Comment on hess-2022-414

We estimate the parameters of a stochastic process model for a macroparasite population within a host using approximate Bayesian computation (ABC). The immunity of the host is an unobserved model variable and only mature macroparasites at sacrifice of the host are counted. With very limited data, process rates are inferred reasonably precisely. Modeling involves a three variable Markov process for which the observed data likelihood is computationally intractable. ABC methods are particularly useful when the likelihood is analytically or computationally intractable. The ABC algorithm we present is based on sequential Monte Carlo, is adaptive in nature, and overcomes some drawbacks of previous approaches to ABC. The algorithm is validated on a test example involving simulated data from an autologistic model before being used to infer parameters of the Markov process model for experimental data. The fitted model explains the observed extra-binomial variation in terms of a zero-one immunity variable, which has a short-lived presence in the host.

Analytically or computationally intractable likelihood functions can arise in complex statistical inferential problems making them inaccessible to standard Bayesian inferential methods. Approximate Bayesian computation (ABC) methods address such inferential problems by replacing direct likelihood evaluations with repeated sampling from the model. ABC methods have been predominantly applied to parameter estimation problems and less to model choice problems due to the added difficulty of handling multiple model spaces. The ABC algorithm proposed here addresses model choice problems by extending Fearnhead and Prangle (2012, Journal of the Royal Statistical Society, Series B 74, 1-28) where the posterior mean of the model parameters estimated through regression formed the summary statistics used in the discrepancy measure. An additional stepwise multinomial logistic regression is performed on the model indicator variable in the regression step and the estimated model probabilities are incorporated into the set of summary statistics for model choice purposes. A reversible jump Markov chain Monte Carlo step is also included in the algorithm to increase model diversity for thorough exploration of the model space. This algorithm was applied to a validating example to demonstrate the robustness of the algorithm across a wide range of true model probabilities. Its subsequent use in three pathogen transmission examples of varying complexity illustrates the utility of the algorithm in inferring preference of particular transmission models for the pathogens.

Markov Chain Monte Carlo (MCMC) is widely applied to fit complex, practical models in various disciplines, such as engineering, physics, agriculture, etc. Indeed, when the target density $f$ is not available in closed form, a Markov chain is constructed with stationary density $f$ for forming Monte Carlo estimators of means with respect to $f$. Although a Harris ergodic Markov chain will converge to the target distribution as the Monte Carlo sample size tends to infinity, and the population means can be consistently estimated by the corresponding MCMC estimators, in practice, it is important to estimate the standard errors associated with these Monte Carlo estimates due to the availability of only a finite sample. Therefore, the geometric ergodicity of a Markov Chain is highly desired as it is the most standard method for guaranteeing a central limit theorem (CLT) for MCMC estimators and finding its standard errors. Among the different MCMC algorithms, Metropolis-Hastings (MH) algorithms are predominant. This thesis establishes conditions under which MH algorithms with a position-dependent proposal covariance matrix will or will not have the geometric convergence rate. Indeed, we provide these results for MH algorithms where the normal proposal density has a general mean function $c(x)$ and a covariance matrix $G(x)$ depending on the current position $x$ of the Markov chain. For modern variants of the popular Metropolis adjusted Langevin algorithms (MALA), like the manifold MALA (MMALA) that adapt to the geometry of the target distributions, the proposal covariance matrix changes in every iteration. Thus, we provide conditions for the geometric ergodicity of different variations of the Langevin algorithms, e.g., MMALA, position-dependent MALA (PMALA), and the pre-conditioned MALA (PCMALA). We also provide conditions guaranteeing geometric ergodicity of the pre-conditioned unadjusted Langevin algorithms (PCULA). Generalized linear mixed models (GLMMs), where the response variable is allowed to follow a non-Gaussian distribution, are popular statistical models, although their likelihood functions are not available in closed form. GLMMs can handle the over-dispersion often present in real-world data, and MCMC methods are generally used to fit frequentist and Bayesian GLMMs. Since the likelihood function for GLMMs is not available in closed form, Monte Carlo EM or Monte Carlo maximum likelihood methods are often used for making inferences from GLMMs. Simulation from the conditional (on the data) distribution of the random effects is, in turn, needed for implementing the Monte Carlo EM or Monte Carlo maximum likelihood methods. In this thesis, our general conditions for geometric ergodicity of variants of Langevin algorithms are also verified in the context of conditional simulation from the two most popular GLMMs, namely the binomial GLMM with the logit link and the Poisson GLMM with the log link. These results have important practical implications as users can now confidently fit these models by attaching asymptotically valid standard errors with their Markov chain-based Monte Carlo estimates. Spatial generalized linear mixed models (SGLMMs) are GLMMs where the random effects form a spatial process and are useful for modeling spatially correlated data. We compare the performance of different variants of MALA mentioned above as well as other popular MH algorithms like Random Walk Metropolis in the context of conditional simulation from SGLMMs. Next, we consider MCMC algorithms for full Bayesian analysis of GLMMs. Blocking and reparameterization are techniques used to improve the efficiency and convergence properties of MCMC algorithms. We combine these strategies with pre-conditioning to develop efficient Langevin algorithms for Bayesian GLMMs and SGLMMs. We illustrate our algorithms using extensive real and simulated data analyses.

Event Abstract Back to Event Statistical uncertainty and sensitivity analysis of intracellular signaling models - through approximate Bayesian computation and variance based global sensitivity analysis Olivia Eriksson1, 2*, Alexandra Jauhiainen1, 3, Sara Maad Sasane4, Anu G Nair5, Carolina Sartorius4 and Jeanette Hellgren Kotaleski2, 5, 6 1 Contributed equally to this work, Sweden 2 Stockholm University, Department of Numerical Analysis and Computer Science, Sweden 3 AstraZeneca AB R&D, Early Clinical Biometrics, Sweden 4 Lund University, Centre for Mathematical Sciences, Sweden 5 KTH Royal Institute of Technology, School of Computer Science and Communication, Sweden 6 Karolinska Institute, Department of Neuroscience, Sweden Computational dynamical models describing intracellular signaling pathways of nerve cells are increasing in size and complexity as more information is obtained from experiments. Models describing protein interactions within neurons can contain over hundred protein reactions [1, 2]. These models are built from knowledge about the interaction topology, inferred from e.g. gene knock-out experiments, as well as from experimental quantitative data describing the input-output relationship of the observed system. The quantitative data are often sparse as compared to the size of the system, and translating the experimental information into dynamical models often results in large uncertainties in the parameter (e.g reaction rates) values. This uncertainty is partly due to the sparseness in experimental time series data (practical unidentifiability), but it is also an intrinsic feature of the modeled system (structural unidentifiability) and could reflect the possibility for biological variation [3]; in many biological systems the same function can be achieved in partly different ways due to degeneracy and redundancy. Here we investigate the extent of this parameter uncertainty, in a model describing calcium (Ca)-dependent activation of Calmodulin (CaM), Protein phosphatase 2B (PP2B) and Ca/CaM-dependent protein kinase II (CamKII) [4], which is an intracellular pathway of importance to synaptic plasticity. We presume that the structure of the model is correct and then characterize the uncertainty in the parameters based on data. This is done by sampling the subspace of parameter values which has an equally good fit to data (corresponding to the “viable space” in [5]), through a statistical approach known as Approximate Bayesian Computation (ABC) with Markov Chain Monte Carlo (MCMC) [6]. ABC has been proposed for parameter estimation in system biology models previously, albeit in slightly different settings, e.g. [7, 8], and can be applied to a wide range of problems. In order to characterize the viable space efficiently with several experimental datasets, we employ multivariate probability distributions called copulas as a part of the ABC sampling. The result is a multivariate posterior distribution for the parameters, which represents how much they are constrained by the data (i.e. the uncertainty) as illustrated in Figure 1 (pairwise plots of viable space for four parameters indicating constraints and dependencies before and after calibration to data). The next step is to look into how the parameter uncertainty is translated to uncertainty of the predictions made from the model. We also investigate the role and importance of different parameters, with respect to different model outputs including the predictions, by means of global sensitivity analysis [9]. Figure 2 illustrates the sensitivity of one of the outputs calculated by a method based on the decomposition of the variance [10, 11, 12], showing different types of sensitivity measures. Finally, we explore how the sensitivity of different subsets of parameters change as different parts of the viable space are investigated, which is shown in Figure 3, where sensitivity profiles are clustered into groups with different sensitivity characteristics. Figure 1 Figure 2 Figure 3 Acknowledgements This research was supported by funding from the Swedish e-Science Research Centre and the Human Brain Project References [1] Gutierrez-Arenas O, Eriksson O, Hellgren Kotaleski J (2014) Segregation and Crosstalk of D1 Receptor-Mediated Activation of ERK in Striatal Medium Spiny Neurons upon Acute Administration of Psychostimulants. PLoS Comput Biol 10, e1003445. [2] Nair AG, Gutierrez-Arenas O, Eriksson O, Vincent P, and Hellgren Kotaleski J (2015) Sensing Positive versus Negative Reward Signals through Adenylyl Cyclase-Coupled GPCRs in Direct and Indirect Pathway Striatal Medium Spiny Neurons. J. Neuroscience 35, 14017-14030. [3] Marder E, Goeritz ML, Otopalik AG (2015) Robust circuit rhythms in small circuits arise from variable circuit components and mechanisms. Curr Opin Neurobiol 31, 156-163. [4] Nair AG, Gutierrez-Arenas O, Eriksson O, Jauhiainen A, Blackwell KT and Kotaleski, JH (2014). Modeling intracellular signaling underlying striatal function in health and disease. Progress in molecular biology and translational science, 123, 277 [5] Zamora-Sillero E, Hafner M, Ibig A, Stelling J, and Wagner, A. (2011). Efficient characterization of high-dimensional parameter spaces for systems biology. BMC systems biology 5, 142. [6] Marjoram P, Molitor J, Plagnol V, and Tavare S (2003) Markov chain Monte Carlo without likelihoods. Proc. Natl. Acad. Sci. U.S.A. 100, 15324–15328. [7] Toni T, Welch D, Strelkowa N, Ipsen A, and Stumpf MP. Approximate Bayesian computation scheme for parameter inference and model selection in dynamical systems. J R Soc Interface, 6, 187–202. [8] Liepe J, Kirk P, Filippi S, Toni T, Barnes CP, and Stumpf MP. A framework for parameter estimation and model selection from experimental data in systems biology using approximate Bayesian computation. Nat Protoc, 9, 439–456. [9] Saltelli A, Ratto M, Andres T, Campolongo F, Cariboni J, Gatelli D, Saisana M, Tarantola S Global sensitivity analysis: the primer. In Wiley 2008 New York, NY:Wiley. [10] Sobol IM (2001) Global sensitivity indices for nonlinear mathematical models and their Monte Carlo estimates, Math. Comput. Simul. 55, 271–280. [11] Saltelli A (2002) Making best use of model evaluations to compute sensitivity indices. Comp Phys Comm 145, 280 – 297. [12] Halnes G, Ulfhielm E Ljunggren EE, Kotaleski JH and Rospars JP (2009) Modelling and sensitivity analysis of the reactions involving receptor, G-protein and effector in vertebrate olfactory receptor neurons. Journal of computational neuroscience 27, 471-491. Keywords: sensitivity analysis, Approximate Bayesian Computation, copulas, intracellular signalling, Dynamical Modeling, global sensitivity analysis, Markov chain Monte Carlo, variance decomposition Conference: Neuroinformatics 2016, Reading, United Kingdom, 3 Sep - 4 Sep, 2016. Presentation Type: Investigator presentations Topic: Computational neuroscience Citation: Eriksson O, Jauhiainen A, Maad Sasane S, Nair A, Sartorius C and Hellgren Kotaleski J (2016). Statistical uncertainty and sensitivity analysis of intracellular signaling models - through approximate Bayesian computation and variance based global sensitivity analysis. Front. Neuroinform. Conference Abstract: Neuroinformatics 2016. doi: 10.3389/conf.fninf.2016.20.00014 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 31 May 2016; Published Online: 18 Jul 2016. * Correspondence: PhD. Olivia Eriksson, Contributed equally to this work, Stockholm, Sweden, olivia@kth.se Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Olivia Eriksson Alexandra Jauhiainen Sara Maad Sasane Anu G Nair Carolina Sartorius Jeanette Hellgren Kotaleski Google Olivia Eriksson Alexandra Jauhiainen Sara Maad Sasane Anu G Nair Carolina Sartorius Jeanette Hellgren Kotaleski Google Scholar Olivia Eriksson Alexandra Jauhiainen Sara Maad Sasane Anu G Nair Carolina Sartorius Jeanette Hellgren Kotaleski PubMed Olivia Eriksson Alexandra Jauhiainen Sara Maad Sasane Anu G Nair Carolina Sartorius Jeanette Hellgren Kotaleski Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

BackgroundModelling disease outbreaks often involves integrating the wealth of data that are gathered during modern outbreaks into complex mathematical or computational models of transmission. Incorporating these data into simple compartmental epidemiological models is often challenging, requiring the use of more complex but also more efficient computational models. In this paper we introduce a new framework that allows for a more systematic and user-friendly way of building and running epidemiological models that efficiently handles disease data and reduces much of the boilerplate code that usually associated to these models. We introduce the framework by developing an SIR model on a simple network as an example.ResultsWe develop Broadwick, a modular, object-oriented epidemiological framework that efficiently handles large epidemiological datasets and provides packages for stochastic simulations, parameter inference using Approximate Bayesian Computation (ABC) and Markov Chain Monte Carlo (MCMC) methods. Each algorithm used is fully customisable with sensible defaults that are easily overridden by custom algorithms as required.ConclusionBroadwick is an epidemiological modelling framework developed to increase the productivity of researchers by providing a common framework with which to develop and share complex models. It will appeal to research team leaders as it allows for models to be created prior to a disease outbreak and has the ability to handle large datasets commonly found in epidemiological modelling.

Wastewater production, like many other engineered and environmental processes, is inherent stochastic in nature and requires the use of complex stochastic models, for example, to predict realistic patterns of down-the-drain chemicals or pharmaceuticals and personal care products. Up until now, a formal method of statistical inference has been lacking for many of those models, where explicit likelihood functions were intractable. In this Article, we investigate Approximate Bayesian Computation (ABC) methods to infer important parameters of stochastic environmental models. ABC methods have been recently suggested to perform model-based inference in a Bayesian setting when model likelihoods are analytically or computationally intractable and have not been applied to environmental systems analysis or water quality modeling before. In a case study, we investigate the performance of three different algorithms to infer the number of wastewater pulses contained in three high-resolution data series of benzotriazole and total nitrogen loads in sewers. We find that all algorithms perform well and that the uncertainty in the inferred number of corresponding wastewater pulses varies between 6% and 28%. In our case, the results are more sensitive to substance characteristics than to catchment properties. Although the application of ABC methods requires careful tuning and attention to detail, they have a great general potential to update stochastic model parameters with monitoring data and improve their predictive capabilities.

Markov Chain Monte Carlo (MCMC) algorithms are employed for accurate uncertainty assessments in non-linear geophysical inverse problems. However, one of their main drawbacks is the considerable number of sampled models needed to attain stable posterior estimations, especially in high-dimensional parameter spaces. We use the Discrete Cosine Transform (DCT) to reparametrize a Bayesian Electrical Resistivity Tomography (ERT) inversion solved through an MCMC sampling. In this framework, the unknown parameters become the series of coefficients associated with the retained DCT base functions. We employ the Differential Evolution Markov Chain (DEMC) algorithm that guarantees a more accurate and rapid sampling of the posterior density than more standard MCMC algorithms (such as the random walk Metropolis). To draw essential conclusions about the reliability of the implemented algorithm, we focus on inversions of a synthetic subsurface block model. We assess the benefits provided by the DCT compression of the model space by comparing the outcomes of the implemented inversion approach with those provided by a DEMC algorithm running in the full, un-reduced model space. Although preliminary, our results are promising and prove that the implemented inversion approach guarantees rapid convergence toward the stationary regime, thereby preserving an accurate sampling of the posterior model.

Knowledge of the Earth's interior relies on indirect information collected at or near the surface. Typically, data do not uniquely constrain the subsurface properties and are contaminated by noise, and therefore the solution of ill-posed inverse problems is required. Geophysicists have traditionally addressed such problems through deterministic approaches, seeking a single 'best-fitting' model defined by optimality criteria that reflect our understanding of the problem at hand. In recent decades, Bayesian approaches have become increasingly common, as they characterise the posterior probability distribution of the model conditioned on the observations, thereby quantifying uncertainty.In this context, Markov chain Monte Carlo (MCMC) methods have emerged as a crucial tool as they allow sampling from posterior distributions of arbitrary complexity. At the core of many MCMC algorithms lies the Metropolis-Hastings scheme. This combines a proposal distribution with a probabilistic acceptance criterion to construct a Markov chain that has the desired target distribution as its stationary distribution. The algorithm is versatile as it rests on mild technical conditions on the proposal, and is thus widely adopted across a broad range of geoscientific inference problems. Yet when the parameter space is large or the forward models are computationally expensive---both common scenarios in geophysical applications---it can become inefficient, resulting in poor chain mixing and slow convergence to the target (posterior) distribution. These challenges underscore the importance of effective proposal mechanisms.In this presentation, we introduce a novel approach to designing Metropolis-Hastings proposals based on adaptive transport maps. The framework is inspired by recent developments from the field of Applied Mathematics linking Bayesian inference with Optimal Transport theory. The idea is to find a monotone, nonlinear transformation to recast a (complex) target probability distribution into a (simpler) reference distribution that is more amenable to standard MCMC steps. Our key contribution is to parameterise these transformations using invertible neural networks, ensuring monotonicity while gaining the flexibility and expressiveness that neural architectures afford.The proposed method progresses iteratively. We begin with a standard sampling strategy (e.g., a random-walk Metropolis) to obtain initial draws from the target distribution. These samples inform the training of an invertible neural network that learns to map from the target to a simpler reference distribution, specifically a standard (multivariate) Gaussian. Subsequent proposals are then generated in the reference space, either as global independence moves or local perturbations, and are accepted or rejected following a suitably modified Metropolis-Hastings criterion. As more samples accumulate, the network's parameters are updated, improving overall sampling efficiency. Ultimately, the approach yields not only an ensemble of samples representative of the desired target distribution---just as in standard MCMC---but also a compact, learned representation of it in the network's weights.We illustrate the proposed paradigm both theoretically and through examples. Preliminary results indicate that transport-map-enhanced MCMC has the potential to significantly accelerate Bayesian sampling across a range of applications.

Approximate Bayesian computation (ABC) is used to estimate unknown parameter values, as well as their uncertainties, in Reynolds-averaged Navier–Stokes (RANS) simulations of turbulent flows. The ABC method approximates posterior distributions of model parameters, but does not require the direct computation, or estimation, of a likelihood function. This method thus enables relatively simple and flexible parameter estimation for complex models and a wide range of reference data. This paper describes the ABC approach, including the use of a calibration step, adaptive proposal, and Markov chain Monte Carlo (MCMC) technique to accelerate the parameter estimation, resulting in an ABC approach with improved MCMC, denoted ABC-IMCMC. As a test of the classic ABC rejection algorithm and ABC-IMCMC, parameters are estimated in a nonequilibrium RANS model using reference data from direct numerical simulations of periodically sheared homogeneous turbulence. The use of ABC-IMCMC is then demonstrated to estimate parameters in the Menter shear-stress-transport (SST) model using experimental reference data for an axisymmetric transonic bump. This paper shows that the accuracy of the SST model for this test case can be improved using ABC-IMCMC, indicating that ABC-IMCMC is a promising method for the calibration of RANS models using a wide range of reference data.

Approximate Bayesian Computation (ABC) methods have a lot of success to accomplish Bayesian inference on the parameters of models for which the calculation of the likelihood is intractable. These algorithms consists in comparing the observed dataset to many simulated datasets. These ones can be generated in different ways. Typically, the rejection ABC scheme consists first of simulating parameters using independent calls to the prior distribution and then, given these values, generating the datasets using independent calls to the model. For such a method, the computation time needed to get a suitable approximation of the posterior distribution can be very long. Also, there exist some sequential Monte Carlo methods replacing simulations from the prior by using successive approximations to the posterior distribution. Here, we recall a sequential simulation algorithm and we compare different parallelization strategies. We notably shown that the parallelization of the sequential ABC sampler is useless when using more than four threads per instance of the program and that the standard rejection ABC sampler has to be used when facing a large number of cores. Indeed, in such a case, the cost of the sequential ABC sampler's parallelization prohibits its use.

Approximate Bayesian Computation for infectious disease modelling

Probabilistic logic programming formalisms permit the definition of potentially very complex probability distributions. This complexity can often make learning hard, even when structure is fixed and learning reduces to parameter estimation. In this paper an approximate Bayesian computation (ABC) method is presented which computes approximations to the posterior distribution over PRISM parameters. The key to ABC approaches is that the likelihood function need not be computed, instead a 'distance' between the observed data and synthetic data generated by candidate parameter values is used to drive the learning. This makes ABC highly appropriate for PRISMprograms which can have an intractable likelihood function, but from which synthetic data can be readily generated. The algorithm is experimentally shown to work well on an easy problem but further work is required to produce acceptable results on harder ones.

Approximate Bayesian computation (ABC) constitutes a class of computational methods rooted in Bayesian statistics. In all model-based statistical inference, the likelihood function is of central importance, since it expresses the probability of the observed data under a particular statistical model, and thus quantifies the support data lend to particular values of parameters and to choices among different models. For simple models, an analytical formula for the likelihood function can typically be derived. However, for more complex models, an analytical formula might be elusive or the likelihood function might be computationally very costly to evaluate. ABC methods bypass the evaluation of the likelihood function. In this way, ABC methods widen the realm of models for which statistical inference can be considered. ABC methods are mathematically well-founded, but they inevitably make assumptions and approximations whose impact needs to be carefully assessed. Furthermore, the wider application domain of ABC exacerbates the challenges of parameter estimation and model selection. ABC has rapidly gained popularity over the last years and in particular for the analysis of complex problems arising in biological sciences (e.g., in population genetics, ecology, epidemiology, and systems biology).

In this paper, we present an approach for evolutionary learning of motif in biopolymer sequences. The focuses in this paper is evolutionary inference of Gaussian model, Differential Evolution for optimization and Markov chain Monte Carlo(MCMC) for sampling are applied in the probability learning of Gaussian model. The framework involves calculations of corresponding weight, mean and covariance. To obtain satisfied effect of MCMC sampling, the fitness function is discussed for MCMC ratio. Comparisons between results of Differential Evolution and Differential Evolution MCMC are provided to show novel effect of our method on synthetic dataset and real world dataset.

Understanding the processes by which new diseases are introduced in previously healthy areas is of major interest in elaborating prevention and management policies, as well as in understanding the dynamics of pathogen diversity at large spatial scale. In this study, we aimed to decipher the dispersal processes that have led to the emergence of the plant pathogenic fungus Microcyclus ulei, which is responsible for the South American Leaf Blight (SALB). This fungus has devastated rubber tree plantations across Latin America since the beginning of the twentieth century. As only imprecise historical information is available, the study of population evolutionary history based on population genetics appeared most appropriate. The distribution of genetic diversity in a continental sampling of four countries (Brazil, Ecuador, Guatemala and French Guiana) was studied using a set of 16 microsatellite markers developed specifically for this purpose. A very strong genetic structure was found (F(st)=0.70), demonstrating that there has been no regular gene flow between Latin American M. ulei populations. Strong bottlenecks probably occurred at the foundation of each population. The most likely scenario of colonization identified by the Approximate Bayesian Computation (ABC) method implemented in DIYABC suggested two independent sources from the Amazonian endemic area. The Brazilian, Ecuadorian and Guatemalan populations might stem from serial introductions through human-mediated movement of infected plant material from an unsampled source population, whereas the French Guiana population seems to have arisen from an independent colonization event through spore dispersal.