What can you explore with your genome?
Your FASTQ/VCF file is raw genomic data, the complete foundation for any analysis you want to run, now or in the future, with any tool you choose.
What is a FASTQ file?
A FASTQ file is the raw transcript of your genome: millions of short DNA reads captured during sequencing, each paired with a quality score. Think of it as the unprocessed recording of your DNA letters (A, T, C, G) straight off the sequencer. It's the universal starting point for any genomic analysis pipeline, and can be re-analyzed indefinitely as science advances.
What is a VCF file?
A VCF (Variant Call Format) file is a structured list of the places where your genome differs from the reference human genome. These differences, called variants, are the basis for most trait, ancestry, and health predisposition analysis. VCF files are smaller and more portable than FASTQ files, and are directly compatible with most consumer genomics tools and research databases.
What people explore
Your FASTQ/VCF file unlocks access to all of the below, and anything the next generation of genomic tools makes possible. Click any topic to learn more.
Explore with AI tools
10 ways to discover your genome
Getting started is simpler than you think
A growing number of AI-powered platforms can take your FASTQ/VCF file and help you explore your genome in plain language. Here's what you'll generally need:
A place to store your file
Cloud storage (Google Drive, Dropbox, iCloud) or your own external drive works fine. Your FASTQ/VCF file is large, typically 60–100 GB, so plan for storage space accordingly.
An analysis tool or platform
AI-powered genomics tools can process your FASTQ/VCF file and surface insights in everyday language. Many are web-based and designed for curious, non-technical users.
Curiosity and patience
Genomics is a fast-moving field. Having your raw data now means you can explore it today and re-analyze it as new discoveries and tools emerge.
Context for what you find
Genomic data reveals tendencies and predispositions, not certainties. For anything medically significant, follow up with a qualified healthcare provider.
Disclaimer: Genewise delivers your raw sequencing data. We do not interpret your FASTQ/VCF file, provide health reports, predict disease risk, or offer medical recommendations. Any analysis of your genomic data is your responsibility. For medical decisions, consult a qualified healthcare provider.
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