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Leveraging genetic ancestry continuum information to interpolate PRS for admixed populations

Ruan, Y.; Bhukar, R.; Patel, A.; Koyama, S.; Hull, L.; Truong, B.; Hornsby, W.; Zhang, H.; Chatterjee, N.; Natarajan, P.

2024-11-10 epidemiology
10.1101/2024.11.09.24316996 medRxiv
Show abstract

The relatively low representation of admixed populations in both discovery and fine-tuning individual-level datasets limits polygenic risk score (PRS) development and equitable clinical translation for admixed populations. Under the assumption that the most informative PRS model for a genetically homogeneous sample varies linearly in an ancestry continuum space, we introduce a Genetic Distance-assisted PRS Combination Pipeline for Diverse Genetic Ancestries (DiscoDivas) to interpolate a harmonized PRS for diverse, especially admixed, genetic ancestries, leveraging multiple PRS models fine-tuned within existing samples, which are mostly of single ancestry, and genetic distance. DiscoDivas treats genetic ancestry as a continuous variable and does not require shifting between different models when calculating PRS for different ancestries. We generated PRS with DiscoDivas and the current conventional method, i.e. fine-tuning multiple GWAS PRS using the matched or similar genetic ancestry samples. DiscoDivas generated a harmonized PRS of the accuracy comparable to or higher than the conventional approach, with the greatest advantage exhibited in admixed individuals.

Published in The American Journal of Human Genetics (predicted rank #1) · training set

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