ABSTRACT
Single-cell technologies have seen rapid advancements in recent years, along with new analytical challenges and opportunities. These high-throughput assays increasingly require special consideration in experimental design, sample multiplexing, batch effect removal, and data interpretation. Here, we describe a lentiviral barcode-based multiplexing approach, ‘CellTag Indexing’, where we transduce and label samples that can then be pooled together for downstream application and analysis. By introducing predefined genetic barcodes that are transcribed and readily detected, we can reliably read out sample identity via genomic or transcriptomic profiling, permitting the simultaneous assessment of cell grouping and transcriptional state. We validate and demonstrate the utility of CellTag Indexing by sequencing transcriptomes at single-cell resolution using a variety of cell types including mouse pre-B cells, primary mouse embryonic fibroblasts, human HEK293T cells, and mouse induced endoderm progenitors. Furthermore, we establish CellTag Indexing as a valuable tool for multiplexing direct lineage reprogramming perturbation experiments. We present CellTag Indexing as a broadly applicable genetic multiplexing tool that is complementary with existing single-cell RNA-sequencing and multiplexing strategies.
