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Circr,一种用于识别微小RNA与环状RNA关联的计算工具。

Circr, a Computational Tool to Identify miRNA:circRNA Associations.

作者信息

Dori Martina, Caroli Jimmy, Forcato Mattia

机构信息

Department of Life Sciences, University of Modena and Reggio Emilia, Modena Italy.

Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.

出版信息

Front Bioinform. 2022 Mar 11;2:852834. doi: 10.3389/fbinf.2022.852834. eCollection 2022.

Abstract

Circular RNAs (circRNAs) are known to act as important regulators of the microRNA (miRNA) activity. Yet, computational resources to identify miRNA:circRNA interactions are mostly limited to already annotated circRNAs or affected by high rates of false positive predictions. To overcome these limitations, we developed Circr, a computational tool for the prediction of associations between circRNAs and miRNAs. Circr combines three publicly available algorithms for prediction of miRNA binding sites on target sequences (miRanda, RNAhybrid, and TargetScan) and annotates each identified miRNA:target pairs with experimentally validated miRNA:RNA interactions and binding sites for Argonaute proteins derived from either ChIPseq or CLIPseq data. The combination of multiple tools for the identification of a single miRNA recognition site with experimental data allows to efficiently prioritize candidate miRNA:circRNA interactions for functional studies in different organisms. Circr can use its internal annotation database or custom annotation tables to enhance the identification of novel and not previously annotated miRNA:circRNA sites in virtually any species. Circr is written in Python 3.6 and is released under the GNU GPL3.0 License at https://github.com/bicciatolab/Circr.

摘要

已知环状RNA(circRNA)可作为微小RNA(miRNA)活性的重要调节因子。然而,用于识别miRNA与circRNA相互作用的计算资源大多仅限于已注释的circRNA,或受到高假阳性预测率的影响。为克服这些限制,我们开发了Circr,这是一种用于预测circRNA与miRNA之间关联的计算工具。Circr结合了三种公开可用的算法来预测靶序列上的miRNA结合位点(miRanda、RNAhybrid和TargetScan),并用实验验证的miRNA与RNA相互作用以及源自ChIPseq或CLIPseq数据的AGO蛋白结合位点注释每个鉴定出的miRNA与靶标对。将多种用于识别单个miRNA识别位点的工具与实验数据相结合,能够有效地对不同生物体功能研究中的候选miRNA与circRNA相互作用进行优先级排序。Circr可以使用其内部注释数据库或自定义注释表,以增强在几乎任何物种中对新的和以前未注释的miRNA与circRNA位点的识别。Circr用Python 3.6编写,并根据GNU GPL3.0许可在https://github.com/bicciatolab/Circr上发布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e13/9580875/99d8564d4c68/fbinf-02-852834-g001.jpg

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