Criteria for Inference of Chromothripsis in Cancer Genomes
Top Cited Papers
- 1 March 2013
- journal article
- research article
- Published by Elsevier BV in Cell
- Vol. 152 (6), 1226-1236
- https://doi.org/10.1016/j.cell.2013.02.023
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- An integrated map of genetic variation from 1,092 human genomesNature, 2012
- Subgroup-specific structural variation across 1,000 medulloblastoma genomesNature, 2012
- Dissecting the genomic complexity underlying medulloblastomaNature, 2012
- The Life History of 21 Breast CancersCell, 2012
- Chromothripsis and Human Disease: Piecing Together the Shattering ProcessCell, 2012
- Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 MutationsCell, 2012
- Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic RearrangementsCell, 2011
- Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer DevelopmentCell, 2011
- Signatures of mutation and selection in the cancer genomeNature, 2010
- Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencingNature Genetics, 2008