Order cells along developmental or regenerative trajectories, using pseudotime to trace how states emerge, diverge, and transition.
Annotate single cells in your sample, automatically or manually (by cluster), to define which cell populations are present.
Identify the biomarkers in your data that indicate a specific biological state, process, or treatment response.
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.
Match your disease gene signature to drugs known to reverse it, or to drugs that produce a similar molecular effect.