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A multiple splitting approach to linkage analysis in large pedigrees identifies a linkage to asthma on chromosome 12.

机译:在大型谱系中进行连锁分析的多重分裂方法可确定与12号染色体上哮喘的连锁。

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摘要

Large genealogies are potentially very informative for linkage analysis. However, the software available for exact non-parametric multipoint linkage analysis is limited with respect to the complexity of the families it can handle. A solution is to split the large pedigrees into sub-families meeting complexity constraints. Different methods have been proposed to "best" split large genealogies. Here, we propose a new procedure in which linkage is performed on several carefully chosen sub-pedigree sets from the genealogy instead of using just a single sub-pedigree set. Our multiple splitting procedure capitalizes on the sensitivity of linkage results to family structure and has been designed to control computational feasibility and global type I error. We describe and apply this procedure to the extreme case of the highly complex Hutterite pedigree and use it to perform a genome-wide linkage analysis on asthma. The detection of a genome-wide significant linkage for asthma on chromosome 12q21 illustrates the potential of this multiple splitting approach.
机译:大型家谱可能对连锁分析很有帮助。但是,就其可以处理的族的复杂性而言,可用于精确的非参数多点链接分析的软件是有限的。一种解决方案是将大型血统分成满足复杂性约束的子系列。已经提出了不同的方法来“最佳”分割大型家谱。在这里,我们提出了一种新的程序,其中对系谱学中几个精心挑选的子谱系集执行链接,而不是仅使用单个子谱系集。我们的多重拆分程序利用了链接结果对家族结构的敏感性,并已设计为控制计算可行性和全局I类错误。我们描述此程序并将其应用于高度复杂的Hutterite谱系的极端情况,并使用它对哮喘进行全基因组连锁分析。在染色体12q21上检测到哮喘的全基因组显着连锁表明了这种多重分裂方法的潜力。

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