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.
RDXplorer is a free software application from the Other subcategory, part of the Education category.
The app is currently available in English and it was last updated on 2011-02-02. The program can be installed on OS X
RDXplorer (version ) is available for download from our website.
Just click the green Download button above to start. Until now the program was downloaded 86 times.
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