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A transcriptome-based classifier to determine molecular subtypes in medulloblastoma.
Rathi, Komal S; Arif, Sherjeel; Koptyra, Mateusz; Naqvi, Ammar S; Taylor, Deanne M; Storm, Phillip B; Resnick, Adam C; Rokita, Jo Lynne; Raman, Pichai.
Afiliación
  • Rathi KS; Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Arif S; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Koptyra M; Division of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Naqvi AS; Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Taylor DM; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Storm PB; Division of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Resnick AC; Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Rokita JL; Division of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
  • Raman P; Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
PLoS Comput Biol ; 16(10): e1008263, 2020 10.
Article en En | MEDLINE | ID: mdl-33119584
ABSTRACT
Medulloblastoma is a highly heterogeneous pediatric brain tumor with five molecular subtypes, Sonic Hedgehog TP53-mutant, Sonic Hedgehog TP53-wildtype, WNT, Group 3, and Group 4, defined by the World Health Organization. The current mechanism for classification into these molecular subtypes is through the use of immunostaining, methylation, and/or genetics. We surveyed the literature and identified a number of RNA-Seq and microarray datasets in order to develop, train, test, and validate a robust classifier to identify medulloblastoma molecular subtypes through the use of transcriptomic profiling data. We have developed a GPL-3 licensed R package and a Shiny Application to enable users to quickly and robustly classify medulloblastoma samples using transcriptomic data. The classifier utilizes a large composite microarray dataset (15 individual datasets), an individual microarray study, and an RNA-Seq dataset, using gene ratios instead of gene expression measures as features for the model. Discriminating features were identified using the limma R package and samples were classified using an unweighted mean of normalized scores. We utilized two training datasets and applied the classifier in 15 separate datasets. We observed a minimum accuracy of 85.71% in the smallest dataset and a maximum of 100% accuracy in four datasets with an overall median accuracy of 97.8% across the 15 datasets, with the majority of misclassification occurring between the heterogeneous Group 3 and Group 4 subtypes. We anticipate this medulloblastoma transcriptomic subtype classifier will be broadly applicable to the cancer research and clinical communities.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_cobertura_universal Asunto principal: Programas Informáticos / Neoplasias Cerebelosas / Perfilación de la Expresión Génica / Transcriptoma / Meduloblastoma Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_cobertura_universal Asunto principal: Programas Informáticos / Neoplasias Cerebelosas / Perfilación de la Expresión Génica / Transcriptoma / Meduloblastoma Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
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