Exome Sequencing of Prostate Cancer Supports the Hypothesis of Independent Tumour Origins
- 1 February 2013
- journal article
- research article
- Published by Elsevier BV in European Urology
- Vol. 63 (2), 347-353
- https://doi.org/10.1016/j.eururo.2012.03.050
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Advancing a clinically relevant perspective of the clonal nature of cancerProceedings of the National Academy of Sciences of the United States of America, 2011
- Use of Whole-Genome Sequencing to Diagnose a Cryptic Fusion OncogeneJAMA, 2011
- Identification of a Novel TP53 Cancer Susceptibility Mutation Through Whole-Genome Sequencing of a Patient With Therapy-Related AMLJAMA, 2011
- A framework for variation discovery and genotyping using next-generation DNA sequencing dataNature Genetics, 2011
- The genomic complexity of primary human prostate cancerNature, 2011
- International network of cancer genome projectsNature, 2010
- Heteroplasmic mitochondrial DNA mutations in normal and tumour cellsNature, 2010
- Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancerNature Medicine, 2009
- Complex patterns of ETS gene alteration arise during cancer development in the human prostateOncogene, 2007
- TMPRSS2-ERG Fusion Heterogeneity in Multifocal Prostate Cancer: Clinical and Biologic ImplicationsUrology, 2007