iPAGE

iPAGE performs integrative, information-theoretic analysis of whole-genome expression and genomic sequence data, operating synergistically with FIRE (Functional Inference from Expression data) to identify perturbed pathways and associated cis-regulatory elements in cancer.


Key Features:

  • Pathway Perturbation Analysis: Identifies pathway perturbations contributing to cancer by analyzing global gene expression profiles from whole-genome datasets.
  • Information-Theoretic Approach: Applies information-theoretic methods to analyze expression levels, pathways, and genomic sequences.
  • De Novo Motif Discovery: Performs de novo motif discovery linking pathways to transcription-factor binding sites and miRNA targets, including associations with E2F, NF-Y, p53, and let-7.
  • Validation of Predictions: Produces cis-regulatory interaction predictions that have been validated by follow-up in vivo experiments.
  • Discovery Beyond Known Pathways: Detects perturbations associated with putative cis-regulatory elements that fall outside known cancer pathways.

Scientific Applications:

  • Cancer Biology Research: Systems-level dissection of regulatory perturbations in cancer to inform mechanistic hypotheses of neoplastic transformation.
  • Drug Target Discovery: Identification of novel regulatory elements and pathways as potential targets for cancer therapy.

Methodology:

Integrates global gene expression data with genomic sequences using information-theoretic analysis, performs de novo motif discovery to associate pathways with transcription-factor binding sites and miRNA targets, and operates synergistically with FIRE (Functional Inference from Expression data).

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Mac
Programming Languages:
Perl
Added:
12/18/2017
Last Updated:
11/25/2024

Operations

Publications

Goodarzi H, Elemento O, Tavazoie S. Revealing Global Regulatory Perturbations across Human Cancers. Molecular Cell. 2009;36(5):900-911. doi:10.1016/j.molcel.2009.11.016. PMID:20005852. PMCID:PMC2900319.

Documentation

Links