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Sample GSM7905281 Query DataSets for GSM7905281
Status Public on Dec 01, 2024
Title Sham Control, rep3
Sample type SRA
 
Source name kidney, glomeruli
Organism Rattus norvegicus
Characteristics tissue: kidney, glomeruli
treatment: Sham Control
Treatment protocol day 0 tail vein injection of 50 mg/kg PAN, treatment thereafter 15mg/kg MP IP injection or 10mg/kg Pio PO daily. Healthy and disease controls received vehicle PO daily.
Growth protocol ad libitum water and standard chow, 12h/12h light/dark cycle, temperature/humidty controlled environment
Extracted molecule total RNA
Extraction protocol Total RNA from the isolated glomeruli was extracted using the RNeasy Mini Kit #74104, Qiagen
350 ng total RNA was prepared to libraries with TruSeq Standard total RNA with Ribo-Zero Globin Complete kit, Illumina
To generate directional signals in RNA seq data, libraries were constructed from first strand cDNA using TruSeq Standard total RNA with Ribo-Zero Globin Complete kit from Epicentre Biotechnologies
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 4000
 
Data processing . Sequencing adapters matching at least 6 bases were then removed from the reads, as well as low-quality bases (<10) using v1.10 of cutadapt (https://cutadapt.readthedocs.io/en/stable/index.html)
An alignment report was also generated, using custom scripts, and manually reviewed to ensure that at least ~80% of reads aligned to the expected reference, and that at least ~50% of the reads aligned to features annotated as protein coding
Each sample was aligned to the Rnor_6.0 assembly of the Rattus norvegicus reference from the National Center for Biotechnology Information (NCBI) using version 2.5.0c of the RNA-Seq aligner STAR (http://bioinformatics.oxfordjournals.org/content/29/1/15)
Transcript features were identified from the general feature format (GFF) file that came with the assembly from the NCBI. Feature coverage counts were calculated using HTSeq (http://www-huber.embl.de/users/anders/HTSeq/doc/count.html).
raw RNA-Seq gene expression data were normalized, and post-alignment statistical analyses and figure generation were performed using DESeq2 (http://genomebiology.com/2014/15/12/550) and custom analysis scripts written in R.
Comparisons of gene expression and associated statistical analyses were made between different conditions of interest using the normalized read counts. All fold-change values were expressed as test condition / control condition, where values <1 were denoted as the negative of its inverse (note that there will be no fold change values between –1 and 1, and that the fold changes of “1” and “-1” represent the same value)
Transcripts were considered significantly differentially expressed using a 10% false discovery rate (DESeq2 adjusted P value < 0.1). Genes were removed from comparisons if they were not expressed above a background threshold (0.5 reads per million) for most samples within each group
Assembly: Rnor_6.0 assembly
Supplementary files format and content: htseq.cov files contain waw counts of reads per gene generated by HTSeq v0.6.1p1.
Supplementary files format and content: AllData_160322_RNASeq_Smoyer_Results_iScience.xlsx contains DESeq2 normalized counts per gene for all samples.
 
Submission date Nov 16, 2023
Last update date Dec 01, 2024
Contact name William E Smoyer
E-mail(s) [email protected]
Organization name Nationwide Children's Hospital, Columbus, Ohio
Department Research
Lab Smoyer
Street address 700 Children's Dr, Research Building 2
City Columbus
State/province OH
ZIP/Postal code 43205
Country USA
 
Platform ID GPL22396
Series (1)
GSE248053 Glucocorticoid- and Pioglitazone-Induced Proteinuria Reduction in Experimental Nephrotic Syndrome Both Correlate with Glomerular ECM Modulation
Relations
BioSample SAMN38286209
SRA SRX22550784

Supplementary file Size Download File type/resource
GSM7905281_119_CONTROL_Dnase.htseq.cov.gz 136.9 Kb (ftp)(http) COV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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