Long insert whole genome sequencing for copy number variant and translocation detection

As next-generation sequencing continues to have an expanding presence in the clinic, the identification of the most cost-effective and robust strategy for identifying copy number changes and translocations in tumor genomes is needed. We hypothesized that performing shallow whole genome sequencing (W...

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Bibliografiske detaljer
Main Authors: Liang, Winnie S., Aldrich, Jessica, Tembe, Waibhav, Kurdoglu, Ahmet, Cherni, Irene, Phillips, Lori, Reiman, Rebecca, Baker, Angela, Weiss, Glen J., Carpten, John D., Craig, David W.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2014
Fag:
Methods Online
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3902897/
https://ncbi.nlm.nih.gov/pubmed/24071583
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkt865
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