Evidence map›Paper›PMID 41959024›Full record

ArticlebioRxiv : the preprint server for biology2026

scProfiterole: Clustering of Single-Cell Proteomic Data Using Graph Contrastive Learning via Spectral Filters.

Mustafa Coşkun, Filipa Blasco Lopes, Pınar Kubilay Tolunay, Mark R Chance, Mehmet Koyutürk

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mustafa CoşkunDepartment of Artificial Intelligence and Data Engineering, Ankara University.
Filipa Blasco LopesCenter for Proteomics and Bioinformatics, Case Western Reserve University.
Pınar Kubilay TolunayDepartment of Medical Oncology, Ankara University School of Medicine.
Mark R ChanceCenter for Proteomics and Bioinformatics, Case Western Reserve University.
Mehmet KoyutürkCenter for Proteomics and Bioinformatics, Case Western Reserve University.

Funding

Construction, Analysis, and Utilization of Co-Phosphorylation Networks to Characterize Cellular SignalingR01LM012980 · NLM · CASE WESTERN RESERVE UNIVERSITY · PI Marzieh Ayati, MARK R CHANCE · 2019 to 2026
$2.1M
NLM NIH HHS R01 LM012980
6 · The paper itself

Abstract

Novel technologies for the acquisition of protein expression data at the single cell level are emerging rapidly. Although there exists a substantial body of computational algorithms and tools for the analysis of single cell gene expression (scRNAseq) data, tools for even basic tasks such as clustering or cell type identification for single cell proteomic (scProteomics) data are relatively scarce. Adoption of algorithms that have been developed for scRNAseq into scProteomics is challenged by the larger number of drop-outs, missing data, and noise in single cell proteomic data. Graph contrastive learning (GCL) on cell-to-cell similarity graphs derived from single cell protein expression profiles show promise in cell type identification. However, missing edges and noise in the cell-to-cell similarity graph requires careful design of convolution matrices to overcome the imperfections in these graphs. Here, we introduce scProfiterole (Single Cell Proteomics Clustering via Spectral Filters), a computational framework to facilitate effective use of spectral graph filters in GCL-based clustering of single cell proteomic data. Since clustering assumes a homophilic network topology, we consider three types of homophilic filters: (i) random walks, (ii) heat kernels, (iii) beta kernels. Direct implementation of these filters is computationally prohibitive, thus the filters are either truncated or approximated in practice. To overcome this limitation, scProfiterole uses Arnoldi orthonormalization to implement polynomial interpolations of any given spectral graph filter. Our results on comprehensive single cell proteomic data show that (i) graph contrastive learning with learnable polynomial coefficients that are carefully initialized improves the effectiveness and robustness of cell type identification, (ii) heat kernels and beta kernels improve clustering performance over adjacency matrices or random walks, and (iii) polynomial interpolation of spectral filters outperforms approximation or truncation. The source code for scProfiterole and Supplementary Materials are available at https://github.com/mustafaCoskunAgu/scProfiterole.

Indexed as

Cell type identificationClusteringGraph contrastive learningPolynomial InterpolationSingle cell proteomicsSpectral graph filters

Identifiers

PMID41959024
PMCPMC13061019

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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.