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Old 11-06-2013, 02:36 AM   #3
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Location: Hong Kong

Join Date: Mar 2010
Posts: 498

Originally Posted by bw. View Post
Also curious about this. Perhaps they are using pooled normals?
If library prep & sequencer are the same, and the pooled samples are copy-number neutral, it should be possible to get decent results using ExomeCNV.
If I understand correctly, pooled normal only helps for calling CNVs on normal samples in the context of ExomeCNV.

I presume they aren't very nosy about accuracy. As long as it works in their clinical trials, then it is ok. One error can bite their ass though....
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