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CusVarDB: A tool for building customized sample-specific variant protein database from next-generation sequencing datasets
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...
Autores principales: | Kasaragod, Sandeep, Mohanty, Varshasnata, Tyagi, Ankur, Behera, Santosh Kumar, Patil, Arun H., Pinto, Sneha M., Prasad, T. S. Keshava, Modi, Prashant Kumar, Gowda, Harsha |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684676/ https://www.ncbi.nlm.nih.gov/pubmed/33274046 http://dx.doi.org/10.12688/f1000research.23214.2 |
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