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Related Concept Videos

State Space Representation01:27

State Space Representation

617
The frequency-domain technique, commonly used in analyzing and designing feedback control systems, is effective for linear, time-invariant systems. However, it falls short when dealing with nonlinear, time-varying, and multiple-input multiple-output systems. The time-domain or state-space approach addresses these limitations by utilizing state variables to construct simultaneous, first-order differential equations, known as state equations, for an nth-order system.
Consider an RLC circuit, a...
617
Model Approaches for Pharmacokinetic Data: Distributed Parameter Models01:06

Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

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Pharmacokinetic models are mathematical constructs that represent and predict the time course of drug concentrations in the body, providing meaningful pharmacokinetic parameters. These models are categorized into compartment, physiological, and distributed parameter models.
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
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Modeling with Differential Equations01:25

Modeling with Differential Equations

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Population dynamics can be described mathematically by considering the population size P(t) as a function of time. The rate of change of the population is then represented by the derivative of P(t). A simple assumption is that the rate of growth is proportional to the size of the population itself. This leads to an exponential growth model, where the population increases rapidly without bound. While this is a useful first approximation, it does not reflect realistic long-term...
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Pharmacodynamic Models: Link Model and Systems Pharmacodynamic Model01:14

Pharmacodynamic Models: Link Model and Systems Pharmacodynamic Model

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The link model is a fundamental pharmacokinetic-pharmacodynamic (PK–PD) approach to account for delayed drug responses when the observed effect does not immediately correlate with the drug's plasma concentration peak. This delay is mathematically addressed by introducing an effect compartment concentration, Ce, which is kinetically linked to the plasma concentration, Cp, via a first-order rate constant, ke0. The linkage allows for a more accurate prediction of drug effects over time. A...
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Mechanistic Models: Compartment Models in Individual and Population Analysis01:23

Mechanistic Models: Compartment Models in Individual and Population Analysis

288
Mechanistic models are utilized in individual analysis using single-source data, but imperfections arise due to data collection errors, preventing perfect prediction of observed data. The mathematical equation involves known values (Xi), observed concentrations (Ci), measurement errors (εi), model parameters (ϕj), and the related function (ƒi) for i number of values. Different least-squares metrics quantify differences between predicted and observed values. The ordinary least...
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Linear Approximation in Time Domain01:21

Linear Approximation in Time Domain

379
Nonlinear systems often require sophisticated approaches for accurate modeling and analysis, with state-space representation being particularly effective. This method is especially useful for systems where variables and parameters vary with time or operating conditions, such as in a simple pendulum or a translational mechanical system with nonlinear springs.
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Inherent Dynamics Visualizer, an Interactive Application for Evaluating and Visualizing Outputs from a Gene Regulatory Network Inference Pipeline
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High-dimensional linear state space models for dynamic microbial interaction networks.

Iris Chen1, Yogeshwar D Kelkar2, Yu Gu1

  • 1Department of Biostatistics and Computational Biology, University of Rochester, Rochester, NY 14642, United States of America.

Plos One
|November 16, 2017
PubMed
Summary
This summary is machine-generated.

Understanding microbial interactions is key to human health. This study introduces a new model to map dynamic microbial interaction networks from microbiome data, revealing complex relationships.

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Area of Science:

  • Microbiology
  • Computational Biology
  • Systems Biology

Background:

  • The human microbiome significantly impacts health, necessitating an understanding of microbial interactions.
  • Microbiome composition dynamically changes due to microbial interdependencies and environmental factors.
  • High-dimensional microbiome data presents challenges for modeling these complex interactions.

Purpose of the Study:

  • To develop a mathematical model for constructing dynamic microbial interaction networks (MINs).
  • To address the challenges posed by high-dimensional microbiome data in network construction.
  • To identify key dynamic interaction networks within the microbiome.

Main Methods:

  • Proposed a high-dimensional linear State Space Model (SSM) with a novel Expectation-Regularization-Maximization (ERM) algorithm.
  • Utilized an adaptive LASSO-based variable selection within the ERM algorithm to handle high-dimensional parameter spaces and preserve network sparsity.
  • Separately specified system and measurement noise within the SSM framework.

Main Results:

  • Simulation studies demonstrated the effectiveness of the proposed ERM algorithm for variable selection.
  • Successfully applied the method to identify a dynamic microbial interaction network from a time-course vaginal microbiome dataset.
  • The model effectively captures the sparsity inherent in microbial interaction networks.

Conclusions:

  • The developed high-dimensional SSM with ERM algorithm provides a robust method for constructing dynamic microbial interaction networks.
  • This approach enables the identification of key bacterial interactions within complex microbiome ecosystems.
  • The methodology is adaptable for future extensions, including the integration of environmental factors into microbial interaction analyses.