Polyomino reconstructs spatial transcriptomic profiles with single-cell resolution via a region-allocation method
- 1Center for Biomedical Digital Science, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangdong-Hong Kong Joint Laboratory for Stem Cell and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China;
- 2University of Chinese Academy of Sciences, Beijing 100049, China;
- 3Guangdong University of Education, School of Mathematics, Guangzhou 510310, China;
- 4Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China;
- 5Guangzhou Medical University, Guangzhou 511436, China;
- 6Centre for Regenerative Medicine and Health, Hong Kong Institute of Science and Innovation, Chinese Academy of Sciences, Hong Kong 999077, China
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↵7 These authors contributed equally to this work.
Abstract
Integration of single-cell and spatial transcriptomes represents a fundamental strategy to enhance spatial data quality. However, existing methods for mapping single-cell data to spatial coordinates struggle with large-scale data sets comprising millions of cells. Here, we introduce Polyomino, an intelligent region-allocation method inspired by the region-of-interest (ROI) concept from image processing. By using gradient descent, Polyomino allocates cells to structured spatial regions that match the most significant biological information, optimizing the integration of data and improving speed and accuracy. Polyomino excels in integrating data even in the presence of various sequencing artifacts, such as cell segmentation errors and imbalanced cell-type representations. Polyomino outperforms state-of-the-art methods by 10 to 1000 times in speed, and it is the only approach capable of integrating data sets containing millions of cells in a single run. As a result, Polyomino uncovers originally hidden gene expression patterns in brain sections and offers new insights into organogenesis and tumor microenvironments, all with exceptional efficiency and accuracy.
Footnotes
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[Supplemental material is available for this article.]
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Article published online before print. Article, supplemental material, and publication date are at https://www.genome.org/cgi/doi/10.1101/gr.280532.125.
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Freely available online through the Genome Research Open Access option.
- Received February 11, 2025.
- Accepted September 18, 2025.
This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.











