|
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 |