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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Software Tool Article
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

Internet

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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