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CircRNAFisher: a systematic computational approach for de novo circular RNA identification.
Jia, Guo-Yi; Wang, Duo-Lin; Xue, Meng-Zhu; Liu, Yu-Wei; Pei, Yu-Chen; Yang, Ying-Qun; Xu, Jing-Mei; Liang, Yan-Chun; Wang, Peng.
Afiliación
  • Jia GY; School of Life Sciences, Shanghai University, Shanghai, 200444, China.
  • Wang DL; Laboratory of Systems Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, China.
  • Xue MZ; Key Laboratory of Symbolic Computation and Knowledge Engineering of Ministry of Education, College of Computer Science and Technology, Jilin University, Changchun, 130012, China.
  • Liu YW; Laboratory of Systems Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, China.
  • Pei YC; Laboratory of Systems Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, China.
  • Yang YQ; Laboratory of Systems Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, China.
  • Xu JM; Laboratory of Systems Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, China.
  • Liang YC; School of Life Science and Technology, Shanghai Tech University, Shanghai, 201210, China.
  • Wang P; Laboratory of Systems Biology, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201210, China.
Acta Pharmacol Sin ; 40(1): 55-63, 2019 Jan.
Article en En | MEDLINE | ID: mdl-30013032
ABSTRACT
Circular RNAs (circRNAs) are emerging species of mRNA splicing products with largely unknown functions. Although several computational pipelines for circRNA identification have been developed, these methods strictly rely on uniquely mapped reads overlapping back-splice junctions (BSJs) and lack approaches to model the statistical significance of the identified circRNAs. Here, we reported a systematic computational approach to identify circRNAs by simultaneously utilizing BSJ overlapping reads and discordant BSJ spanning reads to identify circRNAs. Moreover, we developed a novel procedure to estimate the P-values of the identified circRNAs. A computational cross-validation and experimental validations demonstrated that our method performed favorably compared to existing circRNA detection tools. We created a standalone tool, CircRNAFisher, to implement the method, which might be valuable to computational and experimental scientists studying circRNAs.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN / Análisis de Secuencia de ARN / Biología Computacional Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Acta Pharmacol Sin Asunto de la revista: FARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN / Análisis de Secuencia de ARN / Biología Computacional Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Acta Pharmacol Sin Asunto de la revista: FARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: China