|
Status |
Public on Dec 22, 2020 |
Title |
Identification of 17-DMAG as a novel KDM4B inhibitor for combination therapy |
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) |
33490904 |
|
Submission date |
Jun 01, 2020 |
Last update date |
Jan 27, 2021 |
Contact name |
Hongjian Jin |
E-mail(s) |
hongjian.jin@STJUDE.ORG
|
Organization name |
St Jude Children's Research Hospital
|
Department |
Center for Applied Bioinformatics
|
Street address |
262 Danny Thomas Place
|
City |
Memphis |
State/province |
TN |
ZIP/Postal code |
38015 |
Country |
USA |
|
|
Platforms (2) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
|
Samples (21)
|
|
This SuperSeries is composed of the following SubSeries: |
GSE151493 |
Identification of 17-DMAG as a novel KDM4B inhibitor for combination therapy [ChIP-seq] |
GSE151514 |
Identification of 17-DMAG as a novel KDM4B inhibitor for combination therapy [RNA-seq] |
|
Relations |
BioProject |
PRJNA636501 |