For nonlinear PDEs, this is readily applied to low-dimensional linear parameter-varying (LPV) approximations as they have been exploited for efficient nonlinear controller design via series expansions of the solution to the state-dependent Riccati equation. In this work, we develop a polytopic autoencoder for control applications and show how it outperforms standard linear approaches in view of LPV approximations of nonlinear systems and how the particular architecture enables higher order series expansions at little extra computational effort. We illustrate the properties and potentials of this approach to computational nonlinear controller design for large-scale systems with a thorough numerical study.

In many experiments, the data points collected live in high-dimensional observation spaces, yet can be assigned a set of labels or parameters. In electrophysiological recordings, for instance, the responses of populations of neurons generally depend on mixtures of experimentally controlled parameters. The heterogeneity and diversity of these parameter dependencies can make visualization and interpretation of such data extremely difficult. Standard dimensionality reduction techniques such as principal component analysis (PCA) can provide a succinct and complete description of the data, but the description is constructed independent of the relevant task variables and is often hard to interpret. Here, we start with the assumption that a particularly informative description is one that reveals the dependency of the high-dimensional data on the individual parameters. We show how to modify the loss function of PCA so that the principal components seek to capture both the maximum amount of variance about the data, while also depending on a minimum number of parameters. We call this method demixed principal component analysis (dPCA) as the principal components here segregate the parameter dependencies. We phrase the problem as a probabilistic graphical model, and present a fast Expectation-Maximization (EM) algorithm. We demonstrate the use of this algorithm for electrophysiological data and show that it serves to demix the parameter-dependence of a neural population response.

This paper addresses the $\epsilon$-close parameter tuning problem for Bayesian Networks (BNs): find a minimal $\epsilon$-close amendment of probability entries in a given set of (rows in) conditional probability tables that make a given quantitative constraint on the BN valid. Based on the state-of-the-art "region verification" techniques for parametric Markov chains, we propose an algorithm whose capabilities go beyond any existing techniques. Our experiments show that $\epsilon$-close tuning of large BN benchmarks with up to 8 parameters is feasible. In particular, by allowing (i) varied parameters in multiple CPTs and (ii) inter-CPT parameter dependencies, we treat subclasses of parametric BNs that have received scant attention so far.

In many experiments, the data points collected live in high-dimensional observation spaces, yet can be assigned a set of labels or parameters. In electrophysiological recordings, for instance, the responses of populations of neurons generally depend on mixtures of experimentally controlled parameters. The heterogeneity and diversity of these parameter dependencies can make visualization and interpretation of such data extremely difficult. Standard dimensionality reduction techniques such as principal component analysis (PCA) can provide a succinct and complete description of the data, but the description is constructed independent of the relevant task variables and is often hard to interpret. Here, we start with the assumption that a particularly informative description is one that reveals the dependency of the high-dimensional data on the individual parameters.

In many experiments, the data points collected live in high-dimensional observation spaces, yet can be assigned a set of labels or parameters. In electrophysiological recordings, for instance, the responses of populations of neurons generally depend on mixtures of experimentally controlled parameters. The heterogeneity and diversity of these parameter dependencies can make visualization and interpretation of such data extremely difficult. Standard dimensionality reduction techniques such as principal component analysis (PCA) can provide a succinct and complete description of the data, but the description is constructed independent of the relevant task variables and is often hard to interpret. Here, we start with the assumption that a particularly informative description is one that reveals the dependency of the high-dimensional data on the individual parameters.

In many experiments, the data points collected live in high-dimensional observation spaces, yet can be assigned a set of labels or parameters. In electrophysiological recordings, for instance, the responses of populations of neurons generally depend on mixtures of experimentally controlled parameters. The heterogeneity and diversity of these parameter dependencies can make visualization and interpretation of such data extremely difficult. Standard dimensionality reduction techniques such as principal component analysis (PCA) can provide a succinct and complete description of the data, but the description is constructed independent of the relevant task variables and is often hard to interpret. Here, we start with the assumption that a particularly informative description is one that reveals the dependency of the high-dimensional data on the individual parameters. We show how to modify the loss function of PCA so that the principal components seek to capture both the maximum amount of variance about the data, while also depending on a minimum number of parameters. We call this method demixed principal component analysis (dPCA) as the principal components here segregate the parameter dependencies. We phrase the problem as a probabilistic graphical model, and present a fast Expectation-Maximization (EM) algorithm. We demonstrate the use of this algorithm for electrophysiological data and show that it serves to demix the parameter-dependence of a neural population response.