NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1884990 Query DataSets for GSM1884990
Status Public on Sep 19, 2015
Title Patient 3, CD4+ cells, before second dose of fingolimod [exon-level]
Sample type RNA
 
Source name Peripheral blood CD4+ cells
Organism Homo sapiens
Characteristics patient identifier: YHCG-2832
gender: female
age in years at baseline: 29
disease duration in years at baseline: 5
previous treatment: glatiramer acetate
treatment gap in months: <1
edss at baseline: 2.5
edss after 1 year: 1.5
edss after 2 years: 1.5
edss after 3 years: 1.5
edss after 4 years: 1.5
relapses during the year prior to fingolimod: 3
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 CD4+ cells were separated by magnetic-activated cell sorting using Whole Blood CD4 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 70 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 16, 2015
Last update date Mar 23, 2018
Contact name Michael Hecker
E-mail(s) michael.hecker@rocketmail.com
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)
GSE73080 Transcriptome data of multiple sclerosis patients receiving fingolimod therapy [HTA-2_0, CD4+ cells, exon level]
GSE73174 Transcriptome data of multiple sclerosis patients receiving fingolimod therapy
Relations
Alternative to GSM1884960 (gene-level analysis)

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
JUC01000001.hg.1 5.362667
JUC01000002.hg.1 4.78069
JUC01000003.hg.1 6.08114
JUC01000004.hg.1 6.108554
JUC01000005.hg.1 6.865108
JUC01000006.hg.1 6.66849
JUC01000007.hg.1 3.55069
JUC01000008.hg.1 5.104276
JUC01000009.hg.1 1.758174
JUC01000010.hg.1 1.697841
JUC01000011.hg.1 10.8781
JUC01000012.hg.1 7.860474
JUC01000013.hg.1 9.917726
JUC01000014.hg.1 8.091832
JUC01000015.hg.1 5.18547
JUC01000016.hg.1 6.848608
JUC01000017.hg.1 5.764819
JUC01000018.hg.1 8.222601
JUC01000019.hg.1 6.969639
JUC01000020.hg.1 6.969639

Total number of rows: 914585

Table truncated, full table size 23454 Kbytes.




Supplementary file Size Download File type/resource
GSM1884990_CD4_Pat03_24_hours.CEL.gz 21.1 Mb (ftp)(http) CEL
GSM1884990_CD4_Pat03_24_hours.rma-alt-splice-dabg.chp.gz 9.3 Mb (ftp)(http) CHP
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap