An infection with Epstein-Barr virus is a nonevent for most people. But for a subset, the virus can contribute to chronic ...
Rutgers Develops New Tool for Examining Cancer Genomic Data that Could Improve Treatment When scientists sequence tumor DNA, ...
Ferns, defined by large genomes, high chromosome counts, and pervasive aneuploidy as well as intraspecific polyploid ...
Morning Overview on MSN
New AI model could radically change genetic testing and drug discovery
A new generation of artificial intelligence is starting to read the human genome with a fluency that would have sounded like ...
Researchers at Forschungszentrum Jülich and Heinrich Heine University Düsseldorf have developed a tool that could significantly transform genome research: Helixer identifies genes directly from DNA ...
A newly published paper in Nature describes the complex process of launching a nine-country collaboration in Africa to ...
The complete genome of an ancient Egyptian has been sequenced, revealing genetic links between the Nile and Mesopotamia 5,000 ...
Researchers have unlocked a way to read a baby’s genome in hours, not days, paving the path toward same-day genetic answers for the most fragile patients. Boston researchers sequenced a full human ...
Genomic medicine relies on single reference genomes that miss crucial genetic diversity, creating diagnostic gaps that disproportionately affect underrepresented populations. Pangenome graphs, ...
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