Study: Single Cell Comparison: Cortex data 13783 cells

Systematic comparative analysis of single cell RNA-sequencing methods

Single Cell Comparison: Cortex


A multitude of single-cell RNA sequencing methods have been developed in recent years, with dramatic advances in scale and power, and enabling major discoveries and large scale cell mapping efforts. However, these methods have not been systematically and comprehensively benchmarked. Here, we directly compare seven methods for single cell and/or single nucleus profiling from three types of samples – cell lines, peripheral blood mononuclear cells and brain tissue – generating 36 libraries in six separate experiments in a single center. To analyze these datasets, we developed and applied scumi, a flexible computational pipeline that can be used for any scRNA-seq method. We evaluated the methods for both basic performance and for their ability to recover known biological information in the samples. Our study will help guide experiments with the methods in this study as well as serve as a benchmark for future studies and for computational algorithm development. 


Here, we present the data from the mouse Cortex single nucleus RNA-seq (snRNA-seq) experiments. These consist of two experiments (Cortex1 and Cortex2), each with 4 snRNA-seq methods. This dataset allowed us to better understand the ability of different methods to detect biological differences. This data has been sampled, both in terms of reads and cells to enable a more fair comparison (see details in our preprint). The expression data are log counts per 10,000 (based on UMI counts for all methods except Smart-seq2, which is based on read counts). One can switch between different experiments / methods / annotations by clicking the view options bar and using the tool bar at the right of the screen. By default it displays a joint t-SNE (based on the Harmony joint analysis of all datasets from our preprint) and cell type annotations (the individual level cell type annotations, not the Harmony analysis), though both can be changed easily with the portal. 


More details about the data in this portal can be found in out readme (README_Cortex.docx, available under the download tab) and in our preprint (