Broad Clinical Research Sequencing Platform is now Broad Clinical Labs! Explore our new website to access our trusted services.
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Broad Clinical Research Sequencing Platform is now Broad Clinical Labs! Explore our new website to access our trusted services.
From the world’s first human genome to our 550,000th, we’ve been delivering quality at scale for more than 30 years.
Broad Clinical Labs (BCL), a CLIA licensed and CAP accredited wholly owned subsidiary of the Broad Institute, offers services to power your multi-omic data generation and analysis needs, across a range of research, translational, and clinical Dx applications.
Whole Genome sequencing from $350
Blended Genome-Exome sequencing from $99
BCL develops and offers impactful services to the world, powers transformative projects, and drives adoption of the latest technologies and novel molecular assays. As a non-profit backed by 30+ years of expertise and partnership with thought leaders in the Broad community and beyond, you can trust us to deliver dependable, advanced multi-omic services at competitive prices.
Access whole genome sequencing services backed by 30 years of field-leading experience in providing high-quality, reliable data at scale. With a variety of modalities, outputs, and add-ons, our WGS services offer end-to-end solutions, from research to clinical diagnostic applications, to meet your needs.
Need rapid turnaround sequencing for your pre-constructed libraries and library pools? Our convenient Walk-Up Sequencing (WUS) service provides access to the latest sequencing technologies – including the Illumina® NovaSeq X Plus, PacBio Revio™, and Element AVITI™ – operated by expert staff, whether you “walk up” to drop libraries off in person or ship them to our facility.
Whole Genomes
Sequenced
>550,000
Genomic Specimens
Received and
Processed
>3 million
Whole Exomes
Sequenced
>775,000
Genomic Data
Produced
>95 petabases
Blended Genome-
Exomes sequenced
>100,000
Clinical Diagnostic
Tests Returned
(includes COVID-19
testing)
>32 million
Whole Genomes
Sequenced
>550,000
Whole Exomes
Sequenced
>775,000
Blended Genome-
Exomes sequenced
>100,000
Genomic Specimens Received and Processed
>3 million
Genomic Data Produced
>95 petabases
Clinical Diagnostic
Tests Returned
(includes COVID-19
testing)
>32 million
Tell us about your sequencing needs
Coordinate with a Project Manager
Submit your
samples
Receive results through cloud data platform
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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.
