Off topic:Jointly Detect Somatic Copy Number Variations
0
0
Entering edit mode
11.4 years ago
lyz10302012 ▴ 480

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

• 3.0k views
ADD COMMENT
This thread is not open. No new answers may be added
Traffic: 2414 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6