arXiv subjects

Jiansi Gao

Publications and source records attributed to Jiansi Gao.

4 recordsLinked to original sources

arXiv2026

An adaptive time-tree transition kernel for Bayesian phylogenetic inference

Bayesian phylogenetic and phylodynamic analyses can be very time-consuming, owing to the combination of complex models that are used to estimate key parameters from increasingly large genomic data sets and their associated metadata. The use of high-performance computer hardware can -- to a certain extent -- alleviate the computational burden and markedly decrease the time to results. Still, even converging to the posterior can be a lengthy endeavour, with the burn-in aspect of such analyses potentially taking days or even weeks for large data sets. One of the key aspects that hampers performance in Bayesian phylogenetic inference is the efficiency with which tree topology proposals explore tree space. We here propose a novel adaptive tree transition kernel, which we call `subTreeLeap' (STL), which involves modifying the phylogeny by walking along patristic distance paths in the tree according to an adaptable radius parameter. STL is a general proposal, which can be used with contemporaneous or time-calibrated sequence data, being particularly suited to the latter due to respecting temporal precedence constraints. We carefully assess its impact on convergence and statistical mixing of the exploration of posterior tree space, by comparison to replicate ``golden runs'' obtained from lengthy analyses of empirical data under standard tree transition kernels. We find that STL successfully explores the same posterior tree space as standard kernels, but often does so in a more efficient manner. We discuss limitations as well as future potential improvements to STL that could substantially increase the speed at which Bayesian phylogenetic inferences are obtained.

q-bio.PE↗

arXiv2025

Assessing the Validity of the Fixed Tree Topology Assumption in Phylodynamic Inference

Fixed tree topologies are widely used in phylodynamic analyses to reduce computational burden, yet the consequences of this assumption remain insufficiently understood. Here, we systematically assess the impact of various fixed-topology strategies on phylogenetic and phylodynamic parameter estimates across a diverse set of viral datasets. We compare fully Bayesian joint inference with fixed-topology strategies, including conditioning on maximum likelihood trees subsequently dated with LSD or TreeTime. Our analyses show that global parameters of the substitution and site models are largely robust to the fixed-topology assumption, whereas parameters that depend on the temporal structure of the tree, such as molecular clock rates, node ages, and demographic histories, can exhibit substantial biases. We do treat unconstrained Bayesian analyses as the reference, although we recognize that these too are model-based approximations. Nevertheless, our results highlight serious discordance associated with fixing the topology and underscore the need for faster, time-aware methods that simultaneously integrate topology and parameter estimation. These findings raise important questions about the balance between computational efficiency and inferential accuracy in phylodynamic studies.

q-bio.PE↗

arXiv2025

PhyloVAE: Unsupervised Learning of Phylogenetic Trees via Variational Autoencoders

Learning informative representations of phylogenetic tree structures is essential for analyzing evolutionary relationships. Classical distance-based methods have been widely used to project phylogenetic trees into Euclidean space, but they are often sensitive to the choice of distance metric and may lack sufficient resolution. In this paper, we introduce phylogenetic variational autoencoders (PhyloVAEs), an unsupervised learning framework designed for representation learning and generative modeling of tree topologies. Leveraging an efficient encoding mechanism inspired by autoregressive tree topology generation, we develop a deep latent-variable generative model that facilitates fast, parallelized topology generation. PhyloVAE combines this generative model with a collaborative inference model based on learnable topological features, allowing for high-resolution representations of phylogenetic tree samples. Extensive experiments demonstrate PhyloVAE's robust representation learning capabilities and fast generation of phylogenetic tree topologies.

stat.ML↗

arXiv2024

On the importance of assessing topological convergence in Bayesian phylogenetic inference

Modern phylogenetics research is often performed within a Bayesian framework, using sampling algorithms such as Markov chain Monte Carlo (MCMC) to approximate the posterior distribution. These algorithms require careful evaluation of the quality of the generated samples. Within the field of phylogenetics, one frequently adopted diagnostic approach is to evaluate the effective sample size (ESS) and to investigate trace graphs of the sampled parameters. A major limitation of these approaches is that they are developed for continuous parameters and therefore incompatible with a crucial parameter in these inferences: the tree topology. Several recent advancements have aimed at extending these diagnostics to topological space. In this reflection paper, we present two case studies - one on Ebola virus and one on HIV - illustrating how these topological diagnostics can contain information not found in standard diagnostics, and how decisions regarding which of these diagnostics to compute can impact inferences regarding MCMC convergence and mixing. Our results show the importance of running multiple replicate analyses and of carefully assessing topological convergence using the output of these replicate analyses. To this end, we illustrate different ways of assessing and visualizing the topological convergence of these replicates. Given the major importance of detecting convergence and mixing issues in Bayesian phylogenetic analyses, the lack of a unified approach to this problem warrants further action, especially now that additional tools are becoming available to researchers.

q-bio.PE↗