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A novel quasi-alignment-based method for discovering conserved regions in genetic sequences

机译:一种新的基于准比对的遗传序列保守区发现方法

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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.
机译:本文提出了一种免定位技术,可利用位置敏感的p-mer频率聚类技术有效地发现大型生物序列集中的相似区域。将一组序列分解为片段,然后获得大小为p的所有低聚物(称为p-mers)的频率分布以概括每个片段。这些摘要被聚类,而序列集中的片段顺序保留在Markov型模型中。每个簇中的序列片段具有非常相似的DNA / RNA模式,并形成所谓的准比对。这一事实可用于多种任务,例如物种鉴定和鉴定,系统发育分析,序列功能分析,以及如本文所述的发现保守区的任务。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的数据流聚类算法,该算法在段数上按时间线性运行,因此可以帮助在大量序列中高效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中的保守区。

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