Evidence map›Paper›PMID 33465078›Full record

ArticlePLoS genetics2021

Estimating FST and kinship for arbitrary population structures.

Alejandro Ochoa, John D Storey

Abstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

  1. Population Differentiation and Polygenic Selection in the Finnish Ayrshire Cows Selected on Genomic Information.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2026
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  16. On ARGs, pedigrees, and genetic relatedness matrices.bioRxiv : the preprint server for biology · 2025
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  18. Error rates inbioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Alejandro OchoaDuke Center for Statistical Genetics and Genomics, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0003-4928-3403
John D StoreyLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey, United States of America.ORCID 0000-0001-5992-402X

Funding

Models and Methods for Population GenomicsR01HG006448 · NHGRI · PRINCETON UNIVERSITY · PI STOREY, JOHN D · 2012 to 2025
$3.8M
NHGRI NIH HHS R01 HG006448
6 · The paper itself

Abstract

FST and kinship are key parameters often estimated in modern population genetics studies in order to quantitatively characterize structure and relatedness. Kinship matrices have also become a fundamental quantity used in genome-wide association studies and heritability estimation. The most frequently-used estimators of FST and kinship are method-of-moments estimators whose accuracies depend strongly on the existence of simple underlying forms of structure, such as the independent subpopulations model of non-overlapping, independently evolving subpopulations. However, modern data sets have revealed that these simple models of structure likely do not hold in many populations, including humans. In this work, we analyze the behavior of these estimators in the presence of arbitrarily-complex population structures, which results in an improved estimation framework specifically designed for arbitrary population structures. After generalizing the definition of FST to arbitrary population structures and establishing a framework for assessing bias and consistency of genome-wide estimators, we calculate the accuracy of existing FST and kinship estimators under arbitrary population structures, characterizing biases and estimation challenges unobserved under their originally-assumed models of structure. We then present our new approach, which consistently estimates kinship and FST when the minimum kinship value in the dataset is estimated consistently. We illustrate our results using simulated genotypes from an admixture model, constructing a one-dimensional geographic scenario that departs nontrivially from the independent subpopulations model. Our simulations reveal the potential for severe biases in estimates of existing approaches that are overcome by our new framework. This work may significantly improve future analyses that rely on accurate kinship and FST estimates.

Indexed as

InbreedingModels, GeneticGenetics, PopulationGenome-Wide Association StudyGenotypeHumansPedigreePolymorphism, Single Nucleotide

Identifiers

PMID33465078
PMCPMC7846127

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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.