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增强全基因组筛查中检测低频变异的能力。

Enhancing the power to detect low-frequency variants in genome-wide screens.

作者信息

Lin Chang-Yun, Xing Guan, Ku Hung-Chih, Elston Robert C, Xing Chao

机构信息

McDermott Center of Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas 75390.

出版信息

Genetics. 2014 Apr;196(4):1293-302. doi: 10.1534/genetics.113.160739. Epub 2014 Feb 4.

Abstract

In genetic association studies a conventional test statistic is proportional to the correlation coefficient between the trait and the variant, with the result that it lacks power to detect association for low-frequency variants. Considering the link between the conventional association test statistics and the linkage disequilibrium measure r(2), we propose a test statistic analogous to the standardized linkage disequilibrium D' to increase the power of detecting association for low-frequency variants. By both simulation and real data analysis we show that the proposed D' test is more powerful than the conventional methods for detecting association for low-frequency variants in a genome-wide setting. The optimal coding strategy for the D' test and its asymptotic properties are also investigated. In summary, we advocate using the D' test in a dominant model as a complementary approach to enhancing the power of detecting association for low-frequency variants with moderate to large effect sizes in case-control genome-wide association studies.

摘要

在基因关联研究中,传统的检验统计量与性状和变异之间的相关系数成正比,因此对于低频变异缺乏检测关联的能力。考虑到传统关联检验统计量与连锁不平衡度量r(2)之间的联系,我们提出了一种类似于标准化连锁不平衡D'的检验统计量,以提高检测低频变异关联的能力。通过模拟和实际数据分析,我们表明,在全基因组范围内,所提出的D'检验在检测低频变异关联方面比传统方法更具功效。我们还研究了D'检验的最优编码策略及其渐近性质。总之,我们提倡在显性模型中使用D'检验,作为在病例对照全基因组关联研究中增强检测中等到大效应大小低频变异关联能力的补充方法。

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本文引用的文献

1
Linkage disequilibrium in finite populations.有限群体中的连锁不平衡。
Theor Appl Genet. 1968 Jun;38(6):226-31. doi: 10.1007/BF01245622.
3
Measuring linkage disequilibrium by the partial correlation coefficient.用偏相关系数测量连锁不平衡。
Heredity (Edinb). 2012 Dec;109(6):401-2. doi: 10.1038/hdy.2012.54. Epub 2012 Sep 5.

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