Evidence map›Paper›PMID 38874402›Full record

ArticleMolecular biology and evolution2024

Biases in ARG-Based Inference of Historical Population Size in Populations Experiencing Selection.

Jacob I Marsh, Parul Johri

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. ThebioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Accessible, realistic genome simulation with selection using stdpopsim.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Jacob I MarshDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0003-3734-2023
Parul JohriDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0002-4003-7719

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inferring the demographic history of populations provides fundamental insights into species dynamics and is essential for developing a null model to accurately study selective processes. However, background selection and selective sweeps can produce genomic signatures at linked sites that mimic or mask signals associated with historical population size change. While the theoretical biases introduced by the linked effects of selection have been well established, it is unclear whether ancestral recombination graph (ARG)-based approaches to demographic inference in typical empirical analyses are susceptible to misinference due to these effects. To address this, we developed highly realistic forward simulations of human and Drosophila melanogaster populations, including empirically estimated variability of gene density, mutation rates, recombination rates, purifying, and positive selection, across different historical demographic scenarios, to broadly assess the impact of selection on demographic inference using a genealogy-based approach. Our results indicate that the linked effects of selection minimally impact demographic inference for human populations, although it could cause misinference in populations with similar genome architecture and population parameters experiencing more frequent recurrent sweeps. We found that accurate demographic inference of D. melanogaster populations by ARG-based methods is compromised by the presence of pervasive background selection alone, leading to spurious inferences of recent population expansion, which may be further worsened by recurrent sweeps, depending on the proportion and strength of beneficial mutations. Caution and additional testing with species-specific simulations are needed when inferring population history with non-human populations using ARG-based approaches to avoid misinference due to the linked effects of selection.

Indexed as

Drosophila melanogasterModels, GeneticPopulation DensitySelection, GeneticAnimalsComputer SimulationGenetics, PopulationHumansMutation RateRecombination, Geneticancestral recombination graphbackground selectiondemographic inferenceDrosophila melanogasterhuman population genomicsselective sweeps

Identifiers

PMID38874402
PMCPMC11245712

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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.