Resource Centre
Poster )
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
Workflow )
Workflow overview: direct RNA sequencing
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 )
Spatial isoform sequencing at sub-micrometer single-cell resolution reveals novel patterns of spatial isoform variability in brain cell types
Poster )
Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
Video )
A compendium of human RNA structures and modifications
Case study )
Case study: accurate identification of cancer-predisposing deep intronic variants in tumour-suppressor genes with Oxford Nanopore 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
Case study )
Case study: full-length RNA isoforms deliver new insights into human health and disease
Publication )
Long-read RNA sequencing of archival tissues reveals novel genes and transcripts associated with clear cell renal cell carcinoma recurrence and immune
Publication )
Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumour-suppressor genes
Publication )
Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing
Publication )
Discovery of NRG1-VII: the myeloid-derived class of NRG1
Case study )
Case study: the potential of nanopore cell-free RNA sequencing for earlier cancer detection
