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circVAR database: genome-wide archive of genetic variants for human circular RNAs
Journal article   Open access   Peer reviewed

circVAR database: genome-wide archive of genetic variants for human circular RNAs

Min Zhao and Hong Qu
BMC Genomics, Vol.21, pp.1-8
2020
PMCID: PMC7599103
PMID: 33121433
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circVAR database_ genome-wide archive of genetic variants for human circular RNAs2.28 MBDownloadView
Published Version Open Access CC BY V4.0
url
https://doi.org/10.1186/s12864-020-07172-yView
Published Version

Abstract

Circular RNA Bioinformatics database Genetic variant
Background Circular RNAs (circRNAs) play important roles in regulating gene expression through binding miRNAs and RNA binding proteins. Genetic variation of circRNAs may affect complex traits/diseases by changing their binding efficiency to target miRNAs and proteins. There is a growing demand for investigations of the functions of genetic changes using large-scale experimental evidence. However, there is no online genetic resource for circRNA genes. Results We performed extensive genetic annotation of 295,526 circRNAs integrated from circBase, circNet and circRNAdb. All pre-computed genetic variants were presented at our online resource, circVAR, with data browsing and search functionality. We explored the chromosome-based distribution of circRNAs and their associated variants. We found that, based on mapping to the 1000 Genomes and ClinVAR databases, chromosome 17 has a relatively large number of circRNAs and associated common and health-related genetic variants. Following the annotation of genome wide association studies (GWAS)-based circRNA variants, we found many non-coding variants within circRNAs, suggesting novel mechanisms for common diseases reported from GWAS studies. For cancer-based somatic variants, we found that chromosome 7 has many highly complex mutations that have been overlooked in previous research. Conclusion We used the circVAR database to collect SNPs and small insertions and deletions (INDELs) in putative circRNA regions and to identify their potential phenotypic information. To provide a reusable resource for the circRNA research community, we have published all the pre-computed genetic data concerning circRNAs and associated genes together with data query and browsing functions at http://soft.bioinfo-minzhao.org/circvar.

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