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rNAV 2.0: a visualization tool for bacterial sRNA-mediated regulatory networks mining

机译:rNAV 2.0:用于细菌sRNA介导的调控网络挖掘的可视化工具

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摘要

BackgroundBacterial sRNA-mediated regulatory networks has been introduced as a powerful way to analyze the fast rewiring capabilities of a bacteria in response to changing environmental conditions. The identification of mRNA targets of bacterial sRNAs is essential to investigate their functional activities. However, this step remains challenging with the lack of knowledge of the topological and biological constraints behind the formation of sRNA-mRNA duplexes. Even with the most sophisticated bioinformatics target prediction tools, the large proportion of false predictions may be prohibitive for further analyses. To deal with this issue, sRNA target analyses can be carried out from the resulting gene lists given by RNA-SEQ experiments when available. However, the number of resulting target candidates may be still huge and cannot be easily interpreted by domain experts who need to confront various biological features to prioritize the target candidates. Therefore, novel strategies have to be carried out to improve the specificity of computational prediction results, before proposing new candidates for an expensive experimental validation stage.
机译:背景技术细菌sRNA介导的调控网络已被引入,作为分析细菌对环境条件变化的快速重布线能力的有效方法。细菌sRNA的mRNA靶标的鉴定对于研究其功能活性至关重要。但是,由于缺乏对sRNA-mRNA双链体形成背后的拓扑和生物学限制的了解,这一步骤仍然具有挑战性。即使使用最复杂的生物信息学目标预测工具,错误预测的大部分也可能无法进行进一步的分析。为了解决这个问题,可以从RNA-SEQ实验提供的所得基因列表中进行sRNA靶标分析(如果可用)。但是,生成的目标候选者的数量可能仍然很大,并且领域专家需要面对各种生物学特征来对目标候选者进行优先级排序时,不容易理解。因此,在提出昂贵的实验验证阶段的新候选者之前,必须采取新的策略来提高计算预测结果的特异性。

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