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Hello,
I used snpeff to annotate a set of variants and I would like to only visualize where a particular type of variant (non-synonymous mutations) localize on the chromosomes in the IGV.
Is there a method for doing this from the vcf file or do I need to extract the non-synonymous variants first?
cheers,
Charles
I used snpeff to annotate a set of variants and I would like to only visualize where a particular type of variant (non-synonymous mutations) localize on the chromosomes in the IGV.
Is there a method for doing this from the vcf file or do I need to extract the non-synonymous variants first?
cheers,
Charles