Kintsugi decides, gene by gene, where spatial transcriptomics borrows information.

Subcellular spatial transcriptomics captures where RNA is in tissue, but a single location holds too few molecules of any one gene to estimate composition alone. Every current method fixes in advance where to borrow - a smoothing scale, a cell outline or a factor model - and the fixed choice shapes what is visible. Kintsugi removes the fixed choice and lets held-out molecules decide, gene by gene, how much to borrow from spatial neighbours and from other genes at the same location. On a lung section measured by both Xenium and Visium HD, the data-chosen allocation placed an epithelial programme where the Xenium molecules were, ahead of smoothing, cell segmentation and a factor model; the result replicated across tissues and against protein. Across a 45-core pulmonary fibrosis cohort, separating composition from captured amount shows that a fibroblastic focus is not a place with more RNA but a place with different RNA: 2.8-fold higher in activated-fibroblast composition while segmented nuclear density is at most 1.08-fold higher.