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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Detalles Bibliográficos
Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490749/
https://www.ncbi.nlm.nih.gov/pubmed/18559357
http://dx.doi.org/10.1093/nar/gkn378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490749/
https://www.ncbi.nlm.nih.gov/pubmed/18559357
http://dx.doi.org/10.1093/nar/gkn378

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