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Sample GSM393151 Query DataSets for GSM393151
Status Public on Oct 21, 2009
Title Aspergillus nidulans, glycerol, biological rep3
Sample type RNA
 
Source name Fungal biomass
Organism Aspergillus nidulans
Characteristics strain: FGSC A4
Treatment protocol Fungal biomass from each of the Aspergillus fermentation replicates was harvested in the mid exponential phase of growth, filtered, washed, dryed by squeezing, frozen in liquid nitrogen and stored at -80 °C until further processing.
Growth protocol Aspergillus nidulans, Aspergillus oryzae and Aspergillus niger were grown in batch cultivations.
Extracted molecule total RNA
Extraction protocol A. niger and A. nidulans total RNA was isolated using the Qiagen RNeasy Mini Kit according to the protocol for isolation of total RNA from plant and fungi. A. oryzae total RNA was purified by using the Promega RNAgents Total RNA Isolation system following manufacturer’s recommendations.
Label biotin
Label protocol Biotin-labeled cRNA was prepared from approximately 5 mg of total RNA according to the protocol described in the Affymetrix GeneChipÒ Expression Analysis Technical Manual (Affymetrix and GeneChip. (2007) P/N 702232, Affymetrix, Santa Clara, CA, Revision 2).
 
Hybridization protocol Approximately 15 mg of fragmented cRNA was hybridized for 16 hr at 45 °C on the 3AspergDTU Affymetrix GeneChip Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using an Agilent GeneArrayÒ Scanner 3000. Scanned probe array images (.DAT files) were converted into .CEL files using the Affymetrix GeneChip Operating Software.
Description Gene expression data from A. nidulans grown in batch cultivations
Data processing Affymetrix CEL data files were preprocessed using the statistical language R version 2.7.1 and Bioconductor version 2.2. Normalization was performed using the qspline algorithm and gene expression indexes were calculated from the PM probes with the median polish summary method. All statistical preprocessing methods were implemented in affy package using R scripts and limma package.
 
Submission date Apr 16, 2009
Last update date Oct 21, 2009
Contact name Margarita Salazar Peña
E-mail(s) margarita.salazar@chalmers.se
Phone +46 (031) 7723876
Fax +46 (031) 7723801
Organization name Chalmers University of Technology
Department Chemical and Biological Engineering
Lab Systems Biology
Street address Kemigården 4
City Göteborg
ZIP/Postal code SE-412 96
Country Sweden
 
Platform ID GPL5975
Series (1)
GSE15702 Expression data from batch cultivations with A. niger, A. oryzae and A. nidulans grown on glucose and glycerol

Data table header descriptions
ID_REF
VALUE Gene expression index: qspline, PM probes with the median polish summary method

Data table
ID_REF VALUE
AN0004.3_at 8.74888726517291
AN0005.3_at 5.72542106397571
AN0006.3_at 7.99255464140812
AN0007.3_at 2.13850998397917
AN0008.3_at 3.16615205986084
AN0009.3_at 4.08984029325963
AN0010.3_at 4.67699865713304
AN0011.3_at 2.55583679663858
AN0012.3_at 1.96534811978828
AN0013.3_at 3.33686724805103
AN0014.3_at 3.39874081947717
AN0015.3_at 2.26366631559125
AN0016.3_at 3.54125104552644
AN0017.3_at 5.41662619880778
AN0018.3_at 3.75218492361727
AN0019.3_at 5.68212565280967
AN0020.3_at 4.29281036134874
AN0021.3_at 5.00339261867123
AN0022.3_at 4.2832497760981
AN0023.3_at 5.41846944126747

Total number of rows: 10656

Table truncated, full table size 301 Kbytes.




Supplementary file Size Download File type/resource
GSM393151.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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