Exome sequencing identified six copy number variations as a prediction model for recurrence of primary prostate cancers with distinctive prognosis

BACKGROUND: Prostate cancer (PCa) is a common type of malignancy, which represents one of the leading causes of death among men worldwide. Copy number variations (CNVs) and gene fusions play important roles in PCa and may serve as markers for the prognosis of this condition. METHODS: We have present...

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Detalles Bibliográficos
Autores principales: Liu, Jie, Yan, Jiajun, Mao, Ruifang, Ren, Guoping, Liu, Xiaoyan, Zhang, Yanling, Wang, Jili, Wang, Yan, Li, Meiling, Qiu, Qingchong, Wang, Lin, Liu, Guanfeng, Jin, Shanshan, Ma, Liang, Ma, Yingying, Zhao, Na, Zhang, Hongwei, Lin, Biaoyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798897/
https://www.ncbi.nlm.nih.gov/pubmed/35117583
http://dx.doi.org/10.21037/tcr.2020.03.31

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