Please join us for a live Webcast that we are hosting specifically for members of ABCD, with Dr. Valerie Nedbal, PhD, SAS Institute, on Tuesday, March 18 at 11:00:

Register now for this event

The comprehensive assessment of drug safety is an essential component of clinical trials. The review of the drug's safety has greatly advanced in recent years by access to dynamically interactive graphs from different areas of data safety. During this presentation, we will demonstrate:

• How to segment subgroup of population based on drug effectiveness
• How to identify population structure and relatedness
• How to perform a meta-analysis of Genome Wide Associationto identify biomarkers associated with a particular drugrelated trait
• How to identify a molecular signature of the patients by means of linear regression
• How to predict the outcome of a treatment by means on biological profiles
• How to analyse and visualize cytometric data

Effectively address these topics is only possible through advanced and robust statistics combined with visual graphics. A clinical study of patients who underwent aneurysmal subarachnoid hemorrhage will provide illustration. The analyses from combined JMP Genomics and JMP Clinical, software that combines the analytical power of SAS and a graphic, dynamic and elegant interface of JMP, will demonstrate key concepts.

Register now · Information on JMP Clinical · Information on JMP Genomics