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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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Bibliografiske detaljer
Main Authors: Wang, Jiying, Jiang, Jicai, Fu, Weixuan, Jiang, Li, Ding, Xiangdong, Liu, Jian-Feng, Zhang, Qin
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2012
Fag:
Online adgang: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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