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. Results in 2–3 weeks.

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

• Agricultural producers — improve traits and breeding efficiency

• 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.)

• Crops (wheat, maize, soybean)

• 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

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.