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Small-sample performance of the robust score test and its modifications in generalized estimating equations.稳健得分检验及其在广义估计方程中的修正方法的小样本性能。
Stat Med. 2005 Nov 30;24(22):3479-95. doi: 10.1002/sim.2161.
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Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci.在前列腺癌易感基因座的基因组连锁筛选中微卫星与单核苷酸多态性的比较。
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An efficient Monte Carlo approach to assessing statistical significance in genomic studies.一种用于评估基因组研究中统计显著性的高效蒙特卡罗方法。
Bioinformatics. 2005 Mar;21(6):781-7. doi: 10.1093/bioinformatics/bti053. Epub 2004 Sep 28.
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Genome linkage screen for prostate cancer susceptibility loci: results from the Mayo Clinic Familial Prostate Cancer Study.前列腺癌易感基因座的全基因组连锁分析:梅奥诊所家族性前列腺癌研究结果
Prostate. 2003 Dec 1;57(4):335-46. doi: 10.1002/pros.10308.
7
Regression models for linkage: issues of traits, covariates, heterogeneity, and interaction.连锁分析的回归模型:性状、协变量、异质性及相互作用问题
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Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus.在一个奠基者群体中进行的新型病例对照试验确定P选择素是一个特应性易感基因座。
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9
Detecting gene-gene interactions using affected sib pair analysis with covariates.使用带有协变量的患病同胞对分析来检测基因-基因相互作用。
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通过拟似然得分统计量对亲属对和协变量进行遗传连锁检验。

Testing genetic linkage with relative pairs and covariates by quasi-likelihood score statistics.

作者信息

Schaid Daniel J, Sinnwell Jason P, Thibodeau Stephen N

机构信息

Division of Biostatistics, Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

出版信息

Hum Hered. 2007;64(4):220-33. doi: 10.1159/000103751. Epub 2007 Jun 12.

DOI:10.1159/000103751
PMID:17565225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2880728/
Abstract

BACKGROUND/AIMS: Genetic linkage analysis of common diseases is complicated by the heterogeneity of genetic and environmental factors that increase disease risk, and possibly interactions among them. Most linkage methods that account for covariates are restricted to sib pairs, with the exception of the conditional logistic regression model [1] implemented in LODPAL in the S.A.G.E. software [2]. Although this model can be applied to arbitrary pedigrees, at times it can be difficult to maximize the likelihood due to model constraints, and it does not account for the dependence among the different types of relative pairs in a pedigree.

METHODS

To overcome these limitations, we developed a new approach based on score statistics for quasi- likelihoods, implemented as weighted least squares. Our methods can be used to test three different hypotheses: (1) a test for linkage without covariates; (2) a test for linkage with covariates, and (3) a test for effects of covariates on identity by descent sharing (i.e., heterogeneity). Furthermore, our methods are robust because they account for the dependence among different relative pairs within a pedigree.

RESULTS AND CONCLUSION

Although application of our methods to a prostate cancer linkage study did not find any critical covariates in our data, the results illustrate the utility and interpretation of our methods, and suggest, nonetheless, that our methods will be useful for a broad range of genetic linkage heterogeneity analyses.

摘要

背景/目的:常见疾病的基因连锁分析因增加疾病风险的遗传和环境因素的异质性以及它们之间可能的相互作用而变得复杂。大多数考虑协变量的连锁方法仅限于同胞对,S.A.G.E.软件[2]中的LODPAL所实现的条件逻辑回归模型[1]除外。尽管该模型可应用于任意家系,但有时由于模型限制可能难以使似然最大化,并且它没有考虑家系中不同类型亲属对之间的依赖性。

方法

为克服这些局限性,我们基于拟似然得分统计量开发了一种新方法,通过加权最小二乘法实现。我们的方法可用于检验三种不同的假设:(1)无协变量时的连锁检验;(2)有协变量时的连锁检验;(3)协变量对同源性共享(即异质性)的影响检验。此外,我们的方法具有稳健性,因为它们考虑了家系中不同亲属对之间的依赖性。

结果与结论

尽管将我们的方法应用于前列腺癌连锁研究未在我们的数据中发现任何关键协变量,但结果说明了我们方法的实用性和解释力,并且表明,尽管如此,我们的方法将对广泛的基因连锁异质性分析有用。