bioRxivBioinformaticsPreprint
Detecting Manuscripts Related to Computable Phenotypes Using a Transformer-based Language Model
Junghoon ChaeiD, David HeiseiD, Keith Connatser, Jacqueline P. HonerlawiD, Monika MaripuriiD, Yuk-Lam Anne HoiD, Francesca FontiniD, Vidisha TanukondaiD, Kelly ChoiD
Abstract
ObjectiveThe demand for a comprehensive phenomics library, which requires identifying computable phenotype definitions and associated metadata from an ever-expanding biomedical literature, presents a significant, labor-intensive, and unscalable challenge. To address this, we introduce a transformer-based language model specifically designed for identifying biomedical texts containing computable phenotypes and piloted its use in the Centralized Interactive Phenomics Resource (CIPHER) platform. Materials and MethodsWe fine-tuned a BioBERT model using a labeled dataset of 396 manuscripts. The model incorporates our novel sliding-window approach to effectively overcome token-length limitations, thereby enabling accurate classification of full-length manuscripts. For scalable deployment and continuous refinement, we developed a cohesive framework that integrates a web-based user interface, a control server, and a classification module. ResultsThe staged approach for model development yielded a final model with 95% accuracy. The web-based user interface was deployed on the CIPHER platform and enables user feedback for model retraining. DiscussionWe developed a model and user interface which are currently in use by data curators to identify computable phenotype definitions from the literature. ConclusionThrough this system, users can submit literature, assess classification results, and provide feedback directly influencing future model training, thereby offering an efficient and adaptive solution for accelerating phenotype-driven literature curation.
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- PhenoXtract: combining Large Language Model and Knowledge Graph embedding to extract phenotypes from clinical descriptions
Silvia Berardelli, Galadriel Brière, … Anaı̈s Baudot·bioRxiv·Jun 26, 2026
- PhenoID, a language model normalizer of physical examinations from genetics clinical notes
Davy Weissenbacher, Siddharth Rawal, … Ian M. Campbell·medRxiv·Oct 16, 2023
- Database-Augmented Transformer-Based Large Language Models Achieve High Accuracy in Mapping Gene-Phenotype Relationships
Nicolas Matthew Suhardi, Anastasia Oktarina, … Vincentius Jeremy Suhardi·bioRxiv·Jan 28, 2025
- Evaluating Large Language Models for Gene-to-Phenotype Mapping: The Critical Role of Full-Text Database Access
Nicolas Matthew Suhardi, Anastasia Oktarina, … Vincentius Jeremy Suhardi·bioRxiv·Jun 11, 2025
- Improving Automated Deep Phenotyping Through Large Language Models Using Retrieval Augmented Generation
Brandon T. Garcia, Lauren E. Westerfield, … Jennifer Ellen Posey·Genome MedicinePeer-reviewed·Aug 18, 2025
- Annotation of phenotypes using ontologies: a Gold Standard for the training and evaluation of natural language processing systems
Wasila Dahdul, Prashanti Manda, … Paula M. Mabee·bioRxiv·May 15, 2018