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Fast answers and the most complete view: 24-hour whole-genome sequencing with Oxford Nanopore

This webinar introduces the new 24-hour human whole-genome sequencing workflow — a fast, comprehensive solution for clinical research in neonatal intensive care units (NICUs).

Watch the video to learn:

  • How the Oxford Nanopore 24-hour genome workflow enables you to go from sample to answer in 24 hours, and offers the most complete view of the genome available today

  • How to prepare blood research samples and rapidly sequence them with a PromethION device

  • How to analyse your data using the EPI2ME human variation workflow, wf-human-variation, and prepare your dataset for tertiary analysis

  • Where to find relevant resources for this workflow online

Authors: Jawahar Swaminathan (Director of Informatics, Oxford Nanopore Technologies), Cora Vacher (Associate Director, Segment Marketing — Human Genetics, Oxford Nanopore Technologies), Mark Drost (Laboratory Specialist, Erasmus MC)

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