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Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins
BACKGROUND: Copy number variations (CNVs) are widespread in the human or animal genome and are a significant source of genetic variation, which has been demonstrated to play an important role in phenotypic diversity. Advances in technology have allowed for identification of a large number of CNVs in...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2013
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3639935/ https://ncbi.nlm.nih.gov/pubmed/23442346 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-14-131 |
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