Evidence map›Paper›PMID 42725920›Full record

ArticleBriefings in bioinformatics2026

scASprofiler: profiling single-cell RNA splicing with a deep convolutional generative network.

Pengwei Hu, Pengcheng Song, Bingjie Dai, Chunshen Long, Hanshuang Li, Yongchun Zuo, Yongqiang Xing

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Pengwei HuState 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.
Pengcheng SongState 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.
Bingjie DaiState 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.
Chunshen LongState 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.
Hanshuang LiState 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.
Yongchun ZuoState 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.ORCID 0000-0002-6065-7835
Yongqiang XingInner Mongolia Key Laboratory of Life Health and Bioinformatics, School of Life Science and Technology, Inner Mongolia University of Science and Technology, No. 7, Aerding Street, Kundulun District, Baotou 014010, China.ORCID 0000-0001-6987-7327

Funding

National Natural Science Foundation of China 62371265National Natural Science Foundation of China 62501318National Natural Science Foundation of China 62571279The 2025 Inner Mongolia Key Laboratory of Life Health and Bioinformatics Project 2025KYPT0135The 2026 Inner Mongolia Key Laboratory of Life Health and Bioinformatics Project 2026KYPT0062The China Postdoctoral Science Foundation 2024MD763987 and 2025MD784078The Group Project of Developing Inner Mongolia through Talents 2025TEL25The Natural Science Foundation of Inner Mongolia Autonomous Region 2024JQ10The Natural Science Foundation of Inner Mongolia Autonomous Region 2025QN03080The Natural Science Foundation of Inner Mongolia Autonomous Region 2025QN06021
6 · The paper itself

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.

Indexed as

Alternative SplicingRNA SplicingSingle-Cell AnalysisSoftwareConvolutional Neural NetworksGenerative Adversarial NetworksHumansSequence Analysis, RNASingle-Cell Gene Expression Analysisalternative splicingcell heterogeneityimputationscRNA-seqVAE-GAN

Identifiers

PMID42725920
PMCPMC13563674

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.