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Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits
BACKGROUND: Copy number variations (CNVs) have been shown to account for substantial portions of observed genomic variation and have been associated with qualitative and quantitative traits and the onset of disease in a number of species. Information from high-resolution studies to detect, character...
Autores principales: | da Silva, Joaquim Manoel, Giachetto, Poliana Fernanda, da Silva, Luiz Otávio, Cintra, Leandro Carrijo, Paiva, Samuel Rezende, Yamagishi, Michel Eduardo Beleza, Caetano, Alexandre Rodrigues |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907077/ https://www.ncbi.nlm.nih.gov/pubmed/27297173 http://dx.doi.org/10.1186/s12864-016-2752-9 |
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