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Model fitting and inference under Latent Equilibrium Processes.

Sourabh Bhattacharya1, Alan E Gelfand, Kent E Holsinger

  • 1S. Bhattacharya is a post-doctoral researcher in Department of Probability and Statistics, University of Sheffield, S3 7RH, UK, A. E. Gelfand is a professor in Institute of Statistics and Decision Sciences, Box 90251, Duke University, Durham, NC 27708-0251, K. E. Holsinger is a professor in the Department of Ecology and Evolutionary Biology at the University of Connecticut, Storrs, CT, 06269-3043.

Statistics and Computing
|October 7, 2008
PubMed
Summary
This summary is machine-generated.

This study introduces a new Bayesian methodology for fitting latent equilibrium process (LEP) models. It enables Markov chain Monte Carlo (MCMC) inference for complex population genetics models where equilibrium distributions are unknown.

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Area of Science:

  • Statistics
  • Computational Biology
  • Population Genetics

Background:

  • Bayesian models with latent stationary stochastic processes are common in population genetics.
  • The equilibrium distribution of these processes is often intractable, posing challenges for model fitting.
  • Latent Equilibrium Process (LEP) models are used when data is observed at equilibrium.

Purpose of the Study:

  • To develop a methodology for model fitting and inference in Bayesian Latent Equilibrium Process (LEP) models.
  • To provide a practical implementation of Markov chain Monte Carlo (MCMC) for LEP models.
  • To address the computational challenges associated with fitting these complex models.

Main Methods:

  • Development of a novel methodology for implementing Markov chain Monte Carlo (MCMC) for Latent Equilibrium Process (LEP) models.
  • Application of the methodology to Bayesian inference problems in population genetics.
  • Demonstration using both simulated and real population genetics data sets.

Main Results:

  • Successfully implemented MCMC for Bayesian inference in LEP models, overcoming previous implementation difficulties.
  • The methodology is demonstrated to be effective for problems in population genetics, including parameter estimation (mutation rates, migration rates, population sizes).
  • Computational intensity was noted, leading to a discussion on parallel implementation strategies.

Conclusions:

  • The proposed methodology provides a viable approach for fitting and performing Bayesian inference on Latent Equilibrium Process (LEP) models.
  • This work facilitates the analysis of complex population genetics data where underlying allele frequencies are unobserved.
  • The study highlights the computational demands and suggests parallel computing as a solution for intensive model fitting.