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Workflow Workflow overview: single-cell transcriptomics
Workflow Workflow overview: direct RNA sequencing
Publication )
Widespread occurrence of hybrid internal-terminal exons in human transcriptomes
Publication )
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
Publication )
Transcriptomic reprogramming, alternative splicing and RNA methylation in potato (Solanum tuberosum L.) plants in response to potato virus Y infection
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Transcriptome variation in human tissues revealed by long-read sequencing
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Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib
Publication )
Transcriptional neighborhoods regulate transcript isoform lengths and expression levels
Publication )
TEQUILA-seq: a versatile and low-cost method for targeted long-read RNA sequencing
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Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
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A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
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A systematic benchmark of Nanopore long read RNA sequencing for transcript analysis in human cell lines
Poster )
Study of SPG11’s splicing, in neuronal and non-neuronal cells, by long-read sequencing: implication on phenotype
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Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue
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Single-nuclei isoform RNA sequencing reveals combination patterns of transcript elements across human brain cell types
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Single-molecule, full-length transcript isoform sequencing reveals disease mutation-associated RNA isoforms in cardiomyocytes
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Single-cell multiomics reveal the scale of multi-layered adaptations enabling CLL relapse during venetoclax therapy
Publication )
Single-cell and spatial alternative splicing analysis with nanopore long-read sequencing
Publication )
Selective ablation of 3’ RNA ends and processive RTs facilitate direct cDNA sequencing of full-length host cell and viral transcripts
Publication )
RUNX1 isoform disequilibrium in the development of trisomy 21 associated myeloid leukemia