|
Status |
Public on Nov 23, 2016 |
Title |
Lowered H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
|
|
|
Overall design |
Refer to individual Series
|
|
|
Citation(s) |
27881822 |
|
Submission date |
Nov 02, 2016 |
Last update date |
Jul 14, 2021 |
Contact name |
Sriram Venneti |
E-mail(s) |
svenneti@med.umich.edu
|
Organization name |
University of Michigan
|
Street address |
3520E MSRB 1, 1150 W. Medical Center Dr.
|
City |
Ann Arbor |
State/province |
MI |
ZIP/Postal code |
48109 |
Country |
USA |
|
|
Platforms (2) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
|
Samples (35)
|
|
This SuperSeries is composed of the following SubSeries: |
GSE89446 |
Low H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas |
GSE89448 |
Global reduction in H3K27me3 and DNA hypomethylation define poorly prognostic pediatric posterior fossa ependymomas |
GSE89451 |
Low H3K27me3 define poorly prognostic pediatric posterior fossa ependymomas |
|
Relations |
BioProject |
PRJNA352237 |