Resource Centre
Workflow overview: single-cell transcriptomics
- Splice variation
 - Single cell
 - Transcriptome
 - PromethION 24/48
 - Cancer research
 - Clinical research
 
February 24 2025
Workflow overview: direct RNA sequencing
- Splice variation
 - Workflow
 - RNA
 - cDNA
 - Methylation
 - Epigenetics
 
September 8 2025
Widespread occurrence of hybrid internal-terminal exons in human transcriptomes
- Splice variation
 - Transcriptome
 - Long-read
 - RNA
 - cDNA
 - Isoforms
 
May 29 2021
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
- Splice variation
 - PromethION
 - Transcriptome
 - Neuroscience
 - Transcriptomics
 - Isoforms
 
August 7 2023
Transcriptomic reprogramming, alternative splicing and RNA methylation in potato (Solanum tuberosum L.) plants in response to potato virus Y infection
- Splice variation
 - Plant
 - Long-read
 - Methylation
 - Epigenetics
 - Transcriptome
 
February 25 2022
Transcriptome variation in human tissues revealed by long-read sequencing
- Splice variation
 - Transcriptome
 - RNA
 - cDNA
 - Human genomics
 - MinION
 
August 3 2022
Transcriptional neighborhoods regulate transcript isoform lengths and expression levels
- Splice variation
 - MinION
 - RNA
 - Gene expression
 - Long-read
 - Transcriptome
 
March 3 2022
TEQUILA-seq: a versatile and low-cost method for targeted long-read RNA sequencing
- Splice variation
 - MinION
 - GridION
 - Transcriptome
 - Oncology
 - Sequence capture
 
August 8 2023
Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
- Splice variation
 - Targeted
 - Human genomics
 - Clinical research
 - Long-read
 - Variant calling
 
February 25 2025
A systematic benchmark of nanopore long-read RNA sequencing for transcript-level analysis in human cell lines
- Splice variation
 - Long-read
 - Isoforms
 - Transcriptome
 - cDNA
 - RNA
 
March 13 2025
A systematic benchmark of Nanopore long read RNA sequencing for transcript analysis in human cell lines
- Splice variation
 - Isoforms
 - Transcriptome
 - Human genomics
 - Long-read
 - PromethION
 
April 22 2021
Study of SPG11’s splicing, in neuronal and non-neuronal cells, by long-read sequencing: implication on phenotype
- Splice variation
 - London Calling
 - Bioinformatics
 - Gene expression
 - Human genomics
 - Whole genome
 
May 19 2023
Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue
- Splice variation
 - Long-read
 - Isoforms
 - PromethION
 - RNA
 - cDNA
 
March 7 2022
Single-nuclei isoform RNA sequencing reveals combination patterns of transcript elements across human brain cell types
- Splice variation
 - Transcriptome
 - Human genomics
 - Isoforms
 - PromethION
 - RNA
 
December 30 2021
Single-molecule, full-length transcript isoform sequencing reveals disease mutation-associated RNA isoforms in cardiomyocytes
- Splice variation
 - cDNA
 - MinION
 - Transcriptome
 - Isoforms
 - Long-read
 
June 18 2021
Single-cell multiomics reveal the scale of multi-layered adaptations enabling CLL relapse during venetoclax therapy
- Splice variation
 - Single cell
 - Transcriptome
 - Cancer research
 - Human genomics
 - RNA
 
June 16 2022
Single-cell and spatial alternative splicing analysis with nanopore long-read sequencing
- Splice variation
 - Single cell
 - Long-read
 
July 19 2025
Selective ablation of 3’ RNA ends and processive RTs facilitate direct cDNA sequencing of full-length host cell and viral transcripts
- Splice variation
 - Long-read
 - RNA
 - cDNA
 - Microbiology
 - Clinical research
 
February 2 2022
RUNX1 isoform disequilibrium in the development of trisomy 21 associated myeloid leukemia
- Splice variation
 - RNA
 - cDNA
 - Human genomics
 - Transcriptome
 - Isoforms
 
March 8 2022
Pre-mRNA splicing order is predetermined and maintains splicing fidelity across multi-intronic transcripts
- Splice variation
 - RNA
 - cDNA
 
August 17 2022
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