lot of commentary out there that, ok, yes, it sounds great in theory to do this genomic work and biomarker work, but at the very basic analytical level, are we at the right level? are we mature enough with those analytical tools that we can actually say, ok, we are actually measuring accurately the genetic profile of the patient and being able to make the decisions on that basis? lynn: it comes down to don't throw the baby out with the bathwater. it comes down to the research component of it and the practical patient treatment component of it. right now, yes, it is not what hundred percent certain that it will respond to a receptor like pancreatic cancer. i have no evidence of that, but i have seen it work in other cancers. this patient has very little options. i see no reason to say, well, i really have got to check their genomic dna and they should that this is right. you know, it is the perfect standing in the way of the good and moving forward. in a research setting, yes, we should be doing that. in a research setting, you should be sequencing both the tumor as well as the normal dna,