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Event
NSIGHT explores the implications, challenges and opportunities associated with the possible use of genomic sequence information during the newborn period.
… Related Resources … The Newborn Sequencing in Genomic Medicine and Public Health …
News Release
A new method of targeting specific DNA sequences in zebrafish could accelerate the discovery of gene function and the identification of disease genes in humans.
… in humans, according to scientists at the National Human Genome Research Institute (NHGRI), part of the National … 5, 2015, and to be published in the July 2015 issue of Genome Research , the researchers reported that the … copies of a specific DNA sequence) and high-throughput DNA sequencing, the researchers determined that overall, …
Staff
Dr. Tyra Wolfsberg is the associate director of the Bioinformatics and Scientific Programming Core at the National Human Genome Research Institute. ​
… and retroviral integration sites to the annotation of the genome of the ctenophore Mnemiopsis leidyi . Dr. Wolfsberg … is the co-chair the NIH lecture series Current Topics in Genome Analysis . The lectures, through their availability … JC, O'Hara AJ, Le Gallo M, Urick ME; NISC Comparative Sequencing Program, Cruz P, Zhang S, Hansen NF, Godwin AK, …
Staff
Dr. Sean Conlan is an associate investigator in the Translational and Functional Genomics Branch at the National Human Genome Research Institute.​
… and basic research. The MGS uses a variety of DNA sequencing strategies and platforms to answer basic research … Program, Frank KM, Palmore TN and Segre JA. Whole genome sequencing overrules a suspected case of … Program, Palmore TN, Frank KM and Segre JA. Complete genome sequence of a Klebsiella pneumoniae carrying bla NDM-1 …
News Release
Clinical applications of genomics in neurology and psychiatry will be the focus of the 2014 lecture series Genomics in Medicine at Suburban Hospital.
… an upcoming lecture series sponsored by the National Human Genome Research Institute (NHGRI) in collaboration with …
News Release
Researchers have released a new high-quality collection of reference human genome sequences that captures substantially more diversity from different human populations than what was previously available.
… More complete and sophisticated collection of genome sequences captures significantly more human diversity. … of different genomes from which to compare an individual genome sequence. Like a map of the subway system, the … read. Recent technological advances such as long-read DNA sequencing, which reads longer stretches of the DNA at a …
Staff
Diana Bianchi is an adjunct investigator in the Medical Genetics Branch at the National Human Genome Research Institute. ​
… microchimerism and noninvasive prenatal testing using DNA sequencing of fetal and placental DNA fragments. … Dr. … in pregnant women whose DNA sequencing results demonstrate genome-wide imbalance, which suggests that there may be a … in the Medical Genetics Branch at the National Human Genome Research Institute. … Diana Bianchi, Prenatal testing, …
News Release
The Genetics/Genomics Competency Center (G2C2) resource has been expanded to include a new collection of resources for physicians.
… in genetics and genomics, created by the National Human Genome Research Institute's (NHGRI) Genomic Healthcare …
News
NHGRI launched a new round of strategic planning to establish a 2020 vision for genomics research that will accelerate scientific and medical breakthroughs.
… John Ohab … The National Human Genome Research Institute (NHGRI) today launched a new round … 82nd meeting of the National Advisory Council for Human Genome Research. The process will culminate in the … the 30th anniversary of the launch of the Human Genome Project, the international effort that first mapped a …
News Release
An international team of researchers including NIH has completed the first comprehensive characterization of genomic diversity across sub-Saharan Africa.
… , is the first to use both dense genotyping and whole-genome sequence data to explore the genomic-variation … ethno-linguistic groups. A genotype is a subset of a whole-genome sequence, which is the complete read-out of an … assemble data from genotyping or from whole-genome sequencing to identify the particular pattern of DNA …