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Updated: Jul 1, 2026

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Identification of Circular RNAs using RNA Sequencing
Published on: November 14, 2019
12.7K
BloodCircR: A comprehensive database for human peripheral blood circular RNAs
Shaoxun Yuan1,2, Linwei Li1,2, Xue Bai1,2
1School of Artificial Intelligence and Information Technology, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, China.
Iscience
|November 10, 2025
Summary
We created BloodCircR, a comprehensive database of blood circular RNAs (circRNAs) from human samples across 58 diseases. This resource aids in discovering novel circRNA biomarkers for disease research and potential therapies.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- Circular RNAs (circRNAs) are stable noncoding RNAs with significant biological functions.
- A comprehensive resource for blood-derived circRNAs is currently lacking.
- circRNAs show potential as biomarkers for various diseases.
Purpose of the Study:
- To develop BloodCircR, a centralized database for human blood circRNAs.
- To integrate and analyze a large dataset of circRNAs from diverse disease conditions.
- To provide tools for exploring circRNA expression, function, and interactions.
Main Methods:
- Collected and analyzed 5,430 RNA-sequencing samples from human peripheral blood across 58 diseases.
- Utilized CIRI-full and public datasets for circRNA identification.
- Performed transcript-level annotation, expression analysis, and functional prediction of circRNA-miRNA and circRNA-RBP interactions.
Main Results:
- Identified approximately 2.3 million circRNAs, with over 1.7 million being full-length exonic circRNAs.
- BloodCircR integrates data from a large-scale study, offering extensive circRNA coverage.
- The database provides valuable functional insights into circRNA roles in disease.
Conclusions:
- BloodCircR is a valuable resource for advancing circRNA research in human blood.
- The database facilitates biomarker discovery and understanding of circRNA functions in disease.
- This resource has potential implications for therapeutic strategies involving circRNAs.
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