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A Semantic Web-based System for Mining Genetic Mutations in Cancer Clinical Trials.
Priya, Sambhawa; Jiang, Guoqian; Dasari, Surendra; Zimmermann, Michael T; Wang, Chen; Heflin, Jeff; Chute, Christopher G.
Afiliação
  • Priya S; Mayo Clinic, Rochester, MN ; Lehigh University, Bethlehem, PA.
  • Jiang G; Mayo Clinic, Rochester, MN.
  • Dasari S; Mayo Clinic, Rochester, MN.
  • Zimmermann MT; Mayo Clinic, Rochester, MN.
  • Wang C; Mayo Clinic, Rochester, MN.
  • Heflin J; Lehigh University, Bethlehem, PA.
  • Chute CG; Mayo Clinic, Rochester, MN.
Article em En | MEDLINE | ID: mdl-26306257
ABSTRACT
Textual eligibility criteria in clinical trial protocols contain important information about potential clinically relevant pharmacogenomic events. Manual curation for harvesting this evidence is intractable as it is error prone and time consuming. In this paper, we develop and evaluate a Semantic Web-based system that captures and manages mutation evidences and related contextual information from cancer clinical trials. The system has 2 main components an NLP-based annotator and a Semantic Web ontology-based annotation manager. We evaluated the performance of the annotator in terms of precision and recall. We demonstrated the usefulness of the system by conducting case studies in retrieving relevant clinical trials using a collection of mutations identified from TCGA Leukemia patients and Atlas of Genetics and Cytogenetics in Oncology and Haematology. In conclusion, our system using Semantic Web technologies provides an effective framework for extraction, annotation, standardization and management of genetic mutations in cancer clinical trials.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article