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A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.一项关于唇裂伴或不伴腭裂的全基因组关联研究鉴定了 MAFB 和 ABCA4 附近的风险变异。
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2
Note on the sampling error of the difference between correlated proportions or percentages.关于相关比例或百分比差异的抽样误差说明。
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3
Efficient evaluation of ranking procedures when the number of units is large, with application to SNP identification.当单位数量很大时对排序程序的有效评估及其在单核苷酸多态性识别中的应用。
Biom J. 2010 Feb;52(1):34-49. doi: 10.1002/bimj.200900044.
4
Bayes factors for genome-wide association studies: comparison with P-values.全基因组关联研究的贝叶斯因子:与P值的比较。
Genet Epidemiol. 2009 Jan;33(1):79-86. doi: 10.1002/gepi.20359.
5
Two-stage group sequential robust tests in family-based association studies: controlling type I error.基于家系的关联研究中的两阶段成组序贯稳健检验:控制I型错误
Ann Hum Genet. 2008 Jul;72(Pt 4):557-65. doi: 10.1111/j.1469-1809.2008.00435.x. Epub 2008 Mar 5.
6
A genome-wide association study identifies novel risk loci for type 2 diabetes.一项全基因组关联研究确定了2型糖尿病的新风险位点。
Nature. 2007 Feb 22;445(7130):881-5. doi: 10.1038/nature05616. Epub 2007 Feb 11.
7
Family-based designs in the age of large-scale gene-association studies.大规模基因关联研究时代的基于家系的设计。
Nat Rev Genet. 2006 May;7(5):385-94. doi: 10.1038/nrg1839.
8
Power and related statistical properties of conditional likelihood score tests for association studies in nuclear families with parental genotypes.核心家庭中基于父母基因型的关联研究的条件似然比检验的功效及相关统计特性
Ann Hum Genet. 2005 May;69(Pt 3):296-314. doi: 10.1046/j.1529-8817.2005.00169.x.
9
Exploiting gene-environment independence in family-based case-control studies: increased power for detecting associations, interactions and joint effects.在基于家系的病例对照研究中利用基因-环境独立性:增强检测关联、相互作用和联合效应的效能。
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10
"Power comparisons for genotypic vs. allelic TDT methods with >2 alleles".具有两个以上等位基因的基因型与等位基因传递不平衡检验(TDT)方法的效能比较
Genet Epidemiol. 2002 Nov;23(4):458-61; author reply 462-4. doi: 10.1002/gepi.10192.

基于精确分析参数估计的病例-双亲三联体数据中SNP和基因-环境相互作用的快速检测。

Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation.

作者信息

Schwender Holger, Taub Margaret A, Beaty Terri H, Marazita Mary L, Ruczinski Ingo

机构信息

TU Dortmund University, 44221 Dortmund, Germany.

出版信息

Biometrics. 2012 Sep;68(3):766-73. doi: 10.1111/j.1541-0420.2011.01713.x. Epub 2011 Dec 7.

DOI:10.1111/j.1541-0420.2011.01713.x
PMID:22150644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3387527/
Abstract

Case-parent trio studies concerned with children affected by a disease and their parents aim to detect single nucleotide polymorphisms (SNPs) showing a preferential transmission of alleles from the parents to their affected offspring. A popular statistical test for detecting such SNPs associated with disease in this study design is the genotypic transmission/disequilibrium test (gTDT) based on a conditional logistic regression model, which usually needs to be fitted by an iterative procedure. In this article, we derive exact closed-form solutions for the parameter estimates of the conditional logistic regression models when testing for an additive, a dominant, or a recessive effect of a SNP, and show that such analytic parameter estimates also exist when considering gene-environment interactions with binary environmental variables. Because the genetic model underlying the association between a SNP and a disease is typically unknown, it might further be beneficial to use the maximum over the gTDT statistics for the possible effects of a SNP as test statistic. We therefore propose a procedure enabling a fast computation of the test statistic and the permutation-based p-value of this MAX gTDT. All these methods are applied to whole-genome scans of the case-parent trios from the International Cleft Consortium. These applications show our procedures dramatically reduce the required computing time compared to the conventional iterative methods allowing, for example, the analysis of hundreds of thousands of SNPs in a few minutes instead of several hours.

摘要

病例-双亲三联体研究关注受疾病影响的儿童及其父母,旨在检测单核苷酸多态性(SNP),这些多态性显示出等位基因从父母向其患病后代的优先传递。在该研究设计中,用于检测此类与疾病相关的SNP的一种常用统计检验是基于条件逻辑回归模型的基因型传递/不平衡检验(gTDT),该模型通常需要通过迭代程序进行拟合。在本文中,我们推导了在检验SNP的加性、显性或隐性效应时条件逻辑回归模型参数估计的精确闭式解,并表明在考虑与二元环境变量的基因-环境相互作用时也存在此类解析参数估计。由于SNP与疾病之间关联的潜在遗传模型通常未知,将SNP可能效应的gTDT统计量的最大值用作检验统计量可能会更有益。因此,我们提出了一种程序,能够快速计算该MAX gTDT的检验统计量和基于置换的p值。所有这些方法都应用于国际腭裂联盟病例-双亲三联体的全基因组扫描。这些应用表明,与传统的迭代方法相比,我们的程序显著减少了所需的计算时间,例如,可以在几分钟内而不是几小时内分析数十万SNP。