Master Spatial Transcriptomics: Mapping Gene Expression in 3D Tissue Space in 4 weeks through hands-on, project-based online training with DSTC.
Spatial transcriptomics is transforming biological research by enabling scientists to study gene expression within its native tissue context, preserving spatial relationships between cells. Unlike traditional bulk or single-cell sequencing, spatial methods allow researchers to map where genes are expressed across tissues, providing deeper insights into tumor microenvironments, developmental biology, and disease progression. Every participant receives a verified e-Certificate and e-Marksheet from the Deep Science & Technology Consortium.
Spatial transcriptomics is transforming biological research by enabling scientists to study gene expression within its native tissue context, preserving spatial relationships between cells. Unlike traditional bulk or single-cell sequencing, spatial methods allow researchers to map where genes are expressed across tissues, providing deeper insights into tumor microenvironments, developmental biology, and disease progression.
1. Translate biotechnology theory into practical, reproducible analysis.
2. Assemble a documented case study that evidences your applied capability.
β’ Master's and senior undergraduate students specializing in biotechnology
β’ R&D engineers and working professionals applying biotechnology in industry
β’ Academics and educators building research or teaching capacity in biotechnology
β’ A portfolio-grade biotechnology deliverable you can defend and extend.
β’ A verified e-Certificate of competency and e-Marksheet from the Deep Science & Technology Consortium.
β’ Sequencing-based Visium and imaging-based Xenium, MERFISH and CosMx
β’ The resolution against gene-panel-breadth trade-off that defines the choice
β’ Spot-level capture is not single cell β the point most analyses get wrong
β’ FFPE and fresh-frozen workflows and the RNA integrity each demands
β’ Sectioning, orientation and permeabilisation optimisation
β’ Quality metrics that determine whether a section is worth sequencing at all
β’ Space Ranger output and building objects in Seurat, Squidpy or Scanpy
β’ Normalisation for spatial data and the confound of tissue density
β’ Registering expression to histology and reading the two together
β’ Deconvolution with cell2location or RCTD against a single-cell reference
β’ Spatially variable gene detection and spatial domain identification
β’ Neighbourhood and ligand-receptor analysis, and the co-location fallacy
β’ Tumour microenvironment structure and immune exclusion patterns
β’ Serial section alignment for pseudo-3D reconstruction and its distortions
β’ Validation with immunofluorescence or in situ hybridisation before claiming a finding
| Parameter | Requirement |
|---|---|
| Covered Tool / Platform | BWA |
| Covered Tool / Platform | SAMtools |
| Covered Tool / Platform | GATK |
| Covered Tool / Platform | FastQC |
| Covered Tool / Platform | Trimmomatic |
| Covered Tool / Platform | R/Bioconductor |
| Covered Tool / Platform | IGV |
| Covered Tool / Platform | PLINK |
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