<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Li C</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To compare the performance of clinical factors, FS-T2WI, DWI, T1WI+C based radiomics and a combined clinic-radiomics model in predicting the type of serous ovarian carcinomas (SOCs).&lt;h4>Methods&lt;/h4>In this retrospective analysis, 138 SOC patients were confirmed by histology. Significant clinical factors (&lt;i>P&lt;/i> &lt; 0.05, and with the area under the curve (AUC) > 0.7) was retained to establish a clinical model. The radiomics model included FS-T2WI, DWI, and T1WI+C, and also, a multisequence model was established. A total of 1,316 radiomics features of each sequence were extracted; the univariate and multivariate logistic regressions, cross-validations were performed to reduce valueless features and then radiomics signatures were developed. Nomogram models using clinical fa</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>816982</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9211758</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Nomograms of Combining MRI Multisequences Radiomics and Clinical Factors for Differentiating High-Grade From Low-Grade Serous Ovarian Carcinoma.</pubmed_title><pmcid>PMC9211758</pmcid><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Dong J</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhu C</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nomograms of Combining MRI Multisequences Radiomics and Clinical Factors for Differentiating High-Grade From Low-Grade Serous Ovarian Carcinoma.</name><description>&lt;h4>Objective&lt;/h4>To compare the performance of clinical factors, FS-T2WI, DWI, T1WI+C based radiomics and a combined clinic-radiomics model in predicting the type of serous ovarian carcinomas (SOCs).&lt;h4>Methods&lt;/h4>In this retrospective analysis, 138 SOC patients were confirmed by histology. Significant clinical factors (&lt;i>P&lt;/i> &lt; 0.05, and with the area under the curve (AUC) > 0.7) was retained to establish a clinical model. The radiomics model included FS-T2WI, DWI, and T1WI+C, and also, a multisequence model was established. A total of 1,316 radiomics features of each sequence were extracted; the univariate and multivariate logistic regressions, cross-validations were performed to reduce valueless features and then radiomics signatures were developed. Nomogram models using clinical fa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-26T23:29:10.861Z</modification><creation>2025-04-06T17:33:28.151Z</creation></dates><accession>S-EPMC9211758</accession><cross_references><pubmed>35747838</pubmed><doi>10.3389/fonc.2022.816982</doi></cross_references></HashMap>