I just have a query that ,is it feasible to split the multi sample annotated vcf file for a particular protein (samples are from 1000g) into separate vcf files for clear view because what I need to get is only the mutations and the samples in which they are present . I am very new to the vcf file format .I have annotated the file with vep-ensembel. Now I need to analyze that file for mutation in each sample. Can you kindly give me the way where I can get the sample names for each mutation in a much sorted manner as this annotated file is very huge .Any script or command to filter the file in this way .
Thanks and regards