<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li Z</submitter><funding>XJTLU Key Program Special Fund</funding><funding>National Natural Science Foundation of China</funding><pagination>13493</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9655583</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(21)</volume><pubmed_abstract>One of the most abundant non-canonical bases widely occurring on various RNA molecules is 5-methyluridine (m5U). Recent studies have revealed its influences on the development of breast cancer, systemic lupus erythematosus, and the regulation of stress responses. The accurate identification of m&lt;sup>5&lt;/sup>U sites is crucial for understanding their biological functions. We propose RNADSN, the first transfer learning deep neural network that learns common features between tRNA m&lt;sup>5&lt;/sup>U and mRNA m&lt;sup>5&lt;/sup>U to enhance the prediction of mRNA m&lt;sup>5&lt;/sup>U. Without seeing the experimentally detected mRNA m&lt;sup>5&lt;/sup>U sites, RNADSN has already outperformed the state-of-the-art method, m5UPred. Using mRNA m&lt;sup>5&lt;/sup>U classification as an additional layer of supervision, our model </pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>RNADSN: Transfer-Learning 5-Methyluridine (m&lt;sup>5&lt;/sup>U) Modification on mRNAs from Common Features of tRNA.</pubmed_title><pmcid>PMC9655583</pmcid><funding_grant_id>KSF-P-02</funding_grant_id><funding_grant_id>32100519</funding_grant_id><funding_grant_id>KSF-E-51</funding_grant_id><funding_grant_id>31671373</funding_grant_id><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Huang D</pubmed_authors><pubmed_authors>Song B</pubmed_authors><pubmed_authors>Meng J</pubmed_authors><pubmed_authors>Mao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNADSN: Transfer-Learning 5-Methyluridine (m&lt;sup>5&lt;/sup>U) Modification on mRNAs from Common Features of tRNA.</name><description>One of the most abundant non-canonical bases widely occurring on various RNA molecules is 5-methyluridine (m5U). Recent studies have revealed its influences on the development of breast cancer, systemic lupus erythematosus, and the regulation of stress responses. The accurate identification of m&lt;sup>5&lt;/sup>U sites is crucial for understanding their biological functions. We propose RNADSN, the first transfer learning deep neural network that learns common features between tRNA m&lt;sup>5&lt;/sup>U and mRNA m&lt;sup>5&lt;/sup>U to enhance the prediction of mRNA m&lt;sup>5&lt;/sup>U. Without seeing the experimentally detected mRNA m&lt;sup>5&lt;/sup>U sites, RNADSN has already outperformed the state-of-the-art method, m5UPred. Using mRNA m&lt;sup>5&lt;/sup>U classification as an additional layer of supervision, our model </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T13:30:21.509Z</modification><creation>2024-12-04T03:13:00.53Z</creation></dates><accession>S-EPMC9655583</accession><cross_references><pubmed>36362279</pubmed><doi>10.3390/ijms232113493</doi></cross_references></HashMap>