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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Main Authors: Wang, Jiying, Jiang, Jicai, Fu, Weixuan, Jiang, Li, Ding, Xiangdong, Liu, Jian-Feng, Zhang, Qin
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2012
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3464621/
https://ncbi.nlm.nih.gov/pubmed/22726314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-273
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