A look at the future of health sciences…
Up until now very few genomes had been sequenced and identifying the cause of diseases based on genomic data seemed out of reach. Now two labs working independently have successfully sequenced the genomes of patients suffering from disease, and for only $50 000. This is a huge feat considering only ten years ago it cost $500 million to sequence one genome. Complete Genomics believes they can currently sequence a genome for $25 000 and that it won’t be long until they reach their $5 000 genome goal. [New York Times]
Decreased costs of sequencing means more more genomes sequenced. More genomes sequenced means a better more accurate library of genetic data. A rich genetic library allows for accurate statistical and medical analysis to be performed and will in the end result in better identification and treatment of disease.
