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Series GSE181660 Query DataSets for GSE181660
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.
 
Overall design Genome binding/occupancy profiling of Vehicle- or AG636-treated MN AML cells by high-throughput sequencing.
 
Contributor(s) So J, Gruber E
Citation(s) 35514210
Submission date Aug 08, 2021
Last update date Jul 20, 2022
Contact name Joan So
E-mail(s) [email protected]
Organization name Peter MacCallum Cancer Centre
Street address 305 Grattan St
City Melbourne
State/province Victoria
ZIP/Postal code 3000
Country Australia
 
Platforms (1)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (4)
GSM5508892 Vehicle_1_ATACseq
GSM5508893 Vehicle_2_ATACseq
GSM5508894 AG636_1_ATACseq
This SubSeries is part of SuperSeries:
GSE181666 Inhibition of pyrimidine biosynthesis targets protein translation in AML
Relations
BioProject PRJNA752899
SRA SRP331538

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE181660_drug_merged_bin50_smooth150_e200_CPM_rmBlacklist.bw 191.4 Mb (ftp)(http) BW
GSE181660_veh_merged_bin50_smooth150_e200_CPM_rmBlacklist.bw 184.6 Mb (ftp)(http) BW
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Raw data are available in SRA
Processed data are available on Series record

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