Evidence map›Paper›PMID 40777390›Full record

ArticlebioRxiv : the preprint server for biology2025

Fast variance component analysis using large-scale ancestral recombination graphs.

Jiazheng Zhu, Georgios Kalantzis, Ali Pazokitoroudi, Árni Freyr Gunnarsson, Hrushikesh Loya, Han Chen, Sriram Sankararaman, Pier Francesco Palamara

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In one paragraph

Article in bioRxiv : the preprint server for biology, 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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Georgios KalantzisORCID 0000-0002-0729-1125
Ali Pazokitoroudi
Árni Freyr Gunnarsson
Hrushikesh Loya
Han Chen
Sriram Sankararaman
Pier Francesco PalamaraORCID 0000-0002-7999-1972

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent algorithmic advancements have enabled the inference of genome-wide ancestral recombination graphs (ARGs) from genomic data in large cohorts. These inferred ARGs provide a detailed representation of genealogical relatedness along the genome and have been shown to complement genotype imputation in complex trait analyses by capturing the effects of unobserved genomic variants. An inferred ARG can be used to construct a genetic relatedness matrix, which can be leveraged within a linear mixed model for the analysis of complex traits. However, these analyses are computationally infeasible for large datasets. We introduce a computationally efficient approach, called ARG-RHE, to estimate narrow-sense heritability and perform region-based association testing using an ARG. ARG-RHE leverages a method for computing genotype-matrix products from genealogical data in sublinear time, along with scalable randomized algorithms. This enables fast estimation of variance components and their statistical significance, supports parallel analysis of multiple quantitative traits, and facilitates other linear mixed-model analyses. We conduct extensive simulations to verify the computational efficiency, statistical power, and robustness of this approach. We then apply it to detect associations between 21,159 genes and 52 blood-related traits, using an ARG inferred from genotype data of 337,464 individuals from the UK Biobank. In these analyses, combining ARG-based and imputation-based testing yields 8% more gene-trait associations than using imputation alone, suggesting that inferred genome-wide genealogies may effectively complement genotype imputation in the analysis of complex traits.

Identifiers

PMID40777390
PMCPMC12330685

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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.