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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Bibliografski detalji
Glavni autori: Wang, Jiying, Jiang, Jicai, Fu, Weixuan, Jiang, Li, Ding, Xiangdong, Liu, Jian-Feng, Zhang, Qin
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2012
Teme:
Research Article
Online pristup: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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