Genome-wide identification of significant aberrations in cancer genome

BACKGROUND: Somatic Copy Number Alterations (CNAs) in human genomes are present in almost all human cancers. Systematic efforts to characterize such structural variants must effectively distinguish significant consensus events from random background aberrations. Here we introduce Significant Aberrat...

Descripción completa

Detalles Bibliográficos
Autores principales: Yuan, Xiguo, Yu, Guoqiang, Hou, Xuchu, Shih, Ie-Ming, Clarke, Robert, Zhang, Junying, Hoffman, Eric P, Wang, Roger R, Zhang, Zhen, Wang, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428679/
https://www.ncbi.nlm.nih.gov/pubmed/22839576
http://dx.doi.org/10.1186/1471-2164-13-342

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428679/
https://www.ncbi.nlm.nih.gov/pubmed/22839576
http://dx.doi.org/10.1186/1471-2164-13-342

Ejemplares similares