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Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera
In our previous study [1], we have compared the performance of a number of widely used discrimination methods for classifying ovarian cancer using Matrix Assisted Laser Desorption Ionization (MALDI) mass spectrometry data on serum samples obtained from Reflectron mode. Our results demonstrate good p...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2675484/ https://www.ncbi.nlm.nih.gov/pubmed/19458764 |
_version_ | 1782166698427678720 |
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author | Wu, Baolin Abbott, Tom Fishman, David McMurray, Walter Mor, Gil Stone, Kathryn Ward, David Williams, Kenneth Zhao, Hongyu |
author_facet | Wu, Baolin Abbott, Tom Fishman, David McMurray, Walter Mor, Gil Stone, Kathryn Ward, David Williams, Kenneth Zhao, Hongyu |
author_sort | Wu, Baolin |
collection | PubMed |
description | In our previous study [1], we have compared the performance of a number of widely used discrimination methods for classifying ovarian cancer using Matrix Assisted Laser Desorption Ionization (MALDI) mass spectrometry data on serum samples obtained from Reflectron mode. Our results demonstrate good performance with a random forest classifier. In this follow-up study, to improve the molecular classification power of the MALDI platform for ovarian cancer disease, we expanded the mass range of the MS data by adding data acquired in Linear mode and evaluated the resultant decrease in classification error. A general statistical framework is proposed to obtain unbiased classification error estimates and to analyze the effects of sample size and number of selected m/z features on classification errors. We also emphasize the importance of combining biological knowledge and statistical analysis to obtain both biologically and statistically sound results. Our study shows improvement in classification accuracy upon expanding the mass range of the analysis. In order to obtain the best classification accuracies possible, we found that a relatively large training sample size is needed to obviate the sample variations. For the ovarian MS dataset that is the focus of the current study, our results show that approximately 20–40 m/z features are needed to achieve the best classification accuracy from MALDI-MS analysis of sera. Supplementary information can be found at http://bioinformatics.med.yale.edu/proteomics/BioSupp2.html. |
format | Text |
id | pubmed-2675484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-26754842009-05-20 Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera Wu, Baolin Abbott, Tom Fishman, David McMurray, Walter Mor, Gil Stone, Kathryn Ward, David Williams, Kenneth Zhao, Hongyu Cancer Inform Original Research In our previous study [1], we have compared the performance of a number of widely used discrimination methods for classifying ovarian cancer using Matrix Assisted Laser Desorption Ionization (MALDI) mass spectrometry data on serum samples obtained from Reflectron mode. Our results demonstrate good performance with a random forest classifier. In this follow-up study, to improve the molecular classification power of the MALDI platform for ovarian cancer disease, we expanded the mass range of the MS data by adding data acquired in Linear mode and evaluated the resultant decrease in classification error. A general statistical framework is proposed to obtain unbiased classification error estimates and to analyze the effects of sample size and number of selected m/z features on classification errors. We also emphasize the importance of combining biological knowledge and statistical analysis to obtain both biologically and statistically sound results. Our study shows improvement in classification accuracy upon expanding the mass range of the analysis. In order to obtain the best classification accuracies possible, we found that a relatively large training sample size is needed to obviate the sample variations. For the ovarian MS dataset that is the focus of the current study, our results show that approximately 20–40 m/z features are needed to achieve the best classification accuracy from MALDI-MS analysis of sera. Supplementary information can be found at http://bioinformatics.med.yale.edu/proteomics/BioSupp2.html. Libertas Academica 2007-02-17 /pmc/articles/PMC2675484/ /pubmed/19458764 Text en © 2006 The authors. |
spellingShingle | Original Research Wu, Baolin Abbott, Tom Fishman, David McMurray, Walter Mor, Gil Stone, Kathryn Ward, David Williams, Kenneth Zhao, Hongyu Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera |
title | Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera |
title_full | Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera |
title_fullStr | Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera |
title_full_unstemmed | Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera |
title_short | Ovarian Cancer Classification based on Mass Spectrometry Analysis of Sera |
title_sort | ovarian cancer classification based on mass spectrometry analysis of sera |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2675484/ https://www.ncbi.nlm.nih.gov/pubmed/19458764 |
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