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本文引用的文献

1
Analysis of secondary phenotype involving the interactive effect of the secondary phenotype and genetic variants on the primary disease.对涉及次要表型与遗传变异对原发性疾病的交互作用的次要表型进行分析。
Ann Hum Genet. 2012 Nov;76(6):484-99. doi: 10.1111/j.1469-1809.2012.00725.x. Epub 2012 Aug 10.
2
Efficient adaptively weighted analysis of secondary phenotypes in case-control genome-wide association studies.病例对照全基因组关联研究中次要表型的高效自适应加权分析
Hum Hered. 2012;73(3):159-73. doi: 10.1159/000338943. Epub 2012 Jun 15.
3
A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studies.基于高斯 Copula 的病例对照遗传关联研究中二级表型分析方法。
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Estimation of odds ratios of genetic variants for the secondary phenotypes associated with primary diseases.遗传变异与主要疾病相关次要表型的优势比估计。
Genet Epidemiol. 2011 Apr;35(3):190-200. doi: 10.1002/gepi.20568. Epub 2011 Feb 9.
5
Using cases to strengthen inference on the association between single nucleotide polymorphisms and a secondary phenotype in genome-wide association studies.使用案例加强全基因组关联研究中单个核苷酸多态性与次要表型之间关联的推断。
Genet Epidemiol. 2010 Jul;34(5):427-33. doi: 10.1002/gepi.20495.
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Genome-wide association scans for secondary traits using case-control samples.基于病例对照样本的全基因组关联扫描分析二级特征。
Genet Epidemiol. 2009 Dec;33(8):717-28. doi: 10.1002/gepi.20424.
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Proper analysis of secondary phenotype data in case-control association studies.病例对照关联研究中次级表型数据的恰当分析。
Genet Epidemiol. 2009 Apr;33(3):256-65. doi: 10.1002/gepi.20377.
8
The CHRNA5-A3 region on chromosome 15q24-25.1 is a risk factor both for nicotine dependence and for lung cancer.位于15号染色体q24-25.1区域的CHRNA5-A3基因座是尼古丁依赖和肺癌的一个风险因素。
J Natl Cancer Inst. 2008 Nov 5;100(21):1552-6. doi: 10.1093/jnci/djn363. Epub 2008 Oct 28.
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Estimating odds ratios in genome scans: an approximate conditional likelihood approach.估计基因组扫描中的优势比:一种近似条件似然方法。
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Genome-wide association analysis identifies 20 loci that influence adult height.全基因组关联分析确定了20个影响成人身高的基因座。
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病例对照关联研究中次要性状的统一分析

Unified Analysis of Secondary Traits in Case-Control Association Studies.

作者信息

Ghosh Arpita, Wright Fred A, Zou Fei

机构信息

Public Health Foundation of India, New Delhi, India.

Department of Biostatistics, University of North Carolina at Chapel Hill, North Carolina, USA.

出版信息

J Am Stat Assoc. 2013;108(502). doi: 10.1080/01621459.2013.793121.

DOI:10.1080/01621459.2013.793121
PMID:24409003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3881430/
Abstract

It has been repeatedly shown that in case-control association studies, analysis of a secondary trait which ignores the original sampling scheme can produce highly biased risk estimates. Although a number of approaches have been proposed to properly analyze secondary traits, most approaches fail to reproduce the marginal logistic model assumed for the original case-control trait and/or do not allow for interaction between secondary trait and genotype marker on primary disease risk. In addition, the flexible handling of covariates remains challenging. We present a general retrospective likelihood framework to perform association testing for both binary and continuous secondary traits which respects marginal models and incorporates the interaction term. We provide a computational algorithm, based on a reparameterized approximate profile likelihood, for obtaining the maximum likelihood (ML) estimate and its standard error for the genetic effect on secondary trait, in presence of covariates. For completeness we also present an alternative pseudo-likelihood method for handling covariates. We describe extensive simulations to evaluate the performance of the ML estimator in comparison with the pseudo-likelihood and other competing methods.

摘要

反复表明,在病例对照关联研究中,对次要性状进行分析时若忽略原始抽样方案,可能会产生高度有偏的风险估计。尽管已提出多种方法来正确分析次要性状,但大多数方法无法重现为原始病例对照性状假设的边际逻辑模型,和/或不考虑次要性状与基因型标记对原发性疾病风险的相互作用。此外,协变量的灵活处理仍然具有挑战性。我们提出了一个通用的回顾性似然框架,用于对二元和连续次要性状进行关联检验,该框架尊重边际模型并纳入了交互项。我们提供了一种基于重新参数化的近似轮廓似然的计算算法,用于在存在协变量的情况下获得次要性状遗传效应的最大似然(ML)估计及其标准误差。为了完整性,我们还提出了一种处理协变量的替代伪似然方法。我们描述了广泛的模拟,以评估ML估计器与伪似然及其他竞争方法相比的性能。