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This is is a modular, test driven website that tries to break web clients of all kind. If you are developing applications that interact with websites you might want to throw it at this website first and see if it survives.
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.