RDXplorer 3.2 – CNVs Detection in Whole Human Genome Sequence data

RDXplorer 3.2

:: DESCRIPTION

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.

::DEVELOPER

vlad makarov

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 RDXplorer

:: MORE INFORMATION

Leave a Reply

Your email address will not be published. Required fields are marked *

 

This site uses Akismet to reduce spam. Learn how your comment data is processed.