Evidence map›Paper›PMID 41904656›Full record

ArticleGenetics2026

Genetic prediction with ARG-powered linear algebra.

Hanbin Lee, Nathaniel S Pope, Jerome Kelleher, Gregor Gorjanc, Peter L Ralph

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hanbin LeeDepartment of Statistics, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0002-4545-0027
Nathaniel S PopeInstitute of Ecology & Evolution, University of Oregon, Eugene, OR 97405, United States.ORCID 0000-0001-8409-7812
Jerome KelleherBig Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford OX3 7LF, United Kingdom.ORCID 0000-0002-7894-5253
Gregor GorjancThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.ORCID 0000-0001-8008-2787
Peter L RalphInstitute of Ecology & Evolution, University of Oregon, Eugene, OR 97405, United States.ORCID 0000-0002-9459-6866

Funding

Scaling up computational genomics with tree sequencesR01HG012473 · NHGRI · UNIVERSITY OF OREGON · PI PETER Lochhead RALPH · 2023 to 2026
$2.3M
Ann Arbor through the Departmental FellowshipBBSRC BB/T014067/1ISP BBS/E/D/30002275ISP BBS/E/RL/230001AISP BBS/E/RL/230001CNHGRI NIH HHS HG012473NHGRI NIH HHS R01 HG012473NIHNRC 346741University of Michigan
6 · The paper itself

Abstract

Ancestral recombination graphs (ARGs) are an attractive means for quantitative genetic analysis of complex traits because they encode the realized genetic relatedness between a sample of individuals in the presence of genetic drift, recombination, and mutation. Data structures for efficiently storing ARGs can also be used to rapidly process millions of genomes, and are thus promising for fitting linear mixed models to large phenotype and genome datasets. Here, we study the problems of variance component estimation and prediction of genetic values with ARGs, by describing a generative model of complex traits with additive effects on an ARG, and then developing algorithms that use the ARG to solve these problems efficiently on biobank-scale datasets. We observe nearly linear scaling of runtime with sample size, which is achieved by using the succinct tree sequence representation of the ARG for implicit matrix-vector products, along with modern randomized linear algebra algorithms. We estimate variance components using restricted maximum likelihood, which we find performs substantially better than the Haseman-Elston method. In simulation tests, both variance component estimation and prediction of genetic values (using the best linear unbiased predictor) perform nearly as well with inferred ARGs as with true ARGs. We also discuss interpretations of the variance component estimates as mutational variance and additive genetic variance. We provide an implementation of the algorithms as a Python package tslmm, which leverages the tree sequence library tskit.

Indexed as

AlgorithmsModels, GeneticRecombination, GeneticHumansLinear ModelsPrediction Algorithmsancestral recombination graphgenetic predictiongenomic predictionlinear mixed modelpolygenic score

Identifiers

PMID41904656
PMCPMC13147536

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.