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Status |
Public on Jun 24, 2020 |
Title |
Epigenetic changes in human DIPG cells with histone H3K27M mutations [ATAC-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We assessed changes in chromatin accessibility in H3.3K27M DIPG cell lines on knockdown of metabolic enzymes including HK2, GDH and IDH1
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Overall design |
Hexokinase-2 (HK2), Glutamate dehydrogenase (GLUD1) or insocitrate dehydrogenase (IDH1) were knocked down in H3.3K27M HSJD-DIPG007 cells. Genomic changes in chromatin accessibility were assessed between each shRNA and non-targeted NT controls.
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Contributor(s) |
Venneti S |
Citation(s) |
32795401 |
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Submission date |
Aug 05, 2019 |
Last update date |
Nov 03, 2023 |
Contact name |
Sriram Venneti |
E-mail(s) |
[email protected]
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Organization name |
University of Michigan
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Street address |
3520E MSRB 1, 1150 W. Medical Center Dr.
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City |
Ann Arbor |
State/province |
MI |
ZIP/Postal code |
48109 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE135419 |
Epigenetic changes in mouse neuronal stem cells and human DIPG cells with histone H3K27M mutations |
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Relations |
BioProject |
PRJNA558794 |
SRA |
SRP217515 |