Evidence map›Paper›PMID 40012349›Full record

ArticleMolecular ecology resources2025

Bayesian StairwayPlot for Inferring Single Population Demographic Histories From Site Frequency Spectra.

Sebastian Höhna, Ana Catalán

Abstract read
In one paragraph

Article in Molecular ecology resources, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Sebastian HöhnaGeoBio-Center LMU, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID https://orcid.org/0000-0001-6519-6292
Ana CatalánDivision of Evolutionary Biology, Ludwig-Maximilians-Universität München, Munich, Germany.

Funding

Deutsche Forschungsgemeinschaft HO 6201/1-1Deutsche Forschungsgemeinschaft HO 6201/2-1
6 · The paper itself

Abstract

The StairwayPlot approach provides an elegant, flexible and powerful method to estimate complex demographic histories of single populations from site frequency spectrum data. It uses expected coalescent times to compute the expected site frequency spectrum within a multinomial likelihood function. Population sizes are allowed to vary freely between coalescent events but are constant within each interval. Here, we implement the StairwayPlot approach in the Bayesian software package RevBayes. We use approaches developed for Bayesian Skyline Plots, which include independent and identically distributed (i.i.d.) population sizes, Gaussian Markov random fields and Horseshoe Markov random fields as prior distributions on population sizes. Furthermore, we implement a recently developed approach for computing the leave-one-out cross-validation probability for efficient model selection. We compare inference from our Bayesian implementation to the original Maximum Likelihood implementation, StairwayPlot2. Our results show that our Bayesian implementation in RevBayes performs comparable to StairwayPlot2 in terms of parameter accuracy, which is expected given that both use the same underlying likelihood function. From our set of prior models, the Gaussian Markov random field prior performed best for smoothly varying demographic histories, while the Horseshoe Markov random field performs best for abruptly changing demographic histories. We conclude the study by exploring several choices often faced in empirical studies, including the estimate of the total sequence length, the assumed mutation rate, as well as biases through mis-calling ancestral alleles. We show using our empirical example that as few as 10 diploid individuals are sufficient to infer complex demographic histories, but at least 500 k single nucleotide polymorphisms (SNPs) are required.

Indexed as

Computational BiologyDemographyModels, StatisticalBayes TheoremGenetics, PopulationMarkov ChainsMonte Carlo MethodPopulation DensitySoftwarecoalescentRevBayeswhole genome SNP data

Identifiers

PMID40012349
PMCPMC12225710

What OpenQuestion holds

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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.