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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2008
Matèries:
Research Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars