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Sample GSM558907 Query DataSets for GSM558907
Status Public on Mar 02, 2011
Title Srf [ChIP-seq]
Sample type SRA
 
Source name HL-1 cells
Organism Mus musculus
Characteristics strain: C57BL/6J
cell line: HL-1 cardiac muscle cell line
protocol: Srf fbio ChIP
chip antibody: none
Treatment protocol Confluent HL-1 cells were infected with adenovirus expressing cardiac troponin T promoter driving rtTA and BirA expression, and TRE promoter driving transcription factor Srf for 48 hrs before cells harvest for chromatin preparation
Growth protocol HL-1 cells were cultured routinely, and split 1:3 every 3-4 days until full confluence.
Extracted molecule genomic DNA
Extraction protocol Libraries were generated according to Illumina single-end ChIP-seq library preparation ( Cat# IP-102-1001)
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer
 
Description Srf fbio ChIP
Data processing Alignments was done against build mm9 using bowtie, and peaks detection by Sole-Search ( http://havoc.genomecenter.ucdavis.edu/cgi-bin/chipseq.cgi ). Sole-Search Analysis Summary is available as Series GSE21529 supplementary file.
 
Submission date Jun 22, 2010
Last update date May 15, 2019
Contact name Sek Won Kong
E-mail(s) [email protected]
Phone 617-919-2689
Organization name Boston Children's Hospital
Department Informatics Program
Lab EN137
Street address 300 Longwood Avenue
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platform ID GPL9185
Series (1)
GSE21529 Cardiac transcription factors in HL-1 cells: gene expression and genome binding profiling
Relations
SRA SRX022482
BioSample SAMN00016516

Supplementary file Size Download File type/resource
GSM558907_srf.a05fdr001p5_signifpeaks.gff.gz 326.3 Kb (ftp)(http) GFF
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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