Fuzzy Classification of Genome Sequences Prior to Assembly Based on Similarity Measures

S. Nasser, G. Vert, A. Breland, M. Nicolescu
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引用次数: 1

Abstract

Nucleotide sequencing of genomic data is an important step towards building understanding of gene expression. Current limitations in sequencing limit the number of base pairs that can be processed to only several hundred at a time. Consequently, these sequenced substrings need to be assembled into the overall genome. However, the existence of insertions, deletions and substitutions can complicate the assembly of subsequences and confuse existing methods. What has been needed is an approach that deals with ambiguity in trying to match and assemble a genome from its sequenced subsequences. This research develops fuzzy similarity measures between subsequences that are then incorporated into an assembler based on fuzzy logic and fuzzy similarity measures. The research addresses the problem of extensive computation required by clustering data into meaningful groups. Preliminary evaluation of this approach in conjunction with K-Means clustering suggests that this approach is at least as good as standard approaches and in some cases better.
基于相似性度量的基因组序列装配前模糊分类
基因组数据的核苷酸测序是了解基因表达的重要一步。目前测序的限制限制了一次只能处理几百个碱基对的数量。因此,这些测序的子串需要组装成整个基因组。然而,插入、删除和替换的存在会使子序列的组装复杂化,并使现有的方法混乱。我们所需要的是一种方法,它可以处理在试图匹配和组装基因组序列时的模糊性。本研究开发了子序列之间的模糊相似度度量,然后将其纳入基于模糊逻辑和模糊相似度度量的汇编器中。该研究解决了将数据聚类到有意义的组所需的大量计算问题。结合K-Means聚类对该方法的初步评估表明,该方法至少与标准方法一样好,在某些情况下甚至更好。
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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