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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.
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The skinny
The skinny isn't ready yet — notes appear once the transcript is processed.