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Sample GSM2712464 Query DataSets for GSM2712464
Status Public on Apr 15, 2019
Title INFG_ID_120
Sample type RNA
 
Source name blood
Organism Homo sapiens
Characteristics diagnosis: influenza
tissue: blood
Sex: f
age: 36
severity: flu_svre
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 12.52838521
A_19_P00315529 7.261926862
A_19_P00315668 7.490140191
A_19_P00315716 6.901064952
A_19_P00315804 5.875762158
A_19_P00315824 9.236009029
A_19_P00315843 7.806521907
A_19_P00315922 6.418804104
A_19_P00316107 7.076303915
A_19_P00316225 6.526459881
A_19_P00316326 8.984636096
A_19_P00316375 7.356187706
A_19_P00316396 5.768354859
A_19_P00316427 6.001399815
A_19_P00316533 6.821719134
A_19_P00316625 6.164576255
A_19_P00316675 5.948316817
A_19_P00316701 11.34103228
A_19_P00316726 10.57680485
A_19_P00316753 7.817920039

Total number of rows: 31032

Table truncated, full table size 707 Kbytes.




Supplementary file Size Download File type/resource
GSM2712464_257236313134_Schughart22004_S01_GE1_107_Sep09_1_4.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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