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Sample GSM1888135 Query DataSets for GSM1888135
Status Public on Sep 19, 2015
Title Patient 9, CD8+ cells, after 3 months of fingolimod treatment [exon-level]
Sample type RNA
Source name Peripheral blood CD8+ cells
Organism Homo sapiens
Characteristics patient identifier: RBTM-1672
gender: male
age in years at baseline: 46
disease duration in years at baseline: 15
previous treatment: interferon-beta-1b subcutaneous
treatment gap in months: <1
edss at baseline: 3.5
edss after 1 year: 2.0
edss after 2 years: 2.0
edss after 3 years: 3.0
edss after 4 years: 3.0
relapses during the year prior to fingolimod: 1
relapses during 1-year follow-up: 0
relapses during 2-year follow-up: 0
relapses during 3-year follow-up: 0
relapses during 4-year follow-up: 0
completed years of fingolimod therapy: >=4
Treatment protocol Patients were treated with fingolimod (Gilenya, Novartis) according to the approved label (0.5 mg orally once-daily) and the guidelines and recommendations of the German Society of Neurology.
Growth protocol Patient blood samples were taken immediately before the first dose of fingolimod as well as one day and three months post therapy initiation.
Extracted molecule total RNA
Extraction protocol Peripheral blood CD8+ cells were separated by magnetic-activated cell sorting using Whole Blood CD8 MicroBeads (Miltenyi Biotec) and total RNA was isolated using the mirVana isolation kit (Thermo Fisher Scientific) according to the manufacturers' protocols.
Label Biotin
Label protocol According to the Affymetrix Whole Transcript (WT) manual, cRNA was prepared from 200 ng total RNA. The cRNA was then used to generate single-stranded DNA, which was fragmented and biotinylated.
Hybridization protocol Labeled single-stranded DNA in the sense orientation was hybridized for 16 hours at 45 °C on Affymetrix HTA 2.0 microarrays. The microarrays were washed and stained with a streptavidin-phycoerythrin conjugate in an Affymetrix Fluidics Station 450. Signal amplification with antibodies was applied following the instructions provided by Affymetrix.
Scan protocol The microarrays were scanned with a GeneChip Scanner 3000 7G (Affymetrix).
Description Gene expression data from a multiple sclerosis patient treated with fingolimod
Data processing Data preprocessing of the raw microarray scans was performed using the Affymetrix GeneChip Command Console (AGCC) software version 4.0. The data were then processed using Expression Console version 1.3.1. The robust multi-array average (RMA) algorithm was applied with the default configuration, which includes a log2 data transformation and quantile normalization. In this step, the measured signal intensities of >6 million probes were summarized into gene level probe sets (n=70523) and exon level probe sets (n=914585). The Transcriptome Analysis Console (TAC) software version 1.0 was utilized to analyze the RNA expression dynamics.
Submission date Sep 18, 2015
Last update date Mar 23, 2018
Contact name Michael Hecker
Organization name University of Rostock
Department Department of Neurology
Lab Division of Neuroimmunology
Street address Gehlsheimer Str. 20
City Rostock
ZIP/Postal code 18147
Country Germany
Platform ID GPL17585
Series (2)
GSE73172 Transcriptome data of multiple sclerosis patients receiving fingolimod therapy [HTA-2_0, CD8+ cells, exon level]
GSE73174 Transcriptome data of multiple sclerosis patients receiving fingolimod therapy
Alternative to GSM1885039 (gene-level analysis)

Data table header descriptions
VALUE RMA signal intensity

Data table
JUC01000001.hg.1 5.586334
JUC01000002.hg.1 4.157655
JUC01000003.hg.1 5.952546
JUC01000004.hg.1 6.08127
JUC01000005.hg.1 6.865042
JUC01000006.hg.1 6.665074
JUC01000007.hg.1 3.091666
JUC01000008.hg.1 5.031521
JUC01000009.hg.1 1.219534
JUC01000010.hg.1 1.491603
JUC01000011.hg.1 11.05823
JUC01000012.hg.1 7.601464
JUC01000013.hg.1 10.44369
JUC01000014.hg.1 8.789961
JUC01000015.hg.1 5.571111
JUC01000016.hg.1 7.082415
JUC01000017.hg.1 5.846725
JUC01000018.hg.1 7.836508
JUC01000019.hg.1 7.139914
JUC01000020.hg.1 7.139914

Total number of rows: 914585

Table truncated, full table size 23433 Kbytes.

Supplementary file Size Download File type/resource
GSM1888135_CD8_Pat09_3_months.CEL.gz 22.3 Mb (ftp)(http) CEL
GSM1888135_CD8_Pat09_3_months.rma-alt-splice-dabg.chp.gz 9.3 Mb (ftp)(http) CHP
Processed data included within Sample table

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