<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dou L</submitter><funding>Natural Science Foundation of China</funding><funding>Scientific Research Foundation</funding><funding>Natural Science Foundation of Guangdong Province</funding><funding>Post-doctoral Foundation Project of Shenzhen Polytechnic</funding><pagination>2236-2246</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8632091</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(12)</volume><pubmed_abstract>As one of the common post-transcriptional modifications in tRNAs, dihydrouridine (D) has prominent effects on regulating the flexibility of tRNA as well as cancerous diseases. Facing with the expensive and time-consuming sequencing techniques to detect D modification, precise computational tools can largely promote the progress of molecular mechanisms and medical developments. We proposed a novel predictor, called iRNAD_XGBoost, to identify potential D sites using multiple RNA sequence representations. In this method, by considering the imbalance problem using hybrid sampling method SMOTEEEN, the XGBoost-selected top 30 features are applied to construct model. The optimized model showed high &lt;i>Sn&lt;/i> and &lt;i>Sp&lt;/i> values of 97.13% and 97.38% over jackknife test, respectively. For the inde</pubmed_abstract><journal>RNA biology</journal><pubmed_title>Accurate identification of RNA D modification using multiple features.</pubmed_title><pmcid>PMC8632091</pmcid><funding_grant_id>2018A0303130084</funding_grant_id><funding_grant_id>61902259</funding_grant_id><funding_grant_id>6020330003K</funding_grant_id><funding_grant_id>JCYJ20170818100431895</funding_grant_id><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>Dou L</pubmed_authors><pubmed_authors>Han K</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Accurate identification of RNA D modification using multiple features.</name><description>As one of the common post-transcriptional modifications in tRNAs, dihydrouridine (D) has prominent effects on regulating the flexibility of tRNA as well as cancerous diseases. Facing with the expensive and time-consuming sequencing techniques to detect D modification, precise computational tools can largely promote the progress of molecular mechanisms and medical developments. We proposed a novel predictor, called iRNAD_XGBoost, to identify potential D sites using multiple RNA sequence representations. In this method, by considering the imbalance problem using hybrid sampling method SMOTEEEN, the XGBoost-selected top 30 features are applied to construct model. The optimized model showed high &lt;i>Sn&lt;/i> and &lt;i>Sp&lt;/i> values of 97.13% and 97.38% over jackknife test, respectively. For the inde</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-06-01T02:32:37.077Z</modification><creation>2025-06-01T02:32:37.077Z</creation></dates><accession>S-EPMC8632091</accession><cross_references><pubmed>33729104</pubmed><doi>10.1080/15476286.2021.1898160</doi></cross_references></HashMap>