Evidence map›Paper›PMID 27578422›Full record

ArticleBMC bioinformatics2016

A genetic algorithm-based weighted ensemble method for predicting transposon-derived piRNAs.

Dingfang Li, Longqiang Luo, Wen Zhang, Feng Liu, Fei Luo

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Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

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40citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Guided optimization of ToxPi model weights using a Semi-Automated approach.Computational toxicology (Amsterdam, Netherlands) · 2024
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  18. Mobile genomics: tools and techniques for tackling transposons.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Dingfang LiSchool of Mathematics and Statistics, Wuhan University, Wuhan, 430072, China.
Longqiang LuoSchool of Mathematics and Statistics, Wuhan University, Wuhan, 430072, China.
Wen ZhangState Key Lab of Software Engineering, Wuhan University, Wuhan, 430072, China. zhangwen@whu.edu.cn.
Feng LiuInternational School of Software, Wuhan University, Wuhan, 430072, China.
Fei LuoState Key Lab of Software Engineering, Wuhan University, Wuhan, 430072, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPredicting piwi-interacting RNA (piRNA) is an important topic in the small non-coding RNAs, which provides clues for understanding the generation mechanism of gamete. To the best of our knowledge, several machine learning approaches have been proposed for the piRNA prediction, but there is still room for improvements.

resultsIn this paper, we develop a genetic algorithm-based weighted ensemble method for predicting transposon-derived piRNAs. We construct datasets for three species: Human, Mouse and Drosophila. For each species, we compile the balanced dataset and imbalanced dataset, and thus obtain six datasets to build and evaluate prediction models. In the computational experiments, the genetic algorithm-based weighted ensemble method achieves 10-fold cross validation AUC of 0.932, 0.937 and 0.995 on the balanced Human dataset, Mouse dataset and Drosophila dataset, respectively, and achieves AUC of 0.935, 0.939 and 0.996 on the imbalanced datasets of three species. Further, we use the prediction models trained on the Mouse dataset to identify piRNAs of other species, and the models demonstrate the good performances in the cross-species prediction.

conclusionsCompared with other state-of-the-art methods, our method can lead to better performances. In conclusion, the proposed method is promising for the transposon-derived piRNA prediction. The source codes and datasets are available in https://github.com/zw9977129/piRNAPredictor .

Indexed as

AlgorithmsAnimalsArea Under CurveDNA Transposable ElementsDrosophilaHumansMiceRNA, Small InterferingROC CurveUser-Computer InterfaceDNA Transposable ElementsRNA, Small InterferingEnsemble learningFeatureGenetic algorithmpiRNA

Identifiers

PMID27578422
PMCPMC5006569

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LicenceCC BY
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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.