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

Overview of attention for article published in BMC Bioinformatics, March 2017
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Title
rNAV 2.0: a visualization tool for bacterial sRNA-mediated regulatory networks mining
Published in
BMC Bioinformatics, March 2017
DOI 10.1186/s12859-017-1598-8
Pubmed ID
Authors

Romain Bourqui, Isabelle Dutour, Jonathan Dubois, William Benchimol, Patricia Thébault

Abstract

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. 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. 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.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
New Zealand 1 4%
Unknown 22 96%

Demographic breakdown

Readers by professional status Count As %
Student > Master 6 26%
Student > Ph. D. Student 5 22%
Researcher 3 13%
Student > Bachelor 2 9%
Professor > Associate Professor 1 4%
Other 0 0%
Unknown 6 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 17%
Computer Science 4 17%
Agricultural and Biological Sciences 3 13%
Chemistry 2 9%
Immunology and Microbiology 1 4%
Other 2 9%
Unknown 7 30%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 March 2017.
All research outputs
#20,411,380
of 22,961,203 outputs
Outputs from BMC Bioinformatics
#6,881
of 7,306 outputs
Outputs of similar age
#269,561
of 309,217 outputs
Outputs of similar age from BMC Bioinformatics
#110
of 124 outputs
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