Exploring biological interaction networks with tailored weighted quasi-bicliques

被引:11
|
作者
Chang, Wen-Chieh [1 ]
Vakati, Sudheer [1 ]
Krause, Roland [2 ,3 ]
Eulenstein, Oliver [1 ]
机构
[1] Iowa State Univ, Dept Comp Sci, Ames, IA 50011 USA
[2] Free Univ Berlin, Dept Comp Sci, D-14195 Berlin, Germany
[3] Max Planck Inst Mol Genet, Dept Computat Mol Biol, D-14195 Berlin, Germany
来源
BMC BIOINFORMATICS | 2012年 / 13卷
基金
美国国家科学基金会;
关键词
Bipartite Graph; Integer Program; Edge Weight; Biological Network; Molecular Network;
D O I
10.1186/1471-2105-13-S10-S16
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Biological networks provide fundamental insights into the functional characterization of genes and their products, the characterization of DNA-protein interactions, the identification of regulatory mechanisms, and other biological tasks. Due to the experimental and biological complexity, their computational exploitation faces many algorithmic challenges. Results: We introduce novel weighted quasi-biclique problems to identify functional modules in biological networks when represented by bipartite graphs. In difference to previous quasi-biclique problems, we include biological interaction levels by using edge-weighted quasi-bicliques. While we prove that our problems are NP-hard, we also describe IP formulations to compute exact solutions for moderately sized networks. Conclusions: We verify the effectiveness of our IP solutions using both simulation and empirical data. The simulation shows high quasi-biclique recall rates, and the empirical data corroborate the abilities of our weighted quasi-bicliques in extracting features and recovering missing interactions from biological networks.
引用
收藏
页数:9
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