ChromothripsisDB: a curated database of chromothripsis
 
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PubMed ID   24670920 Publish Date   2014 Mar
Journal   Nature Communications Species   Homo sapiens
Disease Type   Pulmonary carcinoid Technology   Next Generation Sequencing
Case Number   1 Raw Data  
Title   Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Authors   Fernandez-Cuesta L, Peifer M, Lu X, Sun R, Ozretic L, Seidel D, Zander T, Leenders F, George J, Muller C, Dahmen I, Pinther B, Bosco G, Konrad K, Altmuller J, Nurnberg P, Achter V, Lang U, Schneider PM, Bogus M, Soltermann A, Brustugun OT, Helland A, Solberg S, Lund-Iversen M, Ansen S, Stoelben E, Wright GM, Russell P, Wainer Z, Solomon B, Field JK, Hyde R, Davies MP, Heukamp LC, Petersen I, Perner S, Lovly CM, Cappuzzo F, Travis WD, Wolf J, Vingron M, Brambilla E, Haas SA, Buettner R, Thomas RK
Affiliation   Department of Translational Genomics, Center of Integrated Oncology Cologne-Bonn, Medical Faculty, University of Cologne, 50924 Cologne, Germany
Chromothripsis Definition   Close-by breakpoints: >=8
Copy number states: 3
Fragments random joining: Yes
Download   Study Data File
 
Chromothripsis Cases
  S00076
     
  Case ID: S00076
  Chromosome:3,12,13
  Disease type: Pulmonary carcinoid
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq2000
  Affected Gene: Gene List
  Download: Links File
 
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