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A delay in getting sequencing data back can mean a delay in publications, grant milestones, and downstream discoveries. For a translational study, it can mean missing a study cutoff or...Read More
A preprint describing the reference panel behind the All of Us + AnVIL Imputation Service is now available on medRxiv: A 515,579-Genome Reference Panel Improves Rare-Variant Imputation Across Multiple Underrepresented...Read More
Sami Farhi has spent his career convinced that biology needed its own version of the Large Hadron Collider — a way to move past scattered, piecemeal findings and into science...Read More
On June 10, 2026, Broad Clinical Labs hosted a live webinar bringing together clinical and research leaders for an in-depth conversation on how Clinical Blended Genome-Exome Sequencing (cBGE) is reshaping...Read More
As a clinical and translational research service provider, our team at Broad Clinical Labs knows the integrity of your data is everything. You spend months, sometimes years, designing studies, recruiting...Read More
Cloud-native, scalable imputation from Broad Clinical Labs The All of Us + AnVIL Imputation Service helps researchers turn lower-cost genotype array data into richer datasets by filling in missing genetic...Read More
All of Us Research Program Biospecimen Access: An Opportunity to Transform Precision Medicine Through Multi-omics The NIH’s All of Us Research Program has spent 10 years assembling one of the most diverse and richly annotated...Read More
Nomic and Broad Clinical Labs partner to unlock broader applications for proteomics through high-plex, quantitative data that enables cross-study comparable insights. MONTREAL–(BUSINESS WIRE)–Nomic Bio today announced a partnership with...Read More
The National Multi-Omics Accelerator: How Broad Clinical Labs Provides Inclusive Access to Translational Science and Technology For three decades, the genomics field has refined the science and methodology of sequencing....Read More
From Bench to Clinical Scale: Broad Clinical Labs’ Approach to Scaling a Custom Assay Translating a high-performing custom benchtop assay into a reliable, clinical-grade operation at scale is technically challenging....Read More
A delay in getting sequencing data back can mean a delay in publications, grant milestones, and downstream discoveries. For a translational study, it can mean missing a study cutoff...
Sofia Labrecque
A preprint describing the reference panel behind the All of Us + AnVIL Imputation Service is now available on medRxiv: A 515,579-Genome Reference Panel Improves Rare-Variant Imputation Across Multiple...
Sami Farhi has spent his career convinced that biology needed its own version of the Large Hadron Collider — a way to move past scattered, piecemeal findings and into...
On June 10, 2026, Broad Clinical Labs hosted a live webinar bringing together clinical and research leaders for an in-depth conversation on how Clinical Blended Genome-Exome Sequencing (cBGE) is...
As a clinical and translational research service provider, our team at Broad Clinical Labs knows the integrity of your data is everything. You spend months, sometimes years, designing studies,...
Cloud-native, scalable imputation from Broad Clinical Labs The All of Us + AnVIL Imputation Service helps researchers turn lower-cost genotype array data into richer datasets by filling in missing...