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Published on: May 9, 2017
BulkFormer: A large-scale foundation model for bulk transcriptomes
Boming Kang1, Rui Fan1, Meizheng Yi2
1Department of Biomedical Informatics, State Key Laboratory of Vascular Homeostasis and Remodeling, School of Basic Medical Sciences, Peking University, 38 Xueyuan Rd., Beijing 100191, China.
None:
Foundation models are transforming transcriptome analysis, yet most RNA sequencing (RNA-seq) foundation models are pretrained on sparse single-cell RNA-seq data, which typically captures only ∼3,000 genes per cell. This creates a need for models tailored to bulk transcriptomes, a modality that profiles ∼16,000 genes per sample and supports clinical and tissue-level analyses. Here, we present BulkFormer, a foundation model for bulk transcriptome analysis. BulkFormer contains ∼150 million parameters, covers 20,010 protein-coding genes, and is pretrained on 581,503 human bulk RNA-seq profiles. Its hybrid encoder combines a graph neural network to model explicit gene-gene relationships with a Performer module to capture global expression dependencies. Across five downstream tasks, BulkFormer outperformed existing single-cell foundation models while requiring substantially lower training cost. These results identify pretraining data modality as a key determinant of foundation model performance and establish BulkFormer as a framework for bulk transcriptome modeling. A record of this paper's transparent peer review process is included in the supplemental information.
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