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Sample GSM1602927 Query DataSets for GSM1602927
Status Public on Jul 06, 2015
Title intensive-care unit patient [21_03_2013_D11_2545]
Sample type RNA
 
Source name whole blood
Organism Homo sapiens
Characteristics gender: female
age: 82
pneumonia diagnoses: cap
thrombocytopenia: B_medium_low
endotype_cohort: discovery
endotype_class: Mars4
mortality_event_28days: 1
time_to_event_28days: 0
icu_acquired_infection: NA
icu_acquired_infection_paired: NA
diabetes_mellitus: No_DM
abdominal_sepsis_and_controls: NA
Treatment protocol PAXgene blood RNA tubes were left at room temperaturee to defrost (4 hours) while mixing by inversion.
Growth protocol Whole blood was collected in PAXgene blood RNA tubes, mixed by inversion 10X and stored at -80C.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated in accordance with the PAXgene blood RNA isolation (QIAGEN) procedure using the QIAcube workstation.
Label biotin
Label protocol 100ng total RNA was labeled using standard GeneChip® 3' IVT Express Kit (Affymetrix)
 
Hybridization protocol Standard Affymetrix GeneAtlas® Hybridization, Wash, and Stain Kit.
Scan protocol Standard GeneTitan® multi channel instrument.
Description blood gene expression data from healthy subjects and critically-ill patients.
Data processing Raw data scans (.CEL files) were read into the R language and environment for statistical computing (version 2.15.1; R Foundation for Statistical Computing, Vienna, Austria; http://www.R-project.org/). Pre-processing and quality control was performed by using the Affy package version 1.36.1. Array data were background corrected by Robust Multi-array Average, quantiles-normalized and summarized by medianpolish using the expresso function. The resultant 49,386 probe intensities were filtered by means of a 0.5 variance cutoff using the genefilter method to recover 24,646 expressed probes. The occurrence of non-experimental chip effects was evaluated by means of the Surrogate Variable Analysis (R package version 3.4.0) and corrected by the empirical Bayes method ComBat.
 
Submission date Feb 05, 2015
Last update date Jul 12, 2018
Contact name Brendon Scicluna
E-mail(s) brendon.scicluna@um.edu.mt
Organization name University of Malta
Street address Msida campus
City Msida
ZIP/Postal code MSD2020
Country Malta
 
Platform ID GPL13667
Series (1)
GSE65682 Genome-wide blood transcriptional profiling in critically ill patients - MARS consortium

Data table header descriptions
ID_REF
VALUE RMA normalized log2 transformed values

Data table
ID_REF VALUE
11715103_x_at 2.254582676
11715110_at 3.193293815
11715111_s_at 3.18224296
11715113_x_at 2.53947862
11715114_x_at 2.367048677
11715122_at 4.04594237
11715124_s_at 3.151121667
11715125_at 2.563364622
11715126_s_at 2.741125459
11715129_s_at 3.616255556
11715132_x_at 2.265774461
11715135_s_at 3.40121493
11715137_s_at 2.125552444
11715138_s_at 3.254149531
11715140_s_at 2.473856664
11715146_x_at 2.451987162
11715150_s_at 2.877803042
11715155_s_at 2.951454186
11715156_s_at 6.128216609
11715159_at 8.325564588

Total number of rows: 24646

Table truncated, full table size 614 Kbytes.




Supplementary file Size Download File type/resource
GSM1602927_21_03_2013_D11_2545.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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