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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Detalles Bibliográficos
Autores principales: Seroussi, Eyal, Glick, Giora, Shirak, Andrey, Yakobson, Emanuel, Weller, Joel I, Ezra, Ephraim, Zeron, Yoel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091787/
https://www.ncbi.nlm.nih.gov/pubmed/21114805
http://dx.doi.org/10.1186/1471-2164-11-673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091787/
https://www.ncbi.nlm.nih.gov/pubmed/21114805
http://dx.doi.org/10.1186/1471-2164-11-673

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