Resource Centre
Bioinformatics tool )
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Workflow )
Workflow overview: large cohort sequencing
Workflow )
Workflow overview: human variant calling
Workflow )
Workflow overview: direct RNA sequencing
Publication )
Whole human genome 5'-mC methylation analysis using long read nanopore sequencing
Poster )
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
Video )
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
Video )
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video )
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
Publication )
In vivo genetic screen identifies a SLC5A3-dependent myo-inositol auxotrophy in acute myeloid leukemia
Events )
Virtual Nanopore Day, Switzerland
Video )
Virtual Nanopore Day, Australia: Bioinformatics
Knowledge exchange )
Directly detect and phase genomic methylation with high reproducibility and low bias
Publication )
Using long-read sequencing to detect imprinted DNA methylation
Poster )
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
Webinar )
Uncovering hidden variation in rare and complex diseases webinar
Publication )
Publication: Ultra-fast deep-learned CNS tumour classification during surgery
Publication )
Transcriptomic reprogramming, alternative splicing and RNA methylation in potato (Solanum tuberosum L.) plants in response to potato virus Y infection
