KAUSTNMF
KAUSTNMF applies non-negative matrix factorization (NMF) with a maximum correntropy criterion (MCC) to analyze and cluster gene expression data for cancer classification.
Key Features:
- Non-negative matrix factorization (NMF) with MCC: Implements NMF optimized using the maximum correntropy criterion (MCC) for matrix decomposition of gene expression data.
- Maximum correntropy criterion (MCC): Maximizes correntropy as a robust similarity measure that provides stability against outliers and noise.
- Alternative to traditional losses: Replaces minimization of the l2 norm or the Kullback-Leibler distance with a correntropy maximization approach.
- Optimization algorithm: Solves the MCC-based optimization using an expectation conditional maximization algorithm.
- Improved cancer clustering performance: Demonstrated higher accuracy than existing state-of-the-art methods in cancer clustering tasks.
- Benchmark validation: Validated on six benchmark cancer datasets.
- Pattern extraction from gene expression: Extracts meaningful patterns from complex gene expression data to support cancer classification.
Scientific Applications:
- Cancer clustering and classification: Improves clustering of gene expression profiles for cancer subtype identification.
- Robust analysis of noisy data: Provides noise- and outlier-robust decomposition of gene expression matrices for downstream biological interpretation.
- Method comparison in oncology studies: Enables comparison against state-of-the-art NMF methods on cancer datasets.
Methodology:
Performs NMF using the maximum correntropy criterion (MCC), maximizes correntropy rather than minimizing the l2 norm or the Kullback-Leibler distance, and solves the resulting optimization via an expectation conditional maximization algorithm.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- MATLAB
- Added:
- 12/18/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Wang JJ, Wang X, Gao X. Non-negative matrix factorization by maximizing correntropy for cancer clustering. BMC Bioinformatics. 2013;14(1). doi:10.1186/1471-2105-14-107. PMID:23522344. PMCID:PMC3659102.