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Related Experiment Video

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IDBD: infectious disease biomarker database.

In Seok Yang1, Chunsun Ryu, Ki Joon Cho

  • 1Department of Life Sciences & Biotechnology, School of Life Sciences & Biotechnology, Korea University, Seoul, Korea.

Nucleic Acids Research
|November 6, 2007
PubMed
Summary
This summary is machine-generated.

The Infectious Disease Biomarker Database (IDBD) offers a centralized resource for infectious disease biomarkers. This community-driven database facilitates early diagnosis and targeted therapy development for infectious diseases.

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Area of Science:

  • Biomedical Informatics
  • Infectious Diseases
  • Biomarker Discovery

Background:

  • Biomarkers are crucial for early diagnosis, targeted therapy, and monitoring disease response.
  • The development of novel biomarkers has slowed, with a lack of efficient resources for infectious disease biomarkers.
  • Existing literature-derived databases do not adequately address the specific needs of infectious disease biomarker information retrieval and processing.

Purpose of the Study:

  • To develop and present the Infectious Disease Biomarker Database (IDBD), a comprehensive, literature-derived resource for infectious disease biomarkers.
  • To provide an accessible platform for researchers to retrieve, process, and contribute information on infectious disease biomarkers.
  • To support the advancement of infectious disease diagnosis and treatment through efficient biomarker data management.

Main Methods:

  • Developed IDBD as a community annotation database utilizing Web 2.0 features for collaborative data input and revision.
  • Implemented a user-friendly interface for linking infectious diseases/pathogens to protein, gene, or carbohydrate biomarkers.
  • Integrated search tools and application tools for analyzing sequence and structure features of biomarkers.

Main Results:

  • IDBD currently integrates 611 biomarkers associated with 66 infectious diseases and 70 pathogens.
  • The database provides a centralized and accessible repository for literature-derived infectious disease biomarker data.
  • Community annotation features allow for ongoing data refinement and expansion.

Conclusions:

  • IDBD represents a significant step towards addressing the need for a comprehensive infectious disease biomarker resource.
  • The database's collaborative nature and search functionalities can accelerate biomarker discovery and validation.
  • IDBD is publicly accessible, promoting wider use in research and clinical applications for infectious diseases.