Evidence map›Paper›PMID 28335718›Full record

ArticleBMC bioinformatics2017

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

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

Abstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Romain BourquiLaBRI, CNRS UMR5800, Université de Bordeaux, 351, cours de la Libération, Talence cedex, F-33405, France. bourqui@labri.fr.ORCID http://orcid.org/0000-0002-1847-2589
Isabelle DutourLaBRI, CNRS UMR5800, Université de Bordeaux, 351, cours de la Libération, Talence cedex, F-33405, France.
Jonathan DuboisLaBRI, CNRS UMR5800, Université de Bordeaux, 351, cours de la Libération, Talence cedex, F-33405, France.
William BenchimolLaBRI, CNRS UMR5800, Université de Bordeaux, 351, cours de la Libération, Talence cedex, F-33405, France.
Patricia ThébaultLaBRI, CNRS UMR5800, Université de Bordeaux, 351, cours de la Libération, Talence cedex, F-33405, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

resultTo 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.

conclusionThe standalone application implements a set of known algorithms and interaction techniques, and applies them to the new problem of identifying reasonable sRNA target candidates.

Indexed as

Computational BiologyGene Expression Regulation, BacterialRNA, BacterialRNA, BacterialBacterial sRNAsRNA-mediated regulatory networkVisualization and bioinformatics

Identifiers

PMID28335718
PMCPMC5364647

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.