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2.9 years ago
soniabedi.07
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30
I have performed WES with human sample followed by variant calling by Mutect2 and variant annotations. I am looking at few genes of interest, the problem is that even for those few genes I am getting a lot of variants. Is there any basis of shortlisting variants with probable deleterious impact?? Any suggestions??
search this site for VEP, snpEff, annovar....