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Sample GSM746744 Query DataSets for GSM746744
Status Public on Jun 23, 2011
Title Control2
Sample type RNA
 
Source name Human sorted B cells
Organism Homo sapiens
Characteristics individual: Control2
disease state: control
tissue: blood
cell type: Sorted B cell
Treatment protocol Peripheral blood was drawn into heparin-containing sterile tubes and peripheral blood mononuclear cells were prepared by Ficoll (Amersham) density gradient centrifugation for immediate use. B cells were labeled with a biotin anti-CD19 monoclonal antibody (HIB19 clone, Pharmingen) at 4°C and revealed by phycoerythrin-labelled streptavidin (Biomeda) before immediate B cell sorting with high speed cell sorter (FACS Diva, Beckton-Dickinson).
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized on Affymetrix GeneChip human genome U133 plus 2.0 (with probe sets representing 38,572 UniGene clusters) according to the manufacturer’s instructions. After hybridization and washings, arrays were stained with PE-conjugated streptavidin (10 μg/ml) before scanning.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Gene expression data from human sorted B cells.
T02
JLP_T02_U133_2.CEL
Data processing Raw Affymetrix data were analyzed using R (R Development Core Team, 2008; The Comprehensive R Archive Network: http://cran.r-project.org/) and Bioconductor (Bioconductor: http://www.bioconductor.org/) softwares. The quality of the 27 Affymetrix genechips and RNA was assessed using the Bioconductor AffyPLM and simpleaffy packages, with qc, AffyRNAdeg, fitPLM, image, RLE and NUSE functions. For normalization and background correction. Raw values were pre-processed with RMA or GCRMA (library simpleAffy).
The Sample data table shows genes that are considered as expressed by affy (P) at least in one of the patients and controls, thus, reporting ~65% of the data rows in the U133 Plus 2.0 Array.
 
Submission date Jun 22, 2011
Last update date Sep 01, 2016
Contact name Jean-Nicolas SCHICKEL
E-mail(s) [email protected]
Organization name CNRS UPR9021
Street address 15, rue rené descartes
City STRASBOURG
ZIP/Postal code 67084
Country France
 
Platform ID GPL570
Series (1)
GSE30153 B cell signature during inactive systemic lupus
Relations
Reanalyzed by GSE86362

Data table header descriptions
ID_REF
VALUE RMA signal
T2 Detection

Data table
ID_REF VALUE T2 Detection
227030_at 10.5886589 P
215411_s_at 7.452409751 P
222450_at 7.886664542 P
211881_x_at 7.677100672 P
224958_at 8.48223855 P
209772_s_at 8.151395293 P
225535_s_at 8.75971193 P
1598_g_at 6.352460002 A
206693_at 7.846166868 P
209606_at 10.04462751 P
224671_at 7.934247345 P
208674_x_at 8.561114123 P
209469_at 7.267606396 P
209685_s_at 12.07166589 P
227404_s_at 10.08323868 P
205987_at 9.162271602 P
211345_x_at 13.245912 P
228056_s_at 9.59621226 P
201694_s_at 8.901598169 P
202005_at 7.828475888 P

Total number of rows: 34853

Table truncated, full table size 841 Kbytes.




Supplementary file Size Download File type/resource
GSM746744.CEL.gz 8.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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