Maximize your research potential with precision whole genome sequencing, curation, and interpretation.
Our research services are powered by revolutionary technology and backed by a team of world-class experts in medical, genomic science, computer science, and bioinformatics. We offer research use and clinical use (CLIA-certified, CAP-accredited) whole genome sequencing and analytics services in 2 weeks.
Our San Diego lab is CLIA-certified and CAP-accredited, serving both clinical and research demand. Our CLIA-validated tests are eligible for FDA submission for Phase II & III clinical trials.
Get access to the latest Illumina and Ultima sequencers for high-throughput data generation (including NovaseqTM X+, UG 100TM) and somatic and germline whole genome sequencing analysis through our proprietary pipeline.
Our proprietary, automated bioinformatics pipelines, which were developed with 13,000+ cancer and rare disease WGS cases, interpret the WGS data. 15 expert genomic scientists (MD/PhDs in genomic science, computer science and bioinformatics) curate the insights additionally.
Get customized support for what you need. We could provide sequence only, analytics/curation only or full services with either standardized or customized reports. In addition, our experts can offer advisory services upon your requests.
Sequencing only
Bioinformatics only
End-to-end services
Our team of MDs and PhDs specialize in medical, genomic science, computer science and bioinformatics and provide expert advisory services on an hourly or project basis
Our diverse clients and partners span biopharmaceuticals, biotechs, research organizations, biobanks, health techs, academic and clinical labs, health systems and beyond. We provide our services at affordable prices thanks to high-level automation and high-throughput sequencing technology. Unlock the full potential of your research – reliably in 2 weeks.