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Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs
BACKGROUND: Copy number variation (CNV) has been recently identified in human and other mammalian genomes, and there is a growing awareness of CNV's potential as a major source for heritable variation in complex traits. Genomic selection is a newly developed tool based on the estimation of bree...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3091787/ https://ncbi.nlm.nih.gov/pubmed/21114805 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-11-673 |
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