Incorporating exon–exon junction reads enhances differential splicing detection

Abstract Background RNA sequencing (RNA-seq) is a gold standard technology for studying gene and transcript expression. Different transcripts from the same gene are usually determined by varying combinations of exons within the gene, formed by splicing events. One method of studying differential alt...

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Main Authors: Mai T. Pham, Michael J. G. Milevskiy, Jane E. Visvader, Yunshun Chen
Format: Article
Language:English
Published: BMC 2025-07-01
Series:BMC Bioinformatics
Subjects:
Online Access:https://doi.org/10.1186/s12859-025-06210-4
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author Mai T. Pham
Michael J. G. Milevskiy
Jane E. Visvader
Yunshun Chen
author_facet Mai T. Pham
Michael J. G. Milevskiy
Jane E. Visvader
Yunshun Chen
author_sort Mai T. Pham
collection DOAJ
description Abstract Background RNA sequencing (RNA-seq) is a gold standard technology for studying gene and transcript expression. Different transcripts from the same gene are usually determined by varying combinations of exons within the gene, formed by splicing events. One method of studying differential alternative splicing between groups in short-read RNA-seq experiments is through differential exon usage (DEU) analysis, which uses exon-level read counts along with downstream statistical testing strategies. However, the standard exon counting method does not consider exon-junction information, which may reduce the statistical power in detecting splicing alterations. Results We present a new workflow for differential splicing analysis, called differential exon-junction usage (DEJU). This DEJU analysis workflow adopts a new feature quantification approach that jointly summarises exon and exon–exon junction reads, which are then integrated into the established Rsubread-edgeR/limma frameworks. We performed comprehensive simulation studies to benchmark the performance of DEJU against existing methods. We also applied DEJU to a mouse mammary gland RNA-seq dataset, revealing biologically meaningful splicing events that could not be detected previously. Conclusions We demonstrate that incorporating exon–exon junction reads significantly improves the detection of differential splicing events. The proposed DEJU workflow offers increased statistical power and computational efficiency compared to widely used existing approaches, while effectively controlling the false discovery rate.
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spelling doaj-art-5a93139a9c794e079d4e417367ba0efd2025-08-20T04:03:11ZengBMCBMC Bioinformatics1471-21052025-07-0126111510.1186/s12859-025-06210-4Incorporating exon–exon junction reads enhances differential splicing detectionMai T. Pham0Michael J. G. Milevskiy1Jane E. Visvader2Yunshun Chen3ACRF Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical ResearchACRF Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical ResearchACRF Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical ResearchACRF Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical ResearchAbstract Background RNA sequencing (RNA-seq) is a gold standard technology for studying gene and transcript expression. Different transcripts from the same gene are usually determined by varying combinations of exons within the gene, formed by splicing events. One method of studying differential alternative splicing between groups in short-read RNA-seq experiments is through differential exon usage (DEU) analysis, which uses exon-level read counts along with downstream statistical testing strategies. However, the standard exon counting method does not consider exon-junction information, which may reduce the statistical power in detecting splicing alterations. Results We present a new workflow for differential splicing analysis, called differential exon-junction usage (DEJU). This DEJU analysis workflow adopts a new feature quantification approach that jointly summarises exon and exon–exon junction reads, which are then integrated into the established Rsubread-edgeR/limma frameworks. We performed comprehensive simulation studies to benchmark the performance of DEJU against existing methods. We also applied DEJU to a mouse mammary gland RNA-seq dataset, revealing biologically meaningful splicing events that could not be detected previously. Conclusions We demonstrate that incorporating exon–exon junction reads significantly improves the detection of differential splicing events. The proposed DEJU workflow offers increased statistical power and computational efficiency compared to widely used existing approaches, while effectively controlling the false discovery rate.https://doi.org/10.1186/s12859-025-06210-4Exon junctionAlternative splicingRNA-sequencing
spellingShingle Mai T. Pham
Michael J. G. Milevskiy
Jane E. Visvader
Yunshun Chen
Incorporating exon–exon junction reads enhances differential splicing detection
BMC Bioinformatics
Exon junction
Alternative splicing
RNA-sequencing
title Incorporating exon–exon junction reads enhances differential splicing detection
title_full Incorporating exon–exon junction reads enhances differential splicing detection
title_fullStr Incorporating exon–exon junction reads enhances differential splicing detection
title_full_unstemmed Incorporating exon–exon junction reads enhances differential splicing detection
title_short Incorporating exon–exon junction reads enhances differential splicing detection
title_sort incorporating exon exon junction reads enhances differential splicing detection
topic Exon junction
Alternative splicing
RNA-sequencing
url https://doi.org/10.1186/s12859-025-06210-4
work_keys_str_mv AT maitpham incorporatingexonexonjunctionreadsenhancesdifferentialsplicingdetection
AT michaeljgmilevskiy incorporatingexonexonjunctionreadsenhancesdifferentialsplicingdetection
AT janeevisvader incorporatingexonexonjunctionreadsenhancesdifferentialsplicingdetection
AT yunshunchen incorporatingexonexonjunctionreadsenhancesdifferentialsplicingdetection