antiProfiles

antiProfiles identifies stochastic hyper-variability in gene expression and derives genomic anti-profiles for developing cancer diagnostic and prognostic signatures.


Key Features:

  • Gene Expression Anti-Profile Development: Identifies stochastic hyper-variability in gene expression across samples and constructs predictive anti-profiles robust to cancer heterogeneity.
  • Single-Chip Microarray Normalization: Processes microarray data using single-chip normalization and quality assessment to maintain data fidelity across studies.
  • Universal Cancer Signature: Produces a universal cancer anti-profile that discriminates cancerous from normal tissues with ten-fold cross-validation AUC > 0.92 across tissue types.
  • Peripheral Blood-Based Diagnostics: Applies anti-profiles to peripheral blood for colon cancer detection with reported AUC = 0.89 in independent studies compared to AUC = 0.81 for a commercial test.

Scientific Applications:

  • Cancer Diagnosis and Prognosis: Derives genomic signatures from expression heterogeneity for early cancer diagnosis and prediction of disease progression.
  • Non-Invasive Screening: Applies signatures to peripheral blood samples to enable non-invasive cancer screening approaches.
  • Broad Applicability Across Cancer Types: Identifies hyper-variable genes across multiple cancer types to support application of anti-profiles across diverse cancers.

Methodology:

Constructs anti-profiles from experimental findings on gene expression variability, applies single-chip microarray normalization and quality assessment, and evaluates signature performance using ten-fold cross-validation to compute AUC.

Topics

Collections

Details

License:
Artistic-2.0
Tool Type:
command-line tool, library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
1/17/2017
Last Updated:
11/25/2024

Operations

Publications

Corrada Bravo H, Pihur V, McCall M, Irizarry RA, Leek JT. Gene expression anti-profiles as a basis for accurate universal cancer signatures. BMC Bioinformatics. 2012;13(1). doi:10.1186/1471-2105-13-272. PMID:23088656. PMCID:PMC3487959.

Documentation

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