ArticleBMC bioinformatics2019
Identifying protein complexes based on an edge weight algorithm and core-attachment structure.
Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- PCIPG: A comprehensive framework for protein complex identification based on a probabilistic graphical model.PLoS computational biology · 2026Article
- PCIPG2.0: multi-omics fusion and structure-aware graph autoencoding for protein complex identification.Bioinformatics (Oxford, England) · 2026Article
- HPC-Atlas: Computationally Constructing A Comprehensive Atlas of Human Protein Complexes.Genomics, proteomics & bioinformatics · 2023Article
- A supervised protein complex prediction method with network representation learning and gene ontology knowledge.BMC bioinformatics · 2022Article
- Characterization and comparison of gene-centered human interactomes.Briefings in bioinformatics · 2021Article
- Therapeutic RNA Delivery for COVID and Other Diseases.Advanced healthcare materials · 2021Review
- An Improved Memetic Algorithm for Detecting Protein Complexes in Protein Interaction Networks.Frontiers in genetics · 2021Article
- Protein Complexes Form a Basis for Complex Hybrid Incompatibility.Frontiers in genetics · 2021Review
- Identifying Protein Complexes With Clear Module Structure Using Pairwise Constraints in Protein Interaction Networks.Frontiers in genetics · 2021Article
- DPCT: A Dynamic Method for Detecting Protein Complexes From TAP-Aware Weighted PPI Network.Frontiers in genetics · 2020Article
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Authors and funding
3 authors.
Funding
Abstract
backgroundProtein complex identification from protein-protein interaction (PPI) networks is crucial for understanding cellular organization principles and functional mechanisms. In recent decades, numerous computational methods have been proposed to identify protein complexes. However, most of the current state-of-the-art studies still have some challenges to resolve, including their high false-positives rates, incapability of identifying overlapping complexes, lack of consideration for the inherent organization within protein complexes, and absence of some biological attachment proteins.
resultsIn this paper, to overcome these limitations, we present a protein complex identification method based on an edge weight method and core-attachment structure (EWCA) which consists of a complex core and some sparse attachment proteins. First, we propose a new weighting method to assess the reliability of interactions. Second, we identify protein complex cores by using the structural similarity between a seed and its direct neighbors. Third, we introduce a new method to detect attachment proteins that is able to distinguish and identify peripheral proteins and overlapping proteins. Finally, we bind attachment proteins to their corresponding complex cores to form protein complexes and discard redundant protein complexes. The experimental results indicate that EWCA outperforms existing state-of-the-art methods in terms of both accuracy and p-value. Furthermore, EWCA could identify many more protein complexes with statistical significance. Additionally, EWCA could have better balance accuracy and efficiency than some state-of-the-art methods with high accuracy.
conclusionsIn summary, EWCA has better performance for protein complex identification by a comprehensive comparison with twelve algorithms in terms of different evaluation metrics. The datasets and software are freely available for academic research at https://github.com/RongquanWang/EWCA .
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