ArticleGenetics2026
Genetic prediction with ARG-powered linear algebra.
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.
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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.
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Who cites it
1 citing paper in PubMed.
- Tracing the evolutionary histories of ultra-rare variants using variational dating of large ancestral recombination graphs.bioRxiv : the preprint server for biology · 2026Article
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5 authors.
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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.
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