Back

PRANA: A Deep Learning Method for Adapting Polygenic Risk Scores to Diverse Ethnic Groups

Levi, H.; The Breast Cancer Association Consortium, ; Michailidou, K.; Elkon, R.; Shamir, R.

2026-07-15 genetic and genomic medicine
10.64898/2026.07.12.26357860 medRxiv
Show abstract

Polygenic risk scores (PRSs), which quantify inherited susceptibility to complex traits and diseases, have emerged as valuable tools for risk stratification and precision medicine. Despite their promise, PRS developed on European cohorts often demonstrate substantially reduced predictive accuracy in non-European populations, due to differences in genetic architecture. The disproportionate representation of European ancestry cohorts in genome-wide association studies (GWAS) leads to inequitable deployment of PRS technologies across diverse populations. Here, we introduce PRANA (Polygenic Risk Adaptation via Neural-network Architecture), a deep learning framework that adapts an existing PRS developed on one population to other ancestries. Unlike methods that require large-scale GWAS in the target population, PRANA leverages pre-trained PRS models derived from European cohorts and adapts them using modestly sized cohorts from the target population. We evaluated PRANA on seven complex traits in South Asian, East Asian and Ashkenazi Jewish populations, as well as in selected smaller East Asian subpopulations where the scarcity of training data poses a particular challenge. PRANA mostly improved predictive performance of the baseline PRS models by 5%-20% in terms of effect size and Nagelkerke's R^2, and, in most cases, outperformed existing cross-ancestry multi-PRS approaches. These results highlight PRANA as a scalable and practical strategy to reduce disparities in genomic risk prediction and advance the equitable application of PRS in diverse populations.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

1
Nature Communications
5641 papers in training set
Top 11%
15.1%
2
Human Genetics and Genomics Advances
84 papers in training set
Top 0.1%
13.1%
3
Nature Genetics
286 papers in training set
Top 0.5%
10.6%
4
Cell Genomics
172 papers in training set
Top 0.2%
9.8%
5
Bioinformatics
1204 papers in training set
Top 4%
5.5%
50% of probability mass above
6
The American Journal of Human Genetics
234 papers in training set
Top 0.9%
5.2%
7
Briefings in Bioinformatics
354 papers in training set
Top 2%
4.4%
8
Frontiers in Genetics
230 papers in training set
Top 1%
3.2%
9
Genome Medicine
183 papers in training set
Top 1%
3.2%
10
European Journal of Human Genetics
58 papers in training set
Top 0.5%
2.0%
11
Nature Human Behaviour
95 papers in training set
Top 1%
1.7%
12
Bioinformatics Advances
203 papers in training set
Top 3%
1.7%
13
Genome Biology
637 papers in training set
Top 6%
1.5%
14
BMC Genomics
406 papers in training set
Top 5%
1.3%
15
Scientific Reports
3612 papers in training set
Top 62%
1.3%
16
eLife
5828 papers in training set
Top 57%
1.1%
17
Genetic Epidemiology
55 papers in training set
Top 0.5%
1.1%
18
Patterns
78 papers in training set
Top 2%
1.1%
19
Communications Biology
993 papers in training set
Top 21%
1.1%
20
Human Genetics
28 papers in training set
Top 0.4%
1.1%
21
International Journal of Epidemiology
88 papers in training set
Top 1%
1.0%
22
Genome Research
468 papers in training set
Top 6%
0.8%
23
Nature Computational Science
55 papers in training set
Top 2%
0.8%
24
Genetics in Medicine
78 papers in training set
Top 1.0%
0.8%
25
Nature Medicine
125 papers in training set
Top 4%
0.6%