Evidence map›Paper›PMID 42096490›Full record

ArticlePLoS computational biology2026

Fast and interpretable quantification of biological shape heterogeneity via stratified Wasserstein kernel.

Wenjun Zhao, Danica J Sutherland, Khanh Dao Duc

Abstract read
In one paragraph

Article in PLoS computational 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.

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

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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

3 authors.

Wenjun ZhaoDepartment of Mathematics, Wake Forest University, Winston-Salem, North Carolina, United States of America.ORCID https://orcid.org/0000-0001-7499-0084
Danica J SutherlandDepartment of Computer Science, University of British Columbia, Vancouver, Canada.
Khanh Dao DucDepartment of Mathematics, University of British Columbia, Vancouver, Canada‌‌.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modern imaging technologies produce vast collections of cellular and subcellular structures, calling for principled methods that enable shape comparison across individuals and populations. We introduce the stratified Wasserstein framework, which treats each shape as an unstructured point cloud and embeds it into Euclidean space via ranked local distance profiles. This embedding yields an isometry-invariant Euclidean distance and a positive-definite kernel for population analysis, with a consistent sample-based estimator that supports large datasets in near-quadratic time. By leveraging kernel methods, the framework enables statistically rigorous tasks such as nonparametric hypothesis testing, providing theoretical guarantees as well as interpretability. We demonstrate our framework's applicability to large-scale biological datasets. Analyzing 2D cancer cell contours, we quantify population-level discrepancies and identify representative cells contributing most strongly to the observed differences. Using 3D volumes of cell envelope and nucleus, we reveal progression patterns that capture morphological changes across cell populations both at the level of individual shapes. These results establish a simple and principled tool for population-level biological shape analysis, with potential impact across diverse domains of computational imaging and data science.

Indexed as

Cell ShapeComputational BiologyImage Processing, Computer-AssistedAlgorithmsCell Line, TumorHumansImaging, Three-Dimensional

Identifiers

PMID42096490
PMCPMC13167030

What OpenQuestion holds

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LicenceCC BY
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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.