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RNA Secondary Structure Prediction Using High-throughput SHAPE
Published on: May 31, 2013
The RNAsnp web server: predicting SNP effects on local RNA secondary structure
Radhakrishnan Sabarinathan1, Hakim Tafer, Stefan E Seemann
1Center for non-coding RNA in Technology and Health, University of Copenhagen, Grønnegårdsvej 3, 1870 Frederiksberg C, Denmark.
Nucleic Acids Research
|May 1, 2013
Summary
Single nucleotide polymorphisms (SNPs) can alter RNA structure and function, potentially causing disease. RNAsnp predicts these SNP effects on RNA secondary structure, providing valuable insights into genetic variations and their phenotypic consequences.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- RNA secondary structure is crucial for the function of non-coding RNAs and mRNA regulatory elements.
- Single nucleotide polymorphisms (SNPs) and mutations can disrupt RNA structure, leading to altered molecular function and phenotypic effects.
Purpose of the Study:
- To present a web service for predicting the impact of SNPs on local RNA secondary structure using the RNAsnp method.
- To provide a user-friendly interface with graphical output and integration with the UCSC Genome Browser for genomic sequence analysis.
Main Methods:
- Utilizes RNA folding algorithms from the Vienna RNA package.
- Employs empirical P-values derived from pre-computed tables for efficient SNP effect quantification.
- Integrates with a local UCSC Genome Browser mirror for sequence selection and result visualization.
Main Results:
- The RNAsnp web server offers an efficient prediction of SNP effects on RNA secondary structure.
- Provides graphical representations of predicted structural changes.
- Facilitates direct visualization of results within the UCSC Genome Browser.
Conclusions:
- The RNAsnp web server is a valuable tool for researchers studying the functional consequences of genetic variations on RNA structure.
- Enables efficient prediction and visualization of SNP-induced RNA structure alterations.
- Supports the investigation of genotype-phenotype relationships at the molecular level.
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