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Pushing the boundaries of rare disease researchArticle

Pushing the boundaries of rare disease research

  • cDNA
  • Clinical research
  • Human genomics
  • Whole genome
  • Targeted
  • PromethION
  • MinION
  • Bioinformatics
  • Assembly
  • Structural variation
  • SNVs
  • Phasing
  • Amplicons
  • Variant calling
  • Splice variation
  • Transcriptome
  • RNA
June 6 2023
Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanismsArticle

Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms

  • cDNA
  • Cancer research
  • Clinical research
  • Human genomics
  • Single cell
  • Transcriptome
  • RNA
  • Gene fusions
  • Variant calling
  • Targeted
February 13 2024
Characterising alternative splicing in the human cortex with ultra-deep nanopore sequencingArticle

Characterising alternative splicing in the human cortex with ultra-deep nanopore sequencing

  • cDNA
  • Transcriptome
  • Transcriptomics
  • Methylation
  • Human genomics
  • RNA
  • Isoforms
  • Splice variation
  • Epigenetics
  • Clinical research
February 1 2024
London Calling 2024 opens with a day of masterclasses delivering everything you need to know for sample-to-answer nanopore sequencingArticle

London Calling 2024 opens with a day of masterclasses delivering everything you need to know for sample-to-answer nanopore sequencing

  • cDNA
  • 16S
  • Adaptive sampling
  • Amplicons
  • AMR
  • Assembly
  • Basecalling
  • Bacteria
  • Bioinformatics
  • Cancer research
  • Clinical research
  • DNA
  • Direct analysis
  • EPI2ME
  • Epigenetics
  • Extraction
  • Human genomics
  • Identification
  • Infectious disease
  • Kits
  • Masterclass
  • Library prep
  • London Calling
  • Methylation
  • Metagenomics
  • Microbiology
  • MinION
  • MinKNOW
  • P2
  • PromethION
  • RNA
  • Sample prep
  • Scalable
  • Single cell
  • Variant calling
  • Workflow
May 21 2024

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