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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...
Kaydedildi:
| Yayımlandı: | Cancer Sci |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2018
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| Konular: | |
| Online Erişim: | 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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