Discover demonstrated workflows for cancer and genetic disease medical research
Thursday, November 17, 2016
noon–2:45 p.m.
Biodesign Institute A (BDA) auditorium, Tempe campus [map]
Register to attend this free event — space is limited!
This year, next-generation sequencing (NGS) is easier and more affordable than ever. Whether you’re new to NGS or an NGS veteran, Illumina’s latest advancements offer research advantages for labs of any size. These solutions are so simple and intuitive no previous NGS experience is required.
Explore the possibilities and get up to speed on all the updates, including targeted resequencing for oncology, genetic disease medical research and general molecular biology applications, streamlined workflows, and simplified onboard analysis.
- Meet the MiniSeq™ System, Illumina’s simplest, smallest, most affordable sequencing solution yet.
- Explore streamlined, demonstrated workflows from library preparation through easy onboard data analysis.
- See for yourself how easy NGS data analysis is in our live demonstration.
