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Transfer learning with false negative control improves polygenic risk prediction.

Authors :
Jeng XJ
Hu Y
Venkat V
Lu TP
Tzeng JY
Source :
PLoS genetics [PLoS Genet] 2023 Nov 27; Vol. 19 (11), pp. e1010597. Date of Electronic Publication: 2023 Nov 27 (Print Publication: 2023).
Publication Year :
2023

Abstract

Polygenic risk score (PRS) is a quantity that aggregates the effects of variants across the genome and estimates an individual's genetic predisposition for a given trait. PRS analysis typically contains two input data sets: base data for effect size estimation and target data for individual-level prediction. Given the availability of large-scale base data, it becomes more common that the ancestral background of base and target data do not perfectly match. In this paper, we treat the GWAS summary information obtained in the base data as knowledge learned from a pre-trained model, and adopt a transfer learning framework to effectively leverage the knowledge learned from the base data that may or may not have similar ancestral background as the target samples to build prediction models for target individuals. Our proposed transfer learning framework consists of two main steps: (1) conducting false negative control (FNC) marginal screening to extract useful knowledge from the base data; and (2) performing joint model training to integrate the knowledge extracted from base data with the target training data for accurate trans-data prediction. This new approach can significantly enhance the computational and statistical efficiency of joint-model training, alleviate over-fitting, and facilitate more accurate trans-data prediction when heterogeneity level between target and base data sets is small or high.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright: © 2023 Jeng et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

Details

Language :
English
ISSN :
1553-7404
Volume :
19
Issue :
11
Database :
MEDLINE
Journal :
PLoS genetics
Publication Type :
Academic Journal
Accession number :
38011285
Full Text :
https://doi.org/10.1371/journal.pgen.1010597