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Sample GSM1139031 Query DataSets for GSM1139031
Status Public on Mar 12, 2014
Title KYSE70_input
Sample type SRA
 
Source name KYSE70_input
Organism Homo sapiens
Characteristics cell lines: KYSE70
antibody: none
Growth protocol RPMI1640 +10% FBS
Extracted molecule genomic DNA
Extraction protocol Crosslinked with 1% formaldehyde, washed with PBS, lysed in lysis buffer (1% SDS, 10mM EDTA, 50mM Tris-HCl, pH 8.0), sonicated with Covaris E210 to shear DNA to 200-1500bp. After immunoprecipitation or without immunoprecipitation for input, beads were washed, RNase A and Proteinase K treated and reverse crosslinked in elution buffer (1% SDS, 0.1M NaHCO3). DNAs were column purified and subjected to standard Illumina library construction.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2000
 
Description Input
Data processing Bowtie alignment
read counts normalization in 100kb window size
Peak calling (MACS 1.4.1)
Genome_build: hg18
Supplementary_files_format_and_content: MACS_peak files
 
Submission date May 10, 2013
Last update date May 15, 2019
Contact name Shouyong Peng
E-mail(s) shouyongpeng@gmail.com
Organization name Dana-Farber Cancer Institute
Department Medical Oncology
Lab Bass
Street address 450 Brookline Avenue
City Boston
State/province MA
ZIP/Postal code 02215
Country USA
 
Platform ID GPL11154
Series (1)
GSE46837 SOX2 and p63 occupancy in human squamous carcinoma cell lines and embryonic stem cells.
Relations
BioSample SAMN02142030
SRA SRX277130

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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