Cancer subtype identification using somatic mutation data

BACKGROUND: With the onset of next-generation sequencing technologies, we have made great progress in identifying recurrent mutational drivers of cancer. As cancer tissues are now frequently screened for specific sets of mutations, a large amount of samples has become available for analysis. Classif...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuijjer, Marieke Lydia, Paulson, Joseph Nathaniel, Salzman, Peter, Ding, Wei, Quackenbush, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988673/
https://www.ncbi.nlm.nih.gov/pubmed/29765148
http://dx.doi.org/10.1038/s41416-018-0109-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988673/
https://www.ncbi.nlm.nih.gov/pubmed/29765148
http://dx.doi.org/10.1038/s41416-018-0109-7

Ejemplares similares