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Series GSE133621 Query DataSets for GSE133621
Status Public on Jul 02, 2019
Title Transcriptomics analysis of gene expression in wildtype and NSUN2 knockdown T24 cell
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Total RNA was isolated using TRIzol® Reagent (Ambion). The RNA concentration and quality were determined with NanoDrop, Qubit and agarose gel analysis. The Dynabeads® mRNA Purification Kit (Ambion) was used to enrich the mRNAs, which were used as templates for RNA-Seq library construction. RNA-Seq libraries was directly constructed by using KAPA mRNA Stranded mRNA-Seq Kit (KAPA) according to the manufacturer’s instructions. The libraries were sequenced on the Illumina HiSeq X-Ten platform at Novogene (Tianjin, CA) with paired-end 150 bp read length. The different genes expression between the control and NSUN2 knockdown cell were detected.
 
Overall design Examination of gene expressive levels in wildtype and NSUN2 knockdown T24 cell
 
Contributor(s) Chen X, Li A, Sun B, Xie D, Yang Y
Citation(s) 31358969
Submission date Jul 01, 2019
Last update date Apr 23, 2020
Contact name Bao-Fa Sun
E-mail(s) sunbf@big.ac.cn
Organization name Beijing Institute of Genomics (BIG) of Chinese Academy of Sciences (CAS)
Street address Da-Tun Road
City Beijing
ZIP/Postal code 100101
Country China
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (4)
GSM3913327 siControl-T_rep1
GSM3913328 siControl-T_rep2
GSM3913329 siNSUN2-T_rep1
This SubSeries is part of SuperSeries:
GSE133671 m5C Promotes Pathogenesis of the Bladder Cancer Through Stabilizing mRNAs
Relations
BioProject PRJNA552053
SRA SRP212699

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE133621_reads-count-cell-line.txt.gz 363.2 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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