ChromothripsisDB: a curated database of chromothripsis
 
Home Search Browse Download Tutorial Contact  
  Study
PubMed ID   27741277 Publish Date   2016 Oct
Journal   PLoS One Species   Homo sapiens
Disease Type   Myelodysplastic syndrome Technology   Array CGH
Case Number   3 Raw Data   GEO: GSE67682  
Title   Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes
Authors   Abaigar M, Robledo C, Benito R, Ramos F, Diez-Campelo M, Hermosin L, Sanchez-Del-Real J, Alonso JM, Cuello R, Megido M, Rodriguez JN, Martin-Nunez G, Aguilar C, Vargas M, Martin AA, Garcia JL, Kohlmann A, Del Canizo MC, Hernandez-Rivas JM
Affiliation   Unidad de Diagnostico Molecular y Celular del Cancer, Centro de Investigacion del Cancer-IBMCC (USAL-CSIC), Salamanca, Spain
Chromothripsis Definition   Close-by breakpoints: >=22
Copy number states: 2--3
Fragments random joining: NA
Download   Study Data File
 
Chromothripsis Cases
  27741277_026
     
  Case ID: 27741277_026
  Chromosome:13
  Disease type: Myelodysplastic syndrome
  Technology: Array CGH
  Platform: NimbleGen 12x135K Whole-Genome Tiling v3.0 Array
  Affected Gene: Gene List
  Download: Copy Number File   
  27741277_027
     
  Case ID: 27741277_027
  Chromosome:13
  Disease type: Myelodysplastic syndrome
  Technology: Array CGH
  Platform: NimbleGen 12x135K Whole-Genome Tiling v3.0 Array
  Affected Gene: Gene List
  Download: Copy Number File   
  27741277_072
     
  Case ID: 27741277_072
  Chromosome:13
  Disease type: Myelodysplastic syndrome
  Technology: Array CGH
  Platform: NimbleGen 12x135K Whole-Genome Tiling v3.0 Array
  Affected Gene: Gene List
  Download: Copy Number File   
 
© 2015 Cai Laboratory.  Last updated on 13 Mar 2018