Entering edit mode
23 days ago
Chen
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0
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:).
I don't understand your question. a DOC is the average depth , a CNV is a variation.
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!