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Randomized singular value decomposition for integrative subtype analysis of 'omics data' using non-negative matrix

Yonghui Ni1, Jianghua He1, Prabhakar Chalise1

  • 1Department of Biostatistics and Data Science, University of Kansas Medical Center, 3901 Rainbow Blvd, Kansas City, KS 66160, USA.

Statistical Applications in Genetics and Molecular Biology
|November 8, 2023
PubMed
Summary
This summary is machine-generated.

This study introduces intNMF-rsvd, a new method for cancer subtype discovery using multi-omics data. It efficiently identifies subtypes by reducing data dimensionality and computation time, aiding clinical research.

Keywords:
CPIRSVDcancer subtypeseigenvectorintNMFintegrative clustering

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Cancer Research

Background:

  • Multi-omics data integration is crucial for cancer subtype differentiation.
  • Matrix factorization methods like Non-negative Matrix Factorization (NMF) are used for integrative clustering.
  • High dimensionality and long computation times are challenges in multi-omics clustering.

Purpose of the Study:

  • To propose a novel method, intNMF-rsvd, for efficient integrative clustering of multi-omics data.
  • To address the challenges of high dimensionality and computational cost in cancer subtype analysis.
  • To improve the identification of latent subtype structures across diverse omics datasets.

Main Methods:

  • Utilized randomized singular value decomposition (RSVD) for dimensionality reduction.
  • Applied Non-negative Matrix Factorization (NMF) for integrative clustering (intNMF-rsvd).
  • Projected multi-omics data into an eigen vector space with a user-specified lower rank.

Main Results:

  • intNMF-rsvd demonstrated efficient and competitive performance compared to state-of-the-art methods.
  • The method effectively handles large numbers of features and significantly reduces computation time.
  • Evaluated using simulated and The Cancer Genome Atlas (TCGA) datasets.

Conclusions:

  • intNMF-rsvd offers an efficient approach for multi-omics integrative clustering.
  • The method's ability to reduce computation time makes it suitable for large-scale cancer data analysis.
  • Identified subtypes can facilitate further clinical association studies for disease etiology.