CytoPy: An autonomous cytometry analysis framework
Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional...
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Published in | PLoS computational biology Vol. 17; no. 6; p. e1009071 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
01.06.2021
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
ISSN | 1553-7358 1553-734X 1553-7358 |
DOI | 10.1371/journal.pcbi.1009071 |
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Abstract | Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at
https://github.com/burtonrj/CytoPy
, with notebooks accompanying this manuscript (
https://github.com/burtonrj/CytoPyManuscript
) and software documentation at
https://cytopy.readthedocs.io/
. |
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AbstractList | Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at https://github.com/burtonrj/CytoPy, with notebooks accompanying this manuscript (https://github.com/burtonrj/CytoPyManuscript) and software documentation at https://cytopy.readthedocs.io/.Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at https://github.com/burtonrj/CytoPy, with notebooks accompanying this manuscript (https://github.com/burtonrj/CytoPyManuscript) and software documentation at https://cytopy.readthedocs.io/. Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at https://github.com/burtonrj/CytoPy, with notebooks accompanying this manuscript (https://github.com/burtonrj/CytoPyManuscript) and software documentation at https://cytopy.readthedocs.io/. Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at https://github.com/burtonrj/CytoPy , with notebooks accompanying this manuscript ( https://github.com/burtonrj/CytoPyManuscript ) and software documentation at https://cytopy.readthedocs.io/ . Cytometry is a popular technology used to quantify biological material. In recent years, the capabilities of cytometry have expanded, resulting in ever larger datasets. In order to analyse these data, new approaches are required, giving rise to the field of cytometry bioinformatics. Despite the success of numerous algorithms and tools in this domain, widespread adoption by the scientific community has yet to be realised. Here we introduce CytoPy, a comprehensive cytometry data analysis framework deployed in Python, a beginner-friendly programming language. We validate CytoPy’s ability to handle batch effects and identify immune cell populations in human blood. Subsequently, we apply CytoPy to the analysis of drain fluid from patients undergoing peritoneal dialysis and compare the local immune response of stable patients to those presenting with acute peritonitis. CytoPy is open-source and available online: https://cytopy.readthedocs.io/en/latest/ . Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at Cytometry analysis has seen a considerable expansion in recent years in the maximum number of parameters that can be acquired in a single experiment. In response to this technological advance there has been an increased effort to develop new computational methodologies for handling high-dimensional single cell data acquired by flow or mass cytometry. Despite the success of numerous algorithms and published packages to replicate and outperform traditional manual analysis, widespread adoption of these techniques has yet to be realised in the field of immunology. Here we present CytoPy, a Python framework for automated analysis of cytometry data that integrates a document-based database for a data-centric and iterative analytical environment. In addition, our algorithm-agnostic design provides a platform for open-source cytometry bioinformatics in the Python ecosystem. We demonstrate the ability of CytoPy to phenotype T cell subsets in whole blood samples even in the presence of significant batch effects due to technical and user variation. The complete analytical pipeline was then used to immunophenotype the local inflammatory infiltrate in individuals with and without acute bacterial infection. CytoPy is open-source and licensed under the MIT license. CytoPy is available at https://github.com/burtonrj/CytoPy , with notebooks accompanying this manuscript ( https://github.com/burtonrj/CytoPyManuscript ) and software documentation at https://cytopy.readthedocs.io/ . |
Audience | Academic |
Author | Cuff, Simone M. Eberl, Matthias Artemiou, Andreas Burton, Ross J. Baker, Sarah Ahmed, Raya |
AuthorAffiliation | 1 Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom 3 Systems Immunity Research Institute, Cardiff University, Cardiff, United Kingdom 2 School of Mathematics, Cardiff University, Cardiff, United Kingdom bioinformatics, GERMANY |
AuthorAffiliation_xml | – name: 3 Systems Immunity Research Institute, Cardiff University, Cardiff, United Kingdom – name: bioinformatics, GERMANY – name: 1 Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom – name: 2 School of Mathematics, Cardiff University, Cardiff, United Kingdom |
Author_xml | – sequence: 1 givenname: Ross J. orcidid: 0000-0002-1516-7749 surname: Burton fullname: Burton, Ross J. – sequence: 2 givenname: Raya surname: Ahmed fullname: Ahmed, Raya – sequence: 3 givenname: Simone M. orcidid: 0000-0002-0546-3579 surname: Cuff fullname: Cuff, Simone M. – sequence: 4 givenname: Sarah orcidid: 0000-0002-7474-9757 surname: Baker fullname: Baker, Sarah – sequence: 5 givenname: Andreas orcidid: 0000-0002-7501-4090 surname: Artemiou fullname: Artemiou, Andreas – sequence: 6 givenname: Matthias orcidid: 0000-0002-9390-5348 surname: Eberl fullname: Eberl, Matthias |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34101722$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1002_cyto_a_24913 crossref_primary_10_3390_neuroglia5020010 crossref_primary_10_1093_bioadv_vbad103 crossref_primary_10_1002_advs_202207061 crossref_primary_10_1016_j_mcpro_2023_100592 crossref_primary_10_1093_bioinformatics_btac751 crossref_primary_10_1093_cei_uxae019 crossref_primary_10_3389_fimmu_2021_768541 crossref_primary_10_1038_s41581_021_00466_8 |
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ContentType | Journal Article |
Copyright | COPYRIGHT 2021 Public Library of Science 2021 Burton et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2021 Burton et al 2021 Burton et al |
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Title | CytoPy: An autonomous cytometry analysis framework |
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