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Status |
Public on Nov 27, 2024 |
Title |
Control2,rep2 |
Sample type |
SRA |
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Source name |
T24
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Organism |
Homo sapiens |
Characteristics |
cell line: T24 cell type: Human bladder cancer cells genotype: Control
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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
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Description |
Control2
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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
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Submission date |
Oct 20, 2024 |
Last update date |
Nov 27, 2024 |
Contact name |
Changxue Liu |
E-mail(s) |
[email protected]
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Organization name |
The Affiliated Hospital of Qingdao University
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Street address |
Qingdao, Shandong, China
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City |
Qingdao |
State/province |
Shandong |
ZIP/Postal code |
266000 |
Country |
China |
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Platform ID |
GPL24676 |
Series (1) |
GSE279910 |
NOTCH3 Promotes Malignant Progression of Bladder Cancer by Directly Regulating SPP1 and Activating PI3K/AKT Pathway |
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Relations |
BioSample |
SAMN44358570 |
SRA |
SRX26434686 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
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