• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

一种用于检测候选基因或区域中多个单核苷酸多态性(SNP)与遗传关联的统一框架:对比病例组和对照组之间的基因型得分和连锁不平衡模式。

A unified framework for detecting genetic association with multiple SNPs in a candidate gene or region: contrasting genotype scores and LD patterns between cases and controls.

作者信息

Pan Wei

机构信息

Division of Biostatistics, MMC 303, School of Public Health, University of Minnesota, Minneapolis, MN 55455-0392, USA.

出版信息

Hum Hered. 2010;69(1):1-13. doi: 10.1159/000243149. Epub 2009 Oct 2.

DOI:10.1159/000243149
PMID:19797904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2880731/
Abstract

It is critical to develop and apply powerful statistical tests for genetic association studies due to typically weak associations with complex human diseases or phenotypes. For population-based case-control studies with unphased multilocus genotype data, most of the existing methods are based on comparing genotype scores, e.g. allele frequencies, between the case and control groups. Another class of approaches are motivated to contrast linkage disequilibrium (LD) patterns between the two groups. It is expected that no single test can be uniformly most powerful across all situations, and different tests may perform better under different scenarios. A recent effort has been devoted to combining the above two classes of approaches, which however has some potential drawbacks. Here we propose a general and simple framework to unify the above two classes of approaches: it is based on the simple idea to incorporate LD measurements, in addition to genotype scores, as covariates in a logistic regression model, from which various tests can be constructed by taking advantage of the nice properties of the score statistics for the logistic model. It also has an advantage in easily accommodating covariates and other study designs. We use simulated data to show that our proposed tests performed well across several scenarios. In particular, in contrast to either of the two classes of the tests that is only powerful in detecting only one, but not both, of the two types of the distributional differences between cases and controls, our proposed tests are sensitive to both.

摘要

由于与复杂人类疾病或表型的关联通常较弱,因此开发和应用强大的基因关联研究统计检验至关重要。对于基于人群的病例对照研究,若有未分型的多位点基因型数据,现有的大多数方法都是基于比较病例组和对照组之间的基因型得分,例如等位基因频率。另一类方法旨在对比两组之间的连锁不平衡(LD)模式。预计没有单一的检验能在所有情况下都是最强大的,不同的检验在不同的场景下可能表现得更好。最近有人致力于将上述两类方法结合起来,然而这有一些潜在的缺点。在此,我们提出一个通用且简单的框架来统一上述两类方法:它基于一个简单的想法,即在逻辑回归模型中,除了基因型得分外,将LD测量值作为协变量纳入,利用逻辑模型得分统计量的良好性质,可以从中构建各种检验。它在轻松纳入协变量和其他研究设计方面也具有优势。我们使用模拟数据表明,我们提出的检验在几种情况下都表现良好。特别是,与仅能有效检测病例组和对照组之间两种分布差异中的一种(而非两种)的两类检验中的任何一类相比,我们提出的检验对两者都敏感。

相似文献

1
A unified framework for detecting genetic association with multiple SNPs in a candidate gene or region: contrasting genotype scores and LD patterns between cases and controls.一种用于检测候选基因或区域中多个单核苷酸多态性(SNP)与遗传关联的统一框架:对比病例组和对照组之间的基因型得分和连锁不平衡模式。
Hum Hered. 2010;69(1):1-13. doi: 10.1159/000243149. Epub 2009 Oct 2.
2
Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression.强大的多标记关联测试:基于基因组距离的回归和逻辑回归的统一。
Genet Epidemiol. 2010 Nov;34(7):680-8. doi: 10.1002/gepi.20529.
3
Single-marker and two-marker association tests for unphased case-control genotype data, with a power comparison.单标记和双标记关联检验用于非相位病例对照基因型数据,并进行了效能比较。
Genet Epidemiol. 2010 Jan;34(1):67-77. doi: 10.1002/gepi.20436.
4
Contrasting linkage disequilibrium as a multilocus family-based association test.连锁不平衡的多基因座家系关联检验方法比较
Genet Epidemiol. 2011 Sep;35(6):487-98. doi: 10.1002/gepi.20598. Epub 2011 Jul 18.
5
Analysis of single-locus tests to detect gene/disease associations.用于检测基因/疾病关联的单基因座测试分析。
Genet Epidemiol. 2005 Apr;28(3):207-19. doi: 10.1002/gepi.20050.
6
A multilocus linkage disequilibrium measure based on mutual information theory and its applications.基于互信息理论的多基因座连锁不平衡测度及其应用。
Genetica. 2009 Dec;137(3):355-64. doi: 10.1007/s10709-009-9399-2. Epub 2009 Aug 26.
7
Gene-based interaction analysis by incorporating external linkage disequilibrium information.基于基因的交互作用分析,纳入外部连锁不平衡信息。
Eur J Hum Genet. 2011 Feb;19(2):164-72. doi: 10.1038/ejhg.2010.164. Epub 2010 Oct 6.
8
Improving power in contrasting linkage-disequilibrium patterns between cases and controls.提高病例组与对照组之间对比连锁不平衡模式的检验效能。
Am J Hum Genet. 2007 May;80(5):911-20. doi: 10.1086/516794. Epub 2007 Mar 28.
9
Increasing power of genome-wide association studies by collecting additional single-nucleotide polymorphisms.通过收集额外的单核苷酸多态性来提高全基因组关联研究的效力。
Genetics. 2011 Jun;188(2):449-60. doi: 10.1534/genetics.111.128595. Epub 2011 Apr 5.
10
Comparison of linkage disequilibrium estimated from genotypes versus haplotypes for crossbred populations.杂交群体中基于基因型和单倍型估计的连锁不平衡比较。
Genet Sel Evol. 2022 Feb 8;54(1):12. doi: 10.1186/s12711-022-00703-z.

引用本文的文献

1
Two-phase SSU and SKAT in genetic association studies.基因关联研究中的两阶段SSU和SKAT
J Genet. 2020;99.
2
A Bayesian approach to identify genes and gene-level SNP aggregates in a genetic analysis of cancer data.一种用于在癌症数据遗传分析中识别基因和基因水平SNP聚合体的贝叶斯方法。
Stat Interface. 2015;8(2):137-151. doi: 10.4310/SII.2015.v8.n2.a2.
3
Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory.对人类遗传学领域的思考:呼吁加强疾病遗传学理论
Front Genet. 2016 Jun 8;7:106. doi: 10.3389/fgene.2016.00106. eCollection 2016.
4
Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection.通过贝叶斯潜在变量选择进行全基因组关联研究的多单核苷酸多态性集分析
Genet Epidemiol. 2015 Dec;39(8):664-77. doi: 10.1002/gepi.21932. Epub 2015 Oct 30.
5
A Bayesian Partitioning Model for the Detection of Multilocus Effects in Case-Control Studies.用于病例对照研究中多位点效应检测的贝叶斯划分模型。
Hum Hered. 2015;79(2):69-79. doi: 10.1159/000369858. Epub 2015 Jun 3.
6
A composite likelihood approach to latent multivariate Gaussian modeling of SNP data with application to genetic association testing.一种用于SNP数据潜在多变量高斯建模的复合似然方法及其在基因关联测试中的应用。
Biometrics. 2012 Mar;68(1):307-15. doi: 10.1111/j.1541-0420.2011.01649.x. Epub 2011 Aug 12.
7
Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression.强大的多标记关联测试:基于基因组距离的回归和逻辑回归的统一。
Genet Epidemiol. 2010 Nov;34(7):680-8. doi: 10.1002/gepi.20529.
8
Test selection with application to detecting disease association with multiple SNPs.应用于检测疾病与多个单核苷酸多态性(SNP)关联的测试选择。
Hum Hered. 2010;69(2):120-30. doi: 10.1159/000264449. Epub 2009 Dec 4.

本文引用的文献

1
Asymptotic tests of association with multiple SNPs in linkage disequilibrium.与处于连锁不平衡状态的多个单核苷酸多态性(SNP)相关联的渐近检验。
Genet Epidemiol. 2009 Sep;33(6):497-507. doi: 10.1002/gepi.20402.
2
Gains in power for exhaustive analyses of haplotypes using variable-sized sliding window strategy: a comparison of association-mapping strategies.使用可变大小滑动窗口策略对单倍型进行详尽分析时的功效提升:关联映射策略的比较。
Eur J Hum Genet. 2009 Jun;17(6):785-92. doi: 10.1038/ejhg.2008.244. Epub 2008 Dec 17.
3
On combining triads and unrelated subjects data in candidate gene studies: an application to data on testicular cancer.在候选基因研究中合并三联体和无关个体的数据:在睾丸癌数据中的应用
Hum Hered. 2009;67(2):88-103. doi: 10.1159/000179557. Epub 2008 Dec 12.
4
Genetic mapping in human disease.人类疾病中的基因定位
Science. 2008 Nov 7;322(5903):881-8. doi: 10.1126/science.1156409.
5
A new association test to test multiple-marker association.一种用于测试多标记关联的新关联测试。
Genet Epidemiol. 2009 Feb;33(2):164-71. doi: 10.1002/gepi.20369.
6
Analysis of multiple SNPs in a candidate gene or region.对候选基因或区域中的多个单核苷酸多态性进行分析。
Genet Epidemiol. 2008 Sep;32(6):560-6. doi: 10.1002/gepi.20330.
7
Simple association analysis combining data from trios/sibships and unrelated controls.结合三联体/同胞对数据和无关对照数据的简单关联分析。
Genet Epidemiol. 2008 Sep;32(6):520-7. doi: 10.1002/gepi.20325.
8
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.全基因组研究:TRAF1-C5作为类风湿关节炎的一个风险基因座
N Engl J Med. 2007 Sep 20;357(12):1199-209. doi: 10.1056/NEJMoa073491. Epub 2007 Sep 5.
9
Improving power in contrasting linkage-disequilibrium patterns between cases and controls.提高病例组与对照组之间对比连锁不平衡模式的检验效能。
Am J Hum Genet. 2007 May;80(5):911-20. doi: 10.1086/516794. Epub 2007 Mar 28.
10
Improved power by use of a weighted score test for linkage disequilibrium mapping.通过使用加权评分检验进行连锁不平衡定位来提高功效。
Am J Hum Genet. 2007 Feb;80(2):353-60. doi: 10.1086/511312. Epub 2006 Dec 21.