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本文引用的文献

1
The power to detect linkage in complex disease by means of simple LOD-score analyses.通过简单的对数优势分数分析来检测复杂疾病中连锁关系的能力。
Am J Hum Genet. 1998 Sep;63(3):870-9. doi: 10.1086/301997.
2
Exact elods and exact power for affected sib pairs analyzed for linkage under simple right and wrong models.在简单的正确和错误模型下,对受影响的同胞对进行连锁分析时的精确似然比和精确功效。
Am J Med Genet. 1998 Feb 7;81(1):66-72.
3
Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation.核心家庭中用于连锁检测的非参数统计方法比较:单标记评估
Am J Hum Genet. 1997 Dec;61(6):1431-44. doi: 10.1086/301635.
4
Can we find genes for schizophrenia?我们能找到精神分裂症的基因吗?
Am J Med Genet. 1997 Feb 21;74(1):104-11. doi: 10.1002/(sici)1096-8628(19970221)74:1<104::aid-ajmg21>3.0.co;2-u.
5
Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study.单基因座连锁分析在多种模型上最大化时的I型错误大小:一项模拟研究。
Am J Hum Genet. 1997 Jan;60(1):217-27.
6
Parametric and nonparametric linkage analysis: a unified multipoint approach.参数和非参数连锁分析:一种统一的多点方法。
Am J Hum Genet. 1996 Jun;58(6):1347-63.
7
Conclusion of LOD-score analysis for family data generated under two-locus models.基于双基因座模型生成的家系数据的对数优势评分(LOD-score)分析结论。
Am J Hum Genet. 1996 Jun;58(6):1338-46.
8
Affecteds-only linkage methods are not a panacea.仅针对患者的连锁分析方法并非万灵药。
Am J Hum Genet. 1996 Apr;58(4):892-5.
9
Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures.寡基因性状连锁分析中单基因座近似法的充分性:扩展到多代系谱结构
Hum Hered. 1993 Nov-Dec;43(6):329-36. doi: 10.1159/000154155.
10
Conclusions of segregation analysis for family data generated under two-locus models.基于双基因座模型生成的家系数据的分离分析结论。
Am J Hum Genet. 1993 Dec;53(6):1338-46.

与非参数方法相比,LOD 分数功效增加的进一步证据。

Further evidence for the increased power of LOD scores compared with nonparametric methods.

作者信息

Durner M, Vieland V J, Greenberg D A

机构信息

Department of Psychiatry, Mount Sinai Medical Center, New York, USA.

出版信息

Am J Hum Genet. 1999 Jan;64(1):281-9. doi: 10.1086/302181.

DOI:10.1086/302181
PMID:9915967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1377726/
Abstract

In genetic analysis of diseases in which the underlying model is unknown, "model free" methods-such as affected sib pair (ASP) tests-are often preferred over LOD-score methods, although LOD-score methods under the correct or even approximately correct model are more powerful than ASP tests. However, there might be circumstances in which nonparametric methods will outperform LOD-score methods. Recently, Dizier et al. reported that, in some complex two-locus (2L) models, LOD-score methods with segregation analysis-derived parameters had less power to detect linkage than ASP tests. We investigated whether these particular models, in fact, represent a situation that ASP tests are more powerful than LOD scores. We simulated data according to the parameters specified by Dizier et al. and analyzed the data by using a (a) single locus (SL) LOD-score analysis performed twice, under a simple dominant and a recessive mode of inheritance (MOI), (b) ASP methods, and (c) nonparametric linkage (NPL) analysis. We show that SL analysis performed twice and corrected for the type I-error increase due to multiple testing yields almost as much linkage information as does an analysis under the correct 2L model and is more powerful than either the ASP method or the NPL method. We demonstrate that, even for complex genetic models, the most important condition for linkage analysis is that the assumed MOI at the disease locus being tested is approximately correct, not that the inheritance of the disease per se is correctly specified. In the analysis by Dizier et al., segregation analysis led to estimates of dominance parameters that were grossly misspecified for the locus tested in those models in which ASP tests appeared to be more powerful than LOD-score analyses.

摘要

在潜在模型未知的疾病基因分析中,“无模型”方法(如患病同胞对(ASP)检验)通常比对数优势计分法更受青睐,尽管在正确甚至近似正确的模型下,对数优势计分法比ASP检验更具效力。然而,在某些情况下,非参数方法可能会比对数优势计分法表现更优。最近,迪齐耶等人报告称,在一些复杂的双基因座(2L)模型中,采用分离分析得出的参数的对数优势计分法检测连锁的效力低于ASP检验。我们研究了这些特定模型实际上是否代表了ASP检验比对数优势计分更具效力的情况。我们根据迪齐耶等人指定的参数模拟数据,并通过以下方法分析数据:(a)在简单显性和隐性遗传模式(MOI)下进行两次单基因座(SL)对数优势计分分析;(b)ASP方法;(c)非参数连锁(NPL)分析。我们表明,进行两次SL分析并针对多重检验导致的I型错误增加进行校正后,所产生的连锁信息几乎与在正确的2L模型下进行的分析一样多,并且比ASP方法或NPL方法更具效力。我们证明,即使对于复杂的遗传模型,连锁分析的最重要条件是所测试疾病基因座假定的MOI大致正确,而不是疾病本身的遗传被正确指定。在迪齐耶等人的分析中,分离分析得出的显性参数估计值在那些ASP检验似乎比对数优势计分分析更具效力的模型中,对于所测试的基因座存在严重错误指定。