Modeling gene interactions in polygenic prediction via geometric deep learning

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Han Li, Jianyang Zeng, Michael P Snyder, Sai Zhang
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引用次数: 0

Abstract

Polygenic risk score (PRS) is a widely-used approach for predicting individuals' genetic risk of complex diseases, playing a pivotal role in advancing precision medicine. Traditional PRS methods, predominantly following a linear structure, often fall short in capturing the intricate relationships between genotype and phenotype. In this study, we present PRS-Net, an interpretable geometric deep learning-based framework that effectively models the nonlinearity of biological systems for enhanced disease prediction and biological discovery. PRS-Net begins by deconvoluting the genome-wide PRS at the single-gene resolution, and then explicitly encapsulates gene-gene interactions leveraging a graph neural network (GNN) for genetic risk prediction, enabling a systematic characterization of molecular interplay underpinning diseases. An attentive readout module is introduced to facilitate model interpretation. Extensive tests across multiple complex traits and diseases demonstrate the superior prediction performance of PRS-Net compared to conventional PRS methods. The interpretability of PRS-Net further enhances the identification of disease-relevant genes and gene programs. PRS-Net provides a potent tool for concurrent genetic risk prediction and biological discovery for complex diseases.
通过几何深度学习为多基因预测中的基因相互作用建模
多基因风险评分(PRS)是一种广泛应用于预测个体复杂疾病遗传风险的方法,在推进精准医疗方面发挥着举足轻重的作用。传统的多基因风险评分方法主要采用线性结构,往往无法捕捉基因型与表型之间错综复杂的关系。在本研究中,我们提出了一种基于几何深度学习的可解释框架--PRS-Net,它能有效地模拟生物系统的非线性,从而增强疾病预测和生物发现的能力。PRS-Net 首先在单基因分辨率上对全基因组 PRS 进行去卷积,然后利用图神经网络(GNN)明确封装基因与基因之间的相互作用,以进行遗传风险预测,从而系统地描述支撑疾病的分子相互作用。为便于解释模型,还引入了一个细心的读出模块。对多种复杂性状和疾病的广泛测试表明,与传统的 PRS 方法相比,PRS-Net 的预测性能更优越。PRS-Net 的可解释性进一步提高了疾病相关基因和基因程序的鉴定能力。PRS-Net 为同时进行复杂疾病的遗传风险预测和生物学发现提供了有力的工具。
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来源期刊
Genome research
Genome research 生物-生化与分子生物学
CiteScore
12.40
自引率
1.40%
发文量
140
审稿时长
6 months
期刊介绍: Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine. Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies. New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.
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