Copy-Number Evolution Problems: Complexity and Algorithms

被引:14
|
作者
El-Kebir, Mohammed [1 ]
Raphael, Benjamin J. [1 ]
Shamir, Ron [2 ]
Sharan, Roded [2 ]
Zaccaria, Simone [1 ,3 ]
Zehavi, Meirav [2 ]
Zeira, Ron [2 ]
机构
[1] Brown Univ, Dept Comp Sci, Ctr Computat Mol Biol, Providence, RI 02912 USA
[2] Tel Aviv Univ, Sch Comp Sci, IL-69978 Tel Aviv, Israel
[3] Univ Milano Bicocca, Dipartimento Informat Sistemist & Comun, Milan, Italy
来源
ALGORITHMS IN BIOINFORMATICS | 2016年 / 9838卷
基金
美国国家科学基金会;
关键词
TUMOR; INFERENCE; TREES;
D O I
10.1007/978-3-319-43681-4_11
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 are 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. 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. 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. We assess the efficiency and quality of our algorithms on simulated instances.
引用
收藏
页码:137 / 149
页数:13
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