• 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

[人类复杂遗传疾病的QTL分析的理论研究]

[Theoretical studies of QTL analysis of complex genetic diseases in humans].

作者信息

Hu Zhong-Li, Dong Wei-Guo, Song Yun-Chun

机构信息

Key Laboratory of MOE for Developmental Biology, Wuhan University, Wuhan 430072, China.

出版信息

Yi Chuan Xue Bao. 2002 Feb;29(2):101-4.

PMID:11901989
Abstract

Some genes controlling human diseases have been located on the regions less than 1 cM using linkage disequilibrium, and a few of them have been cloned. Z. W. Luo developed a method that can detect and estimate the coefficient of linkage disequilibrium between a marker locus and quantitative trait locus (QTL), and raised the theoretical strategies for high-resolution mapping of complex genetic disorders in humans. Based on the data mentioned above, a method for linkage test between a marker locus and QTL was set up, and a method for linkage test between two marker loci and epistatic QTL was suggested for the first time.

摘要

一些控制人类疾病的基因已通过连锁不平衡定位到小于1厘摩的区域,其中少数已被克隆。罗正伟开发了一种方法,可检测和估计标记位点与数量性状位点(QTL)之间的连锁不平衡系数,并提出了人类复杂遗传疾病高分辨率定位的理论策略。基于上述数据,建立了一种标记位点与QTL之间的连锁检验方法,并首次提出了两个标记位点与上位性QTL之间的连锁检验方法。

相似文献

1
[Theoretical studies of QTL analysis of complex genetic diseases in humans].[人类复杂遗传疾病的QTL分析的理论研究]
Yi Chuan Xue Bao. 2002 Feb;29(2):101-4.
2
High resolution mapping of quantitative trait loci by linkage disequilibrium analysis.通过连锁不平衡分析进行数量性状位点的高分辨率定位。
Eur J Hum Genet. 2002 Oct;10(10):607-15. doi: 10.1038/sj.ejhg.5200843.
3
Combined high resolution linkage and association mapping of quantitative trait loci.数量性状基因座的高分辨率连锁与关联联合图谱绘制
Eur J Hum Genet. 2003 Feb;11(2):125-37. doi: 10.1038/sj.ejhg.5200941.
4
A variance component approach to dichotomous trait linkage analysis using a threshold model.一种使用阈值模型的二分性状连锁分析的方差分量方法。
Genet Epidemiol. 1997;14(6):987-92. doi: 10.1002/(SICI)1098-2272(1997)14:6<987::AID-GEPI71>3.0.CO;2-G.
5
Unified sampling approach for multipoint linkage disequilibrium mapping of qualitative and quantitative traits.定性和定量性状多点连锁不平衡定位的统一抽样方法
Genet Epidemiol. 2002 Apr;22(4):298-312. doi: 10.1002/gepi.0194.
6
Evaluation of linkage disequilibrium measures between multi-allelic markers as predictors of linkage disequilibrium between markers and QTL.评估多等位基因标记之间的连锁不平衡度量,作为标记与数量性状基因座之间连锁不平衡的预测指标。
Genet Res. 2005 Aug;86(1):77-87. doi: 10.1017/S001667230500769X.
7
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.
8
The full EM algorithm for the MLEs of QTL effects and positions and their estimated variances in multiple-interval mapping.用于多区间定位中QTL效应、位置及其估计方差的极大似然估计的完整期望最大化(EM)算法。
Biometrics. 2005 Jun;61(2):474-80. doi: 10.1111/j.1541-0420.2005.00327.x.
9
A population-based latent variable approach for association mapping of quantitative trait loci.一种基于群体的潜在变量方法用于数量性状基因座的关联定位。
Ann Hum Genet. 2006 Jul;70(Pt 4):506-23. doi: 10.1111/j.1469-1809.2006.00264.x.
10
A statistical model for high-resolution mapping of quantitative trait loci determining HIV dynamics.用于确定HIV动态的数量性状基因座高分辨率定位的统计模型。
Stat Med. 2004 Oct 15;23(19):3033-51. doi: 10.1002/sim.1870.