Journal Article DZNE-2025-00036

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Unveiling the power of high-dimensional cytometry data with cyCONDOR.

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2024
Nature Publishing Group UK [London]

Nature Communications 15(1), 10702 () [10.1038/s41467-024-55179-w]

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Abstract: High-dimensional cytometry (HDC) is a powerful technology for studying single-cell phenotypes in complex biological systems. Although technological developments and affordability have made HDC broadly available in recent years, technological advances were not coupled with an adequate development of analytical methods that can take full advantage of the complex data generated. While several analytical platforms and bioinformatics tools have become available for the analysis of HDC data, these are either web-hosted with limited scalability or designed for expert computational biologists, making their use unapproachable for wet lab scientists. Additionally, end-to-end HDC data analysis is further hampered due to missing unified analytical ecosystems, requiring researchers to navigate multiple platforms and software packages to complete the analysis. To bridge this data analysis gap in HDC we develop cyCONDOR, an easy-to-use computational framework covering not only all essential steps of cytometry data analysis but also including an array of downstream functions and tools to expand the biological interpretation of the data. The comprehensive suite of features of cyCONDOR, including guided pre-processing, clustering, dimensionality reduction, and machine learning algorithms, facilitates the seamless integration of cyCONDOR into clinically relevant settings, where scalability and disease classification are paramount for the widespread adoption of HDC in clinical practice. Additionally, the advanced analytical features of cyCONDOR, such as pseudotime analysis and batch integration, provide researchers with the tools to extract deeper insights from their data. We use cyCONDOR on a variety of data from different tissues and technologies demonstrating its versatility to assist the analysis of high-dimensional data from preprocessing to biological interpretation.

Keyword(s): Software (MeSH) ; Flow Cytometry: methods (MeSH) ; Computational Biology: methods (MeSH) ; Humans (MeSH) ; Single-Cell Analysis: methods (MeSH) ; Algorithms (MeSH) ; Animals (MeSH) ; Machine Learning (MeSH) ; Mice (MeSH) ; Cluster Analysis (MeSH)

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Contributing Institute(s):
  1. Clinical Single Cell Omics (CSCO) / Systems Medicine (AG Schultze)
  2. Aging and Immunity (AG Aschenbrenner)
  3. Immunogenomics and Neurodegeneration (AG Beyer)
  4. Clinical Alzheimer’s Disease Research (AG Jessen)
  5. Platform for Single Cell Genomics and Epigenomics (PRECISE)
Research Program(s):
  1. 354 - Disease Prevention and Healthy Aging (POF4-354) (POF4-354)
  2. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)
Experiment(s):
  1. Longitudinal Cognitive Impairment and Dementia Study
  2. Platform for Single Cell Genomics and Epigenomics at DZNE University of Bonn

Database coverage:
Medline ; Creative Commons Attribution CC BY 4.0 ; DOAJ ; OpenAccess ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Agriculture, Biology and Environmental Sciences ; Current Contents - Life Sciences ; Current Contents - Physical, Chemical and Earth Sciences ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF >= 15 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection ; Zoological Record
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The record appears in these collections:
Institute Collections > BN DZNE > BN DZNE-AG Aschenbrenner
Document types > Articles > Journal Article
Institute Collections > BN DZNE > BN DZNE-AG Schultze
Institute Collections > BN DZNE > BN DZNE-AG Jessen
Institute Collections > BN DZNE > BN DZNE-AG Beyer
Institute Collections > BN DZNE > BN DZNE-PRECISE
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 Record created 2025-01-08, last modified 2025-02-03


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