Evidence map›Paper›PMID 42392034›Full record

ArticleAmerican journal of human genetics2026

A transparent and generalizable deep-learning framework for genomic ancestry prediction.

Camille Rochefort-Boulanger, Matthew Scicluna, Raphaël Poujol, Jean-Christophe Grenier, Pierre Luc Carrier, Sébastien Lemieux, Julie G Hussin

Abstract read
In one paragraph

Article in American journal of human genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Camille Rochefort-BoulangerResearch Centre, Montreal Heart Institute, Montreal, QC, Canada; Département de Biochimie et Médecine Moléculaire, Université de Montréal, Montreal, QC, Canada; Mila - Quebec Artificial Intelligence Institute, Montreal, QC, Canada.
Matthew SciclunaResearch Centre, Montreal Heart Institute, Montreal, QC, Canada; Département de Biochimie et Médecine Moléculaire, Université de Montréal, Montreal, QC, Canada; Mila - Quebec Artificial Intelligence Institute, Montreal, QC, Canada.
Raphaël PoujolResearch Centre, Montreal Heart Institute, Montreal, QC, Canada.
Jean-Christophe GrenierResearch Centre, Montreal Heart Institute, Montreal, QC, Canada.
Pierre Luc CarrierMila - Quebec Artificial Intelligence Institute, Montreal, QC, Canada.
Sébastien LemieuxDépartement de Biochimie et Médecine Moléculaire, Université de Montréal, Montreal, QC, Canada; Mila - Quebec Artificial Intelligence Institute, Montreal, QC, Canada; Institute for Research in Immunology and Cancer, Université de Montréal, Montreal, QC, Canada.
Julie G HussinResearch Centre, Montreal Heart Institute, Montreal, QC, Canada; Département de Biochimie et Médecine Moléculaire, Université de Montréal, Montreal, QC, Canada; Mila - Quebec Artificial Intelligence Institute, Montreal, QC, Canada; Département de Médecine, Université de Montréal, Montreal, QC, Canada. Electronic address: julie.hussin@umontreal.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurately characterizing genetic ancestry is critical for ensuring reproducibility and fairness in genomic studies and downstream health research. This study aims to address the prediction of ancestry from genetic data using deep learning, with a focus on generalizability across datasets with diverse populations and on explainability to improve model transparency. We adapt the Diet Network, a deep-learning architecture proven to be effective in handling high-dimensional data, to learn population ancestry from single-nucleotide polymorphism (SNP) data using the populational Thousand Genomes Project dataset. Our results highlight the model's ability to generalize to diverse populations in the CARTaGENE, Montreal Heart Institute, and All of Us biobanks and that predictions remain robust to high levels of missing SNPs. We show that, despite the lack of North African populations in the training dataset, the model learns latent representations that reflect meaningful population structure for North African individuals in the biobanks. To improve model transparency, we apply Saliency Maps, DeepLift, GradientShap, and Integrated Gradients attribution techniques and evaluate their performance in identifying SNPs leveraged by the model. Using DeepLift, we show that the model's predictions are driven by population-specific signals consistent with those identified by traditional population-genetics metrics. This work presents a generalizable and interpretable deep-learning framework for genetic-ancestry inference in large-scale biobanks with genetic data. By enabling more widespread genomic ancestry characterization in these cohorts, this study contributes practical tools for integrating genetic data into downstream biomedical applications, supporting more inclusive and equitable healthcare solutions.

Indexed as

Deep LearningGenetics, PopulationGenome, HumanGenomicsPolymorphism, Single NucleotideHumansPrediction Algorithmsbiobanksdeep learningDiet Networkgeneralizabilitygenetic ancestryinterpretabilitypopulation labels

Identifiers

PMID42392034
PMCPMC13504326

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.