Oxford Nanopore ASHG CoLab


This CoLab session provides an in-depth look at nanopore sequencing — from sample preparation to sequencing and data analysis. Experts form the Oxford Nanopore team will run through demonstrations to provide a full picture of the sequencing experience with nanopore devices.

Using nanopore technology you can fully characterise human genetic variation, sequence whole genomes, targeted regions or full-length RNA transcripts. Long nanopore reads enable comprehensive analysis of structural variation, repetitive regions, haplotype phasing, RNA splice variants, isoforms, fusion transcripts and base modifications.

On Friday 30th October at 12:00 pm (EDT), there will be a live Q&A session with our CoLab team, you can register to attend here (attendees must be registered delegates of the ASHG conference).

Don't worry if you cannot make the Q&A session, our team will be on hand all week to answer any questions you may have, just head on over to the Oxford Nanopore Technologies booth on the ASHG conference platform.

Authors: Oxford Nanopore Technologies