From a single cell to a clinical cohort.
Process, cluster, and annotate single-cell datasets — and integrate them with the rest of your evidence. The same pipelines handle scRNA-seq, CITE-seq, ATAC-seq, TCR/BCR sequencing, and spatial transcriptomics.
For bulk RNA-seq data, the deconvolution engine quantifies up to 64 cell types with seven competing algorithms — so you can see how cellular composition tracks with outcomes across an entire cohort.