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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: 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.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2008
Schlagworte:
Methods Online
Online Zugang: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
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge