Resource Centre
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
- Epigenetics
- Bioinformatics
- Methylation
- RNA
- Plant
- Direct analysis
Workflow overview: tumour-normal sequencing
- Epigenetics
- Workflow
- Structural variation
- SNVs
- Methylation
- Cancer research
Workflow overview: plant genome assembly
- Epigenetics
- Assembly
- DNA
- Kits
- Library prep
- Long-read
Workflow overview: human variant calling
- Epigenetics
- Human genomics
- Clinical research
- Cancer research
- PromethION 24/48
- Whole genome
Workflow overview: direct RNA sequencing
- Epigenetics
- Workflow
- RNA
- cDNA
- Methylation
- Human genomics
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
- Epigenetics
- Whole genome
- Human genomics
- Methylation
- DNA
- gDNA
Whole-genome insights: nanopore sequencing in neuropathology
- Epigenetics
- Epigenetics
- PromethION 2
- PromethION 24/48
- EPI2ME
- Fusion transcript
Resolving complex genomic structures and regulation patterns in cervical cancer
- Epigenetics
- Cancer research
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Epigenetics
- Cancer research
- Clinical research
- Human genomics
- Phasing
- Methylation
Investigating epigenomic alterations in cancer with nanopore sequencing
- Epigenetics
- Cancer research
"...we need a better name than follow through"
- Epigenetics
- Whole genome
- Targeted
- Metagenomics
- RNA
- cDNA
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
- Epigenetics
- Cancer research
- Oncology
- Long-read
- DNA
- GridION
Directly detect and phase genomic methylation with high reproducibility and low bias
- Epigenetics
- Methylation
Using Oxford Nanopore sequencing in grapevine breeding
- Epigenetics
- London Calling
- Plant
- Bioinformatics
- Phasing
- MinION
Using long-read sequencing to detect imprinted DNA methylation
- Epigenetics
- MinION
- PromethION
- Methylation
Untangling heterogeneity in DNA replication with nanopore sequencing
- Epigenetics
- London Calling
- Raw data
- Basecalling
- Whole genome
- Single cell
Understanding the binding of multiple transcription factors by base-pair-resolution chromatin accessibility
- Epigenetics
- Clinical research
- Bioinformatics
- Human genomics
- MinION
- Chromatin conformation
Uncovering hidden variation in rare and complex diseases webinar
- Epigenetics
- Clinical research
- Human genomics
- Webinar
- Whole genome
- Methylation