Hi All,
I have cases and controls the we exome sequenced and the question is what are the variants that we see in cases but not in controls (some these individuals are related). I want to know your opinions and if there are tools out there that can be used to filter the variants and answer the question.
thanks
I have cases and controls the we exome sequenced and the question is what are the variants that we see in cases but not in controls (some these individuals are related). I want to know your opinions and if there are tools out there that can be used to filter the variants and answer the question.
thanks
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