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Sample GSM161099 Query DataSets for GSM161099
Status Public on Feb 12, 2008
Title 36GRa_Blood_GlobinClear_noHRT
Sample type RNA
 
Source name blood samples in PAXgene, globin reduction using GlobinClear kit from ambion, non HRT user
Organism Homo sapiens
Characteristics Postmenopausal women
Extracted molecule total RNA
Extraction protocol PAXgene Blood RNA Kit (PreAnalytiX, Hombrechtikon, Switzerland)
Label digoxigenin
Label protocol NanoAmp™ RT-IVT Labeling Kit from Applied Biosystems
 
Hybridization protocol Applied Biosystems Chemiluminescence Detection Kit
Scan protocol Applied Biosystems Chemiluminescence Detection Kit
Description Briefly, 10 μg of labeled cRNA targets from each sample were first fragmented, mixed with internal control target (24-mer oligo labeled with LIZ® fluorescent dye) and hybridized to a pre-hybridized microarray at 55°C for 16 hr. After washing to remove unhybridized DIG-labeled molecules, an alkaline phosphatase-antibody conjugate was added to bind to the DIG-labeled target. The addition of substrate and a chemiluminescence enhancer initiates the chemiluminescent reaction. Eight images were collected for each microarray using the 1700 analyzer including 2 “short” chemiluminescent images (5 seconds exposure length each) and 2 “long” chemiluminescent images (25 seconds exposure length each) for gene expression analysis, 2 fluorescent images for feature finding and spot normalization and 2 QC images for spectrum cross-talk correction. Applied Biosystems Expression System software was used to extract signal intensities, signal to noise ratios (S/N) and flagging values from the microarray images.
Data processing Using Applera package in R, we set the filtering criteria so that each gene had flagging value < 2 and a signal to noise ratio (S/N) ≥ 3 in at least 50% of the samples. After filtration, we proceed with quantile normalization of the log-intensities.
 
Submission date Feb 08, 2007
Last update date Feb 12, 2008
Contact name Vanessa Dumeaux
E-mail(s) vanessad@rr-research.no
Organization name "The Norwegian Women and Cancer project"
Street address University of Tromsoe
City Tromsoe
ZIP/Postal code 9037
Country Norway
 
Platform ID GPL2986
Series (1)
GSE7008 Comparison of globin RNA processing methods for genome-wide transcriptome analysis from whole-blood

Data table header descriptions
ID_REF
Signal_HB009IA_6/15/06_12:20_PM Signal
SDEV_HB009IA_6/15/06_12:20_PM Standard deviation
CV_HB009IA_6/15/06_12:20_PM Coefficient of variation
S_N_HB009IA_6/15/06_12:20_PM Signal to noise ratio
Flags_HB009IA_6/15/06_12:20_PM Flags
VALUE Quantile normalized log2 intensities

Data table
ID_REF Signal_HB009IA_6/15/06_12:20_PM SDEV_HB009IA_6/15/06_12:20_PM CV_HB009IA_6/15/06_12:20_PM S_N_HB009IA_6/15/06_12:20_PM Flags_HB009IA_6/15/06_12:20_PM VALUE
100002 18339.28 406.86 0.05 45.07 0 13.6
100003 243.28 140.18 0.58 1.74 0
100027 190.63 190.63 0.45 -2.24 1
100036 2017.53 678.45 0.34 2.97 0
100037 6213.63 460.04 0.09 13.51 0 12.04
100039 1255.07 268.3 0.22 4.68 0 9.85
100044 188.4 188.4 3.45 0.29 1
100045 359.39 359.39 6.45 -0.16 1
100051 290.26 290.26 0.8 -1.25 1
100052 242.1 187.74 0.78 1.29 0
100057 2826.07 2826.07 3.77 -0.27 1
100058 22140.7 586.26 0.05 37.77 0 13.87
100060 592.4 592.4 9.4 -0.11 1
100062 1997.57 688 0.35 2.9 0
100064 266.42 140.72 0.53 1.89 0
100079 7076.75 290.77 0.05 24.34 0 12.22
100089 1678.21 397.39 0.24 4.22 0
100093 159.63 159.63 1.21 0.83 1
100095 274.81 274.81 2.09 -0.48 1
100100 15542.05 462.68 0.04 33.59 0 13.33

Total number of rows: 32878

Table truncated, full table size 1195 Kbytes.




Supplementary data files not provided

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