NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM393137 Query DataSets for GSM393137
Status Public on Oct 21, 2009
Title Aspergillus niger, glycerol, biological rep1
Sample type RNA
 
Source name Fungal biomass
Organism Aspergillus niger
Characteristics strain: BO1
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. niger 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
JGI118581_at 7.01720915966784
JGI118598_at 6.27068877870425
JGI118599_at 6.0566583937183
JGI118601_at 5.87897624226034
JGI118617_at 4.04000269033891
JGI118624_at 7.71153694312107
JGI118629_at 5.19129058295406
JGI118635_at 4.2085608600874
JGI118644_at 6.45750561144827
JGI118659_at 5.00610314450677
JGI118662_at 4.70688846920836
JGI118666_at 9.44396555825026
JGI118704_at 9.79145199478087
JGI118744_at 5.05847072022148
JGI118750_at 5.20210918273593
JGI118758_at 5.96942574508048
JGI118832_at 7.9634490027171
JGI118837_at 4.91962538409557
JGI118881_at 7.09187014754083
JGI118888_at 7.06974652819133

Total number of rows: 11122

Table truncated, full table size 318 Kbytes.




Supplementary file Size Download File type/resource
GSM393137.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap