FDA Embraces Personalized Medicine
Food and Drug Administration Acting Director Frank Torti announced Monday in a podcast the creation of a new position in the Office of Chief Scientist: the Senior Genomics Advisor. Dr. Liz Mansfield, a scientist who has worked on scientific policy [...]


Copy number variation refers to the fact that the number of copies of a gene, or deletions from sequences within a person’s DNA, along with the placement of those copies or deletions, contributes to his or her inherited characteristics. That is, the copies or deletions are themselves genetic information. Using sequencing methods, researchers can identify the variation in sequence patterns across a population. Spotting those variations is one challenge, but associating them with observable characteristics is another matter altogether.
Earlier this week, Complete Genomics announced that it will offer complete human genome sequencing for the low, low price of $5000. But as the blog Genetic Future points out, in this industry, profits will to flow to companies that can offer the best interpretation of genetic information, not just the fastest and cheapest sequencing.
Today the FDA released its long-awaited—and in some quarters, long feared—proposed new rules for marketing foods from animals that have been genetically engineered to have particular traits.
At the beginning of the month, NIH pulled pooled GWAS data from its website and began encouraging other institutions to follow suit, because a team of scientists have figured out just how to identify a single person’s DNA from a sample of hundreds.
