Order cells along developmental or regenerative trajectories, using pseudotime to trace how states emerge, diverge, and transition.
Build interaction networks to identify hub genes, key drivers, upstream regulators, and predicted downstream effects.
Uncover the mechanism behind your signature with topology-aware impact analysis: perturbed pathways and the upstream regulators driving them.
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.
Match your disease gene signature to drugs known to reverse it, or to drugs that produce a similar molecular effect.