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Sample GSM320420 Query DataSets for GSM320420
Status Public on Feb 28, 2010
Title EPIC control #9: control
Sample type RNA
 
Source name peripheral blood
Organism Homo sapiens
Characteristics control
Extracted molecule total RNA
Extraction protocol weWe used snap frozen PBMC enriched blood (~ 300 µl) from the EPIC study for RNA extraction. Blood samples were directly thawed in 5ml of TRI Reagent BD (Molecular Research Center, Inc, USA). RNA was extracted according to the manufactures instruction and stored in 70% ethanol until finalization of preparation and dilution in H2O. For further RNA purification we applied Qiagen MinElute columns (Qiagen, Germany). By this method we extracted 960ng RNA (mean; range 120 – 2500ng). One sample contained no RNA. The OD ratio 260/280 was 2.01 in mean (range 1.76-2.06). For the LC-group, we drew 2.5 ml blood directly into PAXgene vials providing stabilization of the gene expression profile. Samples were rested over night at room temperature and then stored at -80°C until further preparation. RNA was extracted according to the manufactures instruction (Qiagen, Hilden, Germany).
Label biotin
Label protocol Biotin labeled cRNA preparation was performed using the Ambion® Illumina RNA amplification kit (Ambion, UK). Quality was controlled using a PCR based system1.
 
Hybridization protocol For hybridization samples were applied to the arrays and assembled into HybCartridges (Illumina). BeadChips were hybridized for 16h at 55°C on the BeadChip Hyb Wheel. 1.5 μg biotin labeled cRNA was hybridized to Sentrix® whole genome bead chips 6 x 2 V1 and V2 (Illumina, USA) according to the manufacturers instruction. Arrays were washed according to Illumina Wash BeadChip 6 x 2 protocol. Signals were developed with streptavidin Cy3.
Scan protocol Scanning was performed on the Illumina(r) BeadStation 500x.
Description All samples were taken from smokers. EPIC cases were taken from the EPIC trial (a large prospective epidemiological trial in Europe, and are incident cases), Cosmos and BC cases are prevalent cases from a Cologne, Germany based epidemiological trial.
Data processing BeadStudio raw data were normalized using R
 
Submission date Sep 13, 2008
Last update date Oct 23, 2009
Contact name Thomas Zander
Organization name University Hospital Cologne
Street address Kerpenerstr. 62
City Cologne
ZIP/Postal code 50924
Country Germany
 
Platform ID GPL6102
Series (1)
GSE12771 Lung cancer prediction

Data table header descriptions
ID_REF
VALUE Normalized Value

Data table
ID_REF VALUE
ILMN_1816125 29.0926298
ILMN_1833258 38.88628779
ILMN_1714952 41.11321488
ILMN_1687193 40.70211291
ILMN_1882087 41.770105
ILMN_1915050 42.60420221
ILMN_1817473 44.41616047
ILMN_1875644 39.65372558
ILMN_1839320 52.08897
ILMN_1763196 39.44291465
ILMN_1799335 43.1736807
ILMN_1671748 34.44483209
ILMN_1865290 41.25162105
ILMN_1750173 40.13071035
ILMN_1687508 45.49444453
ILMN_1828625 41.09486047
ILMN_1853344 39.15572151
ILMN_1869877 40.66632709
ILMN_1789641 36.44803186
ILMN_1916616 43.08066093

Total number of rows: 48702

Table truncated, full table size 1181 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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