Spatial Cell Type Mapping Service

Biological tissues are not random assortments of cells; they are highly organized ecosystems. Spatial Cell Type Mapping allows researchers to transcend the limitations of "bulk" or "dissociated" single-cell analysis. By preserving the physical coordinates of every transcript, we help you build a 3D atlas of gene expression. Whether you are identifying rare cell niches in a tumor or charting neuronal circuits in the brain, our platform provides the spatial context necessary to turn raw data into biological insight.

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Metabolic differences between normal and diseased tissues
  • What is
  • Workflow
  • Deliverables
  • Platform
  • Applications
  • Why choose
  • FAQs

What is Spatial Cell Type Mapping?

Spatial Cell Type Mapping is an advanced analytical framework that integrates Spatial Transcriptomics (ST) with Single-Cell RNA Sequencing (scRNA-seq).

While scRNA-seq provides a high-resolution "parts list" of cell types, it requires tissue dissociation, which destroys the spatial context. Spatial mapping uses computational deconvolution and probabilistic modeling to project those high-resolution cell types back onto a physical tissue slice. This allows us to identify exactly which cells are neighbors, how they communicate, and how their proximity influences disease progression or tissue development.

Our Precision Workflow

We provide an end-to-end solution, moving from your raw tissue block to a fully annotated spatial map.

cell type mapping workflow

Deliverables

Deliverable Module What You Get Solves For You
Publication-Ready Spatial Maps
  • High-res vector graphics (PDF/SVG): Cell type distribution heatmaps
  • Multi-panel composite figures overlaid on H&E background with key regions annotated
  • Insert directly into manuscripts
Complete Data Package
  • Cell composition table (Excel/CSV): Spot ID, cell type, proportion, confidence score
  • Spatial coordinate files: Ready for ImageJ, QuPath, or custom pipelines
  • Seamless integration into downstream analysis
  • Zero technical barriers to exploration
Expert Interpretation Report
  • Key findings summary + QC metrics + biological insights
  • Marker gene validation plots confirming spatia accuracy
  • Quickly grasp scientific value
  • Robust evidence for peer review responses

The Technology Platform

We utilize industry-leading platforms to ensure your data is robust and publication-ready:

  • Visium (10x Genomics): Ideal for whole-transcriptome discovery across large tissue areas.
  • Xenium / MERFISH: High-plex, sub-cellular resolution for targeted gene panels, allowing you to see individual RNA molecules within a cell.
  • Proprietary AI Pipeline: Our custom computational suite handles noise reduction and improves the accuracy of cell-type deconvolution in "dense" tissue environments.

Key Applications

  • Immune Profiling: Map the "Immune Cold" vs. "Immune Hot" zones in tumors to understand immunotherapy resistance.
  • Neurobiology: Define the molecular boundaries of brain regions and identify cell-type specific changes in Alzheimer's or Parkinson's.
  • Developmental Biology: Track lineage commitment and organogenesis in embryonic tissues.
  • Pathology Refinement: Supplement traditional H&E staining with molecular data to identify "hidden" disease states.

Why Choose Our Services?

  • Expertise in Difficult Tissues: We have optimized protocols for "tough" samples, including fatty tissues, highly necrotic tumors, and fibrotic samples.
  • Data Integration: We don't just give you a spreadsheet. We integrate your spatial data with existing scRNA-seq datasets for a "best of both worlds" analysis.
  • Client-Centric Delivery: Every project includes a dedicated project manager and a post-delivery session with a bioinformatician to help you interpret your results.

FAQs

How many cells are in a single "spot"?

Depending on the platform (e.g., Visium), a spot is usually 55 μm in diameter, containing 1 to 10 cells. We use computational deconvolution to estimate the exact cell-type proportions within each spot.

Can I use my own scRNA-seq data as a reference?

Absolutely. In fact, using a matched scRNA-seq reference from the same study significantly increases the accuracy of the spatial mapping.

Learn about other Q&A.

* For Research Use Only. Not for use in diagnostic procedures.
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