Evidence map›Paper›PMID 40366686›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Exact and efficient phylodynamic simulation from arbitrarily large populations.

Michael Celentano, William S DeWitt, Sebastian Prillo, Yun S Song

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Michael CelentanoDepartment of Statistics, University of California, Berkeley, CA 94720.
William S DeWittComputer Science Division, University of California, Berkeley, CA 94720.ORCID 0000-0002-6802-9139
Sebastian PrilloComputer Science Division, University of California, Berkeley, CA 94720.ORCID 0000-0002-2427-8627
Yun S SongDepartment of Statistics, University of California, Berkeley, CA 94720.ORCID 0000-0002-0734-9868

Funding

Scalable Computational Methods for Genealogical Inference: from species level to single cellsR01HG013117 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Ian H Holmes, RASMUS NIELSEN · 2024 to 2026
$1.7M
Scalable Computational Methods for Genealogical Inference: from species level to single cellsR56HG013117 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI HOLMES, IAN H, NIELSEN, RASMUS · 2023 to 2023
$315k
Adolph C. and Mary Sprague Miller Institute for Basic Research in Science, University of California Berkeley (MIBRS) Miller Research FellowshipHHS | NIH | National Institute of General Medical Sciences (NIGMS) R01-HG013117HHS | NIH | National Institute of General Medical Sciences (NIGMS) R56-HG013117James S. McDonnell Foundation (JSMF) Postdoctoral FellowshipNHGRI NIH HHS R01 HG013117NHGRI NIH HHS R56 HG013117
6 · The paper itself

Abstract

Many biological studies involve inferring the evolutionary history of a sample of individuals from a large population and interpreting the reconstructed tree. Such an ascertained tree typically represents only a small part of a comprehensive population tree and is distorted by survivorship and sampling biases. Inferring evolutionary parameters from ascertained trees requires modeling both the underlying population dynamics and the ascertainment process. A crucial component of this phylodynamic modeling involves tree simulation, which is used to benchmark probabilistic inference methods. To simulate an ascertained tree, one must first simulate the full population tree and then prune unobserved lineages. Consequently, the computational cost is determined not by the size of the final simulated tree, but by the size of the population tree in which it is embedded. In most biological scenarios, simulations of the entire population are prohibitively expensive due to computational demands placed on lineages without sampled descendants. Here, we address this challenge by proving that, for any partially ascertained process from a general multitype birth-death-mutation-sampling model, there exists an equivalent process with complete sampling and no death, a property which we leverage to develop a highly efficient algorithm for simulating trees. Our algorithm scales linearly with the size of the final simulated tree and is independent of the population size, enabling simulations from extremely large populations beyond the reach of current methods but essential for various biological applications. We anticipate that this massive speedup will significantly advance the development of novel inference methods that require extensive training data.

Indexed as

Computer SimulationModels, GeneticPhylogenyAlgorithmsBiological EvolutionHumansPopulation DynamicsBDMS modelefficient simulationforward-equivalent modelphylogenetic trees

Identifiers

PMID40366686
PMCPMC12107099

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.