• 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

Extended pedigree patterned covariance matrix mixed models for quantitative phenotype analysis.

作者信息

Schork N J

机构信息

Department of Medicine, University of Michigan, Ann Arbor 48109-0500.

出版信息

Genet Epidemiol. 1992;9(2):73-86. doi: 10.1002/gepi.1370090202.

DOI:10.1002/gepi.1370090202
PMID:1639246
Abstract

Overt computational constraints in the formation of mixed models for the analysis of large extended-pedigree quantitative trait data which allow one to reliably characterize and partition sources of variation resulting from a variety sources have proven difficult to overcome. The present paper suggests that by combining a restricted patterned covariance matrix approach to modeling and partitioning the variation arising from polygenic and environmental forces with an Elston-Stewart like algorithmic approach to modeling variation resulting from a single genetic locus with large phenotypic effects one can produce a model that is at once intuitively appealing, efficient computationally, and reliable numerically. Extensions and variations of this approach are also discussed, as are some simulation and timing studies carried out in an effort to validate the accuracy and computational efficiency of the proposed methodology.

摘要

相似文献

1
Extended pedigree patterned covariance matrix mixed models for quantitative phenotype analysis.
Genet Epidemiol. 1992;9(2):73-86. doi: 10.1002/gepi.1370090202.
2
Efficient computation of patterned covariance matrix mixed models in quantitative segregation analysis.
Genet Epidemiol. 1991;8(1):29-46. doi: 10.1002/gepi.1370080104.
3
Detection of genetic heterogeneity for complex quantitative phenotypes.复杂定量表型的遗传异质性检测。
Genet Epidemiol. 1992;9(3):207-23. doi: 10.1002/gepi.1370090307.
4
Quantitative trait linkage analysis by generalized estimating equations: unification of variance components and Haseman-Elston regression.基于广义估计方程的数量性状连锁分析:方差分量与哈斯曼-埃尔斯顿回归的统一
Genet Epidemiol. 2004 May;26(4):265-72. doi: 10.1002/gepi.10315.
5
Pedigree analysis package (PAP) vs. MORGAN: model selection and hypothesis testing on a large pedigree.
Genet Epidemiol. 1998;15(4):355-69. doi: 10.1002/(SICI)1098-2272(1998)15:4<355::AID-GEPI3>3.0.CO;2-1.
6
A unified approach to joint modeling of multiple quantitative and qualitative traits in gene mapping.基因定位中多个定量和定性性状联合建模的统一方法。
J Theor Biol. 2002 Oct 21;218(4):435-46.
7
Linkage and association studies of QTL for nuclear families by mixed models.利用混合模型对核心家庭数量性状基因座进行连锁和关联研究。
Biostatistics. 2003 Jan;4(1):75-95. doi: 10.1093/biostatistics/4.1.75.
8
Variance components analysis for pedigree-based censored survival data using generalized linear mixed models (GLMMs) and Gibbs sampling in BUGS.使用广义线性混合模型(GLMMs)和BUGS中的吉布斯抽样对基于家系的删失生存数据进行方差成分分析。
Genet Epidemiol. 2000 Sep;19(2):127-48. doi: 10.1002/1098-2272(200009)19:2<127::AID-GEPI2>3.0.CO;2-S.
9
A likelihood approach for quantitative-trait-locus mapping with selected pedigrees.一种利用选定家系进行数量性状基因座定位的似然方法。
Biometrics. 2005 Jun;61(2):465-73. doi: 10.1111/j.1541-0420.2005.031213.x.
10
Pedigree analysis for quantitative traits: variance components without matrix inversion.数量性状的系谱分析:无需矩阵求逆的方差成分
Biometrics. 1990 Jun;46(2):399-413.

引用本文的文献

1
Conservation of Distinct Genetically-Mediated Human Cortical Pattern.独特的基因介导的人类皮质模式的保守性。
PLoS Genet. 2016 Jul 26;12(7):e1006143. doi: 10.1371/journal.pgen.1006143. eCollection 2016 Jul.
2
Mixed-effects models for joint modeling of sequence data in longitudinal studies.纵向研究中序列数据联合建模的混合效应模型。
BMC Proc. 2014 Jun 17;8(Suppl 1):S92. doi: 10.1186/1753-6561-8-S1-S92. eCollection 2014.
3
A comprehensive genetic study on left atrium size in Caribbean Hispanics identifies potential candidate genes in 17p10.
一项针对加勒比西班牙裔左心房大小的全面基因研究在17号染色体短臂10区鉴定出潜在的候选基因。
Circ Cardiovasc Genet. 2010 Aug;3(4):386-92. doi: 10.1161/CIRCGENETICS.110.938381. Epub 2010 Jun 19.
4
Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis.在多米尼加家庭中,新的数量性状基因座被定位到12号染色体短臂11区,与左心室质量相关:中风风险与颈动脉粥样硬化家庭研究。
BMC Med Genet. 2009 Jul 23;10:74. doi: 10.1186/1471-2350-10-74.
5
Heritability and linkage analysis for carotid intima-media thickness: the family study of stroke risk and carotid atherosclerosis.颈动脉内膜中层厚度的遗传力与连锁分析:中风风险与颈动脉粥样硬化的家族研究
Stroke. 2009 Jul;40(7):2307-12. doi: 10.1161/STROKEAHA.109.554121. Epub 2009 Jun 4.
6
Use of multivariate linkage analysis for dissection of a complex cognitive trait.使用多变量连锁分析剖析复杂认知特征。
Am J Hum Genet. 2003 Mar;72(3):561-70. doi: 10.1086/368201. Epub 2003 Feb 13.