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Sample GSM2712433 Query DataSets for GSM2712433
Status Public on Apr 15, 2019
Title INFG_ID_077
Sample type RNA
 
Source name blood
Organism Homo sapiens
Characteristics diagnosis: healthy
tissue: blood
Sex: f
age: 29
severity: hlty_ctrl
Treatment protocol Whole blood was collected into PAXgene Blood RNA tubes (BD systems, NJ, USA), stored at -20oC, and RNA was extracted using (PAXgene Blood RNA kit, Qiagen).
Extracted molecule total RNA
Extraction protocol RNA was prepared using Qiagen RNAeasy Kit. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 0.5 ug RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 1.5 ug of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 250 ml containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 250 ml of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays (G4112A) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Green PMT is set to 100%).
Description Influenza_study
Data processing The scanned images were analyzed with Feature Extraction Software10.5 (Agilent) using default parameters to obtain background subtracted and spatially detrended Processed Signal intensities.
 
Submission date Jul 20, 2017
Last update date Apr 16, 2019
Contact name Klaus Schughart
E-mail(s) labschughart@online.de
Phone +49-159-0483-7911
Organization name University Münster
Department Virology
Street address Von-Esmarch-Str 56
City Münster
ZIP/Postal code 48149
Country Germany
 
Platform ID GPL21185
Series (1)
GSE101702 Host response to IAV infections in human patients

Data table header descriptions
ID_REF
VALUE Background subtracted, offset=50, log2 transformed, normalized (quantile)

Data table
ID_REF VALUE
A_19_P00315506 9.997484947
A_19_P00315529 7.442534669
A_19_P00315668 7.022232884
A_19_P00315716 6.846269246
A_19_P00315804 5.94269846
A_19_P00315824 10.27142049
A_19_P00315843 7.16712405
A_19_P00315922 6.741649759
A_19_P00316107 7.633861795
A_19_P00316225 6.336678431
A_19_P00316326 7.824872295
A_19_P00316375 6.531191827
A_19_P00316396 6.040124975
A_19_P00316427 5.929063569
A_19_P00316533 6.808522766
A_19_P00316625 6.03221074
A_19_P00316675 5.953314785
A_19_P00316701 12.86417661
A_19_P00316726 10.8177186
A_19_P00316753 8.305810894

Total number of rows: 31032

Table truncated, full table size 707 Kbytes.




Supplementary file Size Download File type/resource
GSM2712433_257236313219_Schughart20001_S01_GE1_107_Sep09_1_1.txt.gz 3.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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