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https://github.com/MillironX/nf-core_modules.git
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b5aa12ad3b
* new module: samtools/getrg * add output file to stub * add missing config * Intentionally break prettier linting * [automated] Fix linting with Prettier Co-authored-by: Phil Ewels <phil@seqera.io> Co-authored-by: nf-core-bot <core@nf-co.re>
43 lines
1.2 KiB
YAML
43 lines
1.2 KiB
YAML
name: samtools_getrg
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description: filter/convert SAM/BAM/CRAM file
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keywords:
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- view
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- bam
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- sam
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- cram
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- readgroup
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tools:
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- samtools:
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description: |
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SAMtools is a set of utilities for interacting with and post-processing
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short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li.
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These files are generated as output by short read aligners like BWA.
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homepage: http://www.htslib.org/
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documentation: hhttp://www.htslib.org/doc/samtools.html
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doi: 10.1093/bioinformatics/btp352
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licence: ["MIT"]
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input:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- input:
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type: file
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description: BAM/CRAM/SAM file
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pattern: "*.{bam,cram,sam}"
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output:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- readgroup:
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type: stdout
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description: File containing readgroup string(s)
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- versions:
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type: file
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description: File containing software versions
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pattern: "versions.yml"
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authors:
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- "@matthdsm"
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