Hello all ,
I have a multi sample vcf file of 1000 individuals for one gene . Some of the samples do not have any variants in them like "0/0".I want to filter them out and keep only the samples with variants associated like "0/1" and "1/1".How can I do this .Kindly give a command and tool for the same .
you could use
bcftools viewfor that, check the doc here: http://samtools.github.io/bcftools/bcftools.html#view
Thanks you .What command should I precisely use from that ?