• 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

在编码基因稀疏的物种中,使用两步法从群体基因组数据推断种群统计学和选择历史:对人类数据的应用

Inferring demographic and selective histories from population genomic data using a 2-step approach in species with coding-sparse genomes: an application to human data.

作者信息

Soni Vivak, Jensen Jeffrey D

机构信息

School of Life Sciences, Center for Evolution & Medicine, Arizona State University, Tempe, AZ 85281, USA.

出版信息

G3 (Bethesda). 2025 Apr 17;15(4). doi: 10.1093/g3journal/jkaf019.

DOI:10.1093/g3journal/jkaf019
PMID:39883523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12005166/
Abstract

The demographic history of a population, and the distribution of fitness effects (DFE) of newly arising mutations in functional genomic regions, are fundamental factors dictating both genetic variation and evolutionary trajectories. Although both demographic and DFE inference has been performed extensively in humans, these approaches have generally either been limited to simple demographic models involving a single population, or, where a complex population history has been inferred, without accounting for the potentially confounding effects of selection at linked sites. Taking advantage of the coding-sparse nature of the genome, we propose a 2-step approach in which coalescent simulations are first used to infer a complex multi-population demographic model, utilizing large non-functional regions that are likely free from the effects of background selection. We then use forward-in-time simulations to perform DFE inference in functional regions, conditional on the complex demography inferred and utilizing expected background selection effects in the estimation procedure. Throughout, recombination and mutation rate maps were used to account for the underlying empirical rate heterogeneity across the human genome. Importantly, within this framework it is possible to utilize and fit multiple aspects of the data, and this inference scheme represents a generalized approach for such large-scale inference in species with coding-sparse genomes.

摘要

一个种群的人口统计学历史,以及功能基因组区域中新出现突变的适应性效应分布(DFE),是决定遗传变异和进化轨迹的基本因素。尽管在人类中已经广泛进行了人口统计学和DFE推断,但这些方法通常要么局限于涉及单一群体的简单人口统计学模型,要么在推断出复杂的种群历史时,没有考虑连锁位点选择的潜在混杂效应。利用基因组的编码稀疏特性,我们提出了一种两步法,其中首先使用合并模拟来推断复杂的多群体人口统计学模型,利用可能不受背景选择影响的大型非功能区域。然后,我们使用时间向前模拟在功能区域中进行DFE推断,以推断出的复杂人口统计学为条件,并在估计过程中利用预期的背景选择效应。在整个过程中,重组和突变率图谱被用来解释人类基因组中潜在的经验速率异质性。重要的是,在这个框架内,可以利用和拟合数据的多个方面,并且这种推断方案代表了一种对具有编码稀疏基因组的物种进行此类大规模推断的通用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/f76c7d8b774f/jkaf019f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/4311529d391a/jkaf019f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/0bf217c1c249/jkaf019f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/63bee65c59f5/jkaf019f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/f76c7d8b774f/jkaf019f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/4311529d391a/jkaf019f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/0bf217c1c249/jkaf019f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/63bee65c59f5/jkaf019f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3547/12005166/f76c7d8b774f/jkaf019f4.jpg

相似文献

1
Inferring demographic and selective histories from population genomic data using a 2-step approach in species with coding-sparse genomes: an application to human data.在编码基因稀疏的物种中,使用两步法从群体基因组数据推断种群统计学和选择历史:对人类数据的应用
G3 (Bethesda). 2025 Apr 17;15(4). doi: 10.1093/g3journal/jkaf019.
2
Inferring demographic and selective histories from population genomic data using a two-step approach in species with coding-sparse genomes: an application to human data.在编码基因稀疏的物种中,采用两步法从群体基因组数据推断群体统计学和选择历史:对人类数据的应用
bioRxiv. 2024 Nov 21:2024.09.19.613979. doi: 10.1101/2024.09.19.613979.
3
Biases in ARG-Based Inference of Historical Population Size in Populations Experiencing Selection.基于 ARG 的历史人口规模推断在经历选择的人群中的偏差。
Mol Biol Evol. 2024 Jul 3;41(7). doi: 10.1093/molbev/msae118.
4
The Effects of Mutation and Recombination Rate Heterogeneity on the Inference of Demography and the Distribution of Fitness Effects.突变和重组率异质性对人口推断和适应度效应分布的影响。
Genome Biol Evol. 2024 Feb 1;16(2). doi: 10.1093/gbe/evae004.
5
Genomic inference using diffusion models and the allele frequency spectrum.基于扩散模型和等位基因频率谱的基因组推断。
Curr Opin Genet Dev. 2018 Dec;53:140-147. doi: 10.1016/j.gde.2018.10.001. Epub 2018 Oct 23.
6
Human demographic history has amplified the effects of background selection across the genome.人类人口历史放大了基因组中背景选择的影响。
PLoS Genet. 2018 Jun 18;14(6):e1007387. doi: 10.1371/journal.pgen.1007387. eCollection 2018 Jun.
7
Developing an Evolutionary Baseline Model for Humans: Jointly Inferring Purifying Selection with Population History.为人类建立进化基准模型:共同推断净化选择与种群历史。
Mol Biol Evol. 2023 May 2;40(5). doi: 10.1093/molbev/msad100.
8
The effects of mutation and recombination rate heterogeneity on the inference of demography and the distribution of fitness effects.突变和重组率异质性对种群统计学推断及适合度效应分布的影响。
bioRxiv. 2023 Nov 13:2023.11.11.566703. doi: 10.1101/2023.11.11.566703.
9
Background Selection Does Not Mimic the Patterns of Genetic Diversity Produced by Selective Sweeps.背景选择不会模仿选择清除产生的遗传多样性模式。
Genetics. 2020 Oct;216(2):499-519. doi: 10.1534/genetics.120.303469. Epub 2020 Aug 26.
10
The Promise of Inferring the Past Using the Ancestral Recombination Graph.利用祖先重组图谱推断过去的可能性。
Genome Biol Evol. 2024 Feb 1;16(2). doi: 10.1093/gbe/evae005.

引用本文的文献

1
Accounting for Chimerism in Demographic Inference: Reconstructing the History of Common Marmosets (Callithrix jacchus) from High-Quality, Whole-Genome, Population-Level Data.在人口统计学推断中考虑嵌合体:从高质量、全基因组、群体水平数据重建普通狨猴(Callithrix jacchus)的历史。
Mol Biol Evol. 2025 Jun 4;42(6). doi: 10.1093/molbev/msaf119.
2
A whole-genome scan for evidence of positive and balancing selection in aye-ayes (Daubentonia madagascariensis) utilizing a well-fit evolutionary baseline model.利用拟合良好的进化基线模型,对指猴(Daubentonia madagascariensis)进行全基因组扫描,以寻找正向选择和平衡选择的证据。
G3 (Bethesda). 2025 Apr 10. doi: 10.1093/g3journal/jkaf078.
3

本文引用的文献

1
A whole-genome scan for evidence of positive and balancing selection in aye-ayes (Daubentonia madagascariensis) utilizing a well-fit evolutionary baseline model.利用拟合良好的进化基线模型,对指猴(Daubentonia madagascariensis)进行全基因组扫描,以寻找正向选择和平衡选择的证据。
G3 (Bethesda). 2025 Apr 10. doi: 10.1093/g3journal/jkaf078.
2
Inferring the Demographic History of Aye-Ayes (Daubentonia madagascariensis) from High-Quality, Whole-Genome, Population-Level Data.从高质量的全基因组群体水平数据推断指猴(Daubentonia madagascariensis)的种群历史。
Genome Biol Evol. 2025 Jan 6;17(1). doi: 10.1093/gbe/evae281.
3
Inferring the Demographic History of Aye-Ayes (Daubentonia madagascariensis) from High-Quality, Whole-Genome, Population-Level Data.
从高质量的全基因组群体水平数据推断指猴(Daubentonia madagascariensis)的种群历史。
Genome Biol Evol. 2025 Jan 6;17(1). doi: 10.1093/gbe/evae281.
4
The landscape of structural variation in aye-ayes ().指猴的结构变异图谱()。 (括号内容原文缺失,译文根据已有内容补全括号形式)
bioRxiv. 2024 Nov 11:2024.11.08.622672. doi: 10.1101/2024.11.08.622672.
5
Inferring the demographic history of aye-ayes () from high-quality, whole-genome, population-level data.从高质量的全基因组群体水平数据推断指猴的种群历史。
bioRxiv. 2024 Nov 11:2024.11.08.622659. doi: 10.1101/2024.11.08.622659.
6
A whole-genome scan for evidence of recent positive and balancing selection in aye-ayes () utilizing a well-fit evolutionary baseline model.利用一个拟合良好的进化基线模型,对指猴进行全基因组扫描,以寻找近期正向选择和平衡选择的证据。
bioRxiv. 2024 Nov 11:2024.11.08.622667. doi: 10.1101/2024.11.08.622667.
Population genetic considerations regarding the interpretation of within-patient SARS-CoV-2 polymorphism data.
关于患者体内严重急性呼吸综合征冠状病毒2(SARS-CoV-2)多态性数据解读的群体遗传学考量
Nat Commun. 2024 Apr 16;15(1):3240. doi: 10.1038/s41467-024-46261-4.
4
Temporal challenges in detecting balancing selection from population genomic data.从群体基因组数据中检测平衡选择的时间挑战。
G3 (Bethesda). 2024 Jun 5;14(6). doi: 10.1093/g3journal/jkae069.
5
A quantitative genetic model of background selection in humans.人类背景选择的数量遗传模型。
PLoS Genet. 2024 Mar 20;20(3):e1011144. doi: 10.1371/journal.pgen.1011144. eCollection 2024 Mar.
6
The Effects of Mutation and Recombination Rate Heterogeneity on the Inference of Demography and the Distribution of Fitness Effects.突变和重组率异质性对人口推断和适应度效应分布的影响。
Genome Biol Evol. 2024 Feb 1;16(2). doi: 10.1093/gbe/evae004.
7
A Simulation Framework for Modeling the Within-Patient Evolutionary Dynamics of SARS-CoV-2.用于建模 SARS-CoV-2 患者内进化动态的仿真框架。
Genome Biol Evol. 2023 Nov 1;15(11). doi: 10.1093/gbe/evad204.
8
Genomic inference of a severe human bottleneck during the Early to Middle Pleistocene transition.古人类在早-中更新世过渡期间发生严重瓶颈事件的基因组推断。
Science. 2023 Sep;381(6661):979-984. doi: 10.1126/science.abq7487. Epub 2023 Aug 31.
9
Evaluating power to detect recurrent selective sweeps under increasingly realistic evolutionary null models.评估在越来越现实的进化 null 模型下检测复发性选择扫描的能力。
Evolution. 2023 Oct 3;77(10):2113-2127. doi: 10.1093/evolut/qpad120.
10
SLiM 4: Multispecies Eco-Evolutionary Modeling.SLiM 4:多物种生态进化建模。
Am Nat. 2023 May;201(5):E127-E139. doi: 10.1086/723601. Epub 2023 Mar 21.