Jointly Defining Cell Types from Multiple Single-Cell Datasets Using LIGER

• DOI: 10.1101/2020.04.07.029546
• Publication Date: 2020-04-08T14:05:14Z
• Authors: Jialin Liu; Chao Gao; Joshua Sodicoff; Velina Kozareva; Evan Z. Macosko; Joshua D. Welch
• Keywords: Cell Nucleus; Sequence Analysis, RNA; Gene Expression Profiling; Animals; Cluster Analysis; Humans; Genomics; DNA Methylation; Single-Cell Analysis; Software; Workflow

AbstractHigh-throughput single-cell sequencing technologies hold tremendous potential for defining cell types in an unbiased fashion using gene expression and epigenomic state. A key challenge in realizing this potential is integrating single-cell datasets from multiple protocols, biological contexts, and data modalities into a joint definition of cellular identity. We previously developed an approach called Linked Inference of Genomic Experimental Relationships (LIGER) that uses integrative nonnegative matrix factorization to address this challenge. Here, we provide a step-by-step protocol for using LIGER to jointly define cell types from multiple single-cell datasets. The main steps of the protocol include data preprocessing and normalization, joint factorization, quantile normalization and joint clustering, and visualization. We describe how to jointly define cell types from single-cell RNA-seq and single-nucleus ATAC-seq data, but similar steps apply across a wide range of other settings and data types, including cross-species analysis, single-nucleus DNA methylation, and spatial transcriptomics. Our protocol contains examples of expected results, describes common pitfalls, and relies only on our freely available, open-source R implementation of LIGER. We also provide Rmarkdown tutorials showing the outputs from each individual code segment. The analysis process can be performed in 1 - 4 h depending on dataset size and assumes no specialized bioinformatics training.