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Application of an iterative Bayesian variable selection method in a genome-wide association study of rheumatoid arthritis

机译:贝叶斯迭代选择方法在类风湿关节炎全基因组关联研究中的应用

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摘要

Genome-wide association studies usually involve several hundred thousand of single-nucleotide polymorphisms (SNPs). Conventional approaches face challenges when there are enormous number of SNPs but a relatively small number of samples and, in some cases, are not feasible. We introduce here an iterative Bayesian variable selection method that provides a unique tool for association studies with a large number of SNPs (p) but a relatively small sample size (n). We applied this method to the simulated case-control sample provided by the Genetic Analysis Workshop 15 and compared its performance with stepwise variable selection method. We demonstrated that the results of iterative Bayesian variable selection applied to when p » n are as comparable as those of stepwise variable selection implemented to when n » p. When n > p, the iterative Bayesian variable selection performs better than stepwise variable selection does.
机译:全基因组关联研究通常涉及数十万个单核苷酸多态性(SNP)。当存在大量SNP但样本数量相对较少且在某些情况下不可行时,常规方法面临挑战。我们在这里介绍一种迭代贝叶斯变量选择方法,该方法为具有大量SNP(p)但样本量相对较小(n)的关联研究提供了独特的工具。我们将此方法应用于遗传分析研讨会15提供的模拟病例对照样本,并将其性能与逐步变量选择方法进行了比较。我们证明了适用于p»n的迭代贝叶斯变量选择的结果与适用于适用于n»p的逐步变量选择的结果具有可比性。当n> p时,迭代贝叶斯变量选择的性能优于逐步变量选择。

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