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

Author:

Williams Matthew P1ORCID,Flegontov Pavel23ORCID,Maier Robert3,Huber Christian D1ORCID

Affiliation:

1. Department of Biology, Pennsylvania State University , University Park, PA 16802 , USA

2. Department of Biology and Ecology, University of Ostrava , Ostrava 701 03 , Czechia

3. Department of Human Evolutionary Biology, Harvard University , Cambridge, MA 02138 , USA

Abstract

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.

Funder

National Institute of Health

Czech Science Foundation

Czech Ministry of Education, Youth and Sports

John Templeton Foundation

European Union Operational Programme

European Union

Publisher

Oxford University Press (OUP)

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