Related references
Note: Only part of the references are listed.Pan-cancer analysis of whole genomes
Peter J. Campbell et al.
NATURE (2020)
Patterns of somatic structural variation in human cancer genomes
Yilong Li et al.
NATURE (2020)
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Isidro Cortes-Ciriano et al.
NATURE GENETICS (2020)
Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements
Peter Ly et al.
NATURE GENETICS (2019)
Extrachromosomal oncogene amplification in tumour pathogenesis and evolution
Roel G. W. Verhaak et al.
NATURE REVIEWS CANCER (2019)
Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma
Ana C. deCarvalho et al.
NATURE GENETICS (2018)
Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining
Peter Ly et al.
NATURE CELL BIOLOGY (2017)
Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity
Kristen M. Turner et al.
NATURE (2017)
A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers
Dominik Glodzik et al.
NATURE GENETICS (2017)
ChromEMT: Visualizing 3D chromatin structure and compaction in interphase and mitotic cells
Horng D. Ou et al.
SCIENCE (2017)
Mechanisms of Acquired Resistance to BRAF V600E Inhibition in Colon Cancers Converge on RAF Dimerization and Are Sensitive to Its Inhibition
Rona Yaeger et al.
CANCER RESEARCH (2017)
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
Serena Nik-Zainal et al.
NATURE (2016)
Chromothripsis and Kataegis Induced by Telomere Crisis
John Maciejowski et al.
CELL (2015)
DNA Sequence-Specific Binding of CENP-B Enhances the Fidelity of Human Centromere Function
Daniele Fachinetti et al.
DEVELOPMENTAL CELL (2015)
Visualizing viral protein structures in cells using genetic probes for correlated light and electron microscopy
Horng D. Ou et al.
METHODS (2015)
Chromothripsis from DNA damage in micronuclei
Cheng-Zhong Zhang et al.
NATURE (2015)
The Architecture and Evolution of Cancer Neochromosomes
Dale W. Garsed et al.
CANCER CELL (2014)
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
Suhas S. P. Rao et al.
CELL (2014)
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
Yilong Li et al.
NATURE (2014)
Targeted Therapy Resistance Mediated by Dynamic Regulation of Extrachromosomal Mutant EGFR DNA
David A. Nathanson et al.
SCIENCE (2014)
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis
Katia Nones et al.
NATURE COMMUNICATIONS (2014)
Criteria for Inference of Chromothripsis in Cancer Genomes
Jan O. Korbel et al.
CELL (2013)
Deciphering Signatures of Mutational Processes Operative in Human Cancer
Ludmil B. Alexandrov et al.
CELL REPORTS (2013)
The Genomic and Transcriptomic Landscape of a HeLa Cell Line
Jonathan J. M. Landry et al.
G3-GENES GENOMES GENETICS (2013)
Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations
Tobias Rausch et al.
CELL (2012)
Fiji: an open-source platform for biological-image analysis
Johannes Schindelin et al.
NATURE METHODS (2012)
Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development
Philip J. Stephens et al.
CELL (2011)
Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting
Tomas Cermak et al.
NUCLEIC ACIDS RESEARCH (2011)
Fast and accurate long-read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2010)
DNA repair pathways as targets for cancer therapy
Thomas Helleday et al.
NATURE REVIEWS CANCER (2008)
Gene amplification in cancer
Donna G. Albertson
TRENDS IN GENETICS (2006)
Resolution of anaphase bridges in cancer cells
DR Hoffelder et al.
CHROMOSOMA (2004)
Induction of multiple double-strand breaks within an hsr by meganuclease I-SceI expression or fragile site activation leads to formation of double minutes and other chromosomal rearrangements
A Coquelle et al.
ONCOGENE (2002)
Amplification of the human dihydrofolate reductase gene via double minutes is initiated by chromosome breaks
MJ Singer et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)