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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Autori principali: Haraksingh, Rajini R., Abyzov, Alexej, Gerstein, Mark, Urban, Alexander E., Snyder, Michael
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2011
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3227574/
https://ncbi.nlm.nih.gov/pubmed/22140474
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0027859
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