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Widespread access to genomic medicine vital to RUNX1 study

Scientists are exploring the genomic and clinical profiles of people with RUNX1 familial platelet disorder.
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To accelerate genomics research, we support scientists at public and private institutions around the world.

“Collaboration and teamwork ensure that our genomic advances improve health for all humans. ”

About the National Human Genome Research Institute

At NHGRI, we are focused on advances in genomics research. Building on our leadership role in the initial sequencing of the human genome, we collaborate with the world's scientific and medical communities to enhance genomic technologies that accelerate breakthroughs and improve lives. By empowering and expanding the field of genomics, we can benefit all of humankind.

Our Mission