OncoBase: a platform for decoding regulatory somatic mutations in human cancers

Whole-exome and whole-genome sequencing have revealed millions of somatic mutations associated with different human cancers, and the vast majority of them are located outside of coding sequences, making it challenging to directly interpret their functional effects. With the rapid advances in high-th...

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Detalles Bibliográficos
Autores principales: Li, Xianfeng, Shi, Leisheng, Wang, Yan, Zhong, Jianing, Zhao, Xiaolu, Teng, Huajing, Shi, Xiaohui, Yang, Haonan, Ruan, Shasha, Li, MingKun, Sun, Zhong Sheng, Zhan, Qimin, Mao, Fengbiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Database Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323961/
https://www.ncbi.nlm.nih.gov/pubmed/30445567
http://dx.doi.org/10.1093/nar/gky1139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323961/
https://www.ncbi.nlm.nih.gov/pubmed/30445567
http://dx.doi.org/10.1093/nar/gky1139

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