Evidence map›Paper›PMID 41279858›Full record

ArticlebioRxiv : the preprint server for biology2025

Uncertainty in joint Ancestral State Reconstruction: Improving accuracy and biological interpretability of ancestral state prediction.

James D Boyko, Kyle J Gontjes, Evan S Snitkin, Stephen A Smith

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

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

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

4 authors.

James D BoykoDepartment of Ecology and Evolutionary Biology, University of Michigan, USA.
Kyle J GontjesDepartment of Microbiology & Immunology, University of Michigan Medical School, USA.
Evan S SnitkinDepartment of Microbiology & Immunology, University of Michigan Medical School, USA.
Stephen A SmithDepartment of Ecology and Evolutionary Biology, University of Michigan, USA.

Funding

University of Michigan Training Program in Genomic ScienceT32HG000040 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Sebastian Zoellner · 1995 to 2026
$16.4M
The Michigan Infectious Disease Genomics (MIDGE) CenterU19AI181767 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAURING, ADAM, SNITKIN, EVAN · 2024 to 2024
$6.2M
Regional genomic epidemiology to identify drivers of resistance, transmission and infection with carbapenem-resistant Klebsiella pneumoniaeR01AI148259 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SNITKIN, EVAN · 2020 to 2023
$2.2M
Genome-driven identification of patient and bacterial drivers of resistance to novel beta-lactam/beta-lactamase inhibitor combination therapiesF31AI186288 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GONTJES, KYLE JAMES · 2024 to 2025
$84k
NHGRI NIH HHS T32 HG000040NIAID NIH HHS F31 AI186288NIAID NIH HHS R01 AI148259NIAID NIH HHS U19 AI181767
6 · The paper itself

Abstract

Ancestral state reconstruction (ASR) is a foundational tool in comparative biology, offering insights into the evolutionary history of lineages. With each new evolutionary model, our ability to estimate ancestral states has improved alongside the increased biological realism of these models. However, the field has primarily relied on reconstructions that focus on individual nodes, known as marginal reconstructions. This framework is analytically tractable but may not accurately represent what biologists want in inference, as evolution is dependent, and phenotypic transitions deeper in time can lead to consistent changes later. We argue that evolutionary history is better represented by joint reconstructions, which estimate the full sequence of states across nodes. Traditionally, joint reconstruction algorithms only estimated the single most likely sequence, but here we develop novel algorithms to estimate all relevant ancestral histories efficiently and provide tools to quantify the uncertainty of joint ASR. Furthermore, through simulations and an empirical case study, we demonstrate that joint reconstructions have higher accuracy than their marginal counterparts, and that the uncertainty surrounding the best joint reconstruction can be biologically meaningful and summarized using novel clustering algorithms. We apply our methods to epidemic multidrug-resistant

Identifiers

PMID41279858
PMCPMC12632483

What Socratic 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 Socratic graph.