VCF To BCF

VCF To BCF supports variant calling, normalization, or annotation so genomic findings can be reproduced from the supplied evidence. In DarwinOmics it is cataloged with variant calls as input and reviewable analysis output 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 entry from the DarwinOmics catalog when it matches the data and analysis path.