COpy number and Mutations Phylogeny from Amplicon Single-cell Sequencing This tool can be used to infer a tree of somatic events (mutations, copy number variants and copy-neutral loss of heterozygosity) that occurred in a tumor. It is specifically designed to be used for MissionBio's Tapestri data, where a small number of amplicons (50-300) are sequenced for thousands of single-cells.
| Label | Latest Version |
|---|---|
| main | 2.0.0 |
