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Sample GSM1309138 Query DataSets for GSM1309138
Status Public on Jun 17, 2015
Title 80-test-NIPP1-RATA-rep2
Sample type genomic
 
Source name HeLa cells, integrated Dam-NIPP1-RATA cassette
Organism Homo sapiens
Characteristics cell line: HeLa
transgene: integrated Dam-NIPP1-RATA cassette
Treatment protocol No additional treatment
Growth protocol Polyclonal stable HeLa cell lines with integrated Dam transgenes were generated and grown following standard cell culture procedures, using G418 as selective agent (also: see Vogel et al. 2007 as cited below)
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted from cells (Sigma GeneElute Mammalian Genomic DNA Minprep kit) and processed according to the DamID protocol published in (Vogel, M.J., Peric-Hupkes, D., and van Steensel, B. 2007. Detection of in vivo protein-DNA interactions using DamID in mammalian cells. Nature protocols 2(6): 1467-1478.)
Label biotin
Label protocol Samples were fragmented and labeled with biotin in a terminal labeling reaction according to the Affymetrix WT Double-Stranded DNA Terminal Labeling Kit.
 
Hybridization protocol A mixture of fragmented biotinylated DNA and hybridisation controls (Affymetrix) was hybridised on Affymetrix GeneChip Human Promoter 1.0 R Arrays followed by staining and washing in a GeneChip® fluidics station 450 (Affymetrix) according to the manufacturer’s procedures.
Scan protocol To assess the raw probe signal intensities, chips were scanned using a GeneChip® scanner 3000 (Affymetrix).
Description NIPP1-RATA.wig
NIPP1-RATA.bed
NIPP1-RATA samples compared to Dam controls
Data processing MAT (Model-based Analysis for Tiling Arrays) analysis algorithm used to detect regions enriched by immunoprecipitation on Affymetrix tiling array. Bed-files are text files containing the enriched genomic regions. MAT algorithm settings: Bandwidth = 300, MaxGap = 300, MinProbes = 5, p-value = 1.00E-04
 
Submission date Jan 16, 2014
Last update date Jun 17, 2015
Contact name Rekin's Janky
E-mail(s) Nucleomics.Bioinformatics@vib.be
Organization name VIB
Department Nucleomics Core
Street address Herestraat 49 Box 816
City Leuven
ZIP/Postal code B-3000
Country Belgium
 
Platform ID GPL5082
Series (1)
GSE54170 Mapping and characterization of promoter-binding sites of protein phosphatase 1

Supplementary file Size Download File type/resource
GSM1309138_hyb10548_Hs_PromPR_v02_.CEL.gz 18.7 Mb (ftp)(http) CEL
Processed data are available on Series record

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