CompaRNA: a server for continuous benchmarking of automated methods for RNA secondary structure prediction

被引:78
作者
Puton, Tomasz [1 ,2 ]
Kozlowski, Lukasz P. [2 ]
Rother, Kristian M. [1 ,2 ]
Bujnicki, Janusz M. [1 ,2 ]
机构
[1] Adam Mickiewicz Univ, Fac Biol, Inst Mol Biol & Biotechnol, Bioinformat Lab, PL-61614 Poznan, Poland
[2] Int Inst Mol & Cell Biol Warsaw, Lab Bioinformat & Prot Engn, PL-02109 Warsaw, Poland
基金
欧洲研究理事会;
关键词
WEB SERVER; MULTIPLE ALIGNMENT; ACCURATE PREDICTION; INTERNAL LOOPS; PROTEIN; ALGORITHM; PSEUDOKNOTS; COMMON; CLASSIFICATION; SOFTWARE;
D O I
10.1093/nar/gkt101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present a continuous benchmarking approach for the assessment of RNA secondary structure prediction methods implemented in the CompaRNA web server. As of 3 October 2012, the performance of 28 single-sequence and 13 comparative methods has been evaluated on RNA sequences/structures released weekly by the Protein Data Bank. We also provide a static benchmark generated on RNA 2D structures derived from the RNAstrand database. Benchmarks on both data sets offer insight into the relative performance of RNA secondary structure prediction methods on RNAs of different size and with respect to different types of structure. According to our tests, on the average, the most accurate predictions obtained by a comparative approach are generated by CentroidAlifold, MXScarna, RNAalifold and TurboFold. On the average, the most accurate predictions obtained by single-sequence analyses are generated by CentroidFold, ContextFold and IPknot. The best comparative methods typically outperform the best single-sequence methods if an alignment of homologous RNA sequences is available. This article presents the results of our benchmarks as of 3 October 2012, whereas the rankings presented online are continuously updated. We will gladly include new prediction methods and new measures of accuracy in the new editions of CompaRNA benchmarks.
引用
收藏
页码:4307 / 4323
页数:17
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