Suppr超能文献

校正由单核苷酸多态性发现过程导致的确定偏差的θ和 Tajima's D估计量。

Correcting estimators of theta and Tajima's D for ascertainment biases caused by the single-nucleotide polymorphism discovery process.

作者信息

Ramírez-Soriano Anna, Nielsen Rasmus

机构信息

Department of Biology, University of Copenhagen, 2100 Kbh Ø, Copenhagen, Denmark.

出版信息

Genetics. 2009 Feb;181(2):701-10. doi: 10.1534/genetics.108.094060. Epub 2008 Dec 15.

Abstract

Most single-nucleotide polymorphism (SNP) data suffer from an ascertainment bias caused by the process of SNP discovery followed by SNP genotyping. The final genotyped data are biased toward an excess of common alleles compared to directly sequenced data, making standard genetic methods of analysis inapplicable to this type of data. We here derive corrected estimators of the fundamental population genetic parameter = 4N(e)mu (N(e), effective population size; mu, mutation rate) on the basis of the average number of pairwise differences and on the basis of the number of segregating sites. We also derive the variances and covariances of these estimators and provide a corrected version of Tajima's D statistic. We reanalyze a human genomewide SNP data set and find substantial differences in the results with or without ascertainment bias correction.

摘要

大多数单核苷酸多态性(SNP)数据都存在由SNP发现过程随后,随后SNP基因分型所导致的确认偏倚。与直接测序数据相比,最终的基因分型数据偏向于常见等位基因过多,使得标准的遗传分析方法不适用于这类数据。我们在此基于成对差异的平均数和基于分离位点的数量,推导出基本群体遗传参数 = 4N(e)μ(N(e),有效群体大小;μ,突变率)的校正估计值。我们还推导了这些估计值的方差和协方差,并提供了Tajima's D统计量的校正版本。我们重新分析了一个人类全基因组SNP数据集,发现校正或未校正确认偏倚时结果存在显著差异。

相似文献

8
How array design creates SNP ascertainment bias.基因芯片设计如何导致 SNP 确认偏倚。
PLoS One. 2021 Mar 30;16(3):e0245178. doi: 10.1371/journal.pone.0245178. eCollection 2021.

引用本文的文献

3
Population genomics of the eastern cottonwood ().东部杨属植物()的群体基因组学
Ecol Evol. 2017 Oct 10;7(22):9426-9440. doi: 10.1002/ece3.3466. eCollection 2017 Nov.
5
Inferring positive selection in humans from genomic data.从基因组数据推断人类的正选择。
Investig Genet. 2015 Apr 1;6:5. doi: 10.1186/s13323-015-0023-1. eCollection 2015.
10
Rare variant density across the genome and across populations.全基因组及不同人群中的罕见变异密度。
BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S39. doi: 10.1186/1753-6561-5-S9-S39.

本文引用的文献

3
Autosomal recessive hypercholesterolemia in Spanish kindred due to a large deletion in the ARH gene.
Mol Genet Metab. 2007 Nov;92(3):243-8. doi: 10.1016/j.ymgme.2007.06.012. Epub 2007 Aug 7.
5
Localizing recent adaptive evolution in the human genome.定位人类基因组中近期的适应性进化
PLoS Genet. 2007 Jun;3(6):e90. doi: 10.1371/journal.pgen.0030090. Epub 2007 Apr 20.
6
Positive natural selection in the human lineage.人类谱系中的正向自然选择。
Science. 2006 Jun 16;312(5780):1614-20. doi: 10.1126/science.1124309.
9
A map of recent positive selection in the human genome.人类基因组中近期正选择图谱。
PLoS Biol. 2006 Mar;4(3):e72. doi: 10.1371/journal.pbio.0040072. Epub 2006 Mar 7.

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