Human Genetics, Genome Institute of Singapore, Singapore, Singapore.
BMC Genomics. 2013 Aug 21;14:569. doi: 10.1186/1471-2164-14-569.
Although single-SNP analysis has proven to be useful in identifying many disease-associated loci, region-based analysis has several advantages. Empirically, it has been shown that region-based genotype and haplotype approaches may possess much higher power than single-SNP statistical tests. Both high quality haplotypes and genotypes may be available for analysis given the development of next generation sequencing technologies and haplotype assembly algorithms.
As generally it is unknown whether genotypes or haplotypes are more relevant for identifying an association, we propose to use both of them with the purpose of preserving high power under both genotype and haplotype disease scenarios. We suggest two approaches for a combined association test and investigate the performance of these two approaches based on a theoretical model, population genetics simulations and analysis of a real data set.
Based on a theoretical model, population genetics simulations and analysis of a central corneal thickness (CCT) Genome Wide Association Study (GWAS) data set we have shown that combined genotype and haplotype approach has a high potential utility for applications in association studies.
尽管单核苷酸多态性分析已被证明在识别许多疾病相关基因座方面非常有用,但基于区域的分析具有几个优势。经验表明,基于区域的基因型和单倍型方法可能比单核苷酸多态性统计检验具有更高的功效。鉴于下一代测序技术和单倍型组装算法的发展,可能有高质量的单倍型和基因型可供分析。
由于通常未知基因型或单倍型对于识别关联是否更相关,我们建议同时使用这两种方法,目的是在基因型和单倍型疾病情况下均保持高功效。我们提出了两种联合关联检验方法,并基于理论模型、群体遗传学模拟和对真实数据集的分析来研究这两种方法的性能。
基于理论模型、群体遗传学模拟和对中央角膜厚度(CCT)全基因组关联研究(GWAS)数据集的分析,我们表明,联合基因型和单倍型方法在关联研究中的应用具有很高的潜在效用。