Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.

Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.

Accurate and efficient genome-wide detection of copy number variants (CNVs) is essential for understanding human genomic variation, genome-wide CNV association type studies, cytogenetics research and diagnostics, and independent validation of CNVs identified from sequencing based technologies. Numer...

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Bibliographic Details
Main Authors: Rajini R Haraksingh, Alexej Abyzov, Mark Gerstein, Alexander E Urban, Michael Snyder
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3227574?pdf=render

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