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Sample GSM1713665 Query DataSets for GSM1713665
Status Public on Jun 18, 2015
Title IM101_VN1203_2d_RNA_2
Sample type RNA
Source name Lung_VN1203-inoculated_2 days
Organism Mus musculus
Characteristics strain: C57Bl/6J
age: 22 weeks
virus: VN1203
time (d.p.i): 2
tissue: lung
biological_replicate: 2
Treatment protocol Mice were anesthetized with isofllurane and inoculated with PBS or PBS containing virus in a volume of 50 μl.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from TRIzol homogenate of mouse lung.
Label Cy3
Label protocol Total RNA was labeled according to Agilent’s Quick Amp Labeling protocol as part of the Agilent One-Color Microarray-Based Gene Expression Analysis Protocol (Agilent Technology). Total RNA from each sample was linearly amplified and labeled with Cy3-UTP.
Hybridization protocol Hybridization was performed according to Agilent One-Color Microarray-Based Gene Expression Analysis Protocol (Agilent Technology). The labeled cRNAs were purified by RNeasy Mini Kit (Qiagen). The concentration and specific activity of the labeled cRNAs (pmol Cy3/μg cRNA) were measured by NanoDrop ND-1000. 1 μg of each labeled cRNA was fragmented by adding 11 μl 10 × Blocking Agent and 2.2 μl of 25×Fragmentation Buffer, then heated at 60 °C for 30 min, and finally 55 μl 2 × GE Hybridization buffer was added to dilute the labeled cRNA. 100μl of hybridization solution was dispensed into the gasket slide and assembled to the gene expression microarray slide. The slides were incubated for 17 hours at 65°C in an Agilent Hybridization Oven.
Scan protocol The hybridized arrays were washed, fixed and scanned with using the Agilent DNA Microarray Scanner (part number G2505C).
Description IM101_VN1203_2d_2
Data processing Scanned images were analyzed using Agilent Feature Extraction Software (v11.0.1.1). The limma package for R (available on Bioconductor) was used to perform background correction, quantile normalization (normalizeBetweenArrays), and summarization (avereps) to derive a single normalized intensity value per probe. Outlier samples were detected using PCA and by visual inspection of heatmaps, and all data was re-processed after removing outlier samples. All data processing for each of the biological replicates was performed independently of the other.
Submission date Jun 17, 2015
Last update date Aug 31, 2016
Contact name Natalie Heller
Organization name PNNL
Street address 902 Battelle Blvd.
City Richland
ZIP/Postal code 99354
Country USA
Platform ID GPL11202
Series (2)
GSE65575 Modeling Host Responses to Understand Severe Human Virus Infections
GSE69945 Mouse lung tissue transcriptome response to H1N1, H5N1, and mutants [mRNA]

Data table header descriptions
VALUE normalized

Data table
A_55_P1989846 10.05493247
A_55_P1991598 7.042590876
A_55_P2022211 14.00668993
A_55_P1980764 7.156158889
A_55_P1964375 10.56510244
A_51_P128876 17.3367626
A_55_P2121042 7.111699118
A_52_P219230 7.121996113
A_51_P207591 12.31015364
A_55_P2131920 9.853545196
A_55_P2404223 8.067105574
A_55_P2101944 14.33615326
A_52_P358860 8.459056135
A_51_P119031 10.4831661
A_51_P309854 7.201819138
A_51_P343900 11.15475743
A_51_P234359 11.60728187
A_51_P487813 13.65973237
A_52_P613977 11.70498382
A_55_P1957209 8.416455673

Total number of rows: 39429

Table truncated, full table size 982 Kbytes.

Supplementary file Size Download File type/resource
GSM1713665_IM101_VN1203_2d_RNA_2.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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