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Sample GSM1611871 Query DataSets for GSM1611871
Status Public on Feb 12, 2018
Title Brd7oe_ChIP-seq
Sample type SRA
 
Source name embryonic kidney cells
Organism Homo sapiens
Characteristics cell type: human embryonic kidney cell line transformed with adenovirus 5 DNA
tissue: kidney
genotype: BRD7 overexpression
antibody: Monoclonal ANTI-FLAGĀ® M2 antibody (Sigma Aldrich, Cat# F1804)
cell line: HEK293
Treatment protocol Overexpression of BRD7 gene
Growth protocol HEK293 cells were grown in DMEM media containing 10% FBS
Extracted molecule genomic DNA
Extraction protocol Lysates were clarified from sonicated nuclei and the FLAG fusion Brd7 protein-DNA complexes were isolated with mouse-anti-human, Monoclonal ANTI-FLAGĀ® M2 antibody (Sigma Aldrich, Cat# F1804)
Illumina Paired-End DNA Sample Prep kit (Part#1005063) was used to perform end repair, adenylate 3' ends and to ligate adapters.The purified adapter-ligated DNA fragments were then PCR amplified and the products with length of 100bp - 300bp(including adapters) were used for library construction.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2000
 
Data processing Raw data was generated and processed through standard Illumina pipeline.
Reads were cleaned by wiping 3' adaptor, empty and low-quality reads, and then were aligned to human genome database hg19 using SOAP 2.21.
Peak-calling using MACS 1.4.0
Genome_build: hg19
Supplementary_files_format_and_content: Wig files for each chromosome were gzipped, separately, and packed into 1 tar file of each lane. Fold enrichment represents reads on peak region against random Poisson distribution with local lambda.
 
Submission date Feb 17, 2015
Last update date May 15, 2019
Contact name Wei Xiong
E-mail(s) xiongwei@csu.edu.cn
Organization name Central South University
Department Cancer Research Institute
Street address 110 Xiangya Road
City Changsha
State/province Hunan
ZIP/Postal code 410078
Country China
 
Platform ID GPL11154
Series (2)
GSE65974 Genome-wide maps of Brd7 binding sites in control and BRD7 overexpressed cells.
GSE65981 BRD7 overexpression cells
Relations
BioSample SAMN03351750
SRA SRX878830

Supplementary file Size Download File type/resource
GSM1611871_HEK293_BRD7oe.wig.gz.tar.gz 117.6 Mb (ftp)(http) TAR
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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