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:
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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