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Sample GSM1108097 Query DataSets for GSM1108097
Status Public on Jul 09, 2013
Title NT2 input 2
Sample type SRA
 
Source name NT2 input 2
Organism Homo sapiens
Characteristics cell line: Ntera2
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted from NT2 cells and was either fragmented using HindIII, EcoRI, BsrGI, XbaI and SspI (DRIP-seq 1) or BamHI, NcoI, ApaLI, NheI and PvuII (DRIP-seq 2). Monoclonal S9.6 antibody was used to enrich for RNA/DNA hybrids.
Sequencing library was constructed using standard Illumina protocol.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2000
 
Description gDNA digested with BamHI, NcoI, ApaLI, NheI and PvuII
Data processing Library strategy: DRIP-seq
Fastq reads were aligned to hg19 using BWA version 0.6.1
Peak calling was performed using MACS 1.4.2
Genome_build: hg19
Supplementary_files_format_and_content: wig files were generated by MACS
 
Submission date Mar 27, 2013
Last update date May 15, 2019
Contact name Yoong Wearn Lim
E-mail(s) ywlim@ucdavis.edu
Organization name University of California, Davis
Department Molecular and Cellular Biology
Lab Chedin
Street address One Shields Avenue
City Davis
State/province CA
ZIP/Postal code 95616
Country USA
 
Platform ID GPL11154
Series (1)
GSE45530 DNA-RNA Immunoprecipitation sequencing (DRIP-seq) of human NT2 cells
Relations
SRA SRX255722
BioSample SAMN01992771

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data not applicable for this record

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