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Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies

A significant challenge facing high-throughput phenotyping of in-vivo knockout mice is ensuring phenotype calls are robust and reliable. Central to this problem is selecting an appropriate statistical analysis that models both the experimental design (the workflow and the way control mice are select...

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Autores principales: Karp, Natasha A., Speak, Anneliese O., White, Jacqueline K., Adams, David J., Hrabé de Angelis, Martin, Hérault, Yann, Mott, Richard F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208881/
https://www.ncbi.nlm.nih.gov/pubmed/25343444
http://dx.doi.org/10.1371/journal.pone.0111239
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author Karp, Natasha A.
Speak, Anneliese O.
White, Jacqueline K.
Adams, David J.
Hrabé de Angelis, Martin
Hérault, Yann
Mott, Richard F.
author_facet Karp, Natasha A.
Speak, Anneliese O.
White, Jacqueline K.
Adams, David J.
Hrabé de Angelis, Martin
Hérault, Yann
Mott, Richard F.
author_sort Karp, Natasha A.
collection PubMed
description A significant challenge facing high-throughput phenotyping of in-vivo knockout mice is ensuring phenotype calls are robust and reliable. Central to this problem is selecting an appropriate statistical analysis that models both the experimental design (the workflow and the way control mice are selected for comparison with knockout animals) and the sources of variation. Recently we proposed a mixed model suitable for small batch-oriented studies, where controls are not phenotyped concurrently with mutants. Here we evaluate this method both for its sensitivity to detect phenotypic effects and to control false positives, across a range of workflows used at mouse phenotyping centers. We found the sensitivity and control of false positives depend on the workflow. We show that the phenotypes in control mice fluctuate unexpectedly between batches and this can cause the false positive rate of phenotype calls to be inflated when only a small number of batches are tested, when the effect of knockout becomes confounded with temporal fluctuations in control mice. This effect was observed in both behavioural and physiological assays. Based on this analysis, we recommend two approaches (workflow and accompanying control strategy) and associated analyses, which would be robust, for use in high-throughput phenotyping pipelines. Our results show the importance in modelling all sources of variability in high-throughput phenotyping studies.
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spelling pubmed-42088812014-10-27 Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies Karp, Natasha A. Speak, Anneliese O. White, Jacqueline K. Adams, David J. Hrabé de Angelis, Martin Hérault, Yann Mott, Richard F. PLoS One Research Article A significant challenge facing high-throughput phenotyping of in-vivo knockout mice is ensuring phenotype calls are robust and reliable. Central to this problem is selecting an appropriate statistical analysis that models both the experimental design (the workflow and the way control mice are selected for comparison with knockout animals) and the sources of variation. Recently we proposed a mixed model suitable for small batch-oriented studies, where controls are not phenotyped concurrently with mutants. Here we evaluate this method both for its sensitivity to detect phenotypic effects and to control false positives, across a range of workflows used at mouse phenotyping centers. We found the sensitivity and control of false positives depend on the workflow. We show that the phenotypes in control mice fluctuate unexpectedly between batches and this can cause the false positive rate of phenotype calls to be inflated when only a small number of batches are tested, when the effect of knockout becomes confounded with temporal fluctuations in control mice. This effect was observed in both behavioural and physiological assays. Based on this analysis, we recommend two approaches (workflow and accompanying control strategy) and associated analyses, which would be robust, for use in high-throughput phenotyping pipelines. Our results show the importance in modelling all sources of variability in high-throughput phenotyping studies. Public Library of Science 2014-10-24 /pmc/articles/PMC4208881/ /pubmed/25343444 http://dx.doi.org/10.1371/journal.pone.0111239 Text en © 2014 Karp et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Karp, Natasha A.
Speak, Anneliese O.
White, Jacqueline K.
Adams, David J.
Hrabé de Angelis, Martin
Hérault, Yann
Mott, Richard F.
Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies
title Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies
title_full Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies
title_fullStr Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies
title_full_unstemmed Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies
title_short Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies
title_sort impact of temporal variation on design and analysis of mouse knockout phenotyping studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208881/
https://www.ncbi.nlm.nih.gov/pubmed/25343444
http://dx.doi.org/10.1371/journal.pone.0111239
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