NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1224751 Query DataSets for GSM1224751
Status Public on Sep 05, 2013
Title c-FostetON Keratinocyte. 6h. Replicate 1.
Sample type RNA
 
Source name Keratinocytes from the tail
Organism Mus musculus
Characteristics strain: C57BL/6
cell type: c-FostetON keratinocytes
treatment: untreated
time: 6h
Treatment protocol c-FostetON keratinocytes were cultured in the presence/abscence of 1ug/ml of Doxicycline.
Growth protocol Isolation and culture of mouse primary tail keratinocytes was performed as described elsewhere (Zenz et al., 2003). 24h after plating, keratinocyte media was changed to KC-SFM (Gibco). Keratinocytes were cultured at 32ºC. Medium was changed every other day and, if needed, supplemented with Dox at 1μg/L. Cells were collected at different time points after Dox treatment.
Extracted molecule total RNA
Extraction protocol RNA was extracted using Trizol.
Label biotin
Label protocol Standard Illumina protocol
 
Hybridization protocol RNA of samples was hybridized to the Illumina MouseRef-8 V2 R3 BeadChip array according to the manufacturer's instructions (Illumina, Inc., San Diego, CA).
Scan protocol Microarray scanning was done using a Beadstation array scanner.
Description A6h_Fos-dox
Data processing Raw data files from the Illumina chip quantification.
Data preprocessing and quality control was conducted using packages of the Bioconductor project implemented in our in-house developed ChipYard framework for microarray data analysis (http://www.dkfz.de/genetics/ChipYard/). In summary microarray probes were annotated based on Ensembl (version 58) using an in house BLAST-based pipeline. Before normalization with variance-stabilizing transformation (VST) and robust spline normalization (RSN) algorithms beads with signals below the negative controls were removed and positive negative and hybridization controls were excluded.
 
Submission date Sep 05, 2013
Last update date Sep 05, 2013
Contact name Marc Zapatka
Organization name German Cancer Research Center
Department B060 Molecular Genetics
Street address Im Neuenheimer Feld 580
City 69120
ZIP/Postal code Heidelberg
Country Germany
 
Platform ID GPL6885
Series (1)
GSE50621 Expression analyses of inducible c-Fos expressing kerationcytes

Data table header descriptions
ID_REF
VALUE VST transformed, RSN normalized signal
Detection Pval

Data table
ID_REF VALUE Detection Pval
ILMN_2659724 6.773315434 0.315789474
ILMN_2706226 6.705081564 0.862155388
ILMN_1217123 6.721856848 0.763157895
ILMN_2780205 11.45675444 0
ILMN_2713160 6.746239222 0.555137845
ILMN_2650094 6.747571673 0.543859649
ILMN_2703479 6.770953529 0.329573935
ILMN_2952493 6.795057087 0.15914787
ILMN_2731592 6.821243526 0.04887218
ILMN_2729743 6.887731482 0
ILMN_1252621 8.035464191 0
ILMN_3162407 10.36701365 0
ILMN_2692952 6.831466494 0.030075188
ILMN_2910076 6.716480775 0.802005013
ILMN_2709047 7.821763267 0
ILMN_2718462 7.100674039 0
ILMN_2882078 7.868115981 0
ILMN_2882079 6.87132491 0.001253133
ILMN_2771368 6.691009781 0.919799499
ILMN_2724039 6.791775606 0.179197995

Total number of rows: 25697

Table truncated, full table size 844 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap