REIA
REIA catalogs and analyzes adenosine-to-inosine (A-to-I) RNA editing sites and integrates multi-omic data to investigate their roles in human cancers.
Key Features:
- Extensive Database: Curates 8,447,588 A-to-I RNA editing sites (RESs) from 9,895 patients across 34 cancer types with primary sources including TCGA and GEO.
- Multi-Omic Integration: Integrates 13 distinct types of multi-omic data to enable cross-layer analyses of RNA editing in cancer.
- Site-specific and Quantitative Analyses: Provides site-specific querying and annotation, quantification of editing levels, and profiling of cancer-specific edits.
- Comparative and Proteogenomic Analysis: Performs comparative analyses of multi-omic features between edited and non-edited groups and identifies novel peptides, reporting 658 mass spectrometry-supported peptides not previously documented.
Scientific Applications:
- Functional Studies: Investigating the functional implications of A-to-I RNA editing in cancer development and progression.
- Multi-Omic Correlation: Correlating RNA editing status with genomic, transcriptomic, and proteomic alterations across cancer types.
- Biomarker and Peptide Discovery: Identifying mass spectrometry-supported novel peptides and potential biomarkers or therapeutic targets arising from RNA editing events.
Methodology:
Integrates A-to-I RNA editing calls curated from TCGA and GEO (8,447,588 RESs from 9,895 patients across 34 cancers) with 13 types of multi-omic data, quantifies editing levels, profiles cancer-specific edits, conducts comparative analyses between edited and non-edited groups, and identifies peptides supported by mass spectrometry.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Mac, Linux, Windows
- Added:
- 7/25/2022
- Last Updated:
- 7/25/2022
Operations
Publications
Zhu H, Huang L, Liu S, Dai Z, Songyang Z, Weng Z, Xiong Y. REIA: A database for cancer A-to-I RNA editing with interactive analysis. International Journal of Biological Sciences. 2022;18(6):2472-2483. doi:10.7150/ijbs.69458. PMID:35414795. PMCID:PMC8990463.