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Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”

Proteomic patterns derived from mass spectrometry have recently been put forth as potential biomarkers for the early diagnosis of cancer. This approach has generated much excitement, particularly as initial results reported on SELDI profiling of serum suggested that near perfect sensitivity and spec...

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Detalles Bibliográficos
Autores principales: Baggerly, Keith A., Coombes, Kevin R., Morris, Jeffrey S.
Formato: Texto
Lenguaje:English
Publicado: Libertas Academica 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657654/
https://www.ncbi.nlm.nih.gov/pubmed/19305627
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author Baggerly, Keith A.
Coombes, Kevin R.
Morris, Jeffrey S.
author_facet Baggerly, Keith A.
Coombes, Kevin R.
Morris, Jeffrey S.
author_sort Baggerly, Keith A.
collection PubMed
description Proteomic patterns derived from mass spectrometry have recently been put forth as potential biomarkers for the early diagnosis of cancer. This approach has generated much excitement, particularly as initial results reported on SELDI profiling of serum suggested that near perfect sensitivity and specificity could be achieved in diagnosing ovarian cancer. However, more recent reports have suggested that much of the observed structure could be due to the presence of experimental bias. A rebuttal to the findings of bias, subtitled “Producers and Consumers”, lists several objections. In this paper, we attempt to address these objections. While we continue to find evidence of experimental bias, we emphasize that the problems found are associated with experimental design and processing, and can be avoided in future studies.
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spelling pubmed-26576542009-03-20 Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers” Baggerly, Keith A. Coombes, Kevin R. Morris, Jeffrey S. Cancer Inform Point/Counter-Point Proteomic patterns derived from mass spectrometry have recently been put forth as potential biomarkers for the early diagnosis of cancer. This approach has generated much excitement, particularly as initial results reported on SELDI profiling of serum suggested that near perfect sensitivity and specificity could be achieved in diagnosing ovarian cancer. However, more recent reports have suggested that much of the observed structure could be due to the presence of experimental bias. A rebuttal to the findings of bias, subtitled “Producers and Consumers”, lists several objections. In this paper, we attempt to address these objections. While we continue to find evidence of experimental bias, we emphasize that the problems found are associated with experimental design and processing, and can be avoided in future studies. Libertas Academica 2007-02-26 /pmc/articles/PMC2657654/ /pubmed/19305627 Text en © 2005 The authors. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Point/Counter-Point
Baggerly, Keith A.
Coombes, Kevin R.
Morris, Jeffrey S.
Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”
title Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”
title_full Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”
title_fullStr Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”
title_full_unstemmed Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”
title_short Bias, Randomization, and Ovarian Proteomic Data: A Reply to “Producers and Consumers”
title_sort bias, randomization, and ovarian proteomic data: a reply to “producers and consumers”
topic Point/Counter-Point
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657654/
https://www.ncbi.nlm.nih.gov/pubmed/19305627
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