Whole Genome Sequencing (30x) — Human & Any Organism

Sequence your entire genome at 30x coverage, the gold standard used in clinical research for $599. Includes raw data (FASTQ), aligned reads (BAM), and variant call file (VCF). Available for humans and any organism with a published reference genome.

For a list of eligible fungal genomes, click here.

For now, we do not ship this kit internationally. However, we are working on making this product available in other countries.

Results in 2–3 weeks. Your data is 100% yours, never sold or shared. Choose to retain or permanently delete your data after delivery.
Allow us to retain your animal's genome data for science? We'll email you a $50 Odin gift certificate within 48 hours of sample receipt.

Your complete genome. Decoded.

Your genome contains approximately 3 billion base pairs of DNA. Most consumer DNA tests analyze only a tiny fraction of this.

Whole genome sequencing reads all of it — every base pair at 30× coverage, the gold standard used in clinical research and advanced genomics.

For $599, you receive your complete genetic sequence:

• Raw data

• Aligned reads

• Variant call file

All delivered in industry-standard formats. Your data is yours to keep, explore, and reanalyze as science evolves.

We sequence humans and any organism with a published reference genome — at the same depth, with the same deliverables, at the same price.

What’s included

• Raw sequencing data (FASTQ) — complete sequencer output, base-called and quality-scored

• Aligned reads (BAM file) — reads mapped to the reference genome

• Variant call file (VCF) — all detected differences from the reference genome (SNPs, indels, structural variants)

• 30× genome coverage — each position read ~30 times for statistical confidence

• Illumina PE150 paired-end sequencing — high-accuracy, full-genome sequencing

• Dedicated consultant access — support before, during, and after sequencing 

How it works:

  1. Collect — Use the kit to take a sample (Humans: saliva or blood. Animals: blood or tissue)
  2. Ship — Send the sample back using a prepaid mailer
  3. Consult — Access expert support at any stage
  4. Analyze — Sequencing at 30× coverage using Illumina PE150 (Receive FASTQ, BAM, and VCF files via secure download)
  5. Apply — Use your data for: health research, ancestry, rare disease analysis, breeding and optimization

Who this is for

• Individuals — full genetic insight for health, ancestry, or personal research

• Breeders — screen hereditary conditions and optimize pairings

• Veterinarians — investigate genetic conditions and unexplained traits

• Researchers — generate publication-quality genomic data

• Conservationists — assess genetic diversity and manage populations

Compatible organisms

Any organism with a published reference genome, including:

• Humans

• Horses, dogs, cats

• Livestock (cattle, pigs, sheep, poultry)

• Aquaculture species (salmon, tilapia, etc.)

• Model organisms (mouse, zebrafish, Drosophila)

• Wildlife species (with proper sampling)

Turnaround & delivery

• Standard turnaround: 2–3 weeks from sample receipt

• Delivery via secure download links

• Includes FASTQ, BAM, and VCF files

Expedited processing available on request.

Why 30× coverage?

Coverage determines confidence in your results.

At 30×:

• Each position is read ~30 times

• Reliable variant detection

• Clinical-grade standard

Below 10×, accuracy drops significantly. At 30×, results are robust enough for real decision-making.

Your data — permanently (read our privacy policy)

Your files are delivered in standard formats compatible with tools like:

• IGV

• GATK

• PLINK

• Samtools

• bcftools

Your data doesn’t expire. As genomic science advances, you can reanalyze your existing data without resequencing.