<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>70</viewCount><searchCount>0</searchCount></scores><additional><submitter>Chen Y</submitter><funding>Key Program of Guangdong Basic and Applied Basic Research Fund</funding><funding>Shenzhen Science and Technology</funding><funding>Science, Technology and Innovation Commission of Shenzhen Municipality</funding><funding>Shenzhen City and Longgang District for the Warshel Institute for Computational Biology</funding><funding>National Natural Science Foundation of China</funding><funding>Ganghong Young Scholar Development Fund</funding><funding>Guangdong Young Scholar Development Fund</funding><funding>Guangdong Province Basic and Applied Basic Research Fund</funding><pagination>D93-D101</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8728223</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(D1)</volume><pubmed_abstract>Circular RNAs (circRNAs), which are single-stranded RNA molecules that have individually formed into a covalently closed continuous loop, act as sponges of microRNAs to regulate transcription and translation. CircRNAs are important molecules in the field of cancer diagnosis, as growing evidence suggests that they are closely related to pathological cancer features. Therefore, they have high potential for clinical use as novel cancer biomarkers. In this article, we present our updates to CircNet (version 2.0), into which circRNAs from circAtlas and MiOncoCirc, and novel circRNAs from The Cancer Genome Atlas database have been integrated. In total, 2732 samples from 37 types of cancers were integrated into CircNet 2.0 and analyzed using several of the most reliable circRNA detection algorithms. Furthermore, target miRNAs were predicted from the full-length circRNA sequence using three reliable tools (PITA, miRanda and TargetScan). Additionally, 384 897 experimentally verified miRNA-target interactions from miRTarBase were integrated into our database to facilitate the construction of high-quality circRNA-miRNA-gene regulatory networks. These improvements, along with the user-friendly interactive web interface for data presentation, search, and visualization, showcase the updated CircNet database as a powerful, experimentally validated resource, for providing strong data support in the biomedical fields. CircNet 2.0 is currently accessible at https://awi.cuhk.edu.cn/∼CircNet.</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>CircNet 2.0: an updated database for exploring circular RNA regulatory networks in cancers.</pubmed_title><pmcid>PMC8728223</pmcid><funding_grant_id>32070674</funding_grant_id><funding_grant_id>JCYJ20200109150003938</funding_grant_id><funding_grant_id>2021E0005</funding_grant_id><funding_grant_id>2021E007</funding_grant_id><funding_grant_id>JCYJ20190808102405474</funding_grant_id><funding_grant_id>32070659</funding_grant_id><funding_grant_id>2021A1515012447</funding_grant_id><funding_grant_id>2020B1515120069</funding_grant_id><pubmed_authors>Yao L</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Chang TH</pubmed_authors><pubmed_authors>Cui S</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Jhong JH</pubmed_authors><pubmed_authors>Huang HY</pubmed_authors><pubmed_authors>Lee TY</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Wei F</pubmed_authors><pubmed_authors>Wan J</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Luo Y</pubmed_authors><pubmed_authors>Chang J</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors><pubmed_authors>Cai X</pubmed_authors><pubmed_authors>Huang HD</pubmed_authors><view_count>70</view_count></additional><is_claimable>false</is_claimable><name>CircNet 2.0: an updated database for exploring circular RNA regulatory networks in cancers.</name><description>Circular RNAs (circRNAs), which are single-stranded RNA molecules that have individually formed into a covalently closed continuous loop, act as sponges of microRNAs to regulate transcription and translation. CircRNAs are important molecules in the field of cancer diagnosis, as growing evidence suggests that they are closely related to pathological cancer features. Therefore, they have high potential for clinical use as novel cancer biomarkers. In this article, we present our updates to CircNet (version 2.0), into which circRNAs from circAtlas and MiOncoCirc, and novel circRNAs from The Cancer Genome Atlas database have been integrated. In total, 2732 samples from 37 types of cancers were integrated into CircNet 2.0 and analyzed using several of the most reliable circRNA detection algorithms. Furthermore, target miRNAs were predicted from the full-length circRNA sequence using three reliable tools (PITA, miRanda and TargetScan). Additionally, 384 897 experimentally verified miRNA-target interactions from miRTarBase were integrated into our database to facilitate the construction of high-quality circRNA-miRNA-gene regulatory networks. These improvements, along with the user-friendly interactive web interface for data presentation, search, and visualization, showcase the updated CircNet database as a powerful, experimentally validated resource, for providing strong data support in the biomedical fields. CircNet 2.0 is currently accessible at https://awi.cuhk.edu.cn/∼CircNet.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2024-11-15T11:53:48.083Z</modification><creation>2022-02-11T14:46:08.23Z</creation></dates><accession>S-EPMC8728223</accession><cross_references><pubmed>34850139</pubmed><doi>10.1093/nar/gkab1036</doi></cross_references></HashMap>