Impact of whole genome amplification on analysis of copy number variants

Large-scale copy number variants (CNVs) have recently been recognized to play a role in human genome variation and disease. Approaches for analysis of CNVs in small samples such as microdissected tissues can be confounded by limited amounts of material. To facilitate analyses of such samples, whole...

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Hlavní autoři: Pugh, T. J., Delaney, A. D., Farnoud, N., Flibotte, S., Griffith, M., Li, H. I., Qian, H., Farinha, P., Gascoyne, R. D., Marra, M. A.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2008
Témata:
Methods Online
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2490749/
https://ncbi.nlm.nih.gov/pubmed/18559357
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkn378
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