|
| Status |
Public on Dec 31, 2012 |
| Title |
Clinically significant copy number alterations and complex rearrangements of MYB and NFIB in adenoid cystic carcinoma of the head and neck |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
|
| Summary |
Using high-resolution, array-based comparative genomic hybridization (aCGH), we explored genomic alterations in 40 fresh-frozen ACC samples, the largest cohort to date, with the aims to: (1) identify recurrent CNAs in ACC; (2) identify novel candidate target genes; and (3) correlate recurrent CNAs with tumour grade and other clinical parameters to identify potential clinically useful biomarkers.
|
| |
|
| Overall design |
High-resolution aCGH on fresh frozen tissue from 40 ACCs.
|
| |
|
| Contributor(s) |
Persson M, Andrén Y, Moskaluk CA, Frierson HF, Kling T, Nelander S, Nordkvist A, Persson F, Stenman G |
| Citation(s) |
22505352 |
| |
| Submission date |
Jan 03, 2012 |
| Last update date |
Jun 25, 2020 |
| Contact name |
Marta Persson |
| E-mail(s) |
marta.persson@llcr.med.gu.se
|
| Organization name |
Sahlgrenska Cancer Center
|
| Street address |
Box 425
|
| City |
Gotenburg |
| ZIP/Postal code |
405 90 |
| Country |
Sweden |
| |
|
| Platforms (1) |
| GPL4091 |
Agilent-014693 Human Genome CGH Microarray 244A (Feature number version) |
|
| Samples (40)
|
|
| Relations |
| BioProject |
PRJNA150261 |
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