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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902897/
https://www.ncbi.nlm.nih.gov/pubmed/24071583
http://dx.doi.org/10.1093/nar/gkt865

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902897/
https://www.ncbi.nlm.nih.gov/pubmed/24071583
http://dx.doi.org/10.1093/nar/gkt865

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