ChromothripsisDB: a curated database of chromothripsis
 
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  Study
PubMed ID   28643781 Publish Date   2017 Jun
Journal   Nat Commun Species   Homo sapiens
Disease Type   Osteosarcoma Technology   Next Generation Sequencing
Case Number   1 Raw Data  
Title   Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma
Authors   Behjati S, Tarpey PS, Haase K, Ye H, Young MD, Alexandrov LB, Farndon SJ, Collord G, Wedge DC, Martincorena I, Cooke SL, Davies H, Mifsud W, Lidgren M, Martin S, Latimer C, Maddison M, Butler AP, Teague JW, Pillay N, Shlien A, McDermott U, Futreal PA, Baumhoer D, Zaikova O, Bjerkehagen B, Myklebost O, Amary MF, Tirabosco R, Van Loo P, Stratton MR, Flanagan AM, Campbell PJ
Affiliation   Cancer Genome Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK
Chromothripsis Definition   Close-by breakpoints: >20
Copy number states: 2
Fragments random joining: Yes
Download   Study Data File
 
Chromothripsis Cases
  PD13494a
     
  Case ID: PD13494a
  Chromosome:17
  Disease type: Osteosarcoma
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 2000 or 2500
  Affected Gene: Gene List
  Download: Copy Number File   Links File
 
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