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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2014
Onderwerpen:
Methods Online
Online toegang: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
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items