Your browser doesn't support javascript.
loading
Doublet identification in single-cell sequencing data using scDblFinder.
Germain, Pierre-Luc; Lun, Aaron; Garcia Meixide, Carlos; Macnair, Will; Robinson, Mark D.
Afiliação
  • Germain PL; DMLS Lab of Statistical Bioinformatics, University of Zürich, Zürich, 805, Switzerland.
  • Lun A; D-HEST Institute for Neuroscience, ETH Zürich, Zürich, Switzerland.
  • Garcia Meixide C; Swiss Institute of Bioinformatics, University of Zürich, Zürich, Switzerland.
  • Macnair W; Genentech Inc., South San Francisco, CA, USA.
  • Robinson MD; D-HEST Institute for Neuroscience, ETH Zürich, Zürich, Switzerland.
F1000Res ; 10: 979, 2021.
Article em En | MEDLINE | ID: mdl-35814628
ABSTRACT
Doublets are prevalent in single-cell sequencing data and can lead to artifactual findings. A number of strategies have therefore been proposed to detect them. Building on the strengths of existing approaches, we developed scDblFinder, a fast, flexible and accurate Bioconductor-based doublet detection method. Here we present the method, justify its design choices, demonstrate its performance on both single-cell RNA and accessibility sequencing data, and provide some observations on doublet formation, detection, and enrichment analysis. Even in complex datasets, scDblFinder can accurately identify most heterotypic doublets, and was already found by an independent benchmark to outcompete alternatives.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / RNA Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / RNA Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article