• 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

通过在英国生物银行中的单倍型共享揭示欧洲近期的人口历史。

Revealing the recent demographic history of Europe via haplotype sharing in the UK Biobank.

机构信息

School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons in Ireland, Dublin, D02 YN77, Ireland.

FutureNeuro SFI Research Centre, Royal College of Surgeons in Ireland, Dublin, D02 YN77, Ireland.

出版信息

Proc Natl Acad Sci U S A. 2022 Jun 21;119(25):e2119281119. doi: 10.1073/pnas.2119281119. Epub 2022 Jun 13.

DOI:10.1073/pnas.2119281119
PMID:35696575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9233301/
Abstract

Haplotype-based analyses have recently been leveraged to interrogate the fine-scale structure in specific geographic regions, notably in Europe, although an equivalent haplotype-based understanding across the whole of Europe with these tools is lacking. Furthermore, study of identity-by-descent (IBD) sharing in a large sample of haplotypes across Europe would allow a direct comparison between different demographic histories of different regions. The UK Biobank (UKBB) is a population-scale dataset of genotype and phenotype data collected from the United Kingdom, with established sampling of worldwide ancestries. The exact content of these non-UK ancestries is largely uncharacterized, where study could highlight valuable intracontinental ancestry references with deep phenotyping within the UKBB. In this context, we sought to investigate the sample of European ancestry captured in the UKBB. We studied the haplotypes of 5,500 UKBB individuals with a European birthplace; investigated the population structure and demographic history in Europe, showing in parallel the variety of footprints of demographic history in different genetic regions around Europe; and expand knowledge of the genetic landscape of the east and southeast of Europe. Providing an updated map of European genetics, we leverage IBD-segment sharing to explore the extent of population isolation and size across the continent. In addition to building and expanding upon previous knowledge in Europe, our results show the UKBB as a source of diverse ancestries beyond Britain. These worldwide ancestries sampled in the UKBB may complement and inform researchers interested in specific communities or regions not limited to Britain.

摘要

基于单倍型的分析最近被用于研究特定地理区域的精细结构,特别是在欧洲,尽管这些工具在整个欧洲范围内缺乏基于单倍型的同等理解。此外,对欧洲范围内大量单倍型的同源性(IBD)共享的研究可以在不同地区的不同人口历史之间进行直接比较。英国生物银行(UKBB)是一个基于基因型和表型数据的人群规模数据集,来自英国,对全球血统进行了采样。这些非英国血统的具体内容在很大程度上还没有被描述,研究可以突出具有英国生物银行内深入表型的宝贵的洲际祖先参考。在这种情况下,我们试图研究 UKBB 中捕获的欧洲血统样本。我们研究了 5500 名具有欧洲出生地的 UKBB 个体的单倍型;调查了欧洲的人口结构和人口历史,同时展示了欧洲不同遗传区域人口历史的多样性;并扩展了对东欧和东南欧遗传景观的了解。提供了欧洲遗传学的最新图谱,我们利用 IBD 片段共享来探索整个欧洲大陆的人口隔离和规模程度。除了在欧洲建立和扩展以前的知识外,我们的结果还显示 UKBB 是英国以外多种血统的来源。UKBB 中采样的这些全球血统可能会补充和为对不限于英国的特定社区或地区感兴趣的研究人员提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/999697cbee03/pnas.2119281119fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/6eacf9792fac/pnas.2119281119fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/a7aeb2af84af/pnas.2119281119fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/d163e2b6273c/pnas.2119281119fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/811305517e79/pnas.2119281119fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/999697cbee03/pnas.2119281119fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/6eacf9792fac/pnas.2119281119fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/a7aeb2af84af/pnas.2119281119fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/d163e2b6273c/pnas.2119281119fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/811305517e79/pnas.2119281119fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88fe/9233301/999697cbee03/pnas.2119281119fig05.jpg

相似文献

1
Revealing the recent demographic history of Europe via haplotype sharing in the UK Biobank.通过在英国生物银行中的单倍型共享揭示欧洲近期的人口历史。
Proc Natl Acad Sci U S A. 2022 Jun 21;119(25):e2119281119. doi: 10.1073/pnas.2119281119. Epub 2022 Jun 13.
2
Polygenic scoring accuracy varies across the genetic ancestry continuum.多基因评分准确性在遗传祖先连续体上有所差异。
Nature. 2023 Jun;618(7966):774-781. doi: 10.1038/s41586-023-06079-4. Epub 2023 May 17.
3
Demographic history differences between Hispanics and Brazilians imprint haplotype features.西班牙裔和巴西人之间的人口历史差异影响着单倍型特征。
G3 (Bethesda). 2022 Jul 6;12(7). doi: 10.1093/g3journal/jkac111.
4
Between Lake Baikal and the Baltic Sea: genomic history of the gateway to Europe.在贝加尔湖和波罗的海之间:通往欧洲的门户的基因组历史。
BMC Genet. 2017 Dec 28;18(Suppl 1):110. doi: 10.1186/s12863-017-0578-3.
5
Population Histories of the United States Revealed through Fine-Scale Migration and Haplotype Analysis.通过精细迁移和单倍型分析揭示美国的人口历史。
Am J Hum Genet. 2020 Mar 5;106(3):371-388. doi: 10.1016/j.ajhg.2020.02.002.
6
Personalized genealogical history of UK individuals inferred from biobank-scale IBD segments.从生物库规模的 IBD 片段推断的英国个体的个性化家系史。
BMC Biol. 2021 Feb 16;19(1):32. doi: 10.1186/s12915-021-00964-y.
7
Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences.使用 454,727 份英国生物银行全外显子组序列对跨种族的 CFTR 变体多样性进行特征描述。
Genome Med. 2024 Mar 21;16(1):43. doi: 10.1186/s13073-024-01316-5.
8
Demography and the age of rare variants.人口统计学与罕见变异的时代
PLoS Genet. 2014 Aug 7;10(8):e1004528. doi: 10.1371/journal.pgen.1004528. eCollection 2014 Aug.
9
Length distributions of identity by descent reveal fine-scale demographic history.亲缘关系一致的长度分布揭示了精细的人口历史。
Am J Hum Genet. 2012 Nov 2;91(5):809-22. doi: 10.1016/j.ajhg.2012.08.030. Epub 2012 Oct 25.
10
Fast and Robust Identity-by-Descent Inference with the Templated Positional Burrows-Wheeler Transform.基于模板化位置 Burrows-Wheeler 变换的快速稳健的同宗推断。
Mol Biol Evol. 2021 May 4;38(5):2131-2151. doi: 10.1093/molbev/msaa328.

引用本文的文献

1
SPC: a SPectral Component approach to address recent population structure in genomic analysis.SPC:一种用于解决基因组分析中近期群体结构问题的光谱成分方法。
medRxiv. 2025 Jun 5:2025.06.04.25328990. doi: 10.1101/2025.06.04.25328990.
2
Genetic structure and demographic history of house mice in western Europe inferred using whole-genome sequences.利用全基因组序列推断西欧家鼠的遗传结构和种群历史。
Proc Biol Sci. 2025 Apr;292(2045):20242709. doi: 10.1098/rspb.2024.2709. Epub 2025 Apr 16.
3
Regionally enriched rare deleterious exonic variants in the UK and Ireland.

本文引用的文献

1
Genetic origins, singularity, and heterogeneity of Basques.巴斯克人的遗传起源、奇点和异质性。
Curr Biol. 2021 May 24;31(10):2167-2177.e4. doi: 10.1016/j.cub.2021.03.010. Epub 2021 Mar 25.
2
Personalized genealogical history of UK individuals inferred from biobank-scale IBD segments.从生物库规模的 IBD 片段推断的英国个体的个性化家系史。
BMC Biol. 2021 Feb 16;19(1):32. doi: 10.1186/s12915-021-00964-y.
3
Genetic analysis of ALS cases in the isolated island population of Malta.马耳他孤岛人群中 ALS 病例的遗传分析。
英国和爱尔兰区域富集的罕见有害外显子变异体。
Nat Commun. 2024 Oct 2;15(1):8454. doi: 10.1038/s41467-024-51604-2.
4
The Spectrum of Disease-Associated Alleles in Countries with a Predominantly Slavic Population.主要为斯拉夫人种的国家中与疾病相关的等位基因谱。
Int J Mol Sci. 2024 Aug 28;25(17):9335. doi: 10.3390/ijms25179335.
5
Exploring geometry of genome space via Grassmann manifolds.通过格拉斯曼流形探索基因组空间的几何结构。
Innovation (Camb). 2024 Jul 22;5(5):100677. doi: 10.1016/j.xinn.2024.100677. eCollection 2024 Sep 9.
6
Archaeology meets environmental genomics: implementing sedaDNA in the study of the human past.考古学与环境基因组学相遇:在人类历史研究中应用沉积物DNA
Archaeol Anthropol Sci. 2024;16(7):108. doi: 10.1007/s12520-024-01999-2. Epub 2024 Jun 28.
7
Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain.细胞类型分辨嵌合体揭示人类前脑的克隆动力学。
Nature. 2024 May;629(8011):384-392. doi: 10.1038/s41586-024-07292-5. Epub 2024 Apr 10.
8
Association between a polygenic lipodystrophy genetic risk score and diabetes risk in the high prevalence Maltese population.多基因脂肪营养不良遗传风险评分与高发马耳他人群糖尿病风险的相关性。
Acta Diabetol. 2024 May;61(5):555-564. doi: 10.1007/s00592-023-02230-9. Epub 2024 Jan 27.
9
Whole-Genome Sequencing of 502 Individuals from Latvia: The First Step towards a Population-Specific Reference of Genetic Variation.对 502 名拉脱维亚个体的全基因组测序:迈向特定人群遗传变异参考的第一步。
Int J Mol Sci. 2023 Oct 19;24(20):15345. doi: 10.3390/ijms242015345.
10
Genetic association of hypertension and several other metabolic disorders with Bell's palsy.高血压及其他几种代谢紊乱与贝尔麻痹的遗传关联。
Front Genet. 2023 Jul 18;14:1077438. doi: 10.3389/fgene.2023.1077438. eCollection 2023.
Eur J Hum Genet. 2021 Apr;29(4):604-614. doi: 10.1038/s41431-020-00767-9. Epub 2021 Jan 7.
4
Identity-by-descent detection across 487,409 British samples reveals fine scale population structure and ultra-rare variant associations.对 487409 个英国样本的亲缘关系检测揭示了精细的人口结构和超罕见变异关联。
Nat Commun. 2020 Nov 30;11(1):6130. doi: 10.1038/s41467-020-19588-x.
5
Dutch population structure across space, time and GWAS design.荷兰人口结构在空间、时间和全基因组关联研究设计方面的情况。
Nat Commun. 2020 Sep 11;11(1):4556. doi: 10.1038/s41467-020-18418-4.
6
Differences in local population history at the finest level: the case of the Estonian population.最细微层面的局部人口历史差异:以爱沙尼亚人口为例。
Eur J Hum Genet. 2020 Nov;28(11):1580-1591. doi: 10.1038/s41431-020-0699-4. Epub 2020 Jul 25.
7
Mapping co-ancestry connections between the genome of a Medieval individual and modern Europeans.绘制中世纪个体基因组与现代欧洲人之间的共同祖先关系图谱。
Sci Rep. 2020 Apr 22;10(1):6843. doi: 10.1038/s41598-020-64007-2.
8
Population Histories of the United States Revealed through Fine-Scale Migration and Haplotype Analysis.通过精细迁移和单倍型分析揭示美国的人口历史。
Am J Hum Genet. 2020 Mar 5;106(3):371-388. doi: 10.1016/j.ajhg.2020.02.002.
9
The genetic history of France.法国的遗传历史。
Eur J Hum Genet. 2020 Jul;28(7):853-865. doi: 10.1038/s41431-020-0584-1. Epub 2020 Feb 10.
10
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.在一个孤立的苏格兰人群中,超罕见变异负荷的增加影响外显子和调控区域。
PLoS Genet. 2019 Nov 25;15(11):e1008480. doi: 10.1371/journal.pgen.1008480. eCollection 2019 Nov.