Evidence map›Paper›PMID 41427332›Full record

ArticlebioRxiv : the preprint server for biology2025

evo3D: a generalised framework for structure-informed evolutionary analysis, implemented in R.

Bradley K Broyles, Qixin He

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

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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

5 · Who and what money

Authors and funding

2 authors.

Bradley K BroylesDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA.ORCID 0000-0002-3608-4491
Qixin HeDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA.ORCID 0000-0003-1696-8203

Funding

Introducing a novel computational framework for B-cell epitope prediction based on immune-induced selection signaturesR21AI187928 · NIAID · PURDUE UNIVERSITY · PI HE, QIXIN · 2025 to 2025
$406k
NIAID NIH HHS R21 AI187928
6 · The paper itself

Abstract

Selection pressures often act at the level of protein structure, yet most evolutionary analyses remain confined to linear sequences. Early structure-informed approaches improved interpretation by mapping single-site metrics onto protein structures, and later methods introduced 3D sliding windows to capture spatial neighbourhoods missed by linear analyses. These frameworks, however, are restricted to predefined statistics and narrowly defined 3D window types, limiting the scope of questions that can be addressed. We developed an R package, evo3D, a generalised framework for structure-informed evolutionary analysis that supports any downstream statistic and scales from simple to complex structures. evo3D extracts structure-informed multiple sequence alignment subsets (spatial haplotypes), making the structure-informed unit of analysis directly available to users. The framework provides fixed-count and fixed-distance spatial windows, supports residue and codon analysis modes, and extends across multimers, interfaces, and multiple structural models through a single wrapper, run_evo3d(). We demonstrate evo3D's utility by performing an epitope-level diversity scan of Hepatitis C virus E1/E2 complex, identifying conserved spatial neighbourhoods missed by linear sliding windows, and by evaluating evo3D's scalability on the octameric Chikungunya virus E1/E2 assembly. By formalising the core components of structure-informed genetic analysis and removing the technical barriers, evo3D streamlines the evaluation of evolutionary patterns directly within 3D structural contexts and we anticipate its wide application in molecular evolution studies. The package is available at github.com/bbroyle/evo3D.

Identifiers

PMID41427332
PMCPMC12713595

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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.