A study of whole genome sequencing found that while many people discovered genetic variations linked to rare diseases they didnt overreact to the newsAdvances in technology have made it much easier faster and less expensive to do whole genome sequencing to spell out all three billion letters in a persons genetic code Falling costs have given rise to speculation that it could soon become a routine part of medical care perhaps as routine as checking your blood pressureBut will such tests which can be done for as little as 1000 prove useful or needlessly scaryThe first closely-controlled study aimed at answering that question suggests that doctors and their patients can handle the flood of information the tests would produce The study was published Monday in Annals of Internal MedicineWe can actually do genome sequencing in normal healthy individuals without adverse consequences and actually with identification of some important findings says Teri Manolio director of the division of genomic medicine at the National Human Genome Institute which funded the study Manolio wrote an editorial accompanying the paper More >>