Evidence map›Paper›PMID 41993468›Full record

ArticlebioRxiv : the preprint server for biology2026

Computing coalescence rates for complex demographies and sampling configurations.

Jiatong Liang, Jonathan Terhorst

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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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0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jiatong LiangDepartment of Statistics, University of Michigan.
Jonathan TerhorstDepartment of Statistics, University of Michigan.ORCID 0000-0001-7765-2101

Funding

Large-scale phylodynamics under non-neutral and non-treelike models of evolutionR35GM151145 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jonathan G Terhorst · 2023 to 2026
$1.5M
NIGMS NIH HHS R35 GM151145
6 · The paper itself

Abstract

Inference of population history from genetic data relies, implicitly or explicitly, on the distribution of coalescence times, because population size changes, migration, and admixture all leave characteristic signatures in genealogies. The distribution of pairwise coalescent rates in particular has emerged as a popular target for demographic inference methods. However, pairwise coalescent rates have limited power to resolve recent history, because recent coalescences in samples of size two are rare. In this article, we introduce demestats, a software library for computing first-coalescence and cross-coalescence rate functions for structured demographic models specified in the demes format. The method computes the hazard of the first coalescent event for arbitrary sampling configurations, combines exact calculations with mean-field approximations for larger samples, and is differentiable with respect to model parameters. In simulations, these statistics recover recent population size change and recent migration more accurately than pairwise summaries. Applied to tree sequences inferred from the 1000 Genomes Project, provide new insight into the rate of recent expansion in human populations.

Indexed as

demographic inferencepopulation genetics

Identifiers

PMID41993468
PMCPMC13081972

What OpenQuestion holds

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LicenceCC BY-NC
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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.