scholarly journals iFoldRNA: three-dimensional RNA structure prediction and folding

2008 ◽  
Vol 24 (17) ◽  
pp. 1951-1952 ◽  
Author(s):  
Shantanu Sharma ◽  
Feng Ding ◽  
Nikolay V. Dokholyan
Author(s):  
Grace Meng ◽  
Marva Tariq ◽  
Swati Jain ◽  
Shereef Elmetwaly ◽  
Tamar Schlick

Abstract Summary We launch a webserver for RNA structure prediction and design corresponding to tools developed using our RNA-As-Graphs (RAG) approach. RAG uses coarse-grained tree graphs to represent RNA secondary structure, allowing the application of graph theory to analyze and advance RNA structure discovery. Our webserver consists of three modules: (a) RAG Sampler: samples tree graph topologies from an RNA secondary structure to predict corresponding tertiary topologies, (b) RAG Builder: builds three-dimensional atomic models from candidate graphs generated by RAG Sampler, and (c) RAG Designer: designs sequences that fold onto novel RNA motifs (described by tree graph topologies). Results analyses are performed for further assessment/selection. The Results page provides links to download results and indicates possible errors encountered. RAG-Web offers a user-friendly interface to utilize our RAG software suite to predict and design RNA structures and sequences. Availability and implementation The webserver is freely available online at: http://www.biomath.nyu.edu/ragtop/. Supplementary information Supplementary data are available at Bioinformatics online.


Author(s):  
Riccardo Delli Ponti ◽  
Alexandros Armaos ◽  
Stefanie Marti ◽  
Gian Gaetano Tartaglia

2018 ◽  
Author(s):  
Riccardo Delli ponti ◽  
Alexandros Armaos ◽  
Stefanie Marti ◽  
Gian Gaetano Tartaglia

AbstractTo compare the secondary structures of RNA molecules we developed the CROSSalign method. CROSSalign is based on the combination of the Computational Recognition Of Secondary Structure (CROSS) algorithm to predict the RNA secondary structure at single-nucleotide resolution using sequence information, and the Dynamic Time Warping (DTW) method to align profiles of different lengths. We applied CROSSalign to investigate the structural conservation of long non-coding RNAs such as XIST and HOTAIR as well as ssRNA viruses including HIV. In a pool of sequences with the same secondary structure CROSSalign accurately recognizes repeat A of XIST and domain D2 of HOTAIR and outperforms other methods based on covariance modelling. CROSSalign can be applied to perform pair-wise comparisons and is able to find homologues between thousands of matches identifying the exact regions of similarity between profiles of different lengths. The algorithm is freely available at the webpage http://service.tartaglialab.com//new_submission/CROSSalign.


2013 ◽  
Vol 325-326 ◽  
pp. 1551-1554
Author(s):  
Yi Qi

In this paper, we present an improved BPSO to predict RNA secondary structure to improve the performance with two new strategies. First one is to reduce the searching space of PSO through super stem set construction. Second is to modify the general BPSO updating process to settle stem permutation and combination problems. The experimental results show that the new method is effective for RNA structure prediction in terms of sensitivity and specificity by different sequence datasets including simple pseudoknot.


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