RESEARCH PROBLEM

How can researchers explore clusters, markers and annotations without over-interpreting a two-dimensional embedding?

Connect UMAP neighbourhoods to marker evidence, annotation provenance and the upstream choices that shaped the representation.

WHY THIS IS DIFFICULT

UMAP distance is commonly over-interpreted

Automated cell labels can appear more certain than they are

Batch and QC decisions are hidden by the final figure

RESPONSIBLE APPROACH

1

Inspect annotated and unassigned populations

2

Review marker evidence for selected clusters

3

Treat embeddings as navigation surfaces rather than complete conclusions

RELEVANT FORNEUS RESEARCH

Working demonstration

Single-Cell AI Explorer

Interactive exploration of annotated single-cell populations, UMAP coordinates and marker-gene results.

View evidence and screenshots ↗
Research project

Spatial Transcriptomics Atlas

A production-oriented research framework for spatial neighbourhoods and cell–cell communication across Visium, Xenium and MERFISH data.

View evidence and screenshots ↗

INTERPRETATION BOUNDARY

  • Expert biological validation remains necessary
  • Upstream integration and quality control determine what can be inferred

QUESTIONS THIS PAGE ANSWERS

  • interactive single-cell UMAP
  • review marker gene annotations
  • explore cell populations