This WDL pipeline implements joint calling across multiple samples according to the GATK Best Practices (June 2016) for germline SNP and Indel discovery in human whole-genome sequencing (WGS) data.
- One or more human whole-genome per-sample GVCF files
VCF Output Files
- output vcf
- output vcf index
VCF Metrics
- detail_metrics file
- summary metrics file
Output the interval list generated/used by this run workflow
- output intervals
This is a pre-release version of the pipeline which does not include a fully runnable example dataset.