Evidence map›Paper›PMID 40534544›Full record

ArticleG3 (Bethesda, Md.)2025

Revealing the range of equally likely estimates in the admixture model.

Carola Sophia Heinzel, Franz Baumdicker, Peter Pfaffelhuber

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Carola Sophia HeinzelDepartment of Mathematical Stochastics, Albert-Ludwigs-University Freiburg, Freiburg im Breisgau 79104, Germany.ORCID 0009-0000-9042-949X
Franz BaumdickerCluster of Excellence "Controlling Microbes to Fight Infections", Mathematical and Computational Population Genetics, University of Tübingen, Sand 14, Tübingen 72076, Germany.ORCID 0000-0001-9106-7259
Peter PfaffelhuberDepartment of Mathematical Stochastics, Albert-Ludwigs-University Freiburg, Freiburg im Breisgau 79104, Germany.ORCID 0000-0002-6421-5460

Funding

Deutsche ForschungsgemeinschaftDFGGerman Research Foundation 499552394Germany's Excellence Strategy 390727645Germany's Excellence Strategy 390838134
6 · The paper itself

Abstract

Many ancestry inference tools, including Structure and Admixture, rely on the admixture model to infer both, allele frequencies p and individual admixture proportions q for a collection of individuals relative to a set of hypothetical ancestral populations. We show that under realistic conditions the likelihood in the admixture model is typically flat in some direction around a maximum-likelihood estimate (q^,p^). In particular, the maximum-likelihood estimator is nonunique and there is a complete spectrum of possible estimates. Common inference tools typically identify only a few points within this spectrum. We provide an algorithm which computes the set of equally likely (q~,p~), when starting from (q^,p^). It is analytic for K=2 ancestral populations and numeric for K>2. We apply our algorithm to data from the 1000 genomes project, and show that inter-European estimators of q can come with a large set of equally likely possibilities. In general, markers with large allele frequency differences between populations in combination with individuals with concentrated admixture proportions lead to small areas with a flat likelihood. Our findings imply that care must be taken when interpreting results from STRUCTURE and ADMIXTURE if populations are not separated well enough.

Indexed as

Genetics, PopulationModels, GeneticAlgorithmsGene FrequencyHumansLikelihood FunctionsADMIXTUREadmixture modellabel switchingnonunique estimatorSTRUCTURE

Identifiers

PMID40534544
PMCPMC12341866

What OpenQuestion holds

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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.