NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM747878 Query DataSets for GSM747878
Status Public on Feb 20, 2014
Title T1DControl15_2
Sample type RNA
 
Source name T1DControl15
Organism Homo sapiens
Characteristics case/control pair: 15
age at sample (months): 16
time from seroconversion (months): no seroconversion
time from t1d diagnosis (months): no diagnosis
gender: female
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 6.77479138 0.4097497
ILMN_2055271 7.09024498 0.03952569
ILMN_1736007 6.780530768 0.3965744
ILMN_2383229 6.683820069 0.6469038
ILMN_1806310 6.775227747 0.4084322
ILMN_1779670 6.820921099 0.3003953
ILMN_2321282 6.453657242 0.9670619
ILMN_1671474 7.074797607 0.04347826
ILMN_1772582 6.470601022 0.9604743
ILMN_1735698 6.898899884 0.1541502
ILMN_1653355 7.117145642 0.03689064
ILMN_1717783 7.095499849 0.03952569
ILMN_1705025 6.928452239 0.1225296
ILMN_1814316 6.709319851 0.5797101
ILMN_2359168 6.831861903 0.2727273
ILMN_1731507 6.428463642 0.9762846
ILMN_1787689 6.831614643 0.2740448
ILMN_1745607 6.963376898 0.09222662
ILMN_2136495 6.723660763 0.5401844
ILMN_1668111 6.548876767 0.8919631

Total number of rows: 48803

Table truncated, full table size 1648 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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