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3aacd46da2
* backfilled modules with meta.yml that had no license identifier * harmonized BSD license names * whitespace linting at modules/unzip/meta.yml:12 * harmonized software from US NIH-NCBI/NIST to 'US-Government-Work' * Update modules/bcftools/index/meta.yml `bcftools` is dual-licensed, use associative array to allow for multiple licenses Co-authored-by: Michael L Heuer <heuermh@acm.org> Co-authored-by: Michael L Heuer <heuermh@acm.org>
58 lines
1.6 KiB
YAML
58 lines
1.6 KiB
YAML
name: snpEff
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description: Genetic variant annotation and functional effect prediction toolbox
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keywords:
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- annotation
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tools:
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- snpeff:
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description: |
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SnpEff is a variant annotation and effect prediction tool.
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It annotates and predicts the effects of genetic variants on genes and proteins (such as amino acid changes).
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homepage: https://pcingola.github.io/SnpEff/
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documentation: https://pcingola.github.io/SnpEff/se_introduction/
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licence: ['MIT']
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params:
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- use_cache:
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type: boolean
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description: |
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boolean to enable the usage of containers with cache
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Enable the usage of containers with cache
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Does not work with conda
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- snpeff_tag:
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type: value
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description: |
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Specify the tag for the container
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https://hub.docker.com/r/nfcore/snpeff/tags
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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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- vcf:
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type: file
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description: |
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vcf to annotate
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- db:
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type: value
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description: |
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which db to annotate with
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- cache:
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type: file
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description: |
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path to snpEff cache (optional)
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output:
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- vcf:
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type: file
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description: |
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annotated vcf
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pattern: "*.ann.vcf"
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- report:
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type: file
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description: snpEff report file
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pattern: "*.html"
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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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- "@maxulysse"
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