BryNaxa VCF pre-flights a VCF against the current specification and, critically, against its reference genome — confirming the declared build, contig naming, and REF alleles actually match. A file built on the wrong genome fails at your desk instead of producing silently wrong annotations three steps downstream.
Everything stays on your machine.
Runs fully offline on your own Windows computer. No account, no cloud, no telemetry — your files never leave the desk. Every result comes from a published method computed the same way every time, so the same input always produces the same findings. You keep the report as a plain file in your own systems.
Coming soon.
BryNaxa VCF is part of the BryNaxa R&D line and is in preparation. To talk about access, licensing, or an evaluation for your team, get in touch and we’ll set you up.