Elusive Copy Number Variation in the Mouse Genome

BACKGROUND: Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian genomes has led to a growing awareness of the potential importance of this category of sequence variation as a cause of phenotypic variation. Yet there are large discrepancies between studie...

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Detalles Bibliográficos
Autores principales: Agam, Avigail, Yalcin, Binnaz, Bhomra, Amarjit, Cubin, Matthew, Webber, Caleb, Holmes, Christopher, Flint, Jonathan, Mott, Richard
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943477/
https://www.ncbi.nlm.nih.gov/pubmed/20877625
http://dx.doi.org/10.1371/journal.pone.0012839

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943477/
https://www.ncbi.nlm.nih.gov/pubmed/20877625
http://dx.doi.org/10.1371/journal.pone.0012839

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