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5.7 years ago
cocchi.e89
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290
Dear all,
I have to find the predicted effect of a large sample of variants, I know about GnomAD VEP annotation but some of them are absent in GnomAD. How could I try to retrieve those variants effect? Other Databases etc?
PS: I have to integrate it into a pipeline so I need some source database, can not operate just with some webpage consultation
Thanks a lot in advance for any help!
SNV, SV? Coding, non-coding?
basically SNV/INDEL in exome studies, but I would appreciate so much even broader comments