Start with existing data

Already have data? You can start now.

If you already have raw files, you should not need to buy another test. You need a clear, private path that stays useful over time.

If you already tested with WeGene, 23andMe, BGI, or someone else

This page is for people who already finished the testing part.

Fern Gene does not send you back into a lab flow. It picks up where raw-file ownership starts.

  • You do not need to buy another test
  • The key is getting the raw file back under your control
  • The value starts after import, not when you order sequencing again

What you can import today

On a phone, it makes more sense to start with lighter files instead of heavier sequencing exports.

  • Mobile-first entry points: txt / VCF / gVCF / .genomesprofile
  • Desktop is better for heavier BAM / CRAM workflows
  • FASTQ is not a mobile import target

What you see first after import

After import, the homepage starts with the most useful prompt instead of forcing a long report first.

  • See prompts and summaries first
  • Open detail only when you want more depth
  • Find the partner-review entry point when it matters

When to go deeper

Only go deeper when you want explanation, next steps, and evidence context.

  • Conclusion first, reasoning second
  • More private views stay unlock-gated
  • No need to read a long report up front

Where to start today

iPhone

The main commercial path for phase 1 and the target for the most complete consumer experience.

Android

Already validated on a real device for onboarding, import, results, Vault, partner review, and policy screens.

macOS

Better suited to heavier files and companion desktop workflows than to being the main consumer entry point.

Windows

The Windows client is now in release preparation and will follow the same desktop-companion role as macOS for heavier workflows.