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Adam Felsenfeld: All right. I think Ill just move on in to the concept clearance and Im going to start with a little bit of introduction and just lead in to the common disease variant discovery discussion. So Im going to begin again with the workshop wish list and note that today, even though clinical applications of sequencing was discussed as a central topic, Im not going to discuss that today. Its its own program; it has its own planning process, but obviously those programs -- those groups of programs are going to consider the discussions at the workshop. The same with the big need to enable capture, interpretability, and analysis of the world sequencing data and a bit about creating this virtuous cycle. Those are items that need their own discussion, and we just heard before Phil Bourne talk about some things that bare docHubly on this one. Similarly, were not today going to talk about -- or talk very much about doing genome function especially related to interpretation
