Resource Centre
Workflow )
Workflow overview: single-cell transcriptomics
Workflow )
Workflow overview: direct RNA sequencing
Publication )
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
Poster )
Unlocking Nanopore sequencing for managing food safety in the food industry
Publication )
Transcriptome variation in human tissues revealed by long-read sequencing
Poster )
Transcriptome profiling of Korean colon cancer by cDNA PCR Nanopore sequencing
Poster )
Transcriptome analysis using long nanopore reads
Publication )
Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib
Publication The costimulatory domain influences CD19 CAR-T cell resistance development in B-cell malignancies
Publication )
TEQUILA-seq: a versatile and low-cost method for targeted long-read RNA sequencing
Publication )
Targeting sex determination to suppress mosquito populations
Publication )
Targeted long-read sequencing enriches disease-relevant genomic regions of interest to provide complete Mendelian disease diagnostics
Publication )
Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
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
Poster )
Successful training of laboratories in Asia and Africa to use nanopore sequencing for poliovirus surveillance
Poster )
Study of SPG11’s splicing, in neuronal and non-neuronal cells, by long-read sequencing: implication on phenotype
Publication )
Single-cell rapid capture hybridization sequencing (scRaCH-seq) to reliably detect isoform usage and coding mutations in targeted genes at a single-cell level
Publication )
Single-cell multiomics reveal the scale of multi-layered adaptations enabling CLL relapse during venetoclax therapy
Publication Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
