Cells, the basic units of biological structure and function, vary broadly in type
and state. Single-cell genomics can characterize cell identity and function, but limitations
of ease and scale have prevented its broad application. Here we describe Drop-seq,
a strategy for quickly profiling thousands of individual cells by separating them
into nanoliter-sized aqueous droplets, associating a different barcode with each cell's
RNAs, and sequencing them all together. Drop-seq analyzes mRNA transcripts from thousands
of individual cells simultaneously while remembering transcripts' cell of origin.
We analyzed transcriptomes from 44,808 mouse retinal cells and identified 39 transcriptionally
distinct cell populations, creating a molecular atlas of gene expression for known
retinal cell classes and novel candidate cell subtypes. Drop-seq will accelerate biological
discovery by enabling routine transcriptional profiling at single-cell resolution.
VIDEO ABSTRACT.