Evidence map›Paper›PMID 42286785›Full record

ArticleBioinformatics (Oxford, England)2026

Bayesian hyperparameter optimization improves scGPT fine-tuning for single-cell multi-omics integration.

Darren Yu Jun Tay, Nguyen Quoc Khanh Le, Matthew Chin Heng Chua

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Article in Bioinformatics (Oxford, England), 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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5 · Who and what money

Authors and funding

3 authors.

Darren Yu Jun TayScience Research Programme, Catholic Junior College, Singapore 297822, Singapore.
Nguyen Quoc Khanh LeAIBioMed Lab, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0003-4896-7926
Matthew Chin Heng ChuaDepartment of Biomedical Informatics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119615, Singapore.

Funding

National Science and Technology Council NSTC114-2221-E-038-015National Science and Technology Council NSTC115-2221-E-038-012-MY3
6 · The paper itself

Abstract

motivationFoundation models such as scGPT have demonstrated strong potential for single-cell multi-omics integration; however, their downstream performance is highly sensitive to hyperparameter selection. Manual fine-tuning remains computationally expensive, dataset-dependent, and often irreproducible. Despite the increasing adoption of foundation models in single-cell analysis, systematic strategies for robust hyperparameter optimization remain underexplored.

resultsWe developed a Bayesian optimization framework based on Tree-structured Parzen Estimators (TPE) for automated fine-tuning of scGPT and evaluated its performance on two benchmark bone marrow mononuclear cell (BMMC) multi-omics datasets, including CITE-seq and GSE194122 datasets. Across datasets, Bayesian optimization consistently improved biological conservation and batch integration metrics compared with default scGPT configurations. On the original BMMC benchmark, optimization improved AvgBIO from 0.59 to 0.67 and PCR from 0.33 to 0.52. On the GSE194122 dataset, the default configuration exhibited unstable convergence and weak biological preservation (AvgBIO = 0.19; ARI = 0.007), whereas Bayesian optimization substantially improved integration performance (AvgBIO = 0.60; ARI = 0.63) while reducing validation loss from 137 to 47.1. These findings demonstrate substantial dataset-specific sensitivity of scGPT fine-tuning and highlight the importance of automated optimization for stable deployment across heterogeneous multi-omics datasets. Our study demonstrates that Bayesian optimization provides an effective and reproducible strategy for stabilizing scGPT fine-tuning across diverse single-cell multi-omics datasets. Rather than introducing a new integration architecture, this work emphasizes the importance of systematic optimization for improving robustness and reproducibility of foundation-model applications in computational biology. AVAILABILITY AND IMPLEMENTATION: Our model and dataset are freely available at: https://github.com/daren642/scGPT_multiomic_tuning.

Indexed as

Computational BiologyMultiomicsSingle-Cell AnalysisSoftwareAlgorithmsBayes TheoremHumans

Identifiers

PMID42286785
PMCPMC13360271

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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.