17 September 2020 0 5K Report

I have found a novel variant in my dataset. In order to solidify my finding, I intend to do some more statistical testing on it, like detection of minor allele frequency in various sub populations. However, most of the tools take in already discovered variants present in dbsnp, 1000 genome and other databases. Are there some tools which help us do this analysis for a novel snp?

I would truly appreciate your suggestions on approaching this problem.

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