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Sample GSM1191022 Query DataSets for GSM1191022
Status Public on Jun 30, 2014
Title HF_Pio_Apex_285
Sample type RNA
 
Source name mouse heart
Organism Mus musculus
Characteristics strain: LDL-/-
gender: male
treatment: high fat + pioglitazone
tissue: heart
genetic background: C57BL/6
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from individual hearts (n=8 hearts per group, 48 samples in total) using glass beads and RNAzol (Campro Scientific, Veenendaal, The Netherlands).
Label Biotin
Label protocol The Illumina® TotalPrep™ RNA Amplification Kit (Ambion, art. No. AM-IL1791) was used to synthesize biotin labeled cRNA starting with 500 ng total RNA. Concentration of the labeled cRNA was measured using the Nanodrop spectrophotometer.
 
Hybridization protocol We have used standard Illumina hybridisation protocol. The amount of biotinylated cRNA that was hybridized onto the MouseRef-8 Expression BeadChip was 750 ng
Scan protocol Illumina’s Genomestudio v1.1.1 software with the default settings advised by Illumina, was used for Gene Expression analysis. All the quality control data of this BeadChip were within specifications of the microarray service provider (Service XS, Leiden, the Netherlands).
Data processing Probe-level, background subtracted expression values were used as input for GeneSpring GX11 software (Agilent), which was used for normalization of data; threshold signals below the value of 5 were set at 5. To be considered expressed, the signal detection p-value of the probe had to be lower than 0.01 in at least 1 of 48 experiments. 15505 probes fulfilled these criteria. Differential expression of probes was assessed using unpaired moderated t-test (LIMMA) via The Remote Analysis Computation for gene Expression data (RACE) suite at http://race.unil.ch
Pipeline for illumina arrays (www.arrayanalysis.org) was used to normalize data. Differential expression of probes was assessed using unpaired moderated t-test (LIMMA) via The Remote Analysis Computation for gene Expression data (RACE) suite at http://race.unil.ch
 
Submission date Jul 17, 2013
Last update date Jun 30, 2014
Contact name Lars Verschuren
E-mail(s) lars.verschuren@tno.nl
Phone +31888666039
Organization name TNO
Department Microbiology and Systems Biology
Street address Utrechtseweg 48
City Zeist
ZIP/Postal code 3704HE
Country Netherlands
 
Platform ID GPL6885
Series (1)
GSE48977 A systems biology approach to understand the pathophysiological mechanisms of cardiac pathological hypertrophy associated with rosiglitazone

Data table header descriptions
ID_REF
VALUE quantile normalized

Data table
ID_REF VALUE
ILMN_2896528 12.25032435
ILMN_2721178 10.33715927
ILMN_3033922 9.815169238
ILMN_3092673 11.78678302
ILMN_2816356 6.361592823
ILMN_2808939 6.951365429
ILMN_2634564 7.95491172
ILMN_2737647 6.055560268
ILMN_2734484 9.691615475
ILMN_2952292 5.771725309
ILMN_2699078 5.16955661
ILMN_1213681 9.617672922
ILMN_2735413 4.85235298
ILMN_2735415 5.442351756
ILMN_2891688 10.31903753
ILMN_2637698 9.87459156
ILMN_2674228 7.443822472
ILMN_2601546 5.634252344
ILMN_1230831 5.397355497
ILMN_2848071 5.674618631

Total number of rows: 25697

Table truncated, full table size 624 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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