Skip Navigation

This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (30)
Right arrowRequest Permissions
Google Scholar
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation

Bioinformatics Vol. 18 no. 3 2002
Pages 423-433
© 2002 Oxford University Press

Microarray data warehouse allowing for inclusion of experiment annotations in statistical analysis

Kurt Fellenberg 1,2,*, Nicole C. Hauser 2, Benedikt Brors 1,2, Jörg D. Hoheisel 2 and Martin Vingron 1,3

1 Department of Theoretical Bioinformatics
2 Department of Functional Genome Analysis, German Cancer Research Center, PO Box 101949, D-69009 Heidelberg, Germany

Received on April 18, 2001 ; revised on August 22, 2001 ; accepted on October 29, 2001

Motivation: Microarray technology provides access to expression levels of thousands of genes at once, producing large amounts of data. These datasets are valuable only if they are annotated by sufficiently detailed experiment descriptions. However, in many databases a substantial number of these annotations is in free-text format and not readily accessible to computer-aided analysis.

Results: The Multi-Conditional Hybridization Intensity Processing System (M-CHIPS), a data warehousing concept, focuses on providing both structure and algorithms suitable for statistical analysis of a microarray database’s entire contents including the experiment annotations. It addresses the rapid growth of the amount of hybridization data, more detailed experimental descriptions, and new kinds of experiments in the future. We have developed a storage concept , a particular instance of which is an organism-specific database. Although these databases may contain different ontologies of experiment annotations, they share the same structure and therefore can be accessed by the very same statistical algorithms. Experiment ontologies have not yet reached their final shape, and standards are reduced to minimal conventions that do not yet warrant extensive description. An ontology-independent structure enables updates of annotation hierarchies during normal database operation without altering the structure.

Availability and supplementary information: http://www.dkfz.de/tbi/services/mchips

Contact: k.fellenberg{at}dkfz.de

* To whom correspondence should be addressed.

3 Present address: Max-Planck-Institute for Molecular Genetics, Ihnestr. 73, D-14195 Berlin, Germany.




This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
A. M. Estevez
The RNA-binding protein TbDRBD3 regulates the stability of a specific subset of mRNAs in trypanosomes
Nucleic Acids Res., August 1, 2008; 36(14): 4573 - 4586.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
D. C. Hassane, M. L. Guzman, C. Corbett, X. Li, R. Abboud, F. Young, J. L. Liesveld, M. Carroll, and C. T. Jordan
Discovery of agents that eradicate leukemia stem cells using an in silico screen of public gene expression data
Blood, June 15, 2008; 111(12): 5654 - 5662.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
C. Hartmann, C. Benz, S. Brems, L. Ellis, V.-D. Luu, M. Stewart, I. D'Orso, C. Busold, K. Fellenberg, A. C. C. Frasch, et al.
Small Trypanosome RNA-Binding Proteins TbUBP1 and TbUBP2 Influence Expression of F-Box Protein mRNAs in Bloodstream Trypanosomes
Eukaryot. Cell, November 1, 2007; 6(11): 1964 - 1978.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
N. C. Hauser, R. Martinez, A. Jacob, S. Rupp, J. D. Hoheisel, and S. Matysiak
Utilising the left-helical conformation of L-DNA for analysing different marker types on a single universal microarray platform
Nucleic Acids Res., October 6, 2006; (2006) gkl671v3.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
O. N. Reva, C. Weinel, M. Weinel, K. Bohm, D. Stjepandic, J. D. Hoheisel, and B. Tummler
Functional Genomics of Stress Response in Pseudomonas putida KT2440
J. Bacteriol., June 1, 2006; 188(11): 4079 - 4092.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
C. H. Busold, S. Winter, N. Hauser, A. Bauer, J. Dippon, J. D. Hoheisel, and K. Fellenberg
Integration of GO annotations in Correspondence Analysis: facilitating the interpretation of microarray data
Bioinformatics, May 15, 2005; 21(10): 2424 - 2429.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
M. Bey, K. Stuber, K. Fellenberg, Z. Schwarz-Sommer, H. Sommer, H. Saedler, and S. Zachgo
Characterization of Antirrhinum Petal Development and Identification of Target Genes of the Class B MADS Box Gene DEFICIENS
PLANT CELL, December 1, 2004; 16(12): 3197 - 3215.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Lagorce, N. C. Hauser, D. Labourdette, C. Rodriguez, H. Martin-Yken, J. Arroyo, J. D. Hoheisel, and J. Francois
Genome-wide Analysis of the Response to Cell Wall Mutations in the Yeast Saccharomyces cerevisiae
J. Biol. Chem., May 23, 2003; 278(22): 20345 - 20357.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
T. Barz, K. Ackermann, G. Dubois, R. Eils, and W. Pyerin
Genome-wide expression screens indicate a global role for protein kinase CK2 in chromatin remodeling
J. Cell Sci., April 15, 2003; 116(8): 1563 - 1577.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
F. Diehl, B. Beckmann, N. Kellner, N. C. Hauser, S. Diehl, and J. D. Hoheisel
Manufacturing DNA microarrays from unpurified PCR products
Nucleic Acids Res., August 15, 2002; 30(16): e79 - e79.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.