Abstract
Single-cell sequencing (SCS) enables the inference of tumor phylogenies that provide insights on intra-tumor heterogeneity and evolutionary trajectories. Recently introduced methods perform this task under the infinite-sites assumption, violations of which, due to chromosomal deletions and loss of heterozygosity, necessitate the development of inference methods that utilize finite-site models. We propose a statistical inference method for tumor phylogenies from noisy SCS data under a finite-sites model. The performance of our method on synthetic and experimental datasets from two colorectal cancer patients to trace evolutionary lineages in primary and metastatic tumors suggest that employing a finite-sites model leads to improved inference of tumor phylogenies.
