Map your spatial architecture of a tissue, identifying distinct regions and how their cell types and pathways differ.
Discover subgroups within your population from their molecular profiles to stratify samples and guide decisions.
Order cells along developmental or regenerative trajectories, using pseudotime to trace how states emerge, diverge, and transition.
Match your disease gene signature to drugs known to reverse it, or to drugs that produce a similar molecular effect.
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.