Resource Centre
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
- Methylation
 - Bioinformatics
 - Epigenetics
 - RNA
 - Plant
 - Direct analysis
 
Workflow overview: tumour-normal sequencing
- Methylation
 - Workflow
 - Structural variation
 - SNVs
 - Epigenetics
 - Cancer research
 
Workflow overview: 24-hour human whole-genome sequencing
- Methylation
 - Human genomics
 - Clinical research
 - Whole genome
 - Structural variation
 - Epigenetics
 
Workflow overview: large cohort sequencing
- Methylation
 - Workflow
 - Human genomics
 - Clinical research
 - Population genomics
 - Whole genome
 
Workflow overview: human variant calling
- Methylation
 - Human genomics
 - Clinical research
 - Cancer research
 - PromethION 24/48
 - Whole genome
 
Workflow overview: direct RNA sequencing
- Methylation
 - Workflow
 - RNA
 - cDNA
 - Epigenetics
 - Human genomics
 
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
- Methylation
 - Whole genome
 - Human genomics
 - Epigenetics
 - DNA
 - gDNA
 
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
- Methylation
 - Clinical research
 - PromethION
 - gDNA
 - Whole genome
 - Variant calling
 
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
- Methylation
 - Cancer research
 - Clinical research
 - Human genomics
 - Phasing
 - Epigenetics
 
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
- Methylation
 - Cancer research
 - Neuroscience
 - cfDNA
 
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
- Methylation
 - Cancer research
 - Oncology
 - Long-read
 - DNA
 - GridION
 
Virtual Nanopore Day, Switzerland
- Methylation
 - Bioinformatics
 - Human genomics
 - Transcriptome
 - EPI2ME
 
Virtual Nanopore Day, Australia: Bioinformatics
- Methylation
 - Bioinformatics
 - Long-read
 - Assembly
 - PromethION
 - EPI2ME
 
Directly detect and phase genomic methylation with high reproducibility and low bias
- Methylation
 - Epigenetics
 
Using long-read sequencing to detect imprinted DNA methylation
- Methylation
 - MinION
 - PromethION
 - Epigenetics
 
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
- Methylation
 - Phasing
 - SNVs
 - Long-read
 - PromethION
 - Chromatin conformation
 
Uncovering hidden variation in rare and complex diseases webinar
- Methylation
 - Clinical research
 - Human genomics
 - Webinar
 - Whole genome
 - Epigenetics
 
Publication: Ultra-fast deep-learned CNS tumour classification during surgery
- Methylation
 - Cancer research
 - Epigenetics
 - Clinical research
 - Bioinformatics
 - Real-time
 
Transcriptomic reprogramming, alternative splicing and RNA methylation in potato (Solanum tuberosum L.) plants in response to potato virus Y infection
- Methylation
 - Plant
 - Long-read
 - Epigenetics
 - Splice variation
 - Transcriptome
 
Transcriptional activity and epigenetic regulation of transposable element in the symbiotic fungus Rhizophagus irregularis
- Methylation
 - Whole genome
 - Epigenetics
 - Long-read
 - Fungi
 - gDNA
 
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