Filter Variants

Filter Variants supports variant calling, normalization, or annotation so genomic findings can be reproduced from the supplied evidence. In DarwinOmics it is cataloged with sequencing reads as input and sequencing reads as output, so reviewers can trace how the regenerated artifact was produced and compare it with the submitted analysis.

Use in DarwinOmics

How to use it

Use this workflow element when the submitted analysis needs a multi-step execution path, imported workflow, Darwinomics wrapper, or workflow-scale comparison rather than a single module.