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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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| Główni autorzy: | , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BioMed Central
2012
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| Hasła przedmiotowe: | |
| Dostęp 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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