Single-cell transcriptional diversity is a hallmark of developmental potential

Single-cell RNA sequencing (scRNA-seq) is a powerful approach for reconstructing cellular differentiation trajectories. However, inferring both the state and direction of differentiation is challenging. Here, we demonstrate a simple, yet robust, determinant of developmental potential—the number of expressed genes per cell—and leverage this measure of transcriptional diversity to develop a computational framework (CytoTRACE) for predicting differentiation states from scRNA-seq data. When applied to diverse tissue types and organisms, CytoTRACE outperformed previous methods and nearly 19,000 annotated gene sets for resolving 52 experimentally determined developmental trajectories. Additionally, it facilitated the identification of quiescent stem cells and revealed genes that contribute to breast tumorigenesis. This study thus establishes a key RNA-based feature of developmental potential and a platform for delineation of cellular hierarchies (https://cytotrace.stanford.edu). Single-cell RNA-sequencing (Smart-seq2) profiles (n = 1,902 cells) of human basal (tumor: n = 294, adjacent normal: n = 366), luminal progenitor (tumor: n = 213, adjacent normal: n = 319), and mature luminal cells (tumor: n = 354, adjacent normal: n = 356) from 8 human breast cancer patients (luminal-like: n = 6; basal-like: n = 2) ----------------------------------------- The authors state that they will "upload the remaining raw data to dbGap".