Presented By:
Anton van den Ouden
Speaker Biography:
Anton van den Ouden is a NextGenPCR Field Application Specialist at Molecular Biology Systems, based in the Netherlands. Anton studied Biology and Medical Laboratory Research at the Avans University of Applied Science and is specialized in molecular biology. Currently doing his MscBA with a specialization in health strategy and innovation at the TIAS University for Business and Society, Utrecht, Netherlands. In the past years, Anton traveled around the world and collaborated with top academic hospitals and institutes to develop new and ultra-fast surveillance methods that generate real-time surveillance data which can be used to accelerate public health interventions.
Webinar:
Accelerating Monkeypox and SARS-CoV-2 Virus Whole Genome Sequencing Using Combination of NextGenPCR and Oxford Nanopore…..Towards Real-Time Genomic Surveillance
Webinar Abstract:
Rapid genomic surveillance of pathogens can provide valuable insights, in order to guide public health interventions. Novel workflows using nanopore technology enables for real-time sequencing of clinical samples. However, current library preparation workflows are limited and can take up to 5 hours whereby PCR takes around 3,5 hours.
By using NextGenPCR technology it is possible to decrease the PCR library preparation to 27 minutes for the SARS-CoV-2 Midnight protocol from Nikkie Freed et al. While optimizing this SARS-CoV-2 PCR tiling, the world faced a monkeypox pandemic. At the beginning of the pandemic, public health institutes were limited to metagenomics approaches. Using this method, the coverage depth becomes the limiting factor that prevents to multiplex multiple samples on a single flowcell, making sequencing very costly.
A collaboration between AmsterdamUMC (Netherlands), Rigshospitalet Copenhagen (Denmark), and Molecular Biology Systems (Netherlands) resulted in a successful optimalisation and validation of an amplicon-based sequencing approach, inspired by SARS-CoV-2 Midnight protocol and the ARTIC network. This allows labs to increase depth of coverage and multiplex up to 20 samples per flowcell.
Using this fast developed sequencing workflow, we were able to get fast insights of the spread of monkeypox in the region of Amsterdam, which resulted in a publication in Eurosurveillance about the first pediatric case in the Netherlands.
Earn PACE Credits:
1. Make sure you’re a registered member of Labroots (https://www.labroots.com/webinar/accelerating-monkeypox-sars-cov-2-virus-genome-sequencing-using-combination-nextgenpcr-oxford-nanopo)
2. Watch the webinar on the Labroots Website (https://www.labroots.com/webinar/accelerating-monkeypox-sars-cov-2-virus-genome-sequencing-using-combination-nextgenpcr-oxford-nanopo)
3. Click Here to get your PACE credits (Expiration date – NOV 09, 2024): https://www.labroots.com/credit/pace-credits/7754
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