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Sample GSM779431 Query DataSets for GSM779431
Status Public on Jul 31, 2012
Title THAP11_ChIPSeq
Sample type SRA
 
Source name Suspension HeLa cells
Organism Homo sapiens
Characteristics cell line: HeLa, cycling
chip antibody: THAP11; polyclonal anti-THAP11 (G4275, {Dejosez, 2008 #99})
Treatment protocol HeLa-S cells were crosslinked for 8’ using 1% of formaldehyde, DNA was isolated and sonicated to 100-300 bps using a bioruptor (Bioruptor UCD-200, Diagenode) and 30’’ pulses on and off at maximum power. Sonicated DNA was immunoprecipitated, washed and eluted as described (Shweta 2007). 2-8 x 107 cells were used per antibody.
Growth protocol HeLa-S cells were grown in suspension in Joklik's modified Eagles’s medium (JMEM) with 5% of fetal calf serum.
Extracted molecule genomic DNA
Extraction protocol 5-10ng of ChIP-DNA were transformed into libraries using ChIP-Seq DNA Sample Prep Kit (Illumina) and sequenced on Illumina Genome Analyzer 2 DNA sequencing instrument. Total input DNA was also sequenced.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer II
 
Description Chromatin IP against THAP11
Data processing Alignment : The sequenced tags were mapped onto the unmasked genome build hg18 using the fetchGWI software. Only the tags with a unique and perfect match were kept for the analysis
Peak detection : peaks were determined with the sissrs software (www.rajajothi.com/sissrs/). Peaks common to the control input material and the ChIP material, as well as peaks mapping in satellite and micro-satellite repeats and peaks mapping in 18 and 28S rRNA sequences, were eliminated from the analysis.
 
Submission date Aug 16, 2011
Last update date May 15, 2019
Contact name Nicolo Riggi
Organization name CHUV
Department Département de Pathologie Expérimentale
Lab Institut universitaire de pathologie
Street address Bugnon 25
City Lausanne
State/province VD
ZIP/Postal code 1011
Country Switzerland
 
Platform ID GPL9115
Series (3)
GSE31412 Expression changes in HeLa cells treated with siRNA against HCFC1 or control luciferase
GSE31417 Genome-wide study of HCFC1 binding sites and its associated transcription factors in cycling Human HeLa cells
GSE31419 The epigenetic cell-cycle regulator HCF-1 is recruited to active CpG island-containing promoters together with the ZNF143, THAP11(Ronin), YY-1 and GABP transcription factors.
Relations
SRA SRX092574
BioSample SAMN00710519

Supplementary file Size Download File type/resource
GSM779431_THAP11_cycling_aligned.bed.gz 183.8 Mb (ftp)(http) BED
GSM779431_THAP11_cycling_peaks.bedgraph.gz 673.0 Kb (ftp)(http) BEDGRAPH
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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