OmicsTweezer: A distribution-independent cell deconvolution model for multi-omics Data

Cell deconvolution estimates cell type proportions from bulk omics data, enabling insights into tissue microenvironments and disease. However, practical applications are often hindered by batch effects between bulk data and referenced single-cell data, a challenge that is frequently overlooked. To address this discrepancy, we developed OmicsTweezer, a distribution-independent cell deconvolution model. By integrating optimal transport with deep learning, OmicsTweezer aligns simulated and real data in a shared latent space, effectively mitigating data shifts and inter-omics distribution differences. OmicsTweezer is versatile, capable of deconvolving bulk RNA-seq, bulk proteomics, and spatial transcriptomics. Extensive evaluations on simulated and real-world datasets demonstrate its robustness and accuracy. Furthermore, applications in prostate and colon cancer showcase OmicsTweezer's ability to identify biologically meaningful cell types. As a unified deconvolution framework for multi-omics data, OmicsTweezer offers an efficient and powerful tool for studying disease microenvironments.

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Publication Details

Journal
Cell Genomics
Published
2025-07-16
DOI
https://doi.org/10.1016/j.xgen.2025.100950
Citations
6
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
4.84
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article

OmicsTweezer: A distribution-independent cell deconvolution model for multi-omics Data

Faming Zhao, Gordon Brent Mills, Katelyn T. Byrne, Lisa M. Coussens et al.
6 citations
Cell Genomics
Single-cell and spatial transcriptomics
4.84
article

OmicsTweezer: A distribution-independent cell deconvolution model for multi-omics Data

Faming Zhao, Gordon Brent Mills, Katelyn T. Byrne, Lisa M. Coussens, Alexey Valeryevich Danilov, Peter S. Nelson, Canping Chen, Zheng Xia, Rosalie C. Sears, Tao Ren, Xinxing Yang
article en
6 citations

Abstract

Cell deconvolution estimates cell type proportions from bulk omics data, enabling insights into tissue microenvironments and disease. However, practical applications are often hindered by batch effects between bulk data and referenced single-cell data, a challenge that is frequently overlooked. To address this discrepancy, we developed OmicsTweezer, a distribution-independent cell deconvolution model. By integrating optimal transport with deep learning, OmicsTweezer aligns simulated and real data in a shared latent space, effectively mitigating data shifts and inter-omics distribution differences. OmicsTweezer is versatile, capable of deconvolving bulk RNA-seq, bulk proteomics, and spatial transcriptomics. Extensive evaluations on simulated and real-world datasets demonstrate its robustness and accuracy. Furthermore, applications in prostate and colon cancer showcase OmicsTweezer's ability to identify biologically meaningful cell types. As a unified deconvolution framework for multi-omics data, OmicsTweezer offers an efficient and powerful tool for studying disease microenvironments.

Cell GenomicsVol. 5(9)
City Of Hope National Medical Center (US), Oregon Health & Science University (US), Fred Hutch Cancer Center (US)
Openalex Percentile: Top 5%
Single-cell and spatial transcriptomics
4.84
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