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81ed0e0ff2
* added meta.yml for umitools * Update modules/umitools/dedup/meta.yml type: list --> type: file Co-authored-by: Harshil Patel <drpatelh@users.noreply.github.com> * Update modules/umitools/dedup/meta.yml aww thanks @drpateh :D Co-authored-by: Harshil Patel <drpatelh@users.noreply.github.com> * Update modules/umitools/dedup/meta.yml module can only handle one BAM at a time, ergo BAM files --> BAM file Co-authored-by: Harshil Patel <drpatelh@users.noreply.github.com> * Update meta.yml added `pattern` for input `bam` and `bai` * removed trailing whitespace to appease linter * added license to new meta.yml files * Apply suggestions from code review Co-authored-by: Harshil Patel <drpatelh@users.noreply.github.com>
46 lines
1.4 KiB
YAML
46 lines
1.4 KiB
YAML
name: umitools_extract
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description: Extracts UMI barcode from a read and add it to the read name, leaving any sample barcode in place
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keywords:
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- umitools
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- extract
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tools:
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- umi_tools:
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description: >
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UMI-tools contains tools for dealing with Unique Molecular Identifiers (UMIs)/Random Molecular Tags (RMTs)
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and single cell RNA-Seq cell barcodes
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documentation: https://umi-tools.readthedocs.io/en/latest/
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license: ['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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- reads:
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type: list
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description: |
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List of input FASTQ files whose UMIs will be extracted.
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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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- reads:
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type: file
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description: Extracted FASTQ files. |
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For single-end reads, pattern is \${prefix}.umi_extract.fastq.gz. |
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For paired-end reads, pattern is \${prefix}.umi_extract_{1,2}.fastq.gz.
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pattern: "*.{fastq.gz}"
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- log:
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type: file
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description: Logfile for umi_tools
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pattern: "*.{log}"
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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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- "@drpatelh"
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- "@grst"
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