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Inter-session reproducibility measures for high-throughput data sources

High-throughput biological assays such as micro-arrays and mass spectrometry (MS) have risen as potential clinical tools for disease detection. Multiple potential biomarkers can be rapidly and cheaply evaluated for a large number of patients. Typical research and evaluation studies in these fields h...

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Detalles Bibliográficos
Autores principales: Hauskrecht, Milos, Pelikan, Richard
Formato: Texto
Lenguaje:English
Publicado: American Medical Informatics Association 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041518/
https://www.ncbi.nlm.nih.gov/pubmed/21347125
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author Hauskrecht, Milos
Pelikan, Richard
author_facet Hauskrecht, Milos
Pelikan, Richard
author_sort Hauskrecht, Milos
collection PubMed
description High-throughput biological assays such as micro-arrays and mass spectrometry (MS) have risen as potential clinical tools for disease detection. Multiple potential biomarkers can be rapidly and cheaply evaluated for a large number of patients. Typical research and evaluation studies in these fields have focused primarily on data that were generated from samples in a single data-generation session. However, in the clinical setting, new patients screened by the technology will arrive at different times and data will unavoidably come from multiple data-generation sessions. The understanding and assessment of multi-session effects on data generated by the technology is critical for its application to clinical practice. This paper proposes a methodology for measuring and testing the reproducibility of various aspects of high-throughput data across multiple data-generation sessions. We test and demonstrate the framework on mass-spectrometry data obtained from four different data-generation sessions for the same set of samples.
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spelling pubmed-30415182011-02-23 Inter-session reproducibility measures for high-throughput data sources Hauskrecht, Milos Pelikan, Richard Summit on Translat Bioinforma Articles High-throughput biological assays such as micro-arrays and mass spectrometry (MS) have risen as potential clinical tools for disease detection. Multiple potential biomarkers can be rapidly and cheaply evaluated for a large number of patients. Typical research and evaluation studies in these fields have focused primarily on data that were generated from samples in a single data-generation session. However, in the clinical setting, new patients screened by the technology will arrive at different times and data will unavoidably come from multiple data-generation sessions. The understanding and assessment of multi-session effects on data generated by the technology is critical for its application to clinical practice. This paper proposes a methodology for measuring and testing the reproducibility of various aspects of high-throughput data across multiple data-generation sessions. We test and demonstrate the framework on mass-spectrometry data obtained from four different data-generation sessions for the same set of samples. American Medical Informatics Association 2008-03-01 /pmc/articles/PMC3041518/ /pubmed/21347125 Text en ©2008 AMIA - All rights reserved. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose
spellingShingle Articles
Hauskrecht, Milos
Pelikan, Richard
Inter-session reproducibility measures for high-throughput data sources
title Inter-session reproducibility measures for high-throughput data sources
title_full Inter-session reproducibility measures for high-throughput data sources
title_fullStr Inter-session reproducibility measures for high-throughput data sources
title_full_unstemmed Inter-session reproducibility measures for high-throughput data sources
title_short Inter-session reproducibility measures for high-throughput data sources
title_sort inter-session reproducibility measures for high-throughput data sources
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041518/
https://www.ncbi.nlm.nih.gov/pubmed/21347125
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