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technologiesTechnologyEmerging

Single-cell & spatial profiling

Reading the genes of each individual cell, and mapping where each cell sits in the tumour.

scRNA-seq (10x Genomics) resolves tumour, immune, and stromal populations; spatial transcriptomics (Visium, Xenium, CosMx, MERFISH) and multiplex protein imaging (CODEX, IMC) keep tissue architecture. Revealing how ADC bystander killing, T-cell exclusion, and resistance niches work. Research-grade; entering trials as correlative science.

Schematic · not to scale
Tumour niche · Immune cells, in place

How it works

RNA is captured with barcodes per cell or per spatial location, or read by imaging-based in situ hybridisation for hundreds to thousands of genes.

Strengths
  • Resolves heterogeneity and microenvironment
  • Discovery engine for new targets
Limitations
  • Cost, throughput, analysis burden
  • Not yet clinically actionable

Latest papers

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Literature trend15,315 papers in the last 12 months+30% vs prior 12How this is computed
Latest papers · live from Europe PMC
Open in Europe PMC

Query for this technology: (TITLE:"single-cell RNA sequencing" OR ABSTRACT:"single-cell RNA sequencing" OR TITLE:"spatial transcriptomics" OR ABSTRACT:"spatial transcriptomics" OR TITLE:"single-cell" OR ABSTRACT:"single-cell") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Single-cell & spatial profiling, not a curated reading list.

Connected

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A bone marrow niche on a chip to study human dormancyA global rapid tissue donation network for metastatic diseaseA national rapid research autopsy network for end-stage cancerA short pre-surgery drug window as the default early test of new agentsAn open foundation model of the cancer cell trained on perturbation dataAn open model of every cancer cell state, built from perturbation atlasesBlock the survival signals the tumour's neighbours provideClear the suppressive neutrophils out of pancreatic tumours firstComparability by design: a digital twin and sentinel panel for cell process changesFind the parts of a tumour the drug never reachesGrow immune command posts inside tumoursImplant a tiny device that tests twenty drugs inside the patient's own tumourLink single-cell and spatial tumour atlases to clinical outcomesMake every cold tumour hot: a coordinated programme to reprogramme immune-excluded tumoursMap which tumour clones sit next to which immune cells before choosing therapyMatch therapy to the type of scar-forming cell in the tumourPool every immunotherapy trial's biomarker data into one commonsRe-map the tumour's surface proteins before choosing the next antibody drugReprogramme suppressive macrophages instead of trying to delete themSelect patients for cell therapy by whether their tumour holds reactive T cellsStandards for spatial and multiplex tissue biomarkers before they reach the clinicTest drugs on freshly cut slices of the patient's own tumourTurn the map of immune cells inside a tumour into a standardised testTwo-week pre-operative windows to compare combination biology head to headUse pre-surgery immunotherapy windows as the field's biomarker engineWhat actually holds T cells at the tumour border?What decides which disseminated cells ever colonise?

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