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Series GSE114015 Query DataSets for GSE114015
Status Public on Dec 05, 2019
Title RNA sequencing data of Wild Type and Fmr1 KO hippocampal neuron
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Fragile X syndrome (FXS), caused by mutations in fragile X mental retardation 1 gene (FMR1), is a prevailing genetic disorder of intellectual disability and autism. Analysis of transcriptome outcome (differentially expressed genes between WT and Fmr1 KO hippocampal neuron) associated with FXS reveal promising value of gene signature-based computation in repurposing drugs for potential practical treatment.
 
Overall design Primary DIV (Days in vitro) 14 Hippocampal neuron mRNA profiles of Wild Type (WT) and Fmr1 KO mice were generated in triplicate
 
Contributor(s) Wang H, Sethna F, Ding Q, Wu X, Chen P, Miao Z, Zhang Y, Xiao H, Feng W, Feng Y, Li X
Citation(s) 32179850
Submission date May 03, 2018
Last update date Mar 30, 2020
Contact name Zhuang Miao
E-mail(s) miaozhua@msu.edu
Organization name Michigan State University
Department Physiology
Lab Hongbing Wang
Street address 567 Wilson Road
City East Lansing
State/province Michigan
ZIP/Postal code 48824
Country USA
 
Platforms (1)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
Samples (6)
GSM3130692 WT rep1
GSM3130693 WT rep2
GSM3130694 WT rep3
Relations
BioProject PRJNA454880
SRA SRP144498

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
GSE114015_WTvsFmr1KO.FPKM.DEG.txt.gz 2.4 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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