|
Status |
Public on May 06, 2020 |
Title |
ARID1A gene status shapes cancer immune phenotype and affects cancer immunotherapy |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing Expression profiling by high throughput sequencing
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
|
|
|
Overall design |
Refer to individual Series
|
|
|
Citation(s) |
32027624 |
Submission date |
May 29, 2019 |
Last update date |
May 06, 2020 |
Contact name |
Jing Li |
E-mail(s) |
jingdsli@umich.edu
|
Organization name |
University of Michigan
|
Department |
Surgery
|
Street address |
500 S State St,
|
City |
Ann Arbor, |
State/province |
MI |
ZIP/Postal code |
48109 |
Country |
USA |
|
|
Platforms (2) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
|
Samples (42)
|
|
This SuperSeries is composed of the following SubSeries: |
GSE131915 |
ATAC-seq in ARID1A WT or KO OVCA429 Cells after interferron treatment |
GSE131916 |
RNA-seq in ARID1A WT, KO OVCA429 Cells after IFNγ treatment |
GSE131917 |
Intersection of ARID1A, EZH2 RNA-seq in OVCA429 cells with IFNγ treatment |
|
Relations |
BioProject |
PRJNA545311 |