从基因型关联研究中发现表型网络与肥胖症的应用。

Pub Date : 2015-01-01 DOI:10.1504/ijdmb.2015.069414
Christine W Duarte, Yann C Klimentidis, Jacqueline J Harris, Michelle Cardel, José R Fernández
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引用次数: 3

摘要

全基因组关联研究(GWAS)已经发现了许多与肥胖相关的特征的风险变异。然而,在实现这些发现的临床相关性之前,需要发现这些风险变异的分子或生理机制。一种策略是对表型丰富的数据源进行数据挖掘,例如dbGAP(基因型和表型数据库)中存在的数据,以生成假设。在这里,我们提出了一种技术,将现有贝叶斯网络(BN)学习算法的力量与结构方程建模(SEM)的统计严谨性相结合,以产生具有最佳性能的整体表型网络发现系统。我们通过分析来自AMERICO样本的候选SNP数据集来说明我们的方法,AMERICO样本是一个多种族的横断面队列,大约有300名具有详细的肥胖相关表型的儿童。我们通过展示三个肥胖相关snp的遗传机制来证明我们的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Discovery of phenotypic networks from genotypic association studies with application to obesity.

Genome-wide Association Studies (GWAS) have resulted in many discovered risk variants for several obesity-related traits. However, before clinical relevance of these discoveries can be achieved, molecular or physiological mechanisms of these risk variants needs to be discovered. One strategy is to perform data mining of phenotypically-rich data sources such as those present in dbGAP (database of Genotypes and Phenotypes) for hypothesis generation. Here we propose a technique that combines the power of existing Bayesian Network (BN) learning algorithms with the statistical rigour of Structural Equation Modelling (SEM) to produce an overall phenotypic network discovery system with optimal properties. We illustrate our method using the analysis of a candidate SNP data set from the AMERICO sample, a multi-ethnic cross-sectional cohort of roughly 300 children with detailed obesity-related phenotypes. We demonstrate our approach by showing genetic mechanisms for three obesity-related SNPs.

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