若干置换度量下中值和最近邻问题的参数化复杂度。

IF 1.5 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Algorithms for Molecular Biology Pub Date : 2024-12-24 DOI:10.1186/s13015-024-00269-z
Luís Cunha, Ignasi Sau, Uéverton Souza
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引用次数: 0

摘要

基因组重排是在进化过程中大量DNA交换位置的事件。这些事件的分析是理解进化基因组学的一个有前途的工具,为基于基因组重排措施的系统发育重建提供了数据。许多配对重排距离已被提出,基于寻找重排事件的最小数量,以转换一个基因组到另一个基因组,使用一些预定义的操作。当考虑两个以上的基因组时,我们面临着基于重排的系统发育重建的更具挑战性的问题。给定一组基因组和一个距离概念,至少有两种自然的方法来定义“目标”基因组。一方面,找到一个基因组,它能最小化从这个到任何其他的距离的总和,称为中位数基因组。另一方面,找到一个与任何其他基因组的最大距离最小的基因组,称为最近基因组。考虑到基因组是不同整数的排列,一些距离度量得到了广泛的研究。我们在以下指标上研究排列的中位数和最接近问题:断点距离,交换距离,块交换距离,短块移动距离和转置距离。在生物学应用中,有些值通常非常小,例如解值d或输入排列的个数k。对于这些指标和参数d或k,我们从参数化复杂性的角度分析了最接近和中值问题。我们得到了以下结果:对于某些距离度量,即使只有k = 3个排列,寻找中位数/最接近排列的np -硬度;以目标距离d为参数,求所研究指标的中位数排列的多项式核问题;利用短块移动寻找最接近排列的np -硬度结果FPT算法和多项式核在以目标距离d作为参数时寻找最接近排列的不可行性。
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On the parameterized complexity of the median and closest problems under some permutation metrics.

Genome rearrangements are events where large blocks of DNA exchange places during evolution. The analysis of these events is a promising tool for understanding evolutionary genomics, providing data for phylogenetic reconstruction based on genome rearrangement measures. Many pairwise rearrangement distances have been proposed, based on finding the minimum number of rearrangement events to transform one genome into the other, using some predefined operation. When more than two genomes are considered, we have the more challenging problem of rearrangement-based phylogeny reconstruction. Given a set of genomes and a distance notion, there are at least two natural ways to define the "target" genome. On the one hand, finding a genome that minimizes the sum of the distances from this to any other, called the median genome. On the other hand, finding a genome that minimizes the maximum distance to any other, called the closest genome. Considering genomes as permutations of distinct integers, some distance metrics have been extensively studied. We investigate the median and closest problems on permutations over the following metrics: breakpoint distance, swap distance, block-interchange distance, short-block-move distance, and transposition distance. In biological applications some values are usually very small, such as the solution value d or the number k of input permutations. For each of these metrics and parameters d or k, we analyze the closest and the median problems from the viewpoint of parameterized complexity. We obtain the following results: NP-hardness for finding the median/closest permutation regarding some metrics of distance, even for only k = 3 permutations; Polynomial kernels for the problems of finding the median permutation of all studied metrics, considering the target distance d as parameter; NP-hardness result for finding the closest permutation by short-block-moves; FPT algorithms and infeasibility of polynomial kernels for finding the closest permutation for some metrics when parameterized by the target distance d.

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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
On the parameterized complexity of the median and closest problems under some permutation metrics. TINNiK: inference of the tree of blobs of a species network under the coalescent model. New generalized metric based on branch length distance to compare B cell lineage trees. Metric multidimensional scaling for large single-cell datasets using neural networks. Compression algorithm for colored de Bruijn graphs.
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