| PubMed ID |
|
22622578 |
Publish Date |
|
2012 May |
| Journal |
|
Nature |
Species |
|
Homo sapiens |
| Disease Type |
|
Melanoma |
Technology |
|
Next Generation Sequencing |
| Case Number |
|
2 |
Raw Data |
|
dbGaP: phs000452 |
| Title |
|
Melanoma genome sequencing reveals frequent PREX2 mutations |
| Authors |
|
Berger MF, Hodis E, Heffernan TP, Deribe YL, Lawrence MS, Protopopov A, Ivanova E, Watson IR, Nickerson E, Ghosh P, Zhang H, Zeid R, Ren X, Cibulskis K, Sivachenko AY, Wagle N, Sucker A, Sougnez C, Onofrio R, Ambrogio L, Auclair D, Fennell T, Carter SL, Drier Y, Stojanov P, Singer MA, Voet D, Jing R, Saksena G, Barretina J, Ramos AH, Pugh TJ, Stransky N, Parkin M, Winckler W, Mahan S, Ardlie K, Baldwin J, Wargo J, Schadendorf D, Meyerson M, Gabriel SB, Golub TR, Wagner SN, Lander ES, Getz G, Chin L, Garraway LA |
| Affiliation |
|
The Broad Institute of Harvard and MIT, Cambridge, Massachusetts 02142, USA |
| Chromothripsis Definition |
|
Close-by breakpoints: >=141
Copy number states: 3
Fragments random joining: Yes |
| Download |
|
Study Data File |
| |
| Chromothripsis Cases |
| ME020 |
| |
|
|
| |
Case ID: |
ME020 |
| |
Chromosome: | 6,18 |
| |
Disease type: |
Melanoma |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq2000 |
| |
Affected Gene: |
Gene List |
| |
Download: |
Copy Number File Links File |
| |  | | ME035 |
| |
|
|
| |
Case ID: |
ME035 |
| |
Chromosome: | 5,22 |
| |
Disease type: |
Melanoma |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq2000 |
| |
Affected Gene: |
Gene List |
| |
Download: |
Copy Number File Links File |
| |  |
|
