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A tensor decomposition-based integrated analysis applicable to multiple gene expression profiles without sample

Y-H Taguchi1, Turki Turki2

  • 1Department of Physics, Chuo University, Tokyo, 112-8551, Japan. tag@granular.com.

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|December 9, 2022
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Summary
This summary is machine-generated.

This study introduces a novel tensor decomposition method for integrating diverse gene expression datasets without sample matching or labels. This approach effectively analyzes Alzheimer's disease data and reduces computational memory for single-cell RNA sequencing.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Integrating multiple gene expression profiles from independent studies is challenging due to missing sample matches and common labels.
  • Existing methods often require fully data-driven, unsupervised training, which is hindered by data heterogeneity.

Purpose of the Study:

  • To develop a strategy for integrating multiple gene expression profiles across independent studies without requiring sample matching or common labels.
  • To apply this strategy to Alzheimer's disease (AD) gene expression data, including single-cell RNA sequencing (scRNA-seq) data.

Main Methods:

  • Utilizing tensor decomposition for unsupervised feature extraction to enable data integration.
  • Applying the proposed strategy to Alzheimer's disease-related gene expression profiles lacking precise sample correspondence.

Main Results:

  • Successfully integrated multiple gene expression profiles from independent studies without sample matching or labels.
  • Identified biologically relevant genes through integrated analysis of Alzheimer's disease data.
  • Demonstrated that integrated gene expression profiles can function similarly to transfer-learning strategies.
  • Significantly reduced computational memory requirements for single-cell RNA sequencing data analysis.

Conclusions:

  • The proposed tensor decomposition strategy enables the integration of heterogeneous gene expression profiles across studies.
  • This approach facilitates the selection of biologically meaningful genes and enhances machine learning applications.
  • The method offers a computationally efficient solution for analyzing large-scale gene expression data, particularly scRNA-seq.