通过对高维性状进行多变量潜在因子分析,提高基因发现和精细绘图的分辨率

Feng Zhou, William J Astle, Adam S Butterworth, Jennifer Lea Asimit
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摘要

分子表型或成像特征等高维性状的全基因组关联研究(GWAS)通常使用单变量方法,忽略了相关性状的信息。产生高维性状变异的生物学机制可以通过因子分析中较少数量的潜在因子的 GWAS 准确捕捉。在这里,我们介绍了一种零相关多性状精细绘图方法--flashfmZero,可用于任意数量的潜在因子。在对 INTERVAL 队列中 99 个血细胞性状得出的 25 个潜因子的应用中,我们展示了潜因子的 GWAS 如何能够检测出与多个血细胞性状有亚阈值关联的信号。在87%的比较中,FlashfmZero产生的99%可信集的变异大小与血细胞性状的可信集相同或更少,所有潜在性状精细映射可信集都是flashfmZero产生的可信集的子集。这些分析技术增强了发现和精细绘制许多性状的能力。
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Improved genetic discovery and fine-mapping resolution through multivariate latent factor analysis of high-dimensional traits
Genome-wide association studies (GWAS) of high-dimensional traits, such as molecular phenotypes or imaging features, often use univariate approaches, ignoring information from related traits. Biological mechanisms generating variation in high-dimensional traits can be captured parsimoniously through GWAS of a smaller number of latent factors from factor analysis. Here, we introduce a zero-correlation multi-trait fine-mapping approach, flashfmZero, for any number of latent factors. In our application to 25 latent factors derived from 99 blood cell traits in the INTERVAL cohort, we show how GWAS of latent factors enables detection of signals that have sub-threshold associations with several blood cell traits. FlashfmZero resulted in 99% credible sets with the same size or fewer variants than those for blood cell traits in 87% of our comparisons, and all latent trait fine-mapping credible sets were subsets of those from flashfmZero. These analysis techniques give enhanced power for discovery and fine-mapping for many traits.
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