Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

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

Created on 09 Oct 2026

Authors

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

Published in

Journal of computational biology : a journal of computational molecular cell biology. Pages 15578666261491608. Oct 09, 2026. Epub Oct 09, 2026.

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 (HK), (iii) beta kernels (BK). 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) GCL with learnable polynomial coefficients that are carefully initialized improves the effectiveness and robustness of cell type identification, (ii) HK and BK 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 Data are available at https://github.com/mustafaCoskunAgu/scProfiterole.

PMID:
42853006
Bibliographic data and abstract were imported from PubMed on 09 Oct 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 1
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement