ArticleJournal of computational biology : a journal of computational molecular cell biology2012
Information flow in interaction networks II: channels, path lengths, and potentials.
Article in Journal of computational biology : a journal of computational molecular cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Extensive rewiring of the EGFR network in colorectal cancer cells expressing transforming levels of KRASNature communications · 2020Article
- InfAcrOnt: calculating cross-ontology term similarities using information flow by a random walk.BMC genomics · 2018Article
- Measuring disease similarity and predicting disease-related ncRNAs by a novel method.BMC medical genomics · 2017Article
- IntNetLncSim: an integrative network analysis method to infer human lncRNA functional similarity.Oncotarget · 2016Article
- Using biological networks to integrate, visualize and analyze genomics data.Genetics, selection, evolution : GSE · 2016Review
- DeCoaD: determining correlations among diseases using protein interaction networks.BMC research notes · 2015Article
- Analytical solution and scaling of fluctuations in complex networks traversed by damped, interacting random walkers.Physical review. E, Statistical, nonlinear, and soft matter physics · 2015Article
- Relating diseases by integrating gene associations and information flow through protein interaction network.PloS one · 2014Article
- Building a hierarchical organization of protein complexes out of protein association data.PloS one · 2014Article
- A single source k-shortest paths algorithm to infer regulatory pathways in a gene network.Bioinformatics (Oxford, England) · 2012Article
- CytoITMprobe: a network information flow plugin for Cytoscape.BMC research notes · 2012Article
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2 authors.
Funding
Abstract
In our previous publication, a framework for information flow in interaction networks based on random walks with damping was formulated with two fundamental modes: emitting and absorbing. While many other network analysis methods based on random walks or equivalent notions have been developed before and after our earlier work, one can show that they can all be mapped to one of the two modes. In addition to these two fundamental modes, a major strength of our earlier formalism was its accommodation of context-specific directed information flow that yielded plausible and meaningful biological interpretation of protein functions and pathways. However, the directed flow from origins to destinations was induced via a potential function that was heuristic. Here, with a theoretically sound approach called the channel mode, we extend our earlier work for directed information flow. This is achieved by constructing a potential function facilitating a purely probabilistic interpretation of the channel mode. For each network node, the channel mode combines the solutions of emitting and absorbing modes in the same context, producing what we call a channel tensor. The entries of the channel tensor at each node can be interpreted as the amount of flow passing through that node from an origin to a destination. Similarly to our earlier model, the channel mode encompasses damping as a free parameter that controls the locality of information flow. Through examples involving the yeast pheromone response pathway, we illustrate the versatility and stability of our new framework.
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