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Размер весов
2,4 ГБ
Лицензия
Apache 2.0
Опубликована
15 сен 2025

OpenMed-ZeroShot-NER-Pharma-XLarge-770M

Разметка токеновТекст → label3 профессии

GLiNER-модель OpenMed, дообученная для извлечения химических соединений и лекарств из биомедицинских текстов, включая zero-shot сценарии с пользовательскими типами сущностей.

36 891скачиваний за 30 дней3лайкавеса обновлены18 окт 2025

Бенчмарки

Как модель справилась с задачами пользователей ailist и что о ней публикуют открытые лидерборды

Публичные оценки

Из открытых лидербордов. Сравнивайте результаты одного теста при одинаковых условиях — отсутствие оценки не значит, что модель хуже.

В подключённых источниках результатов для этой модели пока нет.

Что умеет модель

Описание составлено по карточке модели и метаданным Hugging Face

OpenMed-ZeroShot-NER-Pharma-XLarge-770M — модель OpenMed для распознавания химических сущностей в биомедицинских текстах. Она построена на архитектуре GLiNER и дообучена на корпусе BC5CDR-Chem для извлечения названий химических соединений, лекарств и терапевтических веществ. В карточке приведён результат F1 0,9463 на тестовом наборе BC5CDR-Chem.

Модель предназначена для извлечения упоминаний химических веществ из научной литературы и медицинских текстов, в том числе как этап конвейеров фармаконадзора, поиска нежелательных реакций и анализа связей между химическими веществами и заболеваниями. Заявлена возможность zero-shot распознавания пользовательских типов сущностей, однако основное обучение и приведённая оценка относятся к химическим сущностям BC5CDR-Chem. Модель принимает текст и возвращает текстовые упоминания с метками сущностей.

Репозиторий содержит веса PyTorch; лицензия — Apache-2.0. Карточка не сообщает длину контекста. Результаты на BC5CDR-Chem не гарантируют аналогичное качество на других типах сущностей, языках или клинических данных; пользовательские метки могут требовать настройки порога распознавания.

Сценарии применения

  • извлечение названий лекарств из научных аннотаций
  • поиск химических соединений в биомедицинской литературе
  • подготовка упоминаний веществ для фармаконадзора
  • сбор химических сущностей для анализа связей с заболеваниями
  • разметка химических упоминаний в корпусах биомедицинских текстов

Ограничения

Основное обучение и указанная оценка F1 0,9463 относятся к химическим сущностям корпуса BC5CDR-Chem; качество для других сущностей и клинических текстов отдельно не подтверждено. Для пользовательских типов сущностей карточка рекомендует подбирать порог распознавания.

Для каких профессий подходит3

Разделы каталога профессий, в задачах которых используется эта модель

Все профессии

Карточка модели

README от автора на Hugging Face, как он его опубликовал

Открыть на Hugging Face

🧬 OpenMed-ZeroShot-NER-Pharma-XLarge-770M

Specialized model for Chemical Entity Recognition - Chemical entities from the BC5CDR dataset

License Python GliNER OpenMed

📋 Model Overview

Focused on chemical mentions in the BC5CDR domain, capturing pharmaceutical compounds and therapeutic agents in context with diseases.Enables pharmacovigilance, adverse event mining, and chemical–disease relation pipelines when paired with downstream relation extraction.

OpenMed ZeroShot NER is an advanced, domain-adapted Named Entity Recognition (NER) model designed specifically for medical, biomedical, and clinical text mining. Leveraging state-of-the-art zero-shot learning, this model empowers researchers, clinicians, and data scientists to extract expert-level biomedical entities—such as diseases, chemicals, genes, species, and clinical findings—directly from unstructured text, without the need for task-specific retraining.

Built on the robust GLiNER architecture and fine-tuned on curated biomedical corpora, OpenMed ZeroShot NER delivers high-precision entity recognition for critical healthcare and life sciences applications. Its zero-shot capability means you can flexibly define and extract any entity type relevant to your workflow, from standard biomedical categories to custom clinical concepts, supporting rapid adaptation to new research domains and regulatory requirements.

Whether you are working on clinical NLP, biomedical research, electronic health record (EHR) de-identification, or large-scale literature mining, OpenMed ZeroShot NER provides a production-ready, open-source solution that combines expert-level accuracy with unmatched flexibility. Join the OpenMed community to accelerate your medical text analytics with cutting-edge, zero-shot NER technology.

🎯 Key Features

  • Zero-Shot Capability: Can recognize any entity type without specific training
  • High Precision: Optimized for biomedical entity recognition
  • Domain-Specific: Fine-tuned on curated BC5CDR_CHEM dataset
  • Production-Ready: Validated on clinical benchmarks
  • Easy Integration: Compatible with Hugging Face Transformers ecosystem
  • Flexible Entity Recognition: Add custom entity types without retraining

🏷️ Supported Entity Types

This zero-shot model can identify and classify biomedical entities, including but not limited to these entity types. You can also add custom entity types without retraining the model:

  • CHE

💡 Zero-Shot Flexibility: As a GliNER-based model, you can specify any entity types you want to detect, even if they weren't part of the original training. Simply provide the entity labels when using the model, and it will adapt to recognize them.

📊 Dataset

BC5CDR-Chem focuses on chemical entity recognition from the BioCreative V Chemical-Disease Relation extraction task.

The BC5CDR-Chem corpus is part of the BioCreative V Chemical-Disease Relation (CDR) extraction challenge, specifically targeting chemical entity recognition in biomedical texts. This dataset contains 1,500 PubMed abstracts with 4,409 annotated chemical entities, designed to support automated drug discovery and pharmacovigilance applications. The corpus emphasizes chemical compounds, drugs, and therapeutic substances that are relevant for understanding chemical-disease relationships. It serves as a critical resource for developing NER systems that can identify chemical entities for downstream tasks like adverse drug reaction detection and drug repurposing research.

📊 Performance Metrics

Current Model Performance

  • Finetuned F1 vs. Base Model (on test dataset excluded from training): 0.95
  • F1 Improvement vs Base Model: 26.6%

🏆 Top F1 Improvements on BC5CDR_CHEM Dataset

RankModelBase F1Finetuned F1ΔF1ΔF1 %
🥇 1OpenMed-ZeroShot-NER-Pharma-Large-459M0.75370.95420.200526.6%
🥈 2OpenMed-ZeroShot-NER-Pharma-XLarge-770M0.72990.94630.216429.7%
🥉 3OpenMed-ZeroShot-NER-Pharma-Medium-209M0.63580.94570.310048.8%
4OpenMed-ZeroShot-NER-Pharma-Base-220M0.65540.91970.264340.3%
5OpenMed-ZeroShot-NER-Pharma-Multi-209M0.65480.89310.238336.4%

Rankings are sorted by finetuned F1 and show ΔF1% over base model. Test dataset is excluded from training.

OpenMed ZeroShot Clinical & Biomedical NER vs. Original GLiNER models

Figure: OpenMed ZeroShot Clinical & Biomedical NER vs. Original GLiNER models.

🚀 Quick Start

Installation

pip install -q "gliner[tokenizers]"

Usage

from transformers import pipeline

# Load the model and tokenizer
# Model: https://huggingface.co/OpenMed/OpenMed-ZeroShot-NER-Pharma-XLarge-770M
model_name = "OpenMed/OpenMed-ZeroShot-NER-Pharma-XLarge-770M"

from gliner import GLiNER
model = GLiNER.from_pretrained(model_name)

# Example usage with default entity types
text = "Administration of metformin reduced glucose levels significantly."

labels = ['CHE']
entities = model.predict_entities(text, labels, flat_ner=True, threshold=0.5)
for entity in entities:
    print(entity)

Zero-Shot Usage with Custom Entity Types

💡 Tip: If you want to extract entities that are not present in the original training set (i.e., use custom or rare entity types), you may get better results by lowering the threshold parameter in model.predict_entities. For example, try threshold=0.3 or even lower, depending on your use case:

# You can specify custom entity types for zero-shot recognition - for instance:
custom_entities = ["MISC", "CHE", "PERSON", "LOCATION", "MEDICATION", "PROCEDURE"]

entities = model.predict_entities(text, custom_entities, flat_ner=True, threshold=0.1)
for entity in entities:
    print(entity)

Lowering the threshold makes the model more permissive and can help it recognize new or less common entity types, but may also increase false positives. Adjust as needed for your application.

📚 Dataset Information

  • Dataset: BC5CDR_CHEM
  • Description: Chemical Entity Recognition - Chemical entities from the BC5CDR dataset

Training Details

  • Base Model: gliner-x-large
  • Training Framework: Hugging Face Transformers
  • Optimization: AdamW optimizer with learning rate scheduling
  • Validation: Cross-validation on held-out test set

💡 Use Cases

This model is particularly useful for:

  • Clinical Text Mining: Extracting entities from medical records
  • Biomedical Research: Processing scientific literature
  • Drug Discovery: Identifying chemical compounds and drugs
  • Healthcare Analytics: Analyzing patient data and outcomes
  • Academic Research: Supporting biomedical NLP research
  • Custom Entity Recognition: Zero-shot detection of domain-specific entities

🔬 Model Architecture

  • Task: Zero-Shot Classification (Named Entity Recognition)
  • Labels: Dataset-specific entity types
  • Input: Biomedical text
  • Output: Named entity predictions

📜 License

Licensed under the Apache License 2.0. See LICENSE for details.

🤝 Contributing

I welcome contributions of all kinds! Whether you have ideas, feature requests, or want to join my mission to advance open-source Healthcare AI, I'd love to hear from you.

Follow OpenMed Org on Hugging Face 🤗 and click "Watch" to stay updated on my latest releases and developments.

Citation

If you use this model in your research or applications, please cite the following paper:

@misc{panahi2025openmedneropensourcedomainadapted,
      title={OpenMed NER: Open-Source, Domain-Adapted State-of-the-Art Transformers for Biomedical NER Across 12 Public Datasets},
      author={Maziyar Panahi},
      year={2025},
      eprint={2508.01630},
      archivePrefix={arXiv},
      primaryClass={cs.CL},
      url={https://arxiv.org/abs/2508.01630},
}

Proper citation helps support and acknowledge my work. Thank you!

Как запустить

На своей GPU в ailist. Цена — по текущим предложениям провайдеров

GPU в ailist

Универсальный рантайм

Нельзя запустить

Модели GLiNER требуют отдельного рантайма.

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