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WYMM Tour: Bangkok
Thursday 16th January 2025, 09:30 - 16:30 - Bangkok, Thailand (THA/GMT+7) (timings subject to change)
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 16th January 2025 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, and the event language will be in Thai, but some talks will be in English.
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
09:30 — 16:30 | Agenda (subject to change) | Speaker |
---|---|---|
09:30 — 10:00 | Registration | |
10:00 — 10:10 | Opening address | Michael Cheng, Oxford Nanopore Technologies |
10:10 — 10:40 | Genomics research and services in ministry of public health | Surakameth Mahasirimongkol, Department of Medical Sciences, Thailand |
10:40 — 11:10 | Oxford Nanopore sequencing: tools for identifying true pathogens | Orapan Sripichai, National Institute of Health, Thailand |
11:10 — 11:30 | Same-day PGT-A results | Pornwaratt Niyomrattanakit, Jetanin IVF |
11:30 - 12:00 | Oxford Nanopore technical update | Jerald Yam & Stephen Rudd, Oxford Nanopore Technologies |
12:00 — 13:30 | Lunch break & networking | |
13:30 - 14:40 | Rare Disease Expert Talks | |
What You’re Missing Matters: identifying rare diseases by acute care sequencing in New Zealand | Justin O'Sullivan, University of Auckland | |
Application of long-read sequencing in rare diseases | Ni-Chung Lee, National Taiwan University | |
Long-read sequencing in rare diseases | Vorasuk Shotelersuk, Chulalongkorn University | |
14:40 — 15:10 | Coffee break & networking | |
15:10 — 15:40 | Long-read sequencing in clinical research: bridging research and service | Thidathip Wongsurawat, Mahidol University |
15:40 — 16:10 | The potential of long-read sequencing in cancer: Insight from Genomics Thailand cohort | Manop Pithukpakorn, Mahidol University |
16:10 — 16:20 | Closing remarks | Daniel Raciti, Oxford Nanopore Technologies |
Speakers
Genomics research and services in ministry of public health
Surakameth Mahasirimongkol, Department of Medical Sciences, Thailand
Medical doctor, Bioinformatics, SDG3, Cybersecurity...
Oxford Nanopore sequencing: tools for identifying true pathogens
Orapan Sripichai, National Institute of Health, Thailand
Dr.Orapan Sripichai is the Head of the Bacterial Genomic Division and the Head of the Invasive Bacte...
Same-day PGT-A results
Pornwaratt Niyomrattanakit, Jetanin IVF
I'm a scientist with a passion for genomics, specializing in preimplantation genetic testing (PGT) a...
Oxford Nanopore technical update
Jerald Yam, Field Applications Team Lead, Oxford Nanopore Technologies
Jerald is the Field Applications Team Lead at Oxford Nanopore Technologies. In his current role, Jer...
Oxford Nanopore technical update
Stephen Rudd, Director, Bioinformatics Product, Oxford Nanopore Technologies
Stephen has been working with applied genome informatics for over 20 years and has experience in aca...
What You’re Missing Matters: identifying rare diseases by acute care sequencing in New Zealand
Justin O'Sullivan, The University of Aukland
Justin M. O’Sullivan PhD is a Professor and Director of the Liggins Institute at the University of A...
Application of long-read sequencing in rare diseases
Ni-Chung Lee, National Taiwan University Hospital
Dr. Ni-Chung Lee (Nina) is a Pediatrician and a specialist in clinical genetics. She is the Clinical...
Long-read sequencing in rare diseases
Vorasuk Shotelersuk, Chulalongkorn University
Professor Vorasuk Shotelersuk earned his MD from Chulalongkorn University in 1992 and completed pedi...
Long-read sequencing in clinical research: bridging research and service
Thidathip Wongsurawat, Mahidol University
Dr. Thidathip Wongsurawat (Tip) earned her PhD from Nanyang Technological University in Singapore. S...
The potential of long-read sequencing in cancer: Insight from Genomics Thailand cohort
Manop Pithukpakorn, Mahidol University
Dr. Manop Pithukpakorn is an internist, clinical and molecular geneticist. He is currently a Profess...