Hello,
I work on merging GVCF files. Each sample has undergone HaplotypeCaller, and GVCF files were created by chromosome. Now, I have 24 GVCF files per sample and I want to merge them into a single GVCF file per sample. Eventually, I am going to use GVCF files in GenomicsDBImport and then do GenotypeGVCFs for joint calling.
To merge GVCFs, some papers have done this by using MergeVcfs (as in https://www.nature.com/articles/s41586-022-04965-x) and some resources recommend CombineGVCFs. What is the efficient way to merge GVCFs: using CombineGVCFs
or MergeVcfs
?
in the supplemental materials of that UKBB paper they actually do mention MergeVcfs but it must be a typo