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A novel protocol that enables the detection of both SNVs and CNVs from 1-5 cells in a single, low-pass sequencing run that saves time and money.
New to single-cell RNA-seq? These 5 tips will help you get started.
Learn more about how the Allen Institute for Brain Science used our SMART-Seq v4 Ultra Low Input Kit for Sequencing to characterize specific cell types within human brain.
Learn how the many differences between popular scRNA-seq platforms impact your data. Here, we discuss sensitivity, read efficiency, and gene diversity (3' DE expression) data generated by the ABRF Genomics Research Group.
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