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CPEM: Accurate cancer type classification based on somatic alterations using an ensemble of a random forest and a deep neural network.
Lee, Kanggeun; Jeong, Hyoung-Oh; Lee, Semin; Jeong, Won-Ki.
Afiliación
  • Lee K; School of Electrical and Computer Engineering, UNIST, Ulsan, Republic of Korea.
  • Jeong HO; Department of Biomedical Engineering, School of Life Sciences, UNIST, Ulsan, Republic of Korea.
  • Lee S; Department of Biomedical Engineering, School of Life Sciences, UNIST, Ulsan, Republic of Korea. seminlee@unist.ac.kr.
  • Jeong WK; School of Electrical and Computer Engineering, UNIST, Ulsan, Republic of Korea. wkjeong@unist.ac.kr.
Sci Rep ; 9(1): 16927, 2019 11 15.
Article en En | MEDLINE | ID: mdl-31729414
With recent advances in DNA sequencing technologies, fast acquisition of large-scale genomic data has become commonplace. For cancer studies, in particular, there is an increasing need for the classification of cancer type based on somatic alterations detected from sequencing analyses. However, the ever-increasing size and complexity of the data make the classification task extremely challenging. In this study, we evaluate the contributions of various input features, such as mutation profiles, mutation rates, mutation spectra and signatures, and somatic copy number alterations that can be derived from genomic data, and further utilize them for accurate cancer type classification. We introduce a novel ensemble of machine learning classifiers, called CPEM (Cancer Predictor using an Ensemble Model), which is tested on 7,002 samples representing over 31 different cancer types collected from The Cancer Genome Atlas (TCGA) database. We first systematically examined the impact of the input features. Features known to be associated with specific cancers had relatively high importance in our initial prediction model. We further investigated various machine learning classifiers and feature selection methods to derive the ensemble-based cancer type prediction model achieving up to 84% classification accuracy in the nested 10-fold cross-validation. Finally, we narrowed down the target cancers to the six most common types and achieved up to 94% accuracy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Variación Genética / Pruebas Genéticas / Redes Neurales de la Computación / Aprendizaje Automático / Neoplasias Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Variación Genética / Pruebas Genéticas / Redes Neurales de la Computación / Aprendizaje Automático / Neoplasias Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2019 Tipo del documento: Article
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