一种平均情况下高效的两阶段算法,用于枚举基因组对之间最小长度为 k 的所有最长公共子串。

Mattia Prosperi, Simone Marini, Christina Boucher
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摘要

两个文本之间最长公共子串(LCS)问题的扩展是枚举给定最小长度 k 的所有 LCS(ALCS- k)以及它们在每个文本中的位置。在生物信息学中,针对超长文本--基因组或元基因组--的 ALCS- k 的有效解决方案可以为发现生物机制的遗传特征提供有用的见解。与 LCS 问题相比,ALCS- k 问题有两个额外的要求:一个是最小长度 k,另一个是必须报告所有长于 k 的普通字符串。我们提出了一种高效的两阶段 ALCS- k 算法,该算法利用了长度为 k 的文本子串谱(k -mers)。我们的方法在最坏情况下,第一阶段的时间复杂度与 k -mers 的数量成对数线性关系,在平均情况下,第二阶段的时间复杂度与常见 k -mers 的数量成对数线性关系(比总 k -mers 频谱小几个数量级)。空间复杂度在第一阶段(基于磁盘)是线性的,在第二阶段(基于磁盘和内存)平均是线性的。在不同生物体(包括病毒、细菌和动物染色体)基因组上进行的测试表明,运行时间与我们的理论估计值一致;此外,与 MUMmer4 的比较显示,在不同基因组上具有渐进优势。
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An average-case efficient two-stage algorithm for enumerating all longest common substrings of minimum length k between genome pairs.

A problem extension of the longest common substring (LCS) between two texts is the enumeration of all LCSs given a minimum length k (ALCS- k ), along with their positions in each text. In bioinformatics, an efficient solution to the ALCS- k for very long texts -genomes or metagenomes- can provide useful insights to discover genetic signatures responsible for biological mechanisms. The ALCS- k problem has two additional requirements compared to the LCS problem: one is the minimum length k , and the other is that all common strings longer than k must be reported. We present an efficient, two-stage ALCS- k algorithm exploiting the spectrum of text substrings of length k ( k -mers). Our approach yields a worst-case time complexity loglinear in the number of k -mers for the first stage, and an average-case loglinear in the number of common k -mers for the second stage (several orders of magnitudes smaller than the total k -mer spectrum). The space complexity is linear in the first phase (disk-based), and on average linear in the second phase (disk- and memory-based). Tests performed on genomes for different organisms (including viruses, bacteria and animal chromosomes) show that run times are consistent with our theoretical estimates; further, comparisons with MUMmer4 show an asymptotic advantage with divergent genomes.

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