Search bioRxiv⌕ Search

bioRxiv · 10.1101/2022.03.28.484797

Hyperbolic Geometry-Based Deep Learning Methods to Produce Population Trees from Genotype Data

Abstract

The production of population-level trees using the genomic data of individuals is a fundamental task in the field of population genetics. Typically, these trees are produced using methods like hierarchical clustering, neighbor joining, or maximum likelihood. However, such methods are non-parametric: they require all data to be present at the time of tree formation, and the addition of new data points necessitates the regeneration of the entire tree, a potentially expensive process. They also do not easily integrate with larger workflows. In this study, we aim to address these problems by introducing parametric deep learning methods for tree formation from genotype data. Our models specifically create continuous representations of population trees in hyperbolic space, which has previously proven highly effective in embedding hierarchically structured data. We present two different architectures - a multi-layer perceptron (MLP) and a variational autoencoder (VAE) - and we analyze their performance using a variety of metrics along with comparisons to established tree-building methods. Both models tested produce embedding spaces that reflect human evolutionary history. In addition, we demonstrate the generalizability of these models by verifying that addition of new samples to an existing tree occurs in a semantically meaningful manner. Finally, we use Dasguptas Cost to compare the quality of trees generated by our models to those produced by established methods. Despite the fact that the benchmark methods are directly fit on the evaluation data, our models are able to outperform some of these and achieve highly comparable performance overall. Author summaryTree production is a vital task in population genetics, but current approaches fall prey to several common shortfalls. Most notably, they lack the ability to add new data points after tree generation, and they are often difficult to use in larger pipelines. By leveraging cutting-edge advances pairing deep learning with hyperbolic geometry, we develop multiple models designed to rectify these issues. Through experiments on a dataset of humans from globally widespread ancestries, we demonstrate the generalizability of our models to new data, and we also show strong empirical performance with respect to currently used methods. In addition, we show that the data representations produced by our models are semantically meaningful and reflect known facts about human evolutionary history. Finally, we discuss the additional benefits our models could provide, including improved visualization, greater privacy preservation, and improved integration with downstream machine learning tasks. In conclusion, we present models that are accurate, flexible, and generalizable, with the potential to facilitate a variety of further applications.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Patel, A., Mas Montserrat, D., Bustamante, C., Ioannidis, A. G.. 2022-03-29. Hyperbolic Geometry-Based Deep Learning Methods to Produce Population Trees from Genotype Data. https://doi.org/10.1101/2022.03.28.484797

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↗