Evidence map›Paper›PMID 42824423›Full record

ArticleFrontiers in bioinformatics2026

Entropy-driven machine learning for deciphering mRNA rearrangement by splicing in complex microorganisms.

Alessio Mancini, Emanuela Merelli, Marco Piangerelli, Sandra Pucciarelli, Leonardo Vito

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Article in Frontiers 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.

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Alessio ManciniSchool of Biosciences and Veterinary Medicine, Biosciences and Biotechnology Division, University of Camerino, Camerino, Italy.
Emanuela MerelliSchool of Science and Technology, Computer Science Division, University of Camerino, Camerino, Italy.
Marco PiangerelliSchool of Science and Technology, Computer Science Division, University of Camerino, Camerino, Italy.
Sandra PucciarelliSchool of Biosciences and Veterinary Medicine, Biosciences and Biotechnology Division, University of Camerino, Camerino, Italy.
Leonardo VitoSchool of Science and Technology, Computer Science Division, University of Camerino, Camerino, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Alternative splicing allows a single gene to produce multiple messenger RNA (mRNA) variants by differential RNA processing, resulting in the translation of distinct protein isoforms. Intron retention (IR) is a specific type of alternative splicing in which introns remain unspliced in the mature mRNA. The exact regulatory code behind intron splicing remains not fully deciphered, and unraveling these mechanisms is critical to uncovering the foundations of genetic disorders: a substantial fraction of disease-causing mutations disrupt intron splicing. Methods: We applied explainable machine learning (xML) models to intronic sequences from four species of the ciliate genus Tetrahymena ( Results: Across 289.6 k analysed introns, the C5.0 decision tree gave the best and most consistent performance, ranking first in three of the four species (accuracy 0.948-0.984). The key distinguishing features of retained introns were a higher entropy (Shannon entropy above 1.67, versus below 1.53 for constitutively spliced introns, against a theoretical maximum of 2) and more complex secondary structures near the 3' splice sites, together with a greater effective branch-point-to-3'-splice-site distance and a relative enrichment of the GC dinucleotide. Discussion: These features converge on weaker, less accessible splicing signals, which may impair splice-site recognition and bias the outcome towards retention. Our work identifies key sequence-level features predictive of intron retention in Tetrahymena and could provide a generalizable, explainable ML framework for investigating splicing regulation in other eukaryotes.

Indexed as

cis-regulatory elementsexplainable machine learningintron retentionLempel–Ziv (LZ) measuremultiple mRNA variantsShannon entropyTetrahymena

Identifiers

PMID42824423
PMCPMC13627988

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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.