Comparative study on gene set and pathway topology-based enrichment methods

2015 | journal article. A publication with affiliation to the University of Göttingen.

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​Comparative study on gene set and pathway topology-based enrichment methods​
Bayerlová, M. ; Jung, K. ; Kramer, F. ; Klemm, F. ; Bleckmann, A.   & Beißbarth, T. ​ (2015) 
BMC Bioinformatics16 art. 334​.​ DOI: https://doi.org/10.1186/s12859-015-0751-5 

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Authors
Bayerlová, Michaela ; Jung, Klaus ; Kramer, Frank ; Klemm, Florian ; Bleckmann, Annalen ; Beißbarth, Tim 
Abstract
Background: Enrichment analysis is a popular approach to identify pathways or sets of genes which are significantly enriched in the context of differentially expressed genes. The traditional gene set enrichment approach considers a pathway as a simple gene list disregarding any knowledge of gene or protein interactions. In contrast, the new group of so called pathway topology-based methods integrates the topological structure of a pathway into the analysis. Methods: We comparatively investigated gene set and pathway topology-based enrichment approaches, considering three gene set and four topological methods. These methods were compared in two extensive simulation studies and on a benchmark of 36 real datasets, providing the same pathway input data for all methods. Results: In the benchmark data analysis both types of methods showed a comparable ability to detect enriched pathways. The first simulation study was conducted with KEGG pathways, which showed considerable gene overlaps between each other. In this study with original KEGG pathways, none of the topology-based methods outperformed the gene set approach. Therefore, a second simulation study was performed on non-overlapping pathways created by unique gene IDs. Here, methods accounting for pathway topology reached higher accuracy than the gene set methods, however their sensitivity was lower. Conclusions: We conducted one of the first comprehensive comparative works on evaluating gene set against pathway topology-based enrichment methods. The topological methods showed better performance in the simulation scenarios with non-overlapping pathways, however, they were not conclusively better in the other scenarios. This suggests that simple gene set approach might be sufficient to detect an enriched pathway under realistic circumstances. Nevertheless, more extensive studies and further benchmark data are needed to systematically evaluate these methods and to assess what gain and cost pathway topology information introduces into enrichment analysis. Both types of methods for enrichment analysis require further improvements in order to deal with the problem of pathway overlaps.
Issue Date
2015
Status
published
Publisher
Biomed Central Ltd
Journal
BMC Bioinformatics 
ISSN
1471-2105
Sponsor
Open-Access Publikationsfonds 2015

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