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The 2-Interval Pattern Matching Problems and Its Application to ncRNA Scanning

机译:2间隔模式匹配问题及其在NCRNA扫描中的应用

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This paper focuses on the 2-Interval pattern matching problem for {<, {is contained in}}-structured pattern and applies it on scanning for the ncRNAs without pseudoknots. Vialette [6] gave an O(mn~3 log n) time solution to the problem, where m, n are the number of intervals in the pattern and the given 2-interval set. This solution however is not practical for scanning the secondary structure in a genome-wide or chromosome-wide scale. In this paper, we propose an efficient algorithm to solve the problem in O(mn log n) time. In order to capture more characteristics of the secondary structures of ncRNA families, we define a new problem by considering the distance constraints between the intervals and we can still solve it without increasing the time complexity. Experiment showed that the method to the new defined problem can result in much fewer false positives. Moreover, if we assume the only possible base pairs are { (A,U), (C,G), (U,G)} which are the case for RNA molecule, we can further improve the time complexity to O(m q), where q is the length of the input RNA sequences. From the experiment, our new method requires a reasonable time (2.5 min) to scan the whole chromosome for an ncRNA family.
机译:本文重点介绍了{<,{in}}结构模式的2间隔模式匹配问题,并在没有伪通知的情况下应用它扫描NCRNA。 Vialette [6]给出了问题的O(Mn〜3 log n)时间解决方案,其中M,n是图案中的间隔数和给定的2间隔集。然而,该溶液不实际用于以基因组或染色体尺寸扫描二次结构。在本文中,我们提出了一种有效的算法来解决O(MN Log N)时间中的问题。为了捕获NCRNA家族的二次结构的更多特征,我们通过考虑间隔之间的距离约束来定义一个新问题,并且我们仍然可以在不增加时间复杂度的情况下解决它。实验表明,新定义问题的方法可能导致误报得多。此外,如果我们假设唯一可能的基对是RNA分子的情况的{(a,u),(c,g),(u,g)},我们可以进一步提高O(MQ)的时间复杂度,其中q是输入RNA序列的长度。从实验中,我们的新方法需要合理的时间(2.5分钟)来扫描NCRNA系列的整个染色体。

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