The RNA Secondary Structure Analysis Reveals Potential for Emergence of Pathogenic Flaviviruses

Author(s):  
Bibhudutta Mishra ◽  
Raviprasad Aduri
PLoS ONE ◽  
2017 ◽  
Vol 12 (2) ◽  
pp. e0172848 ◽  
Author(s):  
H. C. Yashavantha Rao ◽  
Devaraju Rakshith ◽  
Ballagere Puttaraju Harini ◽  
Doddahosuru Mahadevappa Gurudatt ◽  
Sreedharamurthy Satish

2021 ◽  
Author(s):  
Maxie Dion Schmidt ◽  
Anna Kirkpatrick ◽  
Christine Heitsch

AbstractSummaryWe present a new graphical tool for RNA secondary structure analysis. The central feature is the ability to visually compare/contrast up to three base pairing configurations for a given sequence in a compact, standardized circular arc diagram layout. This is complemented by a built-in CT-style file viewer and radial layout substructure viewer which are directly linked to the arc diagram window via the zoom selection tool. Additional functionality includes the computation of some numerical information, and the ability to export images and data for later use. This tool should be of use to researchers seeking to better understand similarities and differences between structural alternatives for an RNA sequence.Availability and implementationhttps://github.com/gtDMMB/RNAStructViz/wikiAuthor [email protected], [email protected], and [email protected]


2019 ◽  
Author(s):  
Irena Fischer-Hwang ◽  
Zhipeng Lu ◽  
James Zou ◽  
Tsachy Weissman

AbstractNext generation sequencing and biochemical cross-linking methods have been combined into powerful tools to probe RNA secondary structure. One such method, known as PARIS, has been used to produce near base-pair maps of long-range and alternative RNA structures in living cells. However, the procedure for generating these maps typically relies on laborious manual analysis. We developed an automated method for producing RNA secondary structure maps using network analysis techniques. We produced an analysis pipeline, dubbed cross-linked RNA secondary structure analysis using network techniques (CRSSANT), which automates the grouping of gapped RNA sequencing reads produced using the PARIS assay, and tests the validity of secondary structures implied by the groups. We validated the clusters and secondary structures produced by CRSSANT using manually-produced grouping maps and known secondary structures. We implemented CRSSANT in Python using the network analysis package NetworkX and RNA folding software package ViennaRNA. CRSSANT is fast and efficient, and is available as Python source code at https://github.com/ihwang/CRSSANT.


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