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RNA折叠的快速近似动力学

Fast, approximate kinetics of RNA folding.

作者信息

Senter Evan, Clote Peter

机构信息

Department of Biology, Boston College , Chestnut Hill, Massachusetts.

出版信息

J Comput Biol. 2015 Feb;22(2):124-44. doi: 10.1089/cmb.2014.0193.

Abstract

In this article, we introduce the software suite Hermes, which provides fast, novel algorithms for RNA secondary structure kinetics. Using the fast Fourier transform to efficiently compute the Boltzmann probability that a secondary structure S of a given RNA sequence has base pair distance x (resp. y) from reference structure A (resp. B), Hermes computes the exact kinetics of folding from A to B in this coarse-grained model. In particular, Hermes computes the mean first passage time from the transition probability matrix by using matrix inversion, and also computes the equilibrium time from the rate matrix by using spectral decomposition. Due to the model granularity and the speed of Hermes, it is capable of determining secondary structure refolding kinetics for large RNA sequences, beyond the range of other methods. Comparative benchmarking of Hermes with other methods indicates that Hermes provides refolding kinetics of accuracy suitable for use in the computational design of RNA, an important area of synthetic biology. Source code and documentation for Hermes are available.

摘要

在本文中,我们介绍了软件套件Hermes,它为RNA二级结构动力学提供了快速、新颖的算法。通过使用快速傅里叶变换来高效计算给定RNA序列的二级结构S与参考结构A(或B)的碱基对距离为x(或y)时的玻尔兹曼概率,Hermes在这个粗粒度模型中计算从A到B的精确折叠动力学。具体而言,Hermes通过矩阵求逆从转移概率矩阵计算平均首次通过时间,并通过谱分解从速率矩阵计算平衡时间。由于模型粒度和Hermes的速度,它能够确定大型RNA序列的二级结构重折叠动力学,这超出了其他方法的范围。Hermes与其他方法的比较基准测试表明,Hermes提供的重折叠动力学精度适用于RNA的计算设计,这是合成生物学的一个重要领域。Hermes的源代码和文档均可获取。

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