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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2008
Gaiak:
Research Article
Sarrera elektronikoa: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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