Decoder-FFPE-seq enables sensitive, genome-wide spatial transcriptomics of archival tissues at single-cell resolution
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Updated: Nov 1, 2026

Spatially Resolved, Integrated Single-Cell Multiomic Profiling of the Transcriptome and Epigenomic Targets in Frozen Tissue Sections
Published on: June 12, 2026
Jiao Cao1, Jun Zeng2, Yiwei Meng1
1Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, Department of Urology, Department of pathology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China.
Abstract:
Formalin-fixed paraffin-embedded (FFPE) tissue-compatible spatial transcriptomics (ST) is transforming biology and histopathology, but achieving high sensitivity, genome-wide coverage, single-cell resolution, and researcher accessibility remains challenging. To address these challenges, we here present a dendrimeric DNA coordinate barcoding design for FFPE tissue-adapted spatial RNA sequencing (Decoder-FFPE-seq) by integrating RNA-to-DNA probe conversion with blotting-assisted barcoding. Decoder-FFPE-seq provides single-cell resolution with a >2.6-fold sensitivity increase in whole-transcriptome mouse brain and archived human sample profiling over existing platforms, resolving potential cellular identity of low-abundance genes, finer tissue architecture, and capturing an epithelial-mesenchymal transition-associated signature for prognostic value. With expanded probe libraries, Decoder-FFPE-seq captures long noncoding and viral RNAs, revealing their spatial coregulatory networks with messenger RNAs in oral squamous cell carcinomas (OSCCs). In an OSCC immunotherapy cohort, two CD8+ T cell subpopulations were respectively identified in pre- and postchemoimmunotherapy samples, potentially linked to treatment response. Decoder-FFPE-seq establishes a robust, high-resolution, and accessible framework for sensitive ST profiling of archival tissues in fundamental and translational studies.
