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

Gene selection and clustering for time-course and dose-response microarray experiments using order-restricted

Shyamal D Peddada1, Edward K Lobenhofer, Leping Li

  • 1Biostatistics Branch, Laboratory of Molecular Carcinogenesis, Research Triangle Park, NC 27709, USA. peddada@embryo.niehs.nih.gov

Bioinformatics (Oxford, England)
|May 2, 2003
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

Multi-ancestry transcriptome-wide association studies uncover insights into breast cancer genetics and biology.

Nature communications·2026
Same author

Improved polygenic risk prediction models for breast cancer subtypes in women of African ancestry.

Nature genetics·2026
Same author

Diagnostic labels and clusters based on oxygen requirements in preterm infants with chronic lung disease: a data-driven exploratory cluster analysis in two independent cohorts.

The Lancet. Child & adolescent health·2025
Same author

In utero and early life exposures to smoking are associated with systemic autoimmune rheumatic diseases.

Seminars in arthritis and rheumatism·2025
Same author

Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.

Cancers·2025
Same author

Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer.

Breast (Edinburgh, Scotland)·2025
Same journal

MCFST: Spatial domain identification method based on multi-view graph convolutional network and graph fusion network.

Bioinformatics (Oxford, England)·2026
Same journal

SpaBiT: Enhancing Spatial Transcriptomics Resolution via Bidirectional Attention Transformers.

Bioinformatics (Oxford, England)·2026
Same journal

EDEL: Enhancing Dense Retrievers for Curation of Biomedical Knowledge Bases.

Bioinformatics (Oxford, England)·2026
Same journal

Informative Relational Learning for Adverse Reaction Prediction with Enhanced Generalization to Novel Drugs.

Bioinformatics (Oxford, England)·2026
Same journal

An interpretable deep learning framework uncovers features governing CRISPR-Cas9 genome-editing efficiency.

Bioinformatics (Oxford, England)·2026
Same journal

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

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

We developed a new statistical algorithm to group genes based on their expression patterns over time or treatment. This method identifies significant genes and assigns them to specific temporal profiles, revealing biologically interesting patterns.

Area of Science:

  • Bioinformatics
  • Statistical Genetics
  • Computational Biology

Background:

  • Gene expression data analysis is crucial for understanding biological processes.
  • Identifying genes with specific temporal or dose-response profiles is challenging.
  • Existing methods may miss subtle yet biologically significant gene expression patterns.

Purpose of the Study:

  • To propose a novel algorithm for selecting and clustering genes based on their expression profiles.
  • To apply order-restricted inference for analyzing time-course and dose-response gene expression data.
  • To identify biologically relevant genes missed by previous analyses.

Main Methods:

  • Utilizing order-restricted inference methodology from statistics.
  • Defining candidate temporal profiles using inequalities of mean expression levels.

Related Experiment Videos

  • Employing a bootstrap-based criterion for statistical significance.
  • Assigning selected genes to the best-fitting candidate profile.
  • Main Results:

    • The algorithm successfully selects and clusters genes based on their temporal profiles.
    • Demonstrated applicability using cDNA microarray data from estrogen-stimulated breast cancer cells.
    • Identified several biologically interesting genes not detected by prior analyses.

    Conclusions:

    • The proposed algorithm offers a robust approach for analyzing gene expression dynamics.
    • Order-restricted inference provides a powerful framework for gene expression profile analysis.
    • This method enhances the discovery of biologically significant genes in time-course experiments.