Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Improving Translational Accuracy02:07

Improving Translational Accuracy

15.2K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
15.2K
Improving Translational Accuracy02:07

Improving Translational Accuracy

3.7K
3.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Optimized multichannel 4 mA vs conventional transcranial direct current stimulation for major depressive disorder: A randomized sham-controlled trial.

Molecular psychiatry·2026
Same author

Knowledge-augmented pre-trained language models for biomedical relation extraction.

BMC bioinformatics·2025
Same author

Promoting of Biomechanics' Properties Incisional Wound Repair by Mesenchymal Stem Cell Transplantation.

World journal of plastic surgery·2025
Same author

Explaining care need assessment surveys: qualitative and quantitative evaluation of state-of-the-art local and global explainable artificial intelligence methods.

JAMIA open·2025
Same author

Exploring the gut microbiome's influence on cancer-associated anemia: Mechanisms, clinical challenges, and innovative therapies.

World journal of gastrointestinal pharmacology and therapeutics·2025
Same author

From Molecular Precision to Clinical Practice: A Comprehensive Review of Bispecific and Trispecific Antibodies in Hematologic Malignancies.

International journal of molecular sciences·2025
Same journal

3DICE: Interpretable 3D Cross-Modal Learning for Drug-Target Interaction Prediction and Large-Scale Drug Discovery.

Bioinformatics (Oxford, England)·2026
Same journal

KASSPer: Kinase Active Site Structure Prediction using Protein and Ligand Language Models and Its Application to Virtual Screening.

Bioinformatics (Oxford, England)·2026
Same journal

IDR searcher: a search engine solution for public image resources.

Bioinformatics (Oxford, England)·2026
Same journal

KCFtools: Rapid alignment-free method for introgression screening and GWAS using k-mer profiles.

Bioinformatics (Oxford, England)·2026
Same journal

Meta2DB: Curated shotgun metagenomic feature sets and metadata for health state prediction.

Bioinformatics (Oxford, England)·2026
Same journal

conMItion: an R package adjusting confounding factors for associations in multi-omics.

Bioinformatics (Oxford, England)·2026
See all related articles

Related Experiment Video

Updated: Feb 23, 2026

Augmenting Large Language Models via Vector Embeddings to Improve Domain-Specific Responsiveness
03:14

Augmenting Large Language Models via Vector Embeddings to Improve Domain-Specific Responsiveness

Published on: December 6, 2024

1.2K

Deep learning with word embeddings improves biomedical named entity recognition.

Maryam Habibi1, Leon Weber1, Mariana Neves2

  • 1Computer Science Department, Humboldt-Universität zu Berlin, Berlin, Germany.

Bioinformatics (Oxford, England)
|September 9, 2017
PubMed
Summary
This summary is machine-generated.

A new deep learning method, long short-term memory network-conditional random field (LSTM-CRF), significantly improves biomedical named entity recognition (NER) by outperforming existing entity-specific tools. This generic approach enhances recall for identifying genes, chemicals, and diseases in research texts.

More Related Videos

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
07:35

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports

Published on: October 13, 2023

2.2K
DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
04:17

DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning

Published on: May 10, 2024

1.6K

Related Experiment Videos

Last Updated: Feb 23, 2026

Augmenting Large Language Models via Vector Embeddings to Improve Domain-Specific Responsiveness
03:14

Augmenting Large Language Models via Vector Embeddings to Improve Domain-Specific Responsiveness

Published on: December 6, 2024

1.2K
A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports
07:35

A Knowledge Graph Approach to Elucidate the Role of Organellar Pathways in Disease via Biomedical Reports

Published on: October 13, 2023

2.2K
DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
04:17

DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning

Published on: May 10, 2024

1.6K

Area of Science:

  • Biomedical Informatics
  • Computational Linguistics
  • Bioinformatics

Background:

  • Text mining is crucial for biomedical research, with Named Entity Recognition (NER) as a fundamental task.
  • Current NER methods are often entity-specific, requiring costly development and limiting generalizability.
  • Existing approaches rely on hand-crafted features that are difficult to optimize and transfer across datasets.

Purpose of the Study:

  • To develop and evaluate a generic, deep learning-based method for biomedical NER.
  • To demonstrate the superiority of this new method over existing state-of-the-art entity-specific tools.
  • To assess the performance across diverse biomedical entity types and datasets.

Main Methods:

  • Implemented a long short-term memory network-conditional random field (LSTM-CRF) model.
  • Utilized statistical word embeddings for feature representation.
  • Compared LSTM-CRF performance against entity-specific NER tools and an entity-agnostic CRF on 33 datasets covering five entity classes.

Main Results:

  • The LSTM-CRF model achieved an average F1-score 5% higher than baseline methods.
  • Performance gains were primarily driven by a significant increase in recall.
  • The generic LSTM-CRF approach outperformed specialized NER tools, often by a substantial margin.

Conclusions:

  • A generic deep learning approach (LSTM-CRF) can effectively perform biomedical NER without entity-specific tuning.
  • LSTM-CRF offers a more efficient and broadly applicable solution for extracting biomedical entities from text.
  • This method has the potential to advance biomedical text mining by improving the accuracy and recall of entity recognition.