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Sample GSM1583031 Query DataSets for GSM1583031
Status Public on Jun 23, 2015
Title BAT_cold_Tconv#2_9482914035_B
Sample type RNA
 
Source name Cold-conditioned Brown Adipose Tissue
Organism Mus musculus
Characteristics strain background: C57BL/6
genotype/variation: Foxp3-GFP-DTR-CD90.1
tissue: Brown Adipose Tissue (BAT)
temp.: 12°C
replicate: Replicate 2
cell type: CD4+Foxp3- Tconv
Treatment protocol Mice were housed in a control environment using TSE phenomaster systems
Extracted molecule total RNA
Extraction protocol Spleen and BAT were harvested directly after euthanasia of mice
Label biotin
Label protocol The NuGEN Ovation Pico WTA System (linear isothermal DNA amplification process) was used to generate single-stranded cDNA from small input amounts of 2.5 ng RNA. Labeled cRNA was prepared according to Nugene Encore BiotinIL Module.
 
Hybridization protocol 1.5 µg of cDNA were hybridized for 17hrs at 55.4 °C on Illumina Mouse WG-6-Microarray
Scan protocol Illumina iSCAN-Scanner according to Std Illumina Scanning Protocol Part # 11322355 (Whole-Genome Gene Expression Direct Hybridization Assay Guide). Microarray scanning was done using an iScan array scanner
Description SAMPLE 8
Data processing Microarray scanning was done using an iScan array scanner. Data extraction was done for all beads individually, and outliers are removed when the absolute difference to the median is greater than 2.5 times MAD(2.5 Hampelís method). All remaining bead level data points are than quantile normalized [1]. As test for significance the studentís t-test is used on the bead expression values of the two groups of interest. In the case of significance of expression against background we tested for greater than all negative beads for this sample and in the case of comparing separate groups we tested for inequality of the means of the groups. In both cases Benjamini-Hochberg correction [2] was applied to the complete set of p-values of all 48107 ProbeIDs on the chip. The average expression value is calculated as mean of the measured expressions of beads together with the standard deviation of the beads.
[1] Probe Level Quantile Normalization of High Density Oligonucleotide Array Data, Ben Bolstad, Division of Biostatistics, University of California, Berkeley December 2001
[2] Y. Benjamini and Y. Hochberg (1995). Controlling the false discovery rate: a practical and powerful approach to multiple testing. Journal of the Royal Statistical Society B, Vol. 57, 289-300.
 
Submission date Jan 13, 2015
Last update date Jun 23, 2015
Contact name Michael Delacher
E-mail(s) [email protected]
Phone +49 6131 17 6574
Organization name University Medical Center of the Johannes Gutenberg-University Mainz
Department Institute for Immunology
Lab Immunology
Street address Langenbeckstrasse 1
City Mainz
State/province Rhineland-Palatinate
ZIP/Postal code 55131
Country Germany
 
Platform ID GPL17543
Series (1)
GSE64909 Brown Adipose Tissue Harbors a distinct subpopulation of regulatory T cells

Data table header descriptions
ID_REF
VALUE normalized

Data table
ID_REF VALUE
ILMN_2749327 142.4877172
ILMN_2625626 146.9838461
ILMN_2877059 151.1591987
ILMN_1228839 163.8452659
ILMN_1222339 219.1945488
ILMN_3151270 121.5431942
ILMN_2627041 195.5121176
ILMN_1224020 104.5616528
ILMN_1233116 168.3462628
ILMN_2649363 123.6409243
ILMN_2659804 133.180781
ILMN_2711615 149.4766692
ILMN_1245128 125.3430361
ILMN_2588946 117.9199751
ILMN_2713507 110.2194839
ILMN_2531739 101.4999991
ILMN_1242774 117.7953675
ILMN_1230107 131.6185284
ILMN_2581136 105.0738289
ILMN_2906473 342.6721989

Total number of rows: 46237

Table truncated, full table size 1123 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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