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Sample GSM2699422 Query DataSets for GSM2699422
Status Public on Nov 26, 2019
Title PrimaryNeuron_treatmentJ147_rep1
Sample type SRA
 
Source name PrimaryNeuron_treatmentJ147
Organism Rattus norvegicus
Characteristics cell type: rat primary neuron
treatment: drugJ147
age: embryo
Treatment protocol Mice were fed control diet and diet containing CAD031, CMS 121 and J147 for four months. Primary neurons were treated with 1μM of each compound for 24h.
Growth protocol All experiments with the SAMP8 animals were performed in accordance with the US Public Health Service Guide for Care and Use of Laboratory Animals and protocols approved by the IACUC at the Salk Institute. Primary cortical neurons were prepared from day seventeen rat embryos and grown in culture as described in Soucek, T. Neuron. 2003 Jul 3;39(1):43-56.
Extracted molecule polyA RNA
Extraction protocol RNA from both primary neurons and adult brain hippocampus was isolated using the RNeasy Plus Universal mini kit (Qiagen).
RNA-seq libraries were performed using stranded mRNA kit from Illumina and sequenced in an Illumina HiSeq 2500 device.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description PrimaryNeuron_FPKM.txt
Data processing FastQC v0.11.5 with default parameter was used for quality test.
Reads were mapped to mm10/rn6 reference genome by STAR v2.5.1 with default parameters. Only uniquely mapped reads were considered for downstream analysis.
RNA-Seq gene expression was quantified by HOMER analyzeRepeats command, summing reads mapped across all gene exons of RefSeq genes.
RNA-Seq differential expression was carried out using edgeR v3.16.1 on the raw counts of replicates. FDR < 0.05 and logFC +/- 1.2 was used as cutoff to identify the DE genes.
Genome_build: mm10; rn6
Supplementary_files_format_and_content: tab delimited text file for RNA-Seq FPKM values.
 
Submission date Jul 10, 2017
Last update date Mar 28, 2022
Contact name April Elizabeth Williams
E-mail(s) [email protected], [email protected]
Phone 7345461645
Organization name Salk Institute for Biological Studies
Department IGC
Street address 10010 N Torrey Pines Rd
City San Diego
State/province California
ZIP/Postal code 92037
Country USA
 
Platform ID GPL18694
Series (1)
GSE101112 Whole transcriptome analysis of brain hippocampal tissue from SAMP8 mice and rat primary neurons treated with the Alzheimer's disease drug candidates CMS121 and J147
Relations
BioSample SAMN07340688
SRA SRX2994520

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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