首页> 外文期刊>Annals of Human Genetics >Design and analysis of genetic association studies to finely map a locus identified by linkage analysis: assessment of the extent to which an association can account for the linkage.
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Design and analysis of genetic association studies to finely map a locus identified by linkage analysis: assessment of the extent to which an association can account for the linkage.

机译:遗传关联研究的设计和分析,以精确绘制通过连锁分析确定的基因座:评估连锁可以解释连锁的程度。

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Association studies are often used to finely map quantitative trait loci identified by linkage analysis. Once a polymorphism associated with the trait has been identified, it may be useful to conduct linkage analyses which adjust for this polymorphism to determine the extent to which the association accounts for the linkage signal. However, methods for conducting statistical significance tests for an observed reduction in the linkage signal are not well developed. In the present study we develop methods for assessment of the statistical significance of an observed reduction in the variance due to the linked locus, with variance components or with Haseman-Elston linkage methods. Simulations indicate that these methods have appropriate levels of type I error and that, like other association statistics, their power depends on the magnitude of linkage disequilibrium between functional and marker alleles and on the extent of similarity between the frequency of the functional allele and the frequency of the associated marker allele. These methods can help determine which association results are likely due to strong linkage disequilibrium with functional alleles and, thus, can facilitate the selection of small chromosomal regions for more extensive study.
机译:关联研究通常用于精细绘制通过连锁分析确定的数量性状基因座。一旦识别出与性状相关的多态性,进行连锁分析可能会很有用,该分析针对该多态性进行调整,以确定关联说明连锁信号的程度。然而,对于观察到的连锁信号减少进行统计显着性检验的方法还没有得到很好的发展。在本研究中,我们开发了一种方法,用于评估因链接的基因座,方差分量或Haseman-Elston链接方法而导致的方差减少的统计显着性。仿真表明,这些方法具有适当的I型错误水平,并且像其他关联统计一样,它们的功效取决于功能和等位基因之间的连锁不平衡程度以及功能等位基因频率和频率之间的相似程度相关标记的等位基因。这些方法可以帮助确定哪些关联结果可能是由于与功能性等位基因之间的强烈连锁不平衡所致,因此可以促进小染色体区域的选择,以进行更广泛的研究。

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