name: "rtgtools_vcfeval"
description: The VCFeval tool of RTG tools. It is used to evaluate called variants for agreement with a baseline variant set
keywords:
  - benchmarking
  - vcf
  - rtg-tools
tools:
  - "rtgtools":
      description: "RealTimeGenomics Tools -- Utilities for accurate VCF comparison and manipulation"
      homepage: "https://www.realtimegenomics.com/products/rtg-tools"
      documentation: "https://github.com/RealTimeGenomics/rtg-tools"
      tool_dev_url: "https://github.com/RealTimeGenomics/rtg-tools"
      doi: ""
      licence: "['BSD']"

input:
  - meta:
      type: map
      description: |
        Groovy Map containing sample information
        e.g. [ id:'test', single_end:false ]
  - truth_vcf:
      type: file
      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"
  - bed:
      type: file
      description: The BED file of the called VCF
      pattern: "*.bed"
  - sdf:
      type: folder/file
      description: The SDF (RTG Sequence Data File) of the reference genome. Can be a folder or a tar-zipped folder.
      pattern: "*.{,tar.gz}"

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"
  - results:
      type: file
      description: A text file containing the results of the benchmark
      pattern: "*.txt"

authors:
  - "@nvnieuwk"