While the cost of sequencing declines, use in academic, clinical, biotech, and pharmaceutical labs expands, paving the way for the creation of innovative new markets for bioresearch. By delivering fast, diverse, precise, and large volumes of data, NGS extends our fundamental understanding of genomics, mutation, and gene function and regulation. CHI's Applying Next-Generation Sequencing investigates the applications of next-generation sequencing platforms as they apply to your specific research projects. Sessions will provide insights into the active genome through transcription, as well as the impact of sequencing on personalized medicine.
Day One – Plenary Keynote Sessions
- Plenary Keynote Session
- Plenary Sequencing Selects
Day Two – Combined Sessions
- Sequencing from Personalized Genomics to Personalized Medicine
- Transcription – Insights into the Active Genome
Day Three – Combined Sessions
- Sequencing Cancer from Development to Detection
- Sequencing Cancer from Detection to Diagnosis
- Next-Next Generation Sequencing
Short Courses
Sunday, September 25
Tuesday, September 27
To view the final agenda of each short course, please click here.