NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM747918 Query DataSets for GSM747918
Status Public on Feb 20, 2014
Title T1DCase18_5
Sample type RNA
 
Source name T1DCase18
Organism Homo sapiens
Characteristics case/control pair: 18
age at sample (months): 59
time from seroconversion (months): 53
time from t1d diagnosis (months): -0
gender: male
tissue: peripheral blood
hla-dqb1 genotype: 0302
Growth protocol 2.5 ml of venous blood was drawn into PAXgene Blood RNA tubes (PreAnalytix Switzerland), at the Type 1 Diabetes Prediction and Prevention (DIPP) study clinic, Turku, Finland. The samples were incubated for 2 hours at RT and then stored at -70 °C until analyzed.
Extracted molecule total RNA
Extraction protocol Total whole-blood RNA was extracted from the samples using PAX gene RNA Blood RNA kit (Qiagen, Germany) according to manufacturer's instructions. RNA quality and quantity was determined using Nano Drop ND-1000 (Nano Drop Technologies, USA) and Experion Automated Electrophoresis System (Bio-Rad Laboratories, Finland).
Label Cy3
Label protocol 100 ng total RNA was amplified to cDNA with Ovation RNA Amplification System V2 (NuGEN, cat. no 3100-60), including Ovation Whole Blood Reagent (cat. no 1300-60). The amplified cDNA was labelled according to NuGEN’s Illumina Solution protocol, Application Note #2.
 
Hybridization protocol 750 ng each cDNA was hybridized to Human HT-12 Expression BeadChips, version 3 (Illumina, cat. no BD-103-0603) at 58 °C overnight (18 h) according to Illumina Whole-Genome Gene Expression Direct Hybridization protocol, revision A. Hybridizations were detected with 1 ug/ml Cyanine3-streptavidine (GE Healthcare Biosciences cat. no PA43001).
Scan protocol Chips were scanned with Illumina Bead Array Reader, BeadScan software version 3.5. The numerical results were extracted with GenomeStudio2008 v1 without any normalization or background subtraction.
Data processing The intensities were quantile normalized and log2-transformed using R/Bioconductor.
 
Submission date Jun 24, 2011
Last update date Feb 20, 2014
Contact name Henna Kallionpää
E-mail(s) [email protected]
Phone +358-2-333-8001
Organization name University of Turku
Department Turku Centre for Biotechnology
Lab Riitta Lahesmaa
Street address P.O. Box 123
City Turku
ZIP/Postal code FIN-20521
Country Finland
 
Platform ID GPL6947
Series (2)
GSE30210 Genome-wide espression kinetics of children progressing to clinical Type 1 diabetes (T1D).
GSE30211 Gene expression changes during Type 1 diabetes pathogenesis

Data table header descriptions
ID_REF
VALUE Quantile-normalized and log2 transformed.
Detection Pval

Data table
ID_REF VALUE Detection Pval
ILMN_1762337 6.811241258 0.5125165
ILMN_2055271 7.464734422 0.0342556
ILMN_1736007 6.706868668 0.7496706
ILMN_2383229 6.911924295 0.3030303
ILMN_1806310 6.692701095 0.7760211
ILMN_1779670 6.880115235 0.3478261
ILMN_2321282 6.921194352 0.2938077
ILMN_1671474 6.664503513 0.828722
ILMN_1772582 6.84024248 0.428195
ILMN_1735698 6.905855475 0.3096179
ILMN_1653355 6.962911398 0.2371542
ILMN_1717783 6.727048247 0.7114624
ILMN_1705025 6.738478444 0.6890646
ILMN_1814316 6.799687509 0.5335968
ILMN_2359168 6.731318247 0.7009223
ILMN_1731507 6.848787446 0.4097497
ILMN_1787689 6.948343785 0.2648221
ILMN_1745607 6.931382998 0.2806324
ILMN_2136495 6.485488498 0.9736496
ILMN_1668111 6.600490804 0.9077734

Total number of rows: 48803

Table truncated, full table size 1639 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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