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Revealing the range of maximum likelihood estimates in the admixture model

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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 . In particular, the maximum likelihood estimator is non-unique 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 , when starting from . 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.
Title: Revealing the range of maximum likelihood estimates in the admixture model
Description:
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 .
In particular, the maximum likelihood estimator is non-unique 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 , when starting from .
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.

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