Core webinar: Scalable human genomic characterisation with nanopore sequencing
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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.
Register
Meet the speakers
This webinar will introduce Nanopore’s latest end-to-end workflows for assembly and variant calling with a focus on human genomics.
This webinar will introduce Nanopore’s latest end-to-end workflows for assembly and variant calling with a focus on human genomics.
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Philipp Rescheneder, Snr. Director, Applications Bioinformatics, Oxford Nanopore TechnologiesIn this presentation, Anthony will introduce bioinformatics fundamentals relating to Oxford Nanopore data and speak in detail about the EPI2ME platform, Oxford Nanopore’s bioinformatics analysis platform.
In this presentation, Anthony will introduce bioinformatics fundamentals relating to Oxford Nanopore data and speak in detail about the EPI2ME platform, Oxford Nanopore’s bioinformatics analysis platform.
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Anthony Doran, Associate Director, Bioinformatics Field Applications, Oxford Nanopore Technologies
