Nature CommunicationsGenomicsPeer-reviewed journal article
Improved Allele Frequencies in gnomAD through Local Ancestry Inference
Pragati KoreiD, Michael W. WilsoniD, Grace TiaoiD, Katherine R. ChaoiD, Philip W. Darnowsky, Nicholas A. Watts, Jessica Mauer, Samantha M. BaxteriD, Heidi L. RehmiD, Mark J. DalyiD, Konrad J. KarczewskiiD, Elizabeth G. AtkinsoniD
Abstract
The Genome Aggregation Database (gnomAD) is a foundational resource for allele frequency data, widely used in genomic research and clinical interpretation. However, traditional estimates rely on individual-level genetic ancestry groupings that may obscure variation in recently admixed populations. To improve resolution, we applied local ancestry inference (LAI) to over 27 million variants in two admixed groups: Admixed American (n = 7,612) and African/African American (n = 20,250), deriving ancestry-specific allele frequencies. We show that 78.5% and 85.1% of variants in these groups, respectively, exhibit at least a twofold difference in ancestry-specific frequencies. Moreover, 81.49% of variants with LAI information would be assigned a higher gnomAD-wide maximum frequency after incorporating LAI, potentially altering clinical interpretations. This LAI-informed release reveals clinically relevant frequency differences that are masked in aggregate estimates and may support reclassifying some variants from Uncertain Significance to Benign or Likely Benign.
- organism: human
- assay: whole-genome sequencing
- research focus: variant effect prediction
- research focus: database / resource
- approach: statistical model
- Citations
- 20
- FWCI
- 11.76
- Field percentile
- top 1%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- LoGicAl: Local ancestry and genotype calling uncertainty-aware ancestry-specific allele frequency estimation from admixed samples
Jiongming Wang, Sebastian Zöllner·BioinformaticsPeer-reviewed·Oct 1, 2026
- AFA: Computationally efficient Ancestral Frequency estimation in Admixed populations: the Hispanic Community Health Study/Study of Latinos
Einat Granot Hershkovitz, Quan Sun, … Tamar Sofer·bioRxiv·Aug 6, 2021
- The Clinical Imperative for Inclusivity: Race, Ethnicity, and Ancestry (REA) in Genomics
Alice B. Popejoy, Deborah Ritter, … Carlos D. Bustamante·Human MutationPeer-reviewed·Oct 11, 2018
- Summix: A method for detecting and adjusting for population structure in genetic summary data
Ian Arriaga Mackenzie, Gregory Matesi, … Audrey E. Hendricks·The American Journal of Human GeneticsPeer-reviewed·Jun 21, 2021
- Analyzing globin gene variation in gnomAD: implications for variant interpretation in hemoglobinopathies
Mikaella Kontopoulou, Maria Xenophontos, … Petros Kountouris·bioRxiv·Sep 19, 2026
- The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, … May Okihiro·Communications BiologyPeer-reviewed·Feb 19, 2024