The impact of temporal sampling resolution on parameter inference for biological transport models.

Imaging data has become an essential tool to explore key biological questions at various scales, for example the motile behaviour of bacteria or the transport of mRNA, and it has the potential to transform our understanding of important transport mechanisms. Often these imaging studies require us to...

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Main Authors: Jonathan U Harrison, Ruth E Baker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-06-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC6034909?pdf=render
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spelling doaj-4057e166d67c4cef9da121e4bf863b0f2020-11-25T01:44:39ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582018-06-01146e100623510.1371/journal.pcbi.1006235The impact of temporal sampling resolution on parameter inference for biological transport models.Jonathan U HarrisonRuth E BakerImaging data has become an essential tool to explore key biological questions at various scales, for example the motile behaviour of bacteria or the transport of mRNA, and it has the potential to transform our understanding of important transport mechanisms. Often these imaging studies require us to compare biological species or mutants, and to do this we need to quantitatively characterise their behaviour. Mathematical models offer a quantitative description of a system that enables us to perform this comparison, but to relate mechanistic mathematical models to imaging data, we need to estimate their parameters. In this work we study how collecting data at different temporal resolutions impacts our ability to infer parameters of biological transport models by performing exact inference for simple velocity jump process models in a Bayesian framework. The question of how best to choose the frequency with which data is collected is prominent in a host of studies because the majority of imaging technologies place constraints on the frequency with which images can be taken, and the discrete nature of observations can introduce errors into parameter estimates. In this work, we mitigate such errors by formulating the velocity jump process model within a hidden states framework. This allows us to obtain estimates of the reorientation rate and noise amplitude for noisy observations of a simple velocity jump process. We demonstrate the sensitivity of these estimates to temporal variations in the sampling resolution and extent of measurement noise. We use our methodology to provide experimental guidelines for researchers aiming to characterise motile behaviour that can be described by a velocity jump process. In particular, we consider how experimental constraints resulting in a trade-off between temporal sampling resolution and observation noise may affect parameter estimates. Finally, we demonstrate the robustness of our methodology to model misspecification, and then apply our inference framework to a dataset that was generated with the aim of understanding the localization of RNA-protein complexes.http://europepmc.org/articles/PMC6034909?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jonathan U Harrison
Ruth E Baker
spellingShingle Jonathan U Harrison
Ruth E Baker
The impact of temporal sampling resolution on parameter inference for biological transport models.
PLoS Computational Biology
author_facet Jonathan U Harrison
Ruth E Baker
author_sort Jonathan U Harrison
title The impact of temporal sampling resolution on parameter inference for biological transport models.
title_short The impact of temporal sampling resolution on parameter inference for biological transport models.
title_full The impact of temporal sampling resolution on parameter inference for biological transport models.
title_fullStr The impact of temporal sampling resolution on parameter inference for biological transport models.
title_full_unstemmed The impact of temporal sampling resolution on parameter inference for biological transport models.
title_sort impact of temporal sampling resolution on parameter inference for biological transport models.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2018-06-01
description Imaging data has become an essential tool to explore key biological questions at various scales, for example the motile behaviour of bacteria or the transport of mRNA, and it has the potential to transform our understanding of important transport mechanisms. Often these imaging studies require us to compare biological species or mutants, and to do this we need to quantitatively characterise their behaviour. Mathematical models offer a quantitative description of a system that enables us to perform this comparison, but to relate mechanistic mathematical models to imaging data, we need to estimate their parameters. In this work we study how collecting data at different temporal resolutions impacts our ability to infer parameters of biological transport models by performing exact inference for simple velocity jump process models in a Bayesian framework. The question of how best to choose the frequency with which data is collected is prominent in a host of studies because the majority of imaging technologies place constraints on the frequency with which images can be taken, and the discrete nature of observations can introduce errors into parameter estimates. In this work, we mitigate such errors by formulating the velocity jump process model within a hidden states framework. This allows us to obtain estimates of the reorientation rate and noise amplitude for noisy observations of a simple velocity jump process. We demonstrate the sensitivity of these estimates to temporal variations in the sampling resolution and extent of measurement noise. We use our methodology to provide experimental guidelines for researchers aiming to characterise motile behaviour that can be described by a velocity jump process. In particular, we consider how experimental constraints resulting in a trade-off between temporal sampling resolution and observation noise may affect parameter estimates. Finally, we demonstrate the robustness of our methodology to model misspecification, and then apply our inference framework to a dataset that was generated with the aim of understanding the localization of RNA-protein complexes.
url http://europepmc.org/articles/PMC6034909?pdf=render
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