XPRS: a tool for interpretable and explainable polygenic risk score.

Na Yeon Kim, Seunggeun Lee
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引用次数: 0

Abstract

Summary: The polygenic risk score (PRS) is an important method for assessing genetic susceptibility to diseases; however, its clinical utility is limited by a lack of interpretability tools. To address this problem, we introduce eXplainable PRS (XPRS), an interpretation and visualization tool that decomposes PRSs into genes/regions and single nucleotide polymorphism (SNP) contribution scores via Shapley additive explanations (SHAPs), which provide insights into specific genes and SNPs that significantly contribute to the PRS of an individual. This software features a multilevel visualization approach, including Manhattan plots, LocusZoom-like plots, and tables at the population and individual levels, to highlight important genes and SNPs. By implementing with a user-friendly web interface, XPRS allows for straightforward data input and interpretation. By bridging the gap between complex genetic data and actionable clinical insights, XPRS can improve communication between clinicians and patients.

Availability and implementation: The XPRS software is publicly available on GitHub at https://github.com/nayeonkim93/XPRS and can see the demo through our cloud-based web service at https://xprs.leelabsg.org/.

XPRS:可解释和可解释的多基因风险评分工具。
摘要:多基因风险评分(PRS)是评估疾病遗传易感性的重要方法;然而,由于缺乏可解释性工具,其临床应用受到限制。为了解决这一问题,我们引入了可解释PRS (eXplainable PRS, XPRS),这是一种解释和可视化工具,通过Shapley加性解释(SHAPs)将PRS分解为基因/区域和单核苷酸多态性(SNP)贡献分数,从而深入了解对个体PRS有重要影响的特定基因和SNP。该软件具有多层次可视化方法,包括曼哈顿图,locuszoom样图和人口和个体水平的表格,以突出重要的基因和snp。通过实现用户友好的web界面,XPRS允许直接的数据输入和解释。通过弥合复杂的基因数据和可操作的临床见解之间的差距,XPRS可以改善临床医生和患者之间的沟通。可用性和实施:XPRS软件可在GitHub上公开获取,网址为https://github.com/nayeonkim93/XPRS,并可通过我们基于云的web服务https://xprs.leelabsg.org/.Supplementary查看演示:补充数据可在Bioinformatics在线获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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