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PsiNorm: a scalable normalization for single-cell RNA-seq data.


ABSTRACT:

Motivation

Single-cell RNA sequencing (scRNA-seq) enables transcriptome-wide gene expression measurements at single-cell resolution providing a comprehensive view of the compositions and dynamics of tissue and organism development. The evolution of scRNA-seq protocols has led to a dramatic increase of cells throughput, exacerbating many of the computational and statistical issues that previously arose for bulk sequencing. In particular, with scRNA-seq data all the analyses steps, including normalization, have become computationally intensive, both in terms of memory usage and computational time. In this perspective, new accurate methods able to scale efficiently are desirable.

Results

Here we propose PsiNorm, a between-sample normalization method based on the power-law Pareto distribution parameter estimate. Here we show that the Pareto distribution well resembles scRNA-seq data, especially those coming from platforms that employ unique molecular identifiers (UMIs). Motivated by this result, we implement PsiNorm, a simple and highly scalable normalization method. We benchmark PsiNorm against seven other methods in terms of cluster identification, concordance and computational resources required. We demonstrate that PsiNorm is among the top performing methods showing a good trade-off between accuracy and scalability. Moreover PsiNorm does not need a reference, a characteristic that makes it useful in supervised classification settings, in which new out-of-sample data need to be normalized.

Availability

PsiNorm is implemented in the scone Bioconductor package and available at https://bioconductor.org/packages/scone/.

Supplementary information

Supplementary data are available at Bioinformatics online.

SUBMITTER: Borella M 

PROVIDER: S-EPMC8696108 | biostudies-literature |

REPOSITORIES: biostudies-literature

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