3,603 research outputs found
Distributed Adaptive Learning of Graph Signals
The aim of this paper is to propose distributed strategies for adaptive
learning of signals defined over graphs. Assuming the graph signal to be
bandlimited, the method enables distributed reconstruction, with guaranteed
performance in terms of mean-square error, and tracking from a limited number
of sampled observations taken from a subset of vertices. A detailed mean square
analysis is carried out and illustrates the role played by the sampling
strategy on the performance of the proposed method. Finally, some useful
strategies for distributed selection of the sampling set are provided. Several
numerical results validate our theoretical findings, and illustrate the
performance of the proposed method for distributed adaptive learning of signals
defined over graphs.Comment: To appear in IEEE Transactions on Signal Processing, 201
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Diagnostic Applications for Micro-Synchrophasor Measurements
This report articulates and justifies the preliminary selection of diagnostic applications for data from micro-synchrophasors (µPMUs) in electric power distribution systems that will be further studied and developed within the scope of the three-year ARPA-e award titled Micro-synchrophasors for Distribution Systems
Mutual information in random Boolean models of regulatory networks
The amount of mutual information contained in time series of two elements
gives a measure of how well their activities are coordinated. In a large,
complex network of interacting elements, such as a genetic regulatory network
within a cell, the average of the mutual information over all pairs is a
global measure of how well the system can coordinate its internal dynamics. We
study this average pairwise mutual information in random Boolean networks
(RBNs) as a function of the distribution of Boolean rules implemented at each
element, assuming that the links in the network are randomly placed. Efficient
numerical methods for calculating show that as the number of network nodes
N approaches infinity, the quantity N exhibits a discontinuity at parameter
values corresponding to critical RBNs. For finite systems it peaks near the
critical value, but slightly in the disordered regime for typical parameter
variations. The source of high values of N is the indirect correlations
between pairs of elements from different long chains with a common starting
point. The contribution from pairs that are directly linked approaches zero for
critical networks and peaks deep in the disordered regime.Comment: 11 pages, 6 figures; Minor revisions for clarity and figure format,
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Genomic analysis reveals a tight link between transcription factor dynamics and regulatory network architecture
Although several studies have provided important insights into the general principles of biological networks, the link between network organization and the genome-scale dynamics of the underlying entities (genes, mRNAs, and proteins) and its role in systems behavior remain unclear. Here we show that transcription factor (TF) dynamics and regulatory network organization are tightly linked. By classifying TFs in the yeast regulatory network into three hierarchical layers (top, core, and bottom) and integrating diverse genome-scale datasets, we find that the TFs have static and dynamic properties that are similar within a layer and different across layers. At the protein level, the top-layer TFs are relatively abundant, long-lived, and noisy compared with the core- and bottom-layer TFs. Although variability in expression of top-layer TFs might confer a selective advantage, as this permits at least some members in a clonal cell population to initiate a response to changing conditions, tight regulation of the core- and bottom-layer TFs may minimize noise propagation and ensure fidelity in regulation. We propose that the interplay between network organization and TF dynamics could permit differential utilization of the same underlying network by distinct members of a clonal cell population
Reduction of dynamical biochemical reaction networks in computational biology
Biochemical networks are used in computational biology, to model the static
and dynamical details of systems involved in cell signaling, metabolism, and
regulation of gene expression. Parametric and structural uncertainty, as well
as combinatorial explosion are strong obstacles against analyzing the dynamics
of large models of this type. Multi-scaleness is another property of these
networks, that can be used to get past some of these obstacles. Networks with
many well separated time scales, can be reduced to simpler networks, in a way
that depends only on the orders of magnitude and not on the exact values of the
kinetic parameters. The main idea used for such robust simplifications of
networks is the concept of dominance among model elements, allowing
hierarchical organization of these elements according to their effects on the
network dynamics. This concept finds a natural formulation in tropical
geometry. We revisit, in the light of these new ideas, the main approaches to
model reduction of reaction networks, such as quasi-steady state and
quasi-equilibrium approximations, and provide practical recipes for model
reduction of linear and nonlinear networks. We also discuss the application of
model reduction to backward pruning machine learning techniques
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