基于多模态脑成像遗传学特征选择的快速多任务SCCA学习。

Lei Du, Kefei Liu, Xiaohui Yao, Shannon L Risacher, Junwei Han, Lei Guo, Andrew J Saykin, Li Shen
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引用次数: 14

摘要

脑成像遗传学通过整合单核苷酸多态性(SNP)和成像定量性状(QTs)等基因型数据,研究脑结构和功能的遗传基础。在这一领域,多任务学习(MTL)和稀疏典型相关分析(SCCA)方法由于其优于独立和两两单变量分析而被广泛使用。MTL方法通常包含少量的qt,并且不是为从大量的qt中选择特征而设计的;而现有的SCCA方法通常只采用一种qt模式来研究其与snp的关系。随着snp数量的增加,MTL和SCCA都遇到了计算上的挑战。在本文中,我们结合MTL和SCCA的优点,提出了一个新的多任务SCCA (MTSCCA)学习框架来识别snp和多模态成像qt之间的双多元关联。MTSCCA可以利用不同成像方式所携带的互补信息。使用g2.1范数正则化,MTSCCA将同一组中的所有snp一起处理,以在组级别强制稀疏性。1.1范数惩罚用于snp跨多个任务和qt跨多个模式的联合选择特征。提出了一种利用snp分组信息的快速优化算法。与传统的SCCA方法相比,MTSCCA方法在相关系数和典型权重模式方面都具有更好的性能。此外,我们的方法运行速度快,易于实现,因此可以为全基因组全脑成像遗传学研究提供一个强大的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fast Multi-Task SCCA Learning with Feature Selection for Multi-Modal Brain Imaging Genetics.

Fast Multi-Task SCCA Learning with Feature Selection for Multi-Modal Brain Imaging Genetics.

Fast Multi-Task SCCA Learning with Feature Selection for Multi-Modal Brain Imaging Genetics.

Brain imaging genetics studies the genetic basis of brain structures and functions via integrating both genotypic data such as single nucleotide polymorphism (SNP) and imaging quantitative traits (QTs). In this area, both multi-task learning (MTL) and sparse canonical correlation analysis (SCCA) methods are widely used since they are superior to those independent and pairwise univariate analyses. MTL methods generally incorporate a few of QTs and are not designed for feature selection from a large number of QTs; while existing SCCA methods typically employ only one modality of QTs to study its association with SNPs. Both MTL and SCCA encounter computational challenges as the number of SNPs increases. In this paper, combining the merits of MTL and SCCA, we propose a novel multi-task SCCA (MTSCCA) learning framework to identify bi-multivariate associations between SNPs and multi-modal imaging QTs. MTSCCA could make use of the complementary information carried by different imaging modalities. Using the G 2,1-norm regularization, MTSCCA treats all SNPs in the same group together to enforce sparsity at the group level. The l 2 , 1 -norm penalty is used to jointly select features across multiple tasks for SNPs, and across multiple modalities for QTs. A fast optimization algorithm is proposed using the grouping information of SNPs. Compared with conventional SCCA methods, MTSCCA obtains improved performance regarding both correlation coefficients and canonical weights patterns. In addition, our method runs very fast and is easy-to-implement, and thus could provide a powerful tool for genome-wide brain-wide imaging genetic studies.

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