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本文引用的文献

1
Asymptotic tests of association with multiple SNPs in linkage disequilibrium.与处于连锁不平衡状态的多个单核苷酸多态性(SNP)相关联的渐近检验。
Genet Epidemiol. 2009 Sep;33(6):497-507. doi: 10.1002/gepi.20402.
2
A principal components regression approach to multilocus genetic association studies.一种用于多位点基因关联研究的主成分回归方法。
Genet Epidemiol. 2008 Feb;32(2):108-18. doi: 10.1002/gepi.20266.
3
PLINK: a tool set for whole-genome association and population-based linkage analyses.PLINK:一个用于全基因组关联分析和基于群体的连锁分析的工具集。
Am J Hum Genet. 2007 Sep;81(3):559-75. doi: 10.1086/519795. Epub 2007 Jul 25.
4
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.肌萎缩侧索硬化症及神经功能正常对照人群的全基因组基因分型:第一阶段分析及数据公开发布
Lancet Neurol. 2007 Apr;6(4):322-8. doi: 10.1016/S1474-4422(07)70037-6.
5
Principal components analysis corrects for stratification in genome-wide association studies.主成分分析可校正全基因组关联研究中的分层现象。
Nat Genet. 2006 Aug;38(8):904-9. doi: 10.1038/ng1847. Epub 2006 Jul 23.
6
Use of unphased multilocus genotype data in indirect association studies.在间接关联研究中使用未分型的多位点基因型数据。
Genet Epidemiol. 2004 Dec;27(4):415-28. doi: 10.1002/gepi.20032.
7
Haploview: analysis and visualization of LD and haplotype maps.Haploview:连锁不平衡(LD)和单倍型图谱的分析与可视化
Bioinformatics. 2005 Jan 15;21(2):263-5. doi: 10.1093/bioinformatics/bth457. Epub 2004 Aug 5.
8
TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS.人类遗传学中重组率值的异质性检验
Ann Hum Genet. 1963 Nov;27:175-82. doi: 10.1111/j.1469-1809.1963.tb00210.x.
9
Qualitative semi-parametric test for genetic associations in case-control designs under structured populations.结构化人群中病例对照设计下基因关联的定性半参数检验。
Ann Hum Genet. 2003 May;67(Pt 3):250-64. doi: 10.1046/j.1469-1809.2003.00036.x.
10
Genome association studies of complex diseases by case-control designs.通过病例对照设计对复杂疾病进行全基因组关联研究。
Am J Hum Genet. 2003 Apr;72(4):850-68. doi: 10.1086/373966. Epub 2003 Mar 19.

基于二项混合模型的遗传异质性关联检验

Binomial mixture model-based association tests under genetic heterogeneity.

作者信息

Zhou Hui, Pan Wei

机构信息

Division of Biostatistics, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Ann Hum Genet. 2009 Nov;73(Pt 6):614-30. doi: 10.1111/j.1469-1809.2009.00542.x. Epub 2009 Sep 1.

DOI:10.1111/j.1469-1809.2009.00542.x
PMID:19725835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3354651/
Abstract

Most of the existing association tests for population-based case-control studies are based on comparing the mean genotype scores between the case and control groups, which may not be efficient under genetic heterogeneity. Given that most common diseases are genetically heterogeneous, caused by mutations in multiple loci, it may be beneficial to fully account for genetic heterogeneity in an association test. Here we first propose a binomial mixture model for such a purpose and develop a corresponding mixture likelihood ratio test (MLRT) for a single locus. We also consider two methods to combine single-locus-based MLRTs across multiple loci in linkage disequilibrium to boost power when causal SNPs are not genotyped. We show with a wide spectrum of numerical examples that under genetic heterogeneity the proposed tests are more powerful than some commonly used association tests.

摘要

大多数现有的基于人群的病例对照研究的关联检验是基于比较病例组和对照组之间的平均基因型得分,在遗传异质性情况下这可能效率不高。鉴于大多数常见疾病是遗传异质性的,由多个位点的突变引起,在关联检验中充分考虑遗传异质性可能是有益的。在此,我们首先为此目的提出一个二项混合模型,并针对单个位点开发相应的混合似然比检验(MLRT)。我们还考虑了两种方法,用于在连锁不平衡的多个位点上组合基于单个位点的MLRT,以便在未对因果单核苷酸多态性(SNP)进行基因分型时提高检验效能。我们通过广泛的数值示例表明,在遗传异质性情况下,所提出的检验比一些常用的关联检验更具效能。