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

The human (PEDB) and mouse (mPEDB) Prostate Expression Databases.

Peter S Nelson1, Colin Pritchard, Denise Abbott

  • 1Division of Human Biology and Division of Clinical Research, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, WA 98109-1024, USA. pnelson@fhcrc.org

Nucleic Acids Research
|December 26, 2001
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

Multiomic assessments of LNCaP and derived cell strains reveal determinants of prostate cancer pathobiology.

The Journal of clinical investigation·2025
Same author

Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms.

Journal of medical genetics·2025
Same author

Programmed death-1 inhibition increases vaccine-induced T-cell infiltration in patients with prostate cancer.

Journal for immunotherapy of cancer·2025
Same author

Intestinal human carboxylesterase 2 (CES2) expression rescues drug metabolism and most metabolic syndrome phenotypes in global Ces2 cluster knockout mice.

Acta pharmacologica Sinica·2024
Same author

MADDD-seq, a novel massively parallel sequencing tool for simultaneous detection of DNA damage and mutations.

Nucleic acids research·2024
Same author

Molecular consequences of acute versus chronic CDK12 loss in prostate carcinoma nominates distinct therapeutic strategies.

bioRxiv : the preprint server for biology·2024
Same journal

Neurochondrin promotes U5 snRNP maturation by regulating AAR2 release from PRPF8.

Nucleic acids research·2026
Same journal

Elongationless start-stop elements are stress-resilient translation gates that are more repressive than uTranslons.

Nucleic acids research·2026
Same journal

Evolution of the ribosomal exit tunnel through the eyes of the nascent chain.

Nucleic acids research·2026
Same journal

Enhancing the performance and interpretability of epigenetic clocks.

Nucleic acids research·2026
Same journal

FABIAN-variant 2026: improved prediction of the effects of DNA variants on transcription factor binding.

Nucleic acids research·2026
Same journal

Structural and biochemical characterization of Grimontia hollisae thermostable direct hemolysin with DNA reveals first Vibrio hemolysin with nuclease activity.

Nucleic acids research·2026
See all related articles

The Prostate Expression Databases (PEDB and mPEDB) offer researchers access to human and murine prostate gene expression data. These online resources facilitate the analysis of prostate gene expression profiles and aid in understanding prostate biology.

Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • Gene expression profiling is crucial for understanding prostate function and disease.
  • Existing resources for prostate gene expression data were limited in scope and accessibility.
  • The development of comprehensive databases is essential for advancing prostate research.

Purpose of the Study:

  • To establish and enhance online databases for accessing and analyzing human and murine prostate gene expression data.
  • To provide researchers with tools for comparative analysis of gene expression across different prostate libraries.
  • To facilitate the identification of novel genes and pathways involved in prostate biology.

Main Methods:

  • Curated relational database construction for human prostate Expressed Sequence Tags (ESTs).

Related Experiment Videos

  • Development of a murine prostate expression database (mPEDB) to complement human data.
  • Implementation of a Virtual Expression Analysis Tool (VEAT) for graphical sequence comparisons.
  • Assembly of a non-redundant 'prostate unigene' set.
  • Expansion of search functionalities to include text-based and BLAST queries.
  • Main Results:

    • PEDB archives over 84,000 human prostate ESTs from 38 cDNA libraries.
    • Detailed library information, including tissue source and sequence abundance, is provided.
    • VEAT enables differential expression analysis across libraries.
    • mPEDB expands data accessibility to murine prostate gene expression.
    • The 'prostate unigene' set represents diverse prostate gene expression.

    Conclusions:

    • PEDB and mPEDB serve as valuable, integrated online resources for prostate gene expression research.
    • These databases enhance the ability to analyze and compare gene expression profiles in human and murine prostate.
    • The developed tools and data facilitate deeper insights into prostate biology and disease mechanisms.