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Old 02-20-2012, 06:31 AM   #1
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Location: Berlin

Join Date: Feb 2012
Posts: 1
Default Manipulating normal samples for CNV analysis

Dear all,

I have exome sequence data for about 100 patients. I found some tools like VarScan, ExomeCNV etc for CNV analysis. But they all need normal individual data also. Now I managed to get 10 normal samples. My question is -> should I randomly select any 1 normal sample for CNV analysis or is there any way to use all these normal samples as 1 sample?

Any suggestions?

vikasbansal is offline   Reply With Quote

copy number, exome analysis, varscan

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