Evidence map›Paper›PMID 40321940›Full record

ArticleArXiv2025

Inferring genotype-phenotype maps using attention models.

Krishna Rijal, Caroline M Holmes, Samantha Petti, Gautam Reddy, Michael M Desai, Pankaj Mehta

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In one paragraph

Article in ArXiv, 2025. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Krishna RijalDepartment of Physics, Boston University, Boston, MA.
Caroline M HolmesDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA.
Samantha PettiDepartment of Mathematics, Tufts University, Medford, MA.
Gautam ReddyDepartment of Physics, Princeton University, Princeton, NJ.
Michael M DesaiDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA.
Pankaj MehtaDepartment of Physics, Boston University, Boston, MA.

Funding

Microbial Adaptation and the Statistics of Epistasis and PleiotropyR01GM104239 · NIGMS · HARVARD UNIVERSITY · PI DESAI, MICHAEL M · 2013 to 2025
$4.5M
MODELING EMERGENT BEHAVIORS IN SYSTEMS BIOLOGY: A BIOLOGICAL PHYSICS APPROACHR35GM119461 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Pankaj Mehta · 2016 to 2026
$3.6M
NIGMS NIH HHS R01 GM104239NIGMS NIH HHS R35 GM119461
6 · The paper itself

Abstract

Predicting phenotype from genotype is a central challenge in genetics. Traditional approaches in quantitative genetics typically analyze this problem using methods based on linear regression. These methods generally assume that the genetic architecture of complex traits can be parameterized in terms of an additive model, where the effects of loci are independent, plus (in some cases) pairwise epistatic interactions between loci. However, these models struggle to analyze more complex patterns of epistasis or subtle gene-environment interactions. Recent advances in machine learning, particularly attention-based models, offer a promising alternative. Initially developed for natural language processing, attention-based models excel at capturing context-dependent interactions and have shown exceptional performance in predicting protein structure and function. Here, we apply attention-based models to quantitative genetics. We analyze the performance of this attention-based approach in predicting phenotype from genotype using simulated data across a range of models with increasing epistatic complexity, and using experimental data from a recent quantitative trait locus mapping study in budding yeast. We find that our model demonstrates superior out-of-sample predictions in epistatic regimes compared to standard methods. We also explore a more general multi-environment attention-based model to jointly analyze genotype-phenotype maps across multiple environments and show that such architectures can be used for "transfer learning" - predicting phenotypes in novel environments with limited training data.

Identifiers

PMID40321940
PMCPMC12047939

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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.