Object | Default Values | Description |
---|---|---|
Chemistry | No | Refers to the chemistry that was used to prepare the samples for sequencing. |
Instrument | No | Refers to the instrument that was used to sequence the samples. |
Pathogenicity | Yes | The pathogenicity for a selected variant. Default values are Deleterious, Likely Deleterious, Unknown, Likely Benign, and Benign. |
Pathogenicity Status | Yes | Indicates the status for changing the pathogenicity for a selected variant. Default values are Pending and Confirmed. |
Sample Status | Yes | The status for a sample. Default values are New, QC Passed, Reviewed, and Complete |
Panel Group | No | Separately tracks the pathogenicities of variants that might be found in multiple panels. For example, the pathogenicity of a selected variant is set to Deleterious for multiple cancer panels; however, the pathogenicity can be set to Benign for a cardiac panel. You can create a group for each panel, and then assign the appropriate panels to each group. |
Coverage Region Status | Yes | The Coverage Regions tab (via the Run tab) lists the coverage information for every region in your panel as well as a status for each region. Default values are Passed or Failed to indicate whether a region passed or failed the coverage settings that were set for the run. Note: See Coverage Regions tab. |
Sample Group | No | Used for a group of samples that are to be processed repeatedly over a period of time, for example, a group of control samples for which the coverage or variant frequency is to be tracked. |
Run Status | Yes | The status for a run. Default values are New, QC Passed, Reviewed, and Complete. |
Artifact | No | The artifact type for the sample variant, for example, a Sequencing artifact. A single default value, None, is supplied for artifact type. |
Phenotype | No | The phenotype for a patient. |
Ethnicity | No | The ethnicity for a run patient, for example, Caucasian (Non-Hispanic). |