Evidence map›Paper›PMID 41332568›Full record

ArticlebioRxiv : the preprint server for biology2025

Performance of Information Theory Derived: Semantic Similarity Algorithms for Differential Diagnosis and Clustering.

Ben Coleman, Daniel Danis, Justin Reese, Peter Robinson

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.

Ben ColemanComputational Biology, The Jackson Laboratory for Genomic Medicine, Discovery Dr, CT 06032, USA.ORCID 0000-0002-4422-1708
Daniel DanisBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Charitéplatz 1, Berlin 10117, Germany.ORCID 0000-0003-0900-3411
Justin ReeseLawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.ORCID 0000-0002-2170-2250
Peter RobinsonComputational Biology, The Jackson Laboratory for Genomic Medicine, Discovery Dr, CT 06032, USA.ORCID 0000-0002-0736-9199

Funding

The Monarch Initiative: Linking Diseases to Model Organism ResourcesR24OD011883 · OD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAENDEL, MELISSA A, MUNGALL, CHRISTOPHER J · 2012 to 2024
$16.0M
The Human Phenotype Ontology: Accelerating Computational Integration of Clinical Data for GenomicsU24HG011449 · NHGRI · JACKSON LABORATORY · PI Peter Nicholas Robinson · 2021 to 2026
$6.7M
NHGRI NIH HHS U24 HG011449NIH HHS R24 OD011883
6 · The paper itself

Abstract

Semantic similarity analysis with Human Phenotype Ontology (HPO) enables fuzzy, specificity weighted comparisons of clinical manifestations of individuals and diseases and can be used to support differential diagnostics or to stratify cohorts. Many methods have been proposed to calculate semantic similarity for various applications, including the Phenomizer, which calculates the average best match over all terms in the query and disease, and set-based methods ranging from the Jaccard Intersection to methods that leverage the conditional information content to calculate similarity. However, these methods have not been described under a single mathematical model or robustly compared using a comprehensive data set. Here, we describe several semantic similarity algorithms using derivations based on information theory, propose three of our own variations to these models, and compare the performance of each approach for differential diagnostic ranking and phenotypic clustering. We find that Phenomizer performs better when diseases are ranked by similarity alone, without generating p-values. Additionally, non-normalized algorithms that use conditional information perform similarly to Phenomizer for differential diagnosis. In contrast, normalized algorithms perform best when clustering cohorts.

Indexed as

Differential diagnosisHuman Phenotype OntologyInformation contentPhenomizerPhenotypic clusteringPrecision medicineSemantic similarity

Identifiers

PMID41332568
PMCPMC12667856

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.