Genomic characteristics of cattle copy number variations

BACKGROUND: Copy number variation (CNV) represents another important source of genetic variation complementary to single nucleotide polymorphism (SNP). High-density SNP array data have been routinely used to detect human CNVs, many of which have significant functional effects on gene expression and...

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Detalles Bibliográficos
Autores principales: Hou, Yali, Liu, George E, Bickhart, Derek M, Cardone, Maria Francesca, Wang, Kai, Kim, Eui-soo, Matukumalli, Lakshmi K, Ventura, Mario, Song, Jiuzhou, VanRaden, Paul M, Sonstegard, Tad S, Van Tassell, Curt P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053260/
https://www.ncbi.nlm.nih.gov/pubmed/21345189
http://dx.doi.org/10.1186/1471-2164-12-127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053260/
https://www.ncbi.nlm.nih.gov/pubmed/21345189
http://dx.doi.org/10.1186/1471-2164-12-127

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