How can I identify common variants in siblings with same disorder after joint calling?
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7 weeks ago
pragnapcu • 0

With the help of GATK GenomicsDBImport and Genotypegvcf, I have jointly called variants in siblings and done hardfiltering. I am puzzled about how to find out common variants in these two samples. Could someone please help me out?

joint calling variants common Shared • 240 views
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