NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM879075 Query DataSets for GSM879075
Status Public on Nov 01, 2012
Title D1 11:40_EMF exposure
Sample type RNA
 
Source name ELF-EMF exposure
Organism Homo sapiens
Characteristics tissue source: Healthy volunteers
gender: male
age: 20-30 years
tissue: Peripheral blood
study day: Day1
time-point: 11:40
treatment: ELF-EMF exposure (50 Hz EMF of 62.0 ± 7.1 μT for 2h)
Treatment protocol 17 healthy male subjects age 20 -30 each received an extremely low frequency electromagnetic field exposure (ELF-EMF) on study day 1 repeated on study day 3 (7 days later), a sham exposure ( using counterwound coils in the 1 M cube exposure frames) on study day 2 (the day after study day 1) and a null exposure (no current through coils) on study day 4 (the day after study day 3). All exposures (ELF-EMF, sham or null) were for 2 h at 11.00 - 13.00. 10 ml blood samples were collected at each time point by cannula at 9.00, 11.00, 11.05, 11.10, 11.20,11.40, 12.20, 13.00, 15.00 and 17.00) and transfered directly into PAXgene blood tubes.
Extracted molecule total RNA
Extraction protocol The whole blood samples collected in PAXgene blood tubes were stored a 4C overnight and the RNA was extracted the next day with the PAXgene Blood RNA kit from QIAGEN according to the manufacturer's instructions, including the DNase treatment. A pooling strategy was used to detect significant responses that occur in most or all of the volunteers. Equal amounts of RNA (300 ng/sample) were pooled from the 17 RNA samples samples for each of the 40 time points on study days 1 to 4. The 260/280 nm ratio of all pools was > 2.0. The 40 pooled RNA samples were assayed by Agilent Bioanalyser for RNA Integrity Number (RIN) and all RIN values were >8.0 (38/40>9.0).
Label biotin
Label protocol Biotinylated cRNA samples were prepared with the Illumina TotalPrep RNA Amplification kit from Ambion.
 
Hybridization protocol Standard Illumina hybridization protocol
Scan protocol Standard Illumina scanning protocol using the Beadarray reader.
Description SAMPLE 6
pooled RNA samples using equal amounts of RNA from the 17 volunteers
Data processing Beadstudio v.2.3.47 was used for processing the raw data and the Average method was used for normalization. Averaged data were filtered for probes with detection pvalue < 0.01 in at least one sample.
 
Submission date Feb 22, 2012
Last update date Nov 01, 2012
Contact name James Metcalfe
E-mail(s) [email protected]
Organization name University of Cambridge
Department Biochemistry
Street address 80 Tennis Court Road
City Cambridge
ZIP/Postal code CB2 8PJ
Country United Kingdom
 
Platform ID GPL6097
Series (1)
GSE35999 Gene expression profiles in white blood cells of volunteers exposed to a 50 Hz electromagnetic field

Data table header descriptions
ID_REF
VALUE Average normalized signal intensity
Detection Pval

Data table
ID_REF VALUE Detection Pval
940746 99.79823 0
940731 1303.86 0
940707 503.8197 0
940692 112.953 0
940673 15.91453 0.06394199
940671 491.9555 0
940632 232.8577 0
940600 17.8104 0.0468029
940592 90.54936 0
940577 106.0859 0
940576 26.35067 0.009887937
940546 63.16384 0
940504 324.8325 0
940500 385.9136 0
940494 114.12 0
940487 748.9152 0
940463 1455.581 0
940452 153.778 0
940451 112.3037 0
940435 38.99279 0.000659196

Total number of rows: 16736

Table truncated, full table size 390 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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