Evidence map›Paper›PMID 28559915›Full record

ArticleFrontiers in genetics2017

Combining Results from Distinct MicroRNA Target Prediction Tools Enhances the Performance of Analyses.

Arthur C Oliveira, Luiz A Bovolenta, Pedro G Nachtigall, Marcos E Herkenhoff, Ney Lemke, Danillo Pinhal

Abstract read
In one paragraph

Article in Frontiers in genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed.

  1. miR-29a-3p/Renal failure · 2025
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  9. Frontiers in microbiology · 2024
    Article
  10. AnFrontiers in genetics · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Learning noncoding RNA biology from viruses.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Review
  17. Article
  18. Differences in PLAToxins · 2022
    Article
  19. Article
  20. Machine Learning Using Gene-Sets to Infer miRNA Function.Advances in experimental medicine and biology · 2022
    Article
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

6 authors.

Arthur C OliveiraLaboratory of Genomics and Molecular Evolution, Department of Genetics, Institute of Biosciences of Botucatu, São Paulo State Univesity (UNESP)Botucatu, Brazil.
Luiz A BovolentaLaboratory of Bioinformatics and Computational Biophysics, Department of Physics and Biophysics, Institute of Biosciences of Botucatu, São Paulo State Univesity (UNESP)Botucatu, Brazil.
Pedro G NachtigallLaboratory of Genomics and Molecular Evolution, Department of Genetics, Institute of Biosciences of Botucatu, São Paulo State Univesity (UNESP)Botucatu, Brazil.
Marcos E HerkenhoffLaboratory of Genomics and Molecular Evolution, Department of Genetics, Institute of Biosciences of Botucatu, São Paulo State Univesity (UNESP)Botucatu, Brazil.
Ney LemkeLaboratory of Bioinformatics and Computational Biophysics, Department of Physics and Biophysics, Institute of Biosciences of Botucatu, São Paulo State Univesity (UNESP)Botucatu, Brazil.
Danillo PinhalLaboratory of Genomics and Molecular Evolution, Department of Genetics, Institute of Biosciences of Botucatu, São Paulo State Univesity (UNESP)Botucatu, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Target prediction is generally the first step toward recognition of bona fide microRNA (miRNA)-target interactions in living cells. Several target prediction tools are now available, which use distinct criteria and stringency to provide the best set of candidate targets for a single miRNA or a subset of miRNAs. However, there are many false-negative predictions, and consensus about the optimum strategy to select and use the output information provided by the target prediction tools is lacking. We compared the performance of four tools cited in literature-TargetScan (TS), miRanda-mirSVR (MR), Pita, and RNA22 (R22), and we determined the most effective approach for analyzing target prediction data (individual, union, or intersection). For this purpose, we calculated the sensitivity, specificity, precision, and correlation of these approaches using 10 miRNAs (miR-1-3p, miR-17-5p, miR-21-5p, miR-24-3p, miR-29a-3p, miR-34a-5p, miR-124-3p, miR-125b-5p, miR-145-5p, and miR-155-5p) and 1,400 genes (700 validated and 700 non-validated) as targets of these miRNAs. The four tools provided a subset of high-quality predictions and returned few false-positive predictions; however, they could not identify several known true targets. We demonstrate that union of TS/MR and TS/MR/R22 enhanced the quality of

Indexed as

bioinformaticsin silico predictionmiRanda-mirSVRnon-coding RNAPitaRNA22TargetScan

Identifiers

PMID28559915
PMCPMC5432626

What OpenQuestion holds

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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.