Varora

⚡ Genomic Analysis, Simplified

We provide fast, accurate WES/WGS variant calling and annotation pipelines powered by open-source standards (GATK, VEP, Nextflow) — optimized for labs that don't have time or resources to build bioinformatics infrastructure.

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Who It's For

Clinical labs and IVF centers needing reliable secondary analysis
Rare disease researchers and diagnostics startups
Academic labs with limited bioinformatics support

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Why Varora?

Feature	DRAGEN	Varora
Custom QC filters & variant thresholds	✘	✔
Open, reproducible workflows	✘	✔
Affordable for low sample volumes	✘	✔
Intermediate files + transparency	✘	✔
Direct support from the builder	✘	✔

Let’s Talk

Whether you're exploring WES/WGS or just tired of wrestling with pipelines, we’re happy to help.

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