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Sample GSM6031445 Query DataSets for GSM6031445
Status Public on Jun 29, 2022
Title AT18-Control
Sample type SRA
 
Source name Skeletal muscle
Organism Homo sapiens
Characteristics tissue: Skeletal muscle
cell type: Primary skeletal muscle cells
treatment: unstimulated
Extracted molecule total RNA
Extraction protocol Total RNA from cultured transduced cells was extracted using QIAGEN RNeasy Mini Kit according to the manufacturer’s instructions
A total amount of 1 µg RNA per sample was used as input material for the RNA sample preparations. Sequencing libraries were generated using NEBNext® Ultra TM RNA Library Prep Kit for Illumina® (NEB, USA) following manufacturer’s recommendations and index codes were added to attribute sequences to each sample
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Raw data (raw reads) of FASTQ format were firstly processed through fastp.
Paired-end clean reads were aligned to the reference genome using the Spliced Transcripts Alignment to a Reference (STAR) software v2.5
FeatureCounts was used to count the read numbers mapped of each gene and RPKM was then calculated
Differential expression analysis between control and EPS treated cells was performed using DESeq2 R package v2_1.6.3
Assembly: hg38, GRCh38
Supplementary files format and content: excel file include FPKM values for each sample
 
Submission date Apr 06, 2022
Last update date Jun 29, 2022
Contact name G. Hege Thoresen
E-mail(s) [email protected]
Organization name University of Oslo
Department Section for Pharmacology and Pharmaceutical Biosciences
Street address Sem Sælands vei 3
City Oslo
ZIP/Postal code 0371
Country Norway
 
Platform ID GPL24676
Series (1)
GSE200335 Gene expression profiles of electrically pulse-stimulated human myotubes
Relations
BioSample SAMN27387517
SRA SRX14766595

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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