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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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Wang, Jiying, Jiang, Jicai, Fu, Weixuan, Jiang, Li, Ding, Xiangdong, Liu, Jian-Feng, Zhang, Qin
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2012
Sujets:
Research Article
Accès en ligne: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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