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Sample GSM1716503 Query DataSets for GSM1716503
Status Public on Jun 20, 2015
Title wholeblood_infected_rep2
Sample type RNA
 
Source name peripheral blood, at the beginning of clinical signs
Organism Bos taurus
Characteristics tissue: whole blood
infection status: infected
Treatment protocol no treatment was applied on samples. They were stored at -20°C until shipment at the end of the trial. They were transported in refrigerated boxes from Kenya to France, then stored at -°C for several week until RNA extraction.
Growth protocol whole blood was collected in Tempus tubes
Extracted molecule total RNA
Extraction protocol Total RNA was prepared using the Tempus
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 50 ng RNA using the Agilent Low Input Quick Amplification Labelling kit according to the manufacturer's instructions. Dye incorporation and cRNA yield were checked with a NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 1.65 ug of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented using the Agilent Gene Expression Hybridization kit, according to the manufacturer's instructions, then hybridized to Agilent Bovine Gene expression microarray (V2) for 17h.
Scan protocol Slides were scanned immediately after washing with Agilent Gene Expression wash buffers 1 and 2, according to the manufacturer's instructions. Slides were then scanned on the Agilent C Scanner using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 15µm, Dye channel set to Green and Green PMT set to 100%).
Description Gene expression of animal n°727 at the beginning of the clinical signs in whole blood
Data processing The scanned images were analyzed with Feature Extraction Software 10.7 (Agilent) using default parameters (protocol GE1-107_sep09 and Grid: 023647_D_F_20121015) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded. We processed paired statistical analyses and compared the differential expression between non-infected and infected status.
 
Submission date Jun 19, 2015
Last update date Jun 23, 2015
Contact name Rodrigues Valérie
E-mail(s) [email protected]
Phone +33467593989
Organization name CIRAD
Department BIOS
Lab CMAEE
Street address TA A30/G
City Montpellier
ZIP/Postal code 34398
Country France
 
Platform ID GPL11649
Series (1)
GSE70059 Whole blood transcriptome analysis of Mycoplasma mycoides subsp, mycoides-infected cattle confirms immunosuppression but does not reflect local inflammation

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
GE_BrightCorner -0.30836773
DarkCorner 0.29144526
A_73_112653 -0.8541217
A_73_P034336 -0.19633293
A_73_100764 0.14296865
A_73_P063531 -0.96421146
A_73_P045581 1.4760933
A_73_P064131 1.2022119
A_73_P030916 -0.5286703
A_73_P088811 -0.65157366
A_73_P109491 -0.5012982
A_73_P135701 0.11759186
A_73_P040566 -0.027753353
A_73_P038011 -0.8809948
A_73_P458686 0.5357785
A_73_P206052 1.4081197
A_73_P416581 -0.54548883
A_73_P397461 1.1018586
A_73_P266841 -0.28760958
A_73_P089661 -0.12969756

Total number of rows: 43713

Table truncated, full table size 1002 Kbytes.




Supplementary file Size Download File type/resource
GSM1716503_K727M.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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