merge gVCF files and perform joint variant calling
meta
Groovy Map containing sample information e.g. [ id:‘test’ ]
gvcfs
Input genomic vcf files
*.{gvcf,gvcf.gz,g.vcf,g.vcf.gz}
versions
File containing software versions
versions.yml
bcf
merged BCF file
*.bcf
scalable gVCF merging and joint variant calling for population sequencing projects.
