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Sample GSM674344 Query DataSets for GSM674344
Status Public on Apr 01, 2011
Title non-smoker 302D
Sample type RNA
Source name cord blood, non-smoker
Organism Homo sapiens
Characteristics tissue: cord blood
smoking status: non-smoker
age (years): 20
maternal bmi: 21
parity: 1
gestational age (weeks): 39
mode of delivery: vaginal
placental weight (g): 580
newborn weight (g): 2900
apgar score (5s): 10
maternal blood cotinine (ng/ml): 0.16
cord blood cotinine (ng/ml): 0.33
individual: 302
Extracted molecule total RNA
Extraction protocol Umbilical cord 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 302D
Data processing Bead summary data were imported into the R statistical environment ( 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
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
VALUE Normalized data

Data table
ILMN_1802380 9.3679021
ILMN_1792389 4.488806127
ILMN_2375156 3.592021507
ILMN_1697642 5.918085578
ILMN_1681845 9.129510601
ILMN_1690979 2.768995136
ILMN_1811114 1.674276886
ILMN_1660729 1.055831327
ILMN_2129572 1.933450831
ILMN_1705659 2.104624713
ILMN_1674774 1.06635813
ILMN_1702329 0.838598794
ILMN_1658806 2.339281243
ILMN_2310896 8.470559624
ILMN_1675927 1.06635813
ILMN_2109994 6.846857472
ILMN_1745256 7.830967052
ILMN_2191313 5.77342332
ILMN_1689123 8.751828764
ILMN_1674337 6.242829511

Total number of rows: 24526

Table truncated, full table size 595 Kbytes.

Supplementary data files not provided
Processed data included within Sample table

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