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Interaction network

About: Interaction network is a research topic. Over the lifetime, 2700 publications have been published within this topic receiving 113372 citations.


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Journal ArticleDOI
TL;DR: This paper presents a model for the competition dynamics in the World Wide Web market, representing each site by a vertex in a graph and each competitive interaction as an edge, and evaluates the dynamical evolution of the fraction of the market controlled by the sites through a set of differential equations based on the Lotka–Volterra equations.
Abstract: This paper presents a model for the competition dynamics in the World Wide Web market We show that this problem is suitable to be analyzed in the framework of the theory of complex networks, representing each site by a vertex in a graph and each competitive interaction as an edge Once the topology of the interaction network has been defined, we evaluate the dynamical evolution of the fraction of the market controlled by the sites through a set of differential equations based on the Lotka–Volterra equations We show that, under these assumptions, some interesting and novel nonlinear effects emerge in this kind of markets

18 citations

Journal ArticleDOI
TL;DR: This work explicitly leverage the oscillatory nature of the transcriptional signals and presents a method for reconstructing network interactions tailored to this special but important class of genetic circuits, based on projecting the signal onto a set of oscillatory basis functions using a Discrete Fourier Transform.
Abstract: Motivation: Oscillations lie at the core of many biological processes, from the cell cycle, to circadian oscillations and developmental processes. Time-keeping mechanisms are essential to enable organisms to adapt to varying conditions in environmental cycles, from day/night to seasonal. Transcriptional regulatory networks are one of the mechanisms behind these biological oscillations. However, while identifying cyclically expressed genes from time series measurements is relatively easy, determining the structure of the interaction network underpinning the oscillation is a far more challenging problem. Results: Here, we explicitly leverage the oscillatory nature of the transcriptional signals and present a method for reconstructing network interactions tailored to this special but important class of genetic circuits. Our method is based on projecting the signal onto a set of oscillatory basis functions using a Discrete Fourier Transform. We build a Bayesian Hierarchical model within a frequency domain linear model in order to enforce sparsity and incorporate prior knowledge about the network structure. Experiments on real and simulated data show that the method can lead to substantial improvements over competing approaches if the oscillatory assumption is met, and remains competitive also in cases it is not. Availability: DSS, experiment scripts and data are available at http://homepages.inf.ed.ac.uk/gsanguin/DSS.zip. Contact: ku.ca.de.sms@sonab-ojert.d Supplementary information: Supplementary data are available at Bioinformatics online.

18 citations

Journal ArticleDOI
08 Oct 2019-Chaos
TL;DR: It is demonstrated that, given sufficient observational data on the transient evolution of each oscillator, machine learning can reconstruct the interaction network and identify the intrinsic dynamics.
Abstract: In a complex system, the interactions between individual agents often lead to emergent collective behavior such as spontaneous synchronization, swarming, and pattern formation. Beyond the intrinsic properties of the agents, the topology of the network of interactions can have a dramatic influence over the dynamics. In many studies, researchers start with a specific model for both the intrinsic dynamics of each agent and the interaction network and attempt to learn about the dynamics of the model. Here, we consider the inverse problem: given data from a system, can one learn about the model and the underlying network? We investigate arbitrary networks of coupled phase oscillators that can exhibit both synchronous and asynchronous dynamics. We demonstrate that, given sufficient observational data on the transient evolution of each oscillator, machine learning can reconstruct the interaction network and identify the intrinsic dynamics.

18 citations

Proceedings ArticleDOI
13 Dec 2010
TL;DR: This work proposes a framework for discovery of collaborative community structure in Wiki-based knowledge repositories based on raw-content generation analysis that outperforms existing alternatives in identifying coherent clusters according to objective optimality criteria.
Abstract: —We propose a framework for discovery of collaborative community structure in Wiki-based knowledge repositories based on raw-content generation analysis. We leverage topic modelling in order to capture agreement and opposition of contributors and analyze these multi-modal relations to map communities in the contributor base. The key steps of our approach include (i) modeling of pair wise variable-strength contributor interactions that can be both positive and negative, (ii) synthesis of a global network incorporating all pair wise interactions, and (iii) detection and analysis of community structure encoded in such networks. The global community discovery algorithm we propose outperforms existing alternatives in identifying coherent clusters according to objective optimality criteria. Analysis of the discovered community structure reveals coalitions of common interest editors who back each other in promoting some topics and collectively oppose other coalitions or single authors. We couple contributor interactions with content evolution and reveal the global picture of opposing themes within the self-regulated community base for both controversial and featured articles in Wikipedia.

18 citations

Journal ArticleDOI
Xi Zhou1, Pengcheng Chen1, Qiang Wei1, Xueling Shen1, Xin Chen1 
TL;DR: The human interactome resource and the gene set linkage analysis tool are presented for the functional interpretation of biologically meaningful gene sets observed in experiments and GSLA determines whether an observed gene set has significant functional linkages to established biological processes.
Abstract: MOTIVATION A molecular interaction network can be viewed as a network in which genes with related functions are connected. Therefore, at a systems level, connections between individual genes in a molecular interaction network can be used to infer the collective functional linkages between biologically meaningful gene sets. RESULTS We present the human interactome resource and the gene set linkage analysis (GSLA) tool for the functional interpretation of biologically meaningful gene sets observed in experiments. GSLA determines whether an observed gene set has significant functional linkages to established biological processes. When an observed gene set is not enriched by known biological processes, traditional enrichment-based interpretation methods cannot produce functional insights, but GSLA can still evaluate whether those genes work in concert to regulate specific biological processes, thereby suggesting the functional implications of the observed gene set. The quality of human interactome resource and the utility of GSLA are illustrated with multiple assessments. AVAILABILITY http://www.cls.zju.edu.cn/hir/

18 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202337
202290
2021183
2020221
2019201
2018163