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Series GSE171667 Query DataSets for GSE171667
Status Public on Apr 09, 2021
Title The effect of DMD on THP1 macrophages in response to IMQ.
Organism Homo sapiens
Experiment type Expression profiling by array
Summary To clarify the role of DMD in macrophages in response to IMQ, we performed transcriptomic analysis by a Low Input Quick-Amp Labeling kit (Agilent Technologies, USA) from IMQ-induced THP1 macrophages with or without DMD treatment in vitro.
 
Overall design THP-1 was differentiated into macrophages by treating cells with 100 ng/ml of PMA for 24-36 h, followed by overnight incubation in fresh medium. THP1 cells were pretreated with DMD following in the presence of IMQ. 0.2 μg of total RNA was amplified by a Low Input Quick-Amp Labeling kit (Agilent Technologies, USA) Raw signal data was normalized by quantile normalization for differential expressed genes discovering.For functional assay, we provied enrichment test for differential expressed genes (For most model organisms). Welgen Biotech used clusterProfiler for enrichment test for gene ontology (GO) and pathway (KEGG).
 
Contributor(s) Chuang S
Citation(s) 34054833
Submission date Apr 08, 2021
Last update date Jun 03, 2021
Contact name Shih-Yi Chuang
E-mail(s) clemencechuang@gmail.com
Phone +976232300
Organization name Chang Gung University
Street address No.259, Wenhua 1st Rd., Guishan Dist.
City Taoyuan City
ZIP/Postal code 33302
Country Taiwan
 
Platforms (1)
GPL21185 Agilent-072363 SurePrint G3 Human GE v3 8x60K Microarray 039494 [Probe Name Version]
Samples (3)
GSM5229968 THP1_4hr_Ctrl_rep1
GSM5229969 THP1_4hr_IMQ_rep1
GSM5229970 THP1_4hr_IMQ+X_rep1
Relations
BioProject PRJNA720534

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
GSE171667.txt.gz 7.8 Mb (ftp)(http) TXT
GSE171667_RAW.tar 37.5 Mb (http)(custom) TAR (of TXT)
Processed data provided as supplementary file
Processed data are available on Series record

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