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Massive computational identification of somatic variants in exonic splicing enhancers using The Cancer Genome Atlas

Owing to the development of next‐generation sequencing (NGS) technologies, a large number of somatic variants have been identified in various types of cancer. However, the functional significance of most somatic variants remains unknown. Somatic variants that occur in exonic splicing enhancer (ESE)...

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Detalhes bibliográficos
Publicado no:Cancer Med
Main Authors: Tanimoto, Kousuke, Muramatsu, Tomoki, Inazawa, Johji
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6885893/
https://ncbi.nlm.nih.gov/pubmed/31631560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cam4.2619
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