Hierarchical mixed-model expedites genome-wide longitudinal association analysis

Author(s):  
Ying Zhang ◽  
Yuxin Song ◽  
Jin Gao ◽  
Hengyu Zhang ◽  
Ning Yang ◽  
...  

AbstractA hierarchical random regression model (Hi-RRM) was extended into a genome-wide association analysis for longitudinal data, which significantly reduced the dimensionality of repeated measurements. The Hi-RRM first modeled the phenotypic trajectory of each individual using a RRM and then associated phenotypic regressions with genetic markers using a multivariate mixed model (mvLMM). By spectral decomposition of genomic relationship and regression covariance matrices, the mvLMM was transformed into a multiple linear regression, which improved computing efficiency while implementing mvLMM associations in efficient mixed-model association expedited (EMMAX). Compared with the existing RRM-based association analyses, the statistical utility of Hi-RRM was demonstrated by simulation experiments. The method proposed here was also applied to find the quantitative trait nucleotides controlling the growth pattern of egg weights in poultry data.

Genetics ◽  
2019 ◽  
Vol 213 (4) ◽  
pp. 1225-1236 ◽  
Author(s):  
Weimiao Wu ◽  
Zhong Wang ◽  
Ke Xu ◽  
Xinyu Zhang ◽  
Amei Amei ◽  
...  

Longitudinal phenotypes have been increasingly available in genome-wide association studies (GWAS) and electronic health record-based studies for identification of genetic variants that influence complex traits over time. For longitudinal binary data, there remain significant challenges in gene mapping, including misspecification of the model for phenotype distribution due to ascertainment. Here, we propose L-BRAT (Longitudinal Binary-trait Retrospective Association Test), a retrospective, generalized estimating equation-based method for genetic association analysis of longitudinal binary outcomes. We also develop RGMMAT, a retrospective, generalized linear mixed model-based association test. Both tests are retrospective score approaches in which genotypes are treated as random conditional on phenotype and covariates. They allow both static and time-varying covariates to be included in the analysis. Through simulations, we illustrated that retrospective association tests are robust to ascertainment and other types of phenotype model misspecification, and gain power over previous association methods. We applied L-BRAT and RGMMAT to a genome-wide association analysis of repeated measures of cocaine use in a longitudinal cohort. Pathway analysis implicated association with opioid signaling and axonal guidance signaling pathways. Lastly, we replicated important pathways in an independent cocaine dependence case-control GWAS. Our results illustrate that L-BRAT is able to detect important loci and pathways in a genome scan and to provide insights into genetic architecture of cocaine use.


2020 ◽  
Vol 103 (12) ◽  
pp. 11605-11617
Author(s):  
Maria Gracia Luigi-Sierra ◽  
Vincenzo Landi ◽  
Dailu Guan ◽  
Juan Vicente Delgado ◽  
Anna Castelló ◽  
...  

2016 ◽  
Vol 177 ◽  
pp. 31-40.e6 ◽  
Author(s):  
Joon Seol Bae ◽  
InSong Koh ◽  
Hyun Sub Cheong ◽  
Jeong-Meen Seo ◽  
Dae-Yeon Kim ◽  
...  

animal ◽  
2016 ◽  
Vol 10 (10) ◽  
pp. 1602-1608 ◽  
Author(s):  
H.Y. Ji ◽  
B. Yang ◽  
Z.Y. Zhang ◽  
J. Ouyang ◽  
M. Yang ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document