Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins

BACKGROUND: Copy number variations (CNVs) are widespread in the human or animal genome and are a significant source of genetic variation, which has been demonstrated to play an important role in phenotypic diversity. Advances in technology have allowed for identification of a large number of CNVs in...

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Detalles Bibliográficos
Autores principales: Jiang, Li, Jiang, Jicai, Yang, Jie, Liu, Xuan, Wang, Jiying, Wang, Haifei, Ding, Xiangdong, Liu, Jianfeng, Zhang, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639935/
https://www.ncbi.nlm.nih.gov/pubmed/23442346
http://dx.doi.org/10.1186/1471-2164-14-131

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639935/
https://www.ncbi.nlm.nih.gov/pubmed/23442346
http://dx.doi.org/10.1186/1471-2164-14-131

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