Identifying Robust Subclonal Structures through Tumor Progression Tree Alignment

Abstract Understanding and comparing tumor evolutionary histories is fundamental to cancer genomics. Clonal trees, used to model tumor progression, are rooted, unordered trees in which each node represents a subclone labeled by a set of distinct mutations. To compare two clonal trees, we introduce omlta , the o ptimal m ulti-label tree a lignment, which removes the minimum number of mutation labels from the trees, so that the remaining trees are isomorphic. Computing omlta is NP-hard. Here, we present an algorithm to compute the omlta , with a running time of where L ≥ 1 is the total number of mutation labels occurring in the input trees and k is the minimum possible number of mutation labels that need to be removed for the alignment. Our implementation ( https://github.com/algo-cancer/omlta ) is the first computational tool for determining the optimal alignment between clonal trees. We applied omlta to 126 cases from the TRACERx study on non-small cell lung cancers and some melanoma single-cell data.