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Transcriptome-guided amyloid imaging genetic analysis via a novel structured sparse learning algorithm

机译:通过新型结构化稀疏学习算法的转录组引导淀粉样蛋白成像遗传分析

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摘要

>Motivation: Imaging genetics is an emerging field that studies the influence of genetic variation on brain structure and function. The major task is to examine the association between genetic markers such as single-nucleotide polymorphisms (SNPs) and quantitative traits (QTs) extracted from neuroimaging data. The complexity of these datasets has presented critical bioinformatics challenges that require new enabling tools. Sparse canonical correlation analysis (SCCA) is a bi-multivariate technique used in imaging genetics to identify complex multi-SNP–multi-QT associations. However, most of the existing SCCA algorithms are designed using the soft thresholding method, which assumes that the input features are independent from one another. This assumption clearly does not hold for the imaging genetic data. In this article, we propose a new knowledge-guided SCCA algorithm (KG-SCCA) to overcome this limitation as well as improve learning results by incorporating valuable prior knowledge.>Results: The proposed KG-SCCA method is able to model two types of prior knowledge: one as a group structure (e.g. linkage disequilibrium blocks among SNPs) and the other as a network structure (e.g. gene co-expression network among brain regions). The new model incorporates these prior structures by introducing new regularization terms to encourage weight similarity between grouped or connected features. A new algorithm is designed to solve the KG-SCCA model without imposing the independence constraint on the input features. We demonstrate the effectiveness of our algorithm with both synthetic and real data. For real data, using an Alzheimer’s disease (AD) cohort, we examine the imaging genetic associations between all SNPs in the APOE gene (i.e. top AD gene) and amyloid deposition measures among cortical regions (i.e. a major AD hallmark). In comparison with a widely used SCCA implementation, our KG-SCCA algorithm produces not only improved cross-validation performances but also biologically meaningful results.>Availability: Software is freely available on request.>Contact:
机译:>动机:成像遗传学是一个新兴领域,其研究遗传变异对大脑结构和功能的影响。主要任务是检查遗传标记(例如单核苷酸多态性(SNP))和从神经影像数据中提取的定量特征(QT)之间的关联。这些数据集的复杂性提出了关键的生物信息学挑战,需要新的支持工具。稀疏规范相关分析(SCCA)是用于遗传学成像的双多元技术,用于识别复杂的多SNP-多QT关联。但是,大多数现有的SCCA算法都是使用软阈值方法设计的,该方法假定输入特征彼此独立。该假设显然不适用于成像遗传数据。本文中,我们提出了一种新的知识导向SCCA算法(KG-SCCA),以克服这一局限性,并通过合并有价值的先验知识来提高学习效果。>结果:提出的KG-SCCA方法是能够对两种类型的先验知识进行建模:一种作为组结构(例如SNP之间的连锁不平衡模块),另一种作为网络结构(例如大脑区域之间的基因共表达网络)。新模型通过引入新的正则化项来鼓励分组或连接的特征之间的权重相似性,从而整合了这些先前的结构。设计了一种新算法来求解KG-SCCA模型,而无需在输入特征上施加独立性约束。我们用合成数据和真实数据证明了我们算法的有效性。对于真实数据,我们使用阿尔茨海默氏病(AD)队列,研究了APOE基因(即顶级AD基因)中所有SNP的成像遗传关联以及皮质区域之间的淀粉样蛋白沉积措施(即主要的AD标志)。与广泛使用的SCCA实现相比,我们的KG-SCCA算法不仅可以提高交叉验证性能,而且还可以提供生物学上有意义的结果。>可用性:可根据要求免费提供软件。>联系

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