Evidence map›Paper›PMID 39013011›Full record

ArticleGenetics2024

Testing times: disentangling admixture histories in recent and complex demographies using ancient DNA.

Matthew P Williams, Pavel Flegontov, Robert Maier, Christian D Huber

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In one paragraph

Article in Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Ancient genomes reveal over two thousand years of dingo population structure.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Matthew P WilliamsDepartment of Biology, Pennsylvania State University, University Park, PA 16802, USA.ORCID 0000-0001-7117-193X
Pavel FlegontovDepartment of Biology and Ecology, University of Ostrava, Ostrava 701 03, Czechia.ORCID 0000-0001-9759-4981
Robert MaierDepartment of Human Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA.
Christian D HuberDepartment of Biology, Pennsylvania State University, University Park, PA 16802, USA.ORCID 0000-0002-2267-2604

Funding

The role of admixture in human evolutionR35GM146886 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Christian Huber · 2022 to 2026
$2.0M
Czech Ministry of Education, Youth and Sports LL2103Czech Science Foundation 21-27624SEuropean Union CZ.10.03.01/00/22_003/0000003European Union Operational Programme CZ.10.03.01/00/22_003/0000003John Templeton Foundation 61220National Institute of Health R35GM146886NIGMS NIH HHS R35 GM146886
6 · The paper itself

Abstract

Our knowledge of human evolutionary history has been greatly advanced by paleogenomics. Since the 2020s, the study of ancient DNA has increasingly focused on reconstructing the recent past. However, the accuracy of paleogenomic methods in resolving questions of historical and archaeological importance amidst the increased demographic complexity and decreased genetic differentiation remains an open question. We evaluated the performance and behavior of two commonly used methods, qpAdm and the f3-statistic, on admixture inference under a diversity of demographic models and data conditions. We performed two complementary simulation approaches-firstly exploring a wide demographic parameter space under four simple demographic models of varying complexities and configurations using branch-length data from two chromosomes-and secondly, we analyzed a model of Eurasian history composed of 59 populations using whole-genome data modified with ancient DNA conditions such as SNP ascertainment, data missingness, and pseudohaploidization. We observe that population differentiation is the primary factor driving qpAdm performance. Notably, while complex gene flow histories influence which models are classified as plausible, they do not reduce overall performance. Under conditions reflective of the historical period, qpAdm most frequently identifies the true model as plausible among a small candidate set of closely related populations. To increase the utility for resolving fine-scaled hypotheses, we provide a heuristic for further distinguishing between candidate models that incorporates qpAdm model P-values and f3-statistics. Finally, we demonstrate a significant performance increase for qpAdm using whole-genome branch-length f2-statistics, highlighting the potential for improved demographic inference that could be achieved with future advancements in f-statistic estimations.

Indexed as

GenomicsPaleontologyData AccuracyDemographyModels, GeneticSoftwareadmixtureaDNAancient DNAarchaeogeneticsf-statisticspaleogenomicsqpAdm

Identifiers

PMID39013011
PMCPMC11373510

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.