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

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

What do you want us to do with your data? Retain my data on secure servers Permanently delete my data within 30 days of delivery

Organism Category Human Pet Fungus (see eligible species)

$599.00 USD

See the list of fungal reference genomes we currently support, click here

Width: 10 (in)
Height: 1 (in)
Depth: 6 (in)
Weight: 0.18 (kg)

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

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Product Details

Your genome, sequenced at 30×.

Most consumer DNA tests look at a selected set of variants. Whole genome sequencing reads across the entire genome instead.

We sequence at approximately 30× coverage using Illumina paired-end reads, then deliver the resulting FASTQ, BAM, and VCF files to you.

For $599, you receive the following sequencing files:

Raw data

Aligned reads

Variant call file

All delivered in standard genomics formats. Your files are yours to keep and reanalyze as tools and research evolve.

We sequence humans and other supported organisms with a published reference genome at the same depth, with the same core data files, and at the same price.

Share Animal Genome Data for Research?

We'll email you a $50 Odin gift certificate within 48 hours of sample receipt.

Turnaround & Delivery

Standard Turnaround

Results in 2–3 weeks from sample receipt. Expedited processing available on request.

We do not sell or license customer genomic data. Choose whether we retain your files or delete them after delivery.

Delivery via secure download links.

Includes FASTQ, BAM, and VCF files.

International Shipping

For now, we do not ship this kit internationally.

However, we are working on making this product available in other countries.

Who Is It 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.

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)

Differences identified against the reference genome, including SNPs, insertions, and deletions.

30× Genome Coverage

Average genome coverage of about 30× across the sample.

Illumina PE150
Paired-End Sequencing

Paired-end reads across the whole genome.

Dedicated Consultant Access

Support before, during, and after sequencing.

Collection Kit

Kit for collecting biological material needed for sequencing.

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)

Why 30× Coverage?

Coverage affects confidence in variant calling.

At 30×:

Each position is read ~30 times

Reliable variant detection

Clinical-grade standard

More sequencing depth gives the pipeline more evidence, helping separate real variants from errors.

Your Data, Ready to Reuse

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

IGV

GATK

PLINK

Samtools

bcftools

Because you receive FASTQ, BAM, and VCF files, you can store and reanalyze them later as tools and methods improve.

Read WGS Data & Privacy

How It Works

01

Collect

Use the collection kit to provide the sample type required for your organism.

02

Ship

Send the sample back using a prepaid mailer.

03

Consult

Access expert support at any stage.

04

Process

Your sample is sequenced at approximately 30× coverage, and FASTQ, BAM, and VCF files are prepared for delivery.

05

Apply

Use your data for: health research, ancestry, rare disease analysis, breeding and optimization.

Important

If whole genome sequencing identifies significant microbial contamination in your sample, a repeat sequencing run may be required, and additional sequencing charges may apply.

To help prevent contamination: