用rNAV检测sRNA靶点的全基因组研究

Jonathan Dubois, A. Ghozlane, P. Thébault, I. Dutour, Romain Bourqui
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引用次数: 8

摘要

分子生物学的核心原则是“DNA制造RNA制造蛋白质”,然而,这一原则最近已被扩展到整合涉及小细菌非编码RNA(称为sRNAs)的新生物活动。因此,在过去的十年中,这些分子越来越受到重视,相关的实验工作表明这些分子具有广泛的功能活性。在本文中,我们提出了rNAV (rna NAVigator),这是一种用于视觉探索和分析细菌srna介导的调控网络的新工具。rNAV旨在帮助生物信息学家和生物学家从数以千计的预测列表中识别出相关的、合理的sRNA靶标候选物,以进行实验验证。我们提出了一系列专用算法和交互工具,以促进对此类网络的探索。这些算法可以收集到管道中,然后可以在几个会话中保存和重用。为了支持探测感知,rNAV还提供了一个探测树视图,允许在分析的步骤中导航,也可以选择要可视化和比较的子网。这些比较是由多个和完全链接的视图的整合而促成的。我们通过对大肠杆菌领域专家进行的案例研究证明了我们方法的有用性。
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Genome-wide detection of sRNA targets with rNAV
The central dogma in molecular biology postulated that `DNA makes RNA makes protein', however this dogma has been recently extended to integrate new biological activities involving small bacterial noncoding RNAs, called sRNAs. Accordingly, increasing attention has been given to these molecules over the last decade and related experimental works have shown a wide range of functional activities for these molecules. In this paper, we present rNAV (for rna NAVigator), a new tool for the visual exploration and analysis of bacterial sRNA-mediated regulatory networks. rNAV has been designed to help bioinformaticians and biologists to identify, from lists of thousands of predictions, pertinent and reasonable sRNA target candidates for carrying out experimental validations. We propose a list of dedicated algorithms and interaction tools that facilitate the exploration of such networks. These algorithms can be gathered into pipelines which can then be saved and reused over several sessions. To support exploration awareness, rNAV also provides an exploration tree view that allows to navigate through the steps of the analysis but also to select the sub-networks to visualize and compare. These comparisons are facilitated by the integration of multiple and fully linked views. We demonstrate the usefulness of our approach by a case study on Escherichia coli bacteria performed by domain experts.
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