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Sample GSM266543 Query DataSets for GSM266543
Status Public on Feb 12, 2009
Title Sample_119
Sample type RNA
 
Channel 1
Source name Adipose
Organism Homo sapiens
Characteristics Adipose_Sample_119
Patient#16
Placebo_Fasted
US-1015661
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from the adipose samples by Qiagen RNeasy spin columns with DNAse treatment. 2 µg of each sample was precipitated in ethanol and re-suspended in 14 µl of water. Globin mitigation performed using Ambion's GLOBINclear kit (cat# AM1980; Austin, TX) according to manufacturer’s protocol. Briefly, biotinylated globin-specific oligonucleotides are mixed with total RNA and annealed to α and β globin transcripts; streptavidin-coated paramagnetic beads are then added to bind and capture the bound globin mRNAs; the beads are removed using a magnet. GLOBINclear-treated total RNA samples were adjusted to 150 µl, aliquots of which were used for qRT-PCR and microarray experiments.
Label Cy3,Cy5
Label protocol Custom automated version of the aminoallyl MessageAmp II kit from Ambion
 
Channel 2
Source name Adipose
Organism Homo sapiens
Characteristics US-1021605
common reference
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from the adipose samples by Qiagen RNeasy spin columns with DNAse treatment. 2 µg of each sample was precipitated in ethanol and re-suspended in 14 µl of water. Globin mitigation performed using Ambion's GLOBINclear kit (cat# AM1980; Austin, TX) according to manufacturer’s protocol. Briefly, biotinylated globin-specific oligonucleotides are mixed with total RNA and annealed to α and β globin transcripts; streptavidin-coated paramagnetic beads are then added to bind and capture the bound globin mRNAs; the beads are removed using a magnet. GLOBINclear-treated total RNA samples were adjusted to 150 µl, aliquots of which were used for qRT-PCR and microarray experiments.
Label Cy3,Cy5
Label protocol Custom automated version of the aminoallyl MessageAmp II kit from Ambion
 
 
Hybridization protocol Microarrays are incubated at 40°C for 48 hours in a rotating carousel. Hybridizations to custom Agilent microarrays are completed as previously described (Hughes et al.Nat Biotech (2001), 19(4):342-7). Microarrays are washed to remove non-specific hybridized sample. Afterwards, microarrays are dried in an ozone-free nitrogen chamber.
Scan protocol Microarrays are scanned using the Agilent LP2 laser scanner. The scanner output is a Tiff file, which contains the quantitative hybridization data from each individual microarray. The Tiff files are then processed using Rosetta custom feature extraction software.
Description VALUEs represent averaged data for both channels from a fluor-reverse pair
Data processing Data were processed using the Rosetta Resolver® system. Rosetta's custom feature extraction software performs error modeling before data are loaded into the Resolver system. The Resolver system performs a squeeze operation that combines replicates of the same sequence in an array while applying error weighting. The error weighting consists of adjusting for additive and multiplicative noise. A P-value is generated and propagated throughout the system. The P-value represents the probability that a gene is expressed. The Resolver system allows users to set thresholds, below which genes of a P-value are considered to be significantly expressed. The Resolver system also combines multiple arrays using a squeezing process. If multiple spots reference one sequence, summarization is performed using an error-weighted average as described in Roland Stoughton and Hongyue Dai, Statistical Combining of Cell Expression Profiles. US Patent #6,351,712, February 26, 2002.
 
Submission date Feb 15, 2008
Last update date Feb 15, 2008
Contact name Michael Nebozhyn
Organization name Merck, Inc
Department GpGx/Computational System biology
Street address Mail Stop WP53B-120, 770 Sumneytown Pike, Building 53, P.O. Box 4
City West Point
State/province PA
ZIP/Postal code 19486
Country USA
 
Platform ID GPL3991
Series (1)
GSE10545 Profiling of Human Adipose Tissue and Effect of Sibutramine on Gene Expression

Data table header descriptions
ID_REF
VALUE Corrected, averaged log10(test/ref) ratios for fluor-reverse pair
mlavg averaged raw data for both channels from a fluor-reverse pair
p_value P value that the probe target is differentially expressed in the sample and the reference pool

Data table
ID_REF VALUE mlavg p_value
10025902915 0.018943507 -1.331301332 0.755113184
10023826662 -0.425711155 -0.820579886 1.0509E-11
10025912673 0.117629856 0.243284151 0.02009424
10025904167 -0.021071739 -1.480067253 0.818368256
10023838760 0.154902205 -0.718361259 0.000651557
10025905868 0.010717635 0.979287863 0.833757579
10025904463 0.025476478 0.801523983 0.576952577
10025902815 0.195552453 -0.740130723 0.000152864
10025909974 -0.037309725 -1.022696495 0.462966353
10023816390 0.17322059 0.265107542 0.001749692
10025903812 -0.073308535 0.031772934 0.1730728
10023831151 0.043509997 -0.260570228 0.35121876
10025903503 -0.138591334 -0.459493876 0.011236903
10023833562 0.047480527 -1.647158146 0.712927341
10023844371 0.103399076 -1.394907713 0.202575713
10023811924 0.045352127 -1.412942052 0.712546468
10023826209 -0.021645641 -2.144906282 0.921405494
10023807735 0.083792694 -1.183009624 0.285736978
10025909297 0.459539026 -0.869967461 2.12288E-11
10025912759 -0.039604153 -0.253257364 0.506163955

Total number of rows: 23653

Table truncated, full table size 1124 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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