Varianttools

From Cheaha
Revision as of 15:44, 4 April 2012 by Tanthony@uab.edu (talk | contribs) (added category bioinformatics NGS)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search


Attention: Research Computing Documentation has Moved
https://docs.rc.uab.edu/


Please use the new documentation url https://docs.rc.uab.edu/ for all Research Computing documentation needs.


As a result of this move, we have deprecated use of this wiki for documentation. We are providing read-only access to the content to facilitate migration of bookmarks and to serve as an historical record. All content updates should be made at the new documentation site. The original wiki will not receive further updates.

Thank you,

The Research Computing Team

This page is a Generic stub.

You can help by expanding this page..


variant tools is a software tool for the annotation, selection, and analysis of variants in the context of next-gen sequencing analysis. This tool is designed around the manipulation of variant tables that simplify the tracking of variants (SNV, insertion, deletion, and other complex types) and the samples that they were detected in.

Project website: http://varianttools.sourceforge.net/Main/HomePage

Load SGE module

The following Modules files should be loaded for this package:

module load varianttools/vtools-1.0.1b_patched