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
