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An improved hierarchical variational autoencoder for cell-cell communication estimation using single-cell RNA-seq

Shuhui Liu1, Yupei Zhang1,2, Jiajie Peng1,2

  • 1School of Computer Science, Northwestern Polytechnical University, Xi'an 710129, Shaanxi, China.

Briefings in Functional Genomics
|February 8, 2023
PubMed
Summary
This summary is machine-generated.

This study introduces an improved hierarchical variational autoencoder (HiVAE) model to accurately estimate cell-cell communication (CCC) using single-cell RNA-Seq data, enhancing cancer progression insights.

Keywords:
HiVAE modelcell–cell communicationpairwise ligand–receptorsingle-cell RNA-seq datatransfer entropy

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Area of Science:

  • Computational biology
  • Genomics
  • Cancer research

Background:

  • Cell-cell communication (CCC) in the tumor microenvironment is crucial for understanding cancer progression and drug tolerance.
  • Single-cell RNA sequencing (scRNA-Seq) offers vast data for predicting cellular interactions.
  • Existing methods for inferring CCC rely on limited prior knowledge, leading to inaccuracies.

Purpose of the Study:

  • To develop an improved model for estimating CCC by leveraging comprehensive scRNA-Seq data.
  • To overcome limitations of existing methods that depend on incomplete molecular interaction databases.
  • To provide a more accurate and automated approach for analyzing cellular communication.

Main Methods:

  • Proposed an improved hierarchical variational autoencoder (HiVAE) model.
  • Utilized HiVAE to learn cell representations from both known ligand-receptor genes and all genes in scRNA-Seq data.
  • Employed transfer entropy to quantify information flow and estimate directed communication relationships between cells.

Main Results:

  • The HiVAE model effectively learned meaningful cell representations.
  • Transfer entropy accurately estimated communication scores between cell types.
  • Demonstrated the model's efficacy on human skin disease and melanoma datasets.

Conclusions:

  • The HiVAE model offers a powerful approach for automated CCC estimation from scRNA-Seq data.
  • This method enhances the understanding of cellular interactions in complex biological systems.
  • The findings have implications for cancer research and therapeutic development.