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Status |
Public on Apr 26, 2022 |
Title |
Inhibition of pyrimidine biosynthesis targets protein translation in AML [ATAC-seq_MN-2] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
Investigation of the chromatin accessibility in MN cells. Mice bearing MN tumors were treated with AG636 for 2 days. Leukemic stem cells (cKit high; CD11b low) from bone marrow and spleen were isolated. RNA sequencing and ATAC-seq were performed.
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Overall design |
Genome binding/occupancy profiling of Vehicle- or AG636-treated MN AML cells by high-throughput sequencing.
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Contributor(s) |
So J, Gruber E |
Citation(s) |
35514210 |
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Submission date |
Aug 08, 2021 |
Last update date |
Jul 20, 2022 |
Contact name |
Joan So |
E-mail(s) |
[email protected]
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Organization name |
Peter MacCallum Cancer Centre
|
Street address |
305 Grattan St
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City |
Melbourne |
State/province |
Victoria |
ZIP/Postal code |
3000 |
Country |
Australia |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE181666 |
Inhibition of pyrimidine biosynthesis targets protein translation in AML |
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Relations |
BioProject |
PRJNA752899 |
SRA |
SRP331538 |