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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2374799/
https://ncbi.nlm.nih.gov/pubmed/18373861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-9-27
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