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Sample GSM4216526 Query DataSets for GSM4216526
Status Public on Dec 17, 2019
Title T cells Newcastle Early Arthritis Clinic number 1008
Sample type RNA
 
Source name Disease control T cells
Organism Homo sapiens
Characteristics patient: 1008
gender: M
age: 70
tissue: peripheral blood
cell type: CD4+ T cells
first_diagnosis: Psoriatic Arthritis
working_diagnosis: Psoriatic Arthritis
Growth protocol Monocytes were first depleted by immunorosetting (Rosettesep Human Monocyte depletion cocktail, Stemcell Technologies Inc., Vancouver, non-RA inflammatory arthritisanada), and remaining cells underwent positive selection using Easisep whole blood CD4+ positive selection kit reagents in conjunction with the Robosep automated cell separator (Stemcell). CD4+ T-cell purity was determined using standard flow cytometry techniques; FITC-conjugated anti-CD4 and PE-conjugated anti-CD14 antibodies were used (Beckton Dickinson, New Jersey, USA).
Extracted molecule total RNA
Extraction protocol RNA was immediately extracted from CD4+ T-cell isolates using RNeasy MINI kits (Qiagen GmbH, Germany), incorporating an “on-column” DNA digestion step.
Label biotin
Label protocol 50ng RNA was reverse transcribed into cRNA, and biotin-UTP labeled, using the Illumina TotalPrep RNA Amplification Kit (Ambion, Texas).
 
Hybridization protocol Illumina HT12 BeadChip.
Scan protocol Illumina iScan.
Description Freshly isolated and purified peripheral blood T cells- GEO: GSM2129029
Data processing Samples with mean detection pvalue > 0.05 and probes whose detection p-value was >0.05 in over 25% of samples were excluded prior to background correction and quantile normalization, following which additional probes were removed where they mapped to (i) sex chromosomes, (ii) repeat or intronic/intergenic regions or (iii) unmapped regions.
 
Submission date Dec 12, 2019
Last update date Dec 21, 2019
Contact name Arthur Pratt
E-mail(s) arthur.pratt@newcastle.ac.uk
Organization name Newcastle University
Department Faculty of Medical Sciences
Lab Musculoskeletal Research Group
Street address Framlington Place
City Newcastle upon Tyne
ZIP/Postal code NE2 4HH
Country United Kingdom
 
Platform ID GPL10558
Series (2)
GSE137634 Lymphocyte DNA methylation mediates genetic risk at shared immune mediated disease loci
GSE141934 Transcriptional data of inflamatory arthritis T cells.
Relations
Reanalysis of GSM2129029

Data table header descriptions
ID_REF
VALUE NormExp background correction followed by quantile normalization using negative and positive control probes as implemented by the the neqc function of the Limma package.
Detection Pval

Data table
ID_REF VALUE Detection Pval
ILMN_1796063 10.1468554 0
ILMN_1682799 9.01133664 0
ILMN_1655444 9.768834188 0
ILMN_2121316 5.926865755 0.003896104
ILMN_1761911 6.620106037 0.001298701
ILMN_2313434 6.904535138 0
ILMN_1769158 7.10424675 0
ILMN_1660232 9.420907721 0
ILMN_1763663 7.351753354 0
ILMN_1797082 6.099909326 0.002597403
ILMN_1693210 7.835502885 0
ILMN_1775074 8.966856315 0
ILMN_2309245 11.75288341 0
ILMN_1809344 7.575388936 0
ILMN_1762281 10.57401924 0
ILMN_1734742 11.10540494 0
ILMN_2162234 6.417545261 0.001298701
ILMN_1655684 8.434088798 0
ILMN_3300190 6.085921396 0.002597403
ILMN_1766125 7.976040702 0

Total number of rows: 11710

Table truncated, full table size 344 Kbytes.




Supplementary file Size Download File type/resource
GSM4216526_9477874152_I_Grn.idat.gz 1.6 Mb (ftp)(http) IDAT
Processed data included within Sample table

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