ArticleBMC systems biology2015
Accurate multiple network alignment through context-sensitive random walk.
Article in BMC systems biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 18 citations in OpenAlex.
- ClusterM: a scalable algorithm for computational prediction of conserved protein complexes across multiple protein interaction networks.BMC genomics · 2020Article
- NAPAbench 2: A network synthesis algorithm for generating realistic protein-protein interaction (PPI) network families.PloS one · 2020Article
- CUFID-query: accurate network querying through random walk based network flow estimation.BMC bioinformatics · 2017Article
- SEQUOIA: significance enhanced network querying through context-sensitive random walk and minimization of network conductance.BMC systems biology · 2017Article
- Effective comparative analysis of protein-protein interaction networks by measuring the steady-state network flow using a Markov model.BMC bioinformatics · 2016Article
Corrections and comments
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Authors and funding
2 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundComparative network analysis can provide an effective means of analyzing large-scale biological networks and gaining novel insights into their structure and organization. Global network alignment aims to predict the best overall mapping between a given set of biological networks, thereby identifying important similarities as well as differences among the networks. It has been shown that network alignment methods can be used to detect pathways or network modules that are conserved across different networks. Until now, a number of network alignment algorithms have been proposed based on different formulations and approaches, many of them focusing on pairwise alignment.
resultsIn this work, we propose a novel multiple network alignment algorithm based on a context-sensitive random walk model. The random walker employed in the proposed algorithm switches between two different modes, namely, an individual walk on a single network and a simultaneous walk on two networks. The switching decision is made in a context-sensitive manner by examining the current neighborhood, which is effective for quantitatively estimating the degree of correspondence between nodes that belong to different networks, in a manner that sensibly integrates node similarity and topological similarity. The resulting node correspondence scores are then used to predict the maximum expected accuracy (MEA) alignment of the given networks.
conclusionsPerformance evaluation based on synthetic networks as well as real protein-protein interaction networks shows that the proposed algorithm can construct more accurate multiple network alignments compared to other leading methods.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.