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PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION

Classification of brain tumors using methylation profiling is an important diagnostic advance, reducing subjectivity and improving interpretability of clinical outcome data. Despite the recognized value of methylation profiling in the clinical laboratory, the performance characteristics of different...

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Autores principales: Orr, Brent, Breuer, Alex, Lin, Tong, Tran, Quynh, Suh, Edward, Pounds, Stanley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715456/
http://dx.doi.org/10.1093/neuonc/noaa222.657
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author Orr, Brent
Breuer, Alex
Lin, Tong
Tran, Quynh
Suh, Edward
Pounds, Stanley
author_facet Orr, Brent
Breuer, Alex
Lin, Tong
Tran, Quynh
Suh, Edward
Pounds, Stanley
author_sort Orr, Brent
collection PubMed
description Classification of brain tumors using methylation profiling is an important diagnostic advance, reducing subjectivity and improving interpretability of clinical outcome data. Despite the recognized value of methylation profiling in the clinical laboratory, the performance characteristics of different supervised classification models has not been directly compared. We developed 3 methods using methylation profiles to classify CNS tumors: an exact bootstrap k-nearest neighbor (kNN), a multi-layer perceptron neural net (NN), and a random forest classifier (RF). We trained these methods on the publicly available CNS tumor reference cohort (GSE90496) with 2,801 profiles and 91 classes. We evaluated the performance of these methods by leave-out-25% cross-validation. The relative performance of these methods were evaluated in terms of accuracy, precision, and recall for class or class family. The kNN, RF, and NN classifier had an estimate error rate of 10.74%, 4.01%, and 1.89%, respectively for class prediction and an error rate for family prediction of 5.97%, 0.90%, and 0.6%, respectively. At perfect recall for class assignment, the RF and kNN had a precision of 0.96 and 0.89 while the NN reached 0.98. For family assignment, the precision for the three classifiers was almost 1.0 with recall of nearly 0.8. At the recall rate of 1.0, the precision dropped to 0.94, 0.991 and 0.994 for kNN, RF, and NN, respectively. Overall, the NN showed improved performance metrics compared to the kNN and RF in CNS tumor classification for both class and class family assignment.
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spelling pubmed-77154562020-12-09 PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION Orr, Brent Breuer, Alex Lin, Tong Tran, Quynh Suh, Edward Pounds, Stanley Neuro Oncol Pathology and Molecular Diagnosis Classification of brain tumors using methylation profiling is an important diagnostic advance, reducing subjectivity and improving interpretability of clinical outcome data. Despite the recognized value of methylation profiling in the clinical laboratory, the performance characteristics of different supervised classification models has not been directly compared. We developed 3 methods using methylation profiles to classify CNS tumors: an exact bootstrap k-nearest neighbor (kNN), a multi-layer perceptron neural net (NN), and a random forest classifier (RF). We trained these methods on the publicly available CNS tumor reference cohort (GSE90496) with 2,801 profiles and 91 classes. We evaluated the performance of these methods by leave-out-25% cross-validation. The relative performance of these methods were evaluated in terms of accuracy, precision, and recall for class or class family. The kNN, RF, and NN classifier had an estimate error rate of 10.74%, 4.01%, and 1.89%, respectively for class prediction and an error rate for family prediction of 5.97%, 0.90%, and 0.6%, respectively. At perfect recall for class assignment, the RF and kNN had a precision of 0.96 and 0.89 while the NN reached 0.98. For family assignment, the precision for the three classifiers was almost 1.0 with recall of nearly 0.8. At the recall rate of 1.0, the precision dropped to 0.94, 0.991 and 0.994 for kNN, RF, and NN, respectively. Overall, the NN showed improved performance metrics compared to the kNN and RF in CNS tumor classification for both class and class family assignment. Oxford University Press 2020-12-04 /pmc/articles/PMC7715456/ http://dx.doi.org/10.1093/neuonc/noaa222.657 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Pathology and Molecular Diagnosis
Orr, Brent
Breuer, Alex
Lin, Tong
Tran, Quynh
Suh, Edward
Pounds, Stanley
PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION
title PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION
title_full PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION
title_fullStr PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION
title_full_unstemmed PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION
title_short PATH-22. COMPARISON OF SUPERVISED CLASSIFICATION METHODS FOR CENTRAL NERVOUS SYSTEM TUMORS BASED ON DNA-METHYLATION
title_sort path-22. comparison of supervised classification methods for central nervous system tumors based on dna-methylation
topic Pathology and Molecular Diagnosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715456/
http://dx.doi.org/10.1093/neuonc/noaa222.657
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