TY - GEN
T1 - Fast Multi-Task SCCA Learning with Feature Selection for Multi-Modal Brain Imaging Genetics
AU - Du, Lei
AU - Liu, Kefei
AU - Yao, Xiaohui
AU - Risacher, Shannon L.
AU - Han, Junwei
AU - Guo, Lei
AU - Saykin, Andrew J.
AU - Shen, Li
N1 - Publisher Copyright:
© 2018 IEEE.
PY - 2019/1/21
Y1 - 2019/1/21
N2 - 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) method-s are widely used since they are superior to those independent and pairwise univariate analyses. MTL methods generally incorporate a few 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 G21-norm regularization, MTSCCA treats all SNPs in the same group together to enforce sparsity at the group level. The ℓ2,1-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.
AB - 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) method-s are widely used since they are superior to those independent and pairwise univariate analyses. MTL methods generally incorporate a few 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 G21-norm regularization, MTSCCA treats all SNPs in the same group together to enforce sparsity at the group level. The ℓ2,1-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.
KW - Brain Imaging Genetics
KW - Multi-task SCCA
KW - Sparse Canonical Correlation Analysis
UR - https://www.scopus.com/pages/publications/85062566388
U2 - 10.1109/BIBM.2018.8621298
DO - 10.1109/BIBM.2018.8621298
M3 - 会议稿件
AN - SCOPUS:85062566388
T3 - Proceedings - 2018 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2018
SP - 356
EP - 361
BT - Proceedings - 2018 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2018
A2 - Schmidt, Harald
A2 - Griol, David
A2 - Wang, Haiying
A2 - Baumbach, Jan
A2 - Zheng, Huiru
A2 - Callejas, Zoraida
A2 - Hu, Xiaohua
A2 - Dickerson, Julie
A2 - Zhang, Le
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2018 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2018
Y2 - 3 December 2018 through 6 December 2018
ER -