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Comparison of pre-processing methods for multiplex bead-based immunoassays

BACKGROUND: High throughput protein expression studies can be performed using bead-based protein immunoassays, such as the Luminex® xMAP® technology. Technical variability is inherent to these experiments and may lead to systematic bias and reduced power. To reduce technical variability, data pre-pr...

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Autores principales: Rausch, Tanja K., Schillert, Arne, Ziegler, Andreas, Lüking, Angelika, Zucht, Hans-Dieter, Schulz-Knappe, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982217/
https://www.ncbi.nlm.nih.gov/pubmed/27515389
http://dx.doi.org/10.1186/s12864-016-2888-7
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author Rausch, Tanja K.
Schillert, Arne
Ziegler, Andreas
Lüking, Angelika
Zucht, Hans-Dieter
Schulz-Knappe, Peter
author_facet Rausch, Tanja K.
Schillert, Arne
Ziegler, Andreas
Lüking, Angelika
Zucht, Hans-Dieter
Schulz-Knappe, Peter
author_sort Rausch, Tanja K.
collection PubMed
description BACKGROUND: High throughput protein expression studies can be performed using bead-based protein immunoassays, such as the Luminex® xMAP® technology. Technical variability is inherent to these experiments and may lead to systematic bias and reduced power. To reduce technical variability, data pre-processing is performed. However, no recommendations exist for the pre-processing of Luminex® xMAP® data. RESULTS: We compared 37 different data pre-processing combinations of transformation and normalization methods in 42 samples on 384 analytes obtained from a multiplex immunoassay based on the Luminex® xMAP® technology. We evaluated the performance of each pre-processing approach with 6 different performance criteria. Three performance criteria were plots. All plots were evaluated by 15 independent and blinded readers. Four different combinations of transformation and normalization methods performed well as pre-processing procedure for this bead-based protein immunoassay. CONCLUSIONS: The following combinations of transformation and normalization were suitable for pre-processing Luminex® xMAP® data in this study: weighted Box-Cox followed by quantile or robust spline normalization (rsn), asinh transformation followed by loess normalization and Box-Cox followed by rsn. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2888-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-49822172016-08-13 Comparison of pre-processing methods for multiplex bead-based immunoassays Rausch, Tanja K. Schillert, Arne Ziegler, Andreas Lüking, Angelika Zucht, Hans-Dieter Schulz-Knappe, Peter BMC Genomics Research Article BACKGROUND: High throughput protein expression studies can be performed using bead-based protein immunoassays, such as the Luminex® xMAP® technology. Technical variability is inherent to these experiments and may lead to systematic bias and reduced power. To reduce technical variability, data pre-processing is performed. However, no recommendations exist for the pre-processing of Luminex® xMAP® data. RESULTS: We compared 37 different data pre-processing combinations of transformation and normalization methods in 42 samples on 384 analytes obtained from a multiplex immunoassay based on the Luminex® xMAP® technology. We evaluated the performance of each pre-processing approach with 6 different performance criteria. Three performance criteria were plots. All plots were evaluated by 15 independent and blinded readers. Four different combinations of transformation and normalization methods performed well as pre-processing procedure for this bead-based protein immunoassay. CONCLUSIONS: The following combinations of transformation and normalization were suitable for pre-processing Luminex® xMAP® data in this study: weighted Box-Cox followed by quantile or robust spline normalization (rsn), asinh transformation followed by loess normalization and Box-Cox followed by rsn. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2888-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-11 /pmc/articles/PMC4982217/ /pubmed/27515389 http://dx.doi.org/10.1186/s12864-016-2888-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Rausch, Tanja K.
Schillert, Arne
Ziegler, Andreas
Lüking, Angelika
Zucht, Hans-Dieter
Schulz-Knappe, Peter
Comparison of pre-processing methods for multiplex bead-based immunoassays
title Comparison of pre-processing methods for multiplex bead-based immunoassays
title_full Comparison of pre-processing methods for multiplex bead-based immunoassays
title_fullStr Comparison of pre-processing methods for multiplex bead-based immunoassays
title_full_unstemmed Comparison of pre-processing methods for multiplex bead-based immunoassays
title_short Comparison of pre-processing methods for multiplex bead-based immunoassays
title_sort comparison of pre-processing methods for multiplex bead-based immunoassays
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982217/
https://www.ncbi.nlm.nih.gov/pubmed/27515389
http://dx.doi.org/10.1186/s12864-016-2888-7
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