Evidence map›Paper›PMID 42455870›Full record

ArticlePLoS computational biology2026

Popformer: Learning general signatures of positive selection with a self-supervised transformer.

Leon Zong, Sorelle A Friedler, Sara Mathieson

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Leon ZongDepartment of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0009-0000-3334-2742
Sorelle A FriedlerDepartment of Computer Science, Haverford College, Haverford, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0001-6023-1597
Sara MathiesonDepartment of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-0484-0838

Funding

Adaptive evolutionary inference frameworks for understudied populations using generative neural networksR15HG011528 · NHGRI · HAVERFORD COLLEGE · PI MATHIESON, SARA · 2021 to 2024
$783k
NHGRI NIH HHS R15 HG011528
6 · The paper itself

Abstract

Understanding natural selection can help shed light on the genetics underpinning adaptive evolution. The widespread availability of large-scale human genetic variation data has led to the development of data-driven methods for detecting signatures of selection, many of which are based on deep learning. However, these methods often fail to generalize well to the diversity of selection signatures across a broad range of evolutionary scenarios. We propose a novel transformer-based model, Popformer, for learning encodings of general patterns of genetic variation. Popformer includes site-wise and haplotype-wise attention, allowing us to capture variation among both genetic positions and individuals. It additionally learns relative positional embeddings for inter-SNP distances. The model is pre-trained with an analog of the masked language modeling objective across a range of real human genomic data, similar to the task of genetic imputation. Using dimensionality reduction, we show that the pre-trained model learns meaningful embeddings of genomic windows that correspond with population structure. We also show that the model can accurately perform genotype imputation. We further fine-tune the model on selection classification and demonstrate that our model is more accurate than other selection classification methods, on selection simulations of both well-specified and mis-specified demographic models. Using a novel real data validation approach, we apply Popformer to human data from the 1000 Genomes Project and reveal its ability to generalize from simulated data to the diversity of real data. Overall, our method provides a new direction for population genetic inference methods, with future fine-tuning applications including the inference of recombination rates, introgression, and local ancestry.

Indexed as

Models, GeneticSelection, GeneticSupervised Machine LearningAlgorithmsComputational BiologyGenetics, PopulationGenetic VariationGenome, HumanGenotypeHaplotypesHumansPolymorphism, Single Nucleotide

Identifiers

PMID42455870
PMCPMC13395434

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.