CusVarDB: A tool for building customized sample-specific variant protein database from next-generation sequencing datasets [version 2; peer review: 2 approved]
Cancer genome sequencing studies have revealed a number of variants in coding regions of several genes. Some of these coding variants play an important role in activating specific pathways that drive proliferation. Coding variants present on cancer cell surfaces by the major histocompatibility compl...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
F1000 Research Ltd
2020-11-01
|
| Seri Bilgileri: | F1000Research |
| Online Erişim: | https://f1000research.com/articles/9-344/v2 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|