Extended Data Fig. 3: In situ validation of spatially variable isoform usage of Dtnbp1, related to Extended Data Fig. 2. | Nature Biotechnology

Extended Data Fig. 3: In situ validation of spatially variable isoform usage of Dtnbp1, related to Extended Data Fig. 2.

From: Mapping isoforms and regulatory mechanisms from spatial transcriptomics data with SPLISOSM

Extended Data Fig. 3: In situ validation of spatially variable isoform usage of Dtnbp1, related to Extended Data Fig. 2.The alt text for this image may have been generated using AI.

(a) Spatial distribution of log-normalized expression for Dtnbp1 isoforms in SiT-ONT CBS2 sample. (b) Gene structure of Dtnbp1 with annotated isoforms and Xenium Prime 5K probe sets. Among three ONT-detected Dtnbp1 isoforms (201, 204, 206), codeword 7864 specifically targets 201 and 204, while codeword 11516 recognizes all three. (c) Spatial density of Dtnbp1 codewords (left) and Cluster 2 cells (Slc17a7+ excitatory neurons, right) in Xenium Prime 5K mouse CBS sample. Cell segmentation, clustering and differential expression analysis were performed using Xenium Ranger with default parameters. (d) Dtnbp1-206 spatial variability driven by a subset of Nptxr+ excitatory neurons. Left: Volcano plot of Cluster 2 marker genes. P-values were computed from a negative binomial test and were adjusted via the Benjamini-Hochberg procedure as part of the Xenium Onboard Analysis pipeline. Middle: Comparison of Dtnbp1-11516-only bins (20 × 20 μm) with and without Cluster 2 cells. Right: Volcano plot of marker codewords of Dtnbp1-11516-only Cluster 2 bins.

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