Evidence map›Paper›PMID 39753130›Full record

ArticleAmerican journal of human genetics2025

Characterizing features affecting local ancestry inference performance in admixed populations.

Jessica Honorato-Mauer, Nirav N Shah, Adam X Maihofer, Clement C Zai, Sintia Belangero, Caroline M Nievergelt, Psychiatric Genomics Consortium for PTSD Ancestry Working Group, Marcos Santoro, Elizabeth G Atkinson

Abstract read
In one paragraph

Article in American journal of human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jessica Honorato-MauerDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Nirav N ShahDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Adam X MaihoferDepartment of Psychiatry, School of Medicine, University of California at San Diego, La Jolla, CA 92093, USA.
Clement C ZaiDepartment of Psychiatry, Institute of Medical Science, Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, USA.
Sintia BelangeroDepartment of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil.
Caroline M NievergeltDepartment of Psychiatry, School of Medicine, University of California at San Diego, La Jolla, CA 92093, USA.
Psychiatric Genomics Consortium for PTSD Ancestry Working Group
Marcos SantoroDepartment of Biochemistry, Molecular Biology Division, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil. Electronic address: santoro@unifesp.br.
Elizabeth G AtkinsonDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; The Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA. Electronic address: elizabeth.atkinson@bcm.edu.

Funding

Psychiatric Genomics Consortium for PTSDR01MH106595 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KARESTAN C KOENEN, Caroline M Nievergelt · 2016 to 2026
$8.4M
Empowering gene discovery and accelerating clinical translation for diverse admixed populationsR01HG012869 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI Elizabeth Grace Atkinson · 2023 to 2026
$3.1M
A framework enabling the genomic analysis of psychiatric traits across admixed populations.K01MH121659 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI ATKINSON, ELIZABETH GRACE · 2019 to 2022
$719k
NHGRI NIH HHS R01 HG012869NIMH NIH HHS K01 MH121659NIMH NIH HHS R01 MH106595
6 · The paper itself

Abstract

In recent years, significant efforts have been made to improve methods for genomic studies of admixed populations using local ancestry inference (LAI). Accurate LAI is crucial to ensure that downstream analyses accurately reflect the genetic ancestry of research participants. Here, we test analytic strategies for LAI to provide guidelines for optimal accuracy, focusing on admixed populations reflective of Latin America's primary continental ancestries-African (AFR), Amerindigenous (AMR), and European (EUR). Simulating linkage-disequilibrium-informed admixed haplotypes under a variety of 2- and 3-way admixture models, we implemented a standard LAI pipeline, testing the impact of reference panel composition, DNA data type, demography, and software parameters to quantify ancestry-specific LAI accuracy. We observe that across all models, AMR tracts have notably reduced LAI accuracy as compared to EUR and AFR tracts, with true positive rate means for AMR ranging from 88% to 94%, EUR from 96% to 99%, and AFR from 98% to 99%. When LAI miscalls occurred, they most frequently erroneously called EUR ancestry in true AMR sites. Concerning reference panel curation, we find that using a reference panel well matched to the target population, even with a smaller sample size, was accurate and the most computationally efficient. Imputation did not harm LAI performance in our tests; rather, we observed that higher variant density improved accuracy. While directly responsive to admixed Latin American cohort compositions, these trends are broadly useful for informing best practices for LAI across admixed populations. Our findings reinforce the need for the inclusion of more underrepresented populations in sequencing efforts to improve reference panels.

Indexed as

American Indian or Alaska NativeBlack PeopleGenetics, PopulationWhite PeopleCentral American PeopleGenome, HumanHaplotypesHumansLatin AmericaLinkage DisequilibriumModels, GeneticPolymorphism, Single NucleotideSoftwareSouth American Peopleancestrybioinformaticsgenetic admixturelocal ancestry inferencepopulation geneticsreference panels

Identifiers

PMID39753130
PMCPMC11866949

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.