• 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

相似文献

1
Logarithm of odds (lods) for linkage in complex inheritance.复杂遗传中连锁的优势对数(lods)
Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3471-6. doi: 10.1073/pnas.93.8.3471.
2
Power comparison of parametric and nonparametric linkage tests in small pedigrees.小家族中参数化和非参数化连锁检验的效能比较
Am J Hum Genet. 2000 May;66(5):1661-8. doi: 10.1086/302888. Epub 2000 Apr 11.
3
How to model a complex trait. 1. General considerations and suggestions.如何对复杂性状进行建模。1. 一般考虑因素和建议。
Hum Hered. 2003;55(4):202-10. doi: 10.1159/000073204.
4
[Linkage analysis for complex diseases: a new life for an old method].
Arch Inst Pasteur Tunis. 2000;77(1-4):25-35.
5
Construction of conditional lod tables from multiple-locus linkage data.利用多位点连锁数据构建条件优势对数表。
Genet Epidemiol. 1985;2(4):375-86. doi: 10.1002/gepi.1370020406.
6
Power of multipoint identity-by-descent methods to detect linkage using variance component models.使用方差分量模型的多点同源性方法检测连锁的效能。
Genet Epidemiol. 2001 Dec;21(4):285-98. doi: 10.1002/gepi.1035.
7
Genetic linkage studies.
Lancet. 2005;366(9490):1036-44. doi: 10.1016/S0140-6736(05)67382-5.
8
Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy.精神分裂症和分裂型人格障碍全基因组扫描连锁信号中的显著相关性。
Mol Psychiatry. 2007 Oct;12(10):958-65. doi: 10.1038/sj.mp.4001996. Epub 2007 Apr 17.
9
False disease region identification from identity-by-descent haplotype sharing in the presence of phenocopies.在存在拟表型的情况下,通过同源单倍型共享进行假疾病区域识别。
Twin Res Hum Genet. 2006 Feb;9(1):9-16. doi: 10.1375/183242706776403000.
10
A class of tests for linkage using affected pedigree members.一类使用患病家系成员进行连锁分析的检验方法。
Biometrics. 1994 Mar;50(1):118-27.

引用本文的文献

1
Genetic variants that modify neuroendocrine gene expression and foraging behavior of .改变神经内分泌基因表达和觅食行为的遗传变异。
Sci Adv. 2024 Jun 14;10(24):eadk9481. doi: 10.1126/sciadv.adk9481. Epub 2024 Jun 12.
2
Chromosome-length genome assembly and linkage map of a critically endangered Australian bird: the helmeted honeyeater.极度濒危的澳大利亚鸟类——盔花蜜鸟的染色体长度基因组组装和连锁图谱。
Gigascience. 2022 Mar 29;11. doi: 10.1093/gigascience/giac025.
3
Global Research on Hereditary Hearing Impairment Over the Last 40 Years: A Bibliometric Study.四十年遗传性听力障碍全球研究:文献计量学研究。
J Int Adv Otol. 2021 Nov;17(6):482-491. doi: 10.5152/iao.2021.21276.
4
Genome sequencing-the dawn of a game-changing era.基因组测序——改变游戏规则时代的黎明。
Heredity (Edinb). 2019 Jul;123(1):58-66. doi: 10.1038/s41437-019-0226-y. Epub 2019 Jun 12.
5
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation.SLC9A7 中的一个重复出现的错义变异导致伴高尔基酸化改变和糖基化异常的非综合征性 X 连锁智力残疾。
Hum Mol Genet. 2019 Feb 15;28(4):598-614. doi: 10.1093/hmg/ddy371.
6
Individual disease risk and multimetric analysis of Crohn disease.克罗恩病的个体疾病风险与多指标分析
Proc Natl Acad Sci U S A. 2008 Oct 14;105(41):15843-7. doi: 10.1073/pnas.0808009105. Epub 2008 Oct 8.
7
Testing genetic linkage with relative pairs and covariates by quasi-likelihood score statistics.通过拟似然得分统计量对亲属对和协变量进行遗传连锁检验。
Hum Hered. 2007;64(4):220-33. doi: 10.1159/000103751. Epub 2007 Jun 12.
8
A first trial of retrospective collaboration for positional cloning in complex inheritance: assay of the cytokine region on chromosome 5 by the consortium on asthma genetics (COAG).复杂遗传中用于定位克隆的回顾性合作的首次试验:哮喘遗传学联盟(COAG)对5号染色体上细胞因子区域的分析。
Proc Natl Acad Sci U S A. 2000 Sep 26;97(20):10942-7. doi: 10.1073/pnas.97.20.10942.
9
Pseudoautosomal linkage of Hodgkin disease.霍奇金病的拟常染色体连锁
Am J Hum Genet. 2000 Aug;67(2):535-7. doi: 10.1086/303024.
10
Multipoint linkage analysis of the pseudoautosomal regions, using affected sibling pairs.利用患病同胞对进行假常染色体区域的多点连锁分析。
Am J Hum Genet. 2000 Aug;67(2):462-75. doi: 10.1086/303008. Epub 2000 Jun 26.

本文引用的文献

1
TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS.人类遗传学中重组率值的异质性检验
Ann Hum Genet. 1963 Nov;27:175-82. doi: 10.1111/j.1469-1809.1963.tb00210.x.
2
Sequential tests for the detection of linkage.用于检测连锁的序贯检验。
Am J Hum Genet. 1955 Sep;7(3):277-318.
3
Nonparametric tests for linkage with dependent sib pairs.用于关联分析的非参数检验:基于依存同胞对
Hum Hered. 1995 Nov-Dec;45(6):311-8. doi: 10.1159/000154299.
4
Distribution of the admixture test for the detection of linkage under heterogeneity.
Genet Epidemiol. 1993;10(1):75-83. doi: 10.1002/gepi.1370100108.
5
Asymptotic properties of affected-sib-pair linkage analysis.患病同胞对连锁分析的渐近性质。
Am J Hum Genet. 1993 Feb;52(2):362-74.
6
Linkage detection by the Affected-Pedigree-Member method: what is really tested?通过患病家系成员法进行连锁检测:究竟检测的是什么?
Genet Epidemiol. 1993;10(6):389-94. doi: 10.1002/gepi.1370100610.
7
Efficient strategies for genomic searching using the affected-pedigree-member method of linkage analysis.使用连锁分析的受累家系成员法进行基因组搜索的有效策略。
Am J Hum Genet. 1994 Mar;54(3):544-52.
8
Genetic dissection of complex traits.复杂性状的基因剖析
Science. 1994 Sep 30;265(5181):2037-48. doi: 10.1126/science.8091226.
9
Extreme discordant sib pairs for mapping quantitative trait loci in humans.用于定位人类数量性状基因座的极端不一致同胞对。
Science. 1995 Jun 16;268(5217):1584-9. doi: 10.1126/science.7777857.
10
Complete multipoint sib-pair analysis of qualitative and quantitative traits.对定性和定量性状进行完整的多点同胞对分析。
Am J Hum Genet. 1995 Aug;57(2):439-54.

复杂遗传中连锁的优势对数(lods)

Logarithm of odds (lods) for linkage in complex inheritance.

作者信息

Morton N E

机构信息

Human Genetics, Princess Anne Hospital, Southampton, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3471-6. doi: 10.1073/pnas.93.8.3471.

DOI:10.1073/pnas.93.8.3471
PMID:8622960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC39633/
Abstract

Lod scores provide a method to unify linkage tests based on identity by descent and identity in marker state while permitting selection of the most informative individuals through their disease-related phenotypes and markers in relatives. After parametric lods are reviewed, a nonparametric approach that depends on a single logistic parameter beta is introduced. Lods for parents tested or unknown are derived, multiple pairwise mapping is presented, and power is shown to be good even for moderately small values of beta. Comparison of parametric and nonparametric approaches (yet to be made) will provide for polygenes the efficiency and reliability that lod scores gave to mapping of major loci 40 years ago.

摘要

对数优势分数提供了一种方法,可将基于血统一致性和标记状态一致性的连锁测试统一起来,同时允许通过个体的疾病相关表型及其亲属的标记来选择信息最丰富的个体。在回顾了参数化对数优势分数之后,引入了一种依赖于单个逻辑参数β的非参数方法。推导出了针对已检测或未知亲本的对数优势分数,提出了多重成对映射,并且即使对于β的适度小值,功效也显示良好。参数化方法和非参数化方法的比较(尚未进行)将为多基因提供40年前对数优势分数赋予主要基因座定位的效率和可靠性。