基于新Motif扩展算法的快速Motif发现

Raheleh Mohammadi, Morteza Moradi, Mahmoud Naghibzadeh, Abdorreza Savadi
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引用次数: 0

摘要

在生物学中,蛋白质被建模为一级结构的长链氨基酸。一般来说,每种蛋白质由20种氨基酸组成,不同蛋白质的氨基酸数量和排列方式各不相同。序列基序是蛋白质一级结构中连续氨基酸的重复模式,它可以提供一些重要的生物学特征信息,如转录因子结合和蛋白质-蛋白质相互作用位点。本文提出了一种新的motif扩展算法,以提高最近的motif发现算法之一de Bruijn的性能。提出的算法接收一组初始的候选图案,并尝试使用双边方法将它们扩展到所需的长度。在该算法中,问题状态受到用户给出的相似度阈值的约束。候选基序的开发算法总是选择一个大于指定相似度阈值的字符。我们在真实的硬件和真实的输入上进行了一些实验来评估我们的算法。结果表明,该算法比原de Bruijn算法至少快20倍。此外,鉴定的基序与输入蛋白家族的平均相似性比对应的高28%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fast Motif Discovery Using a New Motif Extension Algorithm
In biology, proteins are modeled as a long chain of amino acids in primary structure. Generally, each protein is composed of 20 types of amino acids and the number and the arrangement of amino acids vary among different proteins. A sequence motif is a repeated pattern of consecutive amino acids in the primary structure of proteins which can provide information about some important biological features such as transcription factor binding and protein-protein interaction sites. In this paper, we proposed a new motif extension algorithm to enhance the performance of de Bruijn which is one of the recent motif discovery algorithms. The proposed algorithm receives an initial set of candidate motifs and tries to extend them to a desired length using a two-sided approach. In the proposed algorithm, the problem state is limited by a similarity threshold which is given by the user as a constraint. The algorithm for the development of candidate motifs always selects a characters whose appearance are greater than that of the specified similarity threshold. We conducted some experiments on real hardware and real inputs to evaluate our algorithm. The results showed that the proposed algorithm is at least 20 times faster than the original de Bruijn algorithm. Furthermore, the average similarity of identified motifs to the input protein family was 28% higher than the counterpart.
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