ArticlebioRxiv : the preprint server for biology2025
Analytical expectations for ancestry junction accumulation in admixed genomes.
Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Complex demographic events have shaped human history, leaving signatures of genetic variation across the genome. Here, we recover the recent evolutionary history of admixed populations formed from multiple ancestral sources. We present a discrete, generalizable model of admixture that leverages ancestry switches, which are recombination breakpoints that mark changes in ancestral origin along a chromosome. We derive analytical expectations for the number of ancestry switches within a genomic segment as functions of recombination rate, ancestry heterozygosity, and effective population size, and extend these expectations to incorporate population-specific recombination maps. Forward-time simulations tracing ancestry junctions for ten generations after admixture show close agreement with theoretical predictions under constant and variable recombination models. We observe minimal variability in switch counts across ten replicates, underscoring the robustness of the theoretical expectation. Furthermore, model-based switch counts agree with empirical observations from African American individuals in the 1000 Genomes Project. For example, when modeling human chromosome 1, we found a mean of approximately six switches per haplotype, which aligns with the theoretical expectation under an initial African ancestry proportion of 0.85, and agrees with published estimates from other African-American cohorts. Overall, the model provides a new route for using ancestry switches to reconstruct how recombination and demography jointly shape ancestry patterns in admixed populations without requiring separation into parental sources.
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