Evidence map›Paper›PMID 41858229›Full record

ArticleBioinformatics (Oxford, England)2026

SpliceHarmonization: an integrated method for identifying RNA splicing events in therapeutics for splicing modulation.

Yirui Chen, Haotian Zhang, Yu H Sun, Soumya Negi, Shaolong Cao, Zhengyu Ouyang, Baohong Zhang, Jessica Hurt, Dann Huh

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

9 authors.

Yirui ChenGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.ORCID 0000-0003-1522-8908
Haotian ZhangGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.
Yu H SunGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.ORCID 0000-0003-0333-2898
Soumya NegiGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.
Shaolong CaoGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.
Zhengyu OuyangData Science, BioInfoRx Inc., Madison, WI 53719, United States.
Baohong ZhangGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.ORCID 0000-0003-4735-4212
Jessica HurtGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.
Dann HuhGenomics and Computational Biology, Biomarkers and Systems Biology, Biogen Inc., Cambridge, MA 02142, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationSplicing, a critical co-transcriptional process in eukaryotes, enhances transcriptome diversity by generating isoforms specific to cell types, tissues, or developmental stages. Recent advancements in splicing modulators have opened new avenues for targeting previously undruggable genes by inducing significant perturbations in splicing events. These developments underscore the need for comprehensive methods to accurately identify and compare splicing events. While several tools have been developed to detect local splice variants, inconsistencies across methods remain a significant challenge. To address this, we present SpliceHarmonization, an integrated approach that combines the strengths of rMATS, LeafCutter, and MAJIQ, enabling robust and reliable splicing analysis with event type annotations.

resultsIn a comprehensive evaluation using diverse simulated datasets, SpliceHarmonization streamlined and standardized the outputs from three detection methods into a unified format, thereby improving splicing detection with event type annotation and outperforming individual methods. By integrating the outputs from rMATS, LeafCutter, and MAJIQ, our approach not only enhanced identification of a wide range of splicing events but also effectively mitigated method-specific discrepancies. This integration led to an accuracy exceeding 0.8 and a recall of up to 0.5, with an observed increase in AUC of up to 10%. Furthermore, SpliceHarmonization demonstrated high sensitivity in detecting low-abundance and complex splicing events, providing annotations including genomic coordinates and event type. AVAILABILITY AND IMPLEMENTATION: SpliceHarmonization is available at https://github.com/interactivereport/SpliceHarmonization.

Indexed as

Computational BiologyRNA SplicingSoftwareHumansSequence Analysis, RNA

Identifiers

PMID41858229
PMCPMC13064980

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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.