G-CNV: A GPU-based Tool for Preparing Data to Detect CNVs with Read Depth Methods
Copy Number Variations (CNVs) are the most prevalent types of structural variations (SVs) in the human genome and are involved in a wide range of common human diseases. Different computational methods have been devised to detect this type of SVs and to study how they are implicated in human diseases...
Main Authors: | Andrea eManconi, Emanuele eManca, Alessandro eOrro, Giuliano eArmano, Matteo eGnocchi, Marco eMoscatelli, Luciano eMilanesi |
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Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2015-03-01
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Series: | Frontiers in Bioengineering and Biotechnology |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fbioe.2015.00028/full |
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