|
Status |
Public on Oct 01, 2014 |
Title |
Genomic analysis of low-grade serous ovarian carcinomas [ILOEF] |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by SNP array
|
Summary |
Low-grade serous ovarian carcinomas are typically Ras-pathway mutated, TP53 wild-type, have limited chromosomal aberration, and are frequently associated with borderline tumors. By contrast, high-grade serous ovarian carcinoma lack Ras-pathway mutations, are invariably TP53 mutated, show widespread genomic change, and are commonly BRCA-pathway disrupted.We sought to identify differences in genomic copy number changes between co-existing borderline and invasive components of serous carcinoma.
|
|
|
Overall design |
Paired co-existing borderline and invasive tumor components were sampled and profiled from formalin-fixed paraffin embedded tumors from 6 patients
|
|
|
Contributor(s) |
deFazio A, Bowtell D, Emmanuel C, Etemadmoghadam D, Chiew Y, George J |
Citation(s) |
25316818 |
|
Submission date |
May 05, 2014 |
Last update date |
Jan 07, 2015 |
Contact name |
Dariush Etemadmoghadam |
E-mail(s) |
dariush.etemadmoghadam@petermac.org
|
Phone |
61396561149
|
Organization name |
Peter MacCallum Cancer Centre
|
Street address |
St Andrew's Place
|
City |
East Melbourne |
ZIP/Postal code |
3002 |
Country |
Australia |
|
|
Platforms (1) |
GPL18643 |
Illumina HumanOmniExpressFFPE-12 BeadChip |
|
Samples (10)
|
|
This SubSeries is part of SuperSeries: |
GSE57280 |
Genomic analysis of low-grade serous ovarian carcinomas |
|
Relations |
BioProject |
PRJNA246156 |