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Cloninger, A.

Publications and source records attributed to Cloninger, A..

2 recordsLinked to original sources

RATS: Unsupervised manifold learning using low-distortion alignment of tangent spaces

With the ubiquity of high-dimensional datasets in various biological fields, identifying low-dimensional topological manifolds within such datasets may reveal principles connecting latent variables to measurable instances in the world. The reliable discovery of such manifold structure in high-dimensional datasets can prove challenging, however, largely due to the introduction of distortion by leading manifold learning methods. The problem is further exacerbated by the lack of consensus on how to evaluate the quality of the recovered manifolds. Here, we present a novel measure of distortion to evaluate low-dimensional representations obtained using different techniques. We additionally develop a novel bottom-up manifold learning technique called Riemannian Alignment of Tangent Spaces (RATS) that aims to recover low-distortion embeddings of data, including the ability to embed closed manifolds into their intrinsic dimension using a unique tearing process. Compared to previous methods, we show that RATS provides low-distortion embeddings that excel in the visualization and deciphering of latent variables across a range of idealized, biological, and surrogate datasets that mimic real-world data. One-sentence summaryWe introduce a novel dimensionality reduction technique that generates low-dimensional embeddings while preserving the global structure within the data for a variety of biological and non-biological datasets.

neuroscience↗

Identifying drug effects in a cardiac model of electrophysiology using kernel-based parameter estimation methods

AbstractCurrent methods for solving inverse problems in cardiac electrophysiology are limited by their accuracy, scalability, practicality, or a combination of these. In this proof-of-concept study we demonstrate the feasibility of using kernel methods to solve the inverse problem of estimating the parameters of ionic membrane currents from observations of corresponding action potential (AP) traces. In particular, we consider AP traces generated by a cardiac cell action potential model, which mimics those obtained experimentally in measurable in vitro cardiac systems. Using synthetic training data from the 1977 Beeler-Reuter AP model of mammalian ventricular cardiomyocytes, we demonstrate our recently proposed boosted kernel ridge regression (KRR) solver StreaMRAK, which is particularly robust and well-adapted for high-complexity functions. We show that this method is less memory demanding, estimates the model parameters with higher accuracy, and is less exposed to parameter sensitivity issues than existing methods, such as standard KRR solvers and loss-minimization schemes based on nearest-neighbor heuristics.

systems biology↗