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Identification of Single Nucleotide Non-coding Driver Mutations in Cancer
Recent whole-genome sequencing studies have identified millions of somatic variants present in tumor samples. Most of these variants reside in non-coding regions of the genome potentially affecting transcriptional and post-transcriptional gene regulation. Although a few hallmark examples of driver m...
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| Publicado no: | Front Genet |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5801294/ https://ncbi.nlm.nih.gov/pubmed/29456552 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00016 |
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