Since its introduction in 2011 the variant call format (VCF) has been widely adopted for processing DNA and RNA variants in practically all population studies-as well as in somatic and germline mutation studies. The VCF format can represent single nucleotide variants. multi-nucleotide variants. insertions and deletions. https://www.hindigyanvishv.com/limited-stock-No-Face-No-Case-Logo-T-Shirt-special-save/