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Sample GSM674218 Query DataSets for GSM674218
Status Public on Apr 01, 2011
Title non-smoker 352M
Sample type RNA
 
Source name maternal peripheral blood, non-smoker
Organism Homo sapiens
Characteristics tissue: maternal peripheral blood
smoking status: non-smoker
age (years): 32.4380561259411
maternal bmi: 21.3839419960573
parity: 3
gestational age (weeks): 39
mode of delivery: vaginal
placental weight (g): 500
newborn weight (g): 2770
apgar score (5s): 10
maternal blood cotinine (ng/ml): 0.185155912584909
cord blood cotinine (ng/ml): 0.380122956169511
individual: 352
Extracted molecule total RNA
Extraction protocol Peripheral blood was sampled and processed using the LeukoLOCK™ Total RNA Isolation System (Ambion, Austin, TX, USA) according to the manufacturer manual. The system employs filter-based leukocyte-depletion technology to isolate leukocytes from whole blood and RNAlater™ (Ambion) to stabilize the cells on the filter. By removal of red blood cells, the RNA purified from captured leukocytes is inherently depleted of globin mRNA, which improves sample quality for expression profiling and other applications. Integrity of the total RNAs was assayed by the Bioanalyzer 2100 (Agilent Technologies, Santa Clara, CA, USA), and only samples with RNA integrity number (RIN) above 7.0 were used for gene expression profiling.
Label biotin
Label protocol Biotinylated cRNA was prepared from 200 ng of total RNA using the Illumina TotalPrep RNA Amplification Kit (Ambion). In vitro transcription (IVT) was performed at 37°C for 14 hours.
 
Hybridization protocol 750 ng of biotinylated cRNA was hybridized to the array for 17 hours according to the manufacturer manual. Final staining was performed with streptavidin conjugated to Cy-3 fluorescent dye.
Scan protocol Arrays were scanned using BeadArray Reader (Illumina), and bead level data were extracted by BeadStudio Software (Illumina).
Description 352M
Data processing Bead summary data were imported into the R statistical environment (www.r-project.org) and normalized by the quantile method in the Lumi package. Only probes that reached detection P-value < 0.01 in all samples were used for further analyses. Differentially expressed genes were analysed in the Limma package. A linear model was fitted for each gene given a series of arrays using the lmFit function. Using the Benjamini and Hochberg method, P-values were corrected for multiple testing. The M, PL, and D groups were normalized separately.
 
Submission date Feb 13, 2011
Last update date Apr 01, 2011
Contact name Hana Bruchova
E-mail(s) Hana.Bruchova@uhkt.cz
Phone +420221977306
Fax +420221977371
Organization name Institute of Hematology and Transfusion
Department Molecular Genetics
Lab Genomics
Street address U nemocnice 1
City Prague 2
ZIP/Postal code 128 20
Country Czech Republic
 
Platform ID GPL6883
Series (1)
GSE27272 Comprehensive Study of Tobacco Smoke-Related Transcriptome Alterations in Maternal and Fetal Cells

Data table header descriptions
ID_REF
VALUE Normalized data

Data table
ID_REF VALUE
ILMN_1802380 9.365722671
ILMN_1792389 5.30213636
ILMN_2375156 3.213711466
ILMN_1697642 6.084573181
ILMN_1681845 8.671199792
ILMN_1690979 3.957862153
ILMN_1811114 1.80275501
ILMN_1660729 1.772936421
ILMN_2129572 1.851363914
ILMN_1705659 2.072765363
ILMN_1674774 1.119255089
ILMN_1702329 1.413531073
ILMN_1658806 1.544599926
ILMN_2310896 8.489130103
ILMN_1675927 2.807183871
ILMN_2109994 7.560605764
ILMN_1745256 8.227969336
ILMN_2191313 6.056074891
ILMN_1689123 8.819385957
ILMN_1674337 7.147995647

Total number of rows: 24526

Table truncated, full table size 596 Kbytes.




Supplementary data files not provided
Raw data are available on Series record
Processed data included within Sample table

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