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Series GSE174678 Query DataSets for GSE174678
Status Public on Jul 01, 2021
Title High-resolution transciptome mapping and N6-methyladenosine modification mapping of RAW264.7 cell lines treated with TCP, TBP or TIP.
Organism Mus musculus
Experiment type Methylation profiling by high throughput sequencing
Summary Purpose:Detect transcriptome-wide mapping of m6A modifications by MeRIP-seq between normal and chemical-treated RAW264.7 cells.
Methods:Total RNA was extracted using TRIzol Reagent followed by chemical fragmentation. The fragmented RNA was incubated with anti-m6A antibody. The desired m6A-enriched RNA eluate was used to construct cDNA library in parallel with input control.
Conclusion: Our study revealed the difference of m6A-methylated RNA between normal and TCP/TBP/TIP-treated cells by RNA-seq and MeRIP-seq technologies.
 
Overall design Compare the difference of m6A-methyalated RNA between normal and TBP/TCP/TIP treated samples.
 
Contributor(s) Huang L, Zhang J
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Submission date May 19, 2021
Last update date Jul 02, 2021
Contact name Zhang Jun
E-mail(s) 3219030654@stu.cpu.edu.cn
Phone 15651718659
Organization name China Pharmaceutical University
Lab zhoulab
Street address longmiandadao
City nanjing
State/province jiangsu
ZIP/Postal code 211198
Country China
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (8)
GSM5322346 Control_IP
GSM5322347 Control_RNAinput
GSM5322348 TBP_IP
Relations
BioProject PRJNA731051
SRA SRP320476

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
GSE174678_RAW.tar 161.4 Mb (http)(custom) TAR (of BW, CSV)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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