ChromothripsisDB: a curated database of chromothripsis
 
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  Study
PubMed ID   25790038 Publish Date   2015 Mar
Journal   Nature Communications Species   Homo sapiens
Disease Type   Renal cancer Technology   Next Generation Sequencing
Case Number   1 Raw Data   EBI: PRJEB7875, ERP008861
Title   Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution
Authors   Kovac M, Navas C, Horswell S, Salm M, Bardella C, Rowan A, Stares M, Castro-Giner F, Fisher R, de Bruin EC, Kovacova M, Gorman M, Makino S, Williams J, Jaeger E, Jones A, Howarth K, Larkin J, Pickering L, Gore M, Nicol DL, Hazell S, Stamp G, O'Brien T, Challacombe B, Matthews N, Phillimore B, Begum S, Rabinowitz A, Varela I, Chandra A, Horsfield C, Polson A, Tran M, Bhatt R, Terracciano L, Eppenberger-Castori S, Protheroe A, Maher E, El Bahrawy M, Fleming S, Ratcliffe P, Heinimann K, Swanton C, Tomlinson I
Affiliation   Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, Nuffield Department of Clinical Medicine, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK
Chromothripsis Definition   Close-by breakpoints: >=200
Copy number states: 3
Fragments random joining: NA
Download   Study Data File
 
Chromothripsis Cases
  P09
     
  Case ID: P09
  Chromosome:2
  Disease type: Renal cancer
  Technology: Next Generation Sequencing
  Platform: Complete Genomics
  Affected Gene: Gene List
  Download: Links File
 
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