|
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.
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|
|
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.
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|
|
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 |