Variant Filter

Variant Filter 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 visualization to regenerate an inspectable figure, report, or interactive view from supplied analysis artifacts so the rendered output can be compared with reported figures or tables.