Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats

Recent work has demonstrated an unexpected prevalence of copy number variation in the human genome, and has highlighted the part this variation may play in predisposition to common phenotypes. Some important genes vary in number over a high range (e.g. DEFB4, which commonly varies between two and se...

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Detalles Bibliográficos
Autores principales: Armour, John A. L., Palla, Raquel, Zeeuwen, Patrick L. J. M., den Heijer, Martin, Schalkwijk, Joost, Hollox, Edward J.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807953/
https://www.ncbi.nlm.nih.gov/pubmed/17175532
http://dx.doi.org/10.1093/nar/gkl1089

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1807953/
https://www.ncbi.nlm.nih.gov/pubmed/17175532
http://dx.doi.org/10.1093/nar/gkl1089

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