Evidence map›Paper›PMID 42180343›Full record

ArticlemedRxiv : the preprint server for health sciences2026

PheBee: A Graph-Aware System for Scalable, Traceable, and Semantic Phenotyping.

David M Gordon, Max Homilius, Austin A Antoniou, Connor Grannis, Grant E Lammi, Adam C Herman, Ashley Kubatko, Bimal P Chaudhari, Peter White

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

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

9 authors.

David M GordonThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.ORCID 0000-0001-7307-6274
Max HomiliusThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Austin A AntoniouThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.ORCID 0000-0003-2952-2673
Connor GrannisThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Grant E LammiThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.ORCID 0009-0004-5127-4658
Adam C HermanThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Ashley KubatkoThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.
Bimal P ChaudhariThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.ORCID 0000-0002-0115-949X
Peter WhiteThe Office of Data Sciences, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.ORCID 0000-0002-5218-5903

Funding

NeoGx-III: Interpretable Machine Learning with Integrated Analysis of Maternal & Infant Electronic Medical Records for Unbiased Prediction of Need for Genome Sequencing in Level III NICUsR21HD119885 · NICHD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI CHAUDHARI, BIMAL PANKAJ, WHITE, PETER · 2025 to 2025
$435k
NICHD NIH HHS R21 HD119885
6 · The paper itself

Abstract

Objectives: Phenotype-driven workflows in clinical and translational research require standardized ontology-based representation, ontology-aware cohort discovery, and provenance inspection for each assertion. Existing approaches optimize either for semantic traversal or scalable batch analytics, but not both. We describe PheBee, a hybrid system that links semantic assertions to scalable evidence storage via a deterministic identifier, preserving provenance while supporting ontology-aware discovery at cohort scale. Materials and Methods: PheBee represents phenotype assertions in a knowledge graph as ontology-linked nodes with clinical modifier context (e.g., negated, family history), and stores supporting evidence records in a scalable row-oriented evidence table for cohort-scale access. The two layers are connected by a deterministic identifier enabling stable joins across repeated ingestions without duplicating high-volume evidence in the graph. We evaluated PheBee using synthetic datasets designed to exercise end-to-end ingestion and query workflows. Results: Functional evaluation validated hierarchical term expansion, qualifier-aware retrieval, duplicate-free assertion handling under re-ingestion, and privacy-conscious management of subjects shared across multiple research projects. At scale (10,000 subjects producing 12M evidence records) PheBee completed ingestion in ~30 minutes and responded to interactive queries within 6 seconds under concurrent load. Discussion: PheBee exposes a unified API for ontology-aware cohort discovery with hierarchical term expansion, subject-centric retrieval of phenotypes and clinical modifiers, and evidence and provenance queries. Its data model aligns with GA4GH Phenopackets, facilitating interoperability with phenotype exchange standards. Conclusion: By combining ontology-aware semantics with scalable, provenance-bearing evidence storage, PheBee provides a practical open-source foundation for phenotype-driven research workflows that demand both semantic precision and cohort-scale traceability.

Indexed as

cohort studiesdata lakeknowledge graphphenotypeprecision medicine

Identifiers

PMID42180343
PMCPMC13193091

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.