Resource Centre
354 results
Workflow: single-cell transcriptomics
- Single cell
- Transcriptome
- PromethION
- Cancer research
- Clinical research
- cDNA
- Workflow
- Human genomics
- Splice variation
- Gene fusions
- Gene expression
- Kits
February 20 2024
Workflow: direct RNA sequencing
- Workflow
- RNA
- cDNA
- Methylation
- Epigenetics
- Human genomics
- Clinical research
- Isoforms
- Splice variation
- Transcriptome
February 26 2024
Widespread occurrence of hybrid internal-terminal exons in human transcriptomes
- Transcriptome
- Long-read
- RNA
- cDNA
- Isoforms
- Splice variation
- Clinical research
- Direct analysis
May 29 2021
Webinar: Rapid leukemia classification using nanopore sequencing
- Cancer research
- Transcriptome
October 7 2022
Wastewater sequencing — an early warning system for infectious disease outbreaks
- Bioinformatics
- Microbiology
- Microbiome
- Environment
- Plant
- Animal
- Human genomics
- Clinical research
- Cancer research
- Population genomics
- Transcriptome
- Infectious disease
November 10 2022
In Vivo Validation of Alternative FDXR Transcripts in Human Blood in Response to Ionizing Radiation
- Human genomics
- Transcriptome
- Isoforms
- Gene expression
- Long-read
- RNA
- cDNA
- PromethION
November 13 2020
Virtual Nanopore Day, Switzerland
- Bioinformatics
- Human genomics
- Transcriptome
- Methylation
- EPI2ME
November 25 2020
Virtual Nanopore Day, Singapore
- Bioinformatics
- RNA
- Environment
- Transcriptome
- Microbiology
- Food safety
January 27 2021
Virtual Nanopore Day, Michigan
- Transcriptome
- RNA
- cDNA
- Infectious disease
- High-throughput
- Targeted
- Plant
- Assembly
October 26 2021
Varicella-zoster virus VLT-ORF63 fusion transcript induces broad viral gene expression during reactivation from neuronal latency
- Microbiology
- Virus
- Gene expression
- cDNA
- RNA
- Transcriptome
- Infectious disease
December 10 2020
Using SPAdes de novo assembler
- Assembly
- Bioinformatics
- Bacteria
- Metagenomics
- Transcriptome
- Microbiology
June 19 2020
Using nanopore RNA-Seq to HLA genotype and correlate donor HLA expression with flow cytometric crossmatch results
- Clinical research
- Human genomics
- Immunology
- RNA
- cDNA
- Gene expression
- Transcriptome
- Isoforms
- MinION
October 24 2019
Using full-length transcript sequencing to reveal the fate of mRNA in aging seeds
- London Calling
- Transcriptome
- RNA
- cDNA
- Plant
February 25 2019
Using direct RNA nanopore sequencing to deconvolute viral transcriptomes
- Microbiology
- Virus
- Protocols
- Direct analysis
- RNA
- cDNA
- Transcriptome
- Gene expression
April 7 2020
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
- RNA
August 7 2023
Uncovering RNA splicing’s cell-specific impact on clonal blood disorders with GoT-Splice
- Human genomics
- Single cell
- Transcriptome
April 8 2024
Uncovering the full-length extracellular transcriptome in human blood plasma using long-read cDNA sequencing
- Cancer research
- Gene expression
- Transcriptome
May 28 2022
Case study: ultra-rich nanopore data offers unprecedented insights into the transcriptomes of single cells
- Single cell
- RNA
- cDNA
- Human genomics
- Clinical research
- Transcriptome
- Cancer research
January 17 2024
Two-pass alignment using machine-learning-filtered splice junctions increases the accuracy of intron detection in long-read RNA sequencing
- Bioinformatics
- Long-read
- Isoforms
- Transcriptome
- RNA
May 29 2020