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DETECTION OF GENETIC FACTORS ASSOCIATED WITH MULTIPLE CORRELATED IMAGING PHENOTYPES BY A SPARSE REGRESSION MODEL
被引:0
|作者:
Lin, Dongdong
[1
,2
]
Li, Jingyao
[1
,2
]
Calhoun, Vince D.
[3
,4
,5
]
Wang, Yu-Ping
[1
,2
]
机构:
[1] Tulane Univ, Dept Biomed Engn, New Orleans, LA 70118 USA
[2] Tulane Univ, Ctr Genom & Bioinformat, New Orleans, LA 70112 USA
[3] Mind Res Network, Albuquerque, NM 87106 USA
[4] LBERI, Albuquerque, NM 87106 USA
[5] Univ New Mexico, Dept Elect & Comp Engn, Albuquerque, NM 87131 USA
关键词:
Sparse low rank regression;
group ridge;
significant test;
imaging genetics;
schizophrenia;
SELECTION;
D O I:
暂无
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Recently, more evidence of polygenicity and pleiotropy has been found in genome-wide association (GWA) studies of complex psychiatric diseases (e.g., schizophrenia), where multiple interacting genetic variants may affect multiple phenotypic traits simultaneously. In this work, we propose a new sparse collaborative group-ridge low-rank regression model (sCGRLR) to study the pleiotropic effects of a group of genetic variants on multiple imaging-derived quantitative traits (i.e., endophenotype). In the method, we enforce sparse and low-rank regularizations to reduce the number of features and then construct an effective gene or gene-set based statistic test to evaluate the significance of selected features. We show the advantage of our method with other gene-set pleiotropy analysis methods and other sparse multivariate regression methods in terms of type I error and power on simulated data. Finally, we demonstrate its application to real data analysis on the study of schizophrenia.
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页码:1368 / 1371
页数:4
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