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Sample GSM544724 Query DataSets for GSM544724
Status Public on May 20, 2010
Title 3T3-L1_24hr_Input
Sample type SRA
 
Source name 24hr_Input
Organism Mus musculus
Characteristics cell line: 3T3-L1
developmental stage: 24 hr after inducing differentiation
chip antibody: --
Treatment protocol ChIP was performed as described using cross-linked 3T3-L1 nuclear lysates.
Growth protocol 3T3-L1 cells were obtained from American Type Culture Collection and differentiated to adipocytes according to standard protocol. All cells were cultured in high-glucose DMEM supplemented with 10% fetal bovine serum and 100 U/ml penicillin and 100 μg/ml streptomycin.
Extracted molecule genomic DNA
Extraction protocol ChIP samples were amplified using the ChIP-Seq Sample Prep Kit (Illumina) according to manufacturer's instructions. Sequence reads of 36 bp were obtained using the Solexa Analysis Pipeline, and mapped to the mouse genome (mm8) using ELAND allowing up to two mismatches. Uniquely positioned reads were included for further analysis such that each start coordinate was represented once.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer II
 
Description Input; no peak file
Data processing Peak detection for H3K9ac ChIPseq data was determined by STAR. CEBPb and GR transcription factor binding data were analyzed with GLITR. Masking file contains regions enriched in input DNA from 3T3-L1 cells.
 
Submission date May 19, 2010
Last update date May 15, 2019
Contact name David Steger
E-mail(s) stegerdj@mail.med.upenn.edu
Organization name University of Pennsylvania
Street address 415 Curie Blvd
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platform ID GPL9250
Series (1)
GSE21898 Propagation of Adipogenic Signals through an Epigenomic Transition State
Relations
SRA SRX020956
BioSample SAMN00013672

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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