Complexity and algorithms for copy-number evolution problems

Mohammed El-Kebir, Benjamin J. Raphael*, Ron Shamir, Roded Sharan, Simone Zaccaria, Meirav Zehavi, Ron Zeira

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

Background: Cancer is an evolutionary process characterized by the accumulation of somatic mutations in a population of cells that form a tumor. One frequent type of mutations is copy number aberrations, which alter the number of copies of genomic regions. The number of copies of each position along a chromosome constitutes the chromosome's copy-number profile. Understanding how such profiles evolve in cancer can assist in both diagnosis and prognosis. Results: We model the evolution of a tumor by segmental deletions and amplifications, and gauge distance from profile a to b by the minimum number of events needed to transform a into b. Given two profiles, our first problem aims to find a parental profile that minimizes the sum of distances to its children. Given k profiles, the second, more general problem, seeks a phylogenetic tree, whose k leaves are labeled by the k given profiles and whose internal vertices are labeled by ancestral profiles such that the sum of edge distances is minimum. Conclusions: For the former problem we give a pseudo-polynomial dynamic programming algorithm that is linear in the profile length, and an integer linear program formulation. For the latter problem we show it is NP-hard and give an integer linear program formulation that scales to practical problem instance sizes. We assess the efficiency and quality of our algorithms on simulated instances. Availability:https://github.com/raphael-group/CNT-ILP.

Original languageEnglish
Article number13
JournalAlgorithms for Molecular Biology
Volume12
Issue number1
DOIs
StatePublished - 16 May 2017

Funding

FundersFunder number
Dotan Hemato‑Oncology Research Center
Simons Institute for the Theory of Computing in Berkeley
National Science Foundation1053753, CCF‑ 1053753
National Institutes of HealthRO1HG005690
Burroughs Wellcome Fund
Israel Science Foundation317/13
Tel Aviv University
Council for Higher Education

    Keywords

    • Cancer
    • Copy-number variant
    • Maximum parsimony
    • Phylogeny
    • Somatic mutation

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