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This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and Indel discovery in human exome sequencing data.

License: BSD 3-Clause "New" or "Revised" License

WDL 100.00%

gatk4-exome-analysis-pipeline's Introduction

gatk4-exome-analysis-pipeline

Purpose :

This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and Indel discovery in human exome sequencing data.

Requirements/expectations :

  • Human exome sequencing data in unmapped BAM (uBAM) format
  • One or more read groups, one per uBAM file, all belonging to a single sample (SM)
  • Input uBAM files must additionally comply with the following requirements:
    • filenames all have the same suffix (we use ".unmapped.bam")
    • files must pass validation by ValidateSamFile
    • reads are provided in query-sorted order
    • all reads must have an RG tag
  • GVCF output names must end in ".g.vcf.gz"
  • Reference genome must be Hg38 with ALT contigs
  • Unique exome calling, target, and bait .interval_list obtained from sequencing provider. Generally the calling, target, and bait files will not be the same.

Output :

  • Cram, cram index, and cram md5
  • GVCF and its gvcf index
  • BQSR Report
  • Several Summary Metrics

Software version notes :

  • GATK 4 or later
  • Cromwell version support
    • Successfully tested on v36
    • Does not work on versions < v23 due to output syntax

Important Note :

LICENSING :

Copyright Broad Institute, 2018 | BSD-3

This script is released under the WDL open source code license (BSD-3) (full license text at https://github.com/openwdl/wdl/blob/master/LICENSE). Note however that the programs it calls may be subject to different licenses. Users are responsible for checking that they are authorized to run all programs before running this script.

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