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Series GSE125356 Query DataSets for GSE125356
Status Public on Nov 12, 2021
Title RNA-seq based transcriptome profiling of Carpesium cernuum extract (CCE) treated MDA-MB-231 cell lines
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary To understand the molecular mechanism of CCE, we performed the RNA-seq analysis. Cells were seeded at 5x10^5 cells/well in 6-well plates then treated with 1μg/mL CCE for 24 h. MDA-MB-231 cells were harvested, and RNA was isolated with TRIzol. The libraries were constructed by using the Quick cDNA Library Preparation Kit and sequenced on an XTEN sequencing system. RNA-seq data were mapped to the reference genome (hg19) by using HISAT2. The reads were counted, and StringTie was used to calculate the FPKM value of the genes. The differentially expressed genes (DEGs) were identified by comparing the experimental group with the control group.
 
Overall design mRNA profiles of control group and CCE group were generated by RNA sequencing.
 
Contributor(s) Dang H, Deng L, Xie L
Citation(s) 31480012
Submission date Jan 18, 2019
Last update date Feb 14, 2022
Contact name Honglei Dang
E-mail(s) hongleidang@capitalbio.com
Organization name National Engineering Research Center for Beijing Biochip Technology
Street address 18 Life Science Parkway, Changping District
City Beijing
ZIP/Postal code 86-010-61777540
Country China
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (2)
GSM3569394 MDA18010029_N709
GSM3569395 MDA18010031_N711
Relations
BioProject PRJNA515909
SRA SRP180304

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
GSE125356_RAW.tar 1.7 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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