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Computational methods for ab initio detection of microRNAs

MicroRNAs are small RNA sequences of 18–24 nucleotides in length, which serve as templates to drive post-transcriptional gene silencing. The canonical microRNA pathway starts with transcription from DNA and is followed by processing via the microprocessor complex, yielding a hairpin structure. Which...

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Detalles Bibliográficos
Autores principales: Allmer, Jens, Yousef, Malik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467617/
https://www.ncbi.nlm.nih.gov/pubmed/23087705
http://dx.doi.org/10.3389/fgene.2012.00209
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author Allmer, Jens
Yousef, Malik
author_facet Allmer, Jens
Yousef, Malik
author_sort Allmer, Jens
collection PubMed
description MicroRNAs are small RNA sequences of 18–24 nucleotides in length, which serve as templates to drive post-transcriptional gene silencing. The canonical microRNA pathway starts with transcription from DNA and is followed by processing via the microprocessor complex, yielding a hairpin structure. Which is then exported into the cytosol where it is processed by Dicer and then incorporated into the RNA-induced silencing complex. All of these biogenesis steps add to the overall specificity of miRNA production and effect. Unfortunately, their modes of action are just beginning to be elucidated and therefore computational prediction algorithms cannot model the process but are usually forced to employ machine learning approaches. This work focuses on ab initio prediction methods throughout; and therefore homology-based miRNA detection methods are not discussed. Current ab initio prediction algorithms, their ties to data mining, and their prediction accuracy are detailed.
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spelling pubmed-34676172012-10-19 Computational methods for ab initio detection of microRNAs Allmer, Jens Yousef, Malik Front Genet Genetics MicroRNAs are small RNA sequences of 18–24 nucleotides in length, which serve as templates to drive post-transcriptional gene silencing. The canonical microRNA pathway starts with transcription from DNA and is followed by processing via the microprocessor complex, yielding a hairpin structure. Which is then exported into the cytosol where it is processed by Dicer and then incorporated into the RNA-induced silencing complex. All of these biogenesis steps add to the overall specificity of miRNA production and effect. Unfortunately, their modes of action are just beginning to be elucidated and therefore computational prediction algorithms cannot model the process but are usually forced to employ machine learning approaches. This work focuses on ab initio prediction methods throughout; and therefore homology-based miRNA detection methods are not discussed. Current ab initio prediction algorithms, their ties to data mining, and their prediction accuracy are detailed. Frontiers Media S.A. 2012-10-10 /pmc/articles/PMC3467617/ /pubmed/23087705 http://dx.doi.org/10.3389/fgene.2012.00209 Text en Copyright © Allmer and Yousef. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Genetics
Allmer, Jens
Yousef, Malik
Computational methods for ab initio detection of microRNAs
title Computational methods for ab initio detection of microRNAs
title_full Computational methods for ab initio detection of microRNAs
title_fullStr Computational methods for ab initio detection of microRNAs
title_full_unstemmed Computational methods for ab initio detection of microRNAs
title_short Computational methods for ab initio detection of microRNAs
title_sort computational methods for ab initio detection of micrornas
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467617/
https://www.ncbi.nlm.nih.gov/pubmed/23087705
http://dx.doi.org/10.3389/fgene.2012.00209
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