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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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2012
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| Θέματα: | |
| Διαθέσιμο Online: | 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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