RDXplorer
The RDXplorer (Read Depth eXplorer) is a computational tool based on LINUX/UNIX/MAC OS X for copy number variants (CNV) detection in whole human genome sequence data using read depth (RD) coverage. It requires SAMtools and Python programming language v 2.6 or further. Registration not required.
Published on 2012-01-18 06:17:49 - Click here to edit or to add informations
Category: Sequencing and assembly software
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