Introduction:

Single-cell transcriptomics is opening new frontiers in biology by allowing researchers to profile gene expression at the resolution of individual cells. This powerful approach reveals cellular diversity, identifies rare cell populations, and uncovers dynamic biological processes that bulk sequencing often cannot capture.

In this beginner-friendly webinar, we will introduce the fundamentals of single-cell RNA sequencing (scRNA-seq) using the cutting-edge 10x Genomics platform. We will walk through the core workflow—from sample preparation and library construction to sequencing and data analysis—while sharing best practices and common pitfalls to avoid. Drawing on Novogene’s extensive experience with projects on various species and tissue and organoid types, we will highlight practical examples that showcase how single-cell technologies can empower discoveries across disease research, developmental biology, and beyond.

Whether you are new to single-cell methods or considering your first project, this session will provide the foundational knowledge, confidence, and actionable insights to help you get started successfully with single-cell transcriptomics.

What you’ll learn:

• How single-cell RNA-seq reveals insights beyond bulk sequencing
• A step-by-step overview of the 10x Genomics workflow
• Key tips and pitfalls for first-time users
• How Novogene helps researchers succeed with single-cell projects