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Identifying quantitative trait loci via group-sparse multitask regression and feature selection: an imaging genetics study of the ADNI cohort

机译:通过群体稀疏多任务回归和特征选择识别数量性状基因座:ADNI队列的影像遗传学研究

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摘要

>Motivation: Recent advances in high-throughput genotyping and brain imaging techniques enable new approaches to study the influence of genetic variation on brain structures and functions. Traditional association studies typically employ independent and pairwise univariate analysis, which treats single nucleotide polymorphisms (SNPs) and quantitative traits (QTs) as isolated units and ignores important underlying interacting relationships between the units. New methods are proposed here to overcome this limitation.>Results: Taking into account the interlinked structure within and between SNPs and imaging QTs, we propose a novel Group-Sparse Multi-task Regression and Feature Selection (G-SMuRFS) method to identify quantitative trait loci for multiple disease-relevant QTs and apply it to a study in mild cognitive impairment and Alzheimer's disease. Built upon regression analysis, our model uses a new form of regularization, group ℓ2,1-norm (G2,1-norm), to incorporate the biological group structures among SNPs induced from their genetic arrangement. The new G2,1-norm considers the regression coefficients of all the SNPs in each group with respect to all the QTs together and enforces sparsity at the group level. In addition, an ℓ2,1-norm regularization is utilized to couple feature selection across multiple tasks to make use of the shared underlying mechanism among different brain regions. The effectiveness of the proposed method is demonstrated by both clearly improved prediction performance in empirical evaluations and a compact set of selected SNP predictors relevant to the imaging QTs.>Availability: Software is publicly available at: >Contact: ; >Supplementary information: are available at Bioinformatics online.
机译:>动机::高通量基因分型和脑成像技术的最新进展为研究遗传变异对脑结构和功能的影响提供了新方法。传统的关联研究通常采用独立的和成对的单变量分析,该分析将单核苷酸多态性(SNP)和数量性状(QT)视为分离的单位,而忽略了这些单位之间重要的潜在相互作用关系。 >结果:考虑到SNP和成像QT之间以及它们之间的相互联系的结构,我们提出了一种新颖的群体稀疏多任务回归和特征选择(G- (SMuRFS)方法来识别多个与疾病相关的QT的定量特征位点,并将其应用于轻度认知障碍和阿尔茨海默氏病的研究。在回归分析的基础上,我们的模型使用一种新的正则化形式1-2,1-范数(G2,1-范数),以将SNPs的遗传排列所引起的生物学基团结构纳入其中。新的G2,1-范数考虑了每个组中所有SNP相对于所有QT的回归系数,并在组一级实施了稀疏性。此外,ℓ2,1-范数正则化用于跨多个任务耦合特征选择,以利用不同大脑区域之间共享的基础机制。建议的方法的有效性通过在经验评估中明显改善的预测性能以及与成像QT相关的一组选定的SNP预测变量的紧凑集来证明。>可用性:该软件在以下位置公开可用:>联系方式:; >补充信息:可在线访问生物信息学。

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