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A multilocus linkage disequilibrium measure based on mutual information theory and its applications

机译:基于互信息理论的多位连锁不平衡测度及其应用

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Evaluating the patterns of linkage disequilibrium (LD) is important for association mapping study as well as for studying the genomic architecture of human genome (e.g., haplotype block structures). Commonly used bi-allelic pairwise measures for assessing LD between two loci, such as r 2 and D′, may not make full and efficient use of modern multilocus data. Though extended to multilocus scenarios, their performance is still questionable. Meanwhile, most existing measures for an entire multilocus region, such as normalized entropy difference, do not consider existence of LD heterogeneity across the region under investigation. Additionally, these existing multilocus measures cannot handle distant regions where long-range LD patterns may exist. In this study, we proposed a novel multilocus LD measure developed based on mutual information theory. Our proposed measure described LD pattern between two chromosome regions each of which may consist of multiple loci (including multi-allele loci). As such, the proposed measure can better characterize LD patterns between two arbitrary regions. As potential applications, we developed algorithms on the proposed measure for partitioning haplotype blocks and for selecting haplotype tagging SNPs (htSNPs), which were helpful for follow-up association tests. The results on both simulated and empirical data showed that our LD measure had distinct advantages over pairwise and other multilocus measures. First, our measure was more robust, and can capture comprehensively the LD information between neighboring as well as disjointed regions. Second, haplotype blocks were better described via our proposed measure. Furthermore, association tests with htSNPs from the proposed algorithm had improved power over tests on single markers and on haplotypes. Keywords Entropy - Mutual information - Linkage disequilibrium (LD) - Multilocus LD - Haplotype block - Haplotype tagging SNPs (htSNPs)
机译:评估连锁不平衡(LD)的模式对于关联作图研究以及研究人类基因组的基因组架构(例如单倍型区块结构)都很重要。用于评估两个基因座之间的LD的常用双等位基因成对测量,例如r 2 和D',可能无法充分有效地利用现代多基因座数据。尽管扩展到多场所方案,但它们的性能仍然值得怀疑。同时,针对整个多基因座区域的大多数现有度量(例如归一化熵差)并未考虑整个调查区域中LD异质性的存在。此外,这些现有的多位置测量无法处理可能存在远程LD模式的遥远区域。在这项研究中,我们提出了一种基于互信息理论开发的新颖的多位点LD测度。我们提出的措施描述了两个染色体区域之间的LD模式,每个染色体区域可能由多个基因座(包括多等位基因基因座)组成。这样,所提出的措施可以更好地表征两个任意区域之间的LD图案。作为潜在的应用程序,我们在建议的度量标准上开发了算法,用于划分单倍型模块和选择单倍型标记SNP(htSNP),这对于后续的关联测试很有帮助。模拟和经验数据的结果都表明,我们的LD度量比成对度量和其他多场所度量具有明显的优势。首先,我们的措施更加可靠,可以全面捕获相邻区域和不相连区域之间的LD信息。其次,通过我们提出的方法可以更好地描述单体型模块。此外,与拟议算法中的htSNPs的关联测试具有比单个标记和单倍型更高的测试能力。熵-互信息-连锁不平衡(LD)-多基因座LD-单倍型模块-单倍型标记SNP(htSNP)

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