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本文引用的文献

1
Comparison of univariate and multivariate linkage analysis of traits related to hypertension.高血压相关性状的单变量和多变量连锁分析比较
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S99. doi: 10.1186/1753-6561-3-s7-s99.
2
A framework for analyzing both linkage and association: an analysis of Genetic Analysis Workshop 16 simulated data.一种用于分析连锁和关联的框架:对遗传分析研讨会16模拟数据的分析
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S98. doi: 10.1186/1753-6561-3-s7-s98.
3
New score tests for age-at-onset linkage analysis in general pedigrees.用于一般家系发病年龄连锁分析的新计分检验。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S97. doi: 10.1186/1753-6561-3-s7-s97.
4
Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results.利用全基因组连锁结果对北美类风湿性关节炎联盟和弗雷明汉心脏研究数据进行全基因组关联分析。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S103. doi: 10.1186/1753-6561-3-s7-s103.
5
Contrasting identity-by-descent estimators, association studies, and linkage analyses using the Framingham Heart Study data.使用弗雷明汉心脏研究数据对比同源性估计方法、关联研究和连锁分析。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S102. doi: 10.1186/1753-6561-3-s7-s102.
6
Identifying association under a previous linkage peak on chromosome 16 for body mass index using cross-sectional and longitudinal data of the Framingham Heart Study.利用弗雷明汉心脏研究的横断面和纵向数据,在16号染色体上先前的连锁峰下鉴定体重指数的关联。
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S101. doi: 10.1186/1753-6561-3-s7-s101.
7
Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood-ratio test and conditional score statistic.数量性状的全基因组关联与连锁分析:似然比检验与条件得分统计量的比较
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S100. doi: 10.1186/1753-6561-3-s7-s100.
8
Calculating asymptotic significance levels of the constrained likelihood ratio test with application to multivariate genetic linkage analysis.计算约束似然比检验的渐近显著性水平及其在多变量遗传连锁分析中的应用
Stat Appl Genet Mol Biol. 2009;8(1):Article 39. doi: 10.2202/1544-6115.1456. Epub 2009 Sep 17.
9
Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies.全基因组连锁研究是否浪费时间?在全基因组关联研究中利用候选区域。
Genet Epidemiol. 2010 Feb;34(2):107-18. doi: 10.1002/gepi.20438.
10
Conditional tests for localizing trait genes.用于定位性状基因的条件检验。
Hum Hered. 2009;68(2):139-50. doi: 10.1159/000218112. Epub 2009 May 11.

结合连锁分析和关联分析方法的信息。

Combining information from linkage and association methods.

机构信息

Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington 98195, USA.

出版信息

Genet Epidemiol. 2009;33 Suppl 1(Suppl 1):S81-7. doi: 10.1002/gepi.20477.

DOI:10.1002/gepi.20477
PMID:19924706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2910520/
Abstract

Group 12 evaluated approaches to incorporate outside information or otherwise optimize traditional linkage and association analyses. The abundance of available data allowed exploration of identity-by-descent (IBD) estimation, score statistics, formal combination of linkage and association testing, significance estimation, and replication. We observed that IBD estimation can be optimized with a subset of marker data while estimation of inheritance vectors can provide both IBD estimates and a measure of their uncertainty. Score statistics incorporating covariates or combining association and linkage information performed at least as well as standard approaches while requiring less computation time. The formal combination of linkage and association methods may be fruitful, although the nature of the simulated data limited our conclusions. Estimation of significance may be improved through simulation, correction for cryptic relatedness, and the inclusion of prior information. Replication using real data provided consistent results, though the same was not true of simulated data replicates. Overall, we found that increasing the amount of available data limits analyses due to computational constraints and motivates the need to improve methods for the identification of complex-trait genes.

摘要

第 12 组评估了将外部信息纳入或优化传统连锁和关联分析的方法。可用数据的丰富性允许探索血缘关系(IBD)估计、评分统计、连锁和关联测试的正式组合、显著性估计和复制。我们观察到,IBD 估计可以通过标记数据的子集进行优化,而遗传向量的估计可以提供 IBD 估计及其不确定性的度量。包含协变量的评分统计或结合关联和连锁信息的方法至少与标准方法一样有效,同时需要更少的计算时间。连锁和关联方法的正式组合可能是富有成效的,尽管模拟数据的性质限制了我们的结论。通过模拟、纠正隐性亲缘关系和纳入先验信息可以提高显著性估计。使用真实数据进行复制提供了一致的结果,尽管模拟数据的复制品并非如此。总的来说,我们发现,可用数据量的增加由于计算限制而限制了分析,并促使需要改进用于识别复杂性状基因的方法。