Resource Centre
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
- cDNA
- Human genomics
- Clinical research
- Assembly
- Multiomics
Workflow overview: direct RNA sequencing
- cDNA
- Workflow
- RNA
- Methylation
- Epigenetics
- Human genomics
Case study: unravelling tumour biology with single-cell Oxford Nanopore sequencing
- cDNA
- Cancer research
- Epigenetics
- Gene expression
- Methylation
- Transcriptomics
Getting started guide: bulk transcriptomics
- cDNA
- RNA
- Transcriptome
- Transcriptomics
- Fusion transcript
- Cancer research
Workflow overview: bulk transcriptomics
- cDNA
- Exome
- Transcriptome
- Transcriptomics
- Cancer research
Spatial isoform sequencing at sub-micrometer single-cell resolution reveals novel patterns of spatial isoform variability in brain cell types
- cDNA
- Single cell
- Transcriptomics
Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
- cDNA
- London Calling
- RNA
- Transcriptomics
A compendium of human RNA structures and modifications
- cDNA
- cDNA
- RNA
- Epigenetics
- Gene expression
- Bioinformatics
Case study: accurate identification of cancer-predisposing deep intronic variants in tumour-suppressor genes with Oxford Nanopore sequencing
- cDNA
- Cancer research
- Oncology
- Adaptive sampling
- DNA
A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
- cDNA
- Long-read
- Isoforms
- Splice variation
- Transcriptome
- RNA
Workflow overview: single-cell transcriptomics
- cDNA
- Single cell
- Transcriptome
- PromethION 24/48
- Cancer research
- Clinical research
Getting started guide: single-cell transcriptomics
- cDNA
- Single cell
- RNA
- Fusion transcript
- Transcriptome
- Transcriptomics
Case study: full-length RNA isoforms deliver new insights into human health and disease
- cDNA
- RNA
- mRNA
- Transcriptome
- Transcriptomics
- Neuroscience
Long-read RNA sequencing of archival tissues reveals novel genes and transcripts associated with clear cell renal cell carcinoma recurrence and immune
- cDNA
- RNA
- Cancer research
- PromethION
- Guppy
Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumour-suppressor genes
- cDNA
- Cancer research
- Targeted
- DNA
- PromethION
Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencing
- cDNA
- Single cell
- Transcriptome
- Transcriptomics
- Workflow
- Scalable
Discovery of NRG1-VII: the myeloid-derived class of NRG1
- cDNA
- Human genomics
- Transcriptomics
- Targeted
- GridION
Case study: the potential of nanopore cell-free RNA sequencing for earlier cancer detection
- cDNA
- Clinical research
- Human genomics
- RNA
- Transcriptome
- Cancer research
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