Scalable high resolution ancestry deconvolution for genomic data

Abstract As genome-wide association studies and genetic risk prediction models extend to globally diverse and admixed biobanks, accurate, scalable ancestry deconvolution, also called local ancestry inference (LAI), has become crucial. LAI assigns ancestry to each genomic segment within an individual, enabling studies of population history and ancestry-associated haplotypic effects. Existing LAI methods scale poorly to biobank-scale data, to the distant past, and to large numbers of ancestries. Here, we introduce several independent LAI methods implemented in the Gnomix software suite, achieving higher accuracy and faster computational performance than all existing approaches and with portable models that can be shared without exposing individual-level training data. Gnomix is paired with Gnofix, a swift, scalable phase correction counterpart. We demonstrate performance on worldwide whole-genome data from humans and canids, leveraging high-resolution accuracy to localise ancient New World haplotypes in the Xoloitzcuintli, dating back over 100 generations. Code is available at https://github.com/AI-sandbox/gnomix .

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Publication Details

Journal
Nature Communications
Published
2026-07-25
DOI
https://doi.org/10.1038/s41467-026-75391-0
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00

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article

Scalable high resolution ancestry deconvolution for genomic data

Míriam Barrabés, Alexander G. Ioannidis, Helgi Hilmarsson, Bustamante Cd et al.
Nature Communications
Genetic Associations and Epidemiology
article

Scalable high resolution ancestry deconvolution for genomic data

Míriam Barrabés, Alexander G. Ioannidis, Helgi Hilmarsson, Bustamante Cd, Daniel Mas Montserrat, Richa Rastogi, Arvind Kumar
article en

Abstract

Abstract As genome-wide association studies and genetic risk prediction models extend to globally diverse and admixed biobanks, accurate, scalable ancestry deconvolution, also called local ancestry inference (LAI), has become crucial. LAI assigns ancestry to each genomic segment within an individual, enabling studies of population history and ancestry-associated haplotypic effects. Existing LAI methods scale poorly to biobank-scale data, to the distant past, and to large numbers of ancestries. Here, we introduce several independent LAI methods implemented in the Gnomix software suite, achieving higher accuracy and faster computational performance than all existing approaches and with portable models that can be shared without exposing individual-level training data. Gnomix is paired with Gnofix, a swift, scalable phase correction counterpart. We demonstrate performance on worldwide whole-genome data from humans and canids, leveraging high-resolution accuracy to localise ancient New World haplotypes in the Xoloitzcuintli, dating back over 100 generations. Code is available at https://github.com/AI-sandbox/gnomix .

Nature Communications
University of California, Santa Cruz (US), Cornell University (US), University of Oklahoma (US), Stanford University (US)
National Human Genome Research Institute
Openalex Percentile: Top 8%
Genetic Associations and Epidemiology
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