Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans

BACKGROUND: High-resolution microarray technology is routinely used in basic research and clinical practice to efficiently detect copy number variants (CNVs) across the entire human genome. A new generation of arrays combining high probe densities with optimized designs will comprise essential tools...

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Publicat a:BMC Genomics
Autors principals: Haraksingh, Rajini R., Abyzov, Alexej, Urban, Alexander Eckehart
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2017
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5402652/
https://ncbi.nlm.nih.gov/pubmed/28438122
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-3658-x
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