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Fast accessibility-based prediction of RNA-RNA interactions.

机译:基于快速可访问性的RNA-RNA相互作用预测。

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Currently, the best RNA-RNA interaction prediction tools are based on approaches that consider both the inter- and intramolecular interactions of hybridizing RNAs. While accurate, these methods are too slow and memory-hungry to be employed in genome-wide RNA target scans. Alternative methods neglecting intramolecular structures are fast enough for genome-wide applications, but are too inaccurate to be of much practical use. RESULTS: A new approach for RNA-RNA interaction was developed, with a prediction accuracy that is similar to that of algorithms that explicitly consider intramolecular structures, but running at least three orders of magnitude faster than RNAup. This is achieved by using a combination of precomputed accessibility profiles with an approximate energy model. This approach is implemented in the new version of RNAplex. The software also provides a variant using multiple sequences alignments as input, resulting in a further increase in specificity. AVAILABILITY: RNAplex is available at www.bioinf.uni-leipzig.de/Software/RNAplex.
机译:当前,最佳的RNA-RNA相互作用预测工具基于同时考虑杂交RNA的分子间和分子内相互作用的方法。尽管准确,但这些方法太慢且需要大量内存,无法在全基因组RNA靶标扫描中使用。忽略分子内结构的替代方法对于全基因组应用来说足够快,但是太不精确了,无法实际应用。结果:开发了一种新的RNA-RNA相互作用方法,其预测精度与明确考虑分子内结构的算法相似,但比RNAup的运行速度至少快三个数量级。这是通过将预计算的可访问性配置文件与近似能量模型结合使用来实现的。在新版本的RNAplex中实现了这种方法。该软件还提供了使用多个序列比对作为输入的变体,从而进一步提高了特异性。可用性:RNAplex可从www.bioinf.uni-leipzig.de/Software/RNAplex获得。

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