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miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures
Decoding the patterns of miRNA regulation in diseases are important to properly realize its potential in diagnostic, prog- nostic, and therapeutic applications. Only a handful of studies computationally predict possible miRNA-miRNA interactions; hence, such interactions require a thorough investigat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206712/ https://www.ncbi.nlm.nih.gov/pubmed/28045122 http://dx.doi.org/10.1038/srep39684 |
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author | Nalluri, Joseph J. Barh, Debmalya Azevedo, Vasco Ghosh, Preetam |
author_facet | Nalluri, Joseph J. Barh, Debmalya Azevedo, Vasco Ghosh, Preetam |
author_sort | Nalluri, Joseph J. |
collection | PubMed |
description | Decoding the patterns of miRNA regulation in diseases are important to properly realize its potential in diagnostic, prog- nostic, and therapeutic applications. Only a handful of studies computationally predict possible miRNA-miRNA interactions; hence, such interactions require a thorough investigation to understand their role in disease progression. In this paper, we design a novel computational pipeline to predict the common signature/core sets of miRNA-miRNA interactions for different diseases using network inference algorithms on the miRNA-disease expression profiles; the individual predictions of these algorithms were then merged using a consensus-based approach to predict miRNA-miRNA associations. We next selected the miRNA-miRNA associations across particular diseases to generate the corresponding disease-specific miRNA-interaction networks. Next, graph intersection analysis was performed on these networks for multiple diseases to identify the common signature/core sets of miRNA interactions. We applied this pipeline to identify the common signature of miRNA-miRNA inter- actions for cancers. The identified signatures when validated using a manual literature search from PubMed Central and the PhenomiR database, show strong relevance with the respective cancers, providing an indirect proof of the high accuracy of our methodology. We developed miRsig, an online tool for analysis and visualization of the disease-specific signature/core miRNA-miRNA interactions, available at: http://bnet.egr.vcu.edu/miRsig. |
format | Online Article Text |
id | pubmed-5206712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52067122017-01-04 miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures Nalluri, Joseph J. Barh, Debmalya Azevedo, Vasco Ghosh, Preetam Sci Rep Article Decoding the patterns of miRNA regulation in diseases are important to properly realize its potential in diagnostic, prog- nostic, and therapeutic applications. Only a handful of studies computationally predict possible miRNA-miRNA interactions; hence, such interactions require a thorough investigation to understand their role in disease progression. In this paper, we design a novel computational pipeline to predict the common signature/core sets of miRNA-miRNA interactions for different diseases using network inference algorithms on the miRNA-disease expression profiles; the individual predictions of these algorithms were then merged using a consensus-based approach to predict miRNA-miRNA associations. We next selected the miRNA-miRNA associations across particular diseases to generate the corresponding disease-specific miRNA-interaction networks. Next, graph intersection analysis was performed on these networks for multiple diseases to identify the common signature/core sets of miRNA interactions. We applied this pipeline to identify the common signature of miRNA-miRNA inter- actions for cancers. The identified signatures when validated using a manual literature search from PubMed Central and the PhenomiR database, show strong relevance with the respective cancers, providing an indirect proof of the high accuracy of our methodology. We developed miRsig, an online tool for analysis and visualization of the disease-specific signature/core miRNA-miRNA interactions, available at: http://bnet.egr.vcu.edu/miRsig. Nature Publishing Group 2017-01-03 /pmc/articles/PMC5206712/ /pubmed/28045122 http://dx.doi.org/10.1038/srep39684 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Nalluri, Joseph J. Barh, Debmalya Azevedo, Vasco Ghosh, Preetam miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures |
title | miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures |
title_full | miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures |
title_fullStr | miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures |
title_full_unstemmed | miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures |
title_short | miRsig: a consensus-based network inference methodology to identify pan-cancer miRNA-miRNA interaction signatures |
title_sort | mirsig: a consensus-based network inference methodology to identify pan-cancer mirna-mirna interaction signatures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206712/ https://www.ncbi.nlm.nih.gov/pubmed/28045122 http://dx.doi.org/10.1038/srep39684 |
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