Blog
5 results
Science unlocked: publication picks from September 2024
- Adaptive sampling
- AMR
- Bacteria
- Cancer research
- cDNA
- Clinical research
- Epigenetics
- Human genomics
- Infectious disease
- Methylation
- Microbiology
- MinION
- Oncology
- Phasing
- Real-time
- rRNA
- Long-read
- Single cell
- SNVs
- Structural variation
- Targeted
- Variant calling
- Whole genome
October 2 2024
Pushing the boundaries of rare disease research
- Clinical research
- Human genomics
- Whole genome
- Targeted
- PromethION
- MinION
- Bioinformatics
- Assembly
- Structural variation
- SNVs
- Phasing
- Amplicons
- Variant calling
- Splice variation
- Transcriptome
- cDNA
- RNA
June 6 2023
Multiomic single-cell cancer analysis — from mutation detection to understanding disease mechanisms
- Cancer research
- Clinical research
- Human genomics
- Single cell
- Transcriptome
- cDNA
- RNA
- Gene fusions
- Variant calling
- Targeted
February 13 2024
Characterising alternative splicing in the human cortex with ultra-deep nanopore sequencing
- Transcriptome
- Transcriptomics
- Methylation
- Human genomics
- RNA
- cDNA
- 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 sequencing
- 16S
- Adaptive sampling
- Amplicons
- AMR
- Assembly
- Basecalling
- Bacteria
- Bioinformatics
- Cancer research
- cDNA
- 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