Your browser doesn't support javascript.
loading
Cyto-Feature Engineering: A Pipeline for Flow Cytometry Analysis to Uncover Immune Populations and Associations with Disease.
Fox, Amy; Dutt, Taru S; Karger, Burton; Rojas, Mauricio; Obregón-Henao, Andrés; Anderson, G Brooke; Henao-Tamayo, Marcela.
Afiliação
  • Fox A; Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, 80523, USA.
  • Dutt TS; Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, 80523, USA.
  • Karger B; Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, 80523, USA.
  • Rojas M; Grupo de Inmunología Celular e Inmunogenética, Facultad de Medicina, Unidad de Citometría de Flujo, Sede de Investigación Universitaria, Universidad de Antioquia, Medellin, Colombia.
  • Obregón-Henao A; Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, 80523, USA.
  • Anderson GB; Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado, 80523, USA.
  • Henao-Tamayo M; Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, 80523, USA. Marcela.Henao_Tamayo@ColoState.edu.
Sci Rep ; 10(1): 7651, 2020 05 06.
Article em En | MEDLINE | ID: mdl-32377001
ABSTRACT
Flow cytometers can now analyze up to 50 parameters per cell and millions of cells per sample; however, conventional methods to analyze data are subjective and time-consuming. To address these issues, we have developed a novel flow cytometry analysis pipeline to identify a plethora of cell populations efficiently. Coupled with feature engineering and immunological context, researchers can immediately extrapolate novel discoveries through easy-to-understand plots. The R-based pipeline uses Fluorescence Minus One (FMO) controls or distinct population differences to develop thresholds for positive/negative marker expression. The continuous data is transformed into binary data, capturing a positive/negative biological dichotomy often of interest in characterizing cells. Next, a filtering step refines the data from all identified cell phenotypes to populations of interest. The data can be partitioned by immune lineages and statistically correlated to other experimental measurements. The pipeline's modularity allows customization of statistical testing, adoption of alternative initial gating steps, and incorporation of other datasets. Validation of this pipeline through manual gating of two datasets (murine splenocytes and human whole blood) confirmed its accuracy in identifying even rare subsets. Lastly, this pipeline can be applied in all disciplines utilizing flow cytometry regardless of cytometer or panel design. The code is available at https//github.com/aef1004/cyto-feature_engineering.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citodiagnóstico / Suscetibilidade a Doenças / Citometria de Fluxo Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Citodiagnóstico / Suscetibilidade a Doenças / Citometria de Fluxo Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article