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Single-cell RNA-seq, cell hashing and spatial transcriptomics
In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.Using CLC Genomics Workbench, you will learn how to perform secondary analysis on your single cell RNA-seq data. Specifically, you will learn how to:Import your raw FASTQ or processed cell-matrix files.Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries.Dimension…
The skinny
The skinny isn't ready yet — notes appear once the transcript is processed.