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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-4982217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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