Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.08.27.671290

On the utility of Deep Learning for model classification and parameter estimation on complex diversification scenarios.

Abstract

Birth-Death models applied to dated phylogenies are a useful tool to study past diversification dynamics. Parameters in these stochastic models are typically inferred using likelihood-based methods such as Maximum Likelihood Estimation (MLE) or Bayesian Inference. However, these approaches exhibit computational tractability issues in the case of models of moderate to high complexity. One approach to increase model complexity while remaining computationally tractable in the context of birth-death modelling is machine learning. So far, these techniques have been explored in the context of serially-sampled phylogenies (phylodynamics) and trait-dependent birth-death models. Here, we explored the power of Convolutional Neural Networks (CNNs), a type of Deep Learning (DL) method, to solve classification and regression (parameter estimation) tasks under constant-rate and time-homogeneous, rate-variable birth-death models. In particular, we compared six diversification scenarios: Constant Birth-Death, High-Extinction, Mass-Extinction, Diversity-Dependent, Stasis-and-Radiate, and Waxing-and-Waning. We simulated 10, 000 phylogenetic trees under each diversification scenario, which were encoded using a vectorization procedure that captures the topology and branch length information. The encoded trees were used to train or test a set of CNNs models that were designed to tailor three empirical case studies differing in the number of tips. We compared CNNs performance with MLE inference. Our results show that CNNs exhibited classification accuracy levels of 93-78%, whereas maximum likelihood estimation achieved levels of 74-70%. The most difficult scenarios to predict for the CNNs were the high-extinction and mass-extinction scenarios, which were often misidentified as one another. For the regression tasks, mean average errors were comparable between CNNs models and MLE inference, and they also coincided in their difficulty estimating ratio parameters such as mass extinction survival and turnover. Finally, we applied our CNNs to three empirical studies (eucalypts, conifers and cetaceans) and discussed potential shortcomings and future avenues for improvement in the application of deep-learning birth-death modelling approaches.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

de la Pena, P. G., Iglesias, G., Talavera, E., Meseguer, A. S., Sanmartin, I.. 2025-08-27. On the utility of Deep Learning for model classification and parameter estimation on complex diversification scenarios.. https://doi.org/10.1101/2025.08.27.671290

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Geometry of antigenic evolution improves influenza vaccine selection

Anticipating antigenic evolution is essential for selecting effective seasonal influenza A/H3N2 vaccine strains. To this end, we integrated hemagglutination-inhibition and neutralization titers spanning 2002 to 2025 into a unified Bayesian antigenic map. The map resolves twelve antigenic clusters advancing in discrete steps, with several clusters co-circulating in most seasons. In 15 of 21 seasons, the WHO-recommended vaccine belonged to an earlier cluster than the dominant circulating cluster. The direction of each vaccine update relative to recent viral drift predicted vaccine effectiveness one season ahead in out-of-sample forecasts. Antigenic distance, the conventional measure of vaccine-virus match, was weakly associated with effectiveness until update direction was accounted for. Retrospectively ranking candidate strains by predicted effectiveness would have selected a strain predicted to outperform the WHO recommendation in every season, raising mean predicted effectiveness by 10 percentage points.

evolutionary biology↗

Evolutionary replay of duplicate-gene retention across independent whole-genome duplications

Whole-genome duplications repeatedly expose ancestral gene lineages to the same broad evolutionary outcome-retention or loss of duplicated copies-but it remains unclear whether this history replays similarly across evolutionary scales. We placed duplicate retention in shared hierarchical orthologous-group coordinates and compared percentile ranks defined within each event-wide mapped universe. Three independent angiosperm whole-genome duplications showed reproducible replay (global rank effect T-replay = 0.210, bootstrap 95% confidence interval 0.172-0.248; permutation P = 1/100,001). A plant reference-panel score specified before target outcomes were examined predicted retention after the Apple/Pear duplication ({rho} = 0.169, n = 373). Deep transfer was heterogeneous: the teleost-genome-duplication estimate was positive but unresolved ({rho} = 0.107, n = 151, 95% confidence interval -0.050 to 0.260), whereas transfer to the ancient budding-yeast whole-genome duplication (yeast WGD) was supported ({rho} = 0.280, n = 186). Independently reconstructed animal outcomes also replayed between teleost and Stylommatophora duplications (r = 0.226, n = 146, P = 0.00326), although the effect remained below a prespecified strong-effect threshold. A strict plant-animal comparison was limited to 25 deeply one-to-one lineages and was unresolved (r = 0.033, 95% confidence interval -0.303 to 0.340). Thus, ancestral gene-lineage identity contributes reproducibly to duplicate retention after independent whole-genome duplications, but replay is structured by evolutionary lineage and modified by event-specific history rather than governed by one universal gene-fate ranking.

evolutionary biology↗

A Hymenoptera-restricted gene mediating ant castes co-opts deeply conserved machinery to control organ size

Lineage-specific genes are widespread and have been implicated as phenotypic innovation inducers, but how they acquire complex developmental functions remains poorly understood. Ant queens and workers develop dramatically different organ sizes from identical genomes under juvenile hormone (JH) control, yet the molecular effectors translating JH signalling into caste-specific organ growth remain unknown. Here we identify torch, a Hymenoptera-restricted gene, as the most consistently gyne-biased and JH-responsive gene across 68 ant species. Knockdown of torch in virgin queens of Monomorium pharaonis produces a worker-like, multi-organ growth-restricted phenotype. Mechanistically, torch harbours an E-box-like motif activated by the JH receptor Gce-Tai and acts as a GA-repeat-binding transcription factor that regulates Hippo signalling, the deeply conserved organ-size control pathway in animals. Expressing torch heterologously in mice and a growth-restricted Drosophila background shows that the gene retained its general growth-promoting activity across more than 700 million years of animal evolution in lineages that lack the gene, establishing that its function is mediated through conserved rather than ant-specific machinery. A lineage-specific gene can therefore acquire complex morphogenetic function by co-opting ancient organ-size circuitry, providing a general route by which novel genes can drive phenotypic innovation.

evolutionary biology↗