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isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants
In plants, post transcriptional regulation by non-coding RNAs (ncRNAs), in particular miRNAs (19–24 nt) has been involved in modulating the transcriptional landscape in developmental, biotic and abiotic interactions. In past few years, considerable focus has been leveraged on delineating and deciphe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359237/ https://www.ncbi.nlm.nih.gov/pubmed/28377776 http://dx.doi.org/10.3389/fpls.2017.00322 |
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author | Yang, Kun Sablok, Gaurav Qiao, Guang Nie, Qiong Wen, Xiaopeng |
author_facet | Yang, Kun Sablok, Gaurav Qiao, Guang Nie, Qiong Wen, Xiaopeng |
author_sort | Yang, Kun |
collection | PubMed |
description | In plants, post transcriptional regulation by non-coding RNAs (ncRNAs), in particular miRNAs (19–24 nt) has been involved in modulating the transcriptional landscape in developmental, biotic and abiotic interactions. In past few years, considerable focus has been leveraged on delineating and deciphering the role of miRNAs and their canonical isomiRs in plants. However, proper classification and accurate prediction of plant isomiRs taking into account the relative features by which we define isomiRs, such as templated or non-templated is still lacking. In the present research, we present isomiR2Function, a standalone easily deployable tool that allows for the robust and high-throughput discovery of templated and non-templated isomiRs. Additionally, isomiR2Function allows for identification of differentially expressed isomiRs and in parallel target prediction based on both transcripts or PARE-Seq either using Targetfinder or Cleaveland. isomiR2Function allows for the functional enrichment of the detected targets using TopGO package. Benchmarking of isomiR2Function revealed highly accurate prediction and classification of isomiRs as compared to the previously developed isomiR prediction tools. Additionally, the downstream implementation of additional features allows isomiR2Function to be classified as a single standalone tool for isomiR profiling from discovery to functional roles. All in all, isomiR2Function allows the streamline processing of the miRNA-seq for the identification and characterization of isomiRs with minimal efforts. isomiR2Function can be accessed through: https://github.com/347033139/isomiR2Function. |
format | Online Article Text |
id | pubmed-5359237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53592372017-04-04 isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants Yang, Kun Sablok, Gaurav Qiao, Guang Nie, Qiong Wen, Xiaopeng Front Plant Sci Plant Science In plants, post transcriptional regulation by non-coding RNAs (ncRNAs), in particular miRNAs (19–24 nt) has been involved in modulating the transcriptional landscape in developmental, biotic and abiotic interactions. In past few years, considerable focus has been leveraged on delineating and deciphering the role of miRNAs and their canonical isomiRs in plants. However, proper classification and accurate prediction of plant isomiRs taking into account the relative features by which we define isomiRs, such as templated or non-templated is still lacking. In the present research, we present isomiR2Function, a standalone easily deployable tool that allows for the robust and high-throughput discovery of templated and non-templated isomiRs. Additionally, isomiR2Function allows for identification of differentially expressed isomiRs and in parallel target prediction based on both transcripts or PARE-Seq either using Targetfinder or Cleaveland. isomiR2Function allows for the functional enrichment of the detected targets using TopGO package. Benchmarking of isomiR2Function revealed highly accurate prediction and classification of isomiRs as compared to the previously developed isomiR prediction tools. Additionally, the downstream implementation of additional features allows isomiR2Function to be classified as a single standalone tool for isomiR profiling from discovery to functional roles. All in all, isomiR2Function allows the streamline processing of the miRNA-seq for the identification and characterization of isomiRs with minimal efforts. isomiR2Function can be accessed through: https://github.com/347033139/isomiR2Function. Frontiers Media S.A. 2017-03-21 /pmc/articles/PMC5359237/ /pubmed/28377776 http://dx.doi.org/10.3389/fpls.2017.00322 Text en Copyright © 2017 Yang, Sablok, Qiao, Nie and Wen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Yang, Kun Sablok, Gaurav Qiao, Guang Nie, Qiong Wen, Xiaopeng isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants |
title | isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants |
title_full | isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants |
title_fullStr | isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants |
title_full_unstemmed | isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants |
title_short | isomiR2Function: An Integrated Workflow for Identifying MicroRNA Variants in Plants |
title_sort | isomir2function: an integrated workflow for identifying microrna variants in plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359237/ https://www.ncbi.nlm.nih.gov/pubmed/28377776 http://dx.doi.org/10.3389/fpls.2017.00322 |
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