MALAT1expression indicates cell quality in single-cell RNA sequencing data

Abstract

AbstractSingle-cell RNA sequencing (scRNA-seq) has revolutionized our understanding of cell types and tissues. However, empty droplets and poor quality cells are often captured in single cell genomics experiments and need to be removed to avoid cell type interpretation errors. Many automated and manual methods exist to identify poor quality cells or empty droplets, such as minimum RNA count thresholds and comparing the gene expression profile of an individual cell to the overall background RNA expression of the experiment. A versatile approach is to use unbalanced overall RNA splice ratios of cells to identify poor quality cells or empty droplets. However, this approach is computationally intensive, requiring a detailed search through all sequence reads in the experiment to quantify spliced and unspliced reads. We found that the expression level ofMALAT1,a non-coding RNA retained in the nucleus and ubiquitously expressed across cell types, is strongly correlated with this splice ratio measure and thus can be used to similarly identify low quality cells in scRNA-seq data. Since it is easy to visualize the expression of a single gene in single-cell maps,MALAT1expression is a simple cell quality measure that can be quickly used during the cell annotation process to improve the interpretation of cells in tissues of human, mouse and other species with a conservedMALAT1function.