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1.
Mol Biol Evol ; 37(6): 1832-1842, 2020 06 01.
Artigo em Inglês | MEDLINE | ID: mdl-32101295

RESUMO

Reconstructing pathogen dynamics from genetic data as they become available during an outbreak or epidemic represents an important statistical scenario in which observations arrive sequentially in time and one is interested in performing inference in an "online" fashion. Widely used Bayesian phylogenetic inference packages are not set up for this purpose, generally requiring one to recompute trees and evolutionary model parameters de novo when new data arrive. To accommodate increasing data flow in a Bayesian phylogenetic framework, we introduce a methodology to efficiently update the posterior distribution with newly available genetic data. Our procedure is implemented in the BEAST 1.10 software package, and relies on a distance-based measure to insert new taxa into the current estimate of the phylogeny and imputes plausible values for new model parameters to accommodate growing dimensionality. This augmentation creates informed starting values and re-uses optimally tuned transition kernels for posterior exploration of growing data sets, reducing the time necessary to converge to target posterior distributions. We apply our framework to data from the recent West African Ebola virus epidemic and demonstrate a considerable reduction in time required to obtain posterior estimates at different time points of the outbreak. Beyond epidemic monitoring, this framework easily finds other applications within the phylogenetics community, where changes in the data-in terms of alignment changes, sequence addition or removal-present common scenarios that can benefit from online inference.


Assuntos
Técnicas Genéticas , Filogenia , Software , África Ocidental/epidemiologia , Teorema de Bayes , Doença pelo Vírus Ebola/epidemiologia
2.
Entropy (Basel) ; 23(5)2021 May 13.
Artigo em Inglês | MEDLINE | ID: mdl-34068364

RESUMO

When humans infer underlying probabilities from stochastic observations, they exhibit biases and variability that cannot be explained on the basis of sound, Bayesian manipulations of probability. This is especially salient when beliefs are updated as a function of sequential observations. We introduce a theoretical framework in which biases and variability emerge from a trade-off between Bayesian inference and the cognitive cost of carrying out probabilistic computations. We consider two forms of the cost: a precision cost and an unpredictability cost; these penalize beliefs that are less entropic and less deterministic, respectively. We apply our framework to the case of a Bernoulli variable: the bias of a coin is inferred from a sequence of coin flips. Theoretical predictions are qualitatively different depending on the form of the cost. A precision cost induces overestimation of small probabilities, on average, and a limited memory of past observations, and, consequently, a fluctuating bias. An unpredictability cost induces underestimation of small probabilities and a fixed bias that remains appreciable even for nearly unbiased observations. The case of a fair (equiprobable) coin, however, is singular, with non-trivial and slow fluctuations in the inferred bias. The proposed framework of costly Bayesian inference illustrates the richness of a 'resource-rational' (or 'bounded-rational') picture of seemingly irrational human cognition.

3.
Philos Trans R Soc Lond B Biol Sci ; 377(1861): 20210242, 2022 10 10.
Artigo em Inglês | MEDLINE | ID: mdl-35989603

RESUMO

Recent advances in Bayesian phylogenetics offer substantial computational savings to accommodate increased genomic sampling that challenges traditional inference methods. In this review, we begin with a brief summary of the Bayesian phylogenetic framework, and then conceptualize a variety of methods to improve posterior approximations via Markov chain Monte Carlo (MCMC) sampling. Specifically, we discuss methods to improve the speed of likelihood calculations, reduce MCMC burn-in, and generate better MCMC proposals. We apply several of these techniques to study the evolution of HIV virulence along a 1536-tip phylogeny and estimate the internal node heights of a 1000-tip SARS-CoV-2 phylogenetic tree in order to illustrate the speed-up of such analyses using current state-of-the-art approaches. We conclude our review with a discussion of promising alternatives to MCMC that approximate the phylogenetic posterior. This article is part of a discussion meeting issue 'Genomic population structures of microbial pathogens'.


Assuntos
COVID-19 , Software , Algoritmos , Teorema de Bayes , Humanos , Cadeias de Markov , Método de Monte Carlo , Filogenia , SARS-CoV-2/genética
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