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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6781296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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