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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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| 發表在: | Cancer Med |
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| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2019
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| 主題: | |
| 在線閱讀: | 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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