Evidence map›Paper›PMID 41325271›Full record

ArticleBioinformatics (Oxford, England)2025

Bayesian reconstruction and differential testing of excised introns.

Marjan Hosseini, Devin McConnell, Derek Aguiar

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Marjan HosseiniSchool of Computing, University of Connecticut, Storrs, CT 06269, United States.
Devin McConnellSchool of Computing, University of Connecticut, Storrs, CT 06269, United States.
Derek AguiarSchool of Computing, University of Connecticut, Storrs, CT 06269, United States.ORCID 0000-0001-9166-8783

Funding

Non-B DNA structure discovery and function assessment using nanopore translocation timesR01HG014255 · NHGRI · UNIVERSITY OF CONNECTICUT STORRS · PI AGUIAR, DEREK C. · 2025 to 2025
$805k
DA's University of Connecticut start-up research fundsNHGRI NIH HHS R01 HG014255NIH NHGRI 1R01HG014255-01NSF IIS 2239870
6 · The paper itself

Abstract

motivationCharacterizing the differential excision of introns is critical for understanding the functional complexity of a cell or tissue, from normal developmental processes to disease pathogenesis. Most transcript reconstruction methods infer full-length transcripts from high-throughput sequencing data. However, this is a challenging task due to incomplete annotations and the heterogeneous expression of transcripts across cell-types, tissues, and experimental conditions. Several recent methods circumvent these difficulties by considering local splicing events, but these methods lose transcript-level splicing information and may conflate similar, but distinct transcripts.

resultsIn this work, we formalize a new transcript reconstruction problem that interpolates between the full-length and local splicing perspectives by considering sequences of exon-exon junctions (SEEJs) that co-occur in transcripts. We then present a hierarchical Bayesian admixture model and posterior inference algorithms for computing SEEJs (BSEEJ), and a generalized linear model for characterizing differential SEEJ usage based on model parameter estimates. We show that BSEEJ achieves high F1 score for reconstruction tasks and improved accuracy and sensitivity in differential splicing when compared with six transcript and local splicing methods on simulated data. Lastly, we evaluate BSEEJ on experimental data based on transcript reconstruction, novelty of transcripts produced, model sensitivity to hyperparameters, and a functional analysis of differentially expressed SEEJs. AVAILABILITY AND IMPLEMENTATION: BSEEJ is freely available at https://github.com/bayesomicslab/BSEEJ.

Indexed as

Computational BiologyIntronsRNA SplicingAlgorithmsBayes TheoremExonsHigh-Throughput Nucleotide SequencingHumans

Identifiers

PMID41325271
PMCPMC12721381

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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.