Data-intensive graph problems abound in the Life Science drug discovery and development process.
An important finding is that by determining the genome sequences of an entire family, one can identify many DNA sequencing errors and thus greatly increase the accuracy of the data. This will ultimately help us understand the role of genetic variations in the diagnosis, treatment, and prevention of disease.
The wellness and prevention market will outgrow the health care market.
Breast cancer isn't one disease - it's probably four or five different types, and without knowing what type a person has, you can't optimize treatment for them.
Your genome sequence will become a vital part of your medical record, thereby providing critical information about how to optimize your wellness.
If you know the mother's genome and the father's genome, and you see that the children have some genes that neither parent has, then you know that difference is either a mutation or a processing error.
