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Single-cell RNA-seq data normalization: A benchmarking study
DOI:10.1371/journal.pone.0335102.png)
Abstract
En 中文
This study examines the noise and biases introduced by technical factors in single-cell RNA sequencing (scRNA-seq) data, presenting a thorough benchmarking analysis of six widely utilized normalization methods. The evaluation of these methods is conducted from three perspectives: cell clustering, differential expression analysis, and computational resource requirements, utilizing seven real datasets alongside four simulated datasets. The findings indicate that Dino excels in clustering 10 x datasets and those with a substantial number of cells, while scTransform demonstrates strong performance with datasets produced through full-length library preparation protocols. Additionally, SCnorm is identified as suitable for small-scale datasets. This research serves as a significant reference for scholars in selecting appropriate normalization tools, thereby enhancing the accuracy and reliability of subsequent analyses of scRNA-seq data.
Keywords:
TECHNOLOGIES
Journal
IF:
2.6
Papers:
2.6W
Citations:
82.6W
Organization
Cited Papers
A scaling normalization method for differential expression analysis of RNA-seq data
GENOME BIOLOGY
IF9.4
Normalization and variance stabilization of single-cell RNA-seq data using regularized negative binomial regression
GENOME BIOLOGY
IF9.4
Integrating single-cell transcriptomic data across different conditions, technologies, and species
NATURE BIOTECHNOLOGY
IF41.7

