Advances in sequencing technologies and the rapid adoption of next-generation sequencing (NGS) in translation oncology and biomedical research have spear-headed the effort worldwide of genome-wide personalized medicine. With greater speed, greater resolution, all at a lower cost, NGS greatly facilitates the in-depth genome-wide search for all mutations, including CNVs, SNVs, and fusions.
Join us for an application seminar to explore the possibilities on how Agilent NGS workflow solution, from sample to data reporting, can help you uncover the answers to drive your research forward.
For more details, please refer to the specific country’s agenda.
Don’t miss out on this opportunity to meet with the experts and network with peers! Register now for the event in your city to reserve a seat.
We hope to see you at our roadshow!
For Research Use Only. Not for use in diagnostic procedures.
