Evidence map›Paper›PMID 40343027›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Detection of patient metadata in published articles for genomic epidemiology using machine learning and large language models.

Ari Z Klein, Davy Weissenbacher, Karen O'Connor, Amir Elyaderani, Ivan Flores Amaro, Takeshi Onishi, Su Golder, Kaelen Spiegel, Matthew Scotch, Graciela Gonzalez-Hernandez

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Ari Z KleinDepartment of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
Davy WeissenbacherDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Karen O'ConnorDepartment of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, USA.
Amir ElyaderaniCollege of Health Solutions, Arizona State University, Phoenix, AZ, USA.
Ivan Flores AmaroDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Takeshi OnishiDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Su GolderDepartment of Health Sciences, University of York, York, UK.
Kaelen SpiegelDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Matthew ScotchCollege of Health Solutions, Arizona State University, Phoenix, AZ, USA.ORCID 0000-0001-5100-9724
Graciela Gonzalez-HernandezDepartment of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Funding

Enriching SARS-CoV-2 sequence data in public repositories with information extracted from full text articlesR01AI164481 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI GONZALEZ HERNANDEZ, GRACIELA, SCOTCH, MATTHEW · 2021 to 2023
$1.9M
NIAID NIH HHS R01 AI164481
6 · The paper itself

Abstract

Objective: Patient metadata exist in published articles, but are often disconnected from genome sequences in databases, limiting their utility for genomic epidemiology. The objective of this study was to develop and evaluate natural language processing methods to facilitate the large-scale detection of patient metadata associated with reports of genome sequencing in published articles, drawing on the case of SARS-CoV-2. Methods: We applied filters to select a sample of 245 PubMed articles (50,918 sentences) in LitCovid for manual annotation of sentences that reported generating SARS-CoV-2 sequences. We trained, deployed, and validated a BERT-based classifier, and selected a sample of 150 predicted articles (22,147 sentences) for manual annotation of sentences that reported patient metadata associated with the sequences. In addition to training BERT-based classifiers, we experimented with a generative AI approach, prompting the Llama-3-70B LLM using zero-shot, role-based, few-shot, chain-of-thought, and reasoning-eliciting prompting. Results: BERT-based models that were pre-trained on corpora in biomedical or, more specifically, COVID-19 domains outperformed those that were pre-trained on corpora in general domains for detecting reports of patient metadata associated with SARS-CoV-2 sequences, achieving the best performance with a classifier based on a BiomedBERT-Large-Abstract model (F Conclusion: Our methods were applied to more than 350,000 published articles and can be used to advance the utility and efficiency of genomic epidemiology for public health responses to virus outbreaks.

Identifiers

PMID40343027
PMCPMC12060954

What OpenQuestion 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 OpenQuestion graph.