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Evaluating the performance of ancient DNA genetic relatedness estimation methods using high-fidelity pedigree simulations.

Lefeuvre Maël, M Marsolier, Marie-Claude MC et al.

41796349 PubMed ID
4 Authors
2026-03-09 Published
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Lefeuvre Maël
MM
M Marsolier
MM
Marie-Claude MC
BC
Bon Céline
Chapter II

Abstract

Summary of the research findings

Recent advancements in paleogenetics, coupled with the emergence of dedicated statistical methods have, in recent years, streamlined the detection of close genetic ties from ancient DNA samples, leading to a substantial surge in scientific publications emphasising the reconstruction of genealogies within archaeological funerary contexts. However, while these methods all claim aptitude for addressing the inherent biases of ancient DNA, assessing their practical reliability can often be challenging, particularly in case studies involving few and/or poorly preserved samples. Furthermore, the genetic heritage and cultural practices of the population studied (e.g., inbreeding, endogamy) are factors which are often both complex to estimate and capable of impacting the accuracy of these methods.We present an in-depth comparative study of six ancient DNA genetic relatedness estimation methods to precisely delineate their respective performance and behaviour across a range of five biological parameters: sample coverage, use of post-mortem damage correction methods, human contamination, genetic diversity, and inbreeding. To this end, we develop BADGER (Benchmark Ancient DNA GEnetic Relatedness), an automated pipeline and software which first simulates pedigrees using randomly selected present-day individuals from the 1000-genomes dataset, and subsequently generates raw ancient DNA sequence data for each individual within these trees.The results of this benchmark enable us to discuss the individual strengths and limitations of these methods, propose a set of prescriptions to consider when interpreting their results and demonstrate that their reliability cannot be predicted from sample coverage alone, and may be subject to multiple sources of bias.

Chapter III

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