Ding Ye, Chan Chi Yu, Lawrence Charles E
Bioinformatics Center, Wadsworth Center, New York State Department of Health, 150 New Scotland Avenue, Albany, NY 12208, USA.
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W135-41. doi: 10.1093/nar/gkh449.
The Sfold web server provides user-friendly access to Sfold, a recently developed nucleic acid folding software package, via the World Wide Web (WWW). The software is based on a new statistical sampling paradigm for the prediction of RNA secondary structure. One of the main objectives of this software is to offer computational tools for the rational design of RNA-targeting nucleic acids, which include small interfering RNAs (siRNAs), antisense oligonucleotides and trans-cleaving ribozymes for gene knock-down studies. The methodology for siRNA design is based on a combination of RNA target accessibility prediction, siRNA duplex thermodynamic properties and empirical design rules. Our approach to target accessibility evaluation is an original extension of the underlying RNA folding algorithm to account for the likely existence of a population of structures for the target mRNA. In addition to the application modules Sirna, Soligo and Sribo for siRNAs, antisense oligos and ribozymes, respectively, the module Srna offers comprehensive features for statistical representation of sampled structures. Detailed output in both graphical and text formats is available for all modules. The Sfold server is available at http://sfold.wadsworth.org and http://www.bioinfo.rpi.edu/applications/sfold.
Sfold网络服务器通过万维网(WWW)为用户提供对Sfold(一个最近开发的核酸折叠软件包)的便捷访问。该软件基于一种用于预测RNA二级结构的新统计抽样范式。该软件的主要目标之一是提供用于合理设计靶向RNA的核酸的计算工具,这些核酸包括用于基因敲除研究的小干扰RNA(siRNA)、反义寡核苷酸和反式切割核酶。siRNA设计方法基于RNA靶标可及性预测、siRNA双链体热力学性质和经验设计规则的组合。我们评估靶标可及性的方法是对基础RNA折叠算法的一种原创扩展,以考虑靶标mRNA可能存在的多种结构。除了分别用于siRNA、反义寡核苷酸和核酶的应用模块Sirna、Soligo和Sribo之外,模块Srna还提供了用于抽样结构统计表示的综合功能。所有模块都提供图形和文本格式的详细输出。Sfold服务器可在http://sfold.wadsworth.org和http://www.bioinfo.rpi.edu/applications/sfold上获取。