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Quantifying variances in comparative RNA secondary structure prediction
BACKGROUND: With the advancement of next-generation sequencing and transcriptomics technologies, regulatory effects involving RNA, in particular RNA structural changes are being detected. These results often rely on RNA secondary structure predictions. However, current approaches to RNA secondary st...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667108/ https://www.ncbi.nlm.nih.gov/pubmed/23634662 http://dx.doi.org/10.1186/1471-2105-14-149 |
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author | Anderson, James WJ Novák, Ádám Sükösd, Zsuzsanna Golden, Michael Arunapuram, Preeti Edvardsson, Ingolfur Hein, Jotun |
author_facet | Anderson, James WJ Novák, Ádám Sükösd, Zsuzsanna Golden, Michael Arunapuram, Preeti Edvardsson, Ingolfur Hein, Jotun |
author_sort | Anderson, James WJ |
collection | PubMed |
description | BACKGROUND: With the advancement of next-generation sequencing and transcriptomics technologies, regulatory effects involving RNA, in particular RNA structural changes are being detected. These results often rely on RNA secondary structure predictions. However, current approaches to RNA secondary structure modelling produce predictions with a high variance in predictive accuracy, and we have little quantifiable knowledge about the reasons for these variances. RESULTS: In this paper we explore a number of factors which can contribute to poor RNA secondary structure prediction quality. We establish a quantified relationship between alignment quality and loss of accuracy. Furthermore, we define two new measures to quantify uncertainty in alignment-based structure predictions. One of the measures improves on the “reliability score” reported by PPfold, and considers alignment uncertainty as well as base-pair probabilities. The other measure considers the information entropy for SCFGs over a space of input alignments. CONCLUSIONS: Our predictive accuracy improves on the PPfold reliability score. We can successfully characterize many of the underlying reasons for and variances in poor prediction. However, there is still variability unaccounted for, which we therefore suggest comes from the RNA secondary structure predictive model itself. |
format | Online Article Text |
id | pubmed-3667108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36671082013-06-05 Quantifying variances in comparative RNA secondary structure prediction Anderson, James WJ Novák, Ádám Sükösd, Zsuzsanna Golden, Michael Arunapuram, Preeti Edvardsson, Ingolfur Hein, Jotun BMC Bioinformatics Research Article BACKGROUND: With the advancement of next-generation sequencing and transcriptomics technologies, regulatory effects involving RNA, in particular RNA structural changes are being detected. These results often rely on RNA secondary structure predictions. However, current approaches to RNA secondary structure modelling produce predictions with a high variance in predictive accuracy, and we have little quantifiable knowledge about the reasons for these variances. RESULTS: In this paper we explore a number of factors which can contribute to poor RNA secondary structure prediction quality. We establish a quantified relationship between alignment quality and loss of accuracy. Furthermore, we define two new measures to quantify uncertainty in alignment-based structure predictions. One of the measures improves on the “reliability score” reported by PPfold, and considers alignment uncertainty as well as base-pair probabilities. The other measure considers the information entropy for SCFGs over a space of input alignments. CONCLUSIONS: Our predictive accuracy improves on the PPfold reliability score. We can successfully characterize many of the underlying reasons for and variances in poor prediction. However, there is still variability unaccounted for, which we therefore suggest comes from the RNA secondary structure predictive model itself. BioMed Central 2013-05-01 /pmc/articles/PMC3667108/ /pubmed/23634662 http://dx.doi.org/10.1186/1471-2105-14-149 Text en Copyright © 2013 Anderson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Anderson, James WJ Novák, Ádám Sükösd, Zsuzsanna Golden, Michael Arunapuram, Preeti Edvardsson, Ingolfur Hein, Jotun Quantifying variances in comparative RNA secondary structure prediction |
title | Quantifying variances in comparative RNA secondary structure prediction |
title_full | Quantifying variances in comparative RNA secondary structure prediction |
title_fullStr | Quantifying variances in comparative RNA secondary structure prediction |
title_full_unstemmed | Quantifying variances in comparative RNA secondary structure prediction |
title_short | Quantifying variances in comparative RNA secondary structure prediction |
title_sort | quantifying variances in comparative rna secondary structure prediction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667108/ https://www.ncbi.nlm.nih.gov/pubmed/23634662 http://dx.doi.org/10.1186/1471-2105-14-149 |
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