| Literature DB >> 31372179 |
Nikolai Karpov1, Salem Malikic2, Md Khaledur Rahman1, S Cenk Sahinalp1.
Abstract
We introduce a new dissimilarity measure between a pair of "clonal trees", each representing the progression and mutational heterogeneity of a tumor sample, constructed by the use of single cell or bulk high throughput sequencing data. In a clonal tree, each vertex represents a specific tumor clone, and is labeled with one or more mutations in a way that each mutation is assigned to the oldest clone that harbors it. Given two clonal trees, our multi-labeled tree dissimilarity (MLTD) measure is defined as the minimum number of mutation/label deletions, (empty) leaf deletions, and vertex (clonal) expansions, applied in any order, to convert each of the two trees to the maximum common tree. We show that the MLTD measure can be computed efficiently in polynomial time and it captures the similarity between trees of different clonal granularity well.Entities:
Keywords: Dynamic programming; Intra-tumor heterogeneity; Multi-labeled tree; Tree edit distance; Tumor evolution
Year: 2019 PMID: 31372179 PMCID: PMC6661107 DOI: 10.1186/s13015-019-0152-9
Source DB: PubMed Journal: Algorithms Mol Biol ISSN: 1748-7188 Impact factor: 1.405