Simple software workflow for your
complex single-cell clonal analysis
Step 1: Input your data
Generate variant calls from single-cell sequencing data
Step 2: Explore your subclones
Identify relevant variants, their zygosity as well as co-occurring & rare mutations
VARIANT FILTERING & SUBCLONE VISUALIZATION
Explore clone distribution with key annotations.
From sequence import to data analysis and publication-ready visualization, this turnkey software ensures you gain meaningful insights into your data.