We deliver deep multi-omic insights that enable better
understanding diagnosis treatment of disease
Multi-Omic Services at Broad Clinical Labs
Broad Clinical Labs (BCL) offers comprehensive CLIA certified and CAP accredited fully integrated multi-omic data generation and advanced analysis services for research and clinical applications.
As a subsidiary of the Broad Institute, a national accelerator for science, technology, and translation, we seek to advance multi-omic research, translational, and clinical diagnostics development and application through access to state-of-the art analytical technologies and bioinformatics analysis services.
Clinical Services
Research Sequencing
Multi-Omics & Advanced Technologies
Specialized Services
Download Our Capabilities Guide
For more than 30 years we have been the trusted partner of researchers around the globe to deliver reliable, reproducible data using the latest cutting-edge technologies and services. See our guide to learn how we can partner with you to extract deeper insights from your data.
Featured Service:
Clinical Blended Genome- Exome Sequencing
Blended Genome Exome (BGE) is a qualitative assay that combines low pass genome and deeper exome sequencing of single nucleotide variants (SNVs) and small insertions and deletions (InDels) in human genome DNA extracted from saliva and blood samples. BGE is ideal for large scale germline gene-disease discovery studies where the low pass genome region is used as an unbiased alternative to microarray genotyping in GWAS applications and the clinical depth exome is used for gene panels for monogenic conditions.
Featured Service:
Whole Genome Sequencing Services
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.
Featured Service:
Sequencing of Customer-Prepared Libraries (Walk-Up Sequencing)
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 Ultima Genomics UG 100™ – operated by expert staff, whether you “walk up” to drop libraries off in person or ship them to our facility.
Delivering quality at scale for over 30 years
Whole Genomes
Sequenced
>850,000
Genomic Specimens
Received and
Processed
>3 million
Whole Exomes
Sequenced
>800,000
Genomic Data
Produced
>100 petabases
Blended Genome-
Exomes sequenced
>200,000
Clinical Diagnostic
Tests Returned
(includes COVID-19
testing)
>37 million
Whole Genomes
Sequenced
>650,000
Whole Exomes
Sequenced
>800,000
Blended Genome-
Exomes sequenced
>150,000
Genomic Specimens Received and Processed
>3 million
Genomic Data Produced
>95 petabases
Clinical Diagnostic
Tests Returned
(includes COVID-19
testing)
>37 million
Fastest DNA Sequencing Technique in the World
Get started with Broad Clinical Labs
Step 1
Tell us about your multi-omics project needs
Step 2
Coordinate with a Project Manager
Step 3
Submit your
samples
Step 4
Receive results through cloud data platform
