arXiv:2603.22477v1 Announce Type: new
Abstract: Spatial transcriptomics data analysis integrates cellular transcriptional activity with spatial coordinates to identify spatial domains, infer cell-type dynamics, and characterize gene expression patterns within tissues. Despite recent advances, significant challenges remain, including the treatment of batch effects, the handling of mixed cell-type signals, and the imputation of poorly measured or missing gene expression. This work addresses these challenges by introducing a novel Subspace Tensor Orthogonal Rotation Model (STORM) that aligns multiple slices which vary in their spatial dimensions and geometry by considering them at the level of physical patterns or microenvironments. To this end, STORM presents an irregular tensor factorization technique for decomposing a collection of gene expression matrices and integrating them into a shared latent space for downstream analysis. In contrast to black-box deep learning approaches, the proposed model is inherently interpretable. Numerical experiments demonstrate state-of-the-art performance in vertical and horizontal batch integration, cell-type deconvolution, and unmeasured gene imputation for spatial transcriptomics data.
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