WYMM Tour: Minneapolis
March 21, 2024, 9:00 - 5:00 pm CT - Minneapolis, Minnesota, United States
Generate ultra-rich data for answers with impact.
Who says you can’t see it all? With a comprehensive view of structural variants and methylation, nanopore technology powers the bigger and bolder research questions you’ve always wanted to ask.
Join us on Thursday, March 21st, 2024 in McNamara Alumni Center at the University of Minnesota to hear from local experts who are breaking new ground in human genomics, using nanopore technology.
What you're missing matters. Stay on top of what's next.
Aside from talks ranging from human genomics for rare disease, to sequencing for cancer research, the full-day agenda will include networking breaks, Q&A, product displays, and opportunities to engage with your peers and nanopore experts.
Please note that this is an in-person event.
There is no delegate fee for this event, but registration is required. Lunch and refreshments will be provided. Your place at this event will be confirmed via email from events@nanoporetech.com.
Agenda
9:00 am — 5:00 pm CT | Agenda (subject to change) | Speaker |
|---|---|---|
9:00 — 9:30 am | Registration/Breakfast | |
9:30 — 9:45 am | Welcome | Oxford Nanopore team |
9:45 — 10:15 am | Nanopore sequencing, the latest and greatest updates | Brandon Blakey, Oxford Nanopore Technologies |
10:15 — 10:45 am | Got snot? Sequencing-based testing for respiratory viruses | Beth Thielen, University of Minnesota |
10:45 — 11:00 am | Coffee Break | |
11:00 — 11:30 am | Resolving “dark” genomic sequences in clinically relevant genes, such as SMN1 and SMN2, using an Oxford Nanopore PromethION | Devin Oglesbee, Mayo Clinic |
11:30 am — 12:00 pm | Answers in hours – A prospective clinical study for rapid detection of pathogens and antibacterial resistance in surgical patients using Oxford Nanopore Sequencing | Emma Whittle, Mayo Clinic |
12:00 — 1:00 pm | Lunch | |
1:00 — 1:30 pm | Enteric pathogens in the neonatal intestine | Kathryn Knoop, Mayo Clinic |
1:30 — 2:00 pm | Development of a single comprehensive genomic test based on long-read sequencing technology for the diagnosis of rare genetic disorders | Siddhartha Sen, University of Minnesota |
2:00 — 2:15 pm | Break | |
2:15 — 2:45 pm | Genome skimming for epigenetics: fast, inexpensive, and precise global DNA methylation | Christopher Faulk, University of Minnesota |
2:45 — 3:00 pm | Closing | |
3:00 - 5:00 pm | Networking |
