Evidence map›Paper›PMID 19091027›Full record

ArticleBMC bioinformatics2008

MiRTif: a support vector machine-based microRNA target interaction filter.

Yuchen Yang, Yu-Ping Wang, Kuo-Bin Li

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

26 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  8. Article
  9. MicroRNAs as predictive biomarkers and therapeutic targets in prostate cancer.American journal of clinical and experimental urology · 2014
    Review
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  11. Article
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  16. Regulation of WNK1 expression by miR-192 and aldosterone.Journal of the American Society of Nephrology : JASN · 2010
    Article
  17. Computational methods to identify miRNA targets.Seminars in cell & developmental biology · 2010
    Review
  18. Article
  19. Article
  20. 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

3 authors at 2 institutions in 2 countries.

Yuchen YangInstitute of Molecular and Cell Biology, 61 Biopolis Drive, 138673, Singapore. ycyang@imcb.a-star.edu.sg
Yu-Ping Wang
Kuo-Bin Li
National Yang Ming Chiao Tung University · TWInstitute of Molecular and Cell Biology · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are a set of small non-coding RNAs serving as important negative gene regulators. In animals, miRNAs turn down protein translation by binding to the 3' UTR regions of target genes with imperfect complementary pairing. The identification of microRNA targets has become one of the major challenges of miRNA research. Bioinformatics investigations on miRNA target have resulted in a number of target prediction tools. Although these tools are capable of predicting hundreds of targets for a given miRNA, many of them suffer from high false positive rates, indicating the need for a post-processing filter for the predicted targets. Once trained with experimentally validated true and false targets, machine learning methods appear to be ideal approaches to distinguish the true targets from the false ones.

resultsWe present a miRNA target filtering system named MiRTif (miRNA:target interaction filter). The system is a support vector machine (SVM) classifier trained with 195 positive and 38 negative miRNA:target interaction pairs, all experimentally validated. Each miRNA:target interaction pair is divided into a seed and a non-seed region. The encoded feature vector contains various k-gram frequencies in the seed, the non-seed and the entire regions. Informative features are selected based on their discriminating abilities. Prediction accuracies are assessed using 10-fold cross-validation experiments. Our system achieves AUC (area under the ROC curve) of 0.86, sensitivity of 83.59%, and specificity of 73.68%. More importantly, the system correctly predicts majority of the false positive miRNA:target interactions (28 out of 38). The possibility of over-fitting due to the relatively small negative sample set has also been investigated using a set of non-validated and randomly selected targets (from miRBase).

conclusionMiRTif is designed as a post-processing filter that takes miRNA:target interactions predicted by other target prediction softwares such as TargetScanS, PicTar and miRanda as inputs, and determines how likely the given interaction is a real or a pseudo one. MiRTif can be accessed from http://bsal.ym.edu.tw/mirtif.

Indexed as

3' Untranslated RegionsAlgorithmsArea Under CurveArtificial IntelligenceComputational BiologyComputersComputer SimulationFalse Positive ReactionsHumansMicroRNAsPattern Recognition, AutomatedReproducibility of ResultsSensitivity and SpecificitySequence Analysis, RNASoftware3' Untranslated RegionsMicroRNAs

Identifiers

PMID19091027
PMCPMC2638144
OpenAlexW2121936213

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.