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Benchmark of computational methods for predicting microRNA-disease associations

BACKGROUND: A series of miRNA-disease association prediction methods have been proposed to prioritize potential disease-associated miRNAs. Independent benchmarking of these methods is warranted to assess their effectiveness and robustness. RESULTS: Based on more than 8000 novel miRNA-disease associa...

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Autores principales: Huang, Zhou, Liu, Leibo, Gao, Yuanxu, Shi, Jiangcheng, Cui, Qinghua, Li, Jianwei, Zhou, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781296/
https://www.ncbi.nlm.nih.gov/pubmed/31594544
http://dx.doi.org/10.1186/s13059-019-1811-3
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author Huang, Zhou
Liu, Leibo
Gao, Yuanxu
Shi, Jiangcheng
Cui, Qinghua
Li, Jianwei
Zhou, Yuan
author_facet Huang, Zhou
Liu, Leibo
Gao, Yuanxu
Shi, Jiangcheng
Cui, Qinghua
Li, Jianwei
Zhou, Yuan
author_sort Huang, Zhou
collection PubMed
description BACKGROUND: A series of miRNA-disease association prediction methods have been proposed to prioritize potential disease-associated miRNAs. Independent benchmarking of these methods is warranted to assess their effectiveness and robustness. RESULTS: Based on more than 8000 novel miRNA-disease associations from the latest HMDD v3.1 database, we perform systematic comparison among 36 readily available prediction methods. Their overall performances are evaluated with rigorous precision-recall curve analysis, where 13 methods show acceptable accuracy (AUPRC > 0.200) while the top two methods achieve a promising AUPRC over 0.300, and most of these methods are also highly ranked when considering only the causal miRNA-disease associations as the positive samples. The potential of performance improvement is demonstrated by combining different predictors or adopting a more updated miRNA similarity matrix, which would result in up to 16% and 46% of AUPRC augmentations compared to the best single predictor and the predictors using the previous similarity matrix, respectively. Our analysis suggests a common issue of the available methods, which is that the prediction results are severely biased toward well-annotated diseases with many associated miRNAs known and cannot further stratify the positive samples by discriminating the causal miRNA-disease associations from the general miRNA-disease associations. CONCLUSION: Our benchmarking results not only provide a reference for biomedical researchers to choose appropriate miRNA-disease association predictors for their purpose, but also suggest the future directions for the development of more robust miRNA-disease association predictors.
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spelling pubmed-67812962019-10-17 Benchmark of computational methods for predicting microRNA-disease associations Huang, Zhou Liu, Leibo Gao, Yuanxu Shi, Jiangcheng Cui, Qinghua Li, Jianwei Zhou, Yuan Genome Biol Research BACKGROUND: A series of miRNA-disease association prediction methods have been proposed to prioritize potential disease-associated miRNAs. Independent benchmarking of these methods is warranted to assess their effectiveness and robustness. RESULTS: Based on more than 8000 novel miRNA-disease associations from the latest HMDD v3.1 database, we perform systematic comparison among 36 readily available prediction methods. Their overall performances are evaluated with rigorous precision-recall curve analysis, where 13 methods show acceptable accuracy (AUPRC > 0.200) while the top two methods achieve a promising AUPRC over 0.300, and most of these methods are also highly ranked when considering only the causal miRNA-disease associations as the positive samples. The potential of performance improvement is demonstrated by combining different predictors or adopting a more updated miRNA similarity matrix, which would result in up to 16% and 46% of AUPRC augmentations compared to the best single predictor and the predictors using the previous similarity matrix, respectively. Our analysis suggests a common issue of the available methods, which is that the prediction results are severely biased toward well-annotated diseases with many associated miRNAs known and cannot further stratify the positive samples by discriminating the causal miRNA-disease associations from the general miRNA-disease associations. CONCLUSION: Our benchmarking results not only provide a reference for biomedical researchers to choose appropriate miRNA-disease association predictors for their purpose, but also suggest the future directions for the development of more robust miRNA-disease association predictors. BioMed Central 2019-10-08 /pmc/articles/PMC6781296/ /pubmed/31594544 http://dx.doi.org/10.1186/s13059-019-1811-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Huang, Zhou
Liu, Leibo
Gao, Yuanxu
Shi, Jiangcheng
Cui, Qinghua
Li, Jianwei
Zhou, Yuan
Benchmark of computational methods for predicting microRNA-disease associations
title Benchmark of computational methods for predicting microRNA-disease associations
title_full Benchmark of computational methods for predicting microRNA-disease associations
title_fullStr Benchmark of computational methods for predicting microRNA-disease associations
title_full_unstemmed Benchmark of computational methods for predicting microRNA-disease associations
title_short Benchmark of computational methods for predicting microRNA-disease associations
title_sort benchmark of computational methods for predicting microrna-disease associations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781296/
https://www.ncbi.nlm.nih.gov/pubmed/31594544
http://dx.doi.org/10.1186/s13059-019-1811-3
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