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* Update README * Rename pytest_software.yml to pytest_modules.yml * Rename main software directory to modules * Remove deprecated modules * Rename tests software to modules * Replace paths for tests in pytest_modules.yml * Replace software with modules in Github Actions * Replace software with modules in main.nf tests * Rename software to modules in test.yml
45 lines
1.3 KiB
YAML
45 lines
1.3 KiB
YAML
name: bowtie_align
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description: Align reads to a reference genome using bowtie
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keywords:
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- align
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- fasta
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- genome
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- reference
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tools:
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- bowtie:
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description: |
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bowtie is a software package for mapping DNA sequences against
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a large reference genome, such as the human genome.
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homepage: http://bowtie-bio.sourceforge.net/index.shtml
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documentation: http://bowtie-bio.sourceforge.net/manual.shtml
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arxiv: arXiv:1303.3997
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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: file
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description: |
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List of input FastQ files of size 1 and 2 for single-end and paired-end data,
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respectively.
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- index:
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type: file
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description: Bowtie genome index files
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pattern: "*.ebwt"
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output:
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- bam:
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type: file
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description: Output BAM file containing read alignments
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pattern: "*.{bam}"
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- version:
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type: file
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description: File containing software version
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pattern: "*.{version.txt}"
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- fastq:
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type: file
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description: Unaligned FastQ files
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pattern: "*.fastq.gz"
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authors:
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- "@kevinmenden"
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