MNDR v3.0: mammal ncRNA–disease repository with increased coverage and annotation

Author:

Ning Lin1,Cui Tianyu2,Zheng Boyang2,Wang Nuo2,Luo Jiaxin2,Yang Beilei2,Du Mengze3,Cheng Jun4,Dou Yiying2,Wang Dong125ORCID

Affiliation:

1. Dermatology Hospital, Southern Medical University, Guangzhou 510091, China

2. Department of Bioinformatics, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China

3. Qingyuan People's Hospital, The Sixth Affiliated Hospital of Guangzhou Medical University, B24 Yinquan South Road, Qingyuan 511518, Guangdong Province, People's Republic of China

4. Affiliated Foshan Maternity & Child Healthcare Hospital, Southern Medical University (Foshan Maternity & Child Healthcare Hospital)

5. Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu 611731, China

Abstract

Abstract Many studies have indicated that non-coding RNA (ncRNA) dysfunction is closely related to numerous diseases. Recently, accumulated ncRNA–disease associations have made related databases insufficient to meet the demands of biomedical research. The constant updating of ncRNA–disease resources has become essential. Here, we have updated the mammal ncRNA–disease repository (MNDR, http://www.rna-society.org/mndr/) to version 3.0, containing more than one million entries, four-fold increment in data compared to the previous version. Experimental and predicted circRNA–disease associations have been integrated, increasing the number of categories of ncRNAs to five, and the number of mammalian species to 11. Moreover, ncRNA–disease related drug annotations and associations, as well as ncRNA subcellular localizations and interactions, were added. In addition, three ncRNA–disease (miRNA/lncRNA/circRNA) prediction tools were provided, and the website was also optimized, making it more practical and user-friendly. In summary, MNDR v3.0 will be a valuable resource for the investigation of disease mechanisms and clinical treatment strategies.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Basic and Applied Basic Research Fund of Guangdong Province

Publisher

Oxford University Press (OUP)

Subject

Genetics

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