PreprintCited by 4Advanced Proteomics Techniques and ApplicationsAnomaly Detection Techniques and ApplicationsGenomics and Rare Diseases

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PROTRIDER: Protein abundance outlier detection from mass spectrometry-based proteomics data with a conditional autoencoder

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Preprint — published as 10.1093/bioinformatics/btaf628

Abstract

Structured abstract: Motivation: Detection of gene regulatory aberrations enhances our ability to interpret the impact of inherited and acquired genetic variation for rare disease diagnostics and tumor characterization. While numerous methods for calling RNA expression outliers from RNA-sequencing data have been proposed, the establishment of protein expression outliers from mass spectrometry data is lacking. Results: Here, we propose and assess various modeling approaches to call protein expression outliers across three datasets from rare disease diagnostics and oncology. We use as independent evidence the enrichment for outlier calls in matched RNA-seq samples and the enrichment for rare variants likely disrupting protein expression. We show that controlling for hidden confounders and technical covariates, while simultaneously modeling the occurrence of missing values, is largely beneficial and can be achieved using conditional autoencoders. Moreover, we find that the differences between experimental and fitted log-transformed intensities by such models exhibit heavy tails that are poorly captured with the Gaussian distribution and report stronger statistical calibration when instead using the Student’s t-distribution. Our resulting method, PROTRIDER, outperformed baseline approaches based on raw log-intensities Z-scores or on differential expression analysis with limma. The application of PROTRIDER reveals significant enrichments of AlphaMissense pathogenic variants in protein expression outliers. Overall, PROTRIDER provides a method to confidently identify aberrantly expressed proteins applicable to rare disease diagnostics and cancer proteomics. Availability and Implementation: PROTRIDER is freely available at github.com/gagneurlab/PROTRIDER and also available on Zenodo under the DOI zenodo. 15569781 . Contact: Julien Gagneur: gagneur at in.tum.de

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Metadata

Authors
Klaproth-Andrade, D., Scheller, I. F., Tsitsiridis, G., Loipfinger, S., Mertes, C., Smirnov, D., Prokisch, H., Yépez, V. A., & Gagneur, J.
Affiliations
  • Technical University of Munich (DE)
  • Helmholtz Munich (DE)
  • TUM School of Computation, Information and Technology, Technical University of Munich, Garching, Germany
  • Institut für Humangenetik (DE)
Corresponding author
Gagneur, Julien
Venue
Bioinformatics
Publisher
openRxiv
Published
2025-02-05
Volume
41
Issue
12
ISSN
1367-4803 (ISSN-L)
OpenAlex
W4416538820
Cited by
4
References
1
Citations by year
2026: 2 · 2025: 2
FWCI
1.01
Type
journal article
Language
en
Open access
Locations
  • Bioinformatics (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • PubMed Central (publishedVersion, cc-by)
Funders
Bundesministerium für Bildung und Forschung
Topics
  • Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
  • Physical Sciences › Computer Science › Artificial Intelligence › Anomaly Detection Techniques and Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
Keywords
conditional autoencoder, mass spectrometry-based proteomics, rare disease diagnosis, cancer proteomics, rare missense variants, protein abundance, t-distribution, missing data
MeSH terms
Autoencoder, Algorithms, Humans, Neoplasms, Software, Mass Spectrometry, Proteomics

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