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BiAEImpute: a robust bidirectional autoencoder framework for High-fidelity dropout imputation in single-cell

Yi Zhang1,2, Xinyuan Liu3,4, Yin Wang1,2

  • 1School of Computer Science and Engineering, Guilin University of Technology, 541004, Guilin, China.

BMC Genomics
|September 27, 2025
PubMed
Summary

BiAEImpute effectively addresses dropout events in single-cell RNA sequencing (scRNA-seq) data. This bidirectional autoencoder model accurately imputes missing values, improving downstream analysis for cell heterogeneity studies.

Keywords:
Bidirectional autoencoderDropout eventsImputationSingle-Cell RNA-seq data

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Single-cell RNA sequencing (scRNA-seq) provides deep insights into cellular heterogeneity.
  • Dropout events, where transcripts go undetected, are a major challenge in scRNA-seq analysis.
  • These missing values compromise the accuracy of downstream analyses.

Purpose of the Study:

  • To develop an effective imputation method for scRNA-seq data.
  • To mitigate the adverse effects of dropout events on data analysis.

Main Methods:

  • A bidirectional autoencoder-based model, BiAEImpute, was developed.
  • The model utilizes row-wise and column-wise autoencoders to learn cellular and genetic features.
  • Synergistic integration of learned features enables robust and accurate imputation.

Main Results:

  • BiAEImpute demonstrated superior performance on four real scRNA-seq datasets compared to existing methods.
  • The model successfully restored missing values.
  • BiAEImpute improved cell subpopulation clustering, marker gene identification, and developmental trajectory inference.

Conclusions:

  • BiAEImpute is an effective and resilient tool for imputing missing data in scRNA-seq.
  • The method enhances the accuracy of downstream scRNA-seq analyses.
  • Source code is publicly available for use and further development.