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Identifying Key Somatic Copy Number Alterations Driving Dysregulation of Cancer Hallmarks in Lower-Grade Glioma

Somatic copy-number alterations (SCNAs) are major contributors to cancer development that are pervasive and highly heterogeneous in human cancers. However, the driver roles of SCNAs in cancer are insufficiently characterized. We combined network propagation and linear regression models to design an...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Zhou, Yao, Wang, Shuai, Yan, Haoteng, Pang, Bo, Zhang, Xinxin, Pang, Lin, Wang, Yihan, Xu, Jinyuan, Hu, Jing, Lan, Yujia, Ping, Yanyan
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8215700/
https://ncbi.nlm.nih.gov/pubmed/34163522
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.654736
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