Resource Centre
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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
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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
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Workflow overview: single-cell transcriptomics
- Splice variation
- Single cell
- Transcriptome
- PromethION 24/48
- Cancer research
- Clinical research
February 24 2025
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Brochure: multiomic sequencing
- Splice variation
- Human genomics
- Clinical research
- DNA
- gDNA
- cDNA
February 24 2025
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MrHAMER2: high-accuracy long-read RNA sequencing to decode isoform-specific variation in viral transcripts during latency
- Splice variation
- Virus
- Long-read
- Isoforms
- RNA
- SNVs
December 22 2024
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Getting started guide: bulk transcriptomics
- Splice variation
- RNA
- cDNA
- Transcriptome
- Transcriptomics
- Fusion transcript
December 9 2024
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Genetic regulation of nascent RNA maturation revealed by direct RNA nanopore sequencing
- Splice variation
- Human genomics
- RNA
- mRNA
- MinION
- MinKNOW
August 29 2024
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Applications of nanopore sequencing in precision cancer medicine
- Splice variation
- Cancer research
- Human genomics
- SNVs
- Methylation
- RNA
July 19 2024
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London Calling 2024 technology update
- Splice variation
- Adaptive sampling
- Assembly
- Automation
- Basecalling
- Bioinformatics
May 24 2024
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Case study: mapping RNA modifications in the human brain with full-length transcript sequencing
- Splice variation
- RNA
- cDNA
- Human genomics
- Transcriptome
- Epigenetics
March 4 2024
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Workflow overview: direct RNA sequencing
- Splice variation
- Workflow
- RNA
- cDNA
- Methylation
- Epigenetics
February 26 2024
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Case study: powered by long nanopore reads, liver transcriptome analysis reveals new clues about cancer
- Splice variation
- Cancer research
- Transcriptome
- Isoforms
- cDNA
- RNA
February 21 2024
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NCM 2023 Houston: Unraveling complex Mendelian diseases with nanopore sequencing
- Splice variation
- Bioinformatics
- Clinical research
- Human genomics
- SNVs
- Structural variation
December 6 2023
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NCM 2023 Houston: Haplotypes, isoforms, and fusions: towards a richer cancer transcriptome
- Splice variation
- Bioinformatics
- Cancer research
- Human genomics
- Phasing
- SNVs
December 6 2023
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NCM 2023 Houston: GoT-Splice: unraveling cell-type-specific impact of splicing factor mutations
- Splice variation
- Bioinformatics
- Cancer research
- Human genomics
- Single cell
- Transcriptome
December 6 2023
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NCM 2023 Houston: Complex phased variants in inherited retinal diseases with long-read sequencing
- Splice variation
- Bioinformatics
- Clinical research
- Human genomics
- Phasing
- SNVs
December 6 2023
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Benchmarking long-read RNA-sequencing analysis tools using in silico mixtures
- Splice variation
- RNA
- cDNA
- Bioinformatics
- Cancer research
- Isoforms
October 2 2023
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NCM 2023 Singapore: Exploring post-transcriptional modifications during myrtle rust pathogen-plant interactions
- Splice variation
- Bioinformatics
- Plant
- Transcriptome
- Nanopore Community Meeting
- MinION
September 27 2023
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NCM 2023 Singapore: Direct detection of DNA modifications in human cancer genomes
- Splice variation
- Bioinformatics
- Cancer research
- Chromatin conformation
- Epigenetics
- Gene expression
September 27 2023
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Coordination of alternative splicing and alternative polyadenylation revealed by targeted long read sequencing
- Splice variation
- Transcriptome
- MinION
September 7 2023