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miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis

Small RNA sequencing is the most widely used tool for microRNA (miRNA) discovery, and shows great potential for the efficient study of miRNA cross-species transport, i.e., by detecting the presence of exogenous miRNA sequences in the host species. Because of the increased appreciation of dietary miR...

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Detalles Bibliográficos
Autores principales: Zhang, Hanyuan, Vieira Resende e Silva, Bruno, Cui, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952930/
https://www.ncbi.nlm.nih.gov/pubmed/28073746
http://dx.doi.org/10.1093/bib/bbw140
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author Zhang, Hanyuan
Vieira Resende e Silva, Bruno
Cui, Juan
author_facet Zhang, Hanyuan
Vieira Resende e Silva, Bruno
Cui, Juan
author_sort Zhang, Hanyuan
collection PubMed
description Small RNA sequencing is the most widely used tool for microRNA (miRNA) discovery, and shows great potential for the efficient study of miRNA cross-species transport, i.e., by detecting the presence of exogenous miRNA sequences in the host species. Because of the increased appreciation of dietary miRNAs and their far-reaching implication in human health, research interests are currently growing with regard to exogenous miRNAs bioavailability, mechanisms of cross-species transport and miRNA function in cellular biological processes. In this article, we present microRNA Discovery (miRDis), a new small RNA sequencing data analysis pipeline for both endogenous and exogenous miRNA detection. Specifically, we developed and deployed a Web service that supports the annotation and expression profiling data of known host miRNAs and the detection of novel miRNAs, other noncoding RNAs, and the exogenous miRNAs from dietary species. As a proof-of-concept, we analyzed a set of human plasma sequencing data from a milk-feeding study where 225 human miRNAs were detected in the plasma samples and 44 show elevated expression after milk intake. By examining the bovine-specific sequences, data indicate that three bovine miRNAs (bta-miR-378, -181* and -150) are present in human plasma possibly because of the dietary uptake. Further evaluation based on different sets of public data demonstrates that miRDis outperforms other state-of-the-art tools in both detection and quantification of miRNA from either animal or plant sources. The miRDis Web server is available at: http://sbbi.unl.edu/miRDis/index.php.
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spelling pubmed-59529302018-05-18 miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis Zhang, Hanyuan Vieira Resende e Silva, Bruno Cui, Juan Brief Bioinform Papers Small RNA sequencing is the most widely used tool for microRNA (miRNA) discovery, and shows great potential for the efficient study of miRNA cross-species transport, i.e., by detecting the presence of exogenous miRNA sequences in the host species. Because of the increased appreciation of dietary miRNAs and their far-reaching implication in human health, research interests are currently growing with regard to exogenous miRNAs bioavailability, mechanisms of cross-species transport and miRNA function in cellular biological processes. In this article, we present microRNA Discovery (miRDis), a new small RNA sequencing data analysis pipeline for both endogenous and exogenous miRNA detection. Specifically, we developed and deployed a Web service that supports the annotation and expression profiling data of known host miRNAs and the detection of novel miRNAs, other noncoding RNAs, and the exogenous miRNAs from dietary species. As a proof-of-concept, we analyzed a set of human plasma sequencing data from a milk-feeding study where 225 human miRNAs were detected in the plasma samples and 44 show elevated expression after milk intake. By examining the bovine-specific sequences, data indicate that three bovine miRNAs (bta-miR-378, -181* and -150) are present in human plasma possibly because of the dietary uptake. Further evaluation based on different sets of public data demonstrates that miRDis outperforms other state-of-the-art tools in both detection and quantification of miRNA from either animal or plant sources. The miRDis Web server is available at: http://sbbi.unl.edu/miRDis/index.php. Oxford University Press 2017-01-10 /pmc/articles/PMC5952930/ /pubmed/28073746 http://dx.doi.org/10.1093/bib/bbw140 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Papers
Zhang, Hanyuan
Vieira Resende e Silva, Bruno
Cui, Juan
miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis
title miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis
title_full miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis
title_fullStr miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis
title_full_unstemmed miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis
title_short miRDis: a Web tool for endogenous and exogenous microRNA discovery based on deep-sequencing data analysis
title_sort mirdis: a web tool for endogenous and exogenous microrna discovery based on deep-sequencing data analysis
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952930/
https://www.ncbi.nlm.nih.gov/pubmed/28073746
http://dx.doi.org/10.1093/bib/bbw140
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