Durruthy-Durruthy Robert, Ray Manisha
Fluidigm Corporation, 7000 Shoreline Court, Suite 100, South San Francisco, CA, 94080, USA.
Methods Mol Biol. 2018;1706:199-221. doi: 10.1007/978-1-4939-7471-9_11.
Single-cell RNA sequencing has evolved into a benchmark application to study cellular heterogeneity, advancing our understanding of cellular differentiation, disease progression, and gene regulation in a multitude of research areas. The generation of high-quality cDNA, an important step in the experimental workflow when generating sequence-ready libraries, is critical to maximizing data quality. Here we describe a strategy that uses a microfluidic device (i.e., the C1™ IFC) to synthesize full-length cDNA from single cells in a fully automated, nanoliter-scale format. The device also facilitates confirmation of the presence of a single, viable cell and recording of phenotypic information, quality control measures that are crucial for streamlining downstream data processing and enhancing overall data validity.
单细胞RNA测序已发展成为研究细胞异质性的基准应用,推动了我们在众多研究领域对细胞分化、疾病进展和基因调控的理解。高质量cDNA的生成是生成可测序文库实验流程中的重要一步,对于最大化数据质量至关重要。在此,我们描述了一种策略,该策略使用微流控设备(即C1™ IFC)以全自动、纳升级的形式从单细胞合成全长cDNA。该设备还便于确认单个活细胞的存在并记录表型信息,这些质量控制措施对于简化下游数据处理和提高整体数据有效性至关重要。