AB CNV Tool

Description

• The SOLiDTM System software tool SOLiD Human Copy Number Variation v0.1 is designed to detect copy number variation using SOLiD data from a single human sample mapped to the human reference sequence hg18. The program detects copy number variations (CNVs) in SOLiD run of a single human sample without the need for a matched reference sample.

Licensing

• This software is being licensed to you under the OSI compliant GNU Public License (GPL). Please read the license in its entirety and ensure that you understand the licensing conditions for use. Your use of this software indicates your acceptance of this licensing agreement. Click on this link to read the licensing agreement.

Support

• This tool is being released as "unsupported software" by Applied Biosystems

Packages

Pre-Bioscope™ Tool

• The current version of the tool can be downloaded here . Download required mappability files and reference sequences here. See documentation for details.
• Documentation and Release notes for this software can be found here
• A sample dataset can be downloaded here

Source Distribution (please note that this is a source ONLY distribution of a Bioscope algorithm and available through SVN checkout)

• Please contact website support to recieve access information
• The current version of the source can be downloaded here
• Documentation and Release notes for this software can be found here
• A sample dataset can be downloaded here