High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians

BACKGROUND: Copy number variants (CNVs) account for a large proportion of genetic variation in the genome. The initial discoveries of long (> 100 kb) CNVs in normal healthy individuals were made on BAC arrays and low resolution oligonucleotide arrays. Subsequent studies that used higher resolutio...

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Detalles Bibliográficos
Autores principales: Matsuzaki, Hajime, Wang, Pei-Hua, Hu, Jing, Rava, Rich, Fu, Glenn K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091319/
https://www.ncbi.nlm.nih.gov/pubmed/19900272
http://dx.doi.org/10.1186/gb-2009-10-11-r125

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091319/
https://www.ncbi.nlm.nih.gov/pubmed/19900272
http://dx.doi.org/10.1186/gb-2009-10-11-r125

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