Question: (Closed) Jointly Detect Somatic Copy Number Variations
0
gravatar for lyz10302012
5.0 years ago by
lyz10302012310
China
lyz10302012310 wrote:

Hi,

Is there any good tools to jointly detect somatic copy number variations (like some tools for SNVs) from tumor-normal paired sequencing data? If not, how can I detect somatic copy number variations using existing common CNV detecting tools?

Thanks

• 2.1k views
ADD COMMENTlink modified 5.0 years ago by Chris Miller20k • written 5.0 years ago by lyz10302012310

Closing this question, as there are many existing threads that answer exactly this query, some of which are linked by Jimbou below.

ADD REPLYlink written 5.0 years ago by Chris Miller20k
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