Next generation sequencing (NGS) has dramatically accelerated the discovery of disease-associated genetic variants. Also known as massively parallel sequencing, this technological tour de force can rapidly “read” a sequence of DNA bases (the “letters” in our genomes) in parallel, making genome sequencing feasible in the research lab. Vanderbilt researchers have developed a “catalog” of human […]
News: Human Mutation
Here are the latest cancer science news nuggets from the Vanderbilt-Ingram Cancer Center, first published in the VUMC Reporter’s Aliquots.
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