首页> 外文期刊>European journal of human genetics: EJHG >Combined high resolution linkage and association mapping of quantitative trait loci.
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Combined high resolution linkage and association mapping of quantitative trait loci.

机译:高分辨率连锁和数量性状基因座的关联映射。

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In this paper, we investigate variance component models of both linkage analysis and high resolution linkage disequilibrium (LD) mapping for quantitative trait loci (QTL). The models are based on both family pedigree and population data. We consider likelihoods which utilize flanking marker information, and carry out an analysis of model building and parameter estimations. The likelihoods jointly include recombination fractions, LD coefficients, the average allele substitution effect and allele dominant effect as parameters. Hence, the model simultaneously takes care of the linkage, LD or association and the effects of the putative trait locus. The models clearly demonstrate that linkage analysis and LD mapping are complementary, not exclusive, methods for QTL mapping. By power calculations and comparisons, we show the advantages of the proposed method: (1) population data can provide information for LD mapping, and family pedigree data can provide information for both linkage analysis and LD mapping; (2) using family pedigree data and a sparse marker map, one may investigate the prior suggestive linkage between trait locus and markers to obtain low resolution of the trait loci, because linkage analysis can locate a broad candidate region; (3) with the prior knowledge of suggestive linkage from linkage analysis, both population and family pedigree data can be used simultaneously in high resolution LD mapping based on a dense marker map, since LD mapping can increase the resolution for candidate regions; (4) models of high resolution LD mappings using two flanking markers have higher power than that of models of using only one marker in the analysis; (5) excluding the dominant variance from the analysis when it does exist would lose power; (6) by performing linkage interval mappings, one may get higher power than by using only one marker in the analysis.European Journal of Human Genetics (2003) 11, 125-137. doi:10.1038/sj.ejhg.5200941
机译:在本文中,我们研究了连锁分析和高分辨率连锁不平衡(LD)作图的定量特征位点(QTL)的方差成分模型。该模型基于家庭血统和人口数据。我们考虑利用侧翼标记信息的可能性,并进行模型构建和参数估计的分析。可能性共同包括重组分数,LD系数,平均等位基因替代效应和等位基因优势效应作为参数。因此,模型同时考虑了连锁,LD或关联以及假定性状位点的影响。这些模型清楚地表明,连锁分析和LD映射是QTL映射的补充而非唯一方法。通过功效计算和比较,我们证明了该方法的优点:(1)人口数据可以为LD映射提供信息,而家族谱系数据可以为连锁分析和LD映射提供信息; (2)利用家族谱系数据和稀疏的标记图,可以研究性状基因座和标记之间先前的暗示性连锁关系,从而获得较低的性状基因座分辨率,因为连锁分析可以找到较宽的候选区域; (3)在具有从连锁分析中暗示连锁的先验知识的基础上,可以基于密集标记图在高分辨率LD映射中同时使用人口和家谱数据,因为LD映射可以提高候选区域的分辨率; (4)在分析中使用两个侧翼标记的高分辨率LD映射模型具有比仅使用一个标记的模型更高的功效; (5)在分析存在时将主导方差从分析中排除会失去能力; (6)通过执行连锁间隔作图,可以得到比仅使用一种标记更高的功效。欧洲人类遗传学杂志(2003)11,125-137。 doi:10.1038 / sj.ejhg.5200941

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