Evidence map›Paper›PMID 40473775›Full record

ArticleHeredity2025

Assessing simulation-based supervised machine learning for demographic parameter inference from genomic data.

Arnaud Quelin, Frédéric Austerlitz, Flora Jay

Abstract read
In one paragraph

Article in Heredity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Arnaud QuelinUMR 7206 Eco-Anthropologie (EA), CNRS, Muséum National d'Histoire Naturelle, Université Paris Cité, Paris, France. arnaud.quelin@mnhn.fr.ORCID 0009-0001-8875-5939
Frédéric Austerlitz *UMR 7206 Eco-Anthropologie (EA), CNRS, Muséum National d'Histoire Naturelle, Université Paris Cité, Paris, France.ORCID 0000-0001-8031-455X
Flora Jay *UMR 9015 - Laboratoire Interdisciplinaire des Sciences du Numérique (LISN), CNRS, INRIA, Université Paris-Saclay, Orsay, France.ORCID 0000-0001-5884-4730

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-CE45-0010-01 RoDAPoG
6 · The paper itself

Abstract

The ever-increasing availability of high-throughput DNA sequences and the development of numerous computational methods have led to considerable advances in our understanding of the evolutionary and demographic history of populations. Several demographic inference methods have been developed to take advantage of these massive genomic data. Simulation-based approaches, such as approximate Bayesian computation (ABC), have proved particularly efficient for complex demographic models. However, taking full advantage of the comprehensive information contained in massive genomic data remains a challenge for demographic inference methods, which generally rely on partial information from these data. Using advanced computational methods, such as machine learning, is valuable for efficiently integrating more comprehensive information. Here, we showed how simulation-based supervised machine learning methods applied to an extensive range of summary statistics are effective in inferring demographic parameters for connected populations. We compared three machine learning (ML) methods: a neural network, the multilayer perceptron (MLP), and two ensemble methods, random forest (RF) and the gradient boosting system XGBoost (XGB), to infer demographic parameters from genomic data under a standard isolation with migration model and a secondary contact model with varying population sizes. We showed that MLP outperformed the other two methods and that, on the basis of permutation feature importance, its predictions involved a larger combination of summary statistics. Moreover, they outperformed all three tested ABC algorithms. Finally, we demonstrated how a method called SHAP, from the field of explainable artificial intelligence, can be used to shed light on the contribution of summary statistics within the ML models.

Indexed as

Computer SimulationGenetics, PopulationGenomicsMachine LearningSupervised Machine LearningAlgorithmsBayes TheoremHumansModels, GeneticNeural Networks, Computer

Identifiers

PMID40473775
PMCPMC12216105

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Registered trials

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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.