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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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Background Bacterial 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. Result To address this issue, we propose a new visualization tool rNAV 2.0 , for detecting and filtering bacterial sRNA targets for regulatory networks. rNAV is designed to cope with a variety of biological constraints, including the gene annotations, the conserved regions of interaction or specific patterns of regulation. Depending on the application, these constraints can be variously combined to analyze the target candidates, prioritized for instance by a known conserved interaction region, or because of a common function. Conclusion The standalone application implements a set of known algorithms and interaction techniques, and applies them to the new problem of identifying reasonable sRNA target candidates.
机译:背景技术细菌sRNA介导的调节网络已被引入,作为分析细菌响应环境条件变化的快速重新连接能力的有力方法。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实验给出的所得基因列表中进行sRNA靶标分析(如果可用)。但是,最终目标候选者的数量可能仍然很大,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,在为昂贵的实验验证阶段提出新的候选方案之前,必须采取新颖的策略来提高计算预测结果的特异性。结果为了解决此问题,我们提出了一种新的可视化工具rNAV 2.0,用于检测和过滤调控网络中的细菌sRNA目标。 rNAV旨在应对多种生物学限制,包括基因注释,相互作用的保守区域或特定调控模式。取决于应用,可以将这些约束条件进行各种组合以分析目标候选对象,例如通过已知的保守交互区域或由于共同的功能而对这些候选对象进行优先级排序。结论独立应用程序实现了一组已知的算法和交互技术,并将它们应用于识别合理的sRNA目标候选物的新问题。

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