4.8 Article

circMine: a comprehensive database to integrate, analyze and visualize human disease-related circRNA transcriptome

期刊

NUCLEIC ACIDS RESEARCH
卷 50, 期 D1, 页码 D83-D92

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkab809

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资金

  1. National Key R&D Program of China [2018YFB0204403]
  2. Guangdong Basic and Applied Basic Research Foundation, China [2020A1515110528]
  3. National Natural Science Foundation of China [32100513]
  4. China Postdoctoral Science Foundation [2021M693302]
  5. Strategic Priority CAS Project [XDB38000000]
  6. Shenzhen Basic Research Fund [RCYX2020071411473419, KQTD20200820113106007, JSGG20201102163800001]
  7. Sanming Project of Medicine (Shenzhen) [SZSM201911016]

向作者/读者索取更多资源

The study introduces circMine as a tool to assist researchers in investigating circRNA transcriptome data. CircMine provides a large amount of data and online analytical functions to assess the clinical and biological significance of circRNA, and additional tools to systematically discover circRNA-miRNA interactions and circRNA translatability.
Many circRNA transcriptome data were deposited in public resources, but these data show great heterogeneity. Researchers without bioinformatics skills have difficulty in investigating these invaluable data or their own data. Here, we specifically designed circMine (http://hpcc.siat.ac.cn/circmine and http://www.biomedical-web.com/circmine/) that provides 1 821 448 entries formed by 136 871 circRNAs, 87 diseases and 120 circRNA transcriptome datasets of 1107 samples across 31 human body sites. circMine further provides 13 online analytical functions to comprehensively investigate these datasets to evaluate the clinical and biological significance of circRNA. To improve the data applicability, each dataset was standardized and annotated with relevant clinical information. All of the 13 analytic functions allow users to group samples based on their clinical data and assign different parameters for different analyses, and enable them to perform these analyses using their own circRNA transcriptomes. Moreover, three additional tools were developed in circMine to systematically discover the circRNA-miRNA interaction and circRNA translatability. For example, we systematically discovered five potential translatable circRNAs associated with prostate cancer progression using circMine. In summary, circMine provides user-friendly web interfaces to browse, search, analyze and download data freely, and submit new data for further integration, and it can be an important resource to discover significant circRNA in different diseases.

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