{"title":"An exact formula for the contribution of sampling error to r2, a common measure of linkage disequilibrium.","authors":"Robin S Waples","doi":"10.1093/jhered/esag087","DOIUrl":null,"url":null,"abstract":"<p><p>Interest in quantifying linkage disequilibrium (LD, non-random associations of alleles at different loci) has skyrocketed in recent years as researchers have focused on use of LD in genome-wide association studies (GWAS), for studying historical demography, and for estimating effective population size (Ne). The most widely used LD metric is r2 = the squared correlation of alleles at a pair of loci. Despite a half century of efforts, developing an unbiased expectation of r2 as a function of the many factors that can affect it (physical linkage, genetic drift, selection, migration, mutation, mating systems) remains elusive. Furthermore, even when all of these other factors are absent, empirical estimates of r2 are upwardly biased by sampling a finite number (S) of individuals, and that must be accounted for if one wants to focus on the desired signal of LD. Previous approaches to estimate ${r}_{sample}^2$ have been shown to be biased to greater or lesser degrees. The purpose of this short paper is to demonstrate that a simple and exact expression for $E\\left({r}_{sample}^2\\right)$ does exist for the special case where sampling error is the only factor contributing to r2, in which case $E\\left({r}_{sample}^2\\right)=1/\\left(S-1\\right)$. When other factors contribute heavily to LD, $E\\left({r}_{sample}^2\\right)$ shrinks toward 0 as empirical r2 ➔ 1. However, for estimating contemporary Ne with unlinked markers, empirical r2 will generally be small and $1/\\left(S-1\\right)$ will provide a robust estimate of $E\\left({r}_{sample}^2\\right)$.</p>","PeriodicalId":54811,"journal":{"name":"Journal of Heredity","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2026-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Heredity","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jhered/esag087","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"EVOLUTIONARY BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Interest in quantifying linkage disequilibrium (LD, non-random associations of alleles at different loci) has skyrocketed in recent years as researchers have focused on use of LD in genome-wide association studies (GWAS), for studying historical demography, and for estimating effective population size (Ne). The most widely used LD metric is r2 = the squared correlation of alleles at a pair of loci. Despite a half century of efforts, developing an unbiased expectation of r2 as a function of the many factors that can affect it (physical linkage, genetic drift, selection, migration, mutation, mating systems) remains elusive. Furthermore, even when all of these other factors are absent, empirical estimates of r2 are upwardly biased by sampling a finite number (S) of individuals, and that must be accounted for if one wants to focus on the desired signal of LD. Previous approaches to estimate ${r}_{sample}^2$ have been shown to be biased to greater or lesser degrees. The purpose of this short paper is to demonstrate that a simple and exact expression for $E\left({r}_{sample}^2\right)$ does exist for the special case where sampling error is the only factor contributing to r2, in which case $E\left({r}_{sample}^2\right)=1/\left(S-1\right)$. When other factors contribute heavily to LD, $E\left({r}_{sample}^2\right)$ shrinks toward 0 as empirical r2 ➔ 1. However, for estimating contemporary Ne with unlinked markers, empirical r2 will generally be small and $1/\left(S-1\right)$ will provide a robust estimate of $E\left({r}_{sample}^2\right)$.
期刊介绍:
Over the last 100 years, the Journal of Heredity has established and maintained a tradition of scholarly excellence in the publication of genetics research. Virtually every major figure in the field has contributed to the journal.
Established in 1903, Journal of Heredity covers organismal genetics across a wide range of disciplines and taxa. Articles include such rapidly advancing fields as conservation genetics of endangered species, population structure and phylogeography, molecular evolution and speciation, molecular genetics of disease resistance in plants and animals, genetic biodiversity and relevant computer programs.