00:00
45 lines
1.3 KiB
YAML
45 lines
1.3 KiB
YAML
|
name: cnvkit_antitarget
|
||
|
description:
|
||
|
keywords:
|
||
|
- cvnkit
|
||
|
- antitarget
|
||
|
tools:
|
||
|
- cnvkit:
|
||
|
description: |
|
||
|
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.
|
||
|
homepage: https://cnvkit.readthedocs.io/en/stable/index.html
|
||
|
documentation: https://cnvkit.readthedocs.io/en/stable/index.html
|
||
|
tool_dev_url: "https://github.com/etal/cnvkit"
|
||
|
doi: 10.1371/journal.pcbi.1004873
|
||
|
licence: ["Apache-2.0"]
|
||
|
|
||
|
input:
|
||
|
- meta:
|
||
|
type: map
|
||
|
description: |
|
||
|
Groovy Map containing sample information
|
||
|
e.g. [ id:'test', single_end:false ]
|
||
|
- targets:
|
||
|
type: file
|
||
|
description: File containing genomic regions
|
||
|
pattern: "*.{bed}"
|
||
|
|
||
|
output:
|
||
|
- meta:
|
||
|
type: map
|
||
|
description: |
|
||
|
Groovy Map containing sample information
|
||
|
e.g. [ id:'test', single_end:false ]
|
||
|
- bed:
|
||
|
type: file
|
||
|
description: File containing off-target regions
|
||
|
pattern: "*.{bed}"
|
||
|
- versions:
|
||
|
type: file
|
||
|
description: File containing software versions
|
||
|
pattern: "versions.yml"
|
||
|
|
||
|
authors:
|
||
|
- "@SusiJo"
|