When data turns to insights

Both CLC Genomics Workbench and Biomedical Genomics Workbench offer an intuitive user experience and require no background in bioinformatics. Our workbenches allow life scientists, clinicians, and bioinformaticians alike to carry out steps crucial for the analysis of RNA-Seq data, easily and compute resource-efficiently:

  • Quality control of data
  • Demultiplexing
  • Quantitative mapping of RNA-Seq reads
  • Normalization and statistical analysis of differential gene expression, and functional annotation of unknown transcripts via the Blast2GO Pro plugin

Results like statistical information, read mappings, as well as differential gene expression are visualized and can be browsed in the context of other genomic information, such as annotations, variants, or epigenetic information like ChIP-Seq results.



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