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Updated: Sep 13, 2026

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
Published on: June 24, 2021
scASprofiler: profiling single-cell RNA splicing with a deep convolutional generative network
Pengwei Hu1, Pengcheng Song1, Bingjie Dai1
1State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, College of Life Sciences, Inner Mongolia University, No. 49, Xilin Gol South Road, Yuquan District, Hohhot 010020, China.
Abstract:
Single-cell RNA sequencing (scRNA-seq) enables the investigation of alternative splicing (AS) at cellular resolution. However, the analysis of AS in scRNA-seq data is constrained by sparse splice-junction coverage, a consequence of low sequencing depth per cell. This limitation is particularly pronounced in 3'-biased, droplet-based protocols. To overcome this, we developed scASprofiler, a tailored deep convolutional generative network designed to decipher AS with single-cell resolution. scASprofiler performs missing-value imputation of junction read counts by leveraging cells generated by a mask-aware variational autoencoder-generative adversarial network (VAE-GAN), reducing oversmoothing of imputed values and preserving biologically meaningful heterogeneity. Across benchmarks, scASprofiler enhances delineation of cell populations and recovery of splicing signals. When applied to datasets generated using plate- and droplet-based platforms, scASprofiler uncovers cryptic AS events and reveals cell-type-specific AS patterns that complement and extend insights derived from gene expression. Together, our study establishes scASprofiler as a robust and versatile tool for dissecting AS landscapes from scRNA-seq data.
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