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Sample GSM393147 Query DataSets for GSM393147
Status Public on Oct 21, 2009
Title Aspergillus nidulans, glucose, biological rep2
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 8.3686511599737
AN0005.3_at 5.71383071522302
AN0006.3_at 6.94327410890392
AN0007.3_at 2.29078279471269
AN0008.3_at 3.20531796273201
AN0009.3_at 4.1961151473747
AN0010.3_at 4.98172422730907
AN0011.3_at 3.1149109787805
AN0012.3_at 3.24610884321165
AN0013.3_at 3.48732472962044
AN0014.3_at 3.12392605035676
AN0015.3_at 2.208785990386
AN0016.3_at 3.98169805819912
AN0017.3_at 5.08483483598568
AN0018.3_at 3.20644572253659
AN0019.3_at 5.13321309048432
AN0020.3_at 3.53526605290608
AN0021.3_at 4.75941113409043
AN0022.3_at 4.2217338883283
AN0023.3_at 3.67613557723562

Total number of rows: 10656

Table truncated, full table size 301 Kbytes.




Supplementary file Size Download File type/resource
GSM393147.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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