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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Hlavní autoři: Armour, John A. L., Palla, Raquel, Zeeuwen, Patrick L. J. M., den Heijer, Martin, Schalkwijk, Joost, Hollox, Edward J.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2007
Témata:
Methods Online
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1807953/
https://ncbi.nlm.nih.gov/pubmed/17175532
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkl1089
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