Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes

BACKGROUND: DNA sequence diversity within the human genome may be more greatly affected by copy number variations (CNVs) than single nucleotide polymorphisms (SNPs). Although the importance of CNVs in genome wide association studies (GWAS) is becoming widely accepted, the optimal methods for identif...

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Detalles Bibliográficos
Autores principales: Shen, Fan, Huang, Jing, Fitch, Karen R, Truong, Vivi B, Kirby, Andrew, Chen, Wenwei, Zhang, Jane, Liu, Guoying, McCarroll, Steven A, Jones, Keith W, Shapero, Michael H
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374799/
https://www.ncbi.nlm.nih.gov/pubmed/18373861
http://dx.doi.org/10.1186/1471-2156-9-27

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374799/
https://www.ncbi.nlm.nih.gov/pubmed/18373861
http://dx.doi.org/10.1186/1471-2156-9-27

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