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Sample GSM6322648 Query DataSets for GSM6322648
Status Public on Jun 11, 2024
Title iMECs cells,BFRTV8d,Day8 [GEF5i8d_2]
Sample type SRA
 
Source name iMECs
Organism Capra hircus
Characteristics cell line: iMECs
cell type: induced Mammary Epithelial Cells
genotype: WT
treatment: reprogramming
Treatment protocol iMECs from fibroblasts with N2B27 and small molecule compounds cocktail induction medium “VTFBR” (500μg/mL VPA, 10 μM Tranylcypromine, 10 μM Forskolin, 1 μM TTNPB, 10 μM RepSox),the induction culture was continued for 8 days.
Growth protocol GEFs were seeded at a density of 5×105 cells per 60 mm dish and cultured in the incubator at 37.5°C in a humidified atmosphere of 5% CO2 with fibroblast culture medium; GMECs were cultured in the incubator at 37.5°C in a humidified atmosphere of 5% CO2 with GMEC culture medium.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from the treated iMECs with BERTV from day 0 and day 8 using TRIzol Reagent according the manufacturer’s instructions (Invitrogen) and genomic DNA was removed using DNase I (TaKara).
RNA-seq transcriptome library was prepared following TruSeqTM RNA sample preparation Kit from Illumina using 1μg of total RNA.
 
Library strategy miRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina NextSeq 500
 
Data processing Illumina seqencing reads were cleaned for quality control and tested the results using FastQC(version0.10.1).
Ribosome RNA were removed again from clean reads
High-quality reads were mapped to the refer genome to obtain BAM files
the read count for each gene in each sample was counted by HTSeq, and the fragments per kilobase of million mapped reads (FPKM) was then calculated
Differential expression analysis was performed using DESeq2 (v1.16.0) with read count
Assembly: CaprahircusARS1
Supplementary files format and content: counts
 
Submission date Jul 11, 2022
Last update date Jun 11, 2024
Contact name ben huang
E-mail(s) benhuang@gxu.edu.cn
Organization name School of Animal Science and Technology, Guangxi University
Street address NO.100. DAXUE EAST RD, Nanning
City Guangxi
ZIP/Postal code 530004
Country China
 
Platform ID GPL21299
Series (1)
GSE207893 Direct Reprogramming of Fibroblasts into Functional Mammary Epithelial cells by small molecules (bulk miRNA-seq)
Relations
BioSample SAMN29630417
SRA SRX16114196

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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