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Sample GSM1716509 Query DataSets for GSM1716509
Status Public on Jun 20, 2015
Title wholeblood_infected_rep5
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°757 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 -0.07747269
DarkCorner -0.54928637
A_73_112653 -0.14907503
A_73_P034336 0.25355148
A_73_100764 0.34824944
A_73_P063531 -0.6121149
A_73_P045581 0.14384079
A_73_P064131 0.08581495
A_73_P030916 0.102786064
A_73_P088811 0.9172764
A_73_P109491 1.0399821
A_73_P135701 -0.10467863
A_73_P040566 0.1360116
A_73_P038011 -0.20024681
A_73_P458686 0.7001834
A_73_P206052 0.23191929
A_73_P416581 -0.27373552
A_73_P397461 0.5531931
A_73_P266841 -0.1435976
A_73_P089661 0.05081582

Total number of rows: 43713

Table truncated, full table size 1025 Kbytes.




Supplementary file Size Download File type/resource
GSM1716509_K757M.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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