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IRIS:A method for predicting in vivo RNA secondary structures using PARIS data

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摘要 Background:RNA secondary structures play a pivotal role in posttranscriptional regulation and the functions of non-coding RNAs,yet in vivo RNA secondary structures remain enigmatic.PARIS(Psoralen Analysis of RNA Interactions and Structures)is a recently developed high-throughput sequencing-based approach that enables direct capture of RNA duplex structures in vivo.However,the existence of incompatible,fuzzy pairing information obstructs the integration of PARIS data with the existing tools for reconstructing RNA secondary structure models at the single-base resolution.Methods:We introduce IRIS,a method for predicting RNA secondary structure ensembles based on PARIS data.IRIS generates a large set of candidate RNA secondary structure models under the guidance of redistributed PARIS reads and then uses a Bayesian model to identify the optimal ensemble,according to both thermodynamic principles and PARIS data.Results:The predicted RNA structure ensembles by IRIS have been verified based on evolutionary conservation information and consistency with other experimental RNA structural data.HIS is implemented in Python and freely available at http://iris.zhanglab.net.Conclusion:IRIS capitalizes upon PARIS data to improve the prediction of in vivo RNA secondary structure ensembles.We expect that IRIS will enhance the application of the PARIS technology and shed more insight on in vivo RNA secondary structures.
出处 《Quantitative Biology》 CAS CSCD 2020年第4期369-381,共13页 定量生物学(英文版)
基金 the Chinese Ministry of Science and Technology(No.2018YFA0107603 to Q.C.Z.) the National Natural Science Foundation ofChina(Nos.91740204 and 31761163007 to Q.C.Z.) the National Natural Science Foundation of China(No.61772197 to T.J.) the National Key Research and Development Program of China(No.2018YFC0910404 to T.J.)。
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