Evidence map›Paper›PMID 40737495›Full record

ArticleG3 (Bethesda, Md.)2025

Estimating allele frequencies, ancestry proportions and genotype likelihoods in the presence of mapping bias.

Torsten Günther, Amy Goldberg, Joshua G Schraiber

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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Torsten GüntherHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala SE-752 36, Sweden.ORCID 0000-0001-9460-390X
Amy GoldbergDepartment of Evolutionary Anthropology, Duke University, Durham, NC 27708, USA.ORCID 0000-0001-9306-1539
Joshua G SchraiberDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, USA.

Funding

Inferring the evolutionary history of admixed populationsR35GM133481 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Amy Goldberg · 2019 to 2026
$2.8M
NIGMS NIH HHS R35 GM133481Svenska Forskningsrådet Formas 2023-01381Vetenskapsrådet 2017-05267
6 · The paper itself

Abstract

Population genomic analyses rely on an accurate and unbiased characterization of the genetic composition of the studied population. For short-read, high-throughput sequencing data, mapping sequencing reads to a linear reference genome can bias population genetic inference due to mismatches in reads carrying non-reference alleles. In this study, we investigate the impact of mapping bias on allele frequency estimates from pseudohaploid data and genotype likelihoods, 2 approaches commonly used in ultra-low to medium coverage sequencing. To mitigate mapping bias, we propose an empirical adjustment to genotype likelihoods. Using data from the 1000 Genomes Project, we find that our new method improves allele frequency estimation. To test a downstream application, we simulate ancient DNA data with realistic post-mortem damage to compare widely used methods for estimating ancestry proportions under different scenarios, including reference genome selection, population divergence, and sequencing depth. Our findings reveal that mapping bias can lead to differences in estimated admixture proportion of up to 4% depending on the reference population. However, the choice of method has a much stronger impact, with some methods showing differences of 10%. qpAdm appears to perform best at estimating simulated ancestry proportions, but it is sensitive to mapping bias and its applicability may vary across species due to its requirement for additional populations beyond the sources and target population. Our adjusted genotype likelihood approach largely mitigates the effect of mapping bias on genome-wide ancestry estimates from genotype likelihood-based tools. However, it cannot account for the bias introduced by the method itself or the noise in individual site allele frequency estimates due to low sequencing depth. Overall, our study provides valuable insights for obtaining more precise estimates of allele frequencies and ancestry proportions in empirical studies.

Indexed as

Chromosome MappingGene FrequencyGenotypeGenetics, PopulationHigh-Throughput Nucleotide SequencingHumansLikelihood FunctionsModels, GeneticPolymorphism, Single Nucleotideadmixtureancestry proportionancient DNAgenotype likelihoodmapping bias

Identifiers

PMID40737495
PMCPMC12506655

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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.