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估计大型家系中方差成分连锁分析的效能。

Estimating the power of variance component linkage analysis in large pedigrees.

作者信息

Chen Wei-Min, Abecasis Gonçalo R

机构信息

Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Genet Epidemiol. 2006 Sep;30(6):471-84. doi: 10.1002/gepi.20160.

Abstract

Variance component linkage analysis is commonly used to map quantitative trait loci (QTLs) in general pedigrees. Large pedigrees are especially attractive for these studies because they provide greater power per genotyped individual than small pedigrees. We propose accurate and computationally efficient methods to calculate the analytical power of variance component linkage analysis that can accommodate large pedigrees. Our analytical power computation involves the approximation of the noncentrality parameter for the likelihood-ratio test by its Taylor expansions. We develop efficient algorithms to compute the second and third moments of the identical by descent (IBD) sharing distribution and enable rapid computation of the Taylor expansions. Our algorithms take advantage of natural symmetries in pedigrees and can accurately analyze many large pedigrees in a few seconds. We verify the accuracy of our power calculation via simulation in pedigrees with 2-5 generations and 2-8 siblings per sibship. We apply this proposed analytical power calculation to 98 quantitative traits in a cohort study of 6,148 Sardinians in which the largest pedigree includes 625 phenotyped individuals. Simulations based on eight representative traits show that the difference between our analytical estimation of the expected LOD score and the average of simulated LOD scores is less than 0.05 (1.5%). Although our analytical calculations are for a fully informative marker locus, in the settings we examined power was similar to what could be attained with a single nucleotide polymorphism (SNP) mapping panel (with >1 SNP/cM). Our algorithms for power analysis together with polygenic analysis are implemented in a freely available computer program, POLY.

摘要

方差成分连锁分析常用于在一般家系中定位数量性状基因座(QTL)。大型家系对这些研究特别有吸引力,因为与小型家系相比,它们为每个基因分型个体提供了更大的功效。我们提出了准确且计算高效的方法来计算方差成分连锁分析的分析功效,该方法能够处理大型家系。我们的分析功效计算涉及通过泰勒展开式对方差比检验的非中心参数进行近似。我们开发了高效算法来计算同源相同(IBD)共享分布的二阶和三阶矩,并能够快速计算泰勒展开式。我们的算法利用了家系中的自然对称性,能够在几秒钟内准确分析许多大型家系。我们通过在具有2至5代且每个同胞组有2至8个兄弟姐妹的家系中进行模拟,验证了我们功效计算的准确性。我们将这种提出的分析功效计算应用于对6148名撒丁岛人的队列研究中的98个数量性状,其中最大的家系包括625个表型个体。基于八个代表性性状的模拟表明,我们对预期LOD得分的分析估计与模拟LOD得分平均值之间的差异小于0.05(1.5%)。尽管我们的分析计算是针对完全信息性标记位点的,但在我们研究的设置中,功效与使用单核苷酸多态性(SNP)图谱面板(每厘摩>1个SNP)所能达到的功效相似。我们的功效分析算法与多基因分析一起在一个免费的计算机程序POLY中实现。

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