Find out about the future of NGS and benefit from critical discussions in the accuracy, cost and coverage of short and long read sequencing. Gain insights from thought-provoking presentations on Long read sequencing for human genomes and De Novo Studies, data analysis in de-novo assembly and structural variants, bioinformatics and mapping tools.
The NextGen Omics Series US includes...
Over 350 end users representing internationally renowned research & academic institutions, clinical research institutions, healthcare organisations as well as leading pharmaceutical and biotech companies.
3 outstanding programmes bringing together Europe’s key genomics experts in Next Generation Sequencing, Single Cell Analysis, Genome Editing.
Over 80 case studies, solution & technology presentations and 2 interactive workshops.
Last Year's Agenda at a Glance
Day One
- Discussion Workshop: Accuracy, cost and coverage of short and long read sequencing
- Future Directions In Long Read Sequencing For Human Genomes And De Novo Studies (part 1)
Day Two
- Future Directions In Long Read Sequencing For Human Genomes And De Novo Studies (part 2)
