Hey everyone! I have obtained the 1092 individual sample vcf files after splitting the ALL.chr3.phase1_release_v3.20101123.snps_indels_svs.genotypes.HG00096.vcf.gz from 1000g .
I have to further process and annotate them using ANNOVAR. How can I do it at once? Do I have to take care of the version of the database while downloading?