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Jelle Van Leene

dblp:52/7063 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2009
0000-0002-4932-8192ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 75% Computational science and engineering · 25%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
functional genomics
0.112009
Gene expression trends and protein features effectively complement each other in gene function prediction · Bioinform. 2009
Bioinformatics and computational biology › functional genomics
gene function prediction
0.112009
Gene expression trends and protein features effectively complement each other in gene function prediction · Bioinform. 2009
Bioinformatics and computational biology
multi-omics data integration
0.112009
Gene expression trends and protein features effectively complement each other in gene function prediction · Bioinform. 2009
Computational science and engineering › pattern recognition
rule-based classification
0.112009
Gene expression trends and protein features effectively complement each other in gene function prediction · Bioinform. 2009

Methods — techniques the papers use, named apart from their topics

rough sets · 0.1if-then rules · 0.1
YearPublicationVenuePosition
2009 Gene expression trends and protein features effectively complement each other in gene function prediction
abstract
MOTIVATION: Genome-scale 'omics' data constitute a potentially rich source of information about biological systems and their function. There is a plethora of tools and methods available to mine omics data. However, the diversity and complexity of different omics data types is a stumbling block for multi-data integration, hence there is a dire need for additional methods to exploit potential synergy from integrated orthogonal data. Rough Sets provide an efficient means to use complex information in classification approaches. Here, we set out to explore the possibilities of Rough Sets to incorporate diverse information sources in a functional classification of unknown genes. RESULTS: We explored the use of Rough Sets for a novel data integration strategy where gene expression data, protein features and Gene Ontology (GO) annotations were combined to describe general and biologically relevant patterns represented by If-Then rules. The descriptive rules were used to predict the function of unknown genes in Arabidopsis thaliana and Schizosaccharomyces pombe. The If-Then rule models showed success rates of up to 0.89 (discriminative and predictive power for both modeled organisms); whereas, models built solely of one data type (protein features or gene expression data) yielded success rates varying from 0.68 to 0.78. Our models were applied to generate classifications for many unknown genes, of which a sizeable number were confirmed either by PubMed literature reports or electronically interfered annotations. Finally, we studied cell cycle protein-protein interactions derived from both tandem affinity purification experiments and in silico experiments in the BioGRID interactome database and found strong experimental evidence for the predictions generated by our models. The results show that our approach can be used to build very robust models that create synergy from integrating gene expression data and protein features. AVAILABILITY: The Rough Set-based method is implemented in the Rosetta toolkit kernel version 1.0.1 available at: http://rosetta.lcb.uu.se/
Krzysztof Wabnik, Torgeir R. Hvidsten, Anna M. Kedzierska, Jelle Van Leene, Geert De Jaeger, Gerrit T. S. Beemster, Jan Komorowski, Martin Kuiper
Bioinform.4