Martinez H M
Department of Biochemistry and Biophysics, University of California, San Franciso 94143.
Nucleic Acids Res. 1988 Mar 11;16(5):1789-98. doi: 10.1093/nar/16.5.1789.
A multiple approach to the study of RNA secondary structure is described which provides for the independent drawing of structures using base-pairing lists, for the generation of local structures in the form of hairpins, and for the generation of global structures by both Monte Carlo and dynamic programming methodologies. User-adjustable parameters provide for limiting the size of hairpin loops, bulges and inner loops, and constraints can be imposed relative to position-dependent base pairing.
本文描述了一种用于研究RNA二级结构的多重方法,该方法可通过碱基配对列表独立绘制结构,以发夹形式生成局部结构,并通过蒙特卡罗方法和动态规划方法生成全局结构。用户可调整的参数用于限制发夹环、凸起和内环的大小,并且可以针对位置依赖性碱基配对施加约束。