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arXiv 2210.12837stat.ME

基于多研究因子分析的多研究数据高斯图模型估计

Estimating Gaussian graphical models of multi-study data with Multi-Study Factor Analysis

Katherine H. Shutta, Denise M. Scholtens, William L. Lowe, Raji Balasubramanian, Roberta De Vito

AI总结:

本文提出MSFA-X方法,用于估计多研究数据中的高斯图模型,通过模拟和实际应用展示了其在识别葡萄糖代谢网络差异方面的有效性。

摘要:

网络模型是从复杂生物数据中获得新见解的强大工具。生物学中最大部分研究涉及在相同预测变量在多个研究或条件下测量(多研究数据)的设置中比较数据集。因此,开发用于多研究数据网络建模的统计工具已成为高度活跃的研究领域。多研究因子分析(MSFA)是一种用于估计多研究数据中潜在变量(因子)的方法。在本文中,我们通过添加估计高斯图模型(GGM)的能力来推广MSFA。我们的新工具MSFA-X是一个用于潜在变量基于的图建模的框架,用于分析多研究数据中的共享和研究特定信号。我们通过模拟证明MSFA-X可以恢复共享和研究特定的GGM,并优于图正则化基准。我们应用MSFA-X分析母体对口服葡萄糖耐量试验的反应,在超糖血症和不良妊娠结局(HAPO)研究中的靶向代谢组学谱中,识别出妊娠糖尿病患者与非妊娠糖尿病患者之间葡萄糖代谢在网络层面的差异。

英文摘要:

Network models are powerful tools for gaining new insights from complex biological data. Most lines of investigation in biology involve comparing datasets in the setting where the same predictors are measured across multiple studies or conditions (multi-study data). Consequently, the development of statistical tools for network modeling of multi-study data is a highly active area of research. Multi-study factor analysis (MSFA) is a method for estimation of latent variables (factors) in multi-study data. In this work, we generalize MSFA by adding the capacity to estimate Gaussian graphical models (GGMs). Our new tool, MSFA-X, is a framework for latent variable-based graphical modeling of shared and study-specific signals in multi-study data. We demonstrate through simulation that MSFA-X can recover shared and study-specific GGMs and outperforms a graphical lasso benchmark. We apply MSFA-X to analyze maternal response to an oral glucose tolerance test in targeted metabolomic profiles from the Hyperglycemia and Adverse Pregnancy Outcomes (HAPO) Study, identifying network-level differences in glucose metabolism between women with and without gestational diabetes mellitus.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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