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The National Human Genome Research Institute conducts genetic and genomic research, funds genetic and genomic research and promotes that research to advance genomics in health care.


Doctor showing sequence data on iPad to patient

New NIH-ACMG fellowship to boost pool of physicians managing genomic medicine programs

The National Institutes of Health (NIH), in partnership with the American College of Medical Genetics and Genomics (ACMG), is seeking qualified physicians interested in acquiring credentials and experience to lead genomic medicine research and implementation programs at the NIH, major medical centers and other organizations. The goal of this fellowship is to increase the pool of physicians trained in managing research and implementation programs in genomic medicine.

Jeffrey Schloss

Jeffery Schloss, a pioneer of genome sequencing technology, retires

Jeffery Schloss, Ph.D., director of the Division of Genome Sciences at NHGRI, has retired after a successful career leading NHGRI's DNA Sequencing Technology Development Program and launching the Centers of Excellence in Genomics Sciences (CEGS) program. Known for his intellect, leadership and dedication, Dr. Schloss shares the story of his career path and the significant contributions he and his team achieved while at NHGRI.


NIH study reveals how melanoma spreads

Newly identified genes and genetic pathways in primary melanoma - the most serious form of skin cancer - could give researchers additional targets for developing new, personalized treatments for melanoma and, potentially, other cancers. Learning how these genes are expressed - turned on or off - could be used in the future to predict how and when the cancer cells will spread to other parts of the body and how fast they will grow. Read the study in the February 6, 2017, online issue of Pigment Cell and Melanoma Research.

Induced pluripotent stem cells (iPSC)

Findings: Induced pluripotent stem cells don't increase genetic mutations

Despite immense promise, adoption of induced pluripotent stem cells (iPSCs) in biomedical research and medicine has been slowed by concerns that these cells are prone to increased numbers of genetic mutations. A new study by NHGRI scientists suggests that iPSCs do not develop more mutations than cells that are duplicated by subcloning. Read the study in the early edition of The Proceedings of the National Academy of Sciences. for February 6, 2017.

Eric Green, M.D., Ph.D.>

Workshop on the Use of Race and Ethnicity in Genomics and Biomedical Research

In the February The Genomics Landscape, NHGRI Director Eric Green reports on an NHGRI and National Institute on Minority Health and Health Disparities (NIMHD) workshop held in October, which addressed the use of race and ethnicity data in genomics, and biomedical and clinical research. Also included: A new policy for the protection of human subjects, newborn sequencing, the next phase of ENCODE and a new fellowship now available in genomic medicine program management.