SEMbap: Bow-free covariance search and data de-correlation

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Mario Grassi, Barbara Tarantino
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Abstract

Large-scale studies of gene expression are commonly influenced by biological and technical sources of expression variation, including batch effects, sample characteristics, and environmental impacts. Learning the causal relationships between observable variables may be challenging in the presence of unobserved confounders. Furthermore, many high-dimensional regression techniques may perform worse. In fact, controlling for unobserved confounding variables is essential, and many deconfounding methods have been suggested for application in a variety of situations. The main contribution of this article is the development of a two-stage deconfounding procedure based on Bow-free Acyclic Paths (BAP) search developed into the framework of Structural Equation Models (SEM), called SEMbap(). In the first stage, an exhaustive search of missing edges with significant covariance is performed via Shipley d-separation tests; then, in the second stage, a Constrained Gaussian Graphical Model (CGGM) is fitted or a low dimensional representation of bow-free edges structure is obtained via Graph Laplacian Principal Component Analysis (gLPCA). We compare four popular deconfounding methods to BAP search approach with applications on simulated and observed expression data. In the former, different structures of the hidden covariance matrix have been replicated. Compared to existing methods, BAP search algorithm is able to correctly identify hidden confounding whilst controlling false positive rate and achieving good fitting and perturbation metrics.
SEMbap:无弓协方差搜索和数据去相关性
大规模的基因表达研究通常会受到表达变异的生物和技术来源的影响,包括批次效应、样本特征和环境影响。在存在未观察到的混杂因素的情况下,学习可观察变量之间的因果关系可能具有挑战性。此外,许多高维回归技术的性能可能会更差。事实上,控制未观察到的混杂变量是非常必要的,而且已经提出了许多适用于各种情况的去混杂方法。本文的主要贡献是基于无鲍无环路径(BAP)搜索,在结构方程模型(SEM)框架内开发了一种两阶段去混淆程序,称为 SEMbap()。在第一阶段,通过 Shipley d-separation 检验对具有显著协方差的缺失边进行穷举搜索;然后,在第二阶段,拟合约束高斯图形模型(CGGM),或通过图形拉普拉斯主成分分析(gLPCA)获得无弓边结构的低维表示。我们比较了四种流行的去嵌方法和 BAP 搜索方法,并将其应用于模拟和观察表达数据。前者复制了隐藏协方差矩阵的不同结构。与现有方法相比,BAP 搜索算法能够正确识别隐藏混杂因素,同时控制假阳性率,并获得良好的拟合和扰动指标。
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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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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