Djordjevic, Djordje and Kusumi, Kenro and Ho, Joshua W K (2016) XGSA: A statistical method for cross-species gene set analysis. Bioinformatics, 32 (17). pp. i620-i628. ISSN 1367-4811 (OA)
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Abstract
MOTIVATION
Gene set analysis is a powerful tool for determining whether an experimentally derived set of genes is statistically significantly enriched for genes in other pre-defined gene sets, such as known pathways, gene ontology terms, or other experimentally derived gene sets. Current gene set analysis methods do not facilitate comparing gene sets across different organisms as they do not explicitly deal with homology mapping between species. There lacks a systematic investigation about the effect of complex gene homology on cross-species gene set analysis.
RESULTS
In this study, we show that not accounting for the complex homology structure when comparing gene sets in two species can lead to false positive discoveries, especially when comparing gene sets that have complex gene homology relationships. To overcome this bias, we propose a straightforward statistical approach, called XGSA, that explicitly takes the cross-species homology mapping into consideration when doing gene set analysis. Simulation experiments confirm that XGSA can avoid false positive discoveries, while maintaining good statistical power compared to other ad hoc approaches for cross-species gene set analysis. We further demonstrate the effectiveness of XGSA with two real-life case studies that aim to discover conserved or species-specific molecular pathways involved in social challenge and vertebrate appendage regeneration.
AVAILABILITY AND IMPLEMENTATION
The R source code for XGSA is available under a GNU General Public License at http://github.com/VCCRI/XGSA CONTACT: jho@victorchang.edu.au.
| Item Type: | Article |
|---|---|
| Subjects: | R Medicine > R Medicine (General) |
| Depositing User: | Repository Administrator |
| Date Deposited: | 04 Sep 2016 23:52 |
| Last Modified: | 04 Sep 2016 23:52 |
| URI: | https://eprints.victorchang.edu.au/id/eprint/483 |
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