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...

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Detalhes bibliográficos
Publicado no:Front Bioeng Biotechnol
Main Authors: Manconi, Andrea, Manca, Emanuele, Moscatelli, Marco, Gnocchi, Matteo, Orro, Alessandro, Armano, Giuliano, Milanesi, Luciano
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2015
Assuntos:
Bioengineering and Biotechnology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4354384/
https://ncbi.nlm.nih.gov/pubmed/25806367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fbioe.2015.00028
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