| PubMed ID |
|
26439695 |
Publish Date |
|
2015 Nov |
| Journal |
|
Oncotarget |
Species |
|
Homo sapiens |
| Disease Type |
|
Breast cancer |
Technology |
|
Next Generation Sequencing |
| Case Number |
|
4 |
Raw Data |
|
|
| Title |
|
Remarkable similarities of chromosomal rearrangements between primary human breast cancers and matched distant metastases as revealed by whole-genome sequencing |
| Authors |
|
Tang MH, Dahlgren M, Brueffer C, Tjitrowirjo T, Winter C, Chen Y, Olsson E, Wang K, Torngren T, Sjostrom M, Grabau D, Bendahl PO, Ryden L, Nimeus E, Saal LH, Borg A, Gruvberger-Saal SK |
| Affiliation |
|
Division of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden |
| Chromothripsis Definition |
|
Close-by breakpoints: >10
Copy number states: >3
Fragments random joining: No |
| |
| Chromothripsis Cases |
| P6 |
| |
|
|
| |
Case ID: |
P6 |
| |
Chromosome: | 17,19 |
| |
Disease type: |
Breast cancer |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq 2000 |
| | | P16 |
| |
|
|
| |
Case ID: |
P16 |
| |
Chromosome: | 16,17 |
| |
Disease type: |
Breast cancer |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq 2000 |
| | | P17 |
| |
|
|
| |
Case ID: |
P17 |
| |
Chromosome: | 11 |
| |
Disease type: |
Breast cancer |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq 2000 |
| | | P20 |
| |
|
|
| |
Case ID: |
P20 |
| |
Chromosome: | 3 |
| |
Disease type: |
Breast cancer |
| |
Technology: |
Next Generation Sequencing |
| |
Platform: |
Illumina HiSeq 2000 |
| | | top |
|
