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Sample GSM624144 Query DataSets for GSM624144
Status Public on Dec 01, 2011
Title Control_ChIPseq
Sample type SRA
 
Source name THP-1, control ChIP-Seq
Organism Homo sapiens
Characteristics cell line: THP-1
cell type: monocytic cells
treatment 1: differentiation with PMA (50ng/ml;40hrs)
treatment 2: 1.5 h of 1microM Rosiglitazone
chip antibody: normal mouse IgG
antibody vendor: Santa Cruz
antibody catalog #: sc-2025
antibody lot #: H0709
Treatment protocol THP-1 cells were differentiated with 50ng/ml of PMA for 40hrs, followed by treatment with Rosiglitazone for 1.5 hrs.
Growth protocol THP-1 cells were passaged in suspension prior to treatment; RPMI medium, 10%FBS, Pen/Strep.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was isolated using phenol/chloroform extraction followed by ethanol precipitation.

10ng of DNA as per manufacturer's protocol. Briefly, using the Solexa ChIP-Seq DNA sample preparation kit, universal linkers were added to the chromatin fragments and DNA was PCR amplified for 15 cycles. DNA was gel-purified and fragments between 200-300bp were selected for sequencing.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer
 
Description Chromatin IP using IgG.
Data processing The raw images have been processed using the Solexa Pipeline and were mapped to the reference genome (NCBI36/hg18) using Eland software with maximal two-mismatches.

Peak detection was performed using CCAT (Xu et al. 2010). Regions enriched in the specific libraries were tested for significance against the tag distribution in a control library (IgG). Peaks with FDR <0.01 were considered for analysis.
 
Submission date Nov 16, 2010
Last update date May 15, 2019
Contact name Sebastian Pott
E-mail(s) spott@uchicago.edu
Organization name University of Chicago
Department Human Genetics
Street address 920 58th Street
City Chicago
State/province Il
ZIP/Postal code 60637
Country USA
 
Platform ID GPL9052
Series (2)
GSE25426 Functional and cellular constraints that shaped the PPARg binding landscape in human and mouse macrophages: human ChIP-Seq
GSE25608 Functional and cellular constraints that shaped the PPARg binding landscape in human and mouse macrophages
Relations
SRA SRX103225
BioSample SAMN00744393

Supplementary file Size Download File type/resource
GSM624144_GA001-SR-R00075_L3.aligned.txt.gz 292.5 Mb (ftp)(http) TXT
GSM624144_GA001-SR-R00075_L4.aligned.txt.gz 290.9 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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