Genome-wide identification of copy number variation using high-density single-nucleotide polymorphism array in Japanese Black cattle

BACKGROUND: Copy number variation (CNV) is an important source of genetic variability associated with phenotypic variation and disease susceptibility. Comprehensive genome-wide CNV maps provide valuable information for genetic and functional studies. To identify CNV in Japanese Black cattle, we perf...

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Detaylı Bibliyografya
Yayımlandı:BMC Genet
Asıl Yazarlar: Sasaki, Shinji, Watanabe, Toshio, Nishimura, Shota, Sugimoto, Yoshikazu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2016
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4727303/
https://ncbi.nlm.nih.gov/pubmed/26809925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12863-016-0335-z
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