Evidence map›Paper›PMID 40093116›Full record

ArticlebioRxiv : the preprint server for biology2025

On ARGs, pedigrees, and genetic relatedness matrices.

Brieuc Lehmann, Hanbin Lee, Luke Anderson-Trocmé, Jerome Kelleher, Gregor Gorjanc, Peter L Ralph

Abstract readPreprint
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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0cells of the map it votes in
0citing papers in PubMed
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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

Who cites it

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.

Brieuc LehmannDepartment of Statistical Science, University College London, WC1E 7HB, UK.ORCID 0000-0002-7302-4391
Hanbin LeeDepartment of Statistics, University of Michigan, Ann Arbor MI 48109, USA.ORCID 0000-0002-4545-0027
Luke Anderson-TrocméDepartment of Human Genetics, University of Chicago, Chicago IL 60637, USA.
Jerome KelleherBig Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, OX3 7LF, UK.
Gregor GorjancThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, UK.ORCID 0000-0001-8008-2787
Peter L RalphInstitute of Ecology and Evolution, University of Oregon, Eugene OR 97402, USA.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
Theory, Methods, and Resources for Understanding and Leveraging Spatial Variation in Population Genetic DataR35GM149521 · NIGMS · UNIVERSITY OF CHICAGO · PI John Novembre · 2023 to 2026
$1.7M
NHGRI NIH HHS R01 HG012473NIGMS NIH HHS R35 GM149521
6 · The paper itself

Abstract

Genetic relatedness is a central concept in genetics, underpinning studies of population and quantitative genetics in human, animal, and plant settings. It is typically stored as a genetic relatedness matrix (GRM), whose elements are pairwise relatedness values between individuals. This relatedness has been defined in various contexts based on pedigree, genotype, phylogeny, coalescent times, and, recently, ancestral recombination graph (ARG). ARG-based GRMs have been found to better capture the structure of a population and improve association studies relative to the genotype GRM. However, calculating GRMs and further operations with them is fundamentally challenging due to inherent quadratic time and space complexity. Here, we first discuss the different definitions of relatedness in a unifying context, making use of the additive model of a quantitative trait to provide a definition of "branch relatedness" and the corresponding "branch GRM". We explore the relationship between branch relatedness and pedigree relatedness through a case study of French-Canadian individuals that have a known pedigree. Through the tree sequence encoding of an ARG, we then derive an efficient algorithm for computing products between the branch GRM and a general vector, without explicitly forming the branch GRM. This algorithm leverages the sparse encoding of genomes with the tree sequence and hence enables large-scale computations with the branch GRM. We demonstrate the power of this algorithm by developing a randomized principal components algorithm for tree sequences that easily scales to millions of genomes. All algorithms are implemented in the open source tskit Python package. Taken together, this work consolidates the different notions of relatedness as branch relatedness and by leveraging the tree sequence encoding of an ARG it provides efficient algorithms that enable computations with the branch GRM that scale to mega-scale genomic datasets.

Identifiers

PMID40093116
PMCPMC11908205

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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.