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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMC Genet |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2016
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| Θέματα: | |
| Διαθέσιμο Online: | 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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