通过超短操作排序有符号循环排列。

IF 1.5 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Algorithms for Molecular Biology Pub Date : 2018-07-26 eCollection Date: 2018-01-01 DOI:10.1186/s13015-018-0131-6
Andre R Oliveira, Guillaume Fertin, Ulisses Dias, Zanoni Dias
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引用次数: 3

摘要

背景:估计两个给定基因组之间进化距离的一种方法是确定将一个基因组转化为另一个基因组所必需的大规模突变或基因组重排的最小数量。在这种情况下,基因组可以表示为有序的基因序列,每个基因用有符号整数表示。如果没有重复的基因,那么基因组就被建模为π=(π1π2…πn)形式的符号排列,在这种情况下,我们可以在不损失一般性的情况下认为其中一个是单位排列ιn=(12…n),我们只需要对另一个排序(即将其转换为ιn)。研究最多的基因组重排事件是逆转,其中基因组的一部分被逆转并在同一位置重新组合;还有调换,两个连续的片段互换。文献中提出了许多变体,例如,结合不同类型的(可能受约束的)重排。其中之一认为,在反转或转位中涉及的基因数量永远不会超过两个,这被称为超短操作排序问题(或SSOs)。结果与结论:除用超短反转和超短转置排序符号圆置换的问题外,所有考虑排列中sso的问题都在P中。在这里,我们通过引入一种称为循环置换图的新图结构来填补这一空白,并提供了一系列中间结果,这允许我们设计一个多项式算法来通过超短反转和超短转置对有符号循环置换进行排序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sorting signed circular permutations by super short operations.

Sorting signed circular permutations by super short operations.

Sorting signed circular permutations by super short operations.

Sorting signed circular permutations by super short operations.

Background: One way to estimate the evolutionary distance between two given genomes is to determine the minimum number of large-scale mutations, or genome rearrangements, that are necessary to transform one into the other. In this context, genomes can be represented as ordered sequences of genes, each gene being represented by a signed integer. If no gene is repeated, genomes are thus modeled as signed permutations of the form π=(π1π2πn) , and in that case we can consider without loss of generality that one of them is the identity permutation ιn=(12n) , and that we just need to sort the other (i.e., transform it into ιn ). The most studied genome rearrangement events are reversals, where a segment of the genome is reversed and reincorporated at the same location; and transpositions, where two consecutive segments are exchanged. Many variants, e.g., combining different types of (possibly constrained) rearrangements, have been proposed in the literature. One of them considers that the number of genes involved, in a reversal or a transposition, is never greater than two, which is known as the problem of sorting by super short operations (or SSOs).

Results and conclusions: All problems considering SSOs in permutations have been shown to be in P , except for one, namely sorting signed circular permutations by super short reversals and super short transpositions. Here we fill this gap by introducing a new graph structure called cyclic permutation graph and providing a series of intermediate results, which allows us to design a polynomial algorithm for sorting signed circular permutations by super short reversals and super short transpositions.

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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.
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