用于预测复杂性状和疾病的统计模型和计算工具。

Q2 Agricultural and Biological Sciences
Genomics and Informatics Pub Date : 2021-12-01 Epub Date: 2021-12-31 DOI:10.5808/gi.21053
Wonil Chung
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引用次数: 4

摘要

从基因变异中预测个体特征和疾病对于实现个性化医疗的承诺至关重要。来自全基因组关联研究(GWAS)的遗传变异,包括远低于GWAS显著性的变异,可以汇总成广泛的复杂性状和疾病的高度重要的预测。最近出现的大样本公共生物库使得基于整个基因组的遗传变异的高度精确的多基因预测成为可能。为了更准确地计算多基因风险评分(PRS),已经引入和开发了各种统计方法和各种计算工具。然而,许多研究人员在使用PRS工具时,并没有彻底了解底层模型以及如何指定参数以获得最佳性能。研究在计算工具中实现的统计模型和要指定的参数的公式是有利的。在这里,我们回顾了最近用于PRS计算的各种统计方法和计算工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Statistical models and computational tools for predicting complex traits and diseases.

Statistical models and computational tools for predicting complex traits and diseases.

Predicting individual traits and diseases from genetic variants is critical to fulfilling the promise of personalized medicine. The genetic variants from genome-wide association studies (GWAS), including variants well below GWAS significance, can be aggregated into highly significant predictions across a wide range of complex traits and diseases. The recent arrival of large-sample public biobanks enables highly accurate polygenic predictions based on genetic variants across the whole genome. Various statistical methodologies and diverse computational tools have been introduced and developed to computed the polygenic risk score (PRS) more accurately. However, many researchers utilize PRS tools without a thorough understanding of the underlying model and how to specify the parameters for the best performance. It is advantageous to study the statistical models implemented in computational tools for PRS estimation and the formulas of parameters to be specified. Here, we review a variety of recent statistical methodologies and computational tools for PRS computation.

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来源期刊
Genomics and Informatics
Genomics and Informatics Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
1.90
自引率
0.00%
发文量
0
审稿时长
12 weeks
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