Workflows
The CLC Genomics Server supports workflows that are created with the CLC Workbenches. A work flow consists of a series of tools where the output of one tool is connected as the input to another tool. As an example, a workflow could pass data through read mapping, use the mapped reads as input for variant detection, and perform some filtering of the variant track. The workflow is created in the CLC Workbench and an installer file is created that can be installed on the CLC Genomics Server. For information about creating a workflow, please see the user manual of CLC Genomics Workbench or CLC Main Workbench at http://www.clcbio.com/usermanuals.
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