Resource Centre
Publication )
DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage
Workflow )
Workflow overview: direct RNA sequencing
Publication )
Isoform-level profiling of m6A epitranscriptomic signatures in human brain
Case study )
Case study: unravelling tumour biology with single-cell Oxford Nanopore sequencing
White paper )
White paper: RNA and cDNA sequencing
Getting started guide )
Getting started guide: bulk transcriptomics
Workflow )
Workflow overview: bulk transcriptomics
Publication )
Combining panel-based and whole-transcriptome-based gene fusion detection by long-read sequencing
Publication )
A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
Workflow )
Workflow overview: single-cell transcriptomics
Getting started guide )
Getting started guide: single-cell transcriptomics
Brochure )
Brochure: multiomic sequencing
Webinar Exploring how alternative splicing and gene isoforms influence disease
Case study )
Case study: revealing hidden biology with isoform-level single-cell transcriptomics
Case study )
Case study: full-length RNA isoforms deliver new insights into human health and disease
Case study )
Case study: delivering ‘unique insights’ into infection with direct RNA sequencing
Publication Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing
Publication )
Exploring the transcriptomic profile of human monkeypox virus via CAGE and native RNA sequencing approaches
Publication )
Nanopore direct RNA sequencing reveals virus-induced changes in the transcriptional landscape in human bronchial epithelial cells
Case study )
Case study: the potential of nanopore cell-free RNA sequencing for earlier cancer detection
