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Limb-Girdle Muscular Dystrophy (LGMD)

The limb-girdle muscular dystrophy (LGMD) branch of the Rare Genomes Project is a partnership with the Muscular Dystrophy Association and the Jain Foundation dedicated to diagnosis and gene discovery through whole genome sequencing for individuals and families with LGMD.

Esteban Miglietta

I am a Biologist by training and an Image Analyst by choice. Microscopy images allow us a unique insight on cells function and respond to stimuli. As a postdoctoral associate in the Cimini Lab, I aim to learn to apply and develop tools to help researchers turn their beautiful microscopy images into...

For Your Physician

The Rare Genomes Project is a research study at The Broad Institute of MIT and Harvard, a non-profit academic research institution focused on using genomic data to better understand human health and disease. Our team, led by investigator Heidi Rehm, has a specific focus on understanding the genetic...