• 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

Lods, wrods, and mods: the interpretation of lod scores calculated under different models.

作者信息

Hodge S E, Elston R C

机构信息

Department of Psychiatry, Columbia University, New York, New York.

出版信息

Genet Epidemiol. 1994;11(4):329-42. doi: 10.1002/gepi.1370110403.

DOI:10.1002/gepi.1370110403
PMID:7813895
Abstract

In this paper we examine the relationships among classical lod scores, "wrod" scores (lod scores calculated under the wrong genetic model), and "mod" scores (lod scores maximized over genetic model parameters). We compare the behavior of these scores when the state of nature is linkage to their behavior when the state of nature is no linkage. We describe sufficient conditions for mod scores to be valid and discuss their use to determine the correct genetic model. We show that lod scores represent a likelihood-ratio test for independence. We explain the "ascertainment-assumption-free" aspect of using mod scores to determine mode of inheritance and we set this aspect into a well-established statistical framework. Finally, we summarize practical guidelines for the use of mod scores.

摘要

相似文献

1
Lods, wrods, and mods: the interpretation of lod scores calculated under different models.
Genet Epidemiol. 1994;11(4):329-42. doi: 10.1002/gepi.1370110403.
2
Determining linkage and mode of inheritance: mode scores and other methods.
Genet Epidemiol. 1996;13(6):575-93. doi: 10.1002/(SICI)1098-2272(1996)13:6<575::AID-GEPI4>3.0.CO;2-#.
3
Multipoint lods provide reliable linkage evidence despite unknown limiting distribution: type I error probabilities decrease with sample size for multipoint lods and mods.尽管极限分布未知,但多点对数优势分数(LODs)仍能提供可靠的连锁证据:对于多点LODs和修正后的LODs,I型错误概率会随着样本量的增加而降低。
Genet Epidemiol. 2008 Dec;32(8):800-15. doi: 10.1002/gepi.20350.
4
Distribution and magnitude of type I error of model-based multipoint lod scores: implications for multipoint mod scores.基于模型的多点对数优势分数的I型错误分布及大小:对多点改良分数的影响
Genet Epidemiol. 2006 Jul;30(5):447-58. doi: 10.1002/gepi.20157.
5
MOD-score analysis with simple pedigrees: an overview of likelihood-based linkage methods.基于简单家系的MOD评分分析:基于似然性的连锁分析方法概述
Hum Hered. 2007;64(3):192-202. doi: 10.1159/000102992. Epub 2007 May 25.
6
Using parametric multipoint lods and mods for linkage analysis requires a shift in statistical thinking.使用参数多点对数优势评分(LODs)和模型进行连锁分析需要统计学思维的转变。
Hum Hered. 2011;72(4):264-75. doi: 10.1159/000331463. Epub 2011 Dec 23.
7
Distribution of lod scores under uncertain mode of inheritance.在不确定遗传模式下对数优势分数的分布。
Am J Hum Genet. 1993 Feb;52(2):354-61.
8
Using lod-score differences to determine mode of inheritance: a simple, robust method even in the presence of heterogeneity and reduced penetrance.使用对数优势比分差来确定遗传模式:一种简单、稳健的方法,即使存在基因异质性和外显率降低的情况。
Am J Hum Genet. 1994 Oct;55(4):834-40.
9
Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases.复杂疾病连锁分析中简单对数优势比分(LOD)分数与正态乘积统计量(NPL)分数之间的直接功效比较。
Am J Hum Genet. 1999 Sep;65(3):847-57. doi: 10.1086/302536.
10
TDT with covariates and genomic screens with mod scores: their behavior on simulated data.带有协变量的传递不平衡检验以及具有修正分数的基因组筛选:它们在模拟数据上的表现。
Genet Epidemiol. 1995;12(6):659-64. doi: 10.1002/gepi.1370120623.

引用本文的文献

1
Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.组合冲突纯合性(CCH)分析能够在存在多种表型模拟的情况下快速识别共享基因组区域。
BMC Genomics. 2015 Mar 10;16(1):163. doi: 10.1186/s12864-015-1360-4.
2
Obtaining accurate p values from a dense SNP linkage scan.从密集单核苷酸多态性(SNP)连锁扫描中获取准确的p值。
Hum Hered. 2012;74(1):12-6. doi: 10.1159/000342754. Epub 2012 Oct 3.
3
Computer simulation is an undervalued tool for genetic analysis: a historical view and presentation of SHIMSHON--a Web-based genetic simulation package.
计算机模拟是基因分析中一种被低估的工具:基于历史视角对SHIMSHON(一个基于网络的基因模拟软件包)的介绍
Hum Hered. 2011;72(4):247-57. doi: 10.1159/000330633. Epub 2011 Dec 23.
4
Estimating gene penetrance from family data.从家族数据估计基因外显率。
Genet Epidemiol. 2010 May;34(4):373-81. doi: 10.1002/gepi.20493.
5
The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches.基于连锁的印记检测的本质:比较两种不同分析方法的效能、一类错误及混杂因素的影响。
Ann Hum Genet. 2010 May;74(3):248-62. doi: 10.1111/j.1469-1809.2010.00568.x. Epub 2010 Mar 31.
6
Estimation of genotype relative risks from pedigree data by retrospective likelihoods.基于回顾性似然法从家系数据估计基因型相对风险。
Genet Epidemiol. 2010 May;34(4):287-98. doi: 10.1002/gepi.20460.
7
Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results.对囊性纤维化胎粪性肠梗阻的修饰基因研究:统计考虑因素和基因定位结果。
Hum Genet. 2009 Dec;126(6):763-78. doi: 10.1007/s00439-009-0724-8.
8
Investigation of parent-of-origin effect in comitant strabismus using MOD score analysis.使用MOD评分分析研究共同性斜视中的亲代起源效应。
Mol Vis. 2009 Jun 9;15:1351-8.
9
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results.非综合征性唇裂伴或不伴腭裂的基因组扫描、精细定位及候选基因分析揭示了连锁和关联结果中特定表型的差异。
Hum Hered. 2009;68(3):151-70. doi: 10.1159/000224636. Epub 2009 Jun 11.
10
Multipoint lods provide reliable linkage evidence despite unknown limiting distribution: type I error probabilities decrease with sample size for multipoint lods and mods.尽管极限分布未知,但多点对数优势分数(LODs)仍能提供可靠的连锁证据:对于多点LODs和修正后的LODs,I型错误概率会随着样本量的增加而降低。
Genet Epidemiol. 2008 Dec;32(8):800-15. doi: 10.1002/gepi.20350.