Computational Tools for Causal Inference in Genetics

被引:4
|
作者
Richardson, Tom G. [1 ]
Zheng, Jie [1 ]
Gaunt, Tom R. [1 ]
机构
[1] Univ Bristol, Bristol Med Sch, MRC Integrat Epidemiol Unit IEU, Populat Hlth Sci, Bristol BS8 2BN, Avon, England
来源
基金
英国医学研究理事会;
关键词
MENDELIAN RANDOMIZATION; SNP HERITABILITY; GWAS; DISEASES; RISK; ASSOCIATIONS; DATABASE; GENES; EQTL;
D O I
10.1101/cshperspect.a039248
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The advent of large-scale, phenotypically rich, and readily accessible data provides an unprecedented opportunity for epidemiologists, statistical geneticists, bioinformaticians, and also behavioral and social scientists to investigate the causes and consequences of disease. Computational tools and resources are an integral component of such endeavors, which will become increasingly important as these data continue to grow exponentially. In this review, we have provided an overview of computational software and databases that have been developed to assist with analyses in causal inference. This includes online tools that can be used to help generate hypotheses, publicly accessible resources that store summary-level information for millions of genetic markers, and computational approaches that can be used to leverage this wealth of data to study causal relationships.
引用
收藏
页数:13
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