Hey, I want to annotate vcf files from 1000G For further processing using ANNOVAR, i want to extract vcf files of each individual from ALL.chr3.phase1_release_v3.20101123.snps_indels_svs.genotypes.vcf.gz using command (someone told me to use vcftools) .....Which command should I use ? PLEASE HELP!!!
Also, I want to further analyse those files using ANNOVAR. Should I do them seperately or should I give the whole mega vcf file (mentioned above) as input?
P.S : My basic question is whether this extraction process necessary for the overall process of annotation?
THANKS in advance!!!