Authors
Lai, W., Li, C., Deng, Q., Zhu, Y., Liu, C., Li, Z., Luo, O. J.
Abstract
The growing availability of single-cell resources creates new opportunities to extract cell-type-resolved information from the vast body of existing bulk omics data through cell-type deconvolution. Conventional deconvolution methods often rely on linear mixture models or specific probabilistic assumptions and can be sensitive to batch effects, whereas many deep-learning approaches are modality-specific or lack a unified end-to-end learning framework. Here, we developed DECIPHER, an end-to-end representation-learning framework for cell-type deconvolution that can be applied across multiple molecular modalities. DECIPHER learns a domain-constant representation (Zc) for deconvolution and a domain-specific representation (Zs) to model domain-associated variation. By integrating nonlinear representation learning with differentiable non-negative least-squares optimization, DECIPHER estimates cell-type proportions from Zc. Across simulated datasets, experimentally generated bulk-cell mixtures, real-world datasets, and multiple molecular modalities, DECIPHER showed robust and competitive cell-type deconvolution performance. Beyond cell-type proportion estimation, the learned Zc supported chronological age prediction across independent cohorts and prognostic stratification in lung adenocarcinoma, demonstrating that DECIPHER can transform high-dimensional bulk omics data into low-dimensional, biologically informative representations. DECIPHER thus broadens the utility of existing bulk omics resources for biological discovery and clinical research.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 30 Sep 2026.
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