A Bayesian Hierarchical Framework for Pathway Analysis in Genome-Wide Association Studies.

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Human Heredity Pub Date : 2019-01-01 Epub Date: 2020-09-23 DOI:10.1159/000508664
Lei Zhang, Charalampos Papachristou, Pankaj K Choudhary, Swati Biswas
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引用次数: 1

Abstract

Background: Pathway analysis allows joint consideration of multiple SNPs belonging to multiple genes, which in turn belong to a biologically defined pathway. This type of analysis is usually more powerful than single-SNP analyses for detecting joint effects of variants in a pathway.

Methods: We develop a Bayesian hierarchical model by fully modeling the 3-level hierarchy, namely, SNP-gene-pathway that is naturally inherent in the structure of the pathways, unlike the currently used ad hoc ways of combining such information. We model the effects at each level conditional on the effects of the levels preceding them within the generalized linear model framework. To deal with the high dimensionality, we regularize the regression coefficients through an appropriate choice of priors. The model is fit using a combination of iteratively weighted least squares and expectation-maximization algorithms to estimate the posterior modes and their standard errors. A normal approximation is used for inference.

Results: We conduct simulations to study the proposed method and find that our method has higher power than some standard approaches in several settings for identifying pathways with multiple modest-sized variants. We illustrate the method by analyzing data from two genome-wide association studies on breast and renal cancers.

Conclusion: Our method can be helpful in detecting pathway association.

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全基因组关联研究中通路分析的贝叶斯层次框架。
背景:通路分析允许联合考虑属于多个基因的多个snp,而这些基因又属于一个生物学定义的通路。这种类型的分析通常比单snp分析更强大,用于检测途径中变体的联合效应。方法:我们开发了一个贝叶斯层次模型,完全模拟了3级层次结构,即snp -基因通路,这是通路结构中自然固有的,不像目前使用的组合这些信息的特别方法。在广义线性模型框架内,我们以前一层的效果为条件,对每一层的效果进行建模。为了处理高维,我们通过适当选择先验来正则化回归系数。采用迭代加权最小二乘法和期望最大化算法对模型进行拟合,估计后验模态及其标准误差。正态近似用于推理。结果:我们进行了模拟来研究所提出的方法,并发现我们的方法在识别具有多个中等大小变量的路径的几个设置中比一些标准方法具有更高的功率。我们通过分析乳腺癌和肾癌两项全基因组关联研究的数据来说明这种方法。结论:该方法有助于检测途径关联。
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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