You can create a MyVariants database when you create an analysis workflow. A MyVariants database can be used research projects for various reasons. For example, separate databases can be useful for projects with interpretations of genomic variants that appear to conflict. If a breast cancer study includes specific gene mutations that are suspected to cause tumors, and a lung cancer study includes the same mutations that are not suspected to cause tumors, two MyVariants databases can be used.
In the Workflows tab, click Create.
In the Research Application step, select the research application and sample group, then click Next.
In the Reference step, select the required files, then click Next.
In the Annotation step, under MyVariants Database, click Create here.
In the Create MyVariant Database dialog box, enter a database name, then click Save. The newly created database is now available for selection in the Annotation step.
Select the new MyVariants database, then click Next.
In the Filters step, select a filter chain from the dropdown list, then click Next. .
In the Copy Number step, select a copy number baseline from the dropdown list, then click Next.
In the Plugins step, select plugins, then click Next.
In the Final Report step, select the final report template in the list, then click Next.
In the Parameters step, select parameters, then click Next.
In the Confirm step, name the analysis workflow, enter an optional description, then click Save Workflow.
To check that the analysis workflow was created, click the Workflows tab, then click Overview, and search for the analysis workflow name.
