Broad Institute of MIT and Harvard

The Broad Institute is a genomic medicine research center located in Cambridge, Massachusetts, United States. Although it is independently governed and supported as a 501(c)(3) nonprofit research organization, the institute is formally affiliated with the Massachusetts Institute of Technology, Harvard University and its affiliated hospitals. The faculty and staff of the Broad Institute include physicians, geneticists, and molecular, chemical, and computational biologists.

Address
Broad Institute scientists and administrators are currently located in three buildings: 7 Cambridge Center, 5 Cambridge Center and 320 Charles Street in Cambridge, MA.
E-mail
news@broadinstitute.org
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Taking on melanoma, one cell at a time

Single-cell analysis is a groundbreaking approach now being used across biological fields to explore a common problem: how to study cellular diversity in cell environments with heterogeneous populations. Such diversity can ...

Apr 08, 2016
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Illuminating the broad spectrum of disease

In a paper published in Nature Biotechnology, researchers from the Broad Institute of MIT and Harvard and the Dana-Farber Cancer Institute describe a new method that dramatically simplifies an arduous experimental process ...

Feb 29, 2016
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Genome misfolding unearthed as new path to cancer

In a landmark study, researchers from the Broad Institute and Massachusetts General Hospital reveal a completely new biological mechanism that underlies cancer. By studying brain tumors that carry mutations in the isocitrate ...

Dec 23, 2015
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Harnessing chemical and genomic data to fight cancer

In the years since the human genome was first sequenced, a trove of genomic data has been amassed, aiding not only in our understanding of how the body works, but also in the search for disease-fighting drugs. Indeed, finding ...

Dec 17, 2015
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Rare gene mutations raise risk of early heart attack

A team of investigators from the Broad Institute, Massachusetts General Hospital and other leading biomedical research institutions has pinpointed rare mutations in a gene called APOA5 that increase a person's risk of having ...

Dec 10, 2014
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