asked 2017-04-26 05:27:54 -0600

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Dear all, Maybe this is a naive question but I want to ask you what theshould you use in read depth to consider that the variant may indeed be worth for further study (sanger sequence)and it's not a false result?

I read about 20, I don't remember where, but I'm not sure if is a good limit or not. Thank you

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