SMetABF: A rapid algorithm for Bayesian GWAS meta-analysis with a large number of studies included

被引:3
|
作者
Sun, Jianle [1 ]
Lyu, Ruiqi [1 ]
Deng, Luojia [1 ]
Li, Qianwen [1 ]
Zhao, Yang [2 ]
Zhang, Yue [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Dept Bioinformat & Biostat, Shanghai, Peoples R China
[2] Nanjing Med Univ, Dept Biostat, Sch Publ Hlth, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
GENOME-WIDE ASSOCIATION; INFLAMMATORY-BOWEL-DISEASE; PARKINSONS-DISEASE; RISK LOCI; GENETIC RISK; SUSCEPTIBILITY LOCI; IDENTIFICATION; VARIANTS; REGION; SNCA;
D O I
10.1371/journal.pcbi.1009948
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bayesian methods are widely used in the GWAS meta-analysis. But the considerable consumption in both computing time and memory space poses great challenges for large-scale meta-analyses. In this research, we propose an algorithm named SMetABF to rapidly obtain the optimal ABF in the GWAS meta-analysis, where shotgun stochastic search (SSS) is introduced to improve the Bayesian GWAS meta-analysis framework, MetABF. Simulation studies confirm that SMetABF performs well in both speed and accuracy, compared to exhaustive methods and MCMC. SMetABF is applied to real GWAS datasets to find several essential loci related to Parkinson's disease (PD) and the results support the underlying relationship between PD and other autoimmune disorders. Developed as an R package and a web tool, SMetABF will become a useful tool to integrate different studies and identify more variants associated with complex traits.
引用
收藏
页数:18
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