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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639935/ https://www.ncbi.nlm.nih.gov/pubmed/23442346 http://dx.doi.org/10.1186/1471-2164-14-131 |