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"Matching" consent to purpose: The example of the Matchmaker Exchange.
Dyke SOM, Knoppers BM, Hamosh A, et al. "Matching" consent to purpose: The example of the Matchmaker Exchange. Hum Mutat. 2017;38(10):1281-1285. doi:10.1002/humu.23278DOIPubMedGoogle Scholar
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Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.
Wolf SM, Amendola LM, Berg JS, et al. Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium. Genet Med. 2018;20(5):545-553. doi:10.1038/gim.2017.137DOIPubMedGoogle Scholar
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A Decade of Genetic and Metabolomic Contributions to Type 2 Diabetes Risk Prediction.
Merino J, Udler MS, Leong A, Meigs JB. A Decade of Genetic and Metabolomic Contributions to Type 2 Diabetes Risk Prediction. Curr Diab Rep. 2017;17(12):135. doi:10.1007/s11892-017-0958-0DOIPubMedGoogle Scholar
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Precision medicine in diabetes: an opportunity for clinical translation.
Merino J, Florez JC. Precision medicine in diabetes: an opportunity for clinical translation. Ann N Y Acad Sci. 2018;1411(1):140-152. doi:10.1111/nyas.13588DOIPubMedGoogle Scholar
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Rapid and deep-scale ubiquitylation profiling for biology and translational research.
Udeshi ND, Mani DC, Satpathy S, et al. Rapid and deep-scale ubiquitylation profiling for biology and translational research. Nat Commun. 2020;11(1):359. doi:10.1038/s41467-019-14175-1DOIPubMedGoogle Scholar
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Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice.
Landry LG, Ali N, Williams DR, Rehm HL, Bonham VL. Lack Of Diversity In Genomic Databases Is A Barrier To Translating Precision Medicine Research Into Practice. Health Aff (Millwood). 2018;37(5):780-785. doi:10.1377/hlthaff.2017.1595DOIPubMedGoogle Scholar
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Genetics of coronary artery disease: discovery, biology and clinical translation.
Khera AV, Kathiresan S. Genetics of coronary artery disease: discovery, biology and clinical translation. Nat Rev Genet. 2017;18(6):331-344. doi:10.1038/nrg.2016.160DOIPubMedGoogle Scholar
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Single-cell analyses to tailor treatments.
Shalek AK, Benson M. Single-cell analyses to tailor treatments. Sci Transl Med. 2017;9(408). doi:10.1126/scitranslmed.aan4730DOIPubMedGoogle Scholar
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The NIH's role in accelerating translational sciences.
Reed JC, White L, Aubé J, et al. The NIH’s role in accelerating translational sciences. Nat Biotechnol. 2012;30(1):16-9. doi:10.1038/nbt.2087DOIPubMedGoogle Scholar
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Precision oncology: an overview.
Garraway LA, Verweij J, Ballman KV. Precision oncology: an overview. J Clin Oncol. 2013;31(15):1803-5. doi:10.1200/JCO.2013.49.4799DOIPubMedGoogle Scholar
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In March of 2020, Broad Institute converted a clinical genetics processing lab into a large-scale COVID-19 testing facility in less than two weeks.

We've screened more than 1,275 cancer cell lines as part of the Cancer Dependency Map (DepMap).

Broad Genomics Platform sequences a whole human genome every four minutes.

More than 11,000 individuals living with cancer in the United States and Canada have partnered with Count Me In to share their experiences and help accelerate cancer research.

The Drug Repurposing Hub is one of the most comprehensive and up-to-date biologically annotated collections of FDA-approved compounds in the world. Researchers anywhere can explore more than 6,000 drugs in the hub and search for possible new uses for them to jump-start new drug discovery.

In 2021, our sustainability efforts sent more than 80 percent of waste from the Genomics Platform to either a recycling facility or to an incineration plant that generates electricity.

Through Broad's Scientists in the Classroom program, Broad researchers visit every 8th grade classroom in Cambridge each year to talk about genetics and evolution.

Every summer, 18 high school students spend six weeks at Broad working side-by-side with mentors on cutting-edge research.

In November 2022, Broad’s Genomics Platform sequenced its 500,000th whole human genome, a mere four years after sequencing its 100,000th.

By the end of 2022, Broad’s COVID-19 testing lab had processed more than 37 million tests.

Working with Addgene, Broad Institute has shared CRISPR genome-editing reagents with researchers at more than 3,200 institutions in 76 countries.

The NeuroGAP-Psychosis project, a collaboration between the Stanley Center for Psychiatric Research and Harvard T.H. Chan School of Public Health to study the genetics of severe mental illness, has recruited more than 42,000 participants in Ethiopia, Kenya, Uganda, and South Africa.

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