In a 2016 National Institutes of Health summer internship at
the National Human Genomic Research Institute, Sappington conducted a third research project in which she demonstrated a fast, alignment - free computational method for identifying orthologs — similar genes from species that are related by descent from a common ancestor.
Not exact matches
The U.S.
National Institutes of Health (NIH) has made major investments in network approaches in many areas, including cancer biology, cardiovascular and metabolic diseases, neurophysiology, and
human genetics and
genomics.
«They are developing the clinical
genomics necessary to foster and support the Precision Medicine Initiative of the
National Institutes of Health, and generating the
genomics data that further drives
human genome research.»
Using
genomic analysis to study cancer in dogs can help develop new therapies for
humans with cancer, according to a proof - of - concept study led by the
National Cancer Institute (NCI) and the Translational Genomics Research Institute (TGen).
But determining which specific genetic changes led to
humans won't be easy, says Asao Fujiyama, of RIKEN
Genomic Sciences Center and the
National Institute of Informatics in Japan, one of the project leaders: «The key proteins are very difficult to iron out because we have so many differences.»
Tamayo and team tested REVEALER using The Cancer Genome Atlas (TCGA), the
National Institutes of Health's database of
genomic information from more than 500
human tumors representing many cancer types.
The U.S.
National Human Genome Research Institute and the
National Academy of Medicine recently brought together 25 of these groups to compare projects, to examine the current state of implementation and desired near - term capabilities, and to identify opportunities for collaboration that promote the responsible practice of
genomic medicine.
In 2003, in «A vision for the future of
genomics research,» Francis Collins — who was then the director of the
National Human Genome Research Institute (NHGRI), part of the
National Institutes of Health — and his co-authors encouraged collaboration between basic scientists and clinical scientists, and between life scientists and social scientists, to address the ethical, legal, and social implications of
genomic and genetic research and the resulting new technologies.
The study analyzed data from The Cancer Genome Atlas (TCGA), a research program supported by the
National Cancer Institute and
National Human Genome Research Institute within the
National Institutes of Health that is looking at
genomic changes in more than 20 different types of cancer.
Robert Wildin, M.D., a clinical geneticist with nearly three decades of experience in private and hospital - based medical practice, joined the
National Human Genome Research Institute (NHGRI) on Nov. 10, 2014 as chief of the
Genomic Healthcare Branch (GHB).
VectorBase is a
National Institute of Allergy and Infectious Diseases (NIAID) Bioinformatics Resource Center (BRC) providing
genomic, phenotypic and population - centric data to the scientific community for invertebrate vectors of
human pathogens.
Teri Manolio, Director, Division of
Genomic Medicine,
National Human Genome Research Institute, USA
Moderator: Teri Manolio, Director, Division of
Genomic Medicine,
National Human Genome Research Institute (USA)
The establishment of the CRGGH, a trans -
National Institutes of Health (NIH) effort, brings about an opportunity for it to be a leader in public awareness regarding how
genomics is informing health and
human history.
BETHESDA, Md., Thurs., Oct. 14, 2004 - The
National Human Genome Research Institute (NHGRI), part of the
National Institutes of Health (NIH), today announced it has awarded more than $ 38 million in grants to spur the development of innovative technologies designed to dramatically reduce the cost of DNA sequencing, a move aimed at broadening the applications of
genomic information in medical research and health care.
09:00 09:30 Teri Manolio, Director, Division of
Genomic Medicine
National Human Genome Research Institute, Baltimore, MA, USA
The Co-Chairs for the 2018 AGBT General Meeting are: Eric Green (
National Human Genome Research Institute /
National Institute of Health) Elaine Mardis (The Institute for
Genomic Medicine at Nationwide Children's Hospital) and Len Pennacchio (Lawrence Berkeley
National Laboratory).
«The new studies complement the current GTEx project in assessing
genomic variation and gene expression,» explained Simona Volpi, Pharm.D., Ph.D., GTEx program director in the Division of Genomic Medicine at the National Human Genome Research Institute (NHGRI), which helps administer the p
genomic variation and gene expression,» explained Simona Volpi, Pharm.D., Ph.D., GTEx program director in the Division of
Genomic Medicine at the National Human Genome Research Institute (NHGRI), which helps administer the p
Genomic Medicine at the
National Human Genome Research Institute (NHGRI), which helps administer the program.
Join us on
National DNA Day 2018 — the 15th anniversary of the completion of the
Human Genome Project — to hear from New York Genome Center scientists about how advances in genetics and
genomics are changing people's lives — and what the future holds.
GENYO is the first
national centre devoted to
genomics that integrates the Public Administration, the University and the biotechnology and pharmaceutical business sector, which would allow the integration of research in all its phases, from the generation of knowledge to its development in clinical and pharmaceutical applications, the development of new projects and services for the prevention, diagnosis and treatment of diseases associated to
human genetic variability, such a cancer and rare diseases, diabetes, hypertension or degenerative diseases, among others.