REAL

Discovering cooperative biomarkers for heterogeneous complex disease diagnoses

Sun, Duanchen and Ren, Xianwen and Ari, Eszter and Korcsmáros Tamás, and Csermely, Péter (2019) Discovering cooperative biomarkers for heterogeneous complex disease diagnoses. BRIEFINGS IN BIOINFORMATICS, 20 (1). pp. 89-101. ISSN 1467-5463

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Abstract

Biomarkers with high reproducibility and accurate prediction performance can contribute to comprehending the underlying pathogenesis of related complex diseases and further facilitate disease diagnosis and therapy. Techniques integrating gene expression profiles and biological networks for the identification of network-based disease biomarkers are receiving increasing interest. The biomarkers for heterogeneous diseases often exhibit strong cooperative effects, which implies that a set of genes may achieve more accurate outcome prediction than any single gene. In this study, we evaluated various biomarker identification methods that consider gene cooperative effects implicitly or explicitly, and proposed the gene cooperation network to explicitly model the cooperative effects of gene combinations. The gene cooperation network- enhanced method, named as MarkRank, achieves superior performance compared with traditional biomarker identification methods in both simulation studies and real data sets. The biomarkers identified by MarkRank not only have a better prediction accuracy but also have stronger topological relationships in the biological network and exhibit high specificity associated with the related diseases. Furthermore, the top genes identified by MarkRank involve crucial biological processes of related diseases and give a good prioritization for known disease genes. In conclusion, MarkRank suggests that explicit modeling of gene cooperative effects can greatly improve biomarker identification for complex diseases, especially for diseases with high heterogeneity.

Item Type: Article
Additional Information: Funding Agency and Grant Number: Strategic Priority Research Program of the Chinese Academy of Sciences [XDB13040600]; National Natural Science Foundation of China [11131009, 11631014, 91330114, 11661141019]; Earlham Institute (Norwich, UK); Institute of Food Research (Norwich, UK); Hungarian National Research, Development and Innovation Office [K115378]; Biotechnological and Biosciences Research Council, UK Funding text: This work was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (grant number XDB13040600) and the National Natural Science Foundation of China (grant numbers 11131009, 11631014, 91330114 and 11661141019). TK's work was supported by a fellowship in computational biology at the Earlham Institute (Norwich, UK) in partnership with the Institute of Food Research (Norwich, UK) and strategically supported by the Biotechnological and Biosciences Research Council, UK. Work in PC's laboratory was supported by the Hungarian National Research, Development and Innovation Office (grant number K115378).
Subjects: Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia
Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia > QH3011 Biochemistry / biokémia
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 24 Nov 2019 14:13
Last Modified: 24 Nov 2019 14:13
URI: http://real.mtak.hu/id/eprint/103670

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