Hi I'm studying about sequencing data analysis. I have performed variant calling pipeline, and finally got two group of variants. one is experimental group, the other is control group. I have to know what kind of changes occurred to the experimental group. so I need to remove overlapping variants in two group. I performed SelectVariants in GATK and vcfremovesample in vcflib. but result showed same variants number after analysis. is there another method to remove overlapping variants in two group? I will be happy if anybody suggest me idea regarding this. Thank you.