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Updated: Sep 6, 2025

Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms
Published on: February 2, 2024
ResPAN: a powerful batch correction model for scRNA-seq data through residual adversarial networks
Yuge Wang1, Tianyu Liu1,2, Hongyu Zhao1
1Department of Biostatistics, Yale School of Public Health, Yale University, New Haven, CT 06520, USA.
Motivation:
With the advancement of technology, we can generate and access large-scale, high dimensional and diverse genomics data, especially through single-cell RNA sequencing (scRNA-seq). However, integrative downstream analysis from multiple scRNA-seq datasets remains challenging due to batch effects.
Results:
In this article, we propose a light-structured deep learning framework called ResPAN for scRNA-seq data integration. ResPAN is based on Wasserstein Generative Adversarial Network (WGAN) combined with random walk mutual nearest neighbor pairing and fully skip-connected autoencoders to reduce the differences among batches. We also discuss the limitations of existing methods and demonstrate the advantages of our model over seven other methods through extensive benchmarking studies on both simulated data under various scenarios and real datasets across different scales. Our model achieves leading performance on both batch correction and biological information conservation and maintains scalable to datasets with over half a million cells.
Availability And Implementation:
An open-source implementation of ResPAN and scripts to reproduce the results can be downloaded from: https://github.com/AprilYuge/ResPAN.
Supplementary Information:
Supplementary data are available at Bioinformatics online.
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