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Status |
Public on Apr 28, 2023 |
Title |
ChIP-seq of in vitro differentiated naïve and Th9 cells |
Organisms |
Homo sapiens; Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
To investigate changes in chromatin accessibility over time, we differentiated Th9 cells in vitro from naïve T cells from human and murine sources, and followed them over an extended time course, during which they gained and then lost capacity for IL-9 production We then performed Chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for histone modifications H3K4me1, K3K4me3, and H3K27Ac in cells from 2 different human donors and from 2 mice at 4 time points.
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Overall design |
Peaks for various histone marks normalized to input
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Contributor(s) |
Schwartz DM, Son A |
Citation(s) |
37106040 |
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Submission date |
Jan 14, 2023 |
Last update date |
Apr 29, 2023 |
Contact name |
Daniella Schwartz |
E-mail(s) |
Daniella.Schwartz@pitt.edu
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Organization name |
University of Pittsburgh
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Street address |
200 Lothrop St
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City |
Pittsburgh |
State/province |
PA |
ZIP/Postal code |
15216 |
Country |
USA |
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Platforms (2) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (64)
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This SubSeries is part of SuperSeries: |
GSE222910 |
ATAC-seq, ChIP-seq and RNA-seq of in vitro differentiated naïve, Th1, and Th9 cells |
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Relations |
BioProject |
PRJNA923820 |