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Sample GSM4838090 Query DataSets for GSM4838090
Status Public on Oct 21, 2020
Title TOP2B_1523_ETO
Sample type SRA
 
Source name Glioma cells
Organism Homo sapiens
Characteristics chip antibody: TOP2B
Treatment protocol 50x10e6 cells were treated with etoposide or DMSO, crosslinked using formaldehyde 1%.
Extracted molecule genomic DNA
Extraction protocol Nuclear extracts were isolated, chromatin fragmented using Covaris sonicator in 1mL tubes for 1min. 10 ug of antibody (TOP2A Abcam TOP2B Abcam) wasc incubated overnight. Washes with RIPA Buffer 4 times and once of TE with 50mM NaCl. Reversed crosslink and DNA purified for sequencing using phenol:chloroform:isoamyl alcohol.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer
 
Data processing ChIP-seq reads were aligned to the hg19 genome assembly using bwa mem.
peaks were called using macs2 with the default setting.
Genome_build: hg19
Supplementary_files_format_and_content: narrowPeak files were generated using macs2.
 
Submission date Oct 20, 2020
Last update date Oct 21, 2020
Contact name Junfei Zhao Zhao
E-mail(s) zjf19870628@gmail.com
Organization name Columbia University
Street address 1130 St. Nicholas Ave
City New York
State/province NY
ZIP/Postal code 10032
Country USA
 
Platform ID GPL9052
Series (1)
GSE133263 TOP2B binding and enzymatic activity on promoters and introns modulates multiple oncogenes in human gliomas [ChIP-seq]
Relations
BioSample SAMN16489400
SRA SRX9318380

Supplementary file Size Download File type/resource
GSM4838090_TOP2B_1523_ETO_peaks.xls.gz 12.5 Kb (ftp)(http) XLS
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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