| Literature DB >> 29423800 |
Robert Durruthy-Durruthy1, Manisha Ray1.
Abstract
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.Keywords: Cell characterization; Full-length cDNA; Gene expression profiling; Single-cell RNA-seq; Single-cell transcriptomics
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Year: 2018 PMID: 29423800 DOI: 10.1007/978-1-4939-7471-9_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745