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Whole genome sequencing analysis for cancer genomics and precision medicine

Explosive advances in next‐generation sequencer (NGS) and computational analyses have enabled exploration of somatic protein‐altered mutations in most cancer types, with coding mutation data intensively accumulated. However, there is limited information on somatic mutations in non‐coding regions, in...

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Dades bibliogràfiques
Publicat a:Cancer Sci
Autors principals: Nakagawa, Hidewaki, Fujita, Masashi
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5834793/
https://ncbi.nlm.nih.gov/pubmed/29345757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cas.13505
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