High throughput sequencing is currently revolutionizing both the cancer research and diagnostics areas. Since the introduction of "next generation sequencing" (NGS) technologies, the field has quickly moved forward, with rapid improvements in sequencing capacity and the time required for data production. As a result, in many studies the sequencing process is no longer the bottleneck. The bottleneck now is the bioinformatic analysis of the data.
CLC Cancer Research Workbench has been developed to address the bioinformatic bottleneck by offering automated workflows that cover all steps from the initial data processing and quality assurance through data analyses, annotation, and reporting.
- Introduction to CLC Cancer Research Workbench
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- The material covered by this manual
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