A genome-wide detection of copy number variations using SNP genotyping arrays in swine

BACKGROUND: Copy Number Variations (CNVs) have been shown important in both normal phenotypic variability and disease susceptibility, and are increasingly accepted as another important source of genetic variation complementary to single nucleotide polymorphism (SNP). Comprehensive identification and...

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Detalles Bibliográficos
Autores principales: Wang, Jiying, Jiang, Jicai, Fu, Weixuan, Jiang, Li, Ding, Xiangdong, Liu, Jian-Feng, Zhang, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464621/
https://www.ncbi.nlm.nih.gov/pubmed/22726314
http://dx.doi.org/10.1186/1471-2164-13-273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464621/
https://www.ncbi.nlm.nih.gov/pubmed/22726314
http://dx.doi.org/10.1186/1471-2164-13-273

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