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Sample GSM1720619 Query DataSets for GSM1720619
Status Public on Jun 30, 2016
Title K562 DRIP-seq
Sample type SRA
 
Source name erythromyeloblastoid leukemia cell line
Organism Homo sapiens
Characteristics cell line: K562
Extracted molecule genomic DNA
Extraction protocol Standard Illumina protocols.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2000
 
Description RNA/DNA hybrids
Genomic DNA was fragmented using HindIII, EcoRI, BsrGI, XbaI and SspI.
Data processing Library strategy: DRIP-Seq
DRIPc-seq, DRIP-seq, MethylC-seq, RNA-seq: All fastq files were trimmed with FastqMcf before mapping.
DRIPc-seq, DRIP-seq: Trimmed fastq reads were mapped to hg19 or mm9 using BWA 0.6.1 and Bowtie2.2.1. Peak calling was performed using a custom HMM algorithm.
RNA-seq: Trimmed fastq reads were mapped to hg19 using TopHat 2.0.5.
MethylC-seq: Trimmed fastq reads were mapped to hg19 using Bismark 0.7.7.
Genome_build: GRCh37 (hg19)
Supplementary_files_format_and_content: wig files, bed files, bedGraph files.
 
Submission date Jun 23, 2015
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)
GSE70189 Human and mouse DRIP-seq and DRIPc-seq
Relations
BioSample SAMN03787480
SRA SRX1070682

Supplementary file Size Download File type/resource
GSM1720619_K562_DRIP.wig.gz 245.4 Mb (ftp)(http) WIG
GSM1720619_K562_DRIP_peaks.bed.gz 417.1 Kb (ftp)(http) BED
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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