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Published on: August 14, 2018
Scaling up Bayesian population phylogenomics through virtual dimension reduction
Tomáš Flouri1, Xiyun Jiao2, Jun Huang3
1Department of Genetics, Evolution, and Environment, University College London, Gower Street, London, UK. t.flouris@ucl.ac.uk.
Population phylogenomics infers genetic history using Bayesian methods. A new parallel computation method, Virtual Dimension Reduction allowing Parallelisation (VDRoP), significantly speeds up analyses and improves accuracy for complex genomic datasets.
Area of Science:
- Population phylogenomics
- Computational biology
- Evolutionary genetics
Background:
- Population phylogenomics jointly infers population genetic processes and phylogenetic trees.
- Bayesian inference under the multispecies coalescent (MSC) model using Markov chain Monte Carlo (MCMC) is the standard approach.
- MCMC methods face challenges with high-dimensional state spaces and lack of parallelization.
Purpose of the Study:
- To develop a novel computational method addressing MCMC limitations in population phylogenomics.
- To improve the efficiency and scalability of phylogenetic and population genetic inference.
Main Methods:
- Development of Virtual Dimension Reduction allowing Parallelisation (VDRoP).
- VDRoP achieves efficient MCMC mixing through analytical parameter integration without restricting priors.
- Implementation within the Bayesian Program for Phylogenetics (BPP) software.
Main Results:
- VDRoP significantly reduces MCMC run-times (3-8 fold) on empirical genomic datasets.
- The method demonstrates substantial improvements in mixing efficiency (up to 50 fold).
- Successful application to diverse datasets including Adansonia, Anopheles, and Heliconius.
Conclusions:
- VDRoP offers a computationally efficient and parallelizable alternative to standard MCMC for population phylogenomics.
- The method enhances the feasibility of analyzing large-scale genomic data for evolutionary inference.
- This advancement facilitates more robust reconstruction of species divergence and demographic histories.
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