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Status |
Public on Jan 25, 2023 |
Title |
Histone variant H3.3 facilitates open chromatin at promoters [ATAC-seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We analyze the contribution of H3.3 to chromatin accessibility, post-translational modification states, and transcription in mouse embryonic stem cells (mESC).
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Overall design |
ATAC-seq analysis in mouse embryonic stem cell lines and embryoid bodies (Control, H33KO).
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Contributor(s) |
Martire S, Banaszynski LA |
Citation(s) |
36782260 |
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Submission date |
Oct 27, 2021 |
Last update date |
Apr 26, 2023 |
Contact name |
Laura Banaszynski |
E-mail(s) |
[email protected]
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Organization name |
UT Southwestern Medical Center
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Department |
Green Center for Reproductive Biology Sciences
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Street address |
5323 Harry Hines Blvd
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City |
Dallas |
State/province |
TX |
ZIP/Postal code |
75390-8511 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE186687 |
Histone variant H3.3 facilitates open chromatin at promoters. |
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Relations |
BioProject |
PRJNA775069 |
SRA |
SRP343431 |