Infer how your cell populations signal to one another, identifying the ligand-receptor interactions in your dataset.
Discover subgroups within your population from their molecular profiles to stratify samples and guide decisions.
Annotate single cells in your sample, automatically or manually (by cluster), to define which cell populations are present.
Build interaction networks to identify hub genes, key drivers, upstream regulators, and predicted downstream effects.
Map your spatial architecture of a tissue, identifying distinct regions and how their cell types and pathways differ.
Uncover the mechanism behind your signature with topology-aware impact analysis: perturbed pathways and the upstream regulators driving them.