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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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| Autors principals: | , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2014
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| Matèries: | |
| Accés en línia: | 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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