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Imprinting detection by extending a regression-based QTL analysis method

机译:通过扩展基于回归的QTL分析方法进行印记检测

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摘要

We present an extension of a regression-based quantitative-trait linkage analysis method to incorporate parent-of-origin effects. We separately regressed total, paternal, and maternal IBD sharing on traits’ squared sums and differences. We also developed a test for imprinting that indicates whether there is any difference between the paternal and maternal regression coefficients. Since this method treats the identity-by-descent information as the dependent variable that is conditioned on the trait, it can be readily applied to data from complex ascertainment processes. We performed a simulation study to examine the performance of the method. We found that when using empirical critical values, the method shows identical or higher power compared to existing methods for evaluation of parent-of-origin effect in linkage analysis of quantitative traits. Missing parental genotypes increase the type I error rate of the linkage test and decrease the power of the imprinting test. When the major gene has a low heritability, the power of the method decreases considerably, but the statistical tests still perform well. We also applied a permutation algorithm, which ensures the appropriate type I error rate for the test for imprinting. The method was applied to a data from a study of 6 body size related measures and 23 loci on chromosome 7 for 255 nuclear families. Multipoint identities-by-descent (IBD) were obtained using a modification of the SIMWALK 2 program. A parent-of-origin effect consistent with maternal imprinting was suggested at 99.67–111.26 Mb for body mass index, bioelectrical impedance analysis, waist circumference, and leptin concentration.
机译:我们提出了一种基于回归的定量特征连锁分析方法的扩展,以结合原产地效应。我们根据特征的平方和和差异分别回归了总IBD,父亲IBD和母亲IBD共享。我们还开发了一种印记测试,该测试表明父亲和母亲回归系数之间是否存在任何差异。由于此方法将后裔身份信息视为以特征为条件的因变量,因此可以轻松地将其应用于来自复杂确定过程的数据。我们进行了仿真研究,以检验该方法的性能。我们发现,使用经验临界值时,该方法与定量性状连锁分析中评估父代效应的现有方法相比具有相同或更高的功效。父母基因型缺失会增加连锁测试的I型错误率,并降低印迹测试的功效。当主要基因的遗传力较低时,该方法的功能会大大降低,但统计检验仍能很好地进行。我们还应用了置换算法,该算法可确保为压印测试提供适当的I类错误率。该方法被应用于来自对255个核心家庭的6种与体重相关的测量和7号染色体上23个基因座的研究数据。使用SIMWALK 2程序的修改获得了按血统的多点身份(IBD)。对于体重指数,生物电阻抗分析,腰围和瘦素浓度,建议在99.67–111.26 Mb时产生与母体印记一致的母体效应。

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  • 来源
    《Human Genetics》 |2007年第2期|159-174|共16页
  • 作者单位

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

    Department of Psychiatry Center for Neurobiology and Behavior University of Pennsylvania Philadelphia PA USA;

    Department of Psychiatry Center for Neurobiology and Behavior University of Pennsylvania Philadelphia PA USA;

    Department of Epidemiology MD Anderson Cancer Center University of Texas Unit 1340 1155 Pressler Street Houston TX 77030 USA;

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