Entering edit mode
10.4 years ago
nilakshafreezon
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120
I have developed a pipeline for variant calling from exome sequence data, and I currently use ANNOVAR to annotate the obtained variants. But I would like to extend my analysis further with pharmacogenomic data as well. PharmGKB is a good source but it does not have any annotation facilities. Anybody know a good tool to do this or any alternative approach is highly appreciated. :)
Thanks in advance.
Thanks I'll look at it