ITI
ITI integrates large-scale protein-protein interaction data with DNA microarray and gene expression datasets to extract genomic signatures that predict clinical outcomes such as distant metastasis in breast cancer.
Key Features:
- Network-Based Integration: Integrates protein-protein interactions with DNA microarray and gene expression data using a network-based framework for classification of transcription profiles.
- Genomic Signature Extraction: Derives genomic signatures, including estrogen receptor-specific signatures, that predict distant metastasis and patient outcomes in breast cancer.
- Stability and Generalization: Enhances the stability and generalizability of genomic signatures, with reported stability increases of 11–35% across datasets.
- Algorithmic Innovation: Employs a superimposition technique that overlays protein-protein interaction networks onto gene expression datasets to improve predictive precision.
- Performance Metrics: Validation on two compendia showed increased stability (11–35%) and superior accuracy (53–74%) for estrogen receptor-specific signatures compared to previously published methods.
Scientific Applications:
- Cancer Research: Applied to breast cancer interactome and transcriptome data to support investigation of mechanisms and markers associated with distant metastasis.
- Clinical Outcome Prediction: Produces genomic signatures for predicting patient outcomes and stratifying clinical risk in breast cancer cohorts.
Methodology:
Integration of large-scale protein-protein interaction data with DNA microarray and gene expression datasets via a superimposition process; validation performed on multiple compendia.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows
- Programming Languages:
- Perl
- Added:
- 12/18/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Garcia M, Millat-Carus R, Bertucci F, Finetti P, Birnbaum D, Bidaut G. Interactome–transcriptome integration for predicting distant metastasis in breast cancer. Bioinformatics. 2012;28(5):672-678. doi:10.1093/bioinformatics/bts025. PMID:22238264.
PMID: 22238264