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基于回归的二分类性状传递/不平衡检验:连锁和关联联合检验的功效。

A regression based transmission/disequilibrium test for binary traits: the power of joint tests for linkage and association.

机构信息

Case Western Reserve University, Department of Epidemiology and Biostatistics, Cleveland, OH 44106, USA.

出版信息

BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S95. doi: 10.1186/1471-2156-6-S1-S95.

Abstract

BACKGROUND

In this analysis we applied a regression based transmission disequilibrium test to the binary trait presence or absence of Kofendred Personality Disorder in the Genetic Analysis Workshop 14 (GAW14) simulated dataset and determined the power and type I error rate of the method at varying map densities and sample sizes. To conduct this transmission disequilibrium test, the logit transformation was applied to a binary outcome and regressed on an indicator variable for the transmitted allele from informative matings. All 100 replicates from chromosomes 1, 3, 5, and 9 for the Aipotu and the combined Aipotu, Karangar, and Danacaa populations were used at densities of 3, 1, and 0.3 cM. Power and type I error were determined by the number of replicates significant at the 0.05 level.

RESULTS

The maximum power to detect linkage and association with the Aipotu population was 93% for chromosome 3 using a 0.3-cM map. For chromosomes 1, 5, and 9 the power was less than 10% at the 3-cM scan and less than 22% for the 0.3-cM map. With the larger sample size, power increased to 38% for chromosome 1, 100% for chromosome 3, 31% for chromosome 5, and 23% for chromosome 9. Type I error was approximately 7%.

CONCLUSION

The power of this method is highly dependent on the amount of information in a region. This study suggests that single-point methods are not particularly effective in narrowing a fine-mapping region, particularly when using single-nucleotide polymorphism data and when linkage disequilibrium in the region is variable.

摘要

背景

在这项分析中,我们将基于回归的传递不平衡检验应用于二进制性状 Kofendred 人格障碍的存在或缺失,在遗传分析工作坊 14(GAW14)模拟数据集中,并确定了在不同图谱密度和样本大小下该方法的功效和Ⅰ型错误率。为了进行这种传递不平衡检验,我们将二项式结果应用于对数转换,并回归于来自信息性交配的传递等位基因的指示变量。在 3、1 和 0.3 cM 的密度下,使用 Aipotu 和合并的 Aipotu、Karangar 和 Danacaa 群体的 100 个染色体 1、3、5 和 9 的重复项进行分析。通过在 0.05 水平显著的重复项数量来确定功效和Ⅰ型错误。

结果

使用 0.3-cM 图谱,Aipotu 群体检测连锁和关联的最大功效为 93%,对于染色体 3。对于染色体 1、5 和 9,在 3-cM 扫描时的功效小于 10%,在 0.3-cM 图谱时的功效小于 22%。随着样本量的增加,对于染色体 1,功效增加到 38%,对于染色体 3,功效增加到 100%,对于染色体 5,功效增加到 31%,对于染色体 9,功效增加到 23%。Ⅰ型错误约为 7%。

结论

这种方法的功效高度依赖于一个区域的信息量。本研究表明,单点方法在缩小精细映射区域方面不是特别有效,特别是在使用单核苷酸多态性数据并且区域内连锁不平衡变化时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc3/1866684/5ee9701bc78b/1471-2156-6-S1-S95-1.jpg

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