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Standardized Workflow for Mass-Spectrometry-Based Single-Cell Proteomics Data Processing and Analysis Using the scp Package.
Grégoire, Samuel; Vanderaa, Christophe; Dit Ruys, Sébastien Pyr; Kune, Christopher; Mazzucchelli, Gabriel; Vertommen, Didier; Gatto, Laurent.
Afiliación
  • Grégoire S; Computational Biology and Bioinformatics Unit, de Duve Institute, UCLouvain, Brussels, Belgium.
  • Vanderaa C; Computational Biology and Bioinformatics Unit, de Duve Institute, UCLouvain, Brussels, Belgium.
  • Dit Ruys SP; Protein Phosphorylation Unit, de Duve Institute, UCLouvain, Brussels, Belgium.
  • Kune C; Laboratory of Mass Spectrometry, MolSys Research Unit, University of Liège, Liège, Belgium.
  • Mazzucchelli G; Laboratory of Mass Spectrometry, MolSys Research Unit, University of Liège, Liège, Belgium.
  • Vertommen D; GIGA Proteomics Facility, University of Liège, Liège, Belgium.
  • Gatto L; Protein Phosphorylation Unit, de Duve Institute, UCLouvain, Brussels, Belgium.
Methods Mol Biol ; 2817: 177-220, 2024.
Article en En | MEDLINE | ID: mdl-38907155
ABSTRACT
Mass-spectrometry (MS)-based single-cell proteomics (SCP) explores cellular heterogeneity by focusing on the functional effectors of the cells-proteins. However, extracting meaningful biological information from MS data is far from trivial, especially with single cells. Currently, data analysis workflows are substantially different from one research team to another. Moreover, it is difficult to evaluate pipelines as ground truths are missing. Our team has developed the R/Bioconductor package called scp to provide a standardized framework for SCP data analysis. It relies on the widely used QFeatures and SingleCellExperiment data structures. In addition, we used a design containing cell lines mixed in known proportions to generate controlled variability for data analysis benchmarking. In this chapter, we provide a flexible data analysis protocol for SCP data using the scp package together with comprehensive explanations at each step of the processing. Our main steps are quality control on the feature and cell level, aggregation of the raw data into peptides and proteins, normalization, and batch correction. We validate our workflow using our ground truth data set. We illustrate how to use this modular, standardized framework and highlight some crucial steps.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría de Masas / Programas Informáticos / Proteómica / Flujo de Trabajo / Análisis de la Célula Individual Límite: Humans Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría de Masas / Programas Informáticos / Proteómica / Flujo de Trabajo / Análisis de la Célula Individual Límite: Humans Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos