Unlocking disease mechanisms with multiomic nanopore sequencing


Webinar Overview

In this Knowledge Exchange, our expert speakers explore the multifaceted applications of multiomic nanopore sequencing in disease research, with best-practice introductions to Oxford Nanopore sequencing workflows and real-world case studies.

Viewers will learn:

  • How multiomic nanopore sequencing approaches — such as integrating genomics, transcriptomics, chromatin conformation capture, genomic variant, and methylation data — can enhance research into mechanisms of disease.

  • How whole-genome and single-cell transcriptome nanopore sequencing can be leveraged for novel antibody discovery and understanding immune response dynamics.

  • How multiomic nanopore sequencing enables exploration of the relationship between 3D chromatin structure, cohesin complexes, and gene regulation in normal and malignant haematopoiesis.

Authors: Sayonika Mohanta (Market Segment Manager - Methylation), Scott Hickey (Director - Genomic Applications), Art Rand (Research Scientist - Machine Learning)