The RDXplorer is a computational tool for copy number variants (CNV) detection in whole human genome sequence data using read depth (RD) coverage. CNV detection is based on the Event-Wise Testing (EWT) algorithm recently published by our group.
VERSION HISTORY
- Version files posted on 2011-02-02
Several fixes and updates - Version N/A posted on 2011-02-02
Program Details
- Category: Education > Other
- Publisher: rdxplorer.sf.net
- License: Free
- Price: N/A
- Version: Array
- Platform: linux