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Estimating population parameters using the structured serial coalescent with Bayesian MCMC inference when some demes
1Allan Wilson Centre for Molecular Ecology and Evolution, Auckland, New Zealand.
Accurate population size inference is possible even with unsampled "ghost demes" if the correct model is used. Including ghost deme sequences at the last sampling time reduces bias and improves parameter estimation, especially with low migration rates.
Area of Science:
- Population genetics
- Computational biology
- Epidemiology
Background:
- Estimating population size is crucial in evolutionary and epidemiological studies.
- Unsampled or
- ghost
- demes
- can complicate accurate demographic inference.
- Previous models often assume complete sampling, which is unrealistic.
Purpose of the Study:
- To investigate the impact of unsampled demes on population size estimation.
- To assess the feasibility of accurate inference when using incorrect models.
- To extend these findings to scenarios with partial sampling of ghost demes at the final time point.
Main Methods:
- Structured serial coalescent simulations.
- Bayesian Markov Chain Monte Carlo (MCMC) methods.
- Analysis of simulated population genetic data with varying sampling schemes.
Main Results:
- Accurate population size and demographic parameter inference is achievable with ghost demes if the correct model is employed.
- Using an incorrect model leads to biased and misleading estimates.
- Including sequences from ghost demes at the last sampling time significantly reduces estimation bias.
- Accurate estimation of ghost deme parameters becomes possible with this extended sampling strategy.
- Migration rate estimates are reliable when migration values are low, even with ghost demes.
Conclusions:
- The structured serial coalescent model provides robust inference even with unobserved population structure.
- Careful model selection is critical to avoid biased demographic estimates.
- Partial sampling of previously unsampled demes at later time points can salvage accurate inference in complex scenarios, relevant to fields like HIV evolution.
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