Webinar overview
Using nanopore technology you can sequence native DNA to accurately identify structural variants and methylation differences, and assemble genomes.
During this webinar, go from sample to answer with Philipp Rescheneder and Anthony Doran and learn about a truly scalable human genomic sequencing and analysis solution.
This webinar will cover:
- The technical fundamentals of implementing production-ready applications and bioinformatic analysis workflows that serve the needs of your research community.
- The level of accuracy nanopore sequencing offers for the detection of genomics variations to deliver comprehensive insights.
- The usage of pre-packed bioinformatic workflows to run data analysis and retrieve key genomic information.
- Examples used in research settings to investigate genetic disorders, cancer genomics, or population genetics.
This webinar will take place at 4pm (BST) or 11:00am EDT. Please register below to attend.
Meet the speakers
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Scalable human genomic characterisation with nanopore sequencing.
Philipp Rescheneder, Snr. Director, Applications Bioinformatics, Oxford Nanopore Technologies
Philipp Rescheneder and his teams identify, benchmark, and adapt the most appropriate tools and work...
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Bioinformatics from beginner to production: EPI2ME, Oxford Nanopore’s data analysis platform
Anthony Doran, Associate Director, Bioinformatics Field Applications, Oxford Nanopore Technologies
Anthony joined Oxford Nanopore Technologies in May 2019 having previously spent nearly 10 years work...
