Evidence map›Paper›PMID 41293525›Full record

ArticleArXiv2026

Which Similarity-Sensitive Entropy (Sentropy)?

Phuc Nguyen, Josiah Couch, Rahul Bansal, Alexandra Morgan, Chris Tam, Miao Li, Rima Arnaout, Ramy Arnaout

Abstract readPreprint
In one paragraph

Article in ArXiv, 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

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

8 authors.

Phuc NguyenDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0000-0001-9993-8434
Josiah CouchDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0000-0002-7416-5858
Rahul BansalDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0009-0006-0626-7752
Alexandra MorganDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0000-0001-7787-0547
Chris TamDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0000-0002-9126-4276
Miao LiDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0009-0004-4951-2899
Rima ArnaoutDepartment of Medicine, UCSF.ORCID 0000-0002-7134-0040
Ramy ArnaoutDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215.ORCID 0000-0001-6955-9310

Funding

Toward efficient performance for deep learning on medical imagingR01HL150394 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Rima Arnaout · 2020 to 2026
$6.2M
An Integrated Multilevel Modeling Framework for Repertoire-Based DiagnosticsR01AI148747 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ARNAOUT, RAMY · 2020 to 2024
$2.8M
NHLBI NIH HHS R01 HL150394NIAID NIH HHS R01 AI148747
6 · The paper itself

Abstract

Shannon entropy is not the only entropy that is relevant to machine-learning datasets, nor possibly even the most important one. Traditional entropies such as Shannon entropy capture information represented by elements' frequencies but not the richer information encoded by their similarities and differences. Capturing the latter requires similarity-sensitive entropy ("sentropy"). Sentropy can be measured using either the recently developed Leinster-Cobbold-Reeve framework (LCR) or the newer Vendi score (VS). This raises the practical question of which one to use: LCR or VS. Here we address this question theoretically and numerically, using 53 large and well-known imaging and tabular datasets. We find that LCR and VS values can differ by orders of magnitude and are complementary, except in limiting cases. We show that both LCR and VS results depend on how similarities are scaled, and introduce the notion of "half-distance" to parameterize this dependence. We prove the VS provides an upper bound on LCR for all non-negative values of the Rényi-Hill order parameter, as well as for negative values in the special case that the similarity matrix is full rank. We conclude that VS is preferable only when a dataset's elements can be usefully interpreted as linear combinations of a more fundamental set of "ur-elements" or when the system that the dataset describes has a quantum-mechanical character. In the broader case where one simply wishes to capture the rich information encoded by elements' similarities and differences as well as their frequencies, we propose that LCR should be favored; nevertheless, for certain half-distances the two methods can complement each other.

Identifiers

PMID41293525
PMCPMC12642762

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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.