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| Status |
Public on May 14, 2024 |
| Title |
H3K27ac ChIP-seq for lung ILC2 and CD4 T cells in HDM induced asthma |
| Organism |
Mus musculus |
| Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
| Summary |
Lung ILC2 and Th2 cells exhibited similar chromatin activation. However, small fraction of super-enhancers showed ILC2-specific, or T cell specific activation.
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| |
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| Overall design |
H3K27ac ChIP-seq were performed in ILC2 and CD4 T cells obtained from HDM-induced murine asthma models and control mice.
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| Contributor(s) |
Iwata A, Furuya H, Toda Y |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
| |
| Submission date |
Nov 16, 2022 |
| Last update date |
May 15, 2024 |
| Contact name |
Arifumi Iwata |
| Organization name |
Chiba University
|
| Department |
Department of Allergy and Clinical Immunology
|
| Street address |
1-8-1 Inohana, Chuou-ku
|
| City |
Chiba-shi |
| State/province |
Chiba |
| ZIP/Postal code |
260-8670 |
| Country |
Japan |
| |
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| Platforms (1) |
| GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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| Samples (4)
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| This SubSeries is part of SuperSeries: |
| GSE218155 |
ILC2 development requires GATA3-related super-enhancers after lineage commitment |
|
| Relations |
| BioProject |
PRJNA902401 |
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