一种基于准比对的发现基因序列保守区域的新方法

Anurag Nagar, Michael Hahsler
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引用次数: 2

摘要

本文提出了一种利用位置敏感p-mer频率聚类技术在大量生物序列中有效地发现相似区域的无比对技术。将一组序列分解成片段,然后得到大小为p的所有低聚物(称为p-mers)的频率分布,以总结每个片段。这些摘要被聚类,而序列集合中片段的顺序在马尔可夫模型中被保留。每个簇内的序列片段具有非常相似的DNA/RNA模式,并形成所谓的准对齐。这一事实可以用于各种任务,如物种表征和鉴定,系统发育分析,序列的功能分析,以及发现保守区域。我们的方法在计算上比多序列比对更有效,因为它可以应用现代数据流聚类算法,该算法在时间上线性地运行片段数量,因此可以帮助在大量序列中有效地发现高度相似的区域。在本文中,我们应用该方法有效地发现和可视化16S rRNA的保守区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel quasi-alignment-based method for discovering conserved regions in genetic sequences
This paper presents an alignment-free technique to efficiently discover similar regions in large sets of biological sequences using position sensitive p-mer frequency clustering. A set of sequences is broken down into segment and then a frequency distribution over all oligomers of size p (referred to as p-mers) is obtained to summarize each segment. These summaries are clustered while the order of segments in the set of sequences is preserved in a Markov-type model. Sequence segments within each cluster have very similar DNA/RNA patterns and form a so called quasi-alignment. This fact can be used for a variety of tasks such as species characterization and identification, phylogenetic analysis, functional analysis of sequences and, as in this paper, for discovering conserved regions. Our method is computationally more efficient than multiple sequences alignment since it can apply modern data stream clustering algorithms which run in time linear in the number of segments and thus can help discover highly similar regions across a large number of sequences efficiently. In this paper, we apply the approach to efficiently discover and visualize conserved regions in 16S rRNA.
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