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bioRxiv · 10.1101/2025.10.08.681071

Optimal Gene Panel Selection for Targeted Spatial Transcriptomics Experiments

Lu, H.·Fang, L.·Zeng, O.·Ma, P.·Zhong, W.·Yuan, G.-C.
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Abstract

Spatial transcriptomics analysis is a powerful approach for dissecting the structure of tissue microenvironment and uncovering the mechanism of cell-cell communications. However, existing technologies are limited by either spatial resolution or gene coverage. Most single-cell resolution technologies target only a few hundreds of pre-selected genes, whose choice plays an important role in the overall analysis. It remains a challenge to optimally design a gene panel to maximize the utility of spatial transcriptomics profiling. To fill this gap, we introduce a novel method, named ReconST, to automatically design optimal gene panels for spatial transcriptomics profiling. ReconST leverages information from existing scRNA-seq data, and identifies the optimal subset of genes by using a gated autoencoder. By using a high-coverage mouse brain MERFISH dataset as the reference benchmark, we showed that ReconST outperforms existing methods in terms of both reconstruction accuracy and spatial pattern preservation. As such, ReconST provides a useful and generally-applicable tool for optimal gene panel design, which in turn can significantly enhance the utility of spatial transcriptomics profiling in a wide range of biomedical investigations.

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Lu, H., Fang, L., Zeng, O., Ma, P., Zhong, W., Yuan, G.-C.. 2025-10-08. Optimal Gene Panel Selection for Targeted Spatial Transcriptomics Experiments. https://doi.org/10.1101/2025.10.08.681071

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