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Inquiry about depth of coverage and copy number variation

Hi, everyone. I was wondering how we could distinguish depth of coverage and copy number variation when it comes to a specific gene when doing the analysis. Thanks:).

number copy cnv sequencing depth variation
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written by Chen 0

I don't understand your question. a DOC is the average depth , a CNV is a variation.

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written by Pierre Lindenbaum 17K

Thanks Pierre, I was actually thinking about the duplicate PCR reads and didn't explain it properly. I have found a post mentioning that question. Thank you!

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written by Chen 0

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