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A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
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RADAR: a rigorously annotated database of A-to-I RNA editing
Gokul Ramaswami1, Jin Billy Li
1Department of Genetics, Stanford University, Stanford, CA 94305, USA.
Nucleic Acids Research
|October 29, 2013
Summary
We created RADAR, a database of adenosine to inosine (A-to-I) RNA editing sites in humans, mice, and flies. This resource provides curated annotations and tissue-specific editing levels to understand RNA editing functions.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- High-throughput RNA sequencing has accelerated the discovery of RNA editing sites.
- Adenosine to inosine (A-to-I) RNA editing is a crucial post-transcriptional modification.
- Understanding RNA editing requires comprehensive and well-annotated datasets.
Purpose of the Study:
- To present RADAR, a rigorously annotated database for A-to-I RNA editing.
- To compile A-to-I RNA editing sites across multiple species (human, mouse, fly).
- To provide manually curated annotations and tissue-specific editing levels.
Main Methods:
- Data compilation from high-throughput RNA sequencing studies.
- Manual curation of identified A-to-I RNA editing sites.
- Development of an expandable database with tissue-specific editing information.
Main Results:
- RADAR includes a comprehensive collection of A-to-I RNA editing sites.
- Extensive manual annotations are provided for each editing site.
- Tissue-specific editing levels are included for functional assignment.
Conclusions:
- RADAR serves as a valuable resource for studying A-to-I RNA editing.
- The database facilitates the assignment of biological functions to RNA editing sites.
- RADAR supports research in molecular biology, genomics, and bioinformatics.
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