Vaeda computationally annotates doublets in single-cell RNA sequencing data

MOTIVATION: Single-cell RNA sequencing (scRNA-seq) continues to expand our knowledge by facilitating the study of transcriptional heterogeneity at the level of single cells. Despite this technology’s utility and success in biomedical research, technical artifacts are present in scRNA-seq data. Doubl...

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Detalles Bibliográficos
Autores principales: Schriever, Hannah, Kostka, Dennis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805559/
https://www.ncbi.nlm.nih.gov/pubmed/36342203
http://dx.doi.org/10.1093/bioinformatics/btac720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805559/
https://www.ncbi.nlm.nih.gov/pubmed/36342203
http://dx.doi.org/10.1093/bioinformatics/btac720

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