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Next Generation Sequencing (NGS) is rapidly becoming an indispensible and widely used tool in clinical genetics settings, and in academic, pharma and biotech research laboratories. NGS has made the concept of personalised medicine and rapid whole genome queries closer to reality, empowering clinicians to make genetically informed decisions. However, the fast pace of NGS technology development and the emerging new applications and platforms can be daunting, in particular for newcomers to the field. Our 2nd Oxford Next Generation Sequencing event, NGS 2014, is aimed at providing a one-stop learning solution to this rapidly evolving technology. NGS2014 will consist of three key components*:
Furthermore, NGS2014 will also provide participants with an excellent opportunity to interact with technology platform and solution providers, exhibiting and presenting at the event. Our sponsors will indeed benefit by interacting with new and old NGS users and by strengthening existing contacts and developing new leads. Therefore, NGS2014 will provide an excellent programme package for everyone interested in NGS.
Places will be allocated on a first-come-first-served basis.
*Delegates will be able to register for individual components or for the whole programme. Discounts will be available for those attending more than one component of NGS2014. See Registration and fees
Alumni discount: As a show of our appreciation we are pleased to offer 10% discount on registration fees to returning participants, in addition to group and multi-component discounts.