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Sample GSM989159 Query DataSets for GSM989159
Status Public on Sep 20, 2013
Title Subject LST026, biological rep1
Sample type RNA
 
Source name Pre
Organism Homo sapiens
Characteristics response: ER
site: Laval
allergen: Cat Hair
Sex: F
ethnicity: Caucasian
age: 28
mch pc20 (mg/ml) at pre-challenge: 9.39
mch pc20 (mg/ml) at post-challenge: 16
% fall in fev1 (early): -27.1
% fall in fev1 (late): -7.1
erythrocytes (x10^12/l): 5.23
hemoglobin (g/l): 137
hematocrit (l/l): 0.421
mean cell volume (fl): 80.5
mean cell hb (pg): 26.1
mean cell hb conc. (g/l): 325
red cell distr. width (%): 14.3
platelets (x10^9/l): 158
leukocytes (x10^9/l): 7.2
neutrophils (x10^9/l): 4.4
lymphocytes (x10^9/l): 1.9
monocytes (x10^9/l): 0.6
eosinophils (x10^9/l): 0.4
basophils (x10^9/l): 0
relative.neutrophils: 0.607
relative.lymphocytes: 0.262
relative.monocytes: 0.077
relative.eosinophils: 0.05
relative.basophils: 0.004
tissue: whole blood
Extracted molecule total RNA
Extraction protocol Samples were stored at -80⁰C until RNA extraction
From PAXgene tube samples, total RNA was purified from 2.5 mL of whole blood using Rneasy mini kit (Qiagen, Chatsworth, CA, USA)
From EDTA tube samples, total RNA was purified from 3.0 mL of whole blood following modified TRIzol-based extraction method.
The yield and quality of RNA was assessed by NanoDrop 8000 Spectrophotometer (Thermo Scientific, Wilmington, DE, USA) and Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA)
Label biotin
Label protocol standard Affymetrix protocol
 
Hybridization protocol Affymetrix Human Gene 1.0 ST array (Affymetrix, Santa Clara, CA)
Scan protocol standard Affymetrix protocol
Data processing Raw data normalization using the 'farms' package consisted of RMA background correction, quantile normalization and summarization of probe-level data using Factor Analysis for Robust Microarray Summarization
Data filtering was also performed using the Informative vs. Non-Informative Calls function in the 'farms' package. Differential gene expression was determined using moderated t-tests in limma using an FDR cut-off of 10%.
All statistical analyses were performed in the statistical computing program R.
 
Submission date Aug 20, 2012
Last update date Sep 20, 2013
Contact name Scott Tebbutt
E-mail(s) [email protected]
Organization name University of British Columbia
Department Medicine
Lab James Hogg Research Centre
Street address Room 166, 1081 Burrard Street
City Vancouver
State/province BC
ZIP/Postal code V6Z 1Y6
Country Canada
 
Platform ID GPL6244
Series (1)
GSE40240 Expression data from peripheral blood - blood draws at Pre and Post time points of Allergen inhalation challenge (ER and DR)

Data table header descriptions
ID_REF
VALUE RMA normalized

Data table
ID_REF VALUE
7892501 1.820182899
7892502 4.420509619
7892503 5.421789324
7892504 8.67694496
7892505 2.412938393
7892506 4.312933109
7892507 5.30226507
7892508 5.228117923
7892509 8.589684859
7892510 4.831242701
7892511 3.558137351
7892512 7.282879223
7892513 3.592137101
7892514 6.371647744
7892515 9.201992373
7892516 4.911905197
7892517 6.279301461
7892518 2.40561338
7892519 4.875599741
7892520 9.053579279

Total number of rows: 32321

Table truncated, full table size 627 Kbytes.




Supplementary file Size Download File type/resource
GSM989159_LST.026.Pre-ER-PAXgene_RNA_HuGene-1_0-st-v1_.CEL.gz 3.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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