挖掘一组协同调节的RNA序列

Yuh-Jyh Hu
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引用次数: 2

摘要

转录后调控是生物信息学中的一个重要研究课题,但研究较少。在一组转录后协同调控的rna中,碱基对相互作用可以将分子组织成结构域,并为功能相互作用提供框架。它们的共识基序可能代表RNA调节蛋白的结合位点。与DNA基序不同,RNA基序在结构上比在序列上更为保守。了解结构基序可以帮助我们更好地理解调控活动。我们提出了一种新的RNA二级结构预测数据挖掘方法。为了证明我们的新方法的性能,我们首先在以前使用和发表在文献中的相同数据集上对其进行了测试。其次,为了展示我们新方法的灵活性,我们还在包含大多数当前系统无法识别的伪结图案的数据集上对其进行了测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mining a set of coregulated RNA sequences
Post-transcriptional regulation, though less studied, is an important research topic in bioinformatics. In a set of post-transcriptionally coregulated RNAs, the basepair interactions can organize the molecules into domains and provide a framework for functional interactions. Their consensus motifs may represent the binding sites of RNA regulatory proteins. Unlike DNA motifs, RNA motifs are more conserved in structures than in sequences. Knowing the structural motifs can help us better understand the regulation activities. We propose a novel data mining approach to RNA secondary structure prediction. To demonstrate the performance of our new approach, we first tested it on the same data sets previously used and published in literature. Secondly, to show the flexibility of our new approach, we also tested it on a data set that contains pseudoknot motifs that most current systems cannot identify.
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