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Through prestigious global partnerships, the Broad Institute works to produce genomic data from the world’s largest biobanks. Our large-scale operation generates high-quality and consistent data that will advance our understanding and treatment of disease.
No organization in the world can offer the infrastructure, services, expertise, or commitment to quality to match that of the Broad Institute.
The Broad CRSP has been really good about implementing tools to make data accessible, browsable, and ready to use to support the scientific community.
We accept a wide range of sample types but will design solutions for unique projects.
We know that they can deliver, and we know that we can trust the data they generate.
Connect to our network via API for secure data transmission. Submit your sample data, follow your sample progress, and receive data in ready-to-use BAM and/or VCF files, pdf, or structured data from our protected system.
Conduct your research. Own your data.
Budget constraints are a reality, but our project management team will work with you to design a plan that fits your budget and maximizes your data.
Discover what reliable, affordable genomic solutions can do for your research.
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As part of our commitment to providing unsurpassed excellence in sequencing, the Broad Institute now offers services utilizing the improved capabilities of the Illumina® NovaSeq X platform.
