Suppr超能文献

当亲本基因型缺失时,连锁不平衡会在多点连锁分析中夸大I型错误率。

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.

作者信息

Boyles Abee L, Scott William K, Martin Eden R, Schmidt Silke, Li Yi-Ju, Ashley-Koch Allison, Bass Meredyth P, Schmidt Michael, Pericak-Vance Margaret A, Speer Marcy C, Hauser Elizabeth R

机构信息

Center for Human Genetics, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Hum Hered. 2005;59(4):220-7. doi: 10.1159/000087122. Epub 2005 Jul 26.

Abstract

OBJECTIVES

Describe the inflation in nonparametric multipoint LOD scores due to inter-marker linkage disequilibrium (LD) across many markers with varied allele frequencies.

METHOD

Using simulated two-generation families with and without parents, we conducted nonparametric multipoint linkage analysis with 2 to 10 markers with minor allele frequencies (MAF) of 0.5 and 0.1.

RESULTS

Misspecification of population haplotype frequencies by assuming linkage equilibrium caused inflated multipoint LOD scores due to inter-marker LD when parental genotypes were not included. Inflation increased as more markers in LD were included and decreased as markers in equilibrium were added. When marker allele frequencies were unequal, the r2 measure of LD was a better predictor of inflation than D'.

CONCLUSION

This observation strongly supports the evaluation of LD in multipoint linkage analyses, and further suggests that unaccounted for LD may be suspected when two-point and multipoint linkage analyses show a marked disparity in regions with elevated r2 measures of LD. Given the increasing popularity of high-density genome-wide SNP screens, inter-marker LD should be a concern in future linkage studies.

摘要

目的

描述由于多个具有不同等位基因频率的标记间的连锁不平衡(LD)导致的非参数多点LOD评分的膨胀情况。

方法

使用有父母和无父母的模拟两代家系,我们对2至10个次要等位基因频率(MAF)为0.5和0.1的标记进行了非参数多点连锁分析。

结果

当不包括亲本基因型时,由于标记间LD,通过假设连锁平衡对群体单倍型频率的错误指定会导致多点LOD评分膨胀。随着包含更多处于LD状态的标记,膨胀增加,而随着添加处于平衡状态的标记,膨胀减少。当标记等位基因频率不相等时,LD的r2度量比D'更能预测膨胀情况。

结论

这一观察结果有力地支持了在多点连锁分析中对LD的评估,并且进一步表明,当两点和多点连锁分析在LD的r2度量升高的区域显示出明显差异时,可能存在未考虑的LD。鉴于高密度全基因组SNP筛查越来越普遍,标记间LD应成为未来连锁研究中的一个关注点。

相似文献

引用本文的文献

4
Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation.全基因组连锁研究荟萃分析男性性取向。
Arch Sex Behav. 2021 Nov;50(8):3371-3375. doi: 10.1007/s10508-021-02035-3. Epub 2021 Jun 2.
6
Mixtures with relatives and linked markers.与亲属和连锁标记的混合物。
Int J Legal Med. 2016 May;130(3):621-34. doi: 10.1007/s00414-015-1288-x. Epub 2015 Nov 27.
8
Can whole-exome sequencing data be used for linkage analysis?全外显子组测序数据能用于连锁分析吗?
Eur J Hum Genet. 2016 Apr;24(4):581-6. doi: 10.1038/ejhg.2015.143. Epub 2015 Jul 15.
10
Parkinson disease loci in the mid-western Amish.中西部阿米什人群中的帕金森病相关基因座。
Hum Genet. 2013 Nov;132(11):1213-21. doi: 10.1007/s00439-013-1316-1. Epub 2013 Jun 21.

本文引用的文献

3
The International HapMap Project.国际人类基因组单体型图计划
Nature. 2003 Dec 18;426(6968):789-96. doi: 10.1038/nature02168.
10

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验