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.
