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 Experiment Videos

Ontology development for a pharmacogenetics knowledge base.

Diane E Oliver1, Daniel L Rubin, Joshua M Stuart

  • 1Stanford Medical Informatics, Stanford University School of Medicine, 251 Campus Drive, MSOB X-215, Stanford, CA 94305-5479, USA. oliver@smi.stanford.edu

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|April 4, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Extraction of distant recurrence sites for breast cancer patients from free-text clinical notes using large language models.

Journal of biomedical informatics·2026
Same author

Creation of Radiology Teaching Content with STELLA-A STandardized Electronic Learning Library and Application Platform.

Academic radiology·2025
Same author

Out-of-the-Box Large Language Models for Detecting and Classifying Critical Findings in Radiology Reports Using Various Prompt Strategies.

AJR. American journal of roentgenology·2025
Same author

Transcriptional profiling clarifies a program of enzalutamide extreme non-response in lethal prostate cancer.

NPJ precision oncology·2025
Same author

Open-Source Hybrid Large Language Model Integrated System for Extraction of Breast Cancer Treatment Pathway From Free-Text Clinical Notes.

JCO clinical cancer informatics·2025
Same author

Protocol for assessing distances in pathway space for classifier feature sets from machine learning methods.

STAR protocols·2025
Same journal

Trust, Reproducibility, and Progress: The Roles of Independent Blind Prediction and Assessment and Benchmarking in Computational Biology.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
Same journal

The Evolving Cyberinfrastructure at the National Institutes of Health to Support Data and AI in Biomedical Research.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
Same journal

Applications of AI & ML in Biomanufacturing of Cell and Gene Therapies.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
Same journal

AI for Health: Leveraging Artificial Intelligence to Revolutionize Healthcare.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
Same journal

Workshop Introduction: Advances of AI Methods in Single Cell Spatial Omics.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
Same journal

DRIVE-KG: Enhancing variant-phenotype association discovery in understudied complex diseases using heterogeneous knowledge graphs.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
See all related articles

Developing a pharmacogenetics knowledge base (PharmGKB) integrates diverse data to understand genetic influences on drug response. This resource facilitates genotype-phenotype correlation research by organizing and sharing crucial pharmacogenetic datasets.

Area of Science:

  • Pharmacogenetics
  • Bioinformatics
  • Computational Biology

Background:

  • Understanding genetic factors influencing drug response is crucial for personalized medicine.
  • Coordinating diverse data from lab, computational, and clinical studies is essential for pharmacogenetics research.
  • A centralized public repository is needed to accelerate progress in pharmacogenetics.

Purpose of the Study:

  • To develop the Pharmacogenetics Knowledge Base (PharmGKB) for storing and retrieving experimental and conceptual pharmacogenetic data.
  • To create an Internet-based resource integrating biological, pharmacological, and clinical data.
  • To facilitate genotype-phenotype correlation investigations by researchers.

Main Methods:

  • Utilizing a frame-based knowledge-representation system for ontology development.

Related Experiment Videos

  • Designing an ontology of concepts and relationships to represent the pharmacogenetics domain.
  • Implementing a system for data submission, storage, and querying.
  • Main Results:

    • Successfully developed an ontology for gene-sequence data.
    • Demonstrated the system's capability to accept, store, and query submitted gene-sequence data.
    • Established a framework for integrating complex pharmacogenetic information.

    Conclusions:

    • The PharmGKB is a valuable resource for organizing and disseminating pharmacogenetic data.
    • The developed ontology enables efficient management and retrieval of gene-sequence data.
    • PharmGKB is poised to accelerate research into genotype-phenotype correlations and personalized drug therapy.