WYMM Tour: Nashville
WYMM Tour: Nashville
June 4, 2024, 9:00 - 5:00 pm CT - Nashville, Tennessee, 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 Tuesday, June 4th, 2024 in at the Vanderbilt University Student Life Center 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.
Register
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 | Gregory Goyne, Oxford Nanopore Technologies |
10:15 — 10:45 am | Long-read sequencing reveals diverse patterns of epigenetic inheritance in mice | Adam Davidovich, Johns Hopkins University School of Medicine |
10:45 — 11:00 am | Coffee Break | |
11:00 — 11:30 am | Long-read RNA sequencing identifies region- and sex-specific C57BL/6J mouse brain mRNA isoform expression and usage | Timothy Howton, University of Alabama at Birmingham |
11:30 am — 12:00 pm | Rapid cytogenomic characterization of pediatric leukemias using adaptive sampling | Jeremy Wang, University of North Carolina at Chapel Hill, USA |
12:00 — 1:00 pm | Lunch | |
1:00 — 1:30 pm | Integrating 10x Genomics single cell and spatial profiling with Oxford Nanopore long read sequencing | Ryan Mote, 10x Genomics |
1:30 — 2:00 pm | Bioinformatic analysis of nanopore long reads: variant calling, T2T assembly, metagenomics, and more | Sean McKenzie, Oxford Nanopore Technologies |
2:00 — 2:15 pm | Break | |
2:15 — 2:55 pm | Uncovering the secrets of chromosome rearrangements in cancer | Michael Dean and Isabel Rodrigez, National Institutes of Health |
2:55 — 3:10 pm | Closing | |
3:10 - 5:00 pm | Networking |
Speakers
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Welcome
Stephanie Abernathy, VP Sales, Americas, Oxford Nanopore Technologies
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Introduction and What’s New
Greg Goyne, Sequencing Specialist , Oxford Nanopore Technologies
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Long-read sequencing reveals diverse patterns of epigenetic inheritance in mice
Adam Davidovich, PhD, Feinberg Lab, Johns Hopkins University, USA
Adam Davidovich is a biomedical engineering PhD candidate in the Feinberg Lab at Johns Hopkins Unive...
)
Long-read RNA sequencing identifies region- and sex-specific C57BL/6J mouse brain mRNA isoform expression and usage
Timothy Howton, University of Alabama at Birmingham, USA
Dr. Howton earned his PhD in Biology from the University of Alabama at Birmingham. During his doctor...
)
Rapid cytogenomic characterization of pediatric leukemias using adaptive sampling
Jeremy Wang, University of North Carolina at Chapel Hill, USA
I am an Assistant Professor of Genetics at the University of North Carolina. My lab develops novel s...
)
Uncovering the secrets of chromosome rearrangements in cancer
Michael Dean, NCI, USA
Chromosome instability is a hallmark of cancer, leading to gene amplification, chromosomal gains and...
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Uncovering the secrets of chromosome rearrangements in cancer
Isabel Rodriguez, NCI, USA
I am currently a fellow at the NCI that is deeply committed to advancing healthcare through cutting-...