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. Our end-to-end multi-omics services cover genomics, transcriptomics, epigenomics, and proteomics, supported by spatial profiling and data sciences.
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. Our scalable services support programs from discovery through clinical validation, including large-scale biopharma and population studies.
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:
Spatial Profiling Technology
Access in situ spatial profiling services that deliver targeted gene expression data with preserved spatial context, driven by 10x Genomics Xenium chemistry. Coming soon: We’re expanding our capabilities by adding the 10x Genomics Atera and Illumina StrataMap platforms for whole transcriptome coverage.
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.
Scalable Sequencing Backed by Over 30 Years of Experience
Whole Genomes
Sequenced
>966,000
Genomic Specimens
Received and
Processed
>3 million
Whole Exomes
Sequenced
>1.2 million
Genomic Data
Produced
>170 petabases
Blended Genome-
Exomes sequenced
>418,000
Clinical Diagnostic
Tests Returned
(includes COVID-19
testing)
>37 million
Whole Genomes
Sequenced
>966,000
Whole Exomes
Sequenced
>1.2 million
Blended Genome-
Exomes sequenced
>418,000
Genomic Specimens Received and Processed
>3 million
Genomic Data Produced
>170 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
