Annotate single cells in your sample, automatically or manually (by cluster), to define which cell populations are present.
Order cells along developmental or regenerative trajectories, using pseudotime to trace how states emerge, diverge, and transition.
Discover subgroups within your population from their molecular profiles to stratify samples and guide decisions.
Uncover the mechanism behind your signature with topology-aware impact analysis: perturbed pathways and the upstream regulators driving them.
Map your spatial architecture of a tissue, identifying distinct regions and how their cell types and pathways differ.
Infer how your cell populations signal to one another, identifying the ligand-receptor interactions in your dataset.