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Change point detection for clustered expression data

BACKGROUND: To detect changes in biological processes, samples are often studied at several time points. We examined expression data measured at different developmental stages, or more broadly, historical data. Hence, the main assumption of our proposed methodology was the independence between the e...

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Autores principales: Sieg, Miriam, Sciesielski, Lina Katrin, Kirschner, Karin Michaela, Kruppa, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261071/
https://www.ncbi.nlm.nih.gov/pubmed/35794534
http://dx.doi.org/10.1186/s12864-022-08680-9
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author Sieg, Miriam
Sciesielski, Lina Katrin
Kirschner, Karin Michaela
Kruppa, Jochen
author_facet Sieg, Miriam
Sciesielski, Lina Katrin
Kirschner, Karin Michaela
Kruppa, Jochen
author_sort Sieg, Miriam
collection PubMed
description BACKGROUND: To detect changes in biological processes, samples are often studied at several time points. We examined expression data measured at different developmental stages, or more broadly, historical data. Hence, the main assumption of our proposed methodology was the independence between the examined samples over time. In addition, however, the examinations were clustered at each time point by measuring littermates from relatively few mother mice at each developmental stage. As each examination was lethal, we had an independent data structure over the entire history, but a dependent data structure at a particular time point. Over the course of these historical data, we wanted to identify abrupt changes in the parameter of interest - change points. RESULTS: In this study, we demonstrated the application of generalized hypothesis testing using a linear mixed effects model as a possible method to detect change points. The coefficients from the linear mixed model were used in multiple contrast tests and the effect estimates were visualized with their respective simultaneous confidence intervals. The latter were used to determine the change point(s). In small simulation studies, we modelled different courses with abrupt changes and compared the influence of different contrast matrices. We found two contrasts, both capable of answering different research questions in change point detection: The Sequen contrast to detect individual change points and the McDermott contrast to find change points due to overall progression. We provide the R code for direct use with provided examples. The applicability of those tests for real experimental data was shown with in-vivo data from a preclinical study. CONCLUSION: Simultaneous confidence intervals estimated by multiple contrast tests using the model fit from a linear mixed model were capable to determine change points in clustered expression data. The confidence intervals directly delivered interpretable effect estimates representing the strength of the potential change point. Hence, scientists can define biologically relevant threshold of effect strength depending on their research question. We found two rarely used contrasts best fitted for detection of a possible change point: the Sequen and McDermott contrasts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12864-022-08680-9).
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spelling pubmed-92610712022-07-08 Change point detection for clustered expression data Sieg, Miriam Sciesielski, Lina Katrin Kirschner, Karin Michaela Kruppa, Jochen BMC Genomics Research BACKGROUND: To detect changes in biological processes, samples are often studied at several time points. We examined expression data measured at different developmental stages, or more broadly, historical data. Hence, the main assumption of our proposed methodology was the independence between the examined samples over time. In addition, however, the examinations were clustered at each time point by measuring littermates from relatively few mother mice at each developmental stage. As each examination was lethal, we had an independent data structure over the entire history, but a dependent data structure at a particular time point. Over the course of these historical data, we wanted to identify abrupt changes in the parameter of interest - change points. RESULTS: In this study, we demonstrated the application of generalized hypothesis testing using a linear mixed effects model as a possible method to detect change points. The coefficients from the linear mixed model were used in multiple contrast tests and the effect estimates were visualized with their respective simultaneous confidence intervals. The latter were used to determine the change point(s). In small simulation studies, we modelled different courses with abrupt changes and compared the influence of different contrast matrices. We found two contrasts, both capable of answering different research questions in change point detection: The Sequen contrast to detect individual change points and the McDermott contrast to find change points due to overall progression. We provide the R code for direct use with provided examples. The applicability of those tests for real experimental data was shown with in-vivo data from a preclinical study. CONCLUSION: Simultaneous confidence intervals estimated by multiple contrast tests using the model fit from a linear mixed model were capable to determine change points in clustered expression data. The confidence intervals directly delivered interpretable effect estimates representing the strength of the potential change point. Hence, scientists can define biologically relevant threshold of effect strength depending on their research question. We found two rarely used contrasts best fitted for detection of a possible change point: the Sequen and McDermott contrasts. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12864-022-08680-9). BioMed Central 2022-07-06 /pmc/articles/PMC9261071/ /pubmed/35794534 http://dx.doi.org/10.1186/s12864-022-08680-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sieg, Miriam
Sciesielski, Lina Katrin
Kirschner, Karin Michaela
Kruppa, Jochen
Change point detection for clustered expression data
title Change point detection for clustered expression data
title_full Change point detection for clustered expression data
title_fullStr Change point detection for clustered expression data
title_full_unstemmed Change point detection for clustered expression data
title_short Change point detection for clustered expression data
title_sort change point detection for clustered expression data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261071/
https://www.ncbi.nlm.nih.gov/pubmed/35794534
http://dx.doi.org/10.1186/s12864-022-08680-9
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