Frederick Sanger, who died recently at the age of 95, won two Nobel prizes in chemistry for his methods for sequencing proteins and DNA. Proteins were of more direct interest to many people because many disease-causing mutations ...
Dec 4, 2013
0
0
The Human Genome Project concluded in 2003, but many of its benefits are only now being realized, according to Alan Guttmacher, director of the National Institutes of Health's Eunice Kennedy Shriver National Institute of ...
Dec 4, 2013
0
0
With their participation in the completion of the largest cloud-based analysis of genome sequence data, researchers from the Baylor College of Medicine Human Genome Sequencing Center are helping to usher genomic scientists ...
Oct 25, 2013
0
0
They were mystery diseases that had stumped doctors for years—adults with strange symptoms and children with neurological problems, mental slowness or muscles too weak to let them stand. Now scientists say they were able ...
Oct 2, 2013
0
0
As new high-throughput "Next Generation" DNA sequencing methods are moving into clinical applications, understanding accuracy of variants is critical. Numerous recent studies have demonstrated that different sequencing and ...
Sep 19, 2013
0
0
Retinitis pigmentosa (RP) is a genetic disease that causes progressive loss of vision and is caused by mutations in more than 50 genes. Conventional methods for identification of both RP mutations and novel RP genes involve ...
Sep 16, 2013
0
0
European scientists, led by researchers from the University of Geneva (UNIGE)'s Faculty of Medicine in the context of the GEUVADIS project, today present a map that points to the genetic causes of differences between people. ...
Sep 15, 2013
0
0
No two human beings are the same. Although we all possess the same genes, our genetic code varies in many places. And since genes provide the blueprint for all proteins, these variants usually result in numerous differences ...
Sep 5, 2013
0
0
Ten years ago, scientists announced the end of the Human Genome Project, the international attempt to learn which combination of four nucleotides—adenine, thymine, cytosine, and guanine—is unique to homo sapien DNA. This ...
Aug 8, 2013
0
0
Hidden in the tangled, repetitious folds of DNA structures called centromeres, researchers from Harvard Medical School and the Broad Institute have discovered the hiding place of 20 million base pairs of genetic sequence, ...
Aug 8, 2013
0
0
