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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Yuan, Xiguo, Yu, Guoqiang, Hou, Xuchu, Shih, Ie-Ming, Clarke, Robert, Zhang, Junying, Hoffman, Eric P, Wang, Roger R, Zhang, Zhen, Wang, Yue
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2012
Matèries:
Methodology Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3428679/
https://ncbi.nlm.nih.gov/pubmed/22839576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-342
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars