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Scalable module detection for attributed networks with applications to breast cancer
Han Yu1, Rachael Hageman Blair2
1Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
This study introduces a Weighted Fast Greedy (WFG) algorithm for attribute-based network module detection. The WFG algorithm effectively integrates network structure with node attributes, identifying significant cancer biomarkers for survival prediction.
Area of Science:
- Bioinformatics
- Computational Biology
- Network Science
Background:
- Network module detection aims to find densely connected groups of nodes.
- Integrating node attributes with network structure is a significant challenge.
- Existing methods often struggle to bridge structural and attribute data effectively.
Purpose of the Study:
- To propose a novel Weighted Fast Greedy (WFG) algorithm for attribute-based module detection.
- To effectively integrate network structure and attribute information for enhanced community detection.
- To demonstrate the utility of attribute-based module detection in a biological context.
Main Methods:
- Developed the Weighted Fast Greedy (WFG) algorithm.
- Utilized logistic regression to bridge network structure and attribute spaces.
- Applied the WFG algorithm to a breast cancer dataset, integrating protein-protein interaction networks, gene expression data, and survival outcomes.
Main Results:
- The WFG algorithm successfully identified five modules significant for survival in breast cancer.
- These significant modules contained known cancer pathways and biomarkers, including cell cycle, p53 pathway, BRCA1, BRCA2, and AURKB.
- Neither network structure nor gene expression data alone yielded these critical cancer signatures.
Conclusions:
- Attribute-based module detection is crucial for uncovering biologically relevant network patterns.
- The WFG algorithm provides an interpretable and effective method for integrating network structure and attributes.
- This approach enhances the discovery of cancer biomarkers and survival-associated pathways.
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