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STOmics Spatial Gene Expression

Comprehensive spatial gene expression analysis to map transcriptomic landscapes across tissue sections and support the discovery of spatially defined cellular organization and function.

STOmics’ flagship technology, Spatial Enhanced REsolution Omics-sequencing (Stereo-seq), is an advanced spatial transcriptomics platform based on DNA Nano Ball (DNB) technology. This cutting-edge system offers unparalleled resolution, throughput, and field of view, enabling comprehensive spatial transcriptomic analysis across multiple scales—tissue, cellular, subcellular, and molecular levels. Using a patterned array chip and Coordinate ID (CID) system, Stereo-seq captures mRNA directly from tissue samples, restoring its precise spatial coordinates. As a transformative tool, Stereo-seq empowers researchers to elucidate the complex relationships between gene expression, cell morphology, and their local microenvironments.

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Benefits of Novogene’s STOmics Spatial Transcriptomics Service

Large Area High Resolution
Large Area High Resolution

500 nm resolution with up to 13 cm × 13 cm capture area for gene and imaging analysis

Broad Sample Compatibility
Broad Sample Compatibility

Compatible with fresh-frozen and FFPE samples across diverse animal and plant tissue types

Pathology Integration
Pathology Integration

Single-section staining enables simultaneous pathological assessment and spatial transcriptomics analysis

Applications

Tumor Microenvironment Research

Characterize the molecular and cellular landscape of the tumor microenvironment.

Immunology

Map the spatial distribution and interactions of immune cells within tissues.

Neuroscience

Investigate neural cell function and expression patterns at unprecedented resolution.

Biomarker Discovery

Identify cell-specific biomarkers for disease diagnosis and therapy development.

Specifications

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Submission Guidelines to learn more. For detailed information, please contact us with your customized requests.


*FFPE glass slides must be positive charged glass slides.

ServiceSample TypeSample AmountPreservationSample QCShipping
Stereo-seq OMNI
(Animal with reference genome)
FFPE block (recommended)1 block, FFPE block must be contained on plastic dehydrating box, otherwise could not be installed on the sectioning devicePreservation After embedding store at 4°C, protected from lightDV200% ≥ 30%Cold pack transportation
FFPE sectionRNA quality control sample: 10-15 sections of 5 μm thick paraffin rolls (at least 10 sections for biopsy samples);
Formal sample: 4-6 sections of 5 μm thick paraffin sections (adjacent sections).
Dry and sealed,storage time at 4°C< 30 days

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Stereo-seq (FFPE)
SpeciesNo species limitation
Resolution500nm
Sequencing platformBGI DNB-SEQ T7
Read lengthPE75
Recommended Data Amount2.5B reads per sample
AnalysisData QC
Mapping and Quantification
Dimensionality Reduction, Clustering, and Differential analysis:
Graphclust clustering
K-means clustering
Seurat Analysis:
PCA analysis
Spatial variable gene expression analysis
Clustering and dimensionality reduction analysis
Differential Expression Gene Analysis (DEG)
DEGs clustering heatmap
Spatial distribution of DEGs
Violine plot
t-SNE and UMAP dimensional reduction visualization
Functional Enrichment Analysis:
GO enrichment
KEGG enrichment
Reactome enrichment

Project Workflow

Project Workflow

Resources

Demo Results

Service flyers

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Novogene Stereo-seq OMNI Spatial Transcriptome Sequencing

Stereo-seq is an advanced technology that combines transcriptomics with spatial information. It enables mapping gene expression in tissue samples while preserving their spatial organization. Stereo-seq OMNI, a revolutionary sequencing-based spatial transcriptomics solution specially designed for studying FFPE samples, provides high-definition spatial whole transcriptome information at single-cell scale.

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