Hi all,
Trying to give sense to the big amount of variants detected after exome sequencing, I was figuring out wether is it possible to append HGMD annotations to my VCF data in order to select only those with reported clinical impact.
I've purchased a copy of HGMD pro.
Thank you in advance,
Best
Luis
Trying to give sense to the big amount of variants detected after exome sequencing, I was figuring out wether is it possible to append HGMD annotations to my VCF data in order to select only those with reported clinical impact.
I've purchased a copy of HGMD pro.
Thank you in advance,
Best
Luis
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