nf-core_modules/modules/rtgtools/vcfeval/meta.yml

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name: "rtgtools_vcfeval"
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description: The VCFeval tool of RTG tools. It is used to evaluate called variants for agreement with a baseline variant set
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keywords:
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- benchmarking
- vcf
- rtg-tools
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tools:
- "rtgtools":
description: "RealTimeGenomics Tools -- Utilities for accurate VCF comparison and manipulation"
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homepage: "https://www.realtimegenomics.com/products/rtg-tools"
documentation: "https://github.com/RealTimeGenomics/rtg-tools"
tool_dev_url: "https://github.com/RealTimeGenomics/rtg-tools"
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doi: ""
licence: "['BSD']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
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- truth_vcf:
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type: file
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description: A standard VCF to compare against
pattern: "*.{vcf,vcf.gz}"
- truth_vcf_index:
type: file
description: The index of the standard VCF (optional)
pattern: "*.tbi"
- query_vcf:
type: file
description: A VCF with called variants to benchmark against the standard
pattern: "*.{vcf,vcf.gz}"
- query_vcf_index:
type: file
description: The index of the called VCF (optional)
pattern: "*.tbi"
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- truth_regions:
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type: file
description: A BED file containining the strict regions where VCFeval should only evaluate the fully overlapping variants (optional)
pattern: "*.bed"
- evaluation_regions:
type: file
description: A BED file containing the regions where VCFeval will evaluate every fully and partially overlapping variant (optional)
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pattern: "*.bed"
- sdf:
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type: file
description: The SDF (RTG Sequence Data File) folder of the reference genome
pattern: "*"
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output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
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- results:
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type: file
description: A folder containing all results of the evaluation
pattern: "*"
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authors:
- "@nvnieuwk"