On the repetitive collection indexing problem

Ali Alatabbi, Carl Barton, C. Iliopoulos
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引用次数: 6

Abstract

In large data sets such as genomes from a single species, large sets of reads, and version control data it is often noted that each entry only differs from another by a very small number of variations. This leads to a large set of data with a great deal of redundancy and repetitiveness. Rapid development in DNA sequencing technologies has caused a drastic growth in the size of publicly available sequence databases with such data. DNA sequencing has become so fast and cost-effective that sequencing individual genomes will soon become a common task [9] making querying and storing such sets of data an important task. In this paper, we propose an indexing structure for highly repetitive collections of sequence data based on a multilevel g-gram model. In particular, the proposed algorithm accommodates variations that may occur in the target sequence with respect to the reference sequence. The paper is organized as follows. Section [1] and [2] introduce the basic concepts and go through the related literature. In Section [3] we present notions and facts. Details of the proposed data structure/algorithm will be given in Section [5] and [4], Section [6] discusses complexity analysis and Section [7] gives conclusions of future work.
关于重复集合索引问题
在大型数据集中,例如来自单一物种的基因组、大型读取集和版本控制数据中,通常会注意到每个条目与另一个条目的差异只有非常小的变化。这将导致大量的数据集具有大量的冗余和重复。DNA测序技术的快速发展导致了包含此类数据的公开序列数据库规模的急剧增长。DNA测序已经变得如此快速和经济,测序个体基因组将很快成为一项常见的任务[9],使查询和存储这些数据集成为一项重要任务。在本文中,我们提出了一种基于多层g-gram模型的高度重复序列数据集合的索引结构。特别地,所提出的算法容纳相对于参考序列在目标序列中可能发生的变化。本文组织如下。[1]和[2]部分介绍了基本概念,并对相关文献进行了梳理。在第[3]节中,我们提出概念和事实。关于所提出的数据结构/算法的细节将在章节[5]和[4]中给出,章节[6]讨论了复杂性分析,章节[7]给出了未来工作的结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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