Annotates and filters variations with SnpEff.
Element type: seff
Parameters
| Parameter | Description | Default value | Parameter in Workflow File | Type |
|---|---|---|---|---|
| Output directory | Select an output directory. Custom - specify the output directory in the 'Custom directory' parameter. Workflow - internal workflow directory. Input file - the directory of the input file. | Input file | out-mode | string |
| Input format | Select the input format of variations. | VCF | inp-format | string |
| Output format | Select the format of annotated output files. | VCF | out-format | string |
| Genome | Select the target genome from the list of SnpEff databases. Genome data will be downloaded if it is not found. The list of databases depends on the SnpEff external tool version. | Homo sapiens | genome | string |
| Upstream/downstream length | Upstream and downstream interval size. Eliminate any upstream and downstream effect by using 0 length. | No upstream/downstream interval (0 bases) | updown-length | numeric |
| Cannonical transcripts | Use only cannonical transcripts. | False | canon | boolean |
| HGVS nomenclature | Annotate using HGVS nomenclature. | False | hgvs | boolean |
| Annotate loss of function | Annotate Loss of function (LOF) and Nonsense mediated decay (NMD). | False | lof | boolean |
| Annotate TFBSs motifs | Annotate transcription factor binding site motifs (only available for latest GRCh37). | False | motif | boolean |
Input/Output Ports
The element has 1 input port:
Name in GUI: Variations
Name in Workflow File: in-file
Slots:
| Slot In GUI | Slot in Workflow File | Type |
|---|---|---|
| Source url | url | string |
And 1 output port:
Name in GUI: Annotated variations
Name in Workflow File: out-file
Slots:
| Slot In GUI | Slot in Workflow File | Type |
|---|---|---|
| Source url | url | variation |