Inference of chromosome-specific copy numbers using population haplotypes

BACKGROUND: Using microarray and sequencing platforms, a large number of copy number variations (CNVs) have been identified in humans. In practice, because our human genome is a diploid, these platforms are limited to or more accurate for detecting total copy numbers rather than chromosome-specific...

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Detalles Bibliográficos
Autores principales: Huang, Yao-Ting, Wu, Min-Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128032/
https://www.ncbi.nlm.nih.gov/pubmed/21605463
http://dx.doi.org/10.1186/1471-2105-12-194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128032/
https://www.ncbi.nlm.nih.gov/pubmed/21605463
http://dx.doi.org/10.1186/1471-2105-12-194

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