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Transcriptome Analysis of Single Cells
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scESI: evolutionary sparse imputation for single-cell transcriptomes from nearest neighbor cells.

Qiaoming Liu1, Ximei Luo2,3, Jie Li1

  • 1School of Computer Science and Technology, Harbin Institute of Technology, Harbin, China.

Briefings in Bioinformatics
|May 5, 2022
PubMed
Summary
This summary is machine-generated.

The evolutionary sparse imputation (ESI) algorithm addresses noise in single-cell RNA sequencing data by learning cell relationships. ESI improves data quality, cell type classification, and biological discovery.

Keywords:
imputationmultiobjective evolutionary algorithmsingle-cell RNA-seqsparse representation

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Single-cell RNA sequencing (scRNA-seq) data is prone to noise from the ubiquitous dropout problem, impacting gene expression profiles.
  • This noise hinders accurate downstream analyses such as cell type classification and trajectory inference.

Purpose of the Study:

  • To develop a novel algorithm, evolutionary sparse imputation (ESI), to address the dropout problem in scRNA-seq data.
  • To improve the quality and reliability of scRNA-seq data by reducing noise and imputing missing gene expression values.

Main Methods:

  • Constructed a sparse representation model for single-cell transcriptomes utilizing gene regulation relationships.
  • Designed an optimization framework based on nondominated sorting genetics to solve the sparse model.
  • Incorporated topological cell relationships and gene expression variability into an iterative global optimization search.

Main Results:

  • The ESI algorithm learned a Pareto optimal cell-cell affinity matrix, effectively modeling sparse relationships.
  • scESI demonstrated superior performance over benchmark methods on simulated datasets across various metrics.
  • Applied to real scRNA-seq data, scESI enhanced cell type classification, visualization, trajectory reconstruction, and differential gene expression analysis.

Conclusions:

  • ESI effectively reduces noise and improves data quality in scRNA-seq datasets.
  • The algorithm facilitates more accurate biological insights, including marker gene expression trend recovery, new cell type discovery, and identification of regulatory pathways.