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Bioinformatics advances · 2026

Accelerating metadata annotation in collaborative research centers: a hybrid AI workflow for biomedical entities.

СтатьяНазвание и аннотация: Перевод пока не подготовлен
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Watter Manuel, Engel Felix, Kalantari Aref, Giuliani Claudia, Schuller Karin, Franzke Claus-Werner, Sperandio Markus, Binder Harald, Kaier Klaus

Аннотация

BACKGROUND: Collaborative Research Centers rely on FAIR-compliant, richly structured metadata, yet manual annotation is a major bottleneck. We implemented a search-augmented large language model (LLM) workflow within a local research data management system to pre-annotate biomedical entities, using human-in-the-loop verification to ensure data quality.

METHODS: The pipeline uses Gemini 3 Pro in a two-step prompting strategy: (1) identify dataset deposits and stable identifiers in articles converted to Markdown; (2) extract structured fields from curated repository landing pages rendered via a headless browser. To handle a highly hierarchical metadata schema, we flattened the schema for prompting and remapped outputs to strict JSON with granular provenance tags. Authors received pre-filled metadata and could accept, edit, or delete entries (TP, FP, FN mapping). Performance metrics (precision, recall, F1) were estimated as proportions and synthesized via random-effects meta-analysis.

RESULTS: Among 51 screened articles, the LLM identified a repository deposit in 31; authors responded for 17 (55% of articles with an identified deposit; 33% of all screened articles), yielding 39 verified datasets. False positives were rare (mean 0.23) and false negatives low (mean 1.46). Precision was consistently high at 99.65% (95% CI 98.42%-100.00%). Recall showed more variability at 93.75% (95% CI 89.79%-96.96%), and the F1 score reached 96.17% (95% CI 93.78%-98.11%).

CONCLUSIONS: The hybrid workflow achieved high author-verified precision with moderate recall, shifting effort from drafting to reviewing while maintaining schema compliance. As these metrics rely on author acceptance and response rates were modest, broader, multi-site validation is needed.