Resource Centre
Publication )
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
Publication )
Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomics
Workflow )
Workflow overview: direct RNA sequencing
Publication )
A single-cell, long-read, isoform-resolved case-control study of FTD reveals cell-type-specific and broad splicing dysregulation in human brain
Getting started guide )
Getting started guide: bulk transcriptomics
Publication )
Systematic characterisation of full-length RNA isoforms in human colorectal cancer at single-cell resolution
Publication )
A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
Getting started guide )
Getting started guide: single-cell transcriptomics
Brochure )
Brochure: multiomic sequencing
Publication )
MrHAMER2: high-accuracy long-read RNA sequencing to decode isoform-specific variation in viral transcripts during latency
Publication Exploring how alternative splicing and gene isoforms influence disease
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
Case study )
Case study: the potential of nanopore cell-free RNA sequencing for earlier cancer detection
Video )
Quality control of gene therapy vectors using nanopore direct RNA sequencing
Video )
Long-read transcriptomics shows synaptic adaptation to amyloid pathology in Alzheimer’s
Video )
Long-read CaptureSeq identifies novel RNA isoforms of psychiatric risk genes
Video )
London Calling 2024 technology update
Video )
Isopod: detecting differential isoform usage from long-read single-cell data
Video )
Igniting single-cell analysis of full-length RNA isoforms in brain development
