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PROTRIDER: Protein abundance outlier detection from mass spectrometry-based proteomics data with a conditional autoencoder
Open accessPreprint — 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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Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Flagged first, then by citations
Research works printed but not linked: 48
- 10.1158/0008-5472.CAN-12-3342 · DOI · Paper page
- Ahlmann-Eltze, Constantin , and Anders, Simon , ‘proDA: Probabilistic Dropout Analysis for Identifying Differentially Abundant Proteins in Label-Free Mass Spectrometry’ (2019) <http://biorxiv.org/lookup/doi/10.1101/661496> [accessed 1 June 2025] · DOI
- Benjamini, Y. , and Hochberg, Y ., ‘Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Hypothesis Testing’, J R Stat Soc B, 57 (1995) · DOI · Paper page
- 2001, The Control of the False Discovery Rate in Multiple Testing under Dependency, The Annals of Statistics, 29, 1165
- Berger-Wolf, Tanya , and Chawla, Nitesh , eds., Proceedings of the 2019 SIAM International Conference on Data Mining (Philadelphia, PA, 2019) <https://epubs.siam.org/doi/book/10.1137/1.9781611975673> [accessed 1 June 2025] · DOI
- 10.1016/j.ajhg.2018.10.025 · DOI
- 10.1074/mcp.RA119.001472 · DOI · Paper page
- Çelik, Muhammed Hasan , Gagneur, Julien , Lim, Ryan G. , Wu, Jie , Thompson, Leslie M. , and Xie, Xiaohui , ‘Identifying Dysregulated Regions in Amyotrophic Lateral Sclerosis through Chromatin Accessibility Outliers’, Human Genetics and Genomics Advances, 5/3 (2024) <https://www.cell.com/hgg-advances/abstract/S2666-2477(24)00057-5> [accessed 20 August 2024] · DOI
- Cheng, Jun , Novati, Guido , Pan, Joshua , Bycroft, Clare , Žemgulytė, Akvilė , Applebaum, Taylor , et al., ‘Accurate Proteome-Wide Missense Variant Effect Prediction with AlphaMissense’, Science, 381/6664 (2023), eadg7492 · DOI · Paper page
- Collier, Mark , Nazabal, Alfredo , and Williams, Christopher K. I. , ‘VAEs in the Presence of Missing Data’ (2020) <https://arxiv.org/abs/2006.05301> [accessed 1 June 2025] · arXiv
- Cummings, Beryl B. , Marshall, Jamie L. , Tukiainen, Taru , Lek, Monkol , Donkervoort, Sandra , Foley, A. Reghan, et al., ‘Improving Genetic Diagnosis in Mendelian Disease with Transcriptome Sequencing’, Science Translational Medicine, 9/386 (2017), eaal5209 ‘DepMap 24Q2 Public’ (2024) <https://plus.figshare.com/articles/dataset/DepMap_24Q2_Public/25880521/1> [accessed 30 August 2024] · DOI · Paper page
- 10.1093/nar/gky955 · DOI
- 10.1038/s41467-020-17336-9 · DOI
- 10.1038/s41591-019-0457-8 · DOI · Paper page
- 10.1109/TIT.2014.2323359 · DOI
- Hock, Daniella H. , Caruana, Nikeisha J. , Semcesen, Liana N. , Lake, Nicole J. , Formosa, Luke E. , Amarasekera, Sumudu S. C. , et al., ‘Untargeted Proteomics Enables Ultra-Rapid Variant Prioritization in Mitochondrial and Other Rare Diseases’, medRxiv, 2024, 2024.08.06.24311318 · DOI
- 10.1093/bioinformatics/btaa259 · DOI
- 10.1038/s41586-020-2308-7 · DOI · Paper page
- 10.1186/1471-2105-13-S16-S5 · DOI · Paper page
- Kingma, Diederik P. , and Ba, Jimmy , ‘Adam: A Method for Stochastic Optimization’ (2017) <http://arxiv.org/abs/1412.6980> [accessed 21 January 2025] · arXiv
- Kong, Weijia , Hui, Harvard Wai Hann , Peng, Hui , and Goh, Wilson Wen Bin , ‘Dealing with Missing Values in Proteomics Data’, PROTEOMICS, 22/23–24 (2022), 2200092 · DOI
- Kopajtich, Robert , Smirnov, Dmitrii , Stenton, Sarah L. , Loipfinger, Stefan , Meng, Chen , Scheller, Ines F. , et al., ‘Integration of Proteomics with Genomics and Transcriptomics Increases the Diagnostic Rate of Mendelian Disorders’, medRxiv, 2021 <https://www.medrxiv.org/content/early/2021/07/03/2021.03.09.21253187>
- 10.1038/ncomms15824 · DOI · Paper page
- Kusnadi, Eric P. , Timpone, Clelia , Topisirovic, Ivan , Larsson, Ola , and Furic, Luc , ‘Regulation of Gene Expression via Translational Buffering’, Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1869/1 (2022), 119140 · DOI
- 10.1093/bioinformatics/btac603 · DOI
- Liu, Fei Tony , Ting, Kai Ming , and Zhou, Zhi-Hua , ‘Isolation-Based Anomaly Detection’, ACM Transactions on Knowledge Discovery from Data, 6/1 (2012), 1–39 · DOI
- 10.1186/s13059-014-0550-8 · DOI · Paper page
- 10.1186/s13059-016-0974-4 · DOI · Paper page
- 10.1038/s41467-020-20573-7 · DOI
- 10.1016/j.patcog.2020.107501 · DOI
- 10.1016/j.csbj.2022.08.022 · DOI · Paper page
- 10.1093/nar/gky1016 · DOI · Paper page
- 10.1093/nar/gkv007 · DOI · Paper page
- 10.1016/j.celrep.2017.08.010 · DOI
- 10.1016/j.jocs.2020.101245 · DOI
- Salkovic, Edin , Sadeghi, Mohammad Amin , Baggag, Abdelkader , Salem, Ahmed Gamal Rashed , and Bensmail, Halima , ‘OutSingle: A Novel Method of Detecting and Injecting Outliers in RNA-Seq Count Data Using the Optimal Hard Threshold for Singular Values’, Bioinformatics, 39/4 (2023), btad142 · DOI
- Scheller, Ines F. , Lutz, Karoline , Mertes, Christian , Yépez, Vicente A. , and Gagneur, Julien , ‘Improved Detection of Aberrant Splicing with FRASER 2.0 and the Intron Jaccard Index’, The American Journal of Human Genetics, 110/12 (2023), 2056–67 · DOI
- Schlegl, Thomas , Seeböck, Philipp , Waldstein, Sebastian M. , Schmidt-Erfurth, Ursula , and Langs, Georg , ‘Unsupervised Anomaly Detection with Generative Adversarial Networks to Guide Marker Discovery’, in Information Processing in Medical Imaging, ed. by Marc Niethammer, Martin Styner, Stephen Aylward, Hongtu Zhu, Ipek Oguz, Pew-Thian Yap, et al., Lecture Notes in Computer Science (Cham, 2017), 146–57 <https://link.springer.com/10.1007/978-3-319-59050-9_12> [accessed 1 June 2025] · DOI · Paper page
- Segers, Alexandre , Gilis, Jeroen , Van Heetvelde, Mattias , De Baere, Elfride , and Clement, Lieven , ‘Juggling Offsets Unlocks RNA-Seq Tools for Fast Scalable Differential Usage, Aberrant Splicing and Expression Analyses’, bioRxiv, 2023, 2023.06.29.547014 · DOI
- Smail, Craig , and Montgomery, Stephen B ., ‘RNA Sequencing in Disease Diagnosis’, Annual Review of Genomics and Human Genetics, 25/Volume 25, 2024 (2024), 353–67 · DOI
- 10.1038/nprot.2016.136 · DOI
- 10.1038/s41593-022-01031-7 · DOI
- 10.1038/s41588-023-01373-3 · DOI
- 10.1093/nar/gkq603 · DOI
- 10.1186/s13059-018-1451-z · DOI
- 10.1186/s13073-022-01019-9 · DOI
- 10.1038/s41596-020-00462-5 · DOI
- 10.1074/mcp.TIR119.001385 · DOI
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
- ORCID
- Venue
- Bioinformatics
- Publisher
- openRxiv
- Published
- 2025-02-05
- Volume
- 41
- Issue
- 12
- ISSN
- 1367-4803 (ISSN-L)
- PMC
- PMC12931418
- OpenAlex
- W4416538820
- Cited by
- 4
- References
- 1
- Citations by year
- 2026: 2 · 2025: 2
- FWCI
- 1.01
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- 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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