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Preparation of Nucleic Acid Libraries for Next-Generation Sequencers with an Automated Molecular Biology Platform for Unknown Pathogen Detection
Challenges Inherent in Designing and Analyzing Experiments Using NGS
Building a Genome Sequencing Center: Managing and Mining Two Years of NGS Data
The rapid emergence of next-generation sequencing (NGS) is revolutionizing biological research. Technology that was once available only for major sequencing centers, is now available to all as price for entry and time for implementation continues to drop. Purchasing a NGS platform, however, is still a major decision. How do you maximize the greatest potential for your investment? Reaching this potential requires efficient pipeline workflow strategies, careful experimental design, comprehensive targeted enrichment technologies, data analysis, management, and integration, in addition to maintaining your platform and people management all at maximum production. The central theme of Cambridge Healthtech Institute’s Second Annual Beyond Sequencing: Managing Resources and Maintaining NGS Platforms for Peak Performance is gaining efficient use of your NGS platform. Sessions will focus on common bottlenecks, case studies, real-world experiences and solutions from experienced users.
June 20
Pre-Conference Short Courses
June 21
Plenary Session
June 22
Deep Sequencing Breakout Sessions
Hear from Keynote Speakers:
Joseph Costello, Ph.D., University of California, San Francisco
Ronald W. Davis, Ph.D., Stanford Genome Technology Center, Stanford University School of Medicine
Kamlesh D. Patel, Ph.D., Biosystems Research Group, Sandia National Laboratories
Michael Snyder, Ph.D., Stanford Center for Genomics and Personalized Medicine, Stanford University