Enhancing portability of trans-ancestral polygenic risk scores through tissue-specific functional genomic data integration.

IF 3.7 2区 生物学 Q1 GENETICS & HEREDITY PLoS Genetics Pub Date : 2024-08-07 eCollection Date: 2024-08-01 DOI:10.1371/journal.pgen.1011356
Bradley Crone, Alan P Boyle
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Abstract

Portability of trans-ancestral polygenic risk scores is often confounded by differences in linkage disequilibrium and genetic architecture between ancestries. Recent literature has shown that prioritizing GWAS SNPs with functional genomic evidence over strong association signals can improve model portability. We leveraged three RegulomeDB-derived functional regulatory annotations-SURF, TURF, and TLand-to construct polygenic risk models across a set of quantitative and binary traits highlighting functional mutations tagged by trait-associated tissue annotations. Tissue-specific prioritization by TURF and TLand provide a significant improvement in model accuracy over standard polygenic risk score (PRS) models across all traits. We developed the Trans-ancestral Iterative Tissue Refinement (TITR) algorithm to construct PRS models that prioritize functional mutations across multiple trait-implicated tissues. TITR-constructed PRS models show increased predictive accuracy over single tissue prioritization. This indicates our TITR approach captures a more comprehensive view of regulatory systems across implicated tissues that contribute to variance in trait expression.

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通过组织特异性功能基因组数据整合,提高跨宗族多基因风险评分的可移植性。
跨祖先多基因风险评分的可移植性往往受到不同祖先间连锁不平衡和遗传结构差异的影响。最近的文献表明,优先考虑具有功能基因组证据的 GWAS SNP,而不是强关联信号,可以提高模型的可移植性。我们利用 RegulomeDB 衍生的三种功能性调控注释--SURF、TURF 和 TLand--构建了一组数量性状和二元性状的多基因风险模型,突出了性状相关组织注释标记的功能性突变。与所有性状的标准多基因风险评分(PRS)模型相比,TURF 和 TLand 的组织特异性优先排序大大提高了模型的准确性。我们开发了跨巢穴迭代组织细化(Trans-ancestral Iterative Tissue Refinement,TITR)算法,用于构建优先考虑多个性状相关组织功能突变的 PRS 模型。与单一组织优先化相比,TITR 构建的 PRS 模型显示出更高的预测准确性。这表明我们的 TITR 方法更全面地捕捉到了导致性状表达差异的各相关组织的调控系统。
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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
期刊最新文献
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