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Status |
Public on Jun 17, 2015 |
Title |
80-test-NIPP1-RATA-rep2 |
Sample type |
genomic |
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Source name |
HeLa cells, integrated Dam-NIPP1-RATA cassette
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Organism |
Homo sapiens |
Characteristics |
cell line: HeLa transgene: integrated Dam-NIPP1-RATA cassette
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Treatment protocol |
No additional treatment
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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)
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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.)
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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.
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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.
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Scan protocol |
To assess the raw probe signal intensities, chips were scanned using a GeneChip® scanner 3000 (Affymetrix).
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Description |
NIPP1-RATA.wig NIPP1-RATA.bed NIPP1-RATA samples compared to Dam controls
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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
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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 |
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|
Platform ID |
GPL5082 |
Series (1) |
GSE54170 |
Mapping and characterization of promoter-binding sites of protein phosphatase 1 |
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