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Sample GSM808893 Query DataSets for GSM808893
Status Public on Oct 06, 2011
Title Control_P1
Sample type RNA
 
Source name Brain_control_replicate1
Organism Danio rerio
Characteristics age: Adults
tissue: Whole Brain
treatment: control
Treatment protocol For microarray screening of fever in zebrafish, RNA extracted of zebrafish brains injected or not with 1mg*Kg-1 of Poly (I:C): zebrafish in thermal gradient (control, n = 9), zebrafish PBS injected in thermal gradient (PBS, n = 9), zebrafish Poly I:C injected without thermal gradient (PIC_sG, n = 9), and zebrafish Poly I:C injected with thermal gradient (PIC_sG, n = 9). Individuals RNAs were grouped into pools from 3 individual for each treatment (3 pools by treatment).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from brains using 500uL of TriReagent (Molecular Research Center) following the manufacturer’s instructions. RNA concentration was quantified using Nanodrop ND-1000 and RNA integrity and quality was assessed using a Bioanalyzer 2100 with the RNA 6000 Nano LabChip kit (Agilent Technologies). The RNA integrity number (RIN) was calculated for each sample using the Agilent 2100 Expert software, only RNAs with a RIN number > 7 were processed (to reduce experimental biases). Total RNA (2μg) was used to synthesize cDNA with SuperScript III Transcriptase (Invitrogen) and oligo-dT primer (Promega).
Label Cy3
Label protocol A loop microarray design approach was taken for the study, all experimental RNA samples were labelled with one dye Cy3 and each stimulated sample was compared to the control sample (pool without stimulation) labelled with the same dye (Cy3). Denatured samples of RNA were reversed transcribed and indirectly labelled with Cy3. RNA labelling, hybridizations, and scanning were performed according to manufacturer’s instructions.
 
Hybridization protocol Briefly, total RNA (500 ng) was amplified and Cy3-labeled with Agilent’s One-Color Microarray-Based Gene Expression Analysis (Quick Amp Labelling kit) along with Agilent’s One-Color RNA SpikeIn Kit. Each sample (1.65 μg of RNA) was hybridized to Zebrafish array (ID 026437, Agilent) at 65 °C for 17 hours using Agilent’s GE Hybridization Kit. Washes were conducted as recommended by the manufacturer using Agilent’s Gene Expression Wash Pack with stabilization and drying solution.
Scan protocol Microarrays slides were scanned with Agilent Technologies Scanner model G2505B. Spot intensities and other quality control features were extracted with Agilent’s Feature Extraction software version 10.4.0.0. One-channel TIFF images were imported into the Gene GeneSpring software GX 11.0.
Description Gene expression after 24 with thermal gradient
Data processing Percentile shift normalization was made to adjust all spot intensities in an array. This normalization takes each column in an experiment independently, and computes the median expression values for this array, across all spots. It then subtracts this value from the expression value of each entity (Bolstad et al, 2003). After Percentile normalization, all data were filtered by comparison of the standard deviation expression among groups (filter by expression). The entities that had values lesser or greater than the standard deviation value were retained. This filter procedure allowed selected genes that have outlier samples, and filter out genes that have a low variation in expression values across all samples.
 
Submission date Oct 05, 2011
Last update date Oct 06, 2011
Contact name Sebastian Boltana
E-mail(s) sboltana@udec.cl
Phone 93 581 3473
Organization name Universidad de Concepcion
Department Oceanografia
Lab Evolutionary Immunology
Street address Edmundo Larenas s/n, Barrio Universitario. Biotechnology Center
City Chile
State/province Bio BIO
ZIP/Postal code 4030000
Country Chile
 
Platform ID GPL6457
Series (1)
GSE32636 Behavioural fever and its underlying molecular mechanisms

Data table header descriptions
ID_REF
VALUE GeneSpring percentile shift normalized signal intensity

Data table
ID_REF VALUE
1 7.580852802
2 4.599500142
3 4.879478223
4 4.360499071
5 null
6 null
7 null
8 null
9 null
10 null
11 null
12 4.108978627
13 4.469402008
14 7.006160664
15 6.463961939
16 5.197197845
17 null
18 5.106823876
19 0.706354578
20 2.273503287

Total number of rows: 45220

Table truncated, full table size 639 Kbytes.




Supplementary file Size Download File type/resource
GSM808893_Control_P1.txt.gz 664.0 Kb (ftp)(http) TXT
GSM808893_US84503584_251916110295_S01_GE1_107_Sep09_1_1_1.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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