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.

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Categories

Bio-Informatics

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Additional Project Details

Operating Systems

Solaris, Linux, Mac

Intended Audience

Science/Research

User Interface

Command-line

Programming Language

Python, S/R

Related Categories

Python Bio-Informatics Software, S/R Bio-Informatics Software

Registered

2009-10-14
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