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Sample GSM4200336 Query DataSets for GSM4200336
Status Public on May 16, 2020
Title pkd1_input
Sample type SRA
 
Source name epithelial cells
Organism Mus musculus
Characteristics tissue: Kidney
cell type: pkd1(PH)
chip antibody: none
Growth protocol pkd1 and null cells were cultured in DMEM-F12 medium supplemented with 3% fetal bovine serum (FBS) and 1% penicillin/streptomycin,1% Insulin-Transferrin-Selenium, IFNγ, Nystatin suspension and T3.
Extracted molecule genomic DNA
Extraction protocol pkd1 and null cells were cross-linked with 1% formaldehyde for 10 min at RT. The crosslink was stopped by adding 1/20 volume of 2.5 M glycine. Cells were washed with PBS and harvested using ChIP lysis buffer. Cells were then sonicated to obtain fragments (100-500 bp) with Bioruptor Sonicator. Immunoprecipitation was performed with H3K27ac antibody (Abcam cat# ab4729). After elution and reversal cross-linking, DNA was purified and sequenced on BGISEQ-500.
Construction of ChIP-seq library was completed by BGI company (Shenzhen,China).
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model BGISEQ-500
 
Data processing ChIP-seq data were mapped to mus musculus genome (mm10) by SOAPaligner/SOAP2
ChIP-Seq peaks were generated using peak finding algorithm MACS (Model-based Analysis for ChIP -Seq, version: MACS-1.4.2)
Reads mapped only once at locus were allowed for peak calling.
Genome_build: mm10
Supplementary_files_format_and_content: Wig files were generated by MACS-1.4.2.
 
Submission date Dec 02, 2019
Last update date May 16, 2020
Contact name Zeyun Mi
E-mail(s) mizeyun@tmu.edu.cn
Phone 15900207057
Organization name Tianjin Medical University
Street address Qi Xiang Tai Road
City Tianjin
ZIP/Postal code 300070
Country China
 
Platform ID GPL23479
Series (2)
GSE141279 SE-driven metabolic reprogramming in ADPKD (ChIP-Seq)
GSE141281 SE-driven metabolic reprogramming in ADPKD
Relations
BioSample SAMN13446748
SRA SRX7255693

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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