Investigating the complexity of the double distance problems

IF 1.5 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Algorithms for Molecular Biology Pub Date : 2024-01-04 DOI:10.1186/s13015-023-00246-y
Marília D. V. Braga, Leonie R. Brockmann, Katharina Klerx, Jens Stoye
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Abstract

Two genomes $$\mathbb {A}$$ and $$\mathbb {B}$$ over the same set of gene families form a canonical pair when each of them has exactly one gene from each family. Denote by $$n_*$$ the number of common families of $$\mathbb {A}$$ and $$\mathbb {B}$$ . Different distances of canonical genomes can be derived from a structure called breakpoint graph, which represents the relation between the two given genomes as a collection of cycles of even length and paths. Let $$c_i$$ and $$p_j$$ be respectively the numbers of cycles of length i and of paths of length j in the breakpoint graph of genomes $$\mathbb {A}$$ and $$\mathbb {B}$$ . Then, the breakpoint distance of $$\mathbb {A}$$ and $$\mathbb {B}$$ is equal to $$n_*-\left( c_2+\frac{p_0}{2}\right)$$ . Similarly, when the considered rearrangements are those modeled by the double-cut-and-join (DCJ) operation, the rearrangement distance of $$\mathbb {A}$$ and $$\mathbb {B}$$ is $$n_*-\left( c+\frac{p_e }{2}\right)$$ , where c is the total number of cycles and $$p_e$$ is the total number of paths of even length. The distance formulation is a basic unit for several other combinatorial problems related to genome evolution and ancestral reconstruction, such as median or double distance. Interestingly, both median and double distance problems can be solved in polynomial time for the breakpoint distance, while they are NP-hard for the rearrangement distance. One way of exploring the complexity space between these two extremes is to consider a $$\sigma _k$$ distance, defined to be $$n_*-\left( c_2+c_4+\ldots +c_k+\frac{p_0+p_2+\ldots +p_{k-2}}{2}\right)$$ , and increasingly investigate the complexities of median and double distance for the $$\sigma _4$$ distance, then the $$\sigma _6$$ distance, and so on. While for the median much effort was done in our and in other research groups but no progress was obtained even for the $$\sigma _4$$ distance, for solving the double distance under $$\sigma _4$$ and $$\sigma _6$$ distances we could devise linear time algorithms, which we present here.
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研究双重距离问题的复杂性
如果两个基因组 $$\mathbb {A}$ 和 $$\mathbb {B}$ 都有来自同一个基因家族的一个基因,那么这两个基因组就形成了一对典型基因组。用 $$n_*$ 表示 $$\mathbb {A}$ 和 $$\mathbb {B}$ 的共同族的数目。典型基因组的不同距离可以从一种叫做断点图(breakpoint graph)的结构中推导出来,这种结构将两个给定基因组之间的关系表示为偶数长度的循环和路径的集合。假设 $$c_i$$ 和 $$p_j$ 分别是基因组 $$\mathbb {A}$ 和 $$\mathbb {B}$ 的断点图中长度为 i 的循环数和长度为 j 的路径数。那么,$$\mathbb {A}$ 和 $$\mathbb {B}$ 的断点距离等于 $$n_*-\left( c_2+\frac{p_0}{2}\right)$$ 。同样,当考虑的重排是由双切-接(DCJ)操作模拟的重排时,$$\mathbb {A}$ 和 $$\mathbb {B}$ 的重排距离为 $$n_*-\left( c+\frac{p_e }{2}\right)$$ ,其中 c 是循环的总数,$$p_e$$ 是偶数长度路径的总数。距离公式是其他几个与基因组进化和祖先重建相关的组合问题(如中值距离或双倍距离)的基本单元。有趣的是,对于断点距离来说,中值距离和双倍距离问题都可以在多项式时间内求解,而对于重排距离来说,它们都是 NP-困难的。探索这两个极端之间复杂性空间的一种方法是考虑 $$\sigma _k$$ 距离,定义为 $$n_*-\left( c_2+c_4+\ldots +c_k+frac{p_0+p_2+\ldots +p_{k-2}}{2}\right)$$ 、并越来越多地研究 $$\sigma _4$$ 距离的中值距离和双倍距离的复杂性,然后是 $$\sigma _6$$ 距离,等等。对于中值距离,我们和其他研究小组做了很多努力,但即使对于 $$\sigma _4$ 距离也没有取得进展,而对于求解 $$\sigma _4$$ 和 $$\sigma _6$ 距离下的双倍距离,我们可以设计出线性时间算法,我们在此介绍这些算法。
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来源期刊
Algorithms for Molecular Biology
Algorithms for Molecular Biology 生物-生化研究方法
CiteScore
2.40
自引率
10.00%
发文量
16
审稿时长
>12 weeks
期刊介绍: Algorithms for Molecular Biology publishes articles on novel algorithms for biological sequence and structure analysis, phylogeny reconstruction, and combinatorial algorithms and machine learning. Areas of interest include but are not limited to: algorithms for RNA and protein structure analysis, gene prediction and genome analysis, comparative sequence analysis and alignment, phylogeny, gene expression, machine learning, and combinatorial algorithms. Where appropriate, manuscripts should describe applications to real-world data. However, pure algorithm papers are also welcome if future applications to biological data are to be expected, or if they address complexity or approximation issues of novel computational problems in molecular biology. Articles about novel software tools will be considered for publication if they contain some algorithmically interesting aspects.
期刊最新文献
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