Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble
As the biomedical impact of small RNAs grows, so does the need to understand competing structural alternatives for regions of functional interest. Suboptimal structure analysis provides significantly more RNA base pairing information than a single minimum free energy prediction. Yet computational en...
Main Authors: | , |
---|---|
Format: | Online |
Language: | English |
Published: |
Oxford University Press
2014
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267672/ |
id |
pubmed-4267672 |
---|---|
recordtype |
oai_dc |
spelling |
pubmed-42676722014-12-23 Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble Rogers, Emily Heitsch, Christine E. Methods Online As the biomedical impact of small RNAs grows, so does the need to understand competing structural alternatives for regions of functional interest. Suboptimal structure analysis provides significantly more RNA base pairing information than a single minimum free energy prediction. Yet computational enhancements like Boltzmann sampling have not been fully adopted by experimentalists since identifying meaningful patterns in this data can be challenging. Profiling is a novel approach to mining RNA suboptimal structure data which makes the power of ensemble-based analysis accessible in a stable and reliable way. Balancing abstraction and specificity, profiling identifies significant combinations of base pairs which dominate low-energy RNA secondary structures. By design, critical similarities and differences are highlighted, yielding crucial information for molecular biologists. The code is freely available via http://gtfold.sourceforge.net/profiling.html. Oxford University Press 2014-12-16 2014-11-11 /pmc/articles/PMC4267672/ /pubmed/25392423 http://dx.doi.org/10.1093/nar/gku959 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 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 |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Rogers, Emily Heitsch, Christine E. |
spellingShingle |
Rogers, Emily Heitsch, Christine E. Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble |
author_facet |
Rogers, Emily Heitsch, Christine E. |
author_sort |
Rogers, Emily |
title |
Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble |
title_short |
Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble |
title_full |
Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble |
title_fullStr |
Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble |
title_full_unstemmed |
Profiling small RNA reveals multimodal substructural signals in a Boltzmann ensemble |
title_sort |
profiling small rna reveals multimodal substructural signals in a boltzmann ensemble |
description |
As the biomedical impact of small RNAs grows, so does the need to understand competing structural alternatives for regions of functional interest. Suboptimal structure analysis provides significantly more RNA base pairing information than a single minimum free energy prediction. Yet computational enhancements like Boltzmann sampling have not been fully adopted by experimentalists since identifying meaningful patterns in this data can be challenging. Profiling is a novel approach to mining RNA suboptimal structure data which makes the power of ensemble-based analysis accessible in a stable and reliable way. Balancing abstraction and specificity, profiling identifies significant combinations of base pairs which dominate low-energy RNA secondary structures. By design, critical similarities and differences are highlighted, yielding crucial information for molecular biologists. The code is freely available via http://gtfold.sourceforge.net/profiling.html. |
publisher |
Oxford University Press |
publishDate |
2014 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267672/ |
_version_ |
1613168036295999488 |