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Sample GSM403444 Query DataSets for GSM403444
Status Public on Mar 29, 2010
Title array Erus 1
Sample type RNA
 
Source name Erus 1
Organism Homo sapiens
Characteristics cell type: HMEC endothelial cells
infection: R. prowazekii Erus strain
Treatment protocol Human endothelial cells (HMEC-1 cell line) were infected with R. prowazekii Erus strain (50:1 bacterium-to-cell ratio) for 6 hours at 37°C.
Growth protocol Human endothelial cells (HMEC-1 cell line) were cultured in MCDB 131 medium (Gibco) supplemented with 10% of SVF and 1% of L-glutamine
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using RNeasy Mini kit (Qiagen).
Label Cy3
Label protocol Labelled cRNA was synthesised from cDNA using T7 RNA polymerase and cyanine 3-labeled CTP (Cy-3) fluorescent dyes with the One-Color Low RNA Input Linear Amplification KitPLUS (Agilent).
 
Hybridization protocol as recommanded by the manufacturer
Scan protocol Slides were scanned at a 5-µm resolution with a G2505B DNA microarray scanner (Agilent)
Description HMEC endothelial cells infected with R. prowazekii Erus strain
Data processing Agilent Feature Extractor Software A.9.1.3 was used for image analysis. The microarray grid was automatically placed, outlier spots were flagged and feature intensities and backgrounds were accurately determined.
Further data processing was performed using Resolver software 7.1 (Rosetta Inpharmatics), and its error model-based transformation pipeline was used to map replicate reporters to genes and to normalise inter-array data sets. The fold change (FC) was calculated using pairs Erus vs. Control, Evir vs. Control and Rp22 vs. Control. Only genes that had an absolute FC over 2.0 (p<0.01) for at least one of them were considered to be regulated and kept for further statistical analysis.
 
Submission date May 15, 2009
Last update date Mar 29, 2010
Contact name Yassina Bechah
E-mail(s) [email protected]
Organization name CNRS
Lab URMITE
Street address 27 bd J. Moulin
City Marseille
ZIP/Postal code 13005
Country France
 
Platform ID GPL4133
Series (1)
GSE16123 Multiomics study to identify virulence factors of Rickettsia prowazekii revealed its adaptive mutation capabilities

Data table header descriptions
ID_REF
SIGNAL_RAW Spot median signal
BKD_RAW Local spot background median signal
VALUE processed spot signal intensity

Data table
ID_REF SIGNAL_RAW BKD_RAW VALUE
1 65257 55 66608.41
2 39.5 56 4.075382
3 45 57 4.100095
4 47.5 57 4.123793
5 47 57 4.144903
6 51 58 4.164538
7 49 57 4.182998
8 51 57 4.199454
9 53 57 4.212783
10 50 57 4.228347
11 51 56 4.24076
12 2222 58 2397.339
13 155 58 108.5768
14 1100 57 1207.212
15 98 57 48.26107
16 17976.5 57 19932.29
17 139.5 57 91.34608
18 376 58 352.5131
19 65128 58 68398.78
20 125 58 78.33338

Total number of rows: 45015

Table truncated, full table size 997 Kbytes.




Supplementary file Size Download File type/resource
GSM403444.txt.gz 6.5 Mb (ftp)(http) TXT
Processed data included within Sample table

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