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Ultra-fast scalable estimation of single-cell differentiation potency from scRNA-Seq data

MOTIVATION: An important task in the analysis of single-cell RNA-Seq data is the estimation of differentiation potency, as this can help identify stem-or-multipotent cells in non-temporal studies or in tissues where differentiation hierarchies are not well established. A key challenge in the estimat...

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Detalles Bibliográficos
Autores principales: Teschendorff, Andrew E, Maity, Alok K, Hu, Xue, Weiyan, Chen, Lechner, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275983/
https://www.ncbi.nlm.nih.gov/pubmed/33244588
http://dx.doi.org/10.1093/bioinformatics/btaa987
Descripción
Sumario:MOTIVATION: An important task in the analysis of single-cell RNA-Seq data is the estimation of differentiation potency, as this can help identify stem-or-multipotent cells in non-temporal studies or in tissues where differentiation hierarchies are not well established. A key challenge in the estimation of single-cell potency is the need for a fast and accurate algorithm, scalable to large scRNA-Seq studies profiling millions of cells. RESULTS: Here, we present a single-cell potency measure, called Correlation of Connectome and Transcriptome (CCAT), which can return accurate single-cell potency estimates of a million cells in minutes, a 100-fold improvement over current state-of-the-art methods. We benchmark CCAT against 8 other single-cell potency models and across 28 scRNA-Seq studies, encompassing over 2 million cells, demonstrating comparable accuracy than the current state-of-the-art, at a significantly reduced computational cost, and with increased robustness to dropouts. AVAILABILITY AND IMPLEMENTATION: CCAT is part of the SCENT R-package, freely available from https://github.com/aet21/SCENT. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.