Evidence map›Paper›PMID 40796134›Full record

ArticleBioinformatics (Oxford, England)2025

IsoBayes: a Bayesian approach for single-isoform proteomics inference.

Jordy Bollon, Michael R Shortreed, Erin Jeffery, Ben T Jordan, Rachel Miller, Andrea Cavalli, Lloyd M Smith, Colin N Dewey, Gloria M Sheynkman, Simone Tiberi

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. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Estimating protein isoform abundances with [Formula: see text].Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

  • Update of
    2025
5 · Who and what money

Authors and funding

10 authors.

Jordy BollonComputational and Chemical Biology, Italian Institute of Technology, Genova 16163, Italy.
Michael R ShortreedDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706, United States.
Erin JefferyDepartment of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22903, United States.
Ben T JordanFrederick National Laboratory for Cancer Research, Frederick, MD 21701, United States.
Rachel MillerDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706, United States.
Andrea CavalliComputational and Chemical Biology, Italian Institute of Technology, Genova 16163, Italy.ORCID 0000-0003-4063-4502
Lloyd M SmithDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI 53706, United States.
Colin N DeweyDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI 53726, United States.ORCID 0000-0003-1498-9254
Gloria M SheynkmanDepartment of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22903, United States.ORCID 0000-0002-4223-9947
Simone TiberiDepartment of Statistical Sciences, University of Bologna, Bologna 40126, Italy.ORCID 0000-0002-3054-9964

Funding

Enhanced Sensitivity and Quantitative Precision for Single Cell ProteomicsR01GM147653 · NIGMS · BRIGHAM YOUNG UNIVERSITY · PI PAYNE, SAMUEL H, SHORTREED, MICHAEL R · 2022 to 2025
$1.6M
NIGMS NIH HHS R01 GM147653NIGMS NIH HHS R01GM147653
6 · The paper itself

Abstract

motivationStudying protein isoforms is an essential step in biomedical research; at present, the main approach for analyzing proteins is via bottom-up mass spectrometry proteomics, which return peptide identifications, that are indirectly used to infer the presence of protein isoforms. However, the detection and quantification processes are noisy; in particular, peptides may be erroneously detected, and most peptides, known as shared peptides, are associated to multiple protein isoforms. As a consequence, studying individual protein isoforms is challenging, and inferred protein results are often abstracted to the gene-level or to groups of protein isoforms.

resultsHere, we introduce IsoBayes, a novel statistical method to perform inference at the isoform level. Our method enhances the information available, by integrating mass spectrometry proteomics and transcriptomics data in a Bayesian probabilistic framework. To account for the uncertainty in the measurement process, we propose a two-layer latent variable approach: first, we sample if a peptide has been correctly detected (or, alternatively filter peptides); second, we allocate the abundance of such selected peptides across the protein(s) they are compatible with. This enables us, starting from peptide-level data, to recover protein-level data; in particular, we: (i) infer the presence/absence of each protein isoform (via a posterior probability), (ii) estimate its abundance (and credible interval), and (iii) target isoforms where transcript and protein relative abundances significantly differ. We benchmarked our approach in simulations, and in two multi-protease real datasets: our method displays good sensitivity and specificity when detecting protein isoforms, its estimated abundances highly correlate with the ground truth, and can detect changes between protein and transcript relative abundances. AVAILABILITY AND IMPLEMENTATION: IsoBayes is freely distributed as a Bioconductor R package, and is accompanied by an example usage vignette.

Indexed as

ProteomicsSoftwareAlgorithmsBayes TheoremDatabases, ProteinMass SpectrometryPeptidesProtein IsoformsPeptidesProtein Isoforms

Identifiers

PMID40796134
PMCPMC12377908

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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.