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Sample GSM8583250 Query DataSets for GSM8583250
Status Public on Nov 27, 2024
Title Control2,rep2
Sample type SRA
 
Source name T24
Organism Homo sapiens
Characteristics cell line: T24
cell type: Human bladder cancer cells
genotype: Control
Extracted molecule total RNA
Extraction protocol RNA was harvested using Trizol reagent. Illumina TruSeq RNA Sample Prep Kit (Cat#FC-122-1001) was used with 1 ug of total RNA for the construction of sequencing libraries.
RNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Description Control2
Data processing Basecalls performed using CASAVA version 1.8
Adapters and low-quality read ends were removed using Trimmomatic, based on quality control statistics generated by FastQC.
Quality filtered reads were then mapped to GRCh38 using Hisat2
The expression level of each transcript was calculated according to the fragments per kilobase of exon per million mapped reads (FRKM) . StringTie was used to quantify gene and isoform abundances.
R statistical package software EdgeR (Empirical analysis of Digital Gene Expression in R) was utilized for differential expression analysis.
Assembly: GRCh38
Supplementary files format and content: Matrix table with raw gene counts for every gene and every sample
 
Submission date Oct 20, 2024
Last update date Nov 27, 2024
Contact name Changxue Liu
E-mail(s) [email protected]
Organization name The Affiliated Hospital of Qingdao University
Street address Qingdao, Shandong, China
City Qingdao
State/province Shandong
ZIP/Postal code 266000
Country China
 
Platform ID GPL24676
Series (1)
GSE279910 NOTCH3 Promotes Malignant Progression of Bladder Cancer by Directly Regulating SPP1 and Activating PI3K/AKT Pathway
Relations
BioSample SAMN44358570
SRA SRX26434686

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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