• 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
Parameters of the human genome.人类基因组参数。
Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7474-6. doi: 10.1073/pnas.88.17.7474.
2
Integration of gene maps: chromosome 21.基因图谱整合:21号染色体
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7210-4. doi: 10.1073/pnas.90.15.7210.
3
Integration of gene maps: chromosome 1.基因图谱整合:1号染色体
Proc Natl Acad Sci U S A. 1992 May 15;89(10):4598-602. doi: 10.1073/pnas.89.10.4598.
4
Lengths of chromosomal segments conserved since divergence of man and mouse.自人类和小鼠分化以来保守的染色体片段长度。
Proc Natl Acad Sci U S A. 1984 Feb;81(3):814-8. doi: 10.1073/pnas.81.3.814.
5
Error filtration, interference, and the human linkage map.错误过滤、干扰与人类连锁图谱。
Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6501-5. doi: 10.1073/pnas.88.15.6501.
6
Genetic linkage map of 46 DNA markers on human chromosome 16.人类16号染色体上46个DNA标记的遗传连锁图谱。
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5754-8. doi: 10.1073/pnas.87.15.5754.
7
Construction of a radiation hybrid map of chicken chromosome 2 and alignment to the chicken draft sequence.鸡2号染色体辐射杂种图谱的构建及其与鸡基因组草图序列的比对。
BMC Genomics. 2005 Feb 4;6:12. doi: 10.1186/1471-2164-6-12.
8
A metric map of humans: 23,500 loci in 850 bands.人类的度量图谱:850个带区中的23,500个基因座。
Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14771-5. doi: 10.1073/pnas.93.25.14771.
9
Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones.通过CEPH酵母人工染色体(YAC)克隆的荧光原位杂交(FISH)图谱绘制实现人类基因组细胞遗传学、遗传学和物理图谱的整合。
Genomics. 1996 Feb 15;32(1):1-14. doi: 10.1006/geno.1996.0070.
10
Physical and genetic maps for chromosome 10.10号染色体的物理图谱和遗传图谱。
Genomics. 1993 May;16(2):320-4. doi: 10.1006/geno.1993.1192.

引用本文的文献

1
Estimating gene conversion rates from population data using multi-individual identity by descent.利用多位个体的同源性从群体数据估计基因转换率。
Am J Hum Genet. 2025 Aug 16. doi: 10.1016/j.ajhg.2025.07.019.
2
Supra-second tracking and live-cell karyotyping reveal principles of mitotic chromosome dynamics.超秒级追踪和活细胞染色体组型分析揭示有丝分裂染色体动力学原理。
Nat Cell Biol. 2025 Apr;27(4):654-667. doi: 10.1038/s41556-025-01637-6. Epub 2025 Apr 4.
3
Estimating gene conversion rates from population data using multi-individual identity by descent.利用多位个体的血缘同一性从群体数据中估计基因转换率。
bioRxiv. 2025 Feb 27:2025.02.22.639693. doi: 10.1101/2025.02.22.639693.
4
Unveiling the mysteries of extrachromosomal circular DNA: from generation to clinical relevance in human cancers and health.揭开染色体外环状DNA的奥秘:从产生到在人类癌症与健康中的临床相关性
Mol Cancer. 2024 Dec 20;23(1):276. doi: 10.1186/s12943-024-02187-5.
5
Cellular and Nuclear Forces: An Overview.细胞与核力:概述
Methods Mol Biol. 2025;2881:3-39. doi: 10.1007/978-1-0716-4280-1_1.
6
Quantitative ctDNA Detection in Hepatoblastoma: Implications for Precision Medicine.肝母细胞瘤中循环肿瘤DNA的定量检测:对精准医学的意义
Cancers (Basel). 2023 Dec 19;16(1):12. doi: 10.3390/cancers16010012.
7
Diagnostic Accuracy of Flow Cytometric DNA Index in Saudi Children with B Cell Acute Lymphoblastic Leukemia.流式细胞术DNA指数在沙特B细胞急性淋巴细胞白血病儿童中的诊断准确性
Children (Basel). 2023 Jul 28;10(8):1299. doi: 10.3390/children10081299.
8
TRPV4 mRNA is elevated in the caudate nucleus with NPH but not in Alzheimer's disease.在正常压力脑积水患者的尾状核中,瞬时受体电位香草酸亚型4(TRPV4)信使核糖核酸(mRNA)水平升高,但在阿尔茨海默病患者中未升高。
Front Genet. 2022 Nov 2;13:936151. doi: 10.3389/fgene.2022.936151. eCollection 2022.
9
Geometrical Properties of the Nucleus and Chromosome Intermingling Are Possible Major Parameters of Chromosome Aberration Formation.核和染色体交织的几何性质可能是染色体畸变形成的主要参数。
Int J Mol Sci. 2022 Aug 3;23(15):8638. doi: 10.3390/ijms23158638.
10
Circular DNA in the human germline and its association with recombination.人类生殖系中环 DNA 及其与重组的关系。
Mol Cell. 2022 Jan 6;82(1):209-217.e7. doi: 10.1016/j.molcel.2021.11.027. Epub 2021 Dec 23.

本文引用的文献

1
Data and theory for a revised chiasma map of man.人类交叉图谱修订版的数据与理论
Hum Genet. 1982;62(3):266-70. doi: 10.1007/BF00333534.
2
The William Allan Memorial Award Address: Gene clusters, Genome organization, and complex phenotypes. When the sequence is known, what will it mean?威廉·艾伦纪念奖演讲:基因簇、基因组组织与复杂表型。当序列已知时,这意味着什么?
Am J Hum Genet. 1981 Sep;33(5):664-82.
3
Quantitative karyotyping of human chromosomes by dual beam flow cytometry.通过双光束流式细胞术对人类染色体进行定量核型分析。
Proc Natl Acad Sci U S A. 1982 Dec;79(24):7876-80. doi: 10.1073/pnas.79.24.7876.
4
The DNA-based human karyotype.基于DNA的人类核型。
Cytometry. 1984 Jul;5(4):376-85. doi: 10.1002/cyto.990050414.
5
DNA content and DNA-based centromeric index of the 24 human chromosomes.24条人类染色体的DNA含量及基于DNA的着丝粒指数
Science. 1973 Mar 16;179(4078):1126-9. doi: 10.1126/science.179.4078.1126.
6
Determination of the DNA content of human chromosomes by flow cytometry.通过流式细胞术测定人类染色体的DNA含量。
Cytogenet Cell Genet. 1986;41(1):14-21. doi: 10.1159/000132190.
7
The centromere index and relative length of human high-resolution G-banded chromosomes.人类高分辨率G带染色体的着丝粒指数和相对长度。
Hum Genet. 1986 Jun;73(2):130-2. doi: 10.1007/BF00291602.
8
Centromeric index versus DNA content flow karyotypes of human chromosomes measured by means of slit-scan flow cytometry.通过狭缝扫描流式细胞术测量的人类染色体着丝粒指数与DNA含量流式核型分析
Cytometry. 1987 May;8(3):273-9. doi: 10.1002/cyto.990080307.
9
Multipoint mapping and the emperor's clothes.
Ann Hum Genet. 1988 Oct;52(4):309-18. doi: 10.1111/j.1469-1809.1988.tb01110.x.
10
Report of the committee on linkage and gene order.
Cytogenet Cell Genet. 1989;51(1-4):459-502. doi: 10.1159/000132805.

人类基因组参数。

Parameters of the human genome.

作者信息

Morton N E

机构信息

CRC Research Group in Genetic Epidemiology, University of Southampton, Southampton General Hospital, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7474-6. doi: 10.1073/pnas.88.17.7474.

DOI:10.1073/pnas.88.17.7474
PMID:1881886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC52322/
Abstract

Chromosome arm lengths are the critical parameters of the human genome. The physical length is required to scale radiation hybrid and other maps to megabases. The genetic lengths in males and females are required for probabilities of exclusion and synteny, choice of well-spaced loci for linkage tests, and comparison with centromeric maps based on nondisjunction. Interpolation of new data into a map is possible only when the length is known, including the distances from centromere and telomeres to the nearest markers. Current evidence on physical parameters including the reliable measurements of relative lengths from flow cytometry but only a crude estimate of genome size (3200 megabases). Evidence on genetic parameters includes chiasma counts and linkage maps corrected for failure to sample telomeres, giving an autosomal size of 2809 centimorgans in males and 4782 centimorgans in females. Estimates of the physical and sex-specific genetic lengths are presented for each chromosome arm. Any linkage analysis that yields substantially larger estimates raises a suspicion of an inappropriate mapping function or typing errors.

摘要

染色体臂长是人类基因组的关键参数。物理长度对于将辐射杂种图谱和其他图谱换算成兆碱基至关重要。男性和女性的遗传长度对于排除概率和同线性、选择用于连锁测试的间隔良好的基因座以及与基于不分离的着丝粒图谱进行比较而言是必需的。只有当长度已知时,包括从着丝粒和端粒到最近标记的距离,才有可能将新数据插入到图谱中。目前关于物理参数的证据包括来自流式细胞术的相对长度的可靠测量,但基因组大小只是一个粗略估计(3200兆碱基)。关于遗传参数的证据包括交叉计数和针对未对端粒进行采样而校正的连锁图谱,得出男性常染色体大小为2809厘摩,女性为4782厘摩。给出了每个染色体臂的物理长度和性别特异性遗传长度的估计值。任何得出明显更大估计值的连锁分析都会引发对不适当的定位函数或分型错误的怀疑。