Home | BioWDL: jointgenotyping

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The workflow can be used to aggregate and genotype GVCF files for multiple samples using GATK’s GenotypeGVCFs.

This workflow is part of BioWDL developed by the SASC team.

Usage

This workflow can be run using Cromwell:

java -jar cromwell-<version>.jar run -i inputs.json jointgenotyping.wdl

Inputs

Inputs are provided through a JSON file. The minimally required inputs are described below and a template containing all possible inputs can be generated using Womtool as described in the WOMtool documentation. See this page for some additional general notes and information about pipeline inputs.

{
  "JointGenotyping.gvcfFiles": "A list of GVCF files and their indexes (see the example)",
  "JointGenotyping.dbsnpVCF": {
    "file": "A dbSNP VCF file",
    "index": "The index (.tbi) for the dbSNP VCF file"
  },
  "JointGenotyping.outputDir": "The path to the output directory",
  "JointGenotyping.reference": {
    "fasta": "A reference fasta file",
    "fai": "The index for the reference fasta",
    "dict": "The dict file for the reference fasta"
  }
}

Some additional inputs that may be of interest are:

{
  "JointGenotyping.mergeGvcfFiles": "Whether or not to output a merged GVCF files, defaults to true",
  "JointGenotyping.scatterSize": "The size of scatter regions (see explanation of scattering below), defaults to 10,000,000",
  "JointGenotyping.vcfBasename": "The basename of the to be outputed VCF files, defaults to 'multisample'",
  "JointGenotyping.scatterList.regions": "The path to a bed file containing the regions be processed"
}

Example

{
  "JointGenotyping.gvcfFiles": [
    {
      "file": "/home/user/analysis/results/s1.vcf.gz",
      "index": "/home/user/analysis/results/s1.vcf.gz.tbi"
    }, {
      "file": "/home/user/analysis/results/s2.vcf.gz",
      "index": "/home/user/analysis/results/s2.vcf.gz.tbi"
    }
  ],
  "JointGenotyping.dbsnpVCF": {
    "file": "/home/user/genomes/human/dbsnp/dbsnp-151.vcf.gz",
    "index": "/home/user/genomes/human/dbsnp/dbsnp-151.vcf.gz.tbi"
  },
  "JointGenotyping.outputDir": "/home/user/analysis/results/genotyping",
  "JointGenotyping.reference": {
    "fasta": "/home/user/genomes/human/GRCh38.fasta",
    "fai": "/home/user/genomes/human/GRCh38.fasta.fai",
    "dict": "/home/user/genomes/human/GRCh38.dict"
  }
}

Dependency requirements and tool versions

Included in the repository is an environment.yml file. This file includes all the tool version on which the workflow was tested. You can use conda and this file to create an environment with all the correct tools.

Output

A multisample VCF file. If mergeGvcfFiles is set to true, also a multisample GVCF file.

scattering

This pipeline performs scattering to speed up analysis on grid computing clusters. This is done by splitting the reference genome into regions of roughly equal size (see the scatterSize input). Each of these regions will be analyzed in separate jobs, allowing them to be processed in parallel.

Contact

For any question about running this workflow or feature requests, please use the github issue tracker or contact the SASC team directly at: sasc@lumc.nl.