Cargando…
The repertoire of copy number alteration signatures in human cancer
Copy number alterations (CNAs) are a predominant source of genetic alterations in human cancer and play an important role in cancer progression. However comprehensive understanding of the mutational processes and signatures of CNA is still lacking. Here we developed a mechanism-agnostic method to ca...
Autores principales: | Tao, Ziyu, Wang, Shixiang, Wu, Chenxu, Wu, Tao, Zhao, Xiangyu, Ning, Wei, Wang, Guangshuai, Wang, Jinyu, Chen, Jing, Diao, Kaixuan, Chen, Fuxiang, Liu, Xue-Song |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025440/ https://www.ncbi.nlm.nih.gov/pubmed/36806386 http://dx.doi.org/10.1093/bib/bbad053 |
Ejemplares similares
-
PEcnv: accurate and efficient detection of copy number variations of various lengths
por: Wang, Xuwen, et al.
Publicado: (2022) -
Accurate prediction of pan-cancer types using machine learning with minimal number of DNA methylation sites
por: Ning, Wei, et al.
Publicado: (2023) -
ExosomePurity: tumour purity deconvolution in serum exosomes based on miRNA signatures
por: Wu, Tao, et al.
Publicado: (2023) -
Tools for fundamental analysis functions of TCR repertoires: a systematic comparison
por: Zhang, Yanfang, et al.
Publicado: (2019) -
Copy number alteration features in pan-cancer homologous recombination deficiency prediction and biology
por: Yao, Huizi, et al.
Publicado: (2023)