Evidence map›Paper›PMID 38261339›Full record

ArticleBriefings in bioinformatics2024

Reconstructing complex admixture history using a hierarchical model.

Shi Zhang, Rui Zhang, Kai Yuan, Lu Yang, Chang Liu, Yuting Liu, Xumin Ni, Shuhua Xu

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shi ZhangSchool of Mathematics and Statistics, Beijing Jiaotong University, Beijing, 100044, China.
Rui ZhangKey Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Kai YuanKey Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Lu YangSchool of Mathematics and Statistics, Beijing Jiaotong University, Beijing, 100044, China.
Chang LiuKey Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Yuting LiuSchool of Mathematics and Statistics, Beijing Jiaotong University, Beijing, 100044, China.
Xumin NiSchool of Mathematics and Statistics, Beijing Jiaotong University, Beijing, 100044, China.
Shuhua XuState Key Laboratory of Genetic Engineering, Human Phenome Institute, Zhangjiang Fudan International Innovation Center, Center for Evolutionary Biology, School of Life Sciences, Department of Liver Surgery and Transplantation Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai 200032 , China.ORCID 0000-0002-1975-1002

Funding

Beijing Natural Science Foundation L222051CFFF Computing Platform and the Human Phenome Data Center of Fudan UniversityFundamental Research Funds for the Central Universities 2023JBMC011Key Projects Development FundNational Key Research and Development Program of China 2023YFC2605400National Natural Science Foundation of China 32288101UK Royal Society-Newton Advanced Fellowship NAF\R1\191094
6 · The paper itself

Abstract

Various methods have been proposed to reconstruct admixture histories by analyzing the length of ancestral chromosomal tracts, such as estimating the admixture time and number of admixture events. However, available methods do not explicitly consider the complex admixture structure, which characterizes the joining and mixing patterns of different ancestral populations during the admixture process, and instead assume a simplified one-by-one sequential admixture model. In this study, we proposed a novel approach that considers the non-sequential admixture structure to reconstruct admixture histories. Specifically, we introduced a hierarchical admixture model that incorporated four ancestral populations and developed a new method, called HierarchyMix, which uses the length of ancestral tracts and the number of ancestry switches along genomes to reconstruct the four-way admixture history. By automatically selecting the optimal admixture model using the Bayesian information criterion principles, HierarchyMix effectively estimates the corresponding admixture parameters. Simulation studies confirmed the effectiveness and robustness of HierarchyMix. We also applied HierarchyMix to Uyghurs and Kazakhs, enabling us to reconstruct the admixture histories of Central Asians. Our results highlight the importance of considering complex admixture structures and demonstrate that HierarchyMix is a useful tool for analyzing complex admixture events.

Indexed as

Central Asian PeopleGenetics, PopulationBayes TheoremChromosomesComputer SimulationHumansadmixture historyancestral tractsancestry switcheshierarchical admixturemodel selectionsequential admixture

Identifiers

PMID38261339
PMCPMC10805183

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