Biotechnology Services | The Open Discovery Institute

Sequence a Genome.

Build Your Project

Get 30× whole genome sequencing with standard data files, or work with our team on custom genetic engineering projects built around your research.

30× Sequencing

Whole Genome Sequencing

We sequence human and other supported genomes at approximately 30× coverage using Illumina paired-end sequencing.

You receive FASTQ, BAM, and VCF files in standard formats, so you can keep the data, analyze it with the tools you choose, or share it with a researcher or clinician.

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Designed for Clinical Accuracy

With 100% Data Protection

Your Data, Your Files

We do not sell or license customer genomic data. Your FASTQ, BAM, and VCF files are delivered directly to you.

Retention Is Your Choice

Choose whether we retain your genomic files for future access or delete them after delivery. The choice is yours.

Clinical Research
Standard

Sequenced at approximately 30× coverage using Illumina paired-end reads, with standard FASTQ, BAM, and VCF outputs.

Standard Data Files

Download FASTQ, BAM, and VCF files for use with standard genomics tools, research pipelines, or your own analysis.

Coming Soon

Custom Genetic

Engineering Services

Some projects need more than an off-the-shelf kit. The ODIN is building a custom genetic engineering service for researchers, startups, labs, breeders, and independent projects with a specific biological problem to solve.

Tell us what you’re trying to make, test, or modify. We’ll look at the organism, the technical requirements, and what the project would actually take, then tell you whether it’s something we can help with.

The service is still in development, but we’re already interested in unusual projects.

What We Expect to Work On: