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CIRI: an efficient and unbiased algorithm for de novo circular RNA identification

Recent studies reveal that circular RNAs (circRNAs) are a novel class of abundant, stable and ubiquitous noncoding RNA molecules in animals. Comprehensive detection of circRNAs from high-throughput transcriptome data is an initial and crucial step to study their biogenesis and function. Here, we pre...

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Detalles Bibliográficos
Autores principales: Gao, Yuan, Wang, Jinfeng, Zhao, Fangqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316645/
https://www.ncbi.nlm.nih.gov/pubmed/25583365
http://dx.doi.org/10.1186/s13059-014-0571-3
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author Gao, Yuan
Wang, Jinfeng
Zhao, Fangqing
author_facet Gao, Yuan
Wang, Jinfeng
Zhao, Fangqing
author_sort Gao, Yuan
collection PubMed
description Recent studies reveal that circular RNAs (circRNAs) are a novel class of abundant, stable and ubiquitous noncoding RNA molecules in animals. Comprehensive detection of circRNAs from high-throughput transcriptome data is an initial and crucial step to study their biogenesis and function. Here, we present a novel chiastic clipping signal-based algorithm, CIRI, to unbiasedly and accurately detect circRNAs from transcriptome data by employing multiple filtration strategies. By applying CIRI to ENCODE RNA-seq data, we for the first time identify and experimentally validate the prevalence of intronic/intergenic circRNAs as well as fragments specific to them in the human transcriptome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-014-0571-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-43166452015-02-05 CIRI: an efficient and unbiased algorithm for de novo circular RNA identification Gao, Yuan Wang, Jinfeng Zhao, Fangqing Genome Biol Method Recent studies reveal that circular RNAs (circRNAs) are a novel class of abundant, stable and ubiquitous noncoding RNA molecules in animals. Comprehensive detection of circRNAs from high-throughput transcriptome data is an initial and crucial step to study their biogenesis and function. Here, we present a novel chiastic clipping signal-based algorithm, CIRI, to unbiasedly and accurately detect circRNAs from transcriptome data by employing multiple filtration strategies. By applying CIRI to ENCODE RNA-seq data, we for the first time identify and experimentally validate the prevalence of intronic/intergenic circRNAs as well as fragments specific to them in the human transcriptome. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-014-0571-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-13 2015 /pmc/articles/PMC4316645/ /pubmed/25583365 http://dx.doi.org/10.1186/s13059-014-0571-3 Text en © Gao et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Method
Gao, Yuan
Wang, Jinfeng
Zhao, Fangqing
CIRI: an efficient and unbiased algorithm for de novo circular RNA identification
title CIRI: an efficient and unbiased algorithm for de novo circular RNA identification
title_full CIRI: an efficient and unbiased algorithm for de novo circular RNA identification
title_fullStr CIRI: an efficient and unbiased algorithm for de novo circular RNA identification
title_full_unstemmed CIRI: an efficient and unbiased algorithm for de novo circular RNA identification
title_short CIRI: an efficient and unbiased algorithm for de novo circular RNA identification
title_sort ciri: an efficient and unbiased algorithm for de novo circular rna identification
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316645/
https://www.ncbi.nlm.nih.gov/pubmed/25583365
http://dx.doi.org/10.1186/s13059-014-0571-3
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