Create an exon tile fusion baseline workflow preset

You must use at least 48 fusion-negative RNA samples to create an exon tile fusion baseline workflow preset.

  1. In the Workflows tab, click Presets, then click Create Preset > Exon Tile Fusion Baseline .
  2. In the Baseline Type step of the Create Exon Tile Fusion Baseline workflow bar, select the Fusion Panel to use for the exon tile fusion baseline.

    Note:

    • The baseline type is set to Exon Tile Fusion Baseline and cannot be changed.

    • The reference genome is set to hg19 and cannot be changed.

  3. Click Next.
  4. In the Parameters step, do not change parameters from the default settings unless you understand how the change can affect the analysis. Click Next.
  5. In the Samples step, select the samples to be used in the baseline creation.

    You must select at least 48 or more fusion-negative RNA samples. If you do not see samples of interest in the table, see Sample definition for information about how to upload or define a sample.

  6. Click Next.
  7. In the Confirm step, enter a name, or accept the default name, then enter an optional description for the baseline.
  8. Click Launch.

The exon tile fusion baseline creation job is started and the baseline with its status now appears on the screen. When the job completes, the exon tile fusion baseline is added to the Workflow Presets screen and is available to add to an analysis workflow. For more information, see Apply an exon tile fusion baseline workflow preset to an analysis workflow.